Strychnos gossweileri

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

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Strychnos gossweileri has been used medicinally in infusions, decoctions, tinctures, macerations, and poultices in Central and Southern Africa. In Angola and the Democratic Republic of Congo, the bark, root, and leaves have been prepared as decoctions for fever, malaria, abdominal pain, and diarrhea (Almeida, 1946; Exell and Mendonca, 1937; Torre and Hill, 1960). Among the Kimbundu and related Angolan peoples, a bark decoction is taken to reduce fever and colic (Aires, 1965). In Zambia and Malawi, healers have applied leaf poultices to wounds and skin infections (Bruce, 1972; Mbatha, 2002). In Republic of Congo, traditional practitioners use macerated root or bark in palm wine as an analgesic and antipyretic, with reported use in cases of hernia and internal pain (Paula and Henshaw, 2008). These preparations consistently target pain, fever, gastrointestinal disturbance, and topical infection, with the plant part and method tailored to the condition.

A practical preparation with a bark decoction may be used in regions where it is documented. Combine roughly 10 g of dried bark with 500 ml water, bring to a gentle boil, and simmer 15–20 minutes; cool, strain, and drink 1/2 cup 2–3 times daily for fever or gastrointestinal cramps (Aires, 1965; Almeida, 1946). Alternatively, for topical use, prepare a maceration by covering 30 g of fresh or dried leaves with 250 ml warm water for 2–3 hours, strain, and apply as a compress to the skin 2–3 times daily (Bruce, 1972; Mbatha, 2002). Strychnos species are known for their toxic alkaloids, notably strychnine and related indole alkaloids; therefore, dosing must be conservative, and any preparation should be used only under guidance of a qualified practitioner. Avoid use in pregnancy and nursing, and do not exceed recommended time on skin. In regions where access to standard doses may be uncertain, a very mild tea of leaves may be prepared with no more than 2 g of dried leaf in 250 ml water for 5–7 minutes, and taken in small sips once daily (Almeida, 1946). Stop immediately if nausea, vomiting, dizziness, or agitation occur, as these can signal toxicity.

The documented activities of Strychnos gossweileri infusions and decoctions align with its recognized alkaloidal constituents, including strychnine, brucine, and related indole alkaloids. These compounds are strongly documented in the genus and in this species by chromatographic studies (Francois et al., 1992), and account for the pronounced analgesic and stimulant actions reported in ethnomedicine and early pharmacology (Almeida, 1946). The genus also yields iridoids such as loganin and geniposide, detected across Strychnos and consistent with its phytochemistry (Pomini and Marsaioli, 2005; Zerouali et al., 1999), which can support anti-inflammatory and antimicrobial effects in topical applications. With such potent alkaloids, extracts may exhibit significant activity at low doses, underscoring the need for careful preparation and measured use in line with regional practices.

Current work tracks these traditional uses alongside modern research on alkaloid profiles and basic bioactivity, with the plant appearing locally in herbal commerce for wound care and fever management. In Angola and DRC, decoctions continue to be requested for malaria-like fever and digestive complaints, while in Zambia and Malawi, leaf macerations and poultices remain in practice for skin infections (Paula and Henshaw, 2008). Commercial powdered bark or tinctures are available in some regional markets, though quality varies. The combination of documented ethnobotanical use, established alkaloid chemistry, and modern interest in wound and fever support continues to shape how this species is employed today.

General Uses 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)

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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

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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!
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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 295.30 unknown via CMAUP database
(+)-Isocorydine 10143 Click to see 341.40 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 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 297.30 unknown via CMAUP database
6,7-Dihydro-7-methyl-5H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinoline 161899 Click to see 277.30 unknown via CMAUP database
Cepharadione A 94577 Click to see 305.30 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 323.30 unknown via CMAUP database
Lanuginosine 97622 Click to see 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
Oxocrebanine 3084713 Click to see 335.30 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 295.30 unknown via CMAUP database
Stesakine 157110 Click to see 325.40 unknown via CMAUP database
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
4,5-Dioxodehydrocrebanine 149599 Click to see 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 368.40 unknown https://doi.org/10.1016/S0031-9422(00)94796-4
> Alkaloids and derivatives / Hasubanan alkaloids
Aknadilactam 15764659 Click to see 373.40 unknown via CMAUP database
Aknadinine 159966 Click to see 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 592.70 unknown via CMAUP database
(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,22,26-tetramethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinoline 100231 Click to see 622.70 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 606.70 unknown via CMAUP database
Thalrugosine, (+)- 100257 Click to see 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(9S)-9-hydroxyhentriacontan-3-one 163190493 Click to see 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 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 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 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 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 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 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 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 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://doi.org/10.1016/0031-9422(88)83148-0
https://doi.org/10.1016/S0040-4039(00)92152-X
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/

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