Strychnopsis thouarsii

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Internal ID UUID6440494da13df901745180
Scientific name Strychnopsis thouarsii
Authority Baill.
First published in Bull. Mens. Soc. Linn. Paris 1: 456 (1885)

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Language Common/alternative name
Malagasy alakamisy
Malagasy amborasaha
Malagasy amboramahitso
Malagasy odiandro
Malagasy telotritry

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001083887
Tropicos 20600285
KEW urn:lsid:ipni.org:names:581499-1
The Plant List tro-20600285
Open Tree Of Life 576466
NCBI Taxonomy 461636
IUCN Red List 128418822
IPNI 581499-1
iNaturalist 705460
GBIF 3830173
EOL 5518006

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
Plant Extracts as a Source of Natural Products with Potential Antimalarial Effects: An Update from 2018 to 2022 Ribeiro GD, Rei Yan SL, Palmisano G, Wrenger C Pharmaceutics 01-Jun-2023
PMCID:PMC10300920
doi:10.3390/pharmaceutics15061638
PMID:37376086
Potent Antiplasmodial Derivatives of Dextromethorphan Reveal the Ent-Morphinan Pharmacophore of Tazopsine-Type Alkaloids Keita A, Franetich JF, Carraz M, Valentin L, Bordessoules M, Baron L, Bigeard P, Dupuy F, Geay V, Tefit M, Sarrasin V, Michel S, Lavazec C, Houzé S, Mazier D, Soulard V, Porée FH, Duval R Pharmaceutics 07-Feb-2022
PMCID:PMC8876632
doi:10.3390/pharmaceutics14020372
PMID:35214104
In vivo antiplasmodial activity of hydromethanolic leaf extract and solvent fractions of Maytenus gracilipes (Celastraceae) against Plasmodium berghei in mice Nureye D, Kedir MS, Muluye RA, Hammeso WW, Tekalign E Heliyon 24-Nov-2021
PMCID:PMC8642609
doi:10.1016/j.heliyon.2021.e08457
PMID:34901504
Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F Malar J 25-Aug-2021
PMCID:PMC8390284
doi:10.1186/s12936-021-03866-0
PMID:34433465
Antimalarial Activity of Plant Metabolites Pan WH, Xu XY, Shi N, Tsang SW, Zhang HJ Int J Mol Sci 06-May-2018
PMCID:PMC5983777
doi:10.3390/ijms19051382
PMID:29734792
Whole plant extracts versus single compounds for the treatment of malaria: synergy and positive interactions Rasoanaivo P, Wright CW, Willcox ML, Gilbert B Malar J 15-Mar-2011
PMCID:PMC3059462
doi:10.1186/1475-2875-10-S1-S4
PMID:21411015
Harnessing biodiversity: the Malagasy Institute of Applied Research (IMRA) Puri M, Masum H, Heys J, Singer PA BMC Int Health Hum Rights 13-Dec-2010
PMCID:PMC3001617
doi:10.1186/1472-698X-10-S1-S9
PMID:21144080
Drug Development Papers in PLoS Medicine: How We Try to Spot a Winner Krishna S PLoS Med 26-Dec-2006
PMCID:PMC1762067
doi:10.1371/journal.pmed.0030547
PMID:17526082
A Plant-Derived Morphinan as a Novel Lead Compound Active against Malaria Liver Stages Carraz M, Jossang A, Franetich JF, Siau A, Ciceron L, Hannoun L, Sauerwein R, Frappier F, Rasoanaivo P, Snounou G, Mazier D PLoS Med 26-Dec-2006
PMCID:PMC1716192
doi:10.1371/journal.pmed.0030513
PMID:17194195
Isoquinoline alkaloid constituents of Spirospermum penduliflorum and Strychnopsis thouarsii (Menispermaceae) P. Rasoanaivo, S. Ratsimamanga-Urverg, A. Rakoto-Ratsimamanga Elsevier BV 12-May-2003
doi:10.1016/0305-1978(95)00051-8
In vitro antimalarial activity and chloroquine potentiating action of two bisbenzylisoquinoline enantiomer alkaloids isolated from Strychnopsis thouarsii and Spirospermum penduliflorum. Ratsimamanga-Urverg S, Rasoanaivo P, Ramiaramanana L, Milijaona R, Rafatro H, Verdier F, Rakoto-Ratsimamanga A, Le Bras J Planta Med 01-Dec-1992
doi:10.1055/S-2006-961545
PMID:1484894

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
(+)-Isocorydine 10143 Click to see 341.40 unknown https://doi.org/10.1055/S-2006-961545
https://doi.org/10.1016/0305-1978(95)00051-8
1,9-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10-diol 390656 Click to see 327.40 unknown https://doi.org/10.1055/S-2006-961545
https://doi.org/10.1016/0305-1978(95)00051-8
CID 91884708 91884708 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)O 327.40 unknown https://doi.org/10.1055/S-2006-961545
https://doi.org/10.1016/0305-1978(95)00051-8
Predicentrine 10042942 Click to see 341.40 unknown https://doi.org/10.1055/S-2006-961545
https://doi.org/10.1016/0305-1978(95)00051-8
> Benzenoids / Phenanthrenes and derivatives
Salutaridine 5408233 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC 327.40 unknown https://doi.org/10.1016/0305-1978(95)00051-8
> Lignans, neolignans and related compounds
(1R,14S)-9,20,25-Trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol 5458555 Click to see 608.70 unknown https://doi.org/10.1016/0305-1978(95)00051-8
Fangchinoline 73481 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 https://doi.org/10.1055/S-2006-961545
https://doi.org/10.1016/0305-1978(95)00051-8
Tetrandrine 73078 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)OC)OC 622.70 unknown https://doi.org/10.1016/0305-1978(95)00051-8

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