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Strychnos gossweileri

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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 UUID644004e33af04678619418
Scientific name Strychnos gossweileri
Authority Exell
First published in J. Bot. 67(Suppl. 2): 102 (1929)

Description Top

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Synonyms Top

Scientific name Authority First published in
Strychnos caespitosa R.D.Good J. Bot. 67(Suppl. 2): 104 (1929)

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
    • South Tropical Africa
      • Zambia
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Congo
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000502737
Tropicos 19000725
KEW urn:lsid:ipni.org:names:547213-1
The Plant List kew-2597871
Open Tree Of Life 6069934
Observations.org 330747
IPNI 547213-1
GBIF 5645879
Elurikkus 562797
USDA GRIN 417572
CMAUP NPO21780

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
Le Dolichantoside, un Alcaloïde Nouveau du Strychnos gossweileri Exell C. Coune, L. Angenot Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1097413
Nouveaux Alcaloïdes des Racines du Strychnos icaja K. Kambu, C. Coune, L Angenot Georg Thieme Verlag KG 15-Jan-2009
doi:10.1055/S-0028-1097317
Matadine, a cytotoxic alkaloid from Strychnos gossweileri J. Quetin-Leclercq, P. Coucke, C. Delaude, R. Warin, R. Bassleer, L. Angenot Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)84236-L
Strychnochromine, an unusual cis indoline alkaloid from strychnos gossweileri Luc Angenot, Claude Coune, Joe¨lle Quetin-Leclercq, Dirk Tavernier Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83148-0
Revision of the structure of strychnochromine J. Quetin-Leclercq, L. Angenot, L. Dupont, O. Dideberg, R. Warin, C. Delaude, C. Coune Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)92152-X
2,7-Dihydroxyapogeissoschizine from root bark of Strychnos gossweileri J. Quetin-Leclercq, G. Dive, C. Delaude, R. Warin, R. Bassleer, L. Angenot Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)94796-4
Revision of the structure of strychnofluorine, an alkaloid of Strychnos gossweileri J. Quetin-Leclercq, C. Coune, C. Delaude, R. Warin, R. Bassleer, L. Angenot Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80472-Q
In vitro activities of strychnos alkaloids and extracts against Plasmodium falciparum. Frederich M, Hayette MP, Tits M, De Mol P, Angenot L Antimicrob Agents Chemother 01-Sep-1999
PMCID:PMC89474
doi:10.1128/AAC.43.9.2328
PMID:10471592

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 / Aporphines
(-)-Phanostenine 12305138 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)O)OC)OCO3 325.40 unknown via CMAUP database
(-)-Roemeroline 15559920 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)O)OCO3 295.30 unknown via CMAUP database
(12S)-15,16-dimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaene 10042806 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5OC)OC)OCO3 339.40 unknown via CMAUP database
(6aS)-1,2-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol 793837 Click to see COC1=C(C2=C3C(CC4=C2C=C(C=C4)O)NCCC3=C1)OC 297.30 unknown via CMAUP database
8H-Benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-8-one, 9,10-dimethoxy- 3084713 Click to see COC1=C(C2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC 335.30 unknown via CMAUP database
Cepharadione A 94577 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC5=C4OCO5)C(=O)C1=O 305.30 unknown via CMAUP database
Dehydroaporheine 161899 Click to see CN1CCC2=CC3=C(C4=C2C1=CC5=CC=CC=C54)OCO3 277.30 unknown via CMAUP database
Dehydrocrebanine 149600 Click to see CN1CCC2=CC3=C(C4=C5C=CC(=C(C5=CC1=C24)OC)OC)OCO3 337.40 unknown via CMAUP database
Dehydrophanostenine 179675 Click to see CN1CCC2=CC3=C(C4=C5C=C(C(=CC5=CC1=C24)OC)O)OCO3 323.30 unknown via CMAUP database
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown via CMAUP database
Lanuginosine 97622 Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O 305.30 unknown via CMAUP database
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown via CMAUP database
Steporphine 155631 Click to see CN1CC(C2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3)O 295.30 unknown via CMAUP database
Stesakine 157110 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5OC)O)OCO3 325.40 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,5-Dioxodehydrocrebanine 149599 Click to see CN1C2=C3C(=CC4=C(C3=C5C=CC(=C(C5=C2)OC)OC)OCO4)C(=O)C1=O 365.30 unknown via CMAUP database
> Alkaloids and derivatives / Corynanthean-type alkaloids
2,7-Dihydroxyapogeissoschizine 10384401 Click to see CC=C1CN2CCC3(C4=CC=CC=C4N5C3(C2CC1C(=C5)C(=O)OC)O)O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)94796-4
Methyl 13-ethylidene-8,17-dihydroxy-1,11-diazapentacyclo[12.3.2.02,7.08,17.011,16]nonadeca-2,4,6,18-tetraene-19-carboxylate 383003 Click to see CC=C1CN2CCC3(C4=CC=CC=C4N5C3(C2CC1C(=C5)C(=O)OC)O)O 368.40 unknown https://doi.org/10.1016/S0031-9422(00)94796-4
> Alkaloids and derivatives / Hasubanan alkaloids
Aknadilactam 15764659 Click to see CN1C(=O)CC23C1(CCC4=C2C(=C(C=C4)OC)O)C(=C(C(=O)C3)OC)OC 373.40 unknown via CMAUP database
Aknadinine 159966 Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)O)C(=C(C(=O)C3)OC)OC 359.40 unknown via CMAUP database
Cepharamine 12302744 Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)O)C=C(C(=O)C3)OC 329.40 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
Pronuciferine 200480 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown via CMAUP database
> Alkaloids and derivatives / Strychnos alkaloids
(11S,12Z,17S)-12-(2-hydroxyethylidene)-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,9-tetraene-10-carbaldehyde 101637550 Click to see C1CN2CC(=CCO)C3CC2C14C5=CC=CC=C5NC4=C3C=O 308.40 unknown https://doi.org/10.1016/0031-9422(92)80472-Q
> Lignans, neolignans and related compounds
(14aS,26aR)-2,3,13,14,14a,15,26,26a-Octahydro-22,30-dimethoxy-14-methyl-1H-4,6:16,19-dietheno-21,25-metheno-12H-[1,3]dioxolo[4,5-g]pyrido[2 inverted exclamation marka,3 inverted exclamation marka:17,18][1,10]dioxacycloeicosino[2,3,4-ij]isoquinoline 14488278 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(O3)C8=C(C=C7CCN6)OCO8)C=C5)OC 592.70 unknown via CMAUP database
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
Cepharanthine 10206 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=C(C=C5)OC6=C(C=CC(=C6)CC7C8=CC(=C(C=C8CCN7C)OC)O4)OC)OCO3 606.70 unknown via CMAUP database
Obaberine 100231 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC 622.70 unknown via CMAUP database
Thalrugosine 100257 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(9S)-9-hydroxyhentriacontan-3-one 163190493 Click to see CCCCCCCCCCCCCCCCCCCCCCC(CCCCCC(=O)CC)O 466.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Dolichantoside 10437390 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 544.60 unknown https://doi.org/10.1016/0031-9422(88)83148-0
methyl (2S,3R,4S)-3-ethenyl-4-[[(1R)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 163185684 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 544.60 unknown https://doi.org/10.1055/S-0028-1097317
methyl (2S,3R,4S)-3-ethenyl-4-[[(1S)-2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl]methyl]-2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 163187360 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 544.60 unknown https://doi.org/10.1055/S-0028-1097413
methyl 3-ethenyl-4-[(2-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-1-yl)methyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 73803915 Click to see CN1CCC2=C(C1CC3C(C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C=C)NC5=CC=CC=C25 544.60 unknown https://doi.org/10.1055/S-0028-1097317
https://doi.org/10.1055/S-0028-1097413
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1R,9S,12S,18S)-9-(2-hydroxyethyl)-8,15-diazapentacyclo[10.5.1.01,9.02,7.015,18]octadeca-2,4,6-trien-10-one 162917390 Click to see C1CN2CCC34C2C1CC(=O)C3(NC5=CC=CC=C45)CCO 298.40 unknown https://doi.org/10.1016/0031-9422(88)83148-0
9-(2-Hydroxyethyl)-8,15-diazapentacyclo[10.5.1.01,9.02,7.015,18]octadeca-2,4,6-trien-10-one 13994619 Click to see C1CN2CCC34C2C1CC(=O)C3(NC5=CC=CC=C45)CCO 298.40 unknown https://doi.org/10.1016/0031-9422(88)83148-0
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(2R)-2-[(2S)-1,2,3,4-tetrahydroindolo[2,3-a]quinolizin-2-yl]but-3-en-1-ol 163194867 Click to see C=CC(CO)C1CCN2C=CC3=C4C=CC=CC4=NC3=C2C1 292.40 unknown https://doi.org/10.1016/0031-9422(91)84236-L
2-(1,2,3,4-Tetrahydroindolo[2,3-a]quinolizin-2-yl)but-3-en-1-ol 4216189 Click to see C=CC(CO)C1CCN2C=CC3=C4C=CC=CC4=NC3=C2C1 292.40 unknown https://doi.org/10.1016/0031-9422(91)84236-L
Matadine 371184 Click to see C=CC(CO)C1CCN2C=CC3=C4C=CC=CC4=NC3=C2C1 292.40 unknown https://doi.org/10.1016/0031-9422(91)84236-L
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-methoxy-3-[4-[[(5S)-11-methoxy-6,19-dimethyl-20-oxo-2,13-dioxa-6,19-diazapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3,9,11,15,21-hexaen-5-yl]methyl]phenoxy]benzaldehyde 389057 Click to see CN1CCC2=CC(=C3C(=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C=O)OC)OC6=C(O3)C=C7CCN(C(=O)C7=C6)C)OC 606.70 unknown via CMAUP database
4-methoxy-3-[4-[[(5S)-4-[(6-methoxy-2-methyl-1-oxo-3,4-dihydroisoquinolin-7-yl)oxy]-6-methyl-7,8-dihydro-5H-[1,3]dioxolo[4,5-g]isoquinolin-5-yl]methyl]phenoxy]benzaldehyde 102157843 Click to see CN1CCC2=CC3=C(C(=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)C=O)OC)OC6=C(C=C7CCN(C(=O)C7=C6)C)OC)OCO3 636.70 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
6,7-Dimethoxy-2-methylisoquinolin-1(2H)-one 11367984 Click to see CN1C=CC2=CC(=C(C=C2C1=O)OC)OC 219.24 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Aminoquinolines and derivatives
9-(2-Hydroxyethyl)-8,11-diazapentacyclo[9.5.2.01,10.02,7.09,14]octadeca-2,4,6-trien-16-one 162924097 Click to see C1CN2CCC34C2C(C1CC3=O)(NC5=CC=CC=C45)CCO 298.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
https://doi.org/10.1016/S0040-4039(00)92152-X
https://doi.org/10.1016/0031-9422(88)83148-0

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