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Coleus xanthanthus

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 UUID68f8f6e145201345141186
Scientific name Coleus xanthanthus
Authority C.Y.Wu & Y.C.Huang
First published in Acta Phytotax. Sin. 10: 241 (1965)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Plectranthus xanthanthus (C.Y.Wu & Y.C.Huang) S.S.Ying New Taxa New Names 2: 234 (2022)

Common names Top

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Language Common/alternative name
Chinese 黄鞘蕊花
Chinese 黃鞘蕊花

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
Tropicos 100244535
KEW urn:lsid:ipni.org:names:77176728-1
The Plant List kew-158601
Observations.org 453496
IPNI 77203685-1
GBIF 7998826
Elurikkus 635725
Open Tree Of Life 1067796
World Flora Online wfo-0000916480
Tropicos 17607525
KEW urn:lsid:ipni.org:names:446219-1
NCBI Taxonomy 662900
IPNI 446219-1
GBIF 5605083

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
The complete chloroplast genome of Periploca forrestii (Apocynaceae), a traditional Chinese medicinal plant Long JL, Zhang N, Wu Y, Zhang YP, Wu ZK Mitochondrial DNA B Resour 09-Mar-2022
PMCID:PMC8920375
doi:10.1080/23802359.2022.2049459
PMID:35295911
An updated tribal classification of Lamiaceae based on plastome phylogenomics Zhao F, Chen YP, Salmaki Y, Drew BT, Wilson TC, Scheen AC, Celep F, Bräuchler C, Bendiksby M, Wang Q, Min DZ, Peng H, Olmstead RG, Li B, Xiang CL BMC Biol 08-Jan-2021
PMCID:PMC7796571
doi:10.1186/s12915-020-00931-z
PMID:33419433
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
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
Eremophilane Sesquiterpenoids from <i>Ligularia fischeri</i> Wei‐Dong Xie, Cheng‐Wu Weng, Xia Li, Kyung‐Ho Row Wiley 20-Oct-2010
doi:10.1002/HLCA.201000010
Diterpenoid quinones of Salvia lanata K.S. Mukherjee, P.K. Ghosh, Sah Badruddoza Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)80064-7
Abietane diterpenoids from Coleus zeylanicus Raj Mehrotra, R.A. Vishwakarma, R.S. Thakur Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80293-6
Abietane diterpenoids from Coleus xanthanthus. Mei SX, Jiang B, Niu XM, Li ML, Yang H, Na Z, Lin ZW, Li CM, Sun HD J Nat Prod 01-May-2002
doi:10.1021/NP0102049
PMID:12027731

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
[(2R)-2-[(4bR)-1,3,4,9-tetrahydroxy-4b,8,8-trimethyl-10-oxo-6,7-dihydro-5H-phenanthren-2-yl]propyl] acetate 101643455 Click to see 404.50 unknown https://doi.org/10.1016/0031-9422(89)80293-6
https://doi.org/10.1021/NP0102049
[(2R)-2-[(4bS)-4-acetyloxy-1,3,9-trihydroxy-4b,8,8-trimethyl-10-oxo-6,7-dihydro-5H-phenanthren-2-yl]propyl] acetate 162953894 Click to see 446.50 unknown https://doi.org/10.1021/NP0102049
[(2S,2'S,3R,4aS)-10-hydroxy-2',4a,8,8-tetramethyl-1,4,9-trioxospiro[3,7-dihydrophenanthrene-2,1'-cyclopropane]-3-yl] acetate 11728714 Click to see CC1CC12C(C(=O)C3(C4=C(C(=O)C(=C3C2=O)O)C(CC=C4)(C)C)C)OC(=O)C 384.40 unknown https://doi.org/10.1021/NP0102049
[(2S,3R,4aS)-10-hydroxy-2',4a,8,8-tetramethyl-1,4,9-trioxospiro[3,7-dihydrophenanthrene-2,1'-cyclopropane]-3-yl] acetate 101188397 Click to see 384.40 unknown https://doi.org/10.1016/0031-9422(89)80293-6
[(2S)-2-[(4bS)-3-acetyloxy-9-hydroxy-4b,8,8-trimethyl-1,4,10-trioxo-6,7-dihydro-5H-phenanthren-2-yl]propyl] acetate 162989978 Click to see 444.50 unknown https://doi.org/10.1021/NP0102049
[(3S,4aS,6R,7S)-6-acetyloxy-10-hydroxy-1,1,2',4a-tetramethyl-5,8,9-trioxospiro[2,3,4,6-tetrahydrophenanthrene-7,1'-cyclopropane]-3-yl] acetate 22297320 Click to see 444.50 unknown https://doi.org/10.1016/0031-9422(89)80293-6
[(3S,4aS)-5-acetyloxy-6,8,10-trihydroxy-1,1,4a-trimethyl-9-oxo-7-(2-propan-2-yloxypropyl)-3,4-dihydro-2H-phenanthren-3-yl] acetate 10864069 Click to see 504.60 unknown https://doi.org/10.1016/0031-9422(89)80293-6
[(3S,4aS)-5-acetyloxy-6,8,10-trihydroxy-1,1,4a-trimethyl-9-oxo-7-[(2S)-2-propan-2-yloxypropyl]-3,4-dihydro-2H-phenanthren-3-yl] acetate 162984691 Click to see 504.60 unknown https://doi.org/10.1021/NP0102049
[(3S,4aS)-5-acetyloxy-6,8,10-trihydroxy-7-[(2R)-2-hydroxypropyl]-1,1,4a-trimethyl-9-oxo-3,4-dihydro-2H-phenanthren-3-yl] acetate 162946246 Click to see 462.50 unknown https://doi.org/10.1021/NP0102049
[(3S,4bS,6R,7S)-6-acetyloxy-9-hydroxy-1,1,2',4b-tetramethyl-5,8,10-trioxospiro[2,3,4,6-tetrahydrophenanthrene-7,1'-cyclopropane]-3-yl] acetate 101188396 Click to see 444.50 unknown https://doi.org/10.1016/0031-9422(89)80293-6
16-O-Acetylcoleon C 630146 Click to see 404.50 unknown https://doi.org/10.1021/NP0102049
Coleon U 333723 Click to see 346.40 unknown https://doi.org/10.1021/NP0102049
https://doi.org/10.1016/0031-9422(89)80293-6
Coleon U 11-acetate 636683 Click to see 388.50 unknown https://doi.org/10.1021/NP0102049
Xanthanthusin H 10094991 Click to see CC(COC(=O)C)C1=C(C(=O)C2=C(C1=O)C(=O)C(=C3C2(CCCC3(C)C)C)O)OC(=O)C 444.50 unknown https://doi.org/10.1016/0031-9422(89)80293-6
Zeysitwnhccrcy-xfjjdfovsa- 636684 Click to see 444.50 unknown https://doi.org/10.1016/0031-9422(89)80293-6
https://doi.org/10.1021/NP0102049
Zlpmihavswbsmf-djfzvpldsa- 10863519 Click to see 462.50 unknown https://doi.org/10.1016/0031-9422(89)80293-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
xanthanthusin E 10247140 Click to see 348.40 unknown https://doi.org/10.1016/0031-9422(89)80293-6
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds
(4R,6R,7Z,10E)-4-hydroxy-13-[(2R)-6-hydroxy-2,8-dimethyl-3,4-dihydrochromen-2-yl]-2,6,10-trimethyltrideca-7,10-dien-5-one 162874327 Click to see 428.60 unknown https://doi.org/10.1016/0031-9422(89)80293-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
3,4a,5-Trimethyl-4,5,6,7-tetrahydrobenzo[f][1]benzofuran-9-one 14830749 Click to see 230.30 unknown https://doi.org/10.1002/HLCA.201000010
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(81)80064-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(81)80064-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3R,3aS,6R,9aS)-3,5,6-trimethyl-9-methylidene-2,3a,6,7,8,9a-hexahydro-1H-cyclopenta[8]annulen-3-ol 162927489 Click to see 220.35 unknown https://doi.org/10.1021/NP0102049

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