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Antiprotozoal Isoflavan Quinones from Abrus precatorius ssp. africanus

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dc.contributor.author Hata, Y
dc.contributor.author Raith, M
dc.contributor.author Ebrahimi, SN
dc.contributor.author Zimmermann, S
dc.contributor.author Mokoka, T
dc.contributor.author Naidoo, Dashnie
dc.contributor.author Fouché, Gerda
dc.contributor.author Maharaj, V
dc.contributor.author Kaiser, M
dc.contributor.author Brun, R
dc.contributor.author Hamburger, M
dc.date.accessioned 2013-09-05T07:51:36Z
dc.date.available 2013-09-05T07:51:36Z
dc.date.issued 2013-04
dc.identifier.citation Hata, Y, Raith, M, Ebrahimi, S.N, Zimmermann, S, Mokoka, T, Naidoo, D, Fouche, G, Maharaj, V, Kaiser, M, Brun, R and Hamburger, M. 2013. Antiprotozoal Isoflavan Quinones from Abrus precatorius ssp. africanus. Planta Medica, vol. 79(6), pp 492-498 en_US
dc.identifier.issn 0032-0943
dc.identifier.uri https://www.thieme-connect.com/ejournals/abstract/10.1055/s-0032-1321293
dc.identifier.uri http://hdl.handle.net/10204/6960
dc.description Copyright: 2013 Georg Thieme Verlag. This is an ABSTRACT ONLY. The definitive version is published in Planta Medica, vol. 79(6), pp 492-498 en_US
dc.description.abstract A library of 206 extracts from selected South African plants was screened in vitro against a panel of protozoan parasites, Plasmodium falciparum, Trypanosoma brucei rhodesiense, and Leishmania donovani. A CH(sub)2Cl(sub)2/MeOH (1:1) extract of Abrus precatorius L. ssp. africanus strongly inhibited P.falciparum (98%), T. b. rhodesiense (100%), and L. donovani (76%) when tested at a concentration of 10.0 μg/mL. The active constituents were tracked by HPLC-based activity profiling and isolated by preparative and semipreparative RPHPLC chromatography. Structures were established by HR-ESIMS, and 1D and 2D NMR ((sup)1H, (sup)13C, COSY, HMBC, HSQC, and NOE difference spectroscopy). Five compounds were obtained and identified as two isoflavan hydroquinones, abruquinone H (1) and abruquinone G (2), and three isoflavan quinones, abruquinone I (3), abruquinone B (4), and 7, 8, 3′‚5′- tetramethoxyisoflavan-1′,4′- quinone (5). Compounds 1 and 3 were new natural products. The absolute configuration of compounds was determined by comparison of electronic circular dichroism spectra with calculated ECD data. Compounds 3 and 4 showed strong activity against T. b. rhodesiense (IC(sub)50 values of 0.30 and 0.16 μM, respectively) and good selectivity (selectivity indices of 73.7 and 50.5, respectively). en_US
dc.language.iso en en_US
dc.publisher Georg Thieme Verlag en_US
dc.relation.ispartofseries Workflow;11380
dc.subject Antiprotozoal en_US
dc.subject Trypanosoma brucei rhodesiense en_US
dc.subject Isoflavan quinone en_US
dc.subject Abrus precatorius en_US
dc.subject Fabaceae en_US
dc.subject Electronic circular dichroism en_US
dc.title Antiprotozoal Isoflavan Quinones from Abrus precatorius ssp. africanus en_US
dc.type Article en_US
dc.identifier.apacitation Hata, Y., Raith, M., Ebrahimi, S., Zimmermann, S., Mokoka, T., Naidoo, D., ... Hamburger, M. (2013). Antiprotozoal Isoflavan Quinones from Abrus precatorius ssp. africanus. http://hdl.handle.net/10204/6960 en_ZA
dc.identifier.chicagocitation Hata, Y, M Raith, SN Ebrahimi, S Zimmermann, T Mokoka, Dashnie Naidoo, Gerda Fouché, et al "Antiprotozoal Isoflavan Quinones from Abrus precatorius ssp. africanus." (2013) http://hdl.handle.net/10204/6960 en_ZA
dc.identifier.vancouvercitation Hata Y, Raith M, Ebrahimi S, Zimmermann S, Mokoka T, Naidoo D, et al. Antiprotozoal Isoflavan Quinones from Abrus precatorius ssp. africanus. 2013; http://hdl.handle.net/10204/6960. en_ZA
dc.identifier.ris TY - Article AU - Hata, Y AU - Raith, M AU - Ebrahimi, SN AU - Zimmermann, S AU - Mokoka, T AU - Naidoo, Dashnie AU - Fouché, Gerda AU - Maharaj, V AU - Kaiser, M AU - Brun, R AU - Hamburger, M AB - A library of 206 extracts from selected South African plants was screened in vitro against a panel of protozoan parasites, Plasmodium falciparum, Trypanosoma brucei rhodesiense, and Leishmania donovani. A CH(sub)2Cl(sub)2/MeOH (1:1) extract of Abrus precatorius L. ssp. africanus strongly inhibited P.falciparum (98%), T. b. rhodesiense (100%), and L. donovani (76%) when tested at a concentration of 10.0 μg/mL. The active constituents were tracked by HPLC-based activity profiling and isolated by preparative and semipreparative RPHPLC chromatography. Structures were established by HR-ESIMS, and 1D and 2D NMR ((sup)1H, (sup)13C, COSY, HMBC, HSQC, and NOE difference spectroscopy). Five compounds were obtained and identified as two isoflavan hydroquinones, abruquinone H (1) and abruquinone G (2), and three isoflavan quinones, abruquinone I (3), abruquinone B (4), and 7, 8, 3′‚5′- tetramethoxyisoflavan-1′,4′- quinone (5). Compounds 1 and 3 were new natural products. The absolute configuration of compounds was determined by comparison of electronic circular dichroism spectra with calculated ECD data. Compounds 3 and 4 showed strong activity against T. b. rhodesiense (IC(sub)50 values of 0.30 and 0.16 μM, respectively) and good selectivity (selectivity indices of 73.7 and 50.5, respectively). DA - 2013-04 DB - ResearchSpace DP - CSIR KW - Antiprotozoal KW - Trypanosoma brucei rhodesiense KW - Isoflavan quinone KW - Abrus precatorius KW - Fabaceae KW - Electronic circular dichroism LK - https://researchspace.csir.co.za PY - 2013 SM - 0032-0943 T1 - Antiprotozoal Isoflavan Quinones from Abrus precatorius ssp. africanus TI - Antiprotozoal Isoflavan Quinones from Abrus precatorius ssp. africanus UR - http://hdl.handle.net/10204/6960 ER - en_ZA


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