Scientific name	Authority	First published in
Kadsura chinensis	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 7: 149 (1837)
Maximowiczia japonica	K.Koch	Dendrologie 1: 386 (1869)
Maximowiczia chinensis	Rupr.	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 31 (1859)
Maximowiczia amurensis	Rupr.	Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 124 (1856)
Schisandra viridicarpa	Y.N.Lee	Fl. Korea ed. 4: 1150. 2002 (2002)
Schisandra chinensis var. leucocarpa	P.H.Huang & L.H.Zhuo	Bull. Bot. Res., Harbin 14(1): 35 (1994)
Sphaerostema japonicum	A.Gray	Mem. Amer. Acad. Arts , n.s., 6: 380 (1859)
Maximowiczia sinensis	Rob.	Garden (London, 1871-1927) 6: 583. 1874 (1874)
Schisandra chinensis var. glabrata	Nakai ex T.Mori	Enum. Pl. Corea 166. 1922

Common names Top

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Filter by language:

Language	Common/alternative name
English	magnolia berry
English	magnolia-vine
Spanish	omija
Arabic	شزندرة صينية
Azerbaijani	Çin cır limonu
Azerbaijani	kadzura sinensis
Azerbaijani	Çin şizandrası
Azerbaijani	Çin cır limon
Belarusian	лімоннік кітайскі
Bulgarian	китайска шизандра
Czech	klanopraška čínská
Czech	schizandra čínská
German	chinesisches spaltkörbchen
German	vitalbeere
German	wu wei zi
Estonian	hiina sidrunväändik
Finnish	sitruunaköynnös
Finnish	palsamiköynnös
Hebrew	שכיזנדרה סינית
Croatian	Šisandra
Hungarian	kínai kúszómagnólia
Armenian	շիզանդրա չինական
Indonesian	omija
Japanese	五味子
Japanese	ゴミシ
Japanese	チョウセンゴミシ
Korean	오미자나무
Korean	오미자
Lithuanian	kininė šizandra
Lithuanian	kininis citrinvytis
Latvian	citronliāna
lzh	五味子
Polish	cytryniec chiński
Russian	китайский лимонник
Russian	лимонник китайский
Slovenian	Šisandra
Ukrainian	лимонник китайський
Vietnamese	ngũ vị tử bắc
Chinese	二色内风消
Chinese	五味子
Chinese	五味子（北五味子）
Chinese	五香血藤
Chinese	北五味子
Chinese	北五味

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
  - Sakhalin

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000495099
UNII	RM13YIU944
Tropicos	19300157
KEW	urn:lsid:ipni.org:names:60456331-2
The Plant List	kew-2585428
Plantarium	34197
PaleoBotany	98938
Open Tree Of Life	639706
Observations.org	121949
NCBI Taxonomy	50507
IPNI	60456331-2
iNaturalist	431608
iNaturalist	431610
GBIF	7335132
Freebase	/m/092j21
EPPO	SHSCH
EOL	5348382
Elurikkus	209951
US Library of Congress	sh88023094
USDA GRIN	70678
Wikipedia	Schisandra_chinensis
CMAUP	NPO8187

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Safety and efficacy of a feed additive consisting of a tincture derived from the dried fruit of Schisandra chinensis (Turcz.) Baill. (omicha tincture) for poultry, horses, dogs and cats (FEFANA asbl)

Bampidis V, Azimonti G, Bastos MD, Christensen H, Durjava M, Kouba M, López‐Alonso M, Puente SL, Marcon F, Mayo B, Pechová A, Petkova M, Ramos F, Villa RE, Woutersen R, Brantom P, Chesson A, Schlatter J, Westendorf J, Dirven Y, Manini P, Dusemund B

EFSA J

10-Apr-2024

PMCID:	PMC11004902
doi:	10.2903/j.efsa.2024.8731
PMID:	38601870

Genome-wide identification of tea plant (Camellia sinensis) BAHD acyltransferases reveals their role in response to herbivorous pests

Qiao D, Yang C, Mi X, Tang M, Liang S, Chen Z

BMC Plant Biol

01-Apr-2024

PMCID:	PMC10985903
doi:	10.1186/s12870-024-04867-2
PMID:	38561653

Gut microbes combined with metabolomics reveal the protective effects of Qijia Rougan decoction against CCl4-induced hepatic fibrosis

Li X, Xu X, Tao S, Su Y, Wen L, Wang D, Liu J, Feng Q

Front Pharmacol

28-Mar-2024

PMCID:	PMC11007057
doi:	10.3389/fphar.2024.1347120
PMID:	38606180

A review of chemotherapeutic drugs-induced arrhythmia and potential intervention with traditional Chinese medicines

Li W, Cheng X, Zhu G, Hu Y, Wang Y, Niu Y, Li H, Aierken A, Li J, Feng L, Liu G

Front Pharmacol

20-Mar-2024

PMCID:	PMC10987752
doi:	10.3389/fphar.2024.1340855
PMID:	38572424

Inhibitory effect of benzocaine from Schisandra chinensis on Alternaria alternata

Long LF, Zhao QF, Zhang FL, Tang R, Wei JB, Guan S, Chen Y

Sci Rep

20-Mar-2024

PMCID:	PMC10954763
doi:	10.1038/s41598-024-57237-1
PMID:	38509170

Dibenzocyclooctadiene Lignans from Schisandra chinensis with Anti-Inflammatory Effects

Rybnikář M, Malaník M, Šmejkal K, Švajdlenka E, Shpet P, Babica P, Dall’Acqua S, Smištík O, Jurček O, Treml J

Int J Mol Sci

19-Mar-2024

PMCID:	PMC10971102
doi:	10.3390/ijms25063465
PMID:	38542438

Traditional Tibetan medicine: therapeutic potential in lung diseases

Li C, Li Y, Huang X, Li S, Sangji K, Gu R

Front Pharmacol

18-Mar-2024

PMCID:	PMC10986185
doi:	10.3389/fphar.2024.1365911
PMID:	38567353

The combination of Schisandrin C and Luteolin synergistically attenuates hepatitis B virus infection via repressing HBV replication and promoting cGAS-STING pathway activation in macrophages

Wu Z, Zhao X, Li R, Wen X, Xiu Y, Long M, Li J, Huang X, Wen J, Dong X, Xu Y, Bai Z, Zhan X, Xiao X

Chin Med

18-Mar-2024

PMCID:	PMC10946137
doi:	10.1186/s13020-024-00888-z
PMID:	38500179

Adulteration of Brain Health (Cognitive, Mood, and Sleep Enhancement) Food Supplements by the Addition of Pharmaceutical Drugs: A Comprehensive Review of Analytical Approaches and Trends

Paiva R, Correia M, Delerue-Matos C, Amaral JS

Foods

16-Mar-2024

PMCID:	PMC10969376
doi:	10.3390/foods13060908
PMID:	38540898

Gut microbiota and its metabolites in Alzheimer’s disease: from pathogenesis to treatment

Zou X, Zou G, Zou X, Wang K, Chen Z

PeerJ

13-Mar-2024

PMCID:	PMC10944166
doi:	10.7717/peerj.17061
PMID:	38495755

Influence of Different Plant Extracts on CYP-Mediated Skatole and Indole Degradation in Pigs

Marro P, Wesoly R, Stefanski V

Animals (Basel)

13-Mar-2024

PMCID:	PMC10967365
doi:	10.3390/ani14060888
PMID:	38539986

Establishment of a pharmacokinetics and pharmacodynamics model of Schisandra lignans against hippocampal neurotransmitters in AD rats based on microdi-alysis liquid chromatography-mass spectrometry

Zhang J, Cui X, Zhao S, Chang Z, Zhang J, Chen Y, Liu J, Sun G, Wang Y, Liu Y

Front Pharmacol

11-Mar-2024

PMCID:	PMC10961592
doi:	10.3389/fphar.2024.1342121
PMID:	38529184

Mechanism of Bazi Bushen capsule in delaying the senescence of mesenchymal stem cells based on network pharmacology and experimental validation

Zhang Y, Wang T, Song Y, Chen M, Hou B, Yao B, Ma K, Song Y, Wang S, Zhang D, Liang J, Wei C

Heliyon

09-Mar-2024

PMCID:	PMC10950659
doi:	10.1016/j.heliyon.2024.e27646
PMID:	38509951

Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy

Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J

Heliyon

06-Mar-2024

PMCID:	PMC10945194
doi:	10.1016/j.heliyon.2024.e27530
PMID:	38501018

Terpenoids derived from Semen Ziziphi Spinosae oil enhance sleep by modulating neurotransmitter signaling in mice

Sun M, Li M, Cui X, Yan L, Pei Y, Wang C, Guan C, Zhang X

Heliyon

01-Mar-2024

PMCID:	PMC10923681
doi:	10.1016/j.heliyon.2024.e26979
PMID:	38463787

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
Cliviasine	558132	Click to see CN1CCC2C1C3C(C(C2)O)OC(=O)C4=CC5=C(C=C34)OCO5	317.34	unknown	https://doi.org/10.1002/JSSC.200800341
Clivonine	12303690	Click to see CN1CCC2C1C3C(C(C2)O)OC(=O)C4=CC5=C(C=C34)OCO5	317.34	unknown	via CMAUP database
> Alkaloids and derivatives / Cephalotaxus alkaloids
1-O-[(2S)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl] 4-O-methyl (2S)-2-hydroxy-2-(3-methylbutyl)butanedioate	56840949	Click to see CC(C)CCC(CC(=O)OC)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O	515.60	unknown	via CMAUP database
> Allenes / Acyclic allenes
3,4-Octadiene, 7-methyl-	142131	Click to see CCC=C=CCC(C)C	124.22	unknown	via CMAUP database
> Benzenoids
Tricyclo[10.4.0.02,7]hexadeca-1,3,5,7,9,11,13,15-octaene	54004248	Click to see C1=CC=C2C=CC=CC2=C3C=CC=CC3=C1	204.27	unknown	https://doi.org/10.1007/S00280-005-0133-1
> Benzenoids / Anthracenes
Anhydroasperflavin	53440463	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2)C=C(C=C3OC)O	270.28	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1248/CPB.40.1191
> Benzenoids / Benzene and substituted derivatives
3-Phenyl-1-propanol	31234	Click to see C1=CC=C(C=C1)CCCO	136.19	unknown	via CMAUP database
Bicyclo[2.2.2]octan-1-ol, 4-phenyl-	327096	Click to see C1CC2(CCC1(CC2)C3=CC=CC=C3)O	202.29	unknown	via CMAUP database
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Anilides
N-(2,5-Dichlorophenyl)cyclohexanecarboxamide	557839	Click to see C1CCC(CC1)C(=O)NC2=C(C=CC(=C2)Cl)Cl	272.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Anilides / Aromatic anilides / Benzanilides
N-(4-Amino-2,5-diethoxyphenyl)benzamide	67108	Click to see CCOC1=CC(=C(C=C1N)OCC)NC(=O)C2=CC=CC=C2	300.35	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate	3026	Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC	278.34	unknown	via CMAUP database
Dimethyl Phthalate	8554	Click to see COC(=O)C1=CC=CC=C1C(=O)OC	194.18	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see C1=CC=C(C=C1)C(=O)O	122.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid	3469	Click to see C1=CC(=C(C=C1O)C(=O)O)O	154.12	unknown	via CMAUP database
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	https://doi.org/10.1021/NP50110A006 https://doi.org/10.3724/SP.J.1008.2010.01120
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid	338	Click to see C1=CC=C(C(=C1)C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
2,4-Dimethylbenzyl alcohol	27809	Click to see CC1=CC(=C(C=C1)CO)C	136.19	unknown	via CMAUP database
3,5-Dimethylbenzyl alcohol	33706	Click to see CC1=CC(=CC(=C1)CO)C	136.19	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzylethers
Benzyl methyl ether	10869	Click to see COCC1=CC=CC=C1	122.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
o-Cymene	10703	Click to see CC1=CC=CC=C1C(C)C	134.22	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
Methyl 4-fluoro-3-phenoxybenzoate	618834	Click to see COC(=O)C1=CC(=C(C=C1)F)OC2=CC=CC=C2	246.23	unknown	https://doi.org/10.1002/JSSC.200800341
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
1,4-Dimethoxy-2,3,5,6-tetramethylbenzene	601765	Click to see CC1=C(C(=C(C(=C1OC)C)C)OC)C	194.27	unknown	via CMAUP database
2-tert-Butyl-1,4-dimethoxybenzene	88792	Click to see CC(C)(C)C1=C(C=CC(=C1)OC)OC	194.27	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-Methyl-1-phenyl-2-propen-1-ol	138211	Click to see CC(=C)C(C1=CC=CC=C1)O	148.20	unknown	https://doi.org/10.1002/JSSC.200800341
3-Phenyldecane	20740	Click to see CCCCCCCC(CC)C1=CC=CC=C1	218.38	unknown	via CMAUP database
Phenylacetone	7678	Click to see CC(=O)CC1=CC=CC=C1	134.17	unknown	via CMAUP database
tert-Butylbenzene	7366	Click to see CC(C)(C)C1=CC=CC=C1	134.22	unknown	via CMAUP database
> Benzenoids / Naphthalenes
1,1,6-Trimethyl-1,2-dihydronaphthalene	121677	Click to see CC1=CC2=C(C=C1)C(CC=C2)(C)C	172.27	unknown	via CMAUP database
Naphthalene	931	Click to see C1=CC=C2C=CC=CC2=C1	128.17	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Deoxyshikonin	98914	Click to see CC(=CCCC1=CC(=O)C2=C(C=CC(=C2C1=O)O)O)C	272.29	unknown	via CMAUP database
> Benzenoids / Phenol ethers
2-(4-Cyclohexylphenoxy)ethanol	160168	Click to see C1CCC(CC1)C2=CC=C(C=C2)OCCO	220.31	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
5,7-Dihydroxy-3,6-dimethoxy-2-(4-methoxyphenyl)-5,8-dihydrochromen-4-one	5319515	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)CC(=C(C3O)OC)O)OC	346.30	unknown	via CMAUP database
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(1,3,5-Trimethylhexyl)phenol	6427088	Click to see CC(C)CC(C)CC(C)C1=CC=C(C=C1)O	220.35	unknown	via CMAUP database
4-Nonylphenol	1752	Click to see CCCCCCCCCC1=CC=C(C=C1)O	220.35	unknown	via CMAUP database
> Benzenoids / Phenols / Cresols / Ortho cresols
4-Amino-2,3-xylenol	76542	Click to see CC1=C(C=CC(=C1C)O)N	137.18	unknown	via CMAUP database
> Hydrocarbon derivatives / Tropones / Tropolones
Nootkatin	238797	Click to see CC(C)C1=CC(=O)C(=CC=C1CC=C(C)C)O	232.32	unknown	via CMAUP database
> Hydrocarbons / Polycyclic hydrocarbons
(-)-Isoledene	91873614	Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C	204.35	unknown	via CMAUP database
(1aR,4R,7R,7bS)-1,1,4,7-Tetramethyl-1a,2,3,4,5,6,7,7b-octahydro-1H-cyclopropa[e]azulene	15431199	Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C	204.35	unknown	via CMAUP database
Isoledene	530426	Click to see CC1CCC2C(C2(C)C)C3=C1CCC3C	204.35	unknown	via CMAUP database
Perhydrofluoranthene	282803	Click to see C1CCC2C(C1)C3CCCC4C3C2CCC4	218.38	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1R,4R,5S)-1,8-Dimethyl-4-(prop-1-en-2-yl)spiro[4.5]dec-7-ene	13743810	Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C	204.35	unknown	via CMAUP database
1-methyl-4-[(E)-prop-1-enyl]cyclohexene	5319725	Click to see CC=CC1CCC(=CC1)C	136.23	unknown	via CMAUP database
1,2,3,4,5-Pentamethylcyclopentadiene	77667	Click to see CC1C(=C(C(=C1C)C)C)C	136.23	unknown	via CMAUP database
1,3,5-Hexatriene, 3-methyl-, (E)-	5367380	Click to see CC(=CC=C)C=C	94.15	unknown	via CMAUP database
2-Methyl-2-bornene	155902	Click to see CC1=CC2CCC1(C2(C)C)C	150.26	unknown	https://doi.org/10.1002/JSSC.200800341
6-Methylenebicyclo[3.1.0]hexane	556304	Click to see C=C1C2C1CCC2	94.15	unknown	https://doi.org/10.1002/JSSC.200800341
Acoradiene	90351	Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C	204.35	unknown	via CMAUP database
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	via CMAUP database
Santolina triene	519872	Click to see CC(=CC(C=C)C(=C)C)C	136.23	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
3-Tridecen-1-yne	538033	Click to see CCCCCCCCCC=CC#C	178.31	unknown	https://doi.org/10.1002/JSSC.200800341
3-Tridecen-1-yne, (E)-	5363493	Click to see CCCCCCCCCC=CC#C	178.31	unknown	via CMAUP database
3-Tridecen-1-yne, (Z)-	5367347	Click to see CCCCCCCCCC=CC#C	178.31	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkadienes
1,3-Pentadiene	62204	Click to see CC=CC=C	68.12	unknown	via CMAUP database
cis-1,3-Pentadiene	643785	Click to see CC=CC=C	68.12	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Cyclic olefins / Cycloalkenes
Cyclohexene	8079	Click to see C1CCC=CC1	82.14	unknown	via CMAUP database
Cyclohexene, 3-(1-hexenyl)-, (E)-	5358331	Click to see CCCCC=CC1CCCC=C1	164.29	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
5-[4-(3-Hydroxy-4,5-dimethoxyphenyl)-2,3-dimethylbutyl]-2,3-dimethoxyphenol	11315296	Click to see CC(CC1=CC(=C(C(=C1)OC)OC)O)C(C)CC2=CC(=C(C(=C2)OC)OC)O	390.50	unknown	https://doi.org/10.1248/BPB.22.265
Anwulignan	13844304	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC	328.40	unknown	https://doi.org/10.1248/BPB.22.265
Dihydroguaiaretic acid, meso-	476856	Click to see CC(CC1=CC(=C(C=C1)O)OC)C(C)CC2=CC(=C(C=C2)O)OC	330.40	unknown	via CMAUP database
erythro-Austrobailignan-6	10381847	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC	328.40	unknown	via CMAUP database
Macelignan	10404245	Click to see CC(CC1=CC2=C(C=C1)OCO2)C(C)CC3=CC(=C(C=C3)O)OC	328.40	unknown	https://doi.org/10.1248/BPB.22.265
Masoprocol	71398	Click to see CC(CC1=CC(=C(C=C1)O)O)C(C)CC2=CC(=C(C=C2)O)O	302.40	unknown	https://doi.org/10.1248/CPB.40.1191
Nordihydroguaiaretic acid	4534	Click to see CC(CC1=CC(=C(C=C1)O)O)C(C)CC2=CC(=C(C=C2)O)O	302.40	unknown	https://doi.org/10.1248/CPB.40.1191
Pregomisin	181796	Click to see CC(CC1=CC(=C(C(=C1)OC)OC)O)C(C)CC2=CC(=C(C(=C2)OC)OC)O	390.50	unknown	https://doi.org/10.1039/C1AN15527J https://doi.org/10.1248/CPB.26.682 https://doi.org/10.1248/CPB.27.1583 https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1007/BF02975223
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
Podofilox	10607	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Isopropyl decanoate	16833	Click to see CCCCCCCCCC(=O)OC(C)C	214.34	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid	6950479	Click to see CCC(C)C(=O)O	102.13	unknown	via CMAUP database
(S)-2-methylbutanoic acid	448893	Click to see CCC(C)C(=O)O	102.13	unknown	via CMAUP database
2-Methylbutanoic acid	8314	Click to see CCC(C)C(=O)O	102.13	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Heterocyclic fatty acids / Furanoid fatty acids
Wyerone	643733	Click to see CCC=CC#CC(=O)C1=CC=C(O1)C=CC(=O)OC	258.27	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Caproic Acid	8892	Click to see CCCCCC(=O)O	116.16	unknown	via CMAUP database
Sorbic Acid	643460	Click to see CC=CC=CC(=O)O	112.13	unknown	https://doi.org/10.1021/NP50110A006
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Docosapentaenoic acid	5497182	Click to see CCC=CCC=CCC=CCC=CCC=CCCCCCC(=O)O	330.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
6-Octen-1-ol, 3,7-dimethyl-, acetate, (3S)-	6999975	Click to see CC(CCC=C(C)C)CCOC(=O)C	198.30	unknown	via CMAUP database
Citronellyl acetate	9017	Click to see CC(CCC=C(C)C)CCOC(=O)C	198.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2,3-Dihydroxypropyl 12-hydroxyoctadecanoate	95408	Click to see CCCCCCC(CCCCCCCCCCC(=O)OCC(CO)O)O	374.60	unknown	https://doi.org/10.1248/CPB.54.542
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
9-Octadecenal	5283381	Click to see CCCCCCCCC=CCCCCCCCC=O	266.50	unknown	via CMAUP database
CID 17029	17029	Click to see CCCCCCCCC=CCCCCCCCC=O	266.50	unknown	via CMAUP database
cis-9-Octadecenal	5364492	Click to see CCCCCCCCC=CCCCCCCCC=O	266.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-Methyl-3-(3,7,11,15-tetramethylhexadecyl)-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalene-1,4-diolate	45357188	Click to see CC1C(C(C2CCCCC2C1[O-])[O-])CCC(C)CCCC(C)CCCC(C)CCCC(C)C	462.80	unknown	via CMAUP database
CID 6711881	6711881	Click to see CC1C(=O)CC2C(CCCC2(C13CCC4(O3)COC=C4)C)(C)C	318.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acid	128570	Click to see CC(=CCCC(=CCCC(=CCCC(=CC(=O)O)C)C)C)C	304.50	unknown	https://doi.org/10.1194/JLR.M300502-JLR200
Geranylgeranic acid	5275521	Click to see CC(=CCCC(=CCCC(=CCCC(=CC(=O)O)C)C)C)C	304.50	unknown	https://doi.org/10.1194/JLR.M300502-JLR200
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,5S,8R,9R,10S,11R,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	10472944	Click to see CC1(CCCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)C	348.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
(1S,2S,3R,5S,8R,9R,10R,13S)-8,12,15,15-tetramethyl-4-methylidenetricyclo[9.3.1.03,8]pentadec-11-ene-1,2,5,9,10,13-hexol	5318040	Click to see CC1=C2C(C(C3(CCC(C(=C)C3C(C(C2(C)C)(CC1O)O)O)O)C)O)O	368.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Dihydromyrcene	10997105	Click to see CC(CCC=C(C)C)C=C	138.25	unknown	via CMAUP database
1,7-Nonadien-4-ol, 4,8-dimethyl-	536461	Click to see CC(=CCCC(C)(CC=C)O)C	168.28	unknown	via CMAUP database
beta-CITRONELLOL, (+/-)-	8842	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
beta-Ocimene	18756	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	via CMAUP database
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	via CMAUP database
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	via CMAUP database
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
D-Citronellol	101977	Click to see CC(CCC=C(C)C)CCO	156.26	unknown	via CMAUP database
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-Isopropyl-5-methylanisole	14104	Click to see CC1=CC(=C(C=C1)C(C)C)OC	164.24	unknown	https://doi.org/10.1002/JSSC.200800341
Cuminaldehyde	326	Click to see CC(C)C1=CC=C(C=C1)C=O	148.20	unknown	https://doi.org/10.1002/JSSC.200800341
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-(1S,4S)-Borneol	6850744	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
(-)-2-Carene	6430755	Click to see CC1=CC2C(C2(C)C)CC1	136.23	unknown	via CMAUP database
(-)-alpha-Neoclovene	605073	Click to see CC1=CCCC2(C13CCC2C(C3)(C)C)C	204.35	unknown	via CMAUP database
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(-)-Sabinene	11051711	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
(+)-2-Carene	78249	Click to see CC1=CC2C(C2(C)C)CC1	136.23	unknown	via CMAUP database
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
(+)-Bornyl acetate	6950274	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(+)-Camphene	92221	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
(1R,2S,4R)-(+)-Bornyl acetate	443131	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(1R,2S,4R)-Borneol	439568	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
(1S-endo)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol	10049	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
(1S,2R,4S)-(-)-Bornyl acetate	442460	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
(1S,2S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol	12242815	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene	12223113	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	via CMAUP database
1,3a-Ethano-3aH-indene, 1,2,3,6,7,7a-hexahydro-2,2,4,7a-tetramethyl-, [1R-(1alpha,3aalpha,7aalpha)]-	6432441	Click to see CC1=CCCC2(C13CCC2C(C3)(C)C)C	204.35	unknown	via CMAUP database
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
2-Carene	79044	Click to see CC1=CC2C(C2(C)C)CC1	136.23	unknown	via CMAUP database
alpha-Bergamotene	86608	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	via CMAUP database
alpha-Fenchyl acetate	6427102	Click to see CC(=O)OC1C(C2CCC1(C2)C)(C)C	196.29	unknown	via CMAUP database
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1002/JSSC.200800341
beta-Neoclovene	595094	Click to see CC1(CC23CCC1C2(CCCC3=C)C)C	204.35	unknown	via CMAUP database
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	via CMAUP database
Bicyclo(4.1.0)hept-2-ene, 3,7,7-trimethyl-, (1S-cis)-	12302456	Click to see CC1=CC2C(C2(C)C)CC1	136.23	unknown	via CMAUP database
Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, exo-	439569	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	via CMAUP database
Bicyclo[3.1.0]hexane, 1-methyl-6-(1-methylethylidene)-	578236	Click to see CC(=C1C2C1(CCC2)C)C	136.23	unknown	via CMAUP database
Borneo camphor	12242824	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Borneol	6552009	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Borneol, (-)-	1201518	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Bornyl acetate, (-)-	93009	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	via CMAUP database
DL-Borneol	10492	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
L-Born-2-yl acetate	44630108	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	via CMAUP database
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
Sumatra camphor	657014	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
trans-alpha-Bergaptene	6428986	Click to see CC1=CCC2CC1C2(C)CCC=C(C)C	204.35	unknown	via CMAUP database
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
Tricyclene	79035	Click to see CC1(C2CC3C1(C3C2)C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Terpinen-4-ol	5325830	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
[(1R,5R,6R,7R,10R)-10-methyl-7-propan-2-yl-3-tricyclo[4.4.0.01,5]dec-3-enyl]methanol	163019916	Click to see CC1CCC(C2C13C2C=C(C3)CO)C(C)C	220.35	unknown	https://doi.org/10.1016/J.BBRC.2009.12.131
3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-, acetate	20960	Click to see CC1=CCC(CC1)(C(C)C)OC(=O)C	196.29	unknown	via CMAUP database
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	via CMAUP database
alpha-Isocubebenol	46224401	Click to see CC1CCC(C2C13C2C=C(C3)CO)C(C)C	220.35	unknown	https://doi.org/10.1016/J.BBRC.2009.12.131
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	via CMAUP database
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
alpha-Terpinyl acetate	111037	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	via CMAUP database
alpha,alpha-Dimethyl-4-methylenecyclohexanemethanol	81722	Click to see CC(C)(C1CCC(=C)CC1)O	154.25	unknown	via CMAUP database
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	via CMAUP database
cis-4-(Isopropyl)-1-methylcyclohex-2-en-1-ol	122485	Click to see CC(C)C1CCC(C=C1)(C)O	154.25	unknown	via CMAUP database
Dihydrocarvyl acetate	30248	Click to see CC1CCC(CC1OC(=O)C)C(=C)C	196.29	unknown	via CMAUP database
Dihydrocarvyl acetate, (-)-	6553874	Click to see CC1CCC(CC1OC(=O)C)C(=C)C	196.29	unknown	via CMAUP database
Isolimonene	521268	Click to see CC1CCC(C=C1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (-)-	439250	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
p-Menth-3-en-1-ol	11468	Click to see CC(C)C1=CCC(CC1)(C)O	154.25	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Cycloheptane, 1-ethenyl-1-methyl-4-methylene-2-(2-methyl-1-propenyl)-	572161	Click to see CC(=CC1CC(=C)CCCC1(C)C=C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
2,5,8-Trimethyl-2-(4,8,12-trimethyltridecyl)-6-chromanol	86052	Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O	416.70	unknown	via CMAUP database
beta-Tocopherol	6857447	Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O	416.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Copaene	442355	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
(-)-alpha-Cubebene	86609	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	via CMAUP database
(-)-beta-Bourbonene	324224	Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C	204.35	unknown	via CMAUP database
(-)-Isolongifolene	11127402	Click to see CC1(CCC=C2C13CCC(C3)C2(C)C)C	204.35	unknown	via CMAUP database
(+)-alpha-Longipinene	520957	Click to see CC1=CCC2C3C1C2(CCCC3(C)C)C	204.35	unknown	via CMAUP database
(+)-alpha-Muurolene	12306049	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	via CMAUP database
(+)-beta-Caryophyllene	20831623	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
(+)-Calamenene	11298625	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	via CMAUP database
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	via CMAUP database
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	via CMAUP database
(+)-Nerolidol	5356544	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
(+)-Sativene	11275742	Click to see CC(C)C1CCC2(C3C1C(C2=C)CC3)C	204.35	unknown	via CMAUP database
(+)-Thujopsene	11401461	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	via CMAUP database
(+)(-)-(E)-beta-caryophyllene	14757966	Click to see CC1(CC2C1CCC(=C)CCCC2=C)C	204.35	unknown	via CMAUP database
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
(1S,2S,7S,8S)-2,6,6,9-tetramethyltricyclo[5.4.0.02,8]undec-9-ene	91753627	Click to see CC1=CCC2C3C1C2(CCCC3(C)C)C	204.35	unknown	via CMAUP database
(1S,3aS,4S,7S)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,6,7-octahydroazulene	91748784	Click to see CC1CCC(C=C2C1CCC2C)C(=C)C	204.35	unknown	via CMAUP database
(2S)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol	6097621	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	via CMAUP database
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
(3R,6R)-6-methyl-7-methylidene-3-propan-2-yltricyclo[4.4.0.02,8]decane	25203247	Click to see CC(C)C1CCC2(C3C1C(C2=C)CC3)C	204.35	unknown	via CMAUP database
(3S,6E)-Nerolidol	5281525	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
(3S,6S)-6-methyl-7-methylidene-3-propan-2-yltricyclo[4.4.0.02,8]decane	71448981	Click to see CC(C)C1CCC2(C3C1C(C2=C)CC3)C	204.35	unknown	via CMAUP database
(4aR)-4,7-dimethylidene-1-propan-2-yl-1,2,3,4a,5,6,8,8a-octahydronaphthalene	5315590	Click to see CC(C)C1CCC(=C)C2C1CC(=C)CC2	204.35	unknown	via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene	5322111	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
(E,Z)-farnesol	1549109	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	via CMAUP database
(E)-beta-farnesene	10407	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	via CMAUP database
(E)-Thujopsene	91749973	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	via CMAUP database
(S)-3alpha-[(S)-1,5-Dimethyl-4-hexenyl]-6-methylenecyclohexene	12315493	Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1	204.35	unknown	via CMAUP database
(Z,E)-alpha-Farnesene	5362889	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	via CMAUP database
(Z)-2-methyl-6-(2-methyl-3-tricyclo[2.2.1.02,6]heptanyl)hept-2-en-1-ol	5352146	Click to see CC(CCC=C(C)CO)C1C2CC3C1(C3C2)C	234.38	unknown	via CMAUP database
(Z)-alpha-Bisabolene	5352653	Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C	204.35	unknown	via CMAUP database
(Z)-caryophyllene	6429301	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene	519346	Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C	202.33	unknown	via CMAUP database
1-Methyl-4-(6-methylhept-5-en-2-yl)cyclohexane	5316889	Click to see CC1CCC(CC1)C(C)CCC=C(C)C	208.38	unknown	via CMAUP database
1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene	403919	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	via CMAUP database
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	via CMAUP database
1,3-Dimethyl-8-(1-methylethyl)-tricyclo[4.4.0.02,7]dec-3-ene	25245021	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
1,4-Methanoindan, hexahydro-7-isopropyl-4-methyl-8-methylene-	530427	Click to see CC(C)C1CCC2(C3C1C(C2=C)CC3)C	204.35	unknown	via CMAUP database
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	via CMAUP database
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl-, (3R,6Z)-	12227246	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
3,4-Dihydrocadalene	528708	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	via CMAUP database
4,7-Dimethyl-7-(4-methylpent-3-enyl)bicyclo[2.2.1]heptan-3-ol	5315645	Click to see CC(=CCCC1(C2CCC1(C(C2)O)C)C)C	222.37	unknown	via CMAUP database
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane	539857	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O	238.37	unknown	via CMAUP database
8-Isopropyl-1,3-dimethyltricyclo(4.4.0.02,7)dec-3-ene	12303902	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
alpha-Bisabolol	10586	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	via CMAUP database
alpha-Cadinene	12306052	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	via CMAUP database
alpha-Copaene	70678558	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Alpha-Farnesene	5281516	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	via CMAUP database
alpha-Isocuparenol	5318539	Click to see CC1=CC=C(C=C1)C2(CCC(C2(C)C)O)C	218.33	unknown	via CMAUP database
alpha-Santalene	94164	Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)C	204.35	unknown	https://doi.org/10.1002/JSSC.200800341
alpha-Santalol	5281531	Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	220.35	unknown	via CMAUP database
beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	via CMAUP database
beta-Bourbonene	62566	Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C	204.35	unknown	via CMAUP database
beta-Cadinene	10657	Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C	204.35	unknown	via CMAUP database
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	via CMAUP database
beta-Farnesene, (6Z)-	5317319	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	via CMAUP database
beta-Guaiene	15560252	Click to see CC1CCC(=C(C)C)CC2=C1CCC2C	204.35	unknown	via CMAUP database
beta-SANTALOL	6857681	Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)CO	220.35	unknown	via CMAUP database
beta-Ylangene	519779	Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C	204.35	unknown	via CMAUP database
Bicyclo[4.4.0]dec-1-ene, 2-isopropyl-5-methyl-9-methylene-	595137	Click to see CC1CCC(=C2C1CCC(=C)C2)C(C)C	204.35	unknown	via CMAUP database
Bisabolol	1549992	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	via CMAUP database
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	via CMAUP database
Cadina-4,9-diene	91748288	Click to see CC1CCC2C(=CCC(C2=C1)C(C)C)C	204.35	unknown	via CMAUP database
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
cis-Nerolidol	5320128	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
cis,cis-Farnesol	1549107	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	via CMAUP database
Cloven	11229486	Click to see CC1(C=CC23C1CCC(C2)(CCC3)C)C	204.35	unknown	via CMAUP database
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Copaene, (+)-	636457	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
Cuparene	86895	Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C	202.33	unknown	via CMAUP database
Cyclohexene, 4-((1Z)-1,5-dimethyl-1,4-hexadienyl)-1-methyl-, (4S)-	24798702	Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C	204.35	unknown	via CMAUP database
Cyclopropa[d]naphthalene, 1,1a,4,4a,5,6,7,8-octahydro-2,4a,8,8-tetramethyl-, (1aS,4aS,8aS)-(-)-	6432451	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	via CMAUP database
d-alpha-Santalol	5368797	Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)CO	220.35	unknown	via CMAUP database
delta-Cadinene	12306054	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	via CMAUP database
Epizonarene	595385	Click to see CC1CCC(=C2C1CCC(=C2)C)C(C)C	204.35	unknown	via CMAUP database
Farnesol	3327	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	via CMAUP database
gamma-Elemene	94254	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	via CMAUP database
gamma-Gurjunene	90805	Click to see CC1CCC(C=C2C1CCC2C)C(=C)C	204.35	unknown	via CMAUP database
Guaiene	6949	Click to see CC1CCC(=C(C)C)CC2=C1CCC2C	204.35	unknown	via CMAUP database
Isocaryophyllene	5281522	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Junipene	5489258	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	via CMAUP database
Levomenol	442343	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	via CMAUP database
Longipinenone	101117096	Click to see CC1=CC(=O)C2C3C1C2(CCCC3(C)C)C	218.33	unknown	via CMAUP database
Naphthalene, 1,2,3,4,4a,5,6,8a-octahydro-7-methyl-4-methylene-1-(1-methylethyl)-, (1alpha,4aalpha,8aalpha)-	6432308	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	via CMAUP database
Naphthalene, 1,2,3,5,6,8a-hexahydro-4,7-dimethyl-1-(1-methylethyl)-, (1S-cis)-	12306059	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	via CMAUP database
Nerolidol	8888	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
Patchoulane	29408	Click to see CC1CCC23C1CC(C2(C)C)CCC3C	206.37	unknown	via CMAUP database
Sativene	11830550	Click to see CC(C)C1CCC2(C3C1C(C2=C)CC3)C	204.35	unknown	via CMAUP database
Selina-4(15),7(11)-diene	10655819	Click to see CC(=C1CCC2(CCCC(=C)C2C1)C)C	204.35	unknown	via CMAUP database
Sesquicarene	11074502	Click to see CC1=CC2C(C2(C)CCC=C(C)C)CC1	204.35	unknown	via CMAUP database
Thujopsen	97829	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	via CMAUP database
Thujopsene	442402	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	via CMAUP database
Toluene, p-(1,2,2-trimethylcyclopentyl)-, (R)-(+)-	11084908	Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C	202.33	unknown	via CMAUP database
trans-Calamenene	6429022	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	via CMAUP database
trans-Nerolidol	5284507	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	via CMAUP database
trans,trans-Farnesol	445070	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	via CMAUP database
Tricyclo[4.4.0.0(2,7)]dec-3-ene, 1,3-dimethyl-8-(1-methylethyl)-, stereoisomer	6432119	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR-(1aalpha,7alpha,7aalpha,7balpha))-	15560278	Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C	204.35	unknown	via CMAUP database
1H-Cyclopropa[a]naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-, (1aR,7R,7aR,7bS)-(+)-	6432176	Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C	204.35	unknown	via CMAUP database
Calarene	28481	Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Alloaromadendrene	10899740	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
(-)-alpha-Gurjunene	521243	Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C	204.35	unknown	via CMAUP database
(+)-Alloaromadendrene	21775889	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
1H-Cycloprop[e]azulene, decahydro-1,1,4,7-tetramethyl-	520381	Click to see CC1CCC2C(C2(C)C)C3C1CCC3C	206.37	unknown	via CMAUP database
1H-Cycloprop[e]azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR,4aS,7R,7aR,7bS)-(-)-	44584667	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
Allo-Aromadendrene	42608158	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
Alloaromadendren	91746537	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
Aromadendrene	91354	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
Aromadendrene oxide	91753455	Click to see CC1CCC2C1C3C(C3(C)C)CCC24CO4	220.35	unknown	via CMAUP database
Aromadendrene oxide 2	16211192	Click to see CC1CCC2C1C3C(C3(C)C)CCC24CO4	220.35	unknown	via CMAUP database
decahydro-1,1,7-trimethylspiro[4H-cycloprop[e]azulene-4,2'-oxirane]	528759	Click to see CC1CCC2C1C3C(C3(C)C)CCC24CO4	220.35	unknown	via CMAUP database
Isoaromadendrene epoxide	534398	Click to see CC1CCC2C1C3C(C3(C)C)CC4C2(O4)C	220.35	unknown	via CMAUP database
Ledane	102239850	Click to see CC1CCC2C(C2(C)C)C3C1CCC3C	206.37	unknown	via CMAUP database
Viridiflorene	10910653	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene	11820258	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	via CMAUP database
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	via CMAUP database
(1S,2E,6E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	13894537	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	via CMAUP database
(1S,2Z,6Z,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	13894533	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	via CMAUP database
Bicyclogermacrene	5315347	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
1H-3a,7-Methanoazulene, 2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl-, (3R,3aS,7S,8aS)-	12302594	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	204.35	unknown	via CMAUP database
alpha-Cedrene	6431015	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	204.35	unknown	via CMAUP database
Cedrene	521207	Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C	204.35	unknown	via CMAUP database
Cedrenol	119831	Click to see CC1CCC2C13CC(C2(C)C)C(=C)C(C3)O	220.35	unknown	via CMAUP database
CID 21119906	21119906	Click to see CC1CCC2C13CC(C2(C)C)C(=C)C(C3)O	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Chamigranes
(-)-beta-Chamigrene	442353	Click to see CC1=CCC2(CC1)C(=C)CCCC2(C)C	204.35	unknown	via CMAUP database
alpha-Chamigrene	519725	Click to see CC1=CCC2(CC1)C(=CCCC2(C)C)C	204.35	unknown	via CMAUP database
beta-Chamigrene	29073	Click to see CC1=CCC2(CC1)C(=C)CCCC2(C)C	204.35	unknown	https://doi.org/10.1002/JSSC.200800341
Chamigrenal	177096	Click to see CC1(CCCC(=C)C12CCC(=CC2)C=O)C	218.33	unknown	https://doi.org/10.1007/BF02975223
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	via CMAUP database
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-	9859094	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	via CMAUP database
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel-	10583	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(6R)-4,4a-dimethyl-6-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one	9794438	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C	218.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene	519361	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	via CMAUP database
beta-Maaliene	521242	Click to see CC1=C2C3C(C3(C)C)CCC2(CCC1)C	204.35	unknown	via CMAUP database
beta-Selinene	442393	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	via CMAUP database
Naphthalene, 1,2,3,4,4a,5,6,8a-octahydro-4a,8-dimethyl-2-(1-methylethenyl)-, [2R-(2alpha,4aalpha,8abeta)]-	6432455	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(+)-germacrene D	24771782	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(1E)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	74764030	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(1Z)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	92003564	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
(6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene	49796490	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
1-Methyl-5-methylene-8-(1-methylethyl)-1,6-cyclodecadiene	6436582	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-, [s-(E,E)]-	5373727	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(1R,6S)-gamma-himachalene	6428535	Click to see CC1=CC2C(CC1)C(=CCCC2(C)C)C	204.35	unknown	via CMAUP database
3,5,5,9-tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo[7]annulene	15095	Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1	204.35	unknown	via CMAUP database
alpha-Himachalene	520909	Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C	204.35	unknown	via CMAUP database
beta-Himachalene	11586487	Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1	204.35	unknown	via CMAUP database
gamma-Himachalene	577062	Click to see CC1=CC2C(CC1)C(=CCCC2(C)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,14bR)-8a-(hydroxymethyl)-4,4,6a,6a,11,11,14b-heptamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol	5319977	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)CO)C	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Schizonepetoside A	49787030	Click to see CC1CCC(C(=O)C1)C(=COC2C(C(C(C(O2)CO)O)O)O)C	330.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Durantoside I	95223135	Click to see CC1(C(CC2(C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)OC(=O)C=CC4=CC=CC=C4)O	552.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1055/S-0030-1249861
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(6S,7R,8S)-8-hydroxy-6,8-dimethyl-3-methylidenespiro[4,5,6,8a-tetrahydro-3aH-cyclohepta[b]furan-7,5'-oxolane]-2,2'-dione	9795694	Click to see CC1CCC2C(C(C13CCC(=O)O3)(C)O)OC(=O)C2=C	280.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
Germacra-1(10),3,11(13)-trien-12-oic acid, 3-alpha,6-alpha,8-alpha-trihydroxy-, 12,8-lactone, diacetate	6436585	Click to see CC1=CCC(C(=CC(C2C(C1)OC(=O)C2=C)OC(=O)C)C)OC(=O)C	348.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,6aR,6bS,8S,8aS,12aS,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,8-diol	23641100	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO)C	458.70	unknown	via CMAUP database
(E,6R)-6-[(3R,5R,10S,13R,14R,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid	101781706	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C	456.70	unknown	https://doi.org/10.1080/10286020.2011.570751
6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid	435761	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C	456.70	unknown	https://doi.org/10.1080/10286020.2011.570751
6-(3,7-dihydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid	78384945	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2C(CC4C3(CCC(C4(C)C)O)C)O)C)C	472.70	unknown	https://doi.org/10.1080/10286020.2011.570751
beta-Citraurin	9845703	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C	432.60	unknown	via CMAUP database
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
Ganoderic acid U	101600072	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2C(CC4C3(CCC(C4(C)C)O)C)O)C)C	472.70	unknown	https://doi.org/10.1080/10286020.2011.570751
Nigranoic acid	10814237	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C	470.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(3S)-10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	6432564	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	via CMAUP database
4,4-Dimethylcholesterol	15137988	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4(C)C)O)C)C	414.70	unknown	via CMAUP database
Cholest-5-en-3-ol	11025495	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	via CMAUP database
Cholest-5-en-3beta-ol, 4,4-dimethyl-	280427	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4(C)C)O)C)C	414.70	unknown	via CMAUP database
Cholesterol	5997	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	via CMAUP database
Lophenol	160482	Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O	400.70	unknown	via CMAUP database
Methostenol	440562	Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)O	400.70	unknown	https://doi.org/10.1002/JSSC.200800341
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergost-8(14)-en-3beta-ol	91744760	Click to see CC(C)C(C)CCC(C)C1CCC2=C3CCC4CC(CCC4(C3CCC12C)C)O	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 16-hydroxysteroids
(8R,9S,13R,17S)-3-(dimethylamino)-9-ethyl-4,4,13,14-tetramethyl-17-[(1S)-1-(methylamino)ethyl]-2,3,5,6,7,8,10,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-16-ol	5316251	Click to see CCC12C=CC3(C(C(CC3(C1CCC4C2CCC(C4(C)C)N(C)C)C)O)C(C)NC)C	430.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
alpha1-Sitosterol	9548595	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C	426.70	unknown	https://doi.org/10.1080/09251619708951283
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Azaniumylhexanoate	517543	Click to see CCCCC(C(=O)[O-])[NH3+]	131.17	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
3,7-Dimethyl-trans-2,6-octadien-1-yl acetate	24832062	Click to see CC(=CCCC(=COC(=O)C)C)C	182.26	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Itaconic anhydride	75110	Click to see C=C1CC(=O)OC1=O	112.08	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
1-Hydroxy-9,9,18-trimethyl-18-[2-methyl-3-(4-methyl-5-oxofuran-2-ylidene)propanoyl]-4,8,15-trioxapentacyclo[11.7.0.03,7.03,10.014,19]icosane-5,16-dione	74076240	Click to see CC1=CC(=CC(C)C(=O)C2(CC(=O)OC3C2CC4(C3CCC5C(OC6C5(C4)OC(=O)C6)(C)C)O)C)OC1=O	528.60	unknown	https://doi.org/10.1021/OL701679N
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron	88113319	Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O	192.12	unknown	via CMAUP database
2-Methylcitric acid	515	Click to see CC(C(=O)O)C(CC(=O)O)(C(=O)O)O	206.15	unknown	https://doi.org/10.3724/SP.J.1008.2010.01120
Schintrilactone A	23643337	Click to see CC1=CC(=CC(C)C(=O)C2(CC(=O)OC3C2CC4(C3CCC5C(OC6C5(C4)OC(=O)C6)(C)C)O)C)OC1=O	528.60	unknown	https://doi.org/10.1021/OL701679N
Schintrilactone B	23643442	Click to see CC1=CC(=CC(C)C(=O)C2(CC(=O)OC3C2CC4(C3CCC5C(OC6C5(C4)OC(=O)C6)(C)C)O)C)OC1=O	528.60	unknown	https://doi.org/10.1021/OL701679N
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(2S)-2-Hydroxybutanedioic acid	222656	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	via CMAUP database
D-malate	92824	Click to see C(C(C(=O)O)O)C(=O)O	134.09	unknown	via CMAUP database
Hydron;2-hydroxybutanedioate	20130941	Click to see [H+].[H+].C(C(C(=O)[O-])O)C(=O)[O-]	134.09	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
cis-Chlorogenic acid	1794425	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
Quinic acid	6508	Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O	192.17	unknown	https://doi.org/10.3724/SP.J.1008.2010.01120
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
(2S,3S)-butane-2,3-diol	439888	Click to see CC(C(C)O)O	90.12	unknown	via CMAUP database
(R,R)-2,3-butanediol	225936	Click to see CC(C(C)O)O	90.12	unknown	via CMAUP database
2,3-Butanediol	262	Click to see CC(C(C)O)O	90.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S)-1-[(E)-2-[(2S)-6-carboxy-2-carboxylato-2,3-dihydropyridin-4-yl]ethenyl]-5-hydroxy-6-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroindole-2-carboxylate	25244723	Click to see C1C(N=C(C=C1C=CN2C(CC3=CC(=C(C=C32)OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)[O-])C(=O)O)C(=O)[O-]	548.50	unknown	via CMAUP database
Zingerone glucoside	74937233	Click to see CC(=O)CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC	356.40	unknown	https://doi.org/10.3724/SP.J.1008.2010.01120
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
3F-alpha-D-Galactosylraffinose	440185	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)CO)O)O)O)O)O)O)O	666.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	unknown	via CMAUP database
5-Methylfurfural	12097	Click to see CC1=CC=C(O1)C=O	110.11	unknown	via CMAUP database
Furfural	7362	Click to see C1=COC(=C1)C=O	96.08	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Octenal	5283324	Click to see CCCCCC=CC=O	126.20	unknown	via CMAUP database
2-Octenal, (2Z)-	6427080	Click to see CCCCCC=CC=O	126.20	unknown	via CMAUP database
Hexanal	6184	Click to see CCCCCC=O	100.16	unknown	via CMAUP database
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	via CMAUP database
trans-2,cis-6-Nonadienal	643731	Click to see CCC=CCCC=CC=O	138.21	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(E)-6,10-Dimethyl-9-methylene-5-undecen-2-one	5318635	Click to see CC(C)C(=C)CCC(=CCCC(=O)C)C	208.34	unknown	via CMAUP database
2-Nonanone	13187	Click to see CCCCCCCC(=O)C	142.24	unknown	via CMAUP database
2-Tetradecanone	75364	Click to see CCCCCCCCCCCCC(=O)C	212.37	unknown	via CMAUP database
2-Undecanone	8163	Click to see CCCCCCCCCC(=O)C	170.29	unknown	via CMAUP database
7-Tridecanone	10015	Click to see CCCCCCC(=O)CCCCCC	198.34	unknown	via CMAUP database
Hexadecan-2-one	29251	Click to see CCCCCCCCCCCCCCC(=O)C	240.42	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Benzoylacetone	7166	Click to see CC(=O)CC(=O)C1=CC=CC=C1	162.18	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
Cyclohexene, 1-(3-ethoxy-1-propenyl)-, (Z)-	5358347	Click to see CCOCC=CC1=CCCCC1	166.26	unknown	via CMAUP database
Oxacyclotetradeca-4,11-diyne	560917	Click to see C1CCC#CCCOCCC#CCC1	190.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Dibenzopyrans
6H-Dibenzo(b,d)pyran-9-carboxylic acid, 1-hydroxy-3-(1-hydroxypentyl)-6,6-dimethyl-	6455303	Click to see CCCCC(C1=CC(=C2C(=C1)OC(C3=C2C=C(C=C3)C(=O)O)(C)C)O)O	356.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrazoles / Indazoles
3,6-Dimethyl-1H-indazole	589741	Click to see CC1=CC2=NNC(=C2C=C1)C	146.19	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Ascorbic Acid	54670067	Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O	176.12	unknown	via CMAUP database
Citraconic anhydride	12012	Click to see CC1=CC(=O)OC1=O	112.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
Rugosal	442391	Click to see CC(C)C1CCC2(C13C(C=C(C(C2)OO3)C=O)O)C	266.33	unknown	via CMAUP database
> Organoheterocyclic compounds / Furofurans
1-hydroxy-18-[1-hydroxy-1-(4-methyl-5-oxo-2H-furan-2-yl)propan-2-yl]-9,9,19-trimethyl-4,8,15-trioxahexacyclo[11.8.0.03,7.03,10.014,16.014,19]henicosan-5-one	73307302	Click to see CC1=CC(OC1=O)C(C(C)C2CC3C4(C2(CCC5(C4CCC6C(OC7C6(C5)OC(=O)C7)(C)C)O)C)O3)O	516.60	unknown	https://doi.org/10.1080/10286020.2011.570751
MicrandilactoneB	16681613	Click to see CC1=CC(OC1=O)C(C(C)C2CC3C4(C2(CCC5(C4CCC6C(OC7C6(C5)OC(=O)C7)(C)C)O)C)O3)O	516.60	unknown	https://doi.org/10.1080/10286020.2011.570751
> Organoheterocyclic compounds / Furopyrans
Lancifodilactone D	12080814	Click to see CC1C2C3C(C(C(=O)O3)C)OC45C2C(C1=O)(CCC6(O4)CC78C(CC=C6C5=O)C(OC7CC(=O)O8)(C)C)C	526.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
3-Butyldihydrofuran-2(3H)-one	86852	Click to see CCCCC1CCOC1=O	142.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxepanes
4,6,6-Trimethyl-2-(3-methylbuta-1,3-dienyl)-3-oxatricyclo[5.1.0.0(2,4)]octane	5369926	Click to see CC(=C)C=CC12C3CC3C(CC1(O2)C)(C)C	218.33	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Methylpyridines
(8R)-2,5-dimethyl-8-prop-1-en-2-yl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridine	5317082	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=C)C	215.33	unknown	via CMAUP database
> Organophosphorus compounds / Alkylhalophosphines
Cyclohexyldichlorophosphine	557869	Click to see C1CCC(CC1)P(Cl)Cl	185.03	unknown	https://doi.org/10.1002/JSSC.200800341
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
3,4-Dihydrocoumarin, 4,4-dimethyl-6-ethyl-	605048	Click to see CCC1=CC2=C(C=C1)OC(=O)CC2(C)C	204.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl-	8784	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	https://doi.org/10.1016/S0731-7085(00)00539-2
Cinnamic acid	444539	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	https://doi.org/10.1016/S0731-7085(00)00539-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid	1549106	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,7-Dimethoxycoumarin	2775	Click to see COC1=CC2=C(C=CC(=O)O2)C(=C1)OC	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
Hexahydrocurcumin	5318039	Click to see COC1=C(C=CC(=C1)CCC(CC(=O)CCC2=CC(=C(C=C2)O)OC)O)O	374.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0731-7085(00)00539-2
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/S0731-7085(00)00539-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	44258154	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	via CMAUP database
Isoscoparin	442611	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(+)Gomisin-M2	16728078	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)OC)O)OCO3	386.40	unknown	via CMAUP database
(10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl) (E)-2-methylbut-2-enoate	5364583	Click to see CC=C(C)C(=O)OC1C2=CC3=C(C(=C2C4=C(C(=C(C=C4CC(C1(C)O)C)OC)OC)OC)OC)OCO3	514.60	unknown	via CMAUP database
(10-Hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl) benzoate	10007357	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	536.60	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1021/NP0503707 https://doi.org/10.1055/S-0030-1249861 https://doi.org/10.1248/CPB.40.1191 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/
(10-Hydroxy-4,5,14,15,16-pentamethoxy-9,10-dimethyl-3-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) 2-methylbut-2-enoate	74491148	Click to see CC=C(C)C(=O)OC1=C2C(=CC(=C1OC)OC)CC(C(CC3=CC(=C(C(=C32)OC)OC)OC)(C)O)C	500.60	unknown	https://doi.org/10.1271/BBB.90597 https://doi.org/10.1021/NP0503707
(10-Hydroxy-4,5,14,15,16-pentamethoxy-9,10-dimethyl-3-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) benzoate	44575227	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC(=O)C4=CC=CC=C4)OC)OC	522.60	unknown	https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1021/NP0503707
(11R,12R,24S,25S)-12-hydroxy-18,19,20-trimethoxy-11,12,24,25-tetramethyl-4,6,9,14-tetraoxapentacyclo[13.7.3.03,7.08,22.016,21]pentacosa-1,3(7),8(22),16,18,20-hexaen-13-one	10436511	Click to see CC1CC2=CC3=C(C4=C2C5=C(C(=C(C=C5C(C1C)OC(=O)C(C(CO4)C)(C)O)OC)OC)OC)OCO3	514.60	unknown	via CMAUP database
(11R,12S,24S,25S)-12,25-dihydroxy-18,19,20-trimethoxy-11,12,24,25-tetramethyl-4,6,9,14-tetraoxapentacyclo[13.7.3.03,7.08,22.016,21]pentacosa-1,3(7),8(22),16,18,20-hexaen-13-one	9984471	Click to see CC1CC2=CC3=C(C4=C2C5=C(C(=C(C=C5C(C1(C)O)OC(=O)C(C(CO4)C)(C)O)OC)OC)OC)OCO3	530.60	unknown	via CMAUP database
(11R)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-ol	45356879	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1C)O)OCO4)OC)OC)OC)OC	416.50	unknown	via CMAUP database
(12S,13S)-3,22-dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.02,10.04,8.017,21]docosa-1(22),2,4(8),9,15,17(21)-hexaene	13652150	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4CC1C)OCO5)OC)OC)OCO3	384.40	unknown	https://doi.org/10.1248/CPB.40.1191
(3,22-Dimethoxy-13-methyl-12-methylidene-5,7,18,20-tetraoxapentacyclo[13.7.0.02,10.04,8.017,21]docosa-1(22),2,4(8),9,15,17(21)-hexaen-11-yl) benzoate	11851244	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1=C)OC(=O)C6=CC=CC=C6)OCO5)OC)OC)OCO3	502.50	unknown	https://doi.org/10.1021/NP0503707
(3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl) (Z)-2-methylbut-2-enoate	5367844	Click to see CC=C(C)C(=O)OC1C(C(CC2=CC(=C(C(=C2C3=C(C4=C(C=C13)OCO4)OC)OC)OC)OC)C)C	498.60	unknown	via CMAUP database
(3,4,5,19-Tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl) benzoate	73819918	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1C)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	520.60	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1055/S-2003-37024
(4,5,14,15,16-Pentamethoxy-9,10-dimethyl-3-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) acetate	5321169	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC(=O)C)OC)OC)OC	444.50	unknown	via CMAUP database
(7S)-6alpha,7beta-Dimethyl-1,2,3,10,11,12-hexamethoxy-5,6,7,8-tetrahydrodibenzo[a,c]cyclooctene-5alpha,6-diol 5-(2-methylcrotonate)	5318795	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C(=C(C=C3CC(C1(C)O)C)OC)OC)OC)OC)OC)OC	530.60	unknown	via CMAUP database
(8R,9R)-3,4,5,14,15,16-hexamethoxy-9,10-dimethyl-8-phenoxytricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaen-9-ol	6326195	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1(C)O)OC4=CC=CC=C4)OC)OC)OC)OC)OC)OC	524.60	unknown	via CMAUP database
(8R,9S,10S)-3,4,5,14,15,16-hexamethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaen-8-ol	5317811	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)O)OC)OC)OC)OC)OC)OC	432.50	unknown	https://doi.org/10.1248/CPB.36.3974
(9,14-Dihydroxy-3,4,5,15,16-pentamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) benzoate	5321177	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1(C)O)OC(=O)C4=CC=CC=C4)OC)OC)OC)OC)OC)O	538.60	unknown	via CMAUP database
(9R,10R)-3,4,5,14,15,16-hexamethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene	10884218	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1016/S0944-7113(97)80072-4 https://doi.org/10.1016/0009-2797(82)90047-3
(9R,10R)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaene	14515707	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)OC)OC)OCO3	400.50	unknown	https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1211/JPP.60.3.0017 https://doi.org/10.1016/S0944-7113(97)80072-4 https://doi.org/10.1016/0009-2797(82)90047-3 https://doi.org/10.1021/NP0503707
(9R,10R)-4,5,14,15,16-pentamethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaen-3-ol	6713072	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)O)OC)OC	402.50	unknown	via CMAUP database
(9R)-3,4,5,19-tetramethoxy-9,10-dimethyl-8-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-9-ol	5321992	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC5=CC=CC=C5)OC)OC)OC)OC)OCO3	508.60	unknown	via CMAUP database
(9S,10S,11R)-3,4,5,19-tetramethoxy-9,10-dimethyl-11-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaene	5321982	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1C)OC5=CC=CC=C5)OCO4)OC)OC)OC)OC	492.60	unknown	via CMAUP database
(9S,10S,11S)-3,4,5,19-tetramethoxy-9,10-dimethyl-11-phenoxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-10-ol	5317802	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC5=CC=CC=C5)OCO4)OC)OC)OC)OC	508.60	unknown	https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1002/RCM.3931 https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1021/NP0503707
(9S,10S)-3,4,5,14,15-pentamethoxy-9,10-dimethyl-16-phenoxytricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaen-9-ol	5321972	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC4=CC=CC=C4)OC)OC	494.60	unknown	https://doi.org/10.1021/NP0503707
(9S,10S)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-10-ol	59203477	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3CC1(C)O)OCO4)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1055/S-2003-37024
[(11R,13R)-3,22-dimethoxy-13-methyl-12-methylidene-5,7,18,20-tetraoxapentacyclo[13.7.0.02,10.04,8.017,21]docosa-1(22),2,4(8),9,15,17(21)-hexaen-11-yl] benzoate	163022418	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1=C)OC(=O)C6=CC=CC=C6)OCO5)OC)OC)OCO3	502.50	unknown	https://doi.org/10.1021/NP0503707
[(11R,13S)-3,22-dimethoxy-13-methyl-12-methylidene-5,7,18,20-tetraoxapentacyclo[13.7.0.02,10.04,8.017,21]docosa-1(22),2,4(8),9,15,17(21)-hexaen-11-yl] benzoate	161253012	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1=C)OC(=O)C6=CC=CC=C6)OCO5)OC)OC)OCO3	502.50	unknown	https://doi.org/10.1021/NP0503707
[(8R,9S,10S)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (Z)-2-methylbut-2-enoate	16745516	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC	514.60	unknown	https://doi.org/10.1016/S0021-9673(00)90280-2 https://doi.org/10.1080/10575639808048288 https://doi.org/10.1016/S0021-9673(96)00685-1
[(8R,9S,10S)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] benzoate	6713205	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	536.60	unknown	https://doi.org/10.1248/BPB.22.265
[(8R)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] acetate	5321020	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)OC(=O)C)OC)OC)OC)OC)OCO3	458.50	unknown	via CMAUP database
[(8S,9S,10R)-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (Z)-2-methylbut-2-enoate	163187539	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC	514.60	unknown	https://doi.org/10.1021/NP0503707
[(8S,9S,10S)-9,19-dihydroxy-3,4,5-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (E)-2-methylbut-2-enoate	45484581	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)O)OC)OC)OC	500.50	unknown	https://doi.org/10.1055/S-0030-1249861
[(8S,9S,10S)-9,19-dihydroxy-3,4,5-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] 2-methylbut-2-enoate	162862673	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)O)OC)OC)OC	500.50	unknown	https://doi.org/10.1055/S-0030-1249861
[(9R,10R,11S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] (E)-2-methylbut-2-enoate	102065620	Click to see CC=C(C)C(=O)OC1C2=CC3=C(C(=C2C4=C(C(=C(C=C4CC(C1(C)O)C)OC)OC)OC)OC)OCO3	514.60	unknown	via CMAUP database
[(9R,10R)-10-hydroxy-4,5,14,15,16-pentamethoxy-9,10-dimethyl-3-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] (Z)-2-methylbut-2-enoate	124355867	Click to see CC=C(C)C(=O)OC1=C2C(=CC(=C1OC)OC)CC(C(CC3=CC(=C(C(=C32)OC)OC)OC)(C)O)C	500.60	unknown	https://doi.org/10.1248/YAKUSHI1947.103.7_743
[(9R,10S,11S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate	124428275	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	536.60	unknown	https://doi.org/10.1021/NP0503707
[(9R,10S)-10-hydroxy-4,5,14,15,16-pentamethoxy-9,10-dimethyl-3-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] benzoate	162898757	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC(=O)C4=CC=CC=C4)OC)OC	522.60	unknown	https://doi.org/10.1021/NP0503707
[(9S,10S,11R)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate	3001661	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	536.60	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1055/S-0030-1249861 https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1021/NP0503707
[(9S,10S,11S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] (E)-2-methylbut-2-enoate	53325466	Click to see CC=C(C)C(=O)OC1C2=CC3=C(C(=C2C4=C(C(=C(C=C4CC(C1(C)O)C)OC)OC)OC)OC)OCO3	514.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1055/S-0030-1249861
[(9S,10S,11S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] 3-methylbut-2-enoate	6325287	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C=C(C)C)OCO4)OC)OC)OC)OC	514.60	unknown	https://doi.org/10.1016/J.CHROMA.2008.09.070 https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1002/RCM.3931
[(9S,10S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate	5480968	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	536.60	unknown	via CMAUP database
[(9S,10S)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate	10006896	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1C)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	520.60	unknown	via CMAUP database
[(9S,10S)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (E)-2-methylbut-2-enoate	6325466	Click to see CC=C(C)C(=O)OC1C(C(CC2=CC3=C(C(=C2C4=C(C(=C(C=C14)OC)OC)OC)OC)OCO3)C)C	498.60	unknown	https://doi.org/10.1002/RCM.3931
1,2,11,12-Tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydrodibenzo[a,c][8]annulene-3,10-diol	73158	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)O)OC)OC)OC)OC)O	388.50	unknown	https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0029-1185685 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1055/S-0030-1249861 https://doi.org/10.1021/NP0503707
3,4,15,16-Tetramethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene-5,9,14-triol	5321168	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)O)OC)OC)OC)OC)O	404.50	unknown	https://doi.org/10.1055/S-2007-967120 https://doi.org/10.1007/S00280-005-0133-1 https://doi.org/10.1007/BF00563602
3,4,5-Trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-19-ol	45782990	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)OC)O)OCO3	386.40	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1248/CPB.40.1191
3,4,5,19-Tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-10-ol	72530274	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3CC1(C)O)OCO4)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1055/S-2003-37024
4,5,14,15,16-Pentamethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene-3,10-diol	11742759	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)O)OC)OC	418.50	unknown	via CMAUP database
4,5,15,16-Tetramethoxy-9,10-dimethyltricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaene-3,14-diol	44481243	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)O)OC)OC)O	388.50	unknown	https://doi.org/10.1055/S-0030-1249861
5,12-Dibromo-schizandrin	3001666	Click to see CC1CC2=C(C3=C(CC1(C)O)C(=C(C(=C3OC)OC)OC)Br)C(=C(C(=C2Br)OC)OC)OC	590.30	unknown	via CMAUP database
5,6,7,8-Tetrahydro-1,2,3,13-tetramethoxy-6,7-dimethylbenzo[3,4]cycloocta[1,2-f][1,3]benzodioxol-5-ol	634472	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)O)OC)OC)OC)OC)OCO3	416.50	unknown	https://doi.org/10.1248/CPB.27.2695
Angeloylgomisin H	26204131	Click to see CC=C(C)C(=O)OC1=C2C(=CC(=C1OC)OC)CC(C(CC3=CC(=C(C(=C32)OC)OC)OC)(C)O)C	500.60	unknown	https://doi.org/10.1271/BBB.90597 https://doi.org/10.1021/NP0503707
Angeloylgomisin O	91864462	Click to see CC=C(C)C(=O)OC1C(C(CC2=CC3=C(C(=C2C4=C(C(=C(C=C14)OC)OC)OC)OC)OCO3)C)C	498.60	unknown	via CMAUP database
Angeloylgomisin P	13844273	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC	514.60	unknown	https://doi.org/10.1016/S0021-9673(96)00685-1
Angeloylisogomisin O	91864463	Click to see CC=C(C)C(=O)OC1C(C(CC2=CC(=C(C(=C2C3=C(C4=C(C=C13)OCO4)OC)OC)OC)OC)C)C	498.60	unknown	via CMAUP database
Arisanschinin F	16099403	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)O)OC)OC)O	388.50	unknown	https://doi.org/10.1055/S-0030-1249861
Arisanschinin K	332607	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	536.60	unknown	https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1007/S00280-005-0133-1 https://doi.org/10.1248/BPB.22.265
Arisanschinin N	5321171	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC	514.60	unknown	via CMAUP database
Benzoylgomisin H	14992069	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC(=O)C4=CC=CC=C4)OC)OC	522.60	unknown	https://doi.org/10.1021/NP0503707 https://doi.org/10.1248/CPB.40.1191
Benzoylgomisin O	91826818	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	520.60	unknown	via CMAUP database
Benzoylisogomisin O	91864464	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1C)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	520.60	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1055/S-2003-37024
Besigomsin	3001662	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1(C)O)OC)OC)OC)OC)OCO3	416.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264271/ https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1111/J.1745-7254.2008.00838.X https://doi.org/10.1055/S-2007-969504 https://doi.org/10.1016/S0021-9673(00)90280-2 https://doi.org/10.1016/0009-2797(82)90047-3 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1016/S0021-9673(01)00556-8 https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1021/NP0503707 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861
CID 133562029	133562029	Click to see CC=C(C)C(=O)OC1C2=CC3=C(C(=C2C4=C(C(=C(C=C4CC(C1(C)O)C)OC)OC)OC)OC)OCO3	514.60	unknown	https://doi.org/10.1016/S0021-9673(96)00685-1
CID 13844278	13844278	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)O)OC)OC	402.50	unknown	https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1021/NP0503707 https://doi.org/10.1055/S-0030-1249861
CID 433451	433451	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)O)OC)OC	402.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1021/NP0503707 https://doi.org/10.1055/S-0030-1249861
CID 5317799	5317799	Click to see CC1CC2=CC3=C(C4=C2C5=C(C(=C(C=C5C(C1(C)O)OC(=O)C(C(CO4)C)(C)O)OC)OC)OC)OCO3	530.60	unknown	https://doi.org/10.1055/S-0030-1249861 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1248/YAKUSHI1947.103.7_743
CID 558009	558009	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC	514.60	unknown	https://doi.org/10.1016/J.BMCL.2007.11.082 https://doi.org/10.1248/CPB.40.1191 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1021/NP0503707 https://doi.org/10.1055/S-0030-1249861
CID 75130910	75130910	Click to see CC1CC2=CC3=C(C4=C2C5=C(C(=C(C=C5C(C1(C)O)OC(=O)C(C(CO4)C)(C)O)OC)OC)OC)OCO3	530.60	unknown	https://doi.org/10.1016/0040-4020(95)00701-9 https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1248/CPB.40.1191 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1055/S-0030-1249861
CID 78385000	78385000	Click to see CC1CC2=CC3=C(C4=C2C5=C(C(=C(C=C5C(C1C)OC(=O)C(C(CO4)C)(C)O)OC)OC)OC)OCO3	514.60	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1248/CPB.27.2695 https://doi.org/10.1055/S-2003-37024
CID 9802006	9802006	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1248/CPB.27.2695 https://doi.org/10.1016/S0021-9673(00)90280-2 https://doi.org/10.1016/S0021-9673(96)00685-1
Deoxyschizandrin	43595	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1055/S-2003-37024 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1021/NP0503707 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861
Deoxyschizandrin,(S)	19020980	Click to see COC1=C(C(=C2C(=C1)CCCCC3=CC(=C(C(=C32)OC)OC)OC)OC)OC	388.50	unknown	via CMAUP database
Epigomisin O	5317081	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)O)OC)OC)OC)OC)OCO3	416.50	unknown	https://doi.org/10.1248/CPB.27.2695
Gomisin A	634470	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1(C)O)OC)OC)OC)OC)OCO3	416.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264271/ https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1016/J.BMCL.2011.08.065 https://doi.org/10.1111/J.1745-7254.2008.00838.X https://doi.org/10.1055/S-0029-1185685 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1007/S00280-005-0133-1 https://doi.org/10.1021/NP0503707 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861
Gomisin D	3085191	Click to see CC1CC2=CC3=C(C4=C2C5=C(C(=C(C=C5C(C1(C)O)OC(=O)C(C(CO4)C)(C)O)OC)OC)OC)OCO3	530.60	unknown	https://doi.org/10.1248/CPB.40.1191
Gomisin E	5317800	Click to see CC1CC2=CC3=C(C4=C2C5=C(C(=C(C=C5C(C1C)OC(=O)C(C(CO4)C)(C)O)OC)OC)OC)OCO3	514.60	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1016/J.CHROMA.2008.09.070 https://doi.org/10.1248/CPB.27.2695 https://doi.org/10.1002/RCM.3931 https://doi.org/10.1055/S-2003-37024
Gomisin F	51003489	Click to see CC=C(C)C(=O)OC1C2=CC3=C(C(=C2C4=C(C(=C(C=C4CC(C1(C)O)C)OC)OC)OC)OC)OCO3	514.60	unknown	via CMAUP database
Gomisin G	14992067	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC	536.60	unknown	https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/
Gomisin H	5317803	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)O)OC)OC	418.50	unknown	https://doi.org/10.1016/J.CHROMA.2008.09.070
Gomisin J	3001686	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)O)OC)OC)OC)OC)O	388.50	unknown	https://doi.org/10.1016/0040-4020(95)00701-9 https://doi.org/10.1248/CPB.27.1583 https://doi.org/10.1248/CPB.26.682 https://doi.org/10.1055/S-0029-1185685 https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1039/C1AN15527J https://doi.org/10.1021/NP0503707
Gomisin K1	78385003	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)O	402.50	unknown	https://doi.org/10.1248/BPB.22.265
Gomisin K2, (+)-	5317805	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)O	402.50	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1248/CPB.36.3974
Gomisin L1, (-)-	5317806	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)O)OC)OCO3	386.40	unknown	https://doi.org/10.1248/BPB.22.265
Gomisin L2, (-)-	5317807	Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3CC1C)OCO4)OC)OC)OC)O	386.40	unknown	via CMAUP database
Gomisin M1, (+/-)-	128150	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)O)OC)OCO3	386.40	unknown	https://doi.org/10.1016/J.CHROMA.2008.09.070 https://doi.org/10.1248/CPB.40.1191
Gomisin M2, (+)-	14992068	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)OC)O)OCO3	386.40	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1248/CPB.40.1191
gomisin N	158103	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)OC)OC)OCO3	400.50	unknown	https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1055/S-2003-37024 https://doi.org/10.1248/CPB.27.2695 https://doi.org/10.1080/10575639808048288 https://doi.org/10.1016/S0021-9673(00)90280-2 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1016/S0021-9673(01)00556-8 https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861
Gomisin O	5317808	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)O)OC)OC)OC)OC)OCO3	416.50	unknown	https://doi.org/10.1248/CPB.27.2695
Gomisin R	11516888	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1C)O)OCO5)OC)OC)OCO3	400.40	unknown	via CMAUP database
Gomisin S	14213995	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)O)OC)OC)OC)OC)OC)O	418.50	unknown	https://doi.org/10.1248/CPB.36.3974
Gomisin-J	3001657	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)O)OC)OC)OC)OC)O	388.50	unknown	via CMAUP database
Isoschisandrin	10455507	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC	432.50	unknown	https://doi.org/10.1016/0031-9422(88)83143-1 https://doi.org/10.1016/S0021-9673(96)00685-1
Marlignan L	46832527	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)O)OC)OC)OC)OC)O	404.50	unknown	via CMAUP database
Propinquanin F	102176162	Click to see CC=C(C)C(=O)OC1=C2C(=CC(=C1OC)OC)CC(C(C(C3=CC(=C(C(=C32)OC)OC)OC)O)C)C	500.60	unknown	via CMAUP database
R(+)-Gomisin M1	5321170	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)O)OC)OCO3	386.40	unknown	via CMAUP database
Rubrisandrin A	16099402	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)O)OC)OC)O	388.50	unknown	https://doi.org/10.1055/S-0030-1249861
Rubschisandrin	174277	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)OC)OC)OCO3	400.50	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1271/BBB.90597
Schisandrene	11613047	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1=C)OC(=O)C6=CC=CC=C6)OCO5)OC)OC)OCO3	502.50	unknown	via CMAUP database
Schisandrin	3001664	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC	432.50	unknown	https://doi.org/10.1111/J.1745-7254.2008.00838.X https://doi.org/10.1055/S-2003-37024 https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1055/S-2007-967120 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264271/ https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1007/BF00563602 https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1016/S0021-9673(00)90280-2 https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1016/S0021-9673(01)00556-8 https://doi.org/10.1055/S-0030-1249861 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1021/NP0503707
schisandrin A	155256	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)OC)OC)OC	416.50	unknown	https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1055/S-2003-37024 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1021/NP0503707 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861
Schisandrin B	108130	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1C)OC)OC)OC)OC)OCO3	400.50	unknown	https://doi.org/10.1055/S-2003-37024 https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1038/JA.2015.48 https://doi.org/10.1016/0009-2797(82)90047-3 https://doi.org/10.1016/S0944-7113(97)80072-4 https://doi.org/10.1007/S00280-005-0133-1 https://doi.org/10.1211/JPP.60.3.0017 https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1055/S-0029-1185685 https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861 https://doi.org/10.1002/RCM.3931 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1016/J.CHROMA.2008.09.070 https://doi.org/10.1021/NP0503707
Schisandrin C	443027	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4CC1C)OCO5)OC)OC)OCO3	384.40	unknown	https://doi.org/10.1111/J.1745-7254.2008.00838.X https://doi.org/10.1055/S-2003-37024 https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1016/0009-2797(82)90047-3 https://doi.org/10.1016/S0944-7113(97)80072-4 https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861 https://doi.org/10.1016/S0021-9673(01)00556-8 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1055/S-2007-969504 https://doi.org/10.1021/NP0503707
SchisandrinB	15608605	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1(C)O)OC)OC)OC)OC)OCO3	416.50	unknown	https://doi.org/10.1248/YAKUSHI1947.103.7_743 https://doi.org/10.1055/S-2007-969504 https://doi.org/10.1016/S0021-9673(00)90280-2 https://doi.org/10.1016/S0021-9673(01)00556-8 https://doi.org/10.1016/S0021-9673(96)00685-1
schisandrinC	119112	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4CC1C)OCO5)OC)OC)OCO3	384.40	unknown	https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1055/S-2003-37024 https://doi.org/10.1111/J.1745-7254.2008.00838.X https://doi.org/10.1055/S-0029-1185685 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1021/NP0503707 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861 https://doi.org/10.3892/IJMM_00000258
Schisandrol A	11102092	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC	432.50	unknown	https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1016/0009-2797(82)90047-3
Schisanhenol	73057	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1C)OC)OC)OC)O)OC)OC	402.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1016/S0021-9673(96)00685-1
SchisanlignaolD	15658448	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1C)O)OCO5)OC)OC)OCO3	400.40	unknown	via CMAUP database
Schisantherin	101769189	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	536.60	unknown	via CMAUP database
Schisantherin A	151529	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	536.60	unknown	https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1016/S0021-9673(00)90280-2 https://doi.org/10.1002/RCM.3931 https://doi.org/10.1007/S00280-005-0133-1 https://doi.org/10.1016/S0021-9673(96)00685-1
Schisantherin B	6438572	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC	514.60	unknown	https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1016/J.BMCL.2007.11.082 https://doi.org/10.1016/0009-2797(82)90047-3 https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1016/S0021-9673(96)00685-1 https://doi.org/10.1080/10575639808048288 https://doi.org/10.1016/S0021-9673(00)90280-2 https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1002/RCM.3931
Schisantherin C	6443826	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC	514.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/
Schisantherin D	163067	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1(C)O)OC(=O)C6=CC=CC=C6)OCO5)OC)OC)OCO3	520.50	unknown	via CMAUP database
Schisantherin E	13844274	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1(C)O)OC(=O)C4=CC=CC=C4)OC)OC)OC)OC)OC)O	538.60	unknown	via CMAUP database
Schisantherin-D	5480967	Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1(C)O)OC(=O)C6=CC=CC=C6)OCO5)OC)OC)OCO3	520.50	unknown	via CMAUP database
Schizandrer A	163338	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3	536.60	unknown	via CMAUP database
Schizandrin	23915	Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC	432.50	unknown	https://doi.org/10.1111/J.1745-7254.2008.00838.X https://doi.org/10.1055/S-2003-37024 https://doi.org/10.1248/BPB.22.265 https://doi.org/10.1055/S-2007-967120 https://doi.org/10.1016/0009-2797(82)90047-3 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264271/ https://doi.org/10.1007/S00280-005-0133-1 https://doi.org/10.1002/PTR.2907 https://doi.org/10.1248/CPB.40.1191 https://doi.org/10.1055/S-0029-1185685 https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0030-1249861 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1021/NP0503707
Schizandrol B	68781	Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1(C)O)OC)OC)OC)OC)OCO3	416.50	unknown	https://doi.org/10.1007/S00280-005-0133-1 https://doi.org/10.1016/0009-2797(82)90048-5 https://doi.org/10.1055/S-0029-1185685 https://doi.org/10.1016/0009-2797(82)90047-3 https://doi.org/10.1016/J.BMCL.2011.08.065 https://doi.org/10.1021/NP0503707
Tigloylgomisin H	5318766	Click to see CC=C(C)C(=O)OC1=C2C(=CC(=C1OC)OC)CC(C(CC3=CC(=C(C(=C32)OC)OC)OC)(C)O)C	500.60	unknown	https://doi.org/10.1271/BBB.90597 https://doi.org/10.1055/S-0029-1185685 https://doi.org/10.1021/NP0503707
Tigloylgomisin O	5318776	Click to see CC=C(C)C(=O)OC1C(C(CC2=CC3=C(C(=C2C4=C(C(=C(C=C14)OC)OC)OC)OC)OCO3)C)C	498.60	unknown	via CMAUP database
Tigloylgomisin P	5318785	Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3CC(C1(C)O)C)OCO4)OC)OC)OC)OC	514.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/ https://doi.org/10.1055/S-0030-1249861

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Schisandra chinensis

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