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Strychnos kasengaensis

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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 UUID644047a367b74128652576
Scientific name Strychnos kasengaensis
Authority De Wild.
First published in Bull. Jard. Bot. État Bruxelles 5: 46 (1915)

Description Top

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Synonyms Top

Scientific name Authority First published in
Strychnos vanderystii De Wild. Bull. Jard. Bot. État Bruxelles 5: 46 (1915)

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
      • Tanzania
    • South Tropical Africa
      • Angola
      • Zambia
    • West-central Tropical Africa
      • Burundi
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001074162
Tropicos 19000886
KEW urn:lsid:ipni.org:names:547252-1
The Plant List tro-19000886
Open Tree Of Life 6069939
IPNI 547252-1
GBIF 5645724

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
Structure of Matopensive, a Novel Dimeric Indole Alkaloid from Strychnos Species Georges Massiot, Bernard Massoussa, Philippe Thepenier, Maris-Jos� Jaquier, Louisette le Men-Olivier, Cl士ent Delaude The Japan Institute of Heterocyclic Chemistry 02-Mar-2009
doi:10.3987/R-1983-12-2339
Antiplasmodial activity of alkaloids from various strychnos species. Frédérich M, Jacquier MJ, Thépenier P, De Mol P, Tits M, Philippe G, Delaude C, Angenot L, Zèches-Hanrot M J Nat Prod 01-Oct-2002
doi:10.1021/NP020070E
PMID:12398531
Dehydroisostrychnobiline, matopensine and other alkaloids from Strychnos kasengaensis Philippe Thepenier, Marie-José Jacquier, Georges Massiot, Louisette Le Men-Olivier, Clément Delaude Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84120-5

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
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (2R)-2-[(2R,3Z,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate 6504264 Click to see CC=C1CN2CCC3=C(C2CC1C(CO)C(=O)OC)NC4=CC=CC=C34 354.40 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
https://doi.org/10.3987/R-1983-12-2339
> Alkaloids and derivatives / Strychnos alkaloids
(1R,9R,10S,11R,13S,17R,25R,26S,27R,28Z,33S,35S,37S,39Z)-28,39-di(ethylidene)-36-oxa-8,14,24,30-tetrazadodecacyclo[25.5.2.211,14.11,26.19,25.110,17.02,7.013,17.018,23.030,33.08,35.024,37]nonatriaconta-2,4,6,18,20,22-hexaene 101208717 Click to see CC=C1CN2CCC34C2CC1C5C3N(C6C7C8CC9C1(C7N(C5O6)C2=CC=CC=C21)CCN9CC8=CC)C1=CC=CC=C41 570.80 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
https://doi.org/10.3987/R-1983-12-2339
1-[(1R,9S,10R,11R,12E,17S)-12-ethylidene-10-(hydroxymethyl)-5-methoxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5-trien-8-yl]ethanone 163189023 Click to see CC=C1CN2CCC34C2CC1C(C3N(C5=C4C=CC(=C5)OC)C(=O)C)CO 368.50 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
1-[(1R,9S,11R,12E,17S)-12-Ethylidene-10-(hydroxymethyl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-8-yl]ethanone 137628408 Click to see CC=C1CN2CCC34C2CC1C(C3N(C5=CC=CC=C45)C(=O)C)CO 338.40 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
1-[(9S,10S,11R,12Z,17S)-12-ethylidene-10-(hydroxymethyl)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-trien-8-yl]ethanone 101297638 Click to see CC=C1CN2CCC34C2CC1C(C3N(C5=CC=CC=C45)C(=O)C)CO 338.40 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
16,17-Dehydroisostrychnobiline 44559878 Click to see CC=C1CN2CCC34C2CC1C(C3N(C5=CC=CC=C45)C(=O)C)C6N7C8C(=CO6)C9CC1C8(CCN1CC9=CC)C1=CC=CC=C17 612.80 unknown https://doi.org/10.1021/NP020070E
8-Acetyl-12-ethylidene-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6-triene-10-carbaldehyde 436039 Click to see CC=C1CN2CCC34C2CC1C(C3N(C5=CC=CC=C45)C(=O)C)C=O 336.40 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
Isoretulinal 5478101 Click to see CC=C1CN2CCC34C2CC1C(C3N(C5=CC=CC=C45)C(=O)C)C=O 336.40 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
O-Acetylretuline 176986 Click to see CC=C1CN2CCC34C2CC1C(C3N(C5=CC=CC=C45)C(=O)C)COC(=O)C 380.50 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
Retulinal 21763838 Click to see CC=C1CN2CCC34C2CC1C(C3N(C5=CC=CC=C45)C(=O)C)C=O 336.40 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2R,3R,4S,5S)-2-[[(1S,2R,3S,4R,7R,9S,12R,14S,17R,18R,19R,21R,22S)-2-hydroxy-22-(2-hydroxypropan-2-yl)-3,8,8,17,19-pentamethyl-23,24-dioxaheptacyclo[19.2.1.01,18.03,17.04,14.07,12.012,14]tetracosan-9-yl]oxy]oxane-3,4,5-triol 163088565 Click to see CC1CC2C(OC3(C1C4(CCC56CC57CCC(C(C7CCC6C4(C3O)C)(C)C)OC8C(C(C(CO8)O)O)O)C)O2)C(C)(C)O 620.80 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Beta amino acids and derivatives
4-[4-(2-Carboxyethylcarbamoyl)phenoxy]-2-methylbutanoic acid 162957734 Click to see CC(CCOC1=CC=C(C=C1)C(=O)NCCC(=O)O)C(=O)O 309.31 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
> Organoheterocyclic compounds / Lactones
(1S,2R,5S,6S,10R,13S)-5,10-dihydroxy-2,6,13-trimethyl-8-oxatricyclo[4.4.3.01,5]tridecane-9,12-dione 12046000 Click to see CC1CCC2(C13CC(=O)C(C2(COC(=O)C3O)C)C)O 282.33 unknown https://doi.org/10.1016/S0031-9422(00)84120-5
> Phenylpropanoids and polyketides / Coumarins and derivatives
Graphislactone B 10686868 Click to see CC1=CC(=C(C2=C1C3=C(C(=CC(=C3)OC)OC)C(=O)O2)O)OC 316.30 unknown https://doi.org/10.1021/NP020070E
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Ethyl 7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-2-carboxylate 76326537 Click to see CCOC(=O)C1CC2=C(C1=O)OC(=O)C3=CC(=C(C(=C23)O)O)O 320.25 unknown https://doi.org/10.1016/S0031-9422(00)84120-5

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