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Isodon gesneroides

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 UUID643fdf7d08172946114730
Scientific name Isodon gesneroides
Authority (J.Sinclair) H.Hara
First published in J. Jap. Bot. 60: 234 (1985)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Plectranthus gesneroides J.Sinclair Notes Roy. Bot. Gard. Edinburgh 20: 124 (1948)
Rabdosia gesneroides (J.Sinclair) H.Hara J. Jap. Bot. 47: 195 (1972)

Common names Top

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Language Common/alternative name
Chinese 苣苔香茶菜

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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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-0000217860
Tropicos 17607182
KEW urn:lsid:ipni.org:names:915127-1
The Plant List kew-102933
Open Tree Of Life 541507
NCBI Taxonomy 662912
IPNI 915127-1
GBIF 5609018
EOL 2898946
CMAUP NPO15057

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
Three New Diterpenoids from <i>Isodon nervosus</i> Zhi‐Xiong Wei, You‐Heng Gao, Fen Yang, Hai‐Xiao Lu, Lin Ni, Xiao‐Hong Zhou Wiley 18-Jul-2011
doi:10.1002/HLCA.201000429
Diterpenoids from Isodon gesneroides Shao-Nong Chen, Hong-Jie Zhang, Zhong-Wen Lin, Yao-Zu Chen, Han-Dong Sun Elsevier BV 01-May-2003
doi:10.1016/S0031-9422(97)00609-2
Cytotoxic ent-kaurene diterpenoids from Isodon gesneroides. Sun HD, Lin ZW, Niu FD, Zhen QT, Wu B, Lin LZ, Cordell GA Phytochemistry 01-Nov-1995
doi:10.1016/0031-9422(95)00373-F
PMID:8534404

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(2-Acetyloxy-3,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 78384977 Click to see 434.50 unknown https://doi.org/10.1016/S0031-9422(97)00609-2
(2,3-Diacetyloxy-11-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 85135901 Click to see 476.60 unknown https://doi.org/10.1016/0031-9422(95)00373-F
(2,3,6-Triacetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 74000945 Click to see 534.60 unknown https://doi.org/10.1016/0031-9422(95)00373-F
(2,3,6,8-Tetraacetyloxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 162979958 Click to see 576.60 unknown https://doi.org/10.1016/S0031-9422(97)00609-2
(5,5,9-Trimethyl-14-methylidene-11,15-dioxo-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 162845894 Click to see CC(=O)OC1CC23CC(CC(=O)C2C4(C1C(CCC4)(C)C)C)C(=C)C3=O 358.50 unknown https://doi.org/10.1016/0031-9422(95)00373-F
[(1R,2R,3R,4R,6S,8S,9S,10S,11S,13S)-2,3,6-triacetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 10602392 Click to see 534.60 unknown https://doi.org/10.1016/0031-9422(95)00373-F
[(1R,2R,3R,4R,6S,8S,9S,10S,11S,13S)-2,3,6,8-tetraacetyloxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 102317488 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)OC(=O)C)(C)C)OC(=O)C)OC(=O)C)C)C(=O)C2=C 576.60 unknown https://doi.org/10.1016/S0031-9422(97)00609-2
[(1R,2R,3R,4S,6S,9S,10S,11S,13S)-2-acetyloxy-3,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 5317641 Click to see 434.50 unknown https://doi.org/10.1016/S0031-9422(97)00609-2
[(1S,2R,3R,4R,6S,8S,9S,10S,11S,13S,15R)-2,3,6,8-tetraacetyloxy-15-hydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 10650858 Click to see 578.60 unknown https://doi.org/10.1002/HLCA.201000429
https://doi.org/10.1016/S0031-9422(97)00609-2
[(1S,2R,3R,4S,6S,9R,10S,13S,15R)-2,3,15-triacetyloxy-5,5,9-trimethyl-14-methylidene-11-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 102317487 Click to see 518.60 unknown https://doi.org/10.1016/S0031-9422(97)00609-2
[(1S,2R,4S,6S,9S,10S,11S,13S,15R)-2,11,15-triacetyloxy-5,5,9-trimethyl-14-methylidene-3-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 10839642 Click to see 518.60 unknown https://doi.org/10.1002/HLCA.201000429
https://doi.org/10.1016/S0031-9422(97)00609-2
[(1S,3S,4R,9R,10S,13S)-5,5,9-trimethyl-14-methylidene-11,15-dioxo-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 10247836 Click to see 358.50 unknown https://doi.org/10.1016/0031-9422(95)00373-F
[(1S,3S,4R,9S,10S,11S,13S)-11-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-3-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 15241155 Click to see 360.50 unknown https://doi.org/10.1016/0031-9422(95)00373-F
Dawoensin A 10412708 Click to see CC(=O)OC1CCC2(C3C(CC4CC3(C(C(C2C1(C)C)OC(=O)C)OC(=O)C)C(=O)C4=C)O)C 476.60 unknown https://doi.org/10.1016/0031-9422(95)00373-F
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
N,N,N-trimethylglycinium 248 Click to see 118.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown via CMAUP database
Methylumbelliferone 10748 Click to see 176.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Cichoriin 442101 Click to see 340.28 unknown via CMAUP database
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database

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