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Isodon henryi

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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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

Suggest others/fix!
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 CC1=CC=CC=C1 92.14 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Cyclobutene, 2-propenylidene- 5368360 Click to see C=CC=C1CC=C1 92.14 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see CC#CC#CC#CC#CC#CC=C 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 CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O 302.50 unknown https://doi.org/10.1007/S10600-007-0103-4
Hinokiol 12310492 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O 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 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
(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 CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 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 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
(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 CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 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 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
(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 CC(=O)OC1C2C(C=CC(=O)C23COC1(C45C3CCC(C4)C(=C)C5OC(=O)C)O)(C)C 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 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
[(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 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
[(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 CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 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 CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C 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 CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C 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 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
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 CC(=O)OC1CC2CC3(C1C45COC3(C(C4C(CCC5O)(C)C)O)O)C(=O)C2=C 406.50 unknown https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L
CID 101157456 101157456 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
Henryin 11741244 Click to see CC(=O)OCC12C3CCC4C(C3(C(CC1C(CCC2O)(C)C)O)C(=O)C4=C)O 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 CC1(C2CC(C34C(C2(C(CC1O)O)C)CCC(C3O)C(=C)C4=O)O)C 350.40 unknown https://doi.org/10.1055/S-0028-1088331
Odonicin 14106499 Click to see CC(=O)OC1C2C(C=CC(=O)C23COC1(C45C3CCC(C4)C(=C)C5OC(=O)C)O)(C)C 430.50 unknown https://doi.org/10.1016/S0040-4039(02)00677-9
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 CC(=O)OC1CC2CC3(C1C45COC3(C(C4C(CCC5O)(C)C)O)O)C(=O)C2=C 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 CC(=O)OC1C(=C)C2CC3C4C1(C2)C(=O)OC5C4(C(C(=O)O3)C(CC5)(C)C)C=O 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 CC1(CCC(C23C1C(OC2OC(=O)C45C3CCC(C4)C(=C)C5O)OC)O)C 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 CC(=O)OCC1C(CCC(C12COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)OC(=O)C)(C)C 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 CC(=O)OC1C(=C)C2CC3C4C1(C2)C(=O)OC5C4(C(C(O3)O)C(CC5)(C)C)C=O 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 CC(=O)OC1C(=C)C2CC3C4C1(C2)C(=O)OC5C4(C(C(=O)O3)C(CC5)(C)C)C=O 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 CC(=O)OC1C(=C)C2CCC3C1(C2)C(=O)OC4C35C(C(OC5OC)O)C(CC4)(C)C 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 CC1(CCC2C3(C1C(=O)OC4C3C5(CC(C4)C(=C)C5O)C(=O)O2)C=O)C 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
Rabdosin C 158213 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
> 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 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
Oleanolic Acid (Caryophyllin) 49867939 Click to see CC1(CC2C(CCC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(C1)C(=O)O)C 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 CCCCOP(=O)(OCCCC)OCCCC 266.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
1-Butanol 263 Click to see CCCCO 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
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1016/S0040-4039(02)00677-9

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