Alpinia zerumbet

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff196d7c65810086672
Scientific name	Alpinia zerumbet
Authority	(Pers.) B.L.Burtt & R.M.Sm.
First published in	Notes Roy. Bot. Gard. Edinburgh 31 (2):204. (1972)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Alpinia fimbriata	Gagnep.	Bull. Soc. Bot. France 51:447. (1905)
Alpinia fluvitialis	Hayata	Icon. pl. formosan. 227
Alpinia schumanniana	Valeton	Bull. Inst. Bot. Buitenzorg 20:84. (1904)
Alpinia speciosa	(J.C.Wendl.) K.Schum.	Fl. Kais. Wilh. Land 29
Alpinia nutans var. longiramosa	Gagnep.	Bull. Soc. Bot. France 48: 87. 1902
Amomum nutans	(Andrews) Schult.	in Roemer, J.J. & Schultes, J.A., Mant. I 40
Catimbium nutans	(Andrews) T.Lestib.	Ann. Sci. Nat. Bot., II 15:342. (1841)
Catimbium speciosum	(J.C.Wendl.) Holttum	Gard. Bull. Singapore 13:152. (1950)
Costus zerumbet	Pers.	Syn. Pl. 1: 3 (1805)
Languas schumanniana	(Valeton) Sasaki	Trans. Nat. Hist. Soc. Taiwan 14:23. (1924)
Languas speciosa	(J.C.Wendl.) Small	Fl. s. e. U. S. Ed. 2 307
Renealmia nutans	Andrews	Bot. repos., pl.360
Renealmia spectabilis	Rusby	Mem. New York Bot. Gard. 7:218. (1927)
Zerumbet speciosum	J.C.Wendl.	Sert. hannov. 3, pl.19
Alpinia speciosa var. longiramosa	Gagnep.	Bull. Soc. Bot. France 48: 87. 1901

Common names Top

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Filter by language:

Language	Common/alternative name
English	shellplant
ami	lengac
Arabic	خولنجان مموه
cdo	tòng-guōi-niŏh-chéu
Czech	galgán velký
Finnish	isogalangajuuri
French	gingembre coquille
Japanese	ゲットウ
Japanese	月桃
Japanese	サンニン
Malayalam	മലയിഞ്ചി
Polish	alpinia zwyczajna
pwn	ngat
Russian	Альпиния церумбет
szy	lalengac
tay	bsyaw
Vietnamese	riềng đẹp
Chinese	虎子花
Chinese	艷山薑
Chinese	枸薑
Chinese	土砂仁
Chinese	月桃
Chinese	艳山姜
Chinese	垂花山姜
Chinese	大良薑
Chinese	良薑
Chinese	大良姜
Chinese	大草寇
Chinese	枸姜
Chinese	箭杆风
Chinese	熊竹兰
Chinese	熊竹蘭
Chinese	良姜
Chinese	良恙
Chinese	艳山红
Chinese	艷山紅
Chinese	草寇
Chinese	草扣

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
- Middle Atlantic Ocean
  - Ascension
  - Saint Helena

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Japan
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Malaya
  - Philippines
- Papuasia
  - Bismarck Archipelago
  - Solomon Islands

Northern America click to expand
- Southeastern U.S.A.
  - Florida

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
- South-central Pacific
  - Cook Islands
  - Tubuai Islands
- Southwestern Pacific
  - Fiji
  - New Caledonia
  - Vanuatu

Southern America click to expand
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - Honduras
- Western South America
  - Bolivia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000338850
UNII	TW1B5UAE5T
Florida Plant Atlas	427
USDA Plants	ALZE
Tropicos	34500581
INPN	447930
KEW	urn:lsid:ipni.org:names:872083-1
The Plant List	kew-219119
Missouri Botanical Garden	287609
Open Tree Of Life	55230
NCBI Taxonomy	97723
Nature Serve	2.160830
IUCN Red List	13507110
IPNI	872083-1
iNaturalist	154776
GBIF	5301979
Freebase	/m/06drtp
EPPO	AIIZE
EOL	1126734
USDA GRIN	101036
Wikipedia	Alpinia_zerumbet
CMAUP	NPO23660

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

Essential oil of Piper hispidum (Piperaceae) has efficacy against monogeneans, and effects on hematology and gill histology of Colossoma macropomum

Alves CM, Baia RR, Farias VA, Farias MA, de Souza FL, Videira MN, Chagas FC, Yoshioka ET, Tavares-Dias M

Rev Bras Parasitol Vet

11-Dec-2023

PMCID:	PMC10782507
doi:	10.1590/S1984-29612024001
PMID:	38088653

Age-dependent dendrobine biosynthesis in Dendrobium nobile: insights into endophytic fungal interactions

Zhao Y, Ji X, Liu X, Qin L, Tan D, Wu D, Bai C, Yang J, Xie J, He Y

Front Microbiol

08-Dec-2023

PMCID:	PMC10749937
doi:	10.3389/fmicb.2023.1294402
PMID:	38149273

Evidence for Dicot Plants as Alternative Hosts of Banana Bunchy Top Virus and Its Alphasatellites in South-East Asia

Guyot V, Ly NS, Trieu TD, Insisiengmay O, Zhang T, Iskra-Caruana ML, Pooggin MM

Pathogens

28-Oct-2023

PMCID:	PMC10675457
doi:	10.3390/pathogens12111289
PMID:	38003755

Comparison of Metabolites and Species Classification of Thirteen Zingiberaceae Spices Based on GC–MS and Multi-Spectral Fusion Technology

Wen H, Yang T, Yang W, Yang M, Wang Y, Zhang J

Foods

10-Oct-2023

PMCID:	PMC10606731
doi:	10.3390/foods12203714
PMID:	37893607

Methyleugenol Has an Antidepressant Effect in a Neuroendocrine Model: In Silico and In Vivo Evidence

Oliveira MC, Cavalcante IL, de Araújo AN, Ferreira dos Santos AM, de Menezes RP, Herrera-Acevedo C, Ferreira de Sousa N, de Souza Aquino J, Barbosa-Filho JM, de Castro RD, Almeida RN, Scotti L, Scotti MT, Da Silva Stiebbe Salvadori MG

Pharmaceuticals (Basel)

04-Oct-2023

PMCID:	PMC10610402
doi:	10.3390/ph16101408
PMID:	37895879

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Larvicidal Potential of Caribbean Plants

Layne-Yarde RN, Sandiford SL

Biomed Res Int

26-Aug-2023

PMCID:	PMC10474962
doi:	10.1155/2023/5518863
PMID:	37663786

Biochar improves the growth and physiological traits of alfalfa, amaranth and maize grown under salt stress

Jabborova D, Abdrakhmanov T, Jabbarov Z, Abdullaev S, Azimov A, Mohamed I, AlHarbi M, Abu-Elsaoud A, Elkelish A

PeerJ

18-Aug-2023

PMCID:	PMC10441527
doi:	10.7717/peerj.15684
PMID:	37609438

Potential Application of the Plant-Derived Essential Oils for Atherosclerosis Treatment: Molecular Mechanisms and Therapeutic Potential

Dabravolski SA, Sukhorukov VN, Melnichenko AA, Khotina VA, Orekhov AN

Molecules

26-Jul-2023

PMCID:	PMC10420188
doi:	10.3390/molecules28155673
PMID:	37570643

Immunomodulatory effects and mechanisms of the extracts and secondary compounds of Zingiber and Alpinia species: a review

Yuandani, Jantan I, Haque MA, Rohani AS, Nugraha SE, Salim E, Septama AW, Juwita NA, Khairunnisa NA, Nasution HR, Utami DS, Ibrahim S

Front Pharmacol

18-Jul-2023

PMCID:	PMC10391552
doi:	10.3389/fphar.2023.1222195
PMID:	37533631

Anticancer Potential of Natural Chalcones: In Vitro and In Vivo Evidence

Michalkova R, Mirossay L, Kello M, Mojzisova G, Baloghova J, Podracka A, Mojzis J

Int J Mol Sci

19-Jun-2023

PMCID:	PMC10299153
doi:	10.3390/ijms241210354
PMID:	37373500

Modulating Effects of Zingiberaceae Phenolic Compounds on Neurotrophic Factors and Their Potential as Neuroprotectants in Brain Disorders and Age-Associated Neurodegenerative Disorders: A Review

Razak AM, Tan JK, Mohd Said M, Makpol S

Nutrients

30-May-2023

PMCID:	PMC10255673
doi:	10.3390/nu15112564
PMID:	37299526

Bobai Hakka weaving: plant diversity, traditional culture, and a model for rural revitalization

Liufu Y, Hu R, Fu Q, Luo B

Environ Dev Sustain

20-May-2023

PMCID:	PMC10199282
doi:	10.1007/s10668-023-03340-8
PMID:	37363008

Ethnobotanical study on herbal tea drinks in Guangxi, China

Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C

J Ethnobiol Ethnomed

31-Mar-2023

PMCID:	PMC10064729
doi:	10.1186/s13002-023-00579-3
PMID:	37004116

Mode of Antifungal Action of Daito-Gettou (Alpinia zerumbet var. exelsa) Essential Oil against Aspergillus brasiliensis

Okazaki K, Sumitani H, Takahashi K, Isegawa Y

Foods

18-Mar-2023

PMCID:	PMC10048414
doi:	10.3390/foods12061298
PMID:	36981224

Phytochemical Profile Top

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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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Maesol	128958	Click to see CC1=C(C=C(C=C1OC)CCCCCCCCCCCCC2=CC(=C(C(=C2)OC)C)O)O	442.60	unknown	https://doi.org/10.1016/J.PHYMED.2009.04.007
> Benzenoids / Tetralins
(4S)-10-Nor-calamenen-10-one	73350586	Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C	202.29	unknown	via CMAUP database
Oxyphyllenotriol A	51041015	Click to see CC(C)C1=C2C(C(CCC2=C(C=C1)O)(C)O)O	236.31	unknown	via CMAUP database
Oxyphyllone G	51041016	Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O	218.29	unknown	via CMAUP database
> Hydrocarbon derivatives / Tropones
Nezukone	570867	Click to see CC(C)C1=CC=CC(=O)C=C1	148.20	unknown	https://doi.org/10.5650/JOS1956.43.424
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[1,3-Dihydroxy-2-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]propyl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11972318	Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC)O)OC)C=CCO	568.60	unknown	https://doi.org/10.5650/JOS1956.44.1012
Citrusin B	131752580	Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC)O)OC)C=CCO	568.60	unknown	https://doi.org/10.5650/JOS1956.44.1012
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid	5280934	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(+)-Zerumin A	10781840	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C	318.40	unknown	https://doi.org/10.1016/0031-9422(96)00887-4
(2E)-2-[2-[(1S,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]butanedial	163068844	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C	302.50	unknown	https://doi.org/10.1016/J.FOODCHEM.2011.04.034
2-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethylidene]butanedial	75094027	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C	302.50	unknown	https://doi.org/10.1248/CPB.28.3452
2-[2-[(1S,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]butanedial	163068847	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C	302.50	unknown	https://doi.org/10.1016/J.FOODCHEM.2011.04.034
5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-formylpent-3-enoic acid	73073987	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C	318.40	unknown	https://doi.org/10.1016/0031-9422(96)00887-4
Labda-8(17),12-diene-15,16-dial	11077520	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C	302.50	unknown	https://doi.org/10.1248/CPB.28.3452
Zerumin A	11723433	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C	318.40	unknown	https://doi.org/10.1016/0031-9422(96)00887-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
3-[2-[(4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]furan	138113847	Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=COC=C3)C)C	284.40	unknown	https://doi.org/10.1016/0031-9422(96)00887-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698417
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698417
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1021/NP50035A037
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Cuminaldehyde	326	Click to see CC(C)C1=CC=C(C=C1)C=O	148.20	unknown	https://doi.org/10.1080/10412905.1993.9698218
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1021/NP50035A037
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698218
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1021/NP50035A037
(1R)-endo-(+)-Fenchyl alcohol	6997371	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698417
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol	12314318	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1021/NP50035A037 https://doi.org/10.1080/10412905.1994.9698417
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane	6429260	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698218
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1080/10412905.1993.9698218
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1021/NP50035A037
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	https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1021/NP50035A037
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1080/10412905.1994.9698417
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.5650/JOS1956.43.424 https://doi.org/10.1080/10412905.1994.9698417
cis-Thujanol	3034320	Click to see CC1C2CC2(CC1O)C(C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698218
Fenchol	15406	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698417
Fenchone	14525	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	https://doi.org/10.5650/JOS1956.43.424 https://doi.org/10.1080/10412905.1994.9698417
Myrtenal	61130	Click to see CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1021/NP50035A037 https://doi.org/10.1080/10412905.1994.9698417
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1080/10412905.1994.9698417
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1021/NP50035A037 https://doi.org/10.1080/10412905.1994.9698417
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
Thujanol	6432367	Click to see CC1C2CC2(CC1O)C(C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698218
Thujone	261491	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1021/NP50035A037
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698417
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol	71423340	Click to see CC(C)C1=CC(C(CC1)(C)O)O	170.25	unknown	via CMAUP database
2-Cyclohexen-1-ol, 3-methyl-6-(1-methylethyl)-, (1R,6S)-rel-	85567	Click to see CC1=CC(C(CC1)C(C)C)O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698218
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1046/J.1472-8206.2003.00150.X https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T
Carvone, (+)-	16724	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1021/NP50035A037
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1021/NP50035A037
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1016/J.PHYMED.2004.04.006 https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
trans-Piperitol	85568	Click to see CC1=CC(C(CC1)C(C)C)O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698218
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one	76285513	Click to see CC1CCC2C1C3(C(=CC(=O)C2(O3)C)C(C)C)O	250.33	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	https://doi.org/10.1080/10412905.1994.9698417
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1248/CPB.44.1603
(E)-4-[(1S,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]but-3-en-2-one	163017578	Click to see CC(=O)C=CC1C(=C)CCC2C1(CCCC2(C)C)C	260.40	unknown	https://doi.org/10.1248/CPB.28.3452
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	https://doi.org/10.1080/10412905.1993.9698218
15,16-Dinor-8(17),11-labdadien-13-one	13994560	Click to see CC(=O)C=CC1C(=C)CCC2C1(CCCC2(C)C)C	260.40	unknown	https://doi.org/10.1248/CPB.28.3452 https://doi.org/10.1016/0031-9422(96)00887-4
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698218
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1080/10412905.1993.9698218
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698218
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1080/10412905.1993.9698218 https://doi.org/10.1021/NP50035A037
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T https://doi.org/10.1080/10412905.1993.9698218
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/J.PHYMED.2004.04.006
cis-Nerolidol	5320128	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1080/10412905.1994.9698417
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
Guaiol	227829	Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1994.9698417
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417 https://doi.org/10.1080/10412905.1993.9698218
Nerolidol	8888	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1248/CPB.44.1603 https://doi.org/10.1080/10412905.1993.9698218
Oxyphyllanene D	57396910	Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O	250.33	unknown	via CMAUP database
Oxyphyllol E	51041018	Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O	250.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	91746456	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
Alloaromadendren	91746537	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
Aromadendrene	91354	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698417
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(11S)-Nootkatone-11,12-diol	15601439	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(CO)O)C	252.35	unknown	via CMAUP database
(1S)-1,2,3,4,4a,5,6,7-Octahydro-4beta,4abeta-dimethyl-6alpha-(1-methylethenyl)naphthalene-1beta-ol	44576208	Click to see CC1CCC(C2=CCC(CC12C)C(=C)C)O	220.35	unknown	via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione	72715093	Click to see CC1CC(=O)C=C2C1(CC(CC2=O)C(=C)C)C	232.32	unknown	via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one	117654813	Click to see CC1CC(=O)C=C2C1(C=C(CC2)C(=O)C)C	218.29	unknown	via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one	89960876	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(C)O)C	236.35	unknown	via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one	53249021	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)CO)C	234.33	unknown	via CMAUP database
(4R)-4beta,4abeta-Dimethyl-6alpha-isopropenyl-8alpha-hydroxy-2,3,4,4a,5,6,7,8-octahydronaphthalene-2-one	11651584	Click to see CC1CC(=O)C=C2C1(CC(CC2O)C(=C)C)C	234.33	unknown	via CMAUP database
Nootkatene	25200342	Click to see CC1CC=CC2=CCC(CC12C)C(=C)C	202.33	unknown	via CMAUP database
Nootkatol	182645	Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O	220.35	unknown	via CMAUP database
Nootkatone	1268142	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C	218.33	unknown	via CMAUP database
oxyphyllol C	10857540	Click to see CC1CCC(C2(C1(CC(CC2)C(=C)C)C)O)O	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol	15560338	Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C	222.37	unknown	via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol	14076604	Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C	220.35	unknown	via CMAUP database
(4aS,7S,8R)-8-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one	57393410	Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=C)C)O	234.33	unknown	via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one	57335617	Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O	234.33	unknown	via CMAUP database
10-epi-gamma-Eudesmol	6430754	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698218
7-Epi-Teucrenone B	57393409	Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C	234.33	unknown	via CMAUP database
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1248/CPB.44.1603 https://doi.org/10.1080/10412905.1993.9698218
beta-Selinene	442393	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698218
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698218
Ligucyperonol	14681770	Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(=C)C	234.33	unknown	via CMAUP database
Oxyphyllol A	637451	Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C	220.35	unknown	via CMAUP database
Rel-Oxyphyllanene E	57400339	Click to see CC(=C)C1(CCC2(CCC(C(=C)C2C1)O)C)O	236.35	unknown	via CMAUP database
Teucrenone	10105443	Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C	234.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2S)-4-[(1R)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-hydroxyethyl]-2-hydroxy-2H-furan-5-one	162957455	Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CC(OC3=O)O)O)C)C	334.40	unknown	https://doi.org/10.1016/0031-9422(96)00887-4
4-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-1-hydroxyethyl]-2-hydroxy-2H-furan-5-one	73234904	Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CC(OC3=O)O)O)C)C	334.40	unknown	https://doi.org/10.1016/0031-9422(96)00887-4
Zerumin	54734314	Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=C(COC3=O)O)C)C	316.40	unknown	https://doi.org/10.1080/10575639508043183
zerumin B	16079165	Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CC(OC3=O)O)O)C)C	334.40	unknown	https://doi.org/10.1016/0031-9422(96)00887-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione	71681246	Click to see CC1=CC(=O)CC2(C1CC3=C(C(=O)OC3C2)C)C	246.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosteryl palmitate	9852570	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C	653.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.5650/JOS1956.44.1012
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.5650/JOS1956.44.1012
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.5650/JOS1956.44.1012
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.5650/JOS1956.44.1012
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.5650/JOS1956.44.1012
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
(2S,3R,4S)-3-hydroxy-2,4-dimethyl-6-[[(E)-2-methylpent-2-enoyl]amino]-5-oxohexanoic acid	163115391	Click to see CCC=C(C)C(=O)NCC(=O)C(C)C(C(C)C(=O)O)O	285.34	unknown	https://doi.org/10.1248/CPB.28.3452 https://doi.org/10.1016/0031-9422(96)00887-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
2-Hexanol	12297	Click to see CCCCC(C)O	102.17	unknown	https://doi.org/10.1080/10412905.1994.9698417
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(4-hydroxy-3-methoxyphenoxy)-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	10528648	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(OC(C(C2O)O)OC3=CC(=C(C=C3)O)OC)CO)O	478.40	unknown	https://doi.org/10.1021/JF991294E
[4,5-Dihydroxy-6-(4-hydroxy-3-methoxyphenoxy)-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	85173008	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(OC(C(C2O)O)OC3=CC(=C(C=C3)O)OC)CO)O	478.40	unknown	https://doi.org/10.1021/JF991294E
Coniferin	5280372	Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O	342.34	unknown	https://doi.org/10.5650/JOS1956.44.1012
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.5650/JOS1956.44.1012
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1080/10412905.1994.9698417
Octanal	454	Click to see CCCCCCCC=O	128.21	unknown	https://doi.org/10.1080/10412905.1994.9698417
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone	102054514	Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O	222.32	unknown	via CMAUP database
Spiro[4.4]nonan-2-one	549163	Click to see C1CCC2(C1)CCC(=O)C2	138.21	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one	71681103	Click to see CC1=CC(=O)CC2(C1(CC(CC2)C(=O)C)O)C	236.31	unknown	via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one	71681245	Click to see CC1=C2C=C(CCC2(CCC1=O)C)C(=O)C	218.29	unknown	via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one	15153217	Click to see CC12CCCC(C1=CC(=O)CC2)(C)O	194.27	unknown	via CMAUP database
OxyphyllaneneA	122402647	Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C	192.25	unknown	via CMAUP database
Oxyphyllenodiol A	10082923	Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O	238.32	unknown	via CMAUP database
Oxyphyllenodiol B	5279294	Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O	238.32	unknown	via CMAUP database
Oxyphyllenone A	10262534	Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O	210.27	unknown	via CMAUP database
Oxyphyllenone B	44310512	Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O	210.27	unknown	via CMAUP database
Oxyphyllone C	44255203	Click to see CC(C)C1CCC(=O)C2=C1C3C(O3)(CC2)C	220.31	unknown	via CMAUP database
Teuhetenone A	15153216	Click to see CC12CCCC(C1=CC(=O)CC2)(C)O	194.27	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Undecanone	8163	Click to see CCCCCCCCCC(=O)C	170.29	unknown	https://doi.org/10.1002/1099-1573(200011)14:7<549::AID-PTR623>3.0.CO;2-T
> Organoheterocyclic compounds / Epoxides
(1R,11S)-1,5,5,8-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene	132587053	Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C	220.35	unknown	https://doi.org/10.1248/CPB.44.1603
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene	12014673	Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C	236.35	unknown	via CMAUP database
1,5,5,8-Tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene	23274265	Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C	220.35	unknown	https://doi.org/10.1080/10412905.1993.9698218
Humulene epoxyde	5463721	Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C	220.35	unknown	https://doi.org/10.1248/CPB.44.1603
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C	57335616	Click to see CC1=C2C3C(O3)(CCC2(CCC1=O)C)C(=O)C	234.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
3-Phenyl-2-propenoic acid methyl ester	7644	Click to see COC(=O)C=CC1=CC=CC=C1	162.18	unknown	https://doi.org/10.1016/0031-9422(81)83082-8
Methyl cinnamate	637520	Click to see COC(=O)C=CC1=CC=CC=C1	162.18	unknown	https://doi.org/10.1016/0031-9422(81)83082-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[6-Ethoxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	85259201	Click to see CCOC1C(C(C(C(O1)CO)OC(=O)C=CC2=CC(=C(C=C2)O)OC)O)O	384.40	unknown	https://doi.org/10.1021/JF991294E
coumaroyl(3-OMe)(-4)Glc(b)-O-Et	10762566	Click to see CCOC1C(C(C(C(O1)CO)OC(=O)C=CC2=CC(=C(C=C2)O)OC)O)O	384.40	unknown	https://doi.org/10.1021/JF991294E
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one	6440365	Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O	310.40	unknown	via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one	72708396	Click to see COC1=CC=C(C=C1)CCCCC(=O)CCC2=C(C(=C(C=C2)O)OC)O	358.40	unknown	via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one	72708395	Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O	328.40	unknown	via CMAUP database
Yakuchinone-A	133145	Click to see COC1=C(C=CC(=C1)CCC(=O)CCCCC2=CC=CC=C2)O	312.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin	182232	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1021/JF991294E
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1021/JF991294E
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1002/(SICI)1099-1573(199809)12:6<442::AID-PTR320>3.0.CO;2-Y
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1002/(SICI)1099-1573(199809)12:6<442::AID-PTR320>3.0.CO;2-Y https://doi.org/10.1021/JF991294E
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R)-	667544	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1076/PHBI.41.1.7.14703
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1016/J.BMC.2009.07.041
5,7-Dihydroxyflavanone	238782	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1016/J.BMC.2009.07.041
Naringenin	439246	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.1016/J.BMC.2009.07.041
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	https://doi.org/10.1016/J.BMC.2009.07.041
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin	5281607	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one	5378823	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O	314.29	unknown	via CMAUP database
Izalpinin	5318691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O	284.26	unknown	via CMAUP database
Kaempferide	5281666	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol-3-O-rutinoside	5318767	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	594.50	unknown	https://doi.org/10.1002/(SICI)1099-1573(199809)12:6<442::AID-PTR320>3.0.CO;2-Y
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	https://doi.org/10.1002/(SICI)1099-1573(199809)12:6<442::AID-PTR320>3.0.CO;2-Y
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide	5280862	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	300.26	unknown	https://doi.org/10.1016/J.BMC.2009.07.041
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
7-Hydroxy-5-methoxy-2-phenylchroman-4-one	4053302	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1016/S0031-9422(00)84672-5 https://doi.org/10.1016/0031-9422(81)83082-8
Alpinetin	154279	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O	270.28	unknown	https://doi.org/10.1016/S0031-9422(00)84672-5 https://doi.org/10.1016/0031-9422(81)83082-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Kavalactones
(1S,6R,7S,8S)-2-methoxy-7-(4-methoxy-6-oxo-pyran-2-yl)-8-phenyl-6-[(E)-styryl]-5-oxabicyclo[4.2.0]oct-2-en-4-one	57400399	Click to see COC1=CC(=O)OC(=C1)C2C(C3C2(OC(=O)C=C3OC)C=CC4=CC=CC=C4)C5=CC=CC=C5	456.50	unknown	https://doi.org/10.1016/S0031-9422(00)97005-5
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)-	160673	Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2	230.26	unknown	https://doi.org/10.1021/JF104813K https://doi.org/10.1016/J.FOODCHEM.2011.04.034 https://doi.org/10.1016/S0031-9422(00)97005-5 https://doi.org/10.1016/0031-9422(81)83082-8
4-Methoxy-6-(2-phenylethenyl)-2h-pyran-2-one	164901	Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2	228.24	unknown	https://doi.org/10.1016/J.FOODCHEM.2011.04.034 https://doi.org/10.1021/JF104813K https://doi.org/10.1016/0031-9422(81)83082-8 https://doi.org/10.1016/J.BMC.2009.07.041
5-Methoxy-8-(4-methoxy-6-oxopyran-2-yl)-7-phenyl-1-(2-phenylethenyl)-2-oxabicyclo[4.2.0]oct-4-en-3-one	4868230	Click to see COC1=CC(=O)OC(=C1)C2C(C3C2(OC(=O)C=C3OC)C=CC4=CC=CC=C4)C5=CC=CC=C5	456.50	unknown	https://doi.org/10.1016/S0031-9422(00)97005-5
Demethoxyyangonin	5273621	Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2	228.24	unknown	https://doi.org/10.1016/0031-9422(81)83082-8 https://doi.org/10.1016/J.BMC.2009.07.041 https://doi.org/10.1016/J.FOODCHEM.2011.04.034 https://doi.org/10.1021/JF104813K
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-(2-Hydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one	270058	Click to see COC1=CC(=C(C(=C1)OC)C(=O)CCC2=CC=CC=C2)O	286.32	unknown	https://doi.org/10.1016/0031-9422(81)83082-8
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one	154102	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O	270.28	unknown	https://doi.org/10.1016/0031-9422(81)83082-8 https://doi.org/10.1016/J.BMC.2009.07.041
6'-Hydroxy-2',4'-dimethoxychalcone	242589	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=CC=C2)O	284.31	unknown	https://doi.org/10.1016/0031-9422(81)83082-8
Cardamonin	641785	Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O	270.28	unknown	https://doi.org/10.1016/0031-9422(81)83082-8 https://doi.org/10.1016/J.BMC.2009.07.041
CID 460718	460718	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O	256.25	unknown	https://doi.org/10.1016/J.BMC.2009.07.041
Flavokawain B	5356121	Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=CC=C2)O	284.31	unknown	https://doi.org/10.1076/PHBI.41.1.7.14703 https://doi.org/10.1016/0031-9422(81)83082-8
Pinocembrin chalcone	6474295	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O	256.25	unknown	https://doi.org/10.1016/J.BMC.2009.07.041

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Alpinia zerumbet

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