Strychnos guianensis

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Internal ID UUID644004e71b8d9715606120
Scientific name Strychnos guianensis
Authority (Aubl.) Mart.
First published in Syst. Mat. Med. Bras. : 121 (1843)

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Synonyms Top

Scientific name Authority First published in
Rouhamon guianense Aubl. Hist. Pl. Guiane 93 1775
Rouhamon curare DC. Prodr. 9: 17 (1845)
Toxicaria americana Schreb. Naturforscher (Halle) 19: 146 (1783)
Strychnos calantha Gilg ex Ule Bot. Jahrb. Syst. 40: 138 (1907)
Strychnos rouhamon Benth. J. Proc. Linn. Soc., Bot. 1: 106. 1856 [1857 publ. 1856]
Strychnos curare Benth. J. Proc. Linn. Soc., Bot. 1: 108 (1856)
Strychnos geoffraeana Baill. Adansonia 11: 378 (1879)
Strychnos lanceolata Spruce ex Benth. J. Proc. Linn. Soc., Bot. 1: 105 (1856)
Strychnos oblonga Gilg Beibl. Bot. Jahrb. Syst. 60: 37 (1898)
Rouhamon guianeesis Aubl. Hist. Pl. Guiane 1: 93. 1775
Strychnos guianensis var. trichina J.F.Macbr. Candollea 5: 401. 1934
Lasiostoma curare Kunth Nov. Gen. Sp. 7: 210 (1825)
Lasiostoma ruhamon J.F.Gmel. Syst. Nat. ed. 13[bis] : 248 (1791)
Lasiostoma cirrhosum Willd. Sp. Pl., ed. 4 , 1: 624 (1798)
Lasiostoma divaricatum G.Mey. Prim. Fl. Esseq. : 83 (1818)
Rouhamon divaricatum DC. Prodr. 9: 17 (1845)
Rouhamon guianensis var. ecirrhosum DC. Prodr. 9: 17 1845
Strychnos rivularia Barb.Rodr. Vellosia ed. 2, 1: 35, pl. fig. B, & 4, fig. C. 1891
Strychnos papilosa Barb.Rodr. Vellosia ed. 2, 1: 36, pl. 4, fig. B. 1891 as papillosa
Strychnos manaoensis Barb.Rodr. Vellosia ed. 2, 1: 36, pl. 5. 1891
Lasiostoma rouhamon Roem. & Schult. Syst. Veg., ed. 15[bis]. 3: 105 (1818)
Rouhamon guianense var. ecirrhosum A.DC. Prodr. 9: 17 (1845)

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Language Common/alternative name
Chinese 圭亚那马钱
Chinese 圭亞那馬錢

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Distribution (via POWO/KEW) Top

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Database ID/link to page
World Flora Online wfo-0000502832
Tropicos 19000619
INPN 733952
KEW urn:lsid:ipni.org:names:547220-1
The Plant List kew-2598063
Open Tree Of Life 420770
NCBI Taxonomy 1040886
GBIF 7289425
USDA GRIN 476663
IPNI 547220-1

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
Feeding ecology of monk sakis (Pithecia monachus) in a seasonally flooded forest in western Amazonia Gottstein M, Morris AL, Heer K, Heymann EW Primates 21-Jun-2023
PMCID:PMC10473984
doi:10.1007/s10329-023-01074-9
PMID:37341865
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
Change the channel: CysLoop receptor antagonists from Nature Tong G, Baker MA, Shenvi RA Pest Manag Sci 22-Nov-2020
PMCID:PMC8087819
doi:10.1002/ps.6166
PMID:33135373
Application of the Asymmetric Pictet–Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds M. Heravi M, Zadsirjan V, Malmir M Molecules 18-Apr-2018
PMCID:PMC6017108
doi:10.3390/molecules23040943
PMID:29670061
General Approach to the Total Synthesis of 9-Methoxy Substituted Indole Alkaloids: Synthesis of Mitragynine, as well as 9-Methoxygeissoschizol and 9-Methoxy-Nb-methylgeissoschizol Ma J, Yin W, Zhou H, Liao X, Cook JM J Org Chem 02-Jan-2009
PMCID:PMC2654583
doi:10.1021/jo801839t
PMID:19046119
Total Synthesis of the Opioid Agonistic Indole Alkaloid, Mitragynine, as well as the First Total Synthesis of 9-Methoxygeissoschizol and 9-Methoxy-Nb-methylgeissoschizol Ma J, Yin W, Zhou H, Cook JM Org Lett 08-Aug-2007
PMCID:PMC2526544
doi:10.1021/ol071220l
PMID:17685530
Lignanas de Strychnos guianensis (Aublet) Mart. Maria Lúcia B. Pinheiro, Arnaldo F. Imbiriba da Rocha, Marco A. do N. Fernandes, Francisco José Queiroz Monte, José Daniel Figueroa Villar, Elizabete Rangel Cruz FapUNIFESP (SciELO) 26-Apr-2005
doi:10.1590/S0100-40422004000200003
Guianensine, a zwitterionic alkaloid from Strychnos guianensis J. Quetin-Leclercq, G. Llabres, R. Warin, M.-I. Belem-Pinheiro, H. Mavar-Manga, L. Angenot Elsevier BV 13-May-2003
doi:10.1016/0031-9422(95)00502-X
9-methoxygeissoschizol, an alkaloid from bark of Strychnos guianensis Hélène Mavar-Manga, Joëlle Quetin-Leclercq, Gabriel Llabres, Maria-Lucia Belem-Pinheiro, Arnaldo F. Imbiriba Da Rocha, Luc Angenot Elsevier BV 13-May-2003
doi:10.1016/S0031-9422(96)00454-2
5',6'-dehydroguiachrysine and 5',6'-dehydroguiaflavine, two curarizing quaternary indole alkaloids from the stem bark of Strychnos guianensis. Penelle J, Christen P, Molgó J, Tits M, Brandt V, Frédérich M, Angenot L Phytochemistry 01-Oct-2001
doi:10.1016/S0031-9422(01)00255-2
PMID:11576611
Quaternary indole alkaloids from the stem bark of Strychnos guianensis. Penelle J, Tits M, Christen P, Molgo J, Brandt V, Frédérich M, Angenot L Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(00)00033-9
PMID:10820831
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
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
Guiaflavine, a new bisindole quaternary alkaloid from the stem bark of Strychnos guianensis. Penelle J, Tits M, Christen P, Brandt V, Frédérich M, Angenot L J Nat Prod 01-Jun-1999
doi:10.1021/NP9804738
PMID:10395514

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 / Macroline alkaloids
[(1S,12S,13S,14R,15E,17R)-15-ethylidene-17-methyl-3-aza-17-azoniapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methanol 124928643 Click to see 309.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
[(1S,13S,14S,15E,17R)-15-Ethylidene-17-methyl-3-aza-17-azoniapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-13-yl]methanol 6441303 Click to see 309.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
> Alkaloids and derivatives / Pleiocarpaman alkaloids
(13Z,14S,16R,17R)-13-ethylidene-18-(hydroxymethyl)-11-methyl-1-aza-11-azoniapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6-triene-16,17-diol 102369793 Click to see 343.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
(8S,11S,13E,14S,16S,17S,18R)-13-ethylidene-18-(hydroxymethyl)-11-methyl-1-aza-11-azoniapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6-triene-8,17-diol 163186243 Click to see 343.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
[(11R,13Z,14R,16R,18S)-13-ethylidene-11-methyl-1-aza-11-azoniapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraen-18-yl]methanol 163184340 Click to see CC=C1C[N+]2(CCC3=C4C2CC1C(N4C5=CC=CC=C35)CO)C 309.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
[(13E,18R)-13-ethylidene-11-methyl-1-aza-11-azoniapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraen-18-yl]methanol 5319313 Click to see 309.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
> Alkaloids and derivatives / Strychnos alkaloids
(1S,11S,12R,13R,14E,16S,19S,21S)-10-(3-ethyl-8-methoxy-6,7-dihydroindolo[2,3-a]quinolizin-2-yl)-14-(2-hydroxyethylidene)-16-methyl-8-aza-16-azoniahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,9-tetraen-11-ol 163185501 Click to see CCC1=CN2CCC3=C4C(=NC3=C2C=C1C5=CN6C7C(C5O)C8CC9C7(CC[N+]9(CC8=CCO)C)C1=CC=CC=C16)C=CC=C4OC 627.80 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
(1S,11S,12R,13R,14E,16S,19S,21S)-10-(3-ethyl-8-methoxyindolo[2,3-a]quinolizin-2-yl)-14-(2-hydroxyethylidene)-16-methyl-8-aza-16-azoniahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,9-tetraen-11-ol 163185500 Click to see 625.80 unknown https://doi.org/10.1016/S0031-9422(01)00255-2
(1S,11S,12R,13R,14Z,19S,21S)-10-(3-ethyl-8-methoxy-6,7-dihydroindolo[2,3-a]quinolizin-2-yl)-14-(2-hydroxyethylidene)-16-methyl-8-aza-16-azoniahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,9-tetraen-11-ol 163194371 Click to see 627.80 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
(2E)-2-[(1R,11R,12R,13R,19S,21S)-10-(3-ethyl-8-methoxyindolo[2,3-a]quinolizin-2-yl)-11-hydroxy-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,9-tetraen-14-ylidene]acetic acid 163190934 Click to see CCC1=CN2C=CC3=C4C(=NC3=C2C=C1C5=CN6C7C(C5O)C8CC9C7(CCN9CC8=CC(=O)O)C1=CC=CC=C16)C=CC=C4OC 624.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/
(2E)-2-[(1R,11S,12R,13R,19S,21S)-10-(3-ethyl-8-methoxyindolo[2,3-a]quinolizin-2-yl)-11-hydroxy-8,16-diazahexacyclo[11.5.2.11,8.02,7.016,19.012,21]henicosa-2,4,6,9-tetraen-14-ylidene]acetic acid 163194796 Click to see 624.70 unknown https://doi.org/10.1016/0031-9422(95)00502-X
(4aR,5aS,6S,8aS,13aS,15aR,15bR)-15-(3-ethyl-8-methoxy-6,7-dihydroindolo[2,3-a]quinolizin-2-yl)-6-methyl-2,4a,5,5a,7,8,13a,15a,15b,16-decahydro4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-6-ium 163187812 Click to see 609.80 unknown https://doi.org/10.1016/S0031-9422(01)00255-2
(4aR,5aS,8aS,13aS,15aR,15bR)-15-(3-ethyl-8-methoxy-6,7-dihydroindolo[2,3-a]quinolizin-2-yl)-6-methyl-2,4a,5,5a,7,8,13a,15a,15b,16-decahydro4,6-methanoindolo[3,2,1-ij]oxepino[2,3,4-de]pyrrolo[2,3-h]quinolin-6-ium 163190932 Click to see 609.80 unknown https://doi.org/10.1021/NP9804738
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isoolivil 5316262 Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown https://doi.org/10.1590/S0100-40422004000200003
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Olivile; Vladinol C 129317076 Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O 376.40 unknown https://doi.org/10.1590/S0100-40422004000200003
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
2-[[4-amino-2-(3-hydroxydodecanoylamino)-4-oxobutanoyl]amino]-N-(1-hydroxy-4-methylpentan-2-yl)pentanediamide 75310444 Click to see CCCCCCCCCC(CC(=O)NC(CC(=O)N)C(=O)NC(CCC(=O)N)C(=O)NC(CC(C)C)CO)O 557.70 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
2-aminoethyl Acetate 112720 Click to see CC(=O)OCCN 103.12 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(13S,15S,16Z)-16-ethylidene-6-methoxy-11-aza-1-azoniapentacyclo[13.2.2.01,13.04,12.05,10]nonadeca-4(12),5(10),6,8-tetraene 102369791 Click to see 309.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
(1R,13S,15S,16E)-16-ethylidene-6-methoxy-11-aza-1-azoniapentacyclo[13.2.2.01,13.04,12.05,10]nonadeca-4(12),5(10),6,8-tetraene 21586987 Click to see 309.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
2-(3-ethylidene-8-methoxy-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl)ethanol 73408882 Click to see 326.40 unknown https://doi.org/10.1016/S0031-9422(96)00454-2
2-[(2R,3E,12bS)-3-ethylidene-8-methoxy-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 17754960 Click to see 326.40 unknown https://doi.org/10.1016/S0031-9422(96)00454-2
2-[(2R,3E,5S,12bS)-3-ethylidene-8-methoxy-5-methyl-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-5-ium-2-yl]ethanol 163193796 Click to see CC=C1C[N+]2(CCC3=C(C2CC1CCO)NC4=C3C(=CC=C4)OC)C 341.50 unknown https://doi.org/10.1016/S0031-9422(01)00255-2
2-[(2R,3Z,12bS)-3-ethylidene-8-methoxy-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 102445612 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=C3C(=CC=C4)OC 326.40 unknown https://doi.org/10.1016/S0031-9422(96)00454-2
> Organoheterocyclic compounds / Indolizidines
(1R,10S,11R,12E,14R,17R)-12-ethylidene-10-(hydroxymethyl)-14-methyl-9-aza-14-azoniapentacyclo[9.5.2.01,9.03,8.014,17]octadeca-3,5,7-trien-2-one 163190263 Click to see CC=C1C[N+]2(CCC34C2CC1C(N3C5=CC=CC=C5C4=O)CO)C 325.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
1-Methyl-2-((2E)-1-hydroxy-3,7-dimethyl-2,6-octenyl)quinoline-4(1H)-one 9883214 Click to see CC(=CCCC(=CC(C1=CC(=O)C2=CC=CC=C2N1C)O)C)C 311.40 unknown https://doi.org/10.1016/S0031-9422(00)00033-9
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Glyceollin Iii 11954193 Click to see 338.40 unknown https://doi.org/10.1016/0031-9422(95)00502-X
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC89474/

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