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Internal ID UUID643fdf7cebeee474743772
Scientific name Isodon forrestii
Authority Kudô
First published in Mem. Fac. Sci. Taihoku Imp. Univ. 2: 130 (1929)

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Synonyms Top

Scientific name Authority First published in
Plectranthus forrestii Diels Notes Roy. Bot. Gard. Edinburgh 5: 229 (1912)
Rabdosia forrestii (Diels) H.Hara J. Jap. Bot. 47: 195 (1972)
Rabdosia forrestii var. intermedia C.Y.Wu & H.W.Li Fl. Yunnanica 1: 769 (1977)

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Language Common/alternative name
Chinese 紫萼香茶菜

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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-0000217859
Tropicos 17607183
KEW urn:lsid:ipni.org:names:448576-1
The Plant List kew-102932
Open Tree Of Life 541512
NCBI Taxonomy 662911
IPNI 448576-1
GBIF 5609019
EOL 2898945

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
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
Libertellenone H, a Natural Pimarane Diterpenoid, Inhibits Thioredoxin System and Induces ROS-Mediated Apoptosis in Human Pancreatic Cancer Cells Zhang W, Zhu Y, Yu H, Liu X, Jiao B, Lu X Molecules 09-Jan-2021
PMCID:PMC7827531
doi:10.3390/molecules26020315
PMID:33435380
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
ent-Isopimarane diterpenoids of the leaves from Rabdosia forrestii. Kubo I, Shimizu K, Xu YL Fitoterapia 01-Dec-2003
doi:10.1016/J.FITOTE.2003.07.006
PMID:14630168
Flavonoids from Isodon oresbius Huang Hao, Sun Handong, Zhao Shouxun Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(96)00084-2
Diterpenoids from Rabdosia forrestii Yunlong Xu, Isao Kubo, Chungshih Tang, Fenglei Zhang, Handong Sun Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)80031-M

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
(1R)-1-[(2R,4aS,4bR,8aR,10aS)-10a-hydroxy-2,4b,8,8-tetramethyl-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthren-2-yl]ethane-1,2-diol 163050194 Click to see CC1(CCCC2(C1CCC3(C2CCC(C3)(C)C(CO)O)O)C)C 324.50 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
(4aR,4bS,7R,8aS,10aR)-7-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-8a-ol 163029699 Click to see CC1(CCCC2(C1CCC3(C2CCC(C3)(C)C4COC(O4)(C)C)O)C)C 364.60 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
[(2R)-2-[(2R,4aS,4bR,8aR,10aS)-10a-hydroxy-2,4b,8,8-tetramethyl-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthren-2-yl]-2-hydroxyethyl] acetate 163189083 Click to see CC(=O)OCC(C1(CCC2C3(CCCC(C3CCC2(C1)O)(C)C)C)C)O 366.50 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
[2-(10a-Hydroxy-2,4b,8,8-tetramethyl-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthren-2-yl)-2-hydroxyethyl] acetate 163007865 Click to see CC(=O)OCC(C1(CCC2C3(CCCC(C3CCC2(C1)O)(C)C)C)C)O 366.50 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
1-(10a-Hydroxy-2,4b,8,8-tetramethyl-1,3,4,4a,5,6,7,8a,9,10-decahydrophenanthren-2-yl)ethane-1,2-diol 163050193 Click to see CC1(CCCC2(C1CCC3(C2CCC(C3)(C)C(CO)O)O)C)C 324.50 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
7-(2,2-Dimethyl-1,3-dioxolan-4-yl)-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-8a-ol 163029698 Click to see CC1(CCCC2(C1CCC3(C2CCC(C3)(C)C4COC(O4)(C)C)O)C)C 364.60 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(2,3,15-Triacetyloxy-5,5,9-trimethyl-14-methylidene-6-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadec-7-enyl) acetate 163036816 Click to see CC(=O)OC1CC2CC3(C1C4(C=CC(=O)C(C4C(C3OC(=O)C)OC(=O)C)(C)C)C)C(C2=C)OC(=O)C 516.60 unknown https://doi.org/10.1016/0031-9422(96)00084-2
https://doi.org/10.1016/0031-9422(93)80031-M
[(1S,2R,3R,4R,6S,8S,9R,10S,11S,13S,15R)-2,8-diacetyloxy-3,6,15-trihydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 101193825 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)O)(C)C)O)OC(=O)C)C)C(C2=C)O 494.60 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
https://doi.org/10.1016/0031-9422(93)80031-M
[(1S,2R,3R,4S,9S,10S,11S,13R,15R)-2,3,15-triacetyloxy-5,5,9-trimethyl-14-methylidene-6-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadec-7-enyl] acetate 163036818 Click to see CC(=O)OC1CC2CC3(C1C4(C=CC(=O)C(C4C(C3OC(=O)C)OC(=O)C)(C)C)C)C(C2=C)OC(=O)C 516.60 unknown https://doi.org/10.1016/0031-9422(96)00084-2
https://doi.org/10.1016/0031-9422(93)80031-M
[(1S,4S,9S,10R)-2,3,8,15-tetraacetyloxy-6-hydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate 129317002 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)OC(=O)C)(C)C)O)OC(=O)C)C)C(C2=C)OC(=O)C 578.60 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
https://doi.org/10.1016/0031-9422(93)80031-M
Forrestin B 44577281 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(C2C1(C)C)O)OC(=O)C)C(C4=C)O)O)C)O 452.50 unknown https://doi.org/10.1016/J.FITOTE.2003.07.006
https://doi.org/10.1016/0031-9422(93)80031-M

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