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Vitex canescens

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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 UUID643ff09028a00306173829
Scientific name Vitex canescens
Authority Kurz
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 42: 101 (1873)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vitex kweichowensis C.Pei Sinensia 2: 71 (1931)

Common names Top

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Language Common/alternative name
Thai ผ่าเสี้ยน
Thai ขี้เห็น
Chinese 蔓荆子
Chinese 灰毛牡荆
Chinese 灰布荆
Chinese 灰牡荆

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000332996
Tropicos 33702218
KEW urn:lsid:ipni.org:names:865635-1
The Plant List kew-213369
Open Tree Of Life 278730
Observations.org 456278
NCBI Taxonomy 413480
IUCN Red List 159073384
IPNI 865635-1
iNaturalist 415619
GBIF 3881963
EOL 2893639
Elurikkus 592512

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
Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones Arif Y, Singh P, Bajguz A, Hayat S Int J Mol Sci 04-Aug-2022
PMCID:PMC9369314
doi:10.3390/ijms23158664
PMID:35955797
The phytochemical, biological, and medicinal attributes of phytoecdysteroids: An updated review Das N, Mishra SK, Bishayee A, Ali ES, Bishayee A Acta Pharm Sin B 16-Oct-2020
PMCID:PMC8343124
doi:10.1016/j.apsb.2020.10.012
PMID:34386319
An interspecific variation in rhizosphere effects on soil anti-erodibility Wang Z, Chiarucci A, Fang H, Chen M Sci Rep 12-Feb-2020
PMCID:PMC7015890
doi:10.1038/s41598-020-58784-z
PMID:32051430
The Administration of Tibetan Precious Pills: Efficacy in Historical and Ritual Contexts Czaja O Asian Med (Lieden) 01-Jan-2015
PMCID:PMC5154374
doi:10.1163/15734218-12341350
PMID:27980504
Novel Ecdysteroids from Serratula wolffii Ványolós A, Béni Z, Dékány M, Simon A, Báthori M ScientificWorldJournal 02-May-2012
PMCID:PMC3354479
doi:10.1100/2012/651275
PMID:22645442
Ecdysteroids from Vitex canescens Apichart Suksamrarn, Chatriwat Sommechai, Panuwat Charulpong, Bordin Chitkul Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(94)00712-3
Ecdysteroids of the root bark of Vitex canescens Apichart Suksamrarn, Nart Promrangsan, Bordin Chitkul, Sureeporn Homvisasevongsa, Achara Sirikate Elsevier BV 25-Mar-2003
doi:10.1016/S0031-9422(97)00102-7
Highly oxygenated ecdysteroids from Vitex canescens root bark. Suksamrarn A, Promrangsan N, Jintasirikul A Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(99)00458-6
PMID:10820804

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(24R)-11alpha,20,24-trihydroxyecdysone 16755634 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(C(C)(C)O)O)O)O)O)O 512.60 unknown https://doi.org/10.1016/S0031-9422(99)00458-6
(25R)-11alpha,20,26-trihydroxyecdysone 16755620 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O)O 512.60 unknown https://doi.org/10.1016/S0031-9422(99)00458-6
(25S)-11alpha,20,26-trihydroxyecdysone 16755647 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O)O 512.60 unknown https://doi.org/10.1016/S0031-9422(99)00458-6
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,5R)-2,3,5,6-tetrahydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 11103069 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(C(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R,5S)-2,3,5,6-tetrahydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 11016518 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(C(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-(2,3,5,6-tetrahydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 73323485 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(C(C)(C)O)O)O)O)O)O 512.60 unknown https://doi.org/10.1016/S0031-9422(99)00458-6
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 4254739 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1016/0031-9422(94)00712-3
https://doi.org/10.1016/S0031-9422(97)00102-7
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-(2,3,6,7-tetrahydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 73323476 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(CO)O)O)O)O)O 512.60 unknown https://doi.org/10.1016/S0031-9422(99)00458-6
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,5,6-tetrahydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 73744749 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CC(C(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
2,3,14-Trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-5,6-dimethylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 12312687 Click to see CC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)(C)O 494.70 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 271605 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
https://doi.org/10.1016/0031-9422(94)00712-3
2,3,6-Trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,11,12,16,17-octahydrocyclopenta[a]phenanthren-7-one 163034315 Click to see CC12CCC3=C(C1=CCC2C(C)(C(CCC(C)(C)O)O)O)C(=O)C(=C4C3(CC(C(C4)O)O)C)O 476.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
https://doi.org/10.1016/0031-9422(94)00712-3
Calonysterone 101281312 Click to see CC12CCC3=C(C1=CCC2C(C)(C(CCC(C)(C)O)O)O)C(=O)C(=C4C3(CC(C(C4)O)O)C)O 476.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
Makisteron-A 12312688 Click to see CC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)(C)O 494.70 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
Turkesterone 14376672 Click to see CC12CC(C3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O)O 496.60 unknown https://doi.org/10.1016/0031-9422(94)00712-3
https://doi.org/10.1016/S0031-9422(97)00102-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
[(3R,6R)-2,6-dihydroxy-2-methyl-6-[(2R,3R,5S,9S,10S,13R,14R,17R)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]heptan-3-yl] 1H-pyrrole-2-carboxylate 162844165 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(CCC(C(C)(C)O)OC(=O)C5=CC=CN5)O)O 573.70 unknown https://doi.org/10.1016/0031-9422(94)00712-3
[(3S,6S)-2,6-dihydroxy-2-methyl-6-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]heptan-3-yl] 1H-pyrrole-2-carboxylate 163186441 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(CCC(C(C)(C)O)OC(=O)C5=CC=CN5)O)O 573.70 unknown https://doi.org/10.1016/0031-9422(94)00712-3
[(6S)-2,6-dihydroxy-2-methyl-6-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]heptan-3-yl] 1H-pyrrole-2-carboxylate 10438055 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(CCC(C(C)(C)O)OC(=O)C5=CC=CN5)O)O 573.70 unknown https://doi.org/10.1016/0031-9422(94)00712-3
[2,6-dihydroxy-2-methyl-6-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)heptan-3-yl] 1H-pyrrole-2-carboxylate 85142938 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(CCC(C(C)(C)O)OC(=O)C5=CC=CN5)O)O 573.70 unknown https://doi.org/10.1016/0031-9422(94)00712-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-17-[(1R)-1-[(2R)-5,5-dimethyloxolan-2-yl]-1-hydroxyethyl]-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 10479483 Click to see CC1(CCC(O1)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C 462.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
Shidasterone 15227299 Click to see CC1(CCC(O1)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C 462.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7
Stachysterone D 634652 Click to see CC1(CCC(O1)C(C)(C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)O)C 462.60 unknown https://doi.org/10.1016/S0031-9422(97)00102-7

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