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Isodon phyllostachys

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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 UUID643fdf81b5c8e645910096
Scientific name Isodon phyllostachys
Authority Kudô
First published in Mem. Fac. Sci. Taihoku Imp. Univ. 2: 121 (1929)

Description Top

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Synonyms Top

Scientific name Authority First published in
Plectranthus phyllostachys Diels Notes Roy. Bot. Gard. Edinburgh 5: 230 (1912)
Rabdosia phyllostachys (Diels) H.Hara J. Jap. Bot. 47: 199 (1972)
Rabdosia phyllostachys var. leptophylla C.Y.Wu & H.W.Li Fl. Yunnanica 1: 766 (1977)

Common names Top

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Language Common/alternative name
Chinese 叶穗香茶菜

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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No forms added yet.

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-0000217938
Tropicos 17607171
KEW urn:lsid:ipni.org:names:448603-1
The Plant List kew-103004
Open Tree Of Life 1017563
Observations.org 451828
NCBI Taxonomy 662923
IPNI 448603-1
iNaturalist 1123413
GBIF 5608888
EOL 2898979
Elurikkus 556182

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
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
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
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
Molecular and morphological evidence for a new species of Isodon (Lamiaceae) from southern China Chen YP, Huang CZ, Zhao Y, Xiang CL Plant Divers 14-Jul-2020
PMCID:PMC7987569
doi:10.1016/j.pld.2020.06.004
PMID:33778225
Natural Products Research in China From 2015 to 2016 Liu H, Zhu G, Fan Y, Du Y, Lan M, Xu Y, Zhu W Front Chem 20-Mar-2018
PMCID:PMC5869933
doi:10.3389/fchem.2018.00045
PMID:29616210
Three New ent-Kauranoids from Isodon phyllostachys Han-Dong Sun, Xian Li, Jianxin Pu, Shenghong Li, Shengxiong Huang, Zhiying Weng, Quanbin Han The Japan Institute of Heterocyclic Chemistry 16-Feb-2009
doi:10.3987/COM-07-11140
<i>ent</i>‐Kaurane Diterpenoids from <i>Isodon phyllostachys</i> Xian Li, Zhi‐Ying Weng, Yong Li, Jian‐Xin Pu, Sheng‐Xiong Huang, Wei‐Lie Xiao, Han‐Dong Sun Wiley 10-Jul-2008
doi:10.1002/HLCA.200890121
Cytotoxic ent-kaurene diterpenoids from Isodon phyllostachys. Li X, Xiao W, Pu J, Ban L, Shen Y, Weng Z, Li S, Sun H Phytochemistry 01-Jul-2006
doi:10.1016/J.PHYTOCHEM.2006.05.002
PMID:16777159
Structure of phyllostachysin A: novel antineoplastic diterpenoid from Rabdosia phyllostachys Tetsuro Fujita, Sun Han-Dong, Yoshio Takeda, Yoshinori Minami, Teruyoshi Marunaka, Lin Zhon-Wen, Xu Yun-Long Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39850001738
Diterpenoid constituents of Rabdosia liangshanica Fenglei Zhang, Yunlong Xu, Handong Sun Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97822-1
Enmein type diterpenoids from Isodon japonica. Li B, Tian X Phytochemistry 01-Oct-2001
doi:10.1016/S0031-9422(01)00245-X
PMID:11576594
A new ent-kaurane diterpenoid from Isodon phyllostachys. Hou AJ, Yang H, Jiang B, Zhao QS, Lin ZW, Sun HD Fitoterapia 01-Aug-2000
doi:10.1016/S0367-326X(00)00148-9
PMID:10925014

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2R,3S,5R,8R,9S,11R,16R,17R)-3,9,16,17-tetrahydroxy-12,12-dimethyl-6-methylidenepentacyclo[7.6.1.15,8.01,11.02,8]heptadecane-7,10-dione 162867678 Click to see CC1(CCCC23C1C(=O)C(C2O)(C45C3C(CC(C4O)C(=C)C5=O)O)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(01)00245-X
(1R,2R,4R,9R,10S,11R,12R,13S,15R,16R)-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,11,12,15,16-pentol 101402141 Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4O)O)O)O)C)C 352.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
(1R,2R,4S,5S,9R,10S,12R,13S,16R)-2,12,16-trihydroxy-5,9-dimethyl-14-methylidene-11,15-dioxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 163010750 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)C=O 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
(1R,2S,3S,5S,8R,9S,10S,11R,18R)-3,9,10,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 10428853 Click to see CC1(CCCC23C1C(C(C45C2C(CC(C4O)C(=C)C5=O)O)(OC3)O)O)C 364.40 unknown https://doi.org/10.1002/HLCA.200890121
(1R,2S,3S,5S,8R,9S,11R,16R,18R)-3,9,16,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,10-dione 163058232 Click to see CC1(CCCC23C1C(=O)C(C45C2C(CC(C4O)C(=C)C5=O)O)(OC3O)O)C 378.40 unknown https://doi.org/10.1002/HLCA.200890121
(1R,2S,3S,5S,8S,9S,11R,16R,17R)-3,9,16,17-tetrahydroxy-12,12-dimethyl-6-methylidenepentacyclo[7.6.1.15,8.01,11.02,8]heptadecane-7,10-dione 101317811 Click to see CC1(CCCC23C1C(=O)C(C2O)(C45C3C(CC(C4O)C(=C)C5=O)O)O)C 362.40 unknown https://doi.org/10.1039/C39850001738
https://doi.org/10.1016/S0031-9422(00)97822-1
(1R,2S,4R,9R,10S,11S,13S,16R)-2,11,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-8,15-dione 16081683 Click to see CC1(CCC(=O)C2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
(1R,2S,4S,5R,8R,9S,10S,11R,18R)-4,9,10,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 24813699 Click to see CC1(CCCC23C1C(C(C45C2CC(C(C4O)C(=C)C5=O)O)(OC3)O)O)C 364.40 unknown https://doi.org/10.3987/COM-07-11140
(1R,2S,5R,8S,9S,10S,11S,13R)-9,10,13-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 102408097 Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)O)C 348.40 unknown https://doi.org/10.1002/HLCA.200890121
(1R,2S,5S,7R,8R,9S,10S,11R,18R)-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,9,10,18-tetrol 162917310 Click to see CC1(CCCC23C1C(C(C45C2CCC(C4O)C(=C)C5O)(OC3)O)O)C 350.40 unknown https://doi.org/10.1002/HLCA.200890121
(1R,2S,5S,8R,9S,10S,11R,12S,18R)-9,10,18-trihydroxy-12-(hydroxymethyl)-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 102382575 Click to see CC1(CCCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)CO 364.40 unknown https://doi.org/10.1002/HLCA.200890121
(1R,2S,5S,8R,9S,10S,11R,15S,16R,18R)-9,10,15,18-tetrahydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 101663493 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3OC)O)O)O)C 394.50 unknown https://doi.org/10.3987/COM-07-11140
(1R,2S,5S,8R,9S,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 102117144 Click to see CC1(CCCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)C 348.40 unknown https://doi.org/10.1002/HLCA.200890121
(1R,2S,5S,8R,9S,10S,11S,13R,18R)-9,10,13,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 102408096 Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1002/HLCA.200890121
(1R,2S,5S,8R,9S,11S,13S,14S,15R,19S)-13,14,19-trihydroxy-16,16-dimethyl-6-methylidene-10,12-dioxahexacyclo[9.8.0.01,15.02,8.05,9.08,13]nonadecan-7-one 92484182 Click to see CC1(CCC(C23C1C(C4(C56C2CCC(C5OC3O4)C(=C)C6=O)O)O)O)C 362.40 unknown https://doi.org/10.1002/HLCA.200890121
https://doi.org/10.3987/COM-07-11140
(1R,5S,8R,9S,10S,11R,15S,18R)-9,10,15,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadec-2-en-7-one 101436261 Click to see CC1(CCC(C23C1C(C(C45C2=CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 362.40 unknown https://doi.org/10.3987/COM-07-11140
(7-Acetyloxy-9,18-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-10-yl) acetate 14564531 Click to see CC(=O)OC1C2C(CCCC23COC1(C45C3CCC(C4O)C(=C)C5OC(=O)C)O)(C)C 434.50 unknown https://doi.org/10.1002/HLCA.200890121
[(1R,2S,3R,5S,6R,8R,9S,10S,11S,12S,14R)-8,10,14-trihydroxy-13,13-dimethyl-7-methylidene-4,18-dioxahexacyclo[8.6.2.16,9.01,12.02,9.03,5]nonadecan-11-yl] acetate 101960703 Click to see CC(=O)OC1C2C(C(CCC23COC1(C45C3C6C(O6)C(C4)C(=C)C5O)O)O)(C)C 406.50 unknown https://doi.org/10.1016/S0367-326X(00)00148-9
[(1R,2S,5S,7R,8R,9S,10S,11R,18R)-7-acetyloxy-9,18-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-10-yl] acetate 101835386 Click to see CC(=O)OC1C2C(CCCC23COC1(C45C3CCC(C4O)C(=C)C5OC(=O)C)O)(C)C 434.50 unknown https://doi.org/10.1002/HLCA.200890121
12,12-Dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,9,10,18-tetrol 14564545 Click to see CC1(CCCC23C1C(C(C45C2CCC(C4O)C(=C)C5O)(OC3)O)O)C 350.40 unknown https://doi.org/10.1002/HLCA.200890121
2,11,12,16-Tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14466845 Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4=O)O)O)O)C)C 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
2,11,16-Trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14563771 Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)CO 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
2,11,16-Trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 73236013 Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
2,11,16-Trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-8,15-dione 73236014 Click to see CC1(CCC(=O)C2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
2,12,16-Trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 14807615 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)CO 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
2,12,16-Trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 56677494 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
2,12,16-Trihydroxy-5,9-dimethyl-14-methylidene-11,15-dioxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 163010749 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)C=O 362.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
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/J.PHYTOCHEM.2006.05.002
2,8,11,16-Tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 14466854 Click to see CC1(CCC(C2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)O)C 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
3,9,10,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 14287139 Click to see CC1(CCCC23C1C(C(C45C2C(CC(C4O)C(=C)C5=O)O)(OC3)O)O)C 364.40 unknown https://doi.org/10.1002/HLCA.200890121
3,9,16,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,10-dione 163058231 Click to see CC1(CCCC23C1C(=O)C(C45C2C(CC(C4O)C(=C)C5=O)O)(OC3O)O)C 378.40 unknown https://doi.org/10.1002/HLCA.200890121
4,9,10,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 74323549 Click to see CC1(CCCC23C1C(C(C45C2CC(C(C4O)C(=C)C5=O)O)(OC3)O)O)C 364.40 unknown https://doi.org/10.3987/COM-07-11140
5,5,9-Trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-2,11,12,15,16-pentol 73236012 Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4O)O)O)O)C)C 352.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
8,11,16-Trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 56674805 Click to see CC1(CCC(C2(C1CCC34C2C(CC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
9,10,13-Trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 74350111 Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)O)C 348.40 unknown https://doi.org/10.1002/HLCA.200890121
9,10,13,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 72752318 Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1002/HLCA.200890121
9,10,15-Trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 9997896 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)O)C 348.40 unknown https://doi.org/10.3987/COM-07-11140
9,10,15,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadec-2-en-7-one 74323640 Click to see CC1(CCC(C23C1C(C(C45C2=CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 362.40 unknown https://doi.org/10.3987/COM-07-11140
9,10,15,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 3576890 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.3987/COM-07-11140
https://doi.org/10.1002/HLCA.200890121
9,10,18-Trihydroxy-12-(hydroxymethyl)-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 74071460 Click to see CC1(CCCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)CO 364.40 unknown https://doi.org/10.1002/HLCA.200890121
Effusanin A 34174827 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)O)C 348.40 unknown https://doi.org/10.3987/COM-07-11140
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/J.PHYTOCHEM.2006.05.002
Longikaurin A 433636 Click to see CC1(CCCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)C 348.40 unknown https://doi.org/10.1002/HLCA.200890121
Oridonin 5321010 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.3987/COM-07-11140
https://doi.org/10.1002/HLCA.200890121
phyllostachysin D 16081682 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
phyllostachysin F 16081680 Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
PhyllostachysinH 16081681 Click to see CC1(CCC(C2(C1CCC34C2C(CC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
Ponicidin 14564539 Click to see CC1(CCC(C23C1C(C4(C56C2CCC(C5OC3O4)C(=C)C6=O)O)O)O)C 362.40 unknown https://doi.org/10.1002/HLCA.200890121
https://doi.org/10.3987/COM-07-11140
rabdoinflexin B 14466855 Click to see CC1(CCC(C2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)O)C 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
rabdokunmin D 45267139 Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)CO 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
rabdoloxin A 45271373 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)CO 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
rabdoloxin B 25195035 Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4=O)O)O)O)C)C 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
Rabdoternin F 74317560 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3OC)O)O)O)C 394.50 unknown https://doi.org/10.3987/COM-07-11140
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,1'S,4'R,5S,6S,7R,7'R,8'R,9S)-7-hydroxy-4'-methyl-10-methylidenespiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,9'-6,10-dioxatricyclo[5.2.1.04,8]decane]-2,11-dione 70698231 Click to see CC12CCC3C4(C1C(O3)OC2)COC(=O)C56C4C(CC(C5)C(=C)C6=O)O 360.40 unknown https://doi.org/10.1016/S0367-326X(00)00148-9
(1S,2S,3R,5S,7R,8S,11S,14R,17S,20R)-3,7-dihydroxy-14-methyl-6-methylidene-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one 20056294 Click to see CC12CCC3C4(C1C(OC2)OC4)C5C(CC6CC5(C(C6=C)O)C(=O)O3)O 362.40 unknown https://doi.org/10.1016/S0367-326X(00)00148-9
(1S,4R,6R,7R,12R,13S,16R,18R)-6,18-dihydroxy-8,8-dimethyl-17-methylidene-3,5-dioxapentacyclo[14.2.1.01,13.04,12.07,12]nonadecan-2-one 15624744 Click to see CC1(CCCC23C1C(OC2OC(=O)C45C3CCC(C4)C(=C)C5O)O)C 348.40 unknown https://doi.org/10.1002/HLCA.200890121
(1S,4R,6R,7S,12R,13S,16R,18R)-6,18-dihydroxy-8,8-dimethyl-17-methylidene-3,5-dioxapentacyclo[14.2.1.01,13.04,12.07,12]nonadec-10-en-2-one 163041064 Click to see CC1(CC=CC23C1C(OC2OC(=O)C45C3CCC(C4)C(=C)C5O)O)C 346.40 unknown https://doi.org/10.3987/COM-07-11140
(1S,4R,6R,7S,12R,13S,16R,18R)-6,18-dihydroxy-8,8-dimethyl-17-methylidene-3,5-dioxapentacyclo[14.2.1.01,13.04,12.07,12]nonadecan-2-one 162943742 Click to see CC1(CCCC23C1C(OC2OC(=O)C45C3CCC(C4)C(=C)C5O)O)C 348.40 unknown https://doi.org/10.3987/COM-07-11140
(1S,4S,8R,12S,13S,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 137705233 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/10.1016/S0367-326X(00)00148-9
6,18-Dihydroxy-8,8-dimethyl-17-methylidene-3,5-dioxapentacyclo[14.2.1.01,13.04,12.07,12]nonadec-10-en-2-one 74323639 Click to see CC1(CC=CC23C1C(OC2OC(=O)C45C3CCC(C4)C(=C)C5O)O)C 346.40 unknown https://doi.org/10.3987/COM-07-11140
6,18-Dihydroxy-8,8-dimethyl-17-methylidene-3,5-dioxapentacyclo[14.2.1.01,13.04,12.07,12]nonadecan-2-one 15624743 Click to see CC1(CCCC23C1C(OC2OC(=O)C45C3CCC(C4)C(=C)C5O)O)C 348.40 unknown https://doi.org/10.3987/COM-07-11140
https://doi.org/10.1002/HLCA.200890121
9,14-Dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione 430943 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/10.1016/S0367-326X(00)00148-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
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/10.1016/S0367-326X(00)00148-9
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0367-326X(00)00148-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.002

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