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Vitex strickeri

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 UUID643ff0a2c4a26743381368
Scientific name Vitex strickeri
Authority Vatke & Hildebr.
First published in Linnaea 43: 532 (1882)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Vitex lamiana W.Piep. Beibl. Bot. Jahrb. Syst. 141: 55 (1928)

Common names Top

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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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Somalia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000333471
Tropicos 33702951
KEW urn:lsid:ipni.org:names:866017-1
The Plant List kew-213807
Open Tree Of Life 6086854
IPNI 866017-1
GBIF 3902724

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
Recent Examples of Natural Products Isolation by Countercurrent Chromatographic Methods Isao Kubo Informa UK Limited 07-Jul-2007
doi:10.1080/10826079208016352
Isolation of ecdysteroids fromVitex strickeri using RLCC and recycling HPLC Zhang Minli, Michael J. Stout, Isao Kubo Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83046-N

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 / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(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 496.60 unknown https://doi.org/10.1080/10826079208016352
https://doi.org/10.1016/0031-9422(91)83046-N
(2S,3R,5R,9S,10R,11R,13R,14S,17R)-17-[(2S,3R)-3,6-dihydroxy-6-methylheptan-2-yl]-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 163090478 Click to see CC(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)C(CCC(C)(C)O)O 480.60 unknown https://doi.org/10.1016/0031-9422(91)83046-N
(2S,3R,5R,9S,10R,11R,13R,14S,17S)-17-[(2R,3R)-2,3-dihydroxy-6-methylheptan-2-yl]-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 163069961 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O 480.60 unknown https://doi.org/10.1016/0031-9422(91)83046-N
(2S,3R,5R,9S,10R,13R,14S,17R)-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 162992206 Click to see 496.60 unknown https://doi.org/10.1016/0031-9422(91)83046-N
17-(2,3-dihydroxy-6-methylheptan-2-yl)-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 4482423 Click to see 480.60 unknown https://doi.org/10.1016/0031-9422(91)83046-N
17-(3,6-dihydroxy-6-methylheptan-2-yl)-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 77199285 Click to see 480.60 unknown https://doi.org/10.1016/0031-9422(91)83046-N
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/10.1016/0031-9422(91)83046-N
2,3,14,20,22,25-Hexahydroxycholest-7-en-6-one 271605 Click to see 480.60 unknown https://doi.org/10.1016/0031-9422(91)83046-N
20-Hydroxyecdysone 5459840 Click to see 480.60 unknown https://doi.org/10.1016/0031-9422(91)83046-N
https://doi.org/10.1080/10826079208016352
Ajugasterone C 441826 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O 480.60 unknown https://doi.org/10.1080/10826079208016352
https://doi.org/10.1016/0031-9422(91)83046-N
Ecdysterone,(S) 12304165 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/10.1016/0031-9422(91)83046-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(2S,3R,5R,9S,10R,11R,13R,14S,17R)-2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[(4R,5S)-2,2,4-trimethyl-5-(3-methylbutyl)-1,3-dioxolan-4-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 163078310 Click to see CC(C)CCC1C(OC(O1)(C)C)(C)C2CCC3(C2(CC(C4C3=CC(=O)C5C4(CC(C(C5)O)O)C)O)C)O 520.70 unknown https://doi.org/10.1016/0031-9422(91)83046-N
(2S,3R,5R,9S,10R,13R,14S,17R)-2,3,14-trihydroxy-17-[(4R,5S)-5-(3-hydroxy-3-methylbutyl)-2,2,4-trimethyl-1,3-dioxolan-4-yl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162991694 Click to see CC1(OC(C(O1)(C)C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)CCC(C)(C)O)C 520.70 unknown https://doi.org/10.1016/0031-9422(91)83046-N
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[2,2,4-trimethyl-5-(3-methylbutyl)-1,3-dioxolan-4-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 85433138 Click to see 520.70 unknown https://doi.org/10.1016/0031-9422(91)83046-N
Ecdysterone 20,22-monoacetonide 3808392 Click to see 520.70 unknown https://doi.org/10.1016/0031-9422(91)83046-N

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