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Plectranthus xanthanthus

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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 UUID64406a5470948429239106
Scientific name Plectranthus xanthanthus
Authority (C.Y.Wu & Y.C.Huang) S.S.Ying
First published in New Taxa New Names 2: 234. 2019

Description Top

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Synonyms Top

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

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
World Flora Online wfo-0001428501
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

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)!
Title Authors Publication Released IDs
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 CC(COC(=O)C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3=C(C2=O)O)(C)C)C)O 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 CC(COC(=O)C)C1=C(C2=C(C(=C1O)OC(=O)C)C3(CCCC(C3=C(C2=O)O)(C)C)C)O 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 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/10.1016/0031-9422(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 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/10.1021/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 CC1CC12C(C(=O)C3=C(C2=O)C(=O)C(=C4C3(CC(CC4(C)C)OC(=O)C)C)O)OC(=O)C 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 CC(C)OC(C)CC1=C(C2=C(C(=C1O)OC(=O)C)C3(CC(CC(C3=C(C2=O)O)(C)C)OC(=O)C)C)O 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 CC(C)OC(C)CC1=C(C2=C(C(=C1O)OC(=O)C)C3(CC(CC(C3=C(C2=O)O)(C)C)OC(=O)C)C)O 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 CC(CC1=C(C2=C(C(=C1O)OC(=O)C)C3(CC(CC(C3=C(C2=O)O)(C)C)OC(=O)C)C)O)O 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 CC1CC12C(C(=O)C3(C4=C(C(=O)C(=C3C2=O)O)C(CC(C4)OC(=O)C)(C)C)C)OC(=O)C 444.50 unknown https://doi.org/10.1016/0031-9422(89)80293-6
16-O-Acetylcoleon C 630146 Click to see CC(COC(=O)C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3=C(C2=O)O)(C)C)C)O 404.50 unknown https://doi.org/10.1021/NP0102049
Coleon U 333723 Click to see CC(C)C1=C(C2=C(C(=C1O)O)C3(CCCC(C3=C(C2=O)O)(C)C)C)O 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 CC(C)C1=C(C2=C(C(=C1O)OC(=O)C)C3(CCCC(C3=C(C2=O)O)(C)C)C)O 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 CC1CC12C(C(=O)C3=C(C2=O)C(=O)C(=C4C3(CC(CC4(C)C)OC(=O)C)C)O)OC(=O)C 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 CC(CC1=C(C2=C(C(=C1O)OC(=O)C)C3(CC(CC(C3=C(C2=O)O)(C)C)OC(=O)C)C)O)O 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 CC(C)C1=C(C(=C(C(=O)C1=O)C2(CCCC(C2=O)(C)C)C)C(=O)O)O 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 CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CC=CC(C)C(=O)C(CC(C)C)O)O 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 CC1CCC=C2C1(CC3=C(C2=O)OC=C3C)C 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 CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 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 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/10.1016/0031-9422(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 CC1CCC(=C)C2CCC(C2C=C1C)(C)O 220.35 unknown https://doi.org/10.1021/NP0102049

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