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Schisandra chinensis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644003da5703e575244789
Scientific name Schisandra chinensis
Authority (Turcz.) Baill.
First published in Hist. Pl. 1: 148 (1868)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Schisandra chinensis, known in Chinese as Wu Wei Zi, has been a staple of traditional medicine for centuries. In the Han‑Chinese pharmacopeia, the dried fruit is boiled into a decoction or steeped as a tea to support liver function, boost stamina, and calm the mind (Chinese Pharmacopoeia, 2020). Korean practitioners similarly prepare a fruit tea and a bark decoction to treat chronic cough and to strengthen the spleen‑qi (Kim et al., 2015). In Japanese Kampo, the fruit is macerated in alcohol to produce a tincture used as an adaptogen for fatigue and as a mild sedative (Sato & Nakamura, 2018). Across these cultures, the fruit is the most common part used for infusions, while the bark and root are reserved for stronger decoctions, and the leaves are occasionally brewed as a light tea for digestive comfort.

A simple, safe way to enjoy Schisandra’s benefits is to make a fruit tea. Take 5 g of dried Schisandra berries and add them to 250 ml of freshly boiled water. Let the mixture steep for 5–10 minutes, then strain and sip. For a stronger tonic, simmer the berries for 20 minutes to produce a decoction; this yields a more concentrated dose of lignans. Pregnant women should avoid large quantities of Schisandra, as the fruit’s uterine stimulant properties are not fully understood, and high doses may affect liver metabolism. As with any herbal preparation, start with a small amount to gauge tolerance.

The therapeutic effects of Schisandra are largely attributed to its rich lignan profile, including schisandrin, schisandrin B, schisandrin C, gomisin A, and deoxyschisandrin, which have demonstrated hepatoprotective, antioxidant, and anti‑inflammatory activity in laboratory studies. Polysaccharides and flavonoids present in the fruit also contribute to its adaptogenic and immune‑modulating properties. These well‑established compounds provide a biochemical basis for the plant’s traditional use as a liver tonic and a stress reducer.

Today, Schisandra extracts are widely available in dietary supplement form, and ongoing research is exploring their potential in treating liver disease, enhancing cognitive function, and mitigating the side effects of chemotherapy. The plant remains a valued component of both traditional practice and modern wellness regimens, bridging ancient wisdom with contemporary science.

General Uses Top

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Common products:
- Fresh fruit used in culinary preparations: pickles, preserves, sauces, desserts, and as a flavoring in beverages.
- Dried fruit used in confectionery, jams, jellies, and as a natural colorant in food products.

Food and beverages (non-medicinal):
- Schisandra berries are incorporated into traditional Chinese and Korean beverages, including fermented wine, liqueur, and non‑alcoholic drinks.
- The fruit is used as a flavoring agent in sauces, desserts, and confectionery items such as candies and pastries.
- Dried berries are used in the production of Schisandra tea (non‑medicinal beverage) and as a natural sweetener in various food products.

Colorants and tanning:
- The high anthocyanin content of the berries provides a deep purple pigment used as a natural food colorant in sauces, desserts, and confectionery.
- The pigment is extracted using aqueous or ethanol‑based solvents and is used in food‑grade colorant applications.

Properties relevant to use:
- Anthocyanin concentration (~200–400 mg/100 g fresh weight) confers intense coloration and antioxidant properties.
- The fruit has a balanced sugar‑acid profile (sugar ~10–12 %, titratable acidity ~0.5–1.0 %) that makes it suitable for preserves and beverages.
- The berries contain volatile compounds such as linalool and terpenes that contribute to aroma in flavoring applications.

Standards and regulation:
- Food‑grade colorants derived from Schisandra must comply with the European Food Safety Authority (EFSA) guidelines for natural colorants and the U.S. Food and Drug Administration (FDA) GRAS status for food additives.
- The use of Schisandra fruit in beverages and confectionery is subject to national food safety regulations, including maximum residue limits for pesticides.

Sustainability and sourcing:
- Schisandra chinensis is cultivated in temperate regions of China, Korea, and Japan, with most commercial production occurring in China’s Yunnan and Sichuan provinces.
- Sustainable cultivation practices include organic farming and integrated pest management to reduce chemical inputs.
- Harvesting is typically performed in late summer to early autumn, and the fruit is processed within 24–48 hours to preserve quality.

Synonyms Top

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
Schisandra chinensis var. typica Nakai Fl. Sylv. Kor. 20: 105 (1933)
Schisandra repanda f. viridicarpa (Y.N.Lee) M.Kim Korean Endemic Pl. : 515 (2017)
Schisandra nigra f. viridicarpa (Y.N.Lee) M.Kim Korean Endemic Pl. : 292 (2004)

Common names Top

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

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
    • 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
Phenolic compound profiling and antioxidant potential of different types of Schisandra henryi in vitro cultures Jafernik K, Kubica P, Sharafan M, Kruk A, Malinowska MA, Granica S, Szopa A Appl Microbiol Biotechnol 07-May-2024
PMCID:PMC11076313
doi:10.1007/s00253-024-13159-6
PMID:38713216
Light-Emitting Diodes and Liquid System Affect the Caffeoylquinic Acid Derivative and Flavonoid Production and Shoot Growth of Rhaponticum carthamoides (Willd.) Iljin Skała E, Olszewska MA, Tabaka P, Kicel A Molecules 05-May-2024
PMCID:PMC11085107
doi:10.3390/molecules29092145
PMID:38731636
Impact of fundamental components of the Mediterranean diet on the microbiota composition in blood pressure regulation Zambrano AK, Cadena-Ullauri S, Ruiz-Pozo VA, Tamayo-Trujillo R, Paz-Cruz E, Guevara-Ramírez P, Frias-Toral E, Simancas-Racines D J Transl Med 03-May-2024
PMCID:PMC11067105
doi:10.1186/s12967-024-05175-x
PMID:38702795
Optimization of Composite Enzymatic Extraction, Structural Characterization and Biological Activity of Soluble Dietary Fiber from Akebia trifoliata Peel Song Y, Sun G, Wang D, Chen J, Lv J, Jiang S, Zhang G, Yu S, Zheng H Molecules 01-May-2024
PMCID:PMC11085559
doi:10.3390/molecules29092085
PMID:38731576
Potential Effects of Traditional Chinese Medicine in Anti-Aging and Aging-Related Diseases: Current Evidence and Perspectives Ding X, Ma X, Meng P, Yue J, Li L, Xu L Clin Interv Aging 01-May-2024
PMCID:PMC11070163
doi:10.2147/CIA.S447514
PMID:38706635
Integrative analysis of the metabolome and transcriptome provides insights into the mechanisms of lignan biosynthesis in Herpetospermum pedunculosum (Cucurbitaceae) Zhu Z, Chen D, Sun M, Xiao M, Huang P, Ren D, Yang Y, Zhang Z, Zhao Q, Li R BMC Genomics 29-Apr-2024
PMCID:PMC11059704
doi:10.1186/s12864-024-10306-1
PMID:38684979
Potential Targets of Natural Products for Improving Cardiac Ischemic Injury: The Role of Nrf2 Signaling Transduction Wang H, Han J, Dmitrii G, Zhang XA Molecules 26-Apr-2024
PMCID:PMC11085255
doi:10.3390/molecules29092005
PMID:38731496
Research progress on the role of macrophages in acne and regulation by natural plant products Zhao D, Wang Y, Wu S, Ji X, Gong K, Zheng H, Zhu M Front Immunol 26-Apr-2024
PMCID:PMC11082307
doi:10.3389/fimmu.2024.1383263
PMID:38736879
Based on HPLC and HS-GC-IMS Techniques, the Changes in the Internal Chemical Components of Schisandra chinensis (Turcz.) Baill. Fruit at Different Harvesting Periods Were Analyzed Sun B, Yan Y, Ma M, Wen J, He Y, Sun Y, Yuan P, Xu P, Yang Y, Zhao Z, Cao L, Lu W Molecules 22-Apr-2024
PMCID:PMC11055173
doi:10.3390/molecules29081893
PMID:38675712
Chinese medicine in the treatment of non-alcoholic fatty liver disease based on network pharmacology: a review Zheng S, Xue C, Li S, Zao X, Li X, Liu Q, Cao X, Wang W, Qi W, Zhang P, Ye Y Front Pharmacol 17-Apr-2024
PMCID:PMC11061375
doi:10.3389/fphar.2024.1381712
PMID:38694920
Gut microbiota-host lipid crosstalk in Alzheimer’s disease: implications for disease progression and therapeutics Luo YX, Yang LL, Yao XQ Mol Neurodegener 16-Apr-2024
PMCID:PMC11020986
doi:10.1186/s13024-024-00720-0
PMID:38627829
Efficacy of probiotics in hair growth and dandruff control: A systematic review and meta-analysis Yin CS, Minh Nguyen TT, Yi EJ, Zheng S, Bellere AD, Zheng Q, Jin X, Kim M, Park S, Oh S, Yi TH Heliyon 16-Apr-2024
PMCID:PMC11064082
doi:10.1016/j.heliyon.2024.e29539
PMID:38698995
Unraveling potential neuroprotective mechanisms of herbal medicine for Alzheimer’s diseases through comprehensive molecular docking analyses Alsenani F Saudi J Biol Sci 15-Apr-2024
PMCID:PMC11053229
doi:10.1016/j.sjbs.2024.103998
PMID:38681227
Examining the Pathogenesis of MAFLD and the Medicinal Properties of Natural Products from a Metabolic Perspective Fu Y, Wang Z, Qin H Metabolites 12-Apr-2024
PMCID:PMC11052500
doi:10.3390/metabo14040218
PMID:38668346
State-of-the-Art Review on Botanical Hybrid Preparations in Phytomedicine and Phytotherapy Research: Background and Perspectives Panossian A, Lemerond T, Efferth T Pharmaceuticals (Basel) 10-Apr-2024
PMCID:PMC11053582
doi:10.3390/ph17040483
PMID:38675443

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
> 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
3(R)-Deoxyharringtonine 56840949 Click to see 515.60 unknown via CMAUP database
> Allenes / Acyclic allenes
3,4-Octadiene, 7-methyl- 142131 Click to see 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 270.28 unknown https://doi.org/10.1248/BPB.22.265
https://doi.org/10.1248/CPB.40.1191
> Benzenoids / Benzene and substituted derivatives
Benzenepropanol 31234 Click to see 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
Benzamide, N-(4-amino-2,5-diethoxyphenyl)- 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 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 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 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1021/NP50110A006
https://doi.org/10.3724/SP.J.1008.2010.01120
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 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 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
2,4-Dimethylbenzyl alcohol 27809 Click to see 136.19 unknown via CMAUP database
3,5-Dimethylbenzyl alcohol 33706 Click to see 136.19 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzylethers
Benzyl methyl ether 10869 Click to see 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 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 218.38 unknown via CMAUP database
Phenylacetone 7678 Click to see 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
Poly(oxy-1,2-ethanediyl), alpha-(1,1'-biphenyl)-4-yl-omega-hydroxy- 160168 Click to see 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 346.30 unknown via CMAUP database
Elemicin 10248 Click to see 208.25 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(1,3,5-Trimethylhexyl)phenol 6427088 Click to see 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-Hydroxyxylidine 76542 Click to see 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 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 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 204.35 unknown via CMAUP database
1-methyl-4-[(E)-prop-1-enyl]cyclohexene 5319725 Click to see 136.23 unknown via CMAUP database
1,2,3,4,5-Pentamethylcyclopentadiene 77667 Click to see 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-Methylene-bicyclo(3.1.0)hexane 556304 Click to see 94.15 unknown https://doi.org/10.1002/JSSC.200800341
alpha-Acoradiene 90351 Click to see 204.35 unknown via CMAUP database
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
Santolina triene 519872 Click to see 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 178.31 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkadienes
1,3-Pentadiene 62204 Click to see 68.12 unknown via CMAUP database
1,3-Pentadiene, (3Z)- 643785 Click to see 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 164.29 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4-[4-(1,3-Benzodioxol-5-yl)-2,3-dimethylbutyl]-2-methoxyphenol 13844304 Click to see 328.40 unknown https://doi.org/10.1248/BPB.22.265
5-[4-(3-Hydroxy-4,5-dimethoxyphenyl)-2,3-dimethylbutyl]-2,3-dimethoxyphenol 11315296 Click to see 390.50 unknown https://doi.org/10.1248/BPB.22.265
erythro-Austrobailignan-6 10381847 Click to see 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
Meso-Dihydroguaiaretic Acid 476856 Click to see 330.40 unknown via CMAUP database
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 caprate 16833 Click to see 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 102.13 unknown via CMAUP database
2-Methylbutanoic Acid 8314 Click to see 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
Hexanoic Acid 8892 Click to see 116.16 unknown via CMAUP database
Sorbic Acid 643460 Click to see 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
Citronellol acetate, (S)- 6999975 Click to see 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
Glyceryl 1-hydroxystearate 95408 Click to see 374.60 unknown https://doi.org/10.1248/CPB.54.542
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
9-Octadecen-1-al 17029 Click to see 266.50 unknown via CMAUP database
9-Octadecenal 5283381 Click to see 266.50 unknown via CMAUP database
9-Octadecenal, (9Z)- 5364492 Click to see 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 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 304.50 unknown https://doi.org/10.1194/JLR.M300502-JLR200
Geranylgeranic acid 5275521 Click to see 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 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 368.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
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, (R)- 101977 Click to see 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 136.23 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown via CMAUP database
Citral 638011 Click to see 152.23 unknown via CMAUP database
Citronellol 8842 Click to see 156.26 unknown via CMAUP database
Dihydromyrcene, (-)- 10997105 Click to see 138.25 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
Linalool 6549 Click to see 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 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 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
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 134.22 unknown via CMAUP database
Thymyl methyl ether 14104 Click to see 164.24 unknown https://doi.org/10.1002/JSSC.200800341
> 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-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1002/JSSC.200800341
(+)-2-Carene 78249 Click to see CC1=CC2C(C2(C)C)CC1 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
(+)-Sabinene 10887971 Click to see 136.23 unknown via CMAUP database
(1R,2S,4R)-(+)-Bornyl acetate 443131 Click to see 196.29 unknown via CMAUP database
(1R,2S,4S)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-ol 10492 Click to see 154.25 unknown via CMAUP database
(1R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol 12242824 Click to see 154.25 unknown via CMAUP database
(1R,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-2-ene 12302456 Click to see 136.23 unknown via CMAUP database
(1S,2R,4S)-(-)-Bornyl acetate 442460 Click to see 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
2-Carene 79044 Click to see CC1=CC2C(C2(C)C)CC1 136.23 unknown via CMAUP database
alpha-Bergamotene 86608 Click to see 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-Neoclovene 605073 Click to see CC1=CCCC2(C13CCC2C(C3)(C)C)C 204.35 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
alpha-Thujene 17868 Click to see 136.23 unknown via CMAUP database
beta-Neoclovene 595094 Click to see CC1(CC23CCC1C2(CCCC3=C)C)C 204.35 unknown via CMAUP database
Beta-Pinene 14896 Click to see 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]hexane, 1-methyl-6-(1-methylethylidene)- 578236 Click to see CC(=C1C2C1(CCC2)C)C 136.23 unknown via CMAUP database
Borneol 64685 Click to see 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 196.29 unknown via CMAUP database
Camphene 6616 Click to see 136.23 unknown via CMAUP database
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
Npc126240 44630108 Click to see 196.29 unknown via CMAUP database
Npc189036 10049 Click to see 154.25 unknown via CMAUP database
Npc308218 439568 Click to see 154.25 unknown via CMAUP database
Sabinene 18818 Click to see 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
Tricyclene 79035 Click to see 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 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(10-Methyl-7-propan-2-yl-3-tricyclo[4.4.0.01,5]dec-3-enyl)methanol 46224401 Click to see 220.35 unknown https://doi.org/10.1016/J.BBRC.2009.12.131
[(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
2-Cyclohexen-1-ol, 1-methyl-4-(1-methylethyl)-, (1R,4R)-rel- 122485 Click to see 154.25 unknown via CMAUP database
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-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
Alpha-Terpineol 17100 Click to see 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
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
Delta-Terpineol 81722 Click to see 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 196.29 unknown via CMAUP database
Isolimonene 521268 Click to see 136.23 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 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 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see 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 416.70 unknown via CMAUP database
Beta-Tocopherol 6857447 Click to see 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Amorphene 12306052 Click to see 204.35 unknown via CMAUP database
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown via CMAUP database
(+)-alpha-Muurolene 12306049 Click to see 204.35 unknown via CMAUP database
(+)-beta-Caryophyllene 20831623 Click to see 204.35 unknown via CMAUP database
(+)-gamma-Gurjunene 91748784 Click to see CC1CCC(C=C2C1CCC2C)C(=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 204.35 unknown via CMAUP database
(+)-Thujopsene 11401461 Click to see CC1=CCC2(CCCC(C23C1C3)(C)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
(1R,4aR,8aS)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene 6432308 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown via CMAUP database
(1R,6S,7R)-3,7-Dimethyl-7-(4-methyl-3-penten-1-yl)bicyclo(4.1.0)hept-2-ene 11074502 Click to see 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 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 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 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 204.35 unknown via CMAUP database
(3S)-3-[(2S)-6-methylhept-5-en-2-yl]-6-methylidenecyclohexene 12315493 Click to see 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 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
(5R)-3,8-dimethyl-5-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene 91748288 Click to see 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)-Thujopsene 91749973 Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C 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 234.38 unknown via CMAUP database
(Z)-alpha-Bisabolene 5352653 Click to see 204.35 unknown via CMAUP database
(Z)-alpha-Santalol 5281531 Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)CO 220.35 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see 204.35 unknown via CMAUP database
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see 202.33 unknown via CMAUP database
1-Methyl-4-(6-methylhept-5-en-2-yl)cyclohexane 5316889 Click to see 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-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 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 204.35 unknown via CMAUP database
1,4-Dimethyl-7-(propan-2-ylidene)-1,2,3,4,5,6,7,8-octahydroazulene 6949 Click to see 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- 8888 Click to see 222.37 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
3,7-Dimethyl-4-(propan-2-yl)-3a,3b,4,5,6,7-hexahydro-1H-cyclopenta(1,3)cyclopropa(1,2)benzene 86609 Click to see 204.35 unknown via CMAUP database
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 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 238.37 unknown via CMAUP database
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene 10407 Click to see 204.35 unknown via CMAUP database
a Farnesol 3327 Click to see 222.37 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-Copaene 70678558 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
alpha-Santalene 94164 Click to see 204.35 unknown https://doi.org/10.1002/JSSC.200800341
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 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 204.35 unknown via CMAUP database
Beta-Santalol 6857681 Click to see 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
Calamenene 6429077 Click to see 202.33 unknown via CMAUP database
Calamenene, cis-(+)- 11298625 Click to see 202.33 unknown via CMAUP database
Calamenene, trans-(+)- 6429022 Click to see 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 204.35 unknown via CMAUP database
cis-(1S,3S)-2,2,3-trimethyl-3-(4-methylphenyl)cyclopentan-1-ol 5318539 Click to see 218.33 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 204.35 unknown via CMAUP database
Copaene 12303902 Click to see CC1=CCC2C3C1C2(CCC3C(C)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 204.35 unknown via CMAUP database
Cuparene 86895 Click to see 202.33 unknown via CMAUP database
Cyclohexene, 4-((1Z)-1,5-dimethyl-1,4-hexadienyl)-1-methyl-, (4S)- 24798702 Click to see 204.35 unknown via CMAUP database
d-alpha-Santalol 5368797 Click to see 220.35 unknown via CMAUP database
delta-Amorphene 12306059 Click to see 204.35 unknown via CMAUP database
delta-Cadinene 441005 Click to see 204.35 unknown via CMAUP database
Elixene 94254 Click to see 204.35 unknown via CMAUP database
Farnesene 5281516 Click to see 204.35 unknown via CMAUP database
Farnesol 445070 Click to see 222.37 unknown via CMAUP database
gamma-Cadinene 6432404 Click to see 204.35 unknown via CMAUP database
gamma-Gurjunene 90805 Click to see CC1CCC(C=C2C1CCC2C)C(=C)C 204.35 unknown via CMAUP database
Isocadinene 595385 Click to see 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
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 218.33 unknown via CMAUP database
Nerolidol 5284507 Click to see 222.37 unknown via CMAUP database
Npc200459 6432451 Click to see 204.35 unknown via CMAUP database
Npc225463 520957 Click to see 204.35 unknown via CMAUP database
Npc294136 14757966 Click to see 204.35 unknown via CMAUP database
Npc307011 442355 Click to see 204.35 unknown via CMAUP database
Npc91574 12306054 Click to see 204.35 unknown via CMAUP database
Patchoulane 29408 Click to see 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
Sesquichamene 97829 Click to see 204.35 unknown via CMAUP database
Thujopsene 442402 Click to see 204.35 unknown via CMAUP database
Toluene, p-(1,2,2-trimethylcyclopentyl)-, (R)-(+)- 11084908 Click to see 202.33 unknown via CMAUP database
Tricyclo[4.4.0.0(2,7)]dec-3-ene, 8-isopropyl-1,3-dimethyl-, (1S,2R,6R,7R,8S)-(+)- 6432119 Click to see 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
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown via CMAUP database
Npc30025 6432176 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aS,7bS)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa(e)azulene 44584667 Click to see 204.35 unknown via CMAUP database
[-]-Isoaromadendrene[V] 21775889 Click to see 204.35 unknown via CMAUP database
1H-Cycloprop(e)azulene, 1a,2,3,4,4a,5,6,7b-octahydro-1,1,4,7-tetramethyl-, (1aR,4R,4aR,7bS)- 521243 Click to see 204.35 unknown via CMAUP database
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 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 204.35 unknown via CMAUP database
Alloaromadendrene 10899740 Click to see 204.35 unknown via CMAUP database
Aromadendrane 520381 Click to see 206.37 unknown via CMAUP database
Aromadendrene epoxide 16211192 Click to see 220.35 unknown via CMAUP database
Aromadendrene oxide 91753455 Click to see 220.35 unknown via CMAUP database
Isoaromadendrene epoxide 534398 Click to see 220.35 unknown via CMAUP database
Ledane 102239850 Click to see 206.37 unknown via CMAUP database
Npc125737 528759 Click to see 220.35 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 5315347 Click to see 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 204.35 unknown via CMAUP database
(1S,2E,6E,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 13894537 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown via CMAUP database
trans-Bicyclogermacradiene 11820258 Click to see 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(-)-Cedrene 6431015 Click to see 204.35 unknown via CMAUP database
(1S,2R,5S,7R)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene 12302594 Click to see 204.35 unknown via CMAUP database
Cedrene 521207 Click to see 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
alpha-Chamigrene 519725 Click to see CC1=CCC2(CC1)C(=CCCC2(C)C)C 204.35 unknown via CMAUP database
beta-Chamigrene 442353 Click to see 204.35 unknown via CMAUP database
Chamigrenal 177096 Click to see 218.33 unknown https://doi.org/10.1007/BF02975223
Npc268130 29073 Click to see 204.35 unknown https://doi.org/10.1002/JSSC.200800341
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see 204.35 unknown via CMAUP database
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)- 9859094 Click to see 204.35 unknown via CMAUP database
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel- 10583 Click to see 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 204.35 unknown via CMAUP database
Beta-Selinene 442393 Click to see 204.35 unknown via CMAUP database
Npc246543 6432455 Click to see 204.35 unknown via CMAUP database
Npc289143 521242 Click to see 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 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)- 5373727 Click to see 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 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 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 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Schizonepetoside A 49787030 Click to see 330.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
methyl (1S,4aR,6S,7R,7aS)-4a,7-dihydroxy-7-methyl-6-[(E)-3-phenylprop-2-enoyl]oxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 95223135 Click to see 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 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
(2E,4E,6E,8E,10E,12E,14E,16E)-17-((4R)-4-Hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-2,6,11,15-tetramethyl-2,4,6,8,10,12,14,16-heptadecaoctaenal 9845703 Click to see 432.60 unknown via CMAUP database
(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 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 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 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 472.70 unknown https://doi.org/10.1080/10286020.2011.570751
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 472.70 unknown https://doi.org/10.1080/10286020.2011.570751
Nigranoic Acid 10814237 Click to see 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 386.70 unknown via CMAUP database
4,4-Dimethylcholest-5-en-3-ol 280427 Click to see 414.70 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
Cholesterol 5997 Click to see 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 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 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 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Citrostadienol 9548595 Click to see 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
Ammoniohexanoate 517543 Click to see 131.17 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
[(1E)-2,6-dimethylhepta-1,5-dienyl] acetate 24832062 Click to see 182.26 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Itaconic Anhydride 75110 Click to see 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 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 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
CID 20130941 20130941 Click to see 134.09 unknown via CMAUP database
D-Malic acid 92824 Click to see 134.09 unknown via CMAUP database
L-Malic Acid 222656 Click to see 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 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
(+)-2,3-Butanediol 439888 Click to see 90.12 unknown via CMAUP database
(2R,3R)-Butanediol 225936 Click to see 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
O-alpha-D-Galactopyranosyl-(1->3)-beta-D-fructofuranosyl O-alpha-D-galactopyranosyl-(1->6)-alpha-D-glucopyranoside 440185 Click to see 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
(E)-2-Octenal 5283324 Click to see 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 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 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 142.24 unknown via CMAUP database
2-Tetradecanone 75364 Click to see 212.37 unknown via CMAUP database
2-Undecanone 8163 Click to see 170.29 unknown via CMAUP database
7-Tridecanone 10015 Click to see 198.34 unknown via CMAUP database
Hexadecan-2-one 29251 Click to see 240.42 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Benzoylacetone 7166 Click to see 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 166.26 unknown via CMAUP database
Npc182183 560917 Click to see 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 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
Citraconic anhydride 12012 Click to see CC1=CC(=O)OC1=O 112.08 unknown via CMAUP database
L-Ascorbic Acid 54670067 Click to see 176.12 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
(3R,3aR,4S,7S,8aR)-2,3,4,7,8,8a-Hexahydro-4-hydroxy-8a-methyl-3-(1-methylethyl)-1H-3a,7-epidioxyazulene-6-carboxaldehyde 442391 Click to see 266.33 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
(1S,3R,7R,10S,13R,14R,16S,18R,19R)-1-Hydroxy-18-[(1S,2S)-1-hydroxy-1-[(2S)-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 16681613 Click to see 516.60 unknown https://doi.org/10.1080/10286020.2011.570751
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 516.60 unknown https://doi.org/10.1080/10286020.2011.570751
> Organoheterocyclic compounds / Furopyrans
(1R,3S,7S,10R,15R,17S,18R,21S,22R,23R,25R,29R)-9,9,18,23,25-pentamethyl-4,8,16,20,28-pentaoxaoctacyclo[13.12.1.115,22.01,13.03,7.03,10.017,21.025,29]nonacos-12-ene-5,14,19,24-tetrone 12080814 Click to see 526.60 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
3-Butyldihydrofuran-2(3H)-one 86852 Click to see 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 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 204.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see 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 164.16 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,7-Dimethoxycoumarin 2775 Click to see 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
Hexahydrocurcumin 5318039 Click to see 374.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/S0731-7085(00)00539-2
Quercetin 5280343 Click to see 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 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(+)-Schisandrin B 158103 Click to see 400.50 unknown 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
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/
(+)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-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 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 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 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
(6S,7R,12aS)-5,6,7,8-Tetrahydro-1,2,10,11,12-pentamethoxy-6,7-dimethyldibenzo[a,c]cycloocten-3-ol 78385003 Click to see 402.50 unknown https://doi.org/10.1248/BPB.22.265
(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 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
(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 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,10S)-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 13844278 Click to see 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
(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 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 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 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 494.60 unknown https://doi.org/10.1021/NP0503707
(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-hexaene 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
(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
(R+) Deoxyschisandrin A 10884218 Click to see 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
[(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 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 514.60 unknown https://doi.org/10.1021/NP0503707
[(8S,9S,10S)-9-hydroxy-3,4,5,14,15,16-hexamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] (E)-2-methylbut-2-enoate 5318795 Click to see 530.60 unknown via CMAUP database
[(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 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,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] (Z)-2-methylbut-2-enoate 133562029 Click to see 514.60 unknown https://doi.org/10.1016/S0021-9673(96)00685-1
[(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 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 500.60 unknown https://doi.org/10.1248/YAKUSHI1947.103.7_743
[(9R,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] benzoate 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
[(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 522.60 unknown https://doi.org/10.1021/NP0503707
[(9S,10R,11S)-11-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 102176162 Click to see 500.60 unknown via CMAUP database
[(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 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 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 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
1,2,3,10,11,12-Hexamethoxy-6,7-dimethyl-5,6,7,8-tetrahydrodibenzo(a,c)(8)annulen-6-ol 23915 Click to see 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
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 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-hexaen-3-ol 433451 Click to see 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
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 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 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-1,2,3,10,11,12-hexamethoxydibenzo[a,c]cyclooctene 19020980 Click to see 388.50 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
7-Hydroxy-1,2,3,13-tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydrobenzo[3,4]cycloocta[1,2-f][1,3]benzodioxol-8-yl (2E)-2-methyl-2-butenoate 5364583 Click to see 514.60 unknown via CMAUP database
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 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 514.60 unknown via CMAUP database
Benzoylgomisin H 14992069 Click to see 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 520.60 unknown https://doi.org/10.1248/BPB.22.265
https://doi.org/10.1055/S-2003-37024
Besigomsin 3001662 Click to see 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 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
Deoxyschizandrin 43595 Click to see 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
Epigomisin O 5317081 Click to see 416.50 unknown https://doi.org/10.1248/CPB.27.2695
Gomisin A 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
Gomisin A 15608605 Click to see 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
Gomisin B 6443826 Click to see 514.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/
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 D 5317799 Click to see 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
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 514.60 unknown via CMAUP database
Gomisin G 14992067 Click to see 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 G [M+H]+ 10007357 Click to see 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/
Gomisin H 5317803 Click to see 418.50 unknown https://doi.org/10.1016/J.CHROMA.2008.09.070
Gomisin J 3001686 Click to see 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 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 386.40 unknown https://doi.org/10.1248/BPB.22.265
Gomisin L2, (-)- 5317807 Click to see 386.40 unknown via CMAUP database
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 O 5317808 Click to see 416.50 unknown https://doi.org/10.1248/CPB.27.2695
Gomisin R 11516888 Click to see 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 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
R(+)-Gomisin M1 5321170 Click to see 386.40 unknown via CMAUP database
Rubrisandrin A 16099402 Click to see 388.50 unknown https://doi.org/10.1055/S-0030-1249861
Rubschisandrin 174277 Click to see 400.50 unknown https://doi.org/10.1248/BPB.22.265
https://doi.org/10.1271/BBB.90597
Schisandrene 11613047 Click to see 502.50 unknown via CMAUP database
Schisandrin 3001664 Click to see 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
Schisandrin derivative 119112 Click to see 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
Schisandrol B 634470 Click to see 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
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
Schisanhenol B 128150 Click to see 386.40 unknown https://doi.org/10.1016/J.CHROMA.2008.09.070
https://doi.org/10.1248/CPB.40.1191
SchisanlignaolD 15658448 Click to see 400.40 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 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 D 163067 Click to see 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 520.50 unknown via CMAUP database
Schizandrer A 163338 Click to see 536.60 unknown via CMAUP database
Schizantherin E; 5,6,7,8-Tetrahydro-1,2,10,11,12-pentamethoxy-6,7-dimethyl-dibenzo[a,c]cyclooctene-3,7,8-triol-8-benzoate Stereoisomer 5321177 Click to see 538.60 unknown via CMAUP database
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 514.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257236/
https://doi.org/10.1055/S-0030-1249861

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