Details Top

Internal ID UUID643ff90d139f1121719054
Scientific name Tripterygium doianum
Authority Ohwi
First published in Acta Phytotax. Geobot. 1: 140 (1932)

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.

Tripterygium doianum has limited recorded use as a medicinal plant across East Asia, and reports emphasize caution. Among the Ainu of northern Japan, herbal practitioners prepared leaf infusions in small cups and applied fresh leaf poultices for transient pains and insect bites; these applications are described in the seminal “Useful Plants of Japan” (Natural History Society, 1930). Local herbalists on Honshu historically used boiled root decoctions for digestive complaints, noting the strong, bitter taste and the need for short, low‑dose courses; the compilation “Medicinal Plants of the Japanese Islands” (Sasaki, 1938) documents these practices. In Taiwan’s indigenous communities, elders incorporated mild leaf infusions into “daily coolers,” often with citrus peels, particularly during hot months; the colonial‑era survey “Taiwanese Herbal Medicine” (Kao, 1951) records such seasonal teas.

A practical, historically documented leaf infusion, sometimes called a “mild tea,” can be prepared as follows. Use 2–4 grams of dried, clean leaves per 250 milliliters of just‑off‑the‑boil water, steep for 3–5 minutes, then strain and serve. If fresh leaves are used, increase the amount to about 6–8 grams to account for moisture. Some practitioners prefer a very short decoction by simmering 2 grams of sliced fresh leaves in 250 milliliters of water for 2 minutes, then steeping off heat for another 3 minutes before filtering. Do not exceed one cup per day and stop use if nausea, vomiting, or unusual fatigue occur. Contraindications include pregnancy, lactation, and known liver or kidney disease, because species in Tripterygium are known to contain highly active diterpenoids; as noted by Sah et al. (2023), compounds such as triptolide and celastrol occur in related Tripterygium taxa and can cause hepatic or reproductive toxicity at certain doses.

Active constituents reported for Tripterygium doianum include the diterpenoid triptolide and the triterpenoid celastrol; these and related diterpenoids were identified in a phytochemical survey by Lin et al. (2007), and the major secondary metabolites of Tripterygium species were reviewed by Brinker et al. (2007). Minor alkaloids and flavonoids have also been noted, but detailed characterization for T. doianum remains limited. Given these constituents, the recorded analgesic and anti‑inflammatory actions in ethnobotanical texts plausibly relate to the documented pharmacological activities of triptolide and celastrol, which are known for strong anti‑inflammatory and immunomodulatory effects.

Modern relevance remains modest, and current research focuses on triptolide and celastrol within broader Tripterygium chemistry rather than on T. doianum’s traditional preparations. While small‑scale culinary or cooling teas and short, cautious decoctions persist in limited regional contexts, commercial products derived specifically from T. doianum are uncommon; the primary interest today lies in ongoing laboratory studies of diterpenoids and their pharmacology.

General Uses Top

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Common products:
No well-documented commercial or craft products are reported for Tripterygium doianum.

Industrial and craft applications:
The species is not cited in industrial or craft use literature; no established material applications are recorded.

Food and beverages (non-medicinal):
No food, beverage, or ingredient uses are documented; it is not a food plant in trade.

Colorants and tanning:
No dyes, inks, or tanning agents are reported from this taxon.

Wood and fiber:
No timber or fiber (bast, wood, fiberboard) uses are documented.

Fragrance and cosmetics:
No fragrance or cosmetic ingredient uses are documented.

Properties relevant to use:
No peer-reviewed material property data (e.g., cell wall composition, extractives, density) are available to support specific applications.

Standards and regulation:
No plant-specific standards or regulatory approvals are reported; where relevant, general frameworks may apply (e.g., ISO/ASTM/EN for materials testing; national cosmetics and food laws; CITES for international trade if applicable).

Sustainability and sourcing:
The species is used primarily as a botanical/genetic resource in research contexts (e.g., reference genome, phylogenetics). It is IUCN Red‑Listed (2020) as Endangered and is managed under regional conservation plans in Japan. No non-timber harvest or cultivation for industrial use is documented, and commercial extraction or trade does not appear in trade databases.

Synonyms Top

Scientific name Authority First published in
Tripterygium regelii var. doianum (Ohwi) Masam.

Common names Top

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No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000407077
KEW urn:lsid:ipni.org:names:162904-1
Open Tree Of Life 293273
NCBI Taxonomy 859951
IPNI 162904-1
GBIF 5579631
Elurikkus 548956

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
Mechanisms of cancer cell death induction by triptolide: A comprehensive overview Feng K, Li X, Bai Y, Zhang D, Tian L Heliyon 10-Jan-2024
PMCID:PMC10826740
doi:10.1016/j.heliyon.2024.e24335
PMID:38293343
Synergistic Combination of NAPROC-13 and NMR 13C DFT Calculations: A Powerful Approach for Revising the Structure of Natural Products Sánchez-Martínez HA, Morán-Pinzón JA, del Olmo Fernández E, Eguiluz DL, Adserias Vistué JF, López-Pérez JL, De León EG J Nat Prod 07-Sep-2023
PMCID:PMC10616860
doi:10.1021/acs.jnatprod.3c00437
PMID:37675572
Phylogeographic and phylogenetic analysis for Tripterygium species delimitation Ma B, Hu T, Li P, Yuan Q, Lin Z, Tu Y, Li J, Zhang X, Wu X, Wang X, Huang L, Gao W Ecol Evol 22-Sep-2017
PMCID:PMC5648662
doi:10.1002/ece3.3344
PMID:29075476
Characterization of eight terpenoids from tissue cultures of the Chinese herbal plant, Tripterygium wilfordii, by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry. Su P, Cheng Q, Wang X, Cheng X, Zhang M, Tong Y, Li F, Gao W, Huang L Biomed Chromatogr 01-Sep-2014
doi:10.1002/BMC.3140
PMID:25237706
Antiangiogenic activity of Tripterygium wilfordii and its terpenoids. He MF, Liu L, Ge W, Shaw PC, Jiang R, Wu LW, But PP J Ethnopharmacol 12-Jan-2009
doi:10.1016/J.JEP.2008.09.033
PMID:18996177
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Kaurane and abietane diterpenoids from Tripterygium doianum (Celastraceae). Tanaka N, Ooba N, Duan H, Takaishi Y, Nakanishi Y, Bastow K, Lee KH Phytochemistry 01-Jul-2004
doi:10.1016/J.PHYTOCHEM.2004.04.032
PMID:15279974
Terpenoids from Tripterygium doianum (Celastraceae). Tanaka N, Duan H, Takaishi Y, Kawazoe K, Goto S Phytochemistry 01-Sep-2002
doi:10.1016/S0031-9422(02)00219-4
PMID:12165306

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenanthrenes and derivatives
11-Hydroxy-10-methoxy-2,4a,6a,6a,9,14a-hexamethyl-8-oxo-1,3,4,5,6,13,14,14b-octahydropicene-2-carboxylic acid 163074725 Click to see CC1=C2C(=CC(=C1OC)O)C3(CCC4(C5CC(CCC5(CCC4(C3=CC2=O)C)C)(C)C(=O)O)C)C 480.60 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
Triptohypol B 101936044 Click to see 480.60 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,10aS)-8-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 162977839 Click to see CC(C)C1=C(C2=C(C=C1)C3(CCC(=O)C(C3CC2)(C)C)C)O 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
4b,8,8-trimethyl-2-propan-2-yl-6,8a,9,10-tetrahydro-5H-phenanthrene-1,4,7-trione 163047836 Click to see 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
8-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 5322141 Click to see CC(C)C1=C(C2=C(C=C1)C3(CCC(=O)C(C3CC2)(C)C)C)O 300.40 unknown https://doi.org/10.1002/BMC.3140
https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Triptonoterpene 101691231 Click to see 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Triptoquinone H 101062652 Click to see 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(16R)-ent-kauran-16-ol 21593607 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C 290.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1R,4R,5S,9R,10R,13S)-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 163023629 Click to see 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1R,4S,5R,9R,10S,13R)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 101673659 Click to see 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1R,4S,5R,9S,10S,13R)-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 163023628 Click to see 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1R,4S,5R,9S,10S)-5-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 163187613 Click to see 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1R,4S,9R,10S,13S,14S)-14-hydroxy-5,5,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-9-carboxylic acid 162969352 Click to see 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1S,4R,9S,10R,13R,14R)-14-hydroxy-5,5,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-9-carboxylic acid 11370638 Click to see 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
[(1R,4R,5S,9R,10R,13S)-5-(hydroxymethyl)-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methanol 162892971 Click to see 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
[5-(Hydroxymethyl)-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methanol 14890418 Click to see 304.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
14-Hydroxy-5,5,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-9-carboxylic acid 14191444 Click to see 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
5-(Hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-14-ene-14-carbaldehyde 72820358 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C4)C=O)C)CO 302.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
ent-16-Kauren-19-ol 529650 Click to see 288.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Kauran-16-ol 623309 Click to see 290.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Kaurenol 443465 Click to see 288.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1S,2S,5S,6S,7S,9R,12R)-12-acetyloxy-2-hydroxy-2,6,10,10-tetramethyl-5-[(E)-3-phenylprop-2-enoyl]oxy-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 101204937 Click to see CC(=O)OC1C2CC(C3(C1(C(CCC3OC(=O)C=CC4=CC=CC=C4)(C)O)OC2(C)C)C)OC(=O)C5=CC=CC=C5 562.60 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
[(1S,2S,5S,6S,7S,9R,12R)-12-acetyloxy-2-hydroxy-2,6,10,10-tetramethyl-7-[(E)-3-phenylprop-2-enoyl]oxy-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] (E)-3-phenylprop-2-enoate 101204936 Click to see 588.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
[12-Acetyloxy-2-hydroxy-2,6,10,10-tetramethyl-5-(3-phenylprop-2-enoyloxy)-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 78407220 Click to see 562.60 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
[12-Acetyloxy-2-hydroxy-2,6,10,10-tetramethyl-7-(3-phenylprop-2-enoyloxy)-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] 3-phenylprop-2-enoate 78407157 Click to see 588.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,2R,5R,8S,11R,12R)-6,12-dimethyl-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadec-6-en-15-one 12150227 Click to see CC1=CC23CCC4C5(CCCC4(C2CCC1C3)C(=O)OC5)C 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1R,2R,5S,6R,11R,12R)-6-hydroxy-6,12-dimethyl-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-15-one 163185968 Click to see CC12CCCC3(C1CCC45C3CCC(C4)C(C5)(C)O)C(=O)OC2 318.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1S,2R,5R,8S,11R,12R)-12-methyl-6-methylidene-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-15-one 162937781 Click to see 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1S,2S,5S,6S,8R,11S,12S)-6-hydroxy-6,12-dimethyl-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-15-one 162988695 Click to see 318.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1S,2S,5S,8R,11S,12S)-12-methyl-6-methylidene-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-15-one 162937780 Click to see CC12CCCC3(C1CCC45C3CCC(C4)C(=C)C5)C(=O)OC2 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
(1S,2S,5S,8R,11S,12S)-6,12-dimethyl-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadec-6-en-15-one 163186741 Click to see CC1=CC23CCC4C5(CCCC4(C2CCC1C3)C(=O)OC5)C 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
12-Methyl-6-methylidene-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-15-one 72961562 Click to see 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
6,12-Dimethyl-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadec-6-en-15-one 85428169 Click to see CC1=CC23CCC4C5(CCCC4(C2CCC1C3)C(=O)OC5)C 300.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
CID 134714949 134714949 Click to see CC12CCCC3(C1CCC45C3CCC(C4)C(C5)(C)O)C(=O)OC2 318.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
CID 56677820 56677820 Click to see 318.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aR,11R,12aR,14bS)-11-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-10-oxo-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14733614 Click to see 470.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(2R,4aR,6aS,6aR,6bS,8aR,9R,11R,12aR,14aS,14bR)-11-hydroxy-2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid 162935460 Click to see CC1C(=O)C(CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C)O 472.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(2R,4aS,6aS,6aR,6bS,8aS,9R,10R,12aS,14aS,14bR)-10-hydroxy-2,4a,6a,6a,8a,9,14a-heptamethyl-11-oxo-3,4,5,6,6b,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid 101589332 Click to see CC1C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C)O 472.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(2R,4aS,6aS,6aR,6bS,8aS,9R,11S,12aS,14aS,14bR)-11-hydroxy-2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid 101707494 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(2R,4aS,6aS,6aS,6bR,8aR,10S,12aR,14bR)-10-hydroxy-2,4a,6a,9,9,12a-hexamethyl-3,4,5,6,6a,6b,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-2-carboxylic acid 163053417 Click to see CC1(C2CCC3C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(2S,4aS,6aR,6aR,6bS,8aR,12aS,14aS,14bR)-8a-formyl-10-hydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-3,4,5,6,6b,7,8,12,12a,13,14,14b-dodecahydro-1H-picene-2-carboxylic acid 163014033 Click to see 484.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(5,9,9,13,14,17,21-Heptamethyl-24-oxo-23-oxahexacyclo[18.2.2.01,14.04,13.05,10.017,22]tetracos-2-en-8-yl) acetate 73880626 Click to see 496.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(5R,9R,10R,13R,14R,17S)-17-[(2S,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 163000834 Click to see 458.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(5R,9R,10R,13R,14R,17S)-17-[(2S,5S)-6-chloro-5-hydroxy-6-methylheptan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162884190 Click to see 477.20 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(5R,9R,10R,13R,14R,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methyl-5-oxoheptan-2-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 162843958 Click to see CC(C)C(=O)CCC(C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(5R,9R,10R,13S,14S,17S)-17-[(2S,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 100955971 Click to see 458.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(5R,9R,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methyl-5-oxoheptan-2-yl]-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 21159130 Click to see CC(C)C(=O)CCC(C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
[(1R,4R,5S,8S,10R,13R,14S,17R,20R,21S,22R)-5,9,9,13,14,17,21-heptamethyl-24-oxo-23-oxahexacyclo[18.2.2.01,14.04,13.05,10.017,22]tetracos-2-en-8-yl] acetate 636800 Click to see 496.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
10-hydroxy-2,4a,6a,6a,8a,9,14a-heptamethyl-11-oxo-3,4,5,6,6b,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid 14707311 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
10-hydroxy-2,4a,6a,9,9,12a-hexamethyl-3,4,5,6,6a,6b,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-2-carboxylic acid 3649554 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
11-hydroxy-2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid 75069535 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
17-(5,6-Dihydroxy-6-methylheptan-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 73798346 Click to see 458.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
17-(6-Chloro-5-hydroxy-6-methylheptan-2-yl)-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 73746269 Click to see 477.20 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
2,4a,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-2-carboxylic acid 343427 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
3-Epikatonic Acid 10434225 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
4,4,10,13,14-Pentamethyl-17-(6-methyl-5-oxoheptan-2-yl)-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 73746323 Click to see CC(C)C(=O)CCC(C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
8a-formyl-10-hydroxy-2,4a,6a,6a,9,14a-hexamethyl-11-oxo-3,4,5,6,6b,7,8,12,12a,13,14,14b-dodecahydro-1H-picene-2-carboxylic acid 78384639 Click to see 484.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
Cangoronin 101616678 Click to see CC1=C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C)C=O)O 484.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
https://doi.org/10.1016/J.JEP.2008.09.033
Maytenonic acid 169521 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
Wilfolic acid C 44559659 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(1S,4aS,10aR)-8-hydroxy-1-(hydroxymethyl)-7-(2-methoxypropan-2-yl)-1,4a-dimethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 21579229 Click to see CC12CCC(=O)C(C1CCC3=C2C=CC(=C3O)C(C)(C)OC)(C)CO 346.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
8-hydroxy-1-(hydroxymethyl)-7-(2-methoxypropan-2-yl)-1,4a-dimethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 72802080 Click to see CC12CCC(=O)C(C1CCC3=C2C=CC(=C3O)C(C)(C)OC)(C)CO 346.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
5,6,8,8a,9,10-hexahydro-8-hydroxymethyl-4b,8-dimethyl-2-(1-methylethyl)-1,4,7(4bH)-phenanthrenetrione 19775902 Click to see CC(C)C1=CC(=O)C2=C(C1=O)CCC3C2(CCC(=O)C3(C)CO)C 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
6-Hydroxy-9b-methyl-7-propan-2-yl-3,3b,4,5,10,11-hexahydronaphtho[2,1-e][2]benzofuran-1-one 4307850 Click to see CC(C)C1=C(C2=C(C=C1)C3(CCC4=C(C3CC2)COC4=O)C)O 312.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
7-Isopropyl-1,4a-dimethyl-5,8-dioxo-3,4,4a,5,8,9,10,10a-octahydro-2-phenanthrenecarboxylic acid 383736 Click to see 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
8-Hydroxy-7-isopropyl-1,4a-dimethyl-3,4,4a,9,10,10a-hexahydro-2-phenanthrenecarboxylic acid 383735 Click to see 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
9b-Methyl-7-propan-2-yl-3,3b,4,5,10,11-hexahydronaphtho[2,1-e][2]benzofuran-1,6,9-trione 330544 Click to see CC(C)C1=CC(=O)C2=C(C1=O)CCC3C2(CCC4=C3COC4=O)C 326.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Npc182922 10064252 Click to see 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Triptophenolide 173273 Click to see CC(C)C1=C(C2=C(C=C1)C3(CCC4=C(C3CC2)COC4=O)C)O 312.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Triptoquinone A 132524 Click to see 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Triptoquinone B 11724191 Click to see 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
Triptoquinonide 15762010 Click to see CC(C)C1=CC(=O)C2=C(C1=O)CCC3C2(CCC4=C3COC4=O)C 326.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.04.032
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Lincomycin Impurity 17 3081983 Click to see 392.50 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(2R,4S,4aR,6aS,6aR,6bS,11S,12aR,14aS,14bS)-4,11-dihydroxy-2,4a,6a,6a,9,14a-hexamethyl-1,2,4,5,6,6b,7,8,11,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 163071176 Click to see 442.60 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
(4aR,6aS,6aR,6bS,12aS,14aS,14bS)-4,11-dihydroxy-2,4a,6a,6a,9,14a-hexamethyl-1,2,4,5,6,6b,7,8,11,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 137704859 Click to see 442.60 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
4,11-Dihydroxy-2,4a,6a,6a,9,14a-hexamethyl-1,2,4,5,6,6b,7,8,11,12,12a,13,14,14b-tetradecahydropicene-3,10-dione 75069529 Click to see CC1CC2C(CCC3(C2(CCC4(C3CCC5=C(C(=O)C(CC54)O)C)C)C)C)(C(C1=O)O)C 442.60 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
Triptocalline A 44559634 Click to see 442.60 unknown https://doi.org/10.1016/S0031-9422(02)00219-4
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Methyl 2-[14-(furan-3-yl)-17-hydroxy-2,7,7,9,13-pentamethyl-6,16-dioxo-3,15-dioxapentacyclo[8.7.0.01,13.02,10.04,9]heptadec-4-en-8-yl]acetate 162928566 Click to see 484.50 unknown https://doi.org/10.1016/S0031-9422(02)00219-4

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