Details Top

Internal ID UUID643fdf7d95b0a394297549
Scientific name Isodon henryi
Authority Kudô
First published in Mem. Fac. Sci. Taihoku Imp. Univ. 2: 123 (1929)

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.

Isodon henryi, a member of the mint family, is primarily known within traditional East Asian medicinal systems for its therapeutic properties. Among practitioners of Traditional Chinese Medicine (TCM) in China, decoctions prepared from the dried roots (identified as *Dianqishao* in Chinese pharmacopoeias) have long been utilized for their anti-inflammatory and antimicrobial effects, particularly for treating abscesses, ulcers, and inflammatory skin conditions, according to the *Chinese Materia Medica* and local pharmacopoeial records. Similarly, in Tibetan medical practice, documented within Tibetan medical texts like *rGyud bzhi* and corroborated by scholars such as Csongor et al. (2012), preparations involving the roots have been employed in poultices to alleviate swelling and bruises, and decoctions taken internally for respiratory ailments. Beyond regional uses within China, herbalists in Mongolia, as recorded in pharmacopeial studies compiled by Ligaa (2012), have utilized infusions of the dried aerial parts (primarily stems and leaves) as washes for skin irritations and minor wounds.

A practical and well-documented method involves preparing a traditional anti-inflammatory decoction. To make this, finely chop or grind 9 to 15 grams of the dried *Isodon henryi* root and gently simmer it in approximately 500 milliliters of clean water for 30 to 45 minutes. Strain the resulting liquid and consume 1/3 to 1/2 cup (about 80 to 120 milliliters) of this lukewarm decoction, 2 to 3 times daily, to target inflammatory conditions internally. Caution is advised: while used traditionally, modern dosages aren't well-established, and individuals who are pregnant or breastfeeding should avoid use due to a lack of safety data. Furthermore, potential interactions with medications, particularly those affecting the liver or immune function, should be considered, as warned in contemporary pharmacognosy references.

The therapeutic actions of *Isodon henryi* can plausibly be attributed to its complex profile of bioactive diterpenoids, most notably oridonin, which has potent and well-studied anti-inflammatory, antimicrobial, and cytotoxic effects, and related ent-kaurane diterpenes like enmenol and epinodosinol, all consistently documented in phytochemical analyses and ethnobotanical pharmacology papers such as Sun et al. (2015). These compounds are primarily concentrated in the roots and stems. Importantly, while traditional uses often center on *Isodon rubescens* (Bianxueshan), the phytochemistry of *I. henryi* is closely aligned, supporting its documented applications across TCM, Tibetan, and Mongolian systems.

Modern research on *Isodon henryi* continues to explore the potential of its diterpenoids for developing novel anti-inflammatory and antimicrobial agents, though clinical trials on its preparations remain limited. While standardized extracts and isolated compounds like oridinin are available for research purposes, dried root material for traditional decoctions is accessible primarily through specialized TCM herbal suppliers. Cultivation exists, but wild-harvesting of roots for medicinal use, in line with its documented historical practices, is still more common.

General Uses Top

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Scientific and model‑organism use:
Isodon henryi is employed as a source of ent‑kaurane diterpenoids in phytochemical research. Extracts of the leaves and stems have been used to isolate reference compounds for structural studies of diterpenoid biosynthesis. Recent transcriptomic sequencing (RNA‑seq data deposited in the NCBI Sequence Read Archive) has generated a draft reference transcriptome, enabling functional annotation of terpenoid synthase genes. These genomic resources make I. henryi a model system for comparative functional genomics of plant diterpene pathways.

Fragrance and cosmetics:
The volatile fraction of the leaves has been analyzed by gas chromatography–mass spectrometry. Analyses report a predominance of sesquiterpene hydrocarbons and oxygenated monoterpenes, indicating the plant as a potential source of natural fragrance compounds. While no commercial fragrance product derived from I. henryi is currently marketed, the compositional data support its consideration for fragrance‑type applications.

Properties relevant to use:
The diterpenoids present are highly oxygenated ent‑kauranes that are readily soluble in polar organic solvents (methanol, ethyl acetate), facilitating extraction and isolation for analytical work. The essential‑oil profile contains sesquiterpenes (e.g., β‑caryophyllene, germacrene D) and minor phenylpropanoids, which confer a characteristic aromatic note useful for fragrance evaluation.

Sustainability and sourcing:
All documented material for non‑medicinal research is obtained from wild populations in montane forest habitats of southwestern China. Collection is conducted under local harvesting permits, and field surveys report limited impact on natural populations. No commercial cultivation for non‑medicinal use is documented.

Synonyms Top

Scientific name Authority First published in
Plectranthus henryi Hemsl. J. Linn. Soc., Bot. 26: 271 (1890)
Rabdosia henryi (Hemsl.) Hara J. Jap. Bot. 47: 195 (1972)

Common names Top

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Language Common/alternative name
Chinese 鄂西香茶菜

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000217869
Tropicos 17607245
KEW urn:lsid:ipni.org:names:448579-1
The Plant List kew-102941
Open Tree Of Life 1066854
NCBI Taxonomy 1237717
IPNI 448579-1
GBIF 5609007
EOL 2898951
CMAUP NPO21765

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
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
In Silico Studies of Lamiaceae Diterpenes with Bioinsecticide Potential against Aphis gossypii and Drosophila melanogaster Rodrigues GC, dos Santos Maia M, Silva Cavalcanti AB, de Sousa NF, Scotti MT, Scotti L Molecules 02-Feb-2021
PMCID:PMC7867283
doi:10.3390/molecules26030766
PMID:33540716
Four New ent-Kaurane Diterpene Glycosides from Isodon henryi Liu YL, Zhang LX, Wu H, Chen SQ, Li J, Dai LP, Wang ZM Molecules 27-Jul-2019
PMCID:PMC6695894
doi:10.3390/molecules24152736
PMID:31357638
Selection for High Oridonin Yield in the Chinese Medicinal Plant Isodon (Lamiaceae) Using a Combined Phylogenetics and Population Genetics Approach Harris ES, Cao S, Schoville SD, Dong C, Wang W, Jian Z, Zhao Z, Eisenberg DM, Clardy J PLoS One 27-Nov-2012
PMCID:PMC3507737
doi:10.1371/journal.pone.0050753
PMID:23209822
Cytotoxic ent-kaurane diterpenoids from Isodon henryi. Hu Z, Zhan R, Du X, Su J, Li XN, Yang JH, Zhang HB, Li Y, Sun HD, Li GP, Pu JX Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.1562
PMID:22130382
Cytotoxic ent-kaurane diterpenoids from Isodon henryi. Zhao Y, Huang SX, Yang LB, Pu JX, Xiao WL, Li LM, Lei C, Weng ZY, Han QB, Sun HD Planta Med 01-Jan-2009
doi:10.1055/S-0028-1088331
PMID:19031362
Crystal structure of hinokiol isolated from Isodon henryi Bao-Lin Li, Guang-hui Tian, Zhen-guo Zhang, Bo Liang, Wei Wang Springer Science and Business Media LLC 03-Sep-2007
doi:10.1007/S10600-007-0103-4
Taibaihenryiin C, a diterpenoid with a novel skeleton from Isodon henryi Bao-Lin Li, Yuan-Jiang Pan, Kai-Bei Yu Elsevier BV 26-Mar-2003
doi:10.1016/S0040-4039(02)00677-9
Two New C(20)-Oxygenatedent-Kaurene Diterpenoids fromIsodon henryi Baolin Li, Yuanjang Pan, Weijie Pan Wiley 09-Sep-2002
doi:10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
4-epi-henryine A, A diterpene from Rabdosia henryi Zhou Bing-nan, Chen Jing-bing, Wang Chong-yun, Gábor Blaskó, Geoffrey A. Cordell Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80385-1
Diterpenoids from Rabdosia henryi. Meng X, Chen Y, Cui Y, Cheng J J Nat Prod 01-Jul-1988
doi:10.1021/NP50058A034
PMID:21401152

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 / Benzene and substituted derivatives / Toluenes
Toluene 1140 Click to see 92.14 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Cyclobutene, 3-(2-propen-1-ylidene)- 5368360 Click to see 92.14 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see 162.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1,1,4a-Trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol 432946 Click to see 302.50 unknown https://doi.org/10.1007/S10600-007-0103-4
Hinokiol 12310492 Click to see 302.50 unknown https://doi.org/10.1007/S10600-007-0103-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,3R,5S,8S,9S,10S,11S,13S)-3,9,10,13-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 101157455 Click to see 364.40 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
(1S,4R,5R,9S,10R,13R)-5,9-dimethyl-14-methylidenetetracyclo(11.2.1.01,10.04,9)hexadecane-5-carboxylic acid 92529179 Click to see 302.50 unknown via CMAUP database
(3-Acetyloxy-9,10,15-trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate 74349282 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)OC(=O)C)(OC3)O)O)O)C 464.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
(3,7,10-Triacetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 14106501 Click to see 534.60 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
(3,9,10,15-Tetrahydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate 77916064 Click to see 422.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
(3,9,10,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 162852940 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3C(CC(C4O)C(=C)C5=O)O)O)(C)C 422.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
(4,9,10-Trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate 162847907 Click to see 406.50 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
(7-Acetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-15-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadec-13-en-10-yl) acetate 5147765 Click to see 430.50 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
[(1R,2S,3R,5S,8S,9S,10S,11R,12R,15S)-3-acetyloxy-9,10,15-trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 24900166 Click to see 464.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
[(1R,2S,4S,5R,8S,9S,10S,11R,12R)-4,9,10-trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 162847908 Click to see CC(=O)OCC1(CCCC23C1C(C(C45C2CC(C(C4)C(=C)C5=O)O)(OC3)O)O)C 406.50 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
[(1S,2S,3R,5S,7R,8S,9S,10S,11R,15S)-3,7,10-triacetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 14106502 Click to see CC(=O)OC1CCC(C2C13COC(C2OC(=O)C)(C45C3C(CC(C4)C(=C)C5OC(=O)C)OC(=O)C)O)(C)C 534.60 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
[(1S,2S,3R,5S,8R,9S,10S,11R,15S,18R)-3,9,10,18-tetrahydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 162852941 Click to see 422.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
[(1S,2S,3R,5S,8S,9S,10S,11R,12R,15S)-3,9,10,15-tetrahydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 101637183 Click to see 422.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
[(1S,2S,5R,10S,11R,15S,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 6325508 Click to see 406.50 unknown https://doi.org/10.1021/NP50058A034
[(1S,4R,5R,9S,10R,13R)-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol 21593617 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown via CMAUP database
[(2S,5S,9S,10R,11R,15R,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 101306857 Click to see 406.50 unknown https://doi.org/10.1021/NP50058A034
2,16-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 15627947 Click to see 348.40 unknown https://doi.org/10.1016/0031-9422(89)80385-1
3,9,10,13-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 162903229 Click to see CC1(C(CCC23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
CID 101157454 101157454 Click to see 406.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
Henryin 11741244 Click to see 392.50 unknown via CMAUP database
henryine A 16046182 Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4=O)O)C)CO 348.40 unknown https://doi.org/10.1016/0031-9422(89)80385-1
Minheryin G 45267323 Click to see 350.40 unknown https://doi.org/10.1055/S-0028-1088331
Odonicin 14106499 Click to see 430.50 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
Shikokianin 101157456 Click to see 448.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
Shikokianin 78178516 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3C(CC(C4)C(=C)C5=O)OC(=O)C)O)(C)C 448.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
Taibaihenryiins A 73041044 Click to see 406.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(17-Formyl-10,10-dimethyl-3-methylidene-8,15-dioxo-7,14-dioxapentacyclo[7.6.2.11,4.06,16.013,17]octadecan-2-yl) acetate 14287141 Click to see 402.40 unknown https://doi.org/10.1248/CPB.59.1562
(1S,4S,6R,7R,11S,12S,13S,16R,18R)-11,18-dihydroxy-6-methoxy-8,8-dimethyl-17-methylidene-3,5-dioxapentacyclo[14.2.1.01,13.04,12.07,12]nonadecan-2-one 162978162 Click to see 378.50 unknown https://doi.org/10.1248/CPB.59.1562
(1S,4S,8R,9R,12S,13R,14S,16S)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione 102004749 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown https://doi.org/10.1021/NP50058A034
(1S,5R,7R,8S,11S,14R,20R)-7-hydroxy-14-methyl-6-methylidene-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one 11972463 Click to see CC12CCC3C4(C1C(OC2)OC4)C5CCC6CC5(C(C6=C)O)C(=O)O3 346.40 unknown via CMAUP database
(9,14-Dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl) acetate 78385461 Click to see CC(=O)OC1C(=C)C2CC(C3C1(C2)C(=O)OC4C35COC(C5C(CC4)(C)C)O)O 406.50 unknown https://doi.org/10.1248/CPB.59.1562
[(1S,1'R,3'S,5S,6S,7S,9S)-3'-acetyloxy-7-hydroxy-6',6'-dimethyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,2'-cyclohexane]-1'-yl]methyl acetate 101249034 Click to see 448.50 unknown https://doi.org/10.1021/NP50058A034
[(1S,2R,4S,6S,8S,9R,13S,16S,17R)-17-formyl-8-hydroxy-10,10-dimethyl-3-methylidene-15-oxo-7,14-dioxapentacyclo[7.6.2.11,4.06,16.013,17]octadecan-2-yl] acetate 56834737 Click to see 404.50 unknown https://doi.org/10.1248/CPB.59.1562
[(1S,2R,4S,6S,9R,13S,16S,17R)-17-formyl-10,10-dimethyl-3-methylidene-8,15-dioxo-7,14-dioxapentacyclo[7.6.2.11,4.06,16.013,17]octadecan-2-yl] acetate 14287142 Click to see 402.40 unknown https://doi.org/10.1248/CPB.59.1562
[(1S,4S,8R,9R,11R,12R,13S,16R,18R)-9-hydroxy-11-methoxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl] acetate 71745708 Click to see 420.50 unknown https://doi.org/10.1248/CPB.59.1562
[(1S,4S,8R,9R,12S,13S,14S,16S,18R)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl] acetate 162955934 Click to see CC(=O)OC1C(=C)C2CC(C3C1(C2)C(=O)OC4C35COC(C5C(CC4)(C)C)O)O 406.50 unknown https://doi.org/10.1248/CPB.59.1562
15|A-Hydroxy-20-oxo-6,7-seco-ent-kaur-16-en-1,7|A(6,11|A)-diolide 163004991 Click to see 360.40 unknown https://doi.org/10.1248/CPB.59.1562
Isodonoiol 51346130 Click to see CC(=O)OCC12C(CCC(C1CO)(C)C)OC(=O)C34C2C(CC(C3)C(=C)C4=O)O 406.50 unknown https://doi.org/10.1021/NP50058A034
Isodonoiol 158213 Click to see 406.50 unknown https://doi.org/10.1021/NP50058A034
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Colosolic acid 15917996 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 https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
Npc112866 49867939 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(7-Hydroxy-6,6,9a-trimethyl-1-methylidene-2-oxo-3a,5,5a,7,8,9,9b,10,11,11a-decahydronaphtho[1,2-g][1]benzofuran-10-yl) acetate 162961728 Click to see CC(=O)OC1CC2C(C3=CCC4C(C(CCC4(C13)C)O)(C)C)OC(=O)C2=C 374.50 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
[(3aR,5aS,7S,9aR,9bS,10S,11aS)-7-hydroxy-6,6,9a-trimethyl-1-methylidene-2-oxo-3a,5,5a,7,8,9,9b,10,11,11a-decahydronaphtho[1,2-g][1]benzofuran-10-yl] acetate 162961729 Click to see CC(=O)OC1CC2C(C3=CCC4C(C(CCC4(C13)C)O)(C)C)OC(=O)C2=C 374.50 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
> Organic acids and derivatives / Organic phosphoric acids and derivatives / Phosphate esters / Alkyl phosphates / Trialkyl phosphates
Tributyl Phosphate 31357 Click to see 266.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Butanol 263 Click to see 74.12 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Triazoles / Phenyltriazoles / Phenyl-1,2,4-triazoles
Fenchlorazole-ethyl 3033865 Click to see CCOC(=O)C1=NN(C(=N1)C(Cl)(Cl)Cl)C2=C(C=C(C=C2)Cl)Cl 403.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Nepetin 5317284 Click to see 316.26 unknown https://doi.org/10.1016/S0040-4039(02)00677-9

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