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Strychnos johnsonii

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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 UUID644004eacaad8277325862
Scientific name Strychnos johnsonii
Authority Hutch. & M.B.Moss
First published in Fl. W. Trop. Afr. 2: 24 (1931)

Description Top

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Synonyms Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Uganda
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000502971
Tropicos 19000731
KEW urn:lsid:ipni.org:names:547248-1
The Plant List kew-2598269
Open Tree Of Life 997968
NCBI Taxonomy 1040892
IPNI 547248-1
GBIF 5645736

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
Psilocybin containing mushrooms: a rapidly developing biotechnology industry in the psychiatry, biomedical and nutraceutical fields Strauss D, Ghosh S, Murray Z, Gryzenhout M 3 Biotech 04-Nov-2022
PMCID:PMC9633885
doi:10.1007/s13205-022-03355-4
PMID:36340802
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Biological Activity of Naturally Derived Naphthyridines Chabowska G, Barg E, Wójcicka A Molecules 16-Jul-2021
PMCID:PMC8306249
doi:10.3390/molecules26144324
PMID:34299599
Recent Advances in the Synthesis of β-Carboline Alkaloids Szabó T, Volk B, Milen M Molecules 27-Jan-2021
PMCID:PMC7866041
doi:10.3390/molecules26030663
PMID:33513936
Plant-Derived Antimalarial Agents: New Leads and Efficient Phytomedicines. Part II. Non-Alkaloidal Natural Products Batista R, de Jesus Silva Júnior A, de Oliveira AB Molecules 13-Aug-2009
PMCID:PMC6254980
doi:10.3390/molecules14083037
PMID:19701144
Total Synthesis of (−)-Normalindine via Addition of Metallated 4-Methyl-3-cyanopyridine to an Enantiopure Sulfinimine Davis FA, Melamed JY, Sharik SS J Org Chem 10-Nov-2006
PMCID:PMC2543119
doi:10.1021/jo061443+
PMID:17081004
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
Janussines a and b from strychnos johnsonii G. Massiot, P. Thépenier, M.J. Jacquier, C. Delaude, L. Le Men-Olivier, R. Verpoorte Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)94848-2
Alkaloids of Strychnos johnsonii Georges Massiot, Philippe Thépenier, Marie-José Jacquier, Louisette Le Men-Olivier, Robert Verpoorte, Clément Delaude Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83601-8

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
> Alkaloids and derivatives / Harmala alkaloids
(1R)-1-[[(5R,7S,9R)-4,9-dimethyl-8-oxo-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl]methyl]-6-hydroxy-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carbaldehyde 163190273 Click to see CC1C(=O)C(CC2C3=C(CCN2C)C4=CC=CC=C4N13)CC5C6=C(CCN5C=O)C7=C(N6)C=CC(=C7)O 496.60 unknown https://doi.org/10.1016/S0040-4039(00)94848-2
(2E,3S)-2-ethylidene-3-[[(1R)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]pentane-1,5-diol 163191114 Click to see CC=C(CO)C(CCO)CC1C2=C(CCN1C)C3=CC=CC=C3N2 328.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(2Z)-2-ethylidene-3-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]pentane-1,5-diol 13892224 Click to see CC=C(CO)C(CCO)CC1C2=C(CCN1C)C3=CC=CC=C3N2 328.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
1-[(4,9-Dimethyl-8-oxo-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl)methyl]-6-hydroxy-1,3,4,9-tetrahydropyrido[3,4-b]indole-2-carbaldehyde 163085878 Click to see CC1C(=O)C(CC2C3=C(CCN2C)C4=CC=CC=C4N13)CC5C6=C(CCN5C=O)C7=C(N6)C=CC(=C7)O 496.60 unknown https://doi.org/10.1016/S0040-4039(00)94848-2
2-Ethylidene-3-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]pentane-1,5-diol 162915154 Click to see CC=C(CO)C(CCO)CC1C2=C(CCN1C)C3=CC=CC=C3N2 328.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
Harmalan 160510 Click to see CC1=NCCC2=C1NC3=CC=CC=C23 184.24 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
15-Hydroxy-dehydroabietic-acid 101225 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
Hookerianamide K 25016412 Click to see CC(C1CC=C2C1(CCC3C2CCC4=CC(CCC34C)N(C)C)C)N(C)C 370.60 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(1R,20R)-1,3,11,12,14,17,18,19,20,21-decahydroyohimban 163195194 Click to see C1CC=C2CN3CCC4=C(C3CC2C1)NC5=CC=CC=C45 278.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(1R)-1,3,11,12,14,21-hexahydroyohimban 163186516 Click to see C1CN2CC3=CC=CC=C3CC2C4=C1C5=CC=CC=C5N4 274.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(1S,15R,16S,18R,20R)-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8-tetraen-18-ol 163190297 Click to see CC1C2CN3CCC4=C(C3CC2CC(O1)O)NC5=CC=CC=C45 312.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(1S,15S,16S,18R,20R)-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8-tetraen-18-ol 163186858 Click to see CC1C2CN3CCC4=C(C3CC2CC(O1)O)NC5=CC=CC=C45 312.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(1S,3S,5R,20S)-20,31-dimethyl-7,17,21,31-tetrazaoctacyclo[19.10.1.03,19.05,17.06,14.08,13.022,27.028,32]dotriaconta-6(14),8(13),9,11,18,22,24,26,28(32)-nonaen-11-ol 163187931 Click to see CC1C2=CN3CCC4=C(C3CC2CC5C6=C(CCN5C)C7=CC=CC=C7N16)NC8=C4C=C(C=C8)O 464.60 unknown https://doi.org/10.1016/S0040-4039(00)94848-2
https://doi.org/10.1016/S0031-9422(00)83601-8
(2R,5E,6R,8S)-5-ethylidene-9-methyl-3-oxa-1,9-diazapentacyclo[10.6.1.12,6.08,19.013,18]icosa-12(19),13,15,17-tetraene 163190267 Click to see CC=C1COC2CC1CC3C4=C(CCN3C)C5=CC=CC=C5N24 308.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(2R)-2-[(2R,12bS)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]but-3-en-1-ol 163195367 Click to see C=CC(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(E)-2-[(5S,7R,9S)-9-ethoxy-4-methyl-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal 163187024 Click to see CCOC1CC(CC2C3=C(CCN2C)C4=CC=CC=C4N13)C(=CC)C=O 352.50 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(E)-2-[(5S,7S,9S)-9-hydroxy-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl]but-2-enal 163187206 Click to see CC=C(C=O)C1CC2C3=C(CCN2)C4=CC=CC=C4N3C(C1)O 310.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
(Z)-2-[(2R,12bS)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]but-2-en-1-ol 13892230 Click to see CC=C(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
1,3,11,12,14,17,18,19,20,21-Decahydroyohimban 13892226 Click to see C1CC=C2CN3CCC4=C(C3CC2C1)NC5=CC=CC=C45 278.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
16-Methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8-tetraen-18-ol 15558558 Click to see CC1C2CN3CCC4=C(C3CC2CC(O1)O)NC5=CC=CC=C45 312.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
2-(1,2,3,4,6,7,12,12b-Octahydroindolo[2,3-a]quinolizin-2-yl)but-2-en-1-ol 163016791 Click to see CC=C(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
2-(3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl)ethanol 372790 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
2-(9-Ethoxy-4-methyl-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl)but-2-enal 162947520 Click to see CCOC1CC(CC2C3=C(CCN2C)C4=CC=CC=C4N13)C(=CC)C=O 352.50 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
2-(9-Hydroxy-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl)but-2-enal 163037081 Click to see CC=C(C=O)C1CC2C3=C(CCN2)C4=CC=CC=C4N3C(C1)O 310.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
2-[(2R,3E,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 5324359 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
2-[(2R,3R,12bS)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]ethanol 22217443 Click to see C=CC1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
3-[(3aS)-1,2,3,3a,4,5alpha,6,7-Octahydro-7alpha-hydroxy-3-methyl-3,7a-diazacyclohepta[jk]fluoren-5-yl]-2(5H)-furanone 13892222 Click to see CN1CCC2=C3C1CC(CC(N3C4=CC=CC=C24)O)C5=CCOC5=O 338.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
4-(1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)-2H-furan-5-one 13892227 Click to see C1CN2CCC3=C(C2CC1C4=CCOC4=O)NC5=CC=CC=C35 308.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
4-(9-ethoxy-4-methyl-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl)-2H-furan-5-one 13892216 Click to see CCOC1CC(CC2C3=C(CCN2C)C4=CC=CC=C4N13)C5=CCOC5=O 366.50 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
4-[(2R,12bS)-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-2H-furan-5-one 13892228 Click to see C1CN2CCC3=C(C2CC1C4=CCOC4=O)NC5=CC=CC=C35 308.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
4-[(5R,7R,9S)-9-ethoxy-4-methyl-4,10-diazatetracyclo[8.6.1.05,17.011,16]heptadeca-1(17),11,13,15-tetraen-7-yl]-2H-furan-5-one 162964865 Click to see CCOC1CC(CC2C3=C(CCN2C)C4=CC=CC=C4N13)C5=CCOC5=O 366.50 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
5-Ethylidene-9-methyl-3-oxa-1,9-diazapentacyclo[10.6.1.12,6.08,19.013,18]icosa-12(19),13,15,17-tetraene 163072498 Click to see CC=C1COC2CC1CC3C4=C(CCN3C)C5=CC=CC=C5N24 308.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
9H-Pyrido[3,4-B]indole 64961 Click to see C1=CC=C2C(=C1)C3=C(N2)C=NC=C3 168.19 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
Akagerine lactone 44559926 Click to see CN1CCC2C3C1CC(CC(N3C4=CC=CC=C24)O)C5=CCOC5=O 340.40 unknown https://doi.org/10.1021/NP020070E
Angustine 441983 Click to see C=CC1=CN=CC2=C1C=C3C4=C(CCN3C2=O)C5=CC=CC=C5N4 313.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
CID 11969719 11969719 Click to see CC=C(C=O)C1CC2C3=C(CCN2C)C4=CC=CC=C4N3C(C1)O 324.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
Corynan-17-ol 164952 Click to see CCC1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 298.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
Demethoxycarbonyl 3,14-dihydrogambirtannine 44559927 Click to see C1CN2CC3=CC=CC=C3CC2C4C1C5=CC=CC=C5N4 276.40 unknown https://doi.org/10.1021/NP020070E
Dihydrogambirtannine, 1-dehydroxycarbonyl- 623554 Click to see C1CN2CC3=CC=CC=C3CC2C4=C1C5=CC=CC=C5N4 274.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
Janussin-A 13892223 Click to see CC1C2=CN3CCC4=C(C3CC2CC5C6=C(CCN5C)C7=CC=CC=C7N16)NC8=C4C=C(C=C8)O 464.60 unknown https://doi.org/10.1016/S0031-9422(00)83601-8
https://doi.org/10.1016/S0040-4039(00)94848-2
janussine A 44559873 Click to see CC1C2=CN3CCC4=C(C3CC2CC5C6N1C7=CC=CC=C7C6CCN5)NC8=C4C=C(C=C8)O 452.60 unknown https://doi.org/10.1021/NP020070E
https://doi.org/10.1016/S0031-9422(00)83601-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Sanggenone H 90681446 Click to see CC1(C=CC2=C(C=CC(=C2O1)C3CC(=O)C4=C(C=C(C=C4O3)O)O)O)C 354.40 unknown https://doi.org/10.1016/S0031-9422(00)83601-8

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