Paenidigyamycin G: 1-Acetyl-2,4-dimethyl-3-phenethyl-1H-imidazol-3-ium

dc.contributor.authorTetevi, G.M.
dc.contributor.authorKwain, S.
dc.contributor.authorMensah, T.
dc.contributor.authorCamas, A.S.
dc.contributor.authorCamas, M.
dc.contributor.authorDofuor, A.K.
dc.contributor.authorAzerigyik, F.A.
dc.contributor.authorOluwabusola, E.
dc.contributor.authorDeng, H.
dc.contributor.authorJaspars, M.
dc.contributor.authorKyeremeh, K.
dc.date.accessioned2019-12-13T16:07:05Z
dc.date.available2019-12-13T16:07:05Z
dc.date.issued2019-11-21
dc.descriptionResearch Articleen_US
dc.description.abstractThe Ghanaian Paenibacillus sp. DE2SH (GenBank Accession Number: MH091697) is a prolific producer of potent antiparasitic alkaloids. Further detailed study of the culture broth of this strain produced the compound Paenidigyamycin G (1), which is a derivative of the known antiparasitic compound PaenidigyamycinA(2). Compound (1) was isolated on HPLC at tR 37.5 min and its structure determined by IR, UV, MS, 1D, and 2D-NMR data. Compound 1 produced weak to moderate antileishmanial and antitrypanosomal activity when tested against Leishmania donovani (Laveran and Mesnil) Ross (D10) and Trypanosoma brucei subsp. brucei strain GUTat 3.1 with IC50 = 115.41 and 28.75 M, respectively. This result is interesting since the parent compound 2 is known to possess consistent and potent antiparasitic activity. However, 1 displayed a promising selectivity profile towards T. brucei subsp. brucei due to its relatively low toxicity against normal mouse macrophages RAW 264.7 cells (SI = 8.70). Given that compound 1 is also the main metabolite found in the hexane fraction of all extracts produced by Paenibacillus sp. DE2SH when it is co-cultured with other bacteria strains, it must possess some unique biological functions which should make it an excellent candidate for further biological activity screening in other bioassays.en_US
dc.description.sponsorshipCentre for AfricanWetlands (CAW), University of Ghana, for providing seed funding to enable the collection of soil samples for microbe isolation and a TWAS Research Grant Award_17-512 RG/CHE/AF/AC_G. K.K. is also very grateful to the Cambridge-Africa Partnership for Research Excellence (CAPREx), which is funded by the Carnegie Corporation of New York, for a Postdoctoral Fellowship. K.K. also appreciates the Cambridge-Africa ALBORADA Research Fund for support. K.K., H.D. and M.J. are grateful for this research which is jointly funded by the UK Medical Research Council (MRC) and the UK Department for International Development (DFID) under the MRC/DFID African Research Leaders Award (MR/S00520X/1). S.K. wishes to thank the Carnegie BANGA-Africa Project Award for a PhD scholarship and M.T. is grateful for an MPhil full scholarship from TWAS Research Grant Award_17-512 RG/CHE/AF/AC_G.en_US
dc.identifier.otherdoi:10.3390/M1094
dc.identifier.urihttp://ugspace.ug.edu.gh/handle/123456789/34189
dc.language.isoenen_US
dc.publishermolbanken_US
dc.relation.ispartofseries;2019
dc.subjectPaenibacillusen_US
dc.subjectalkaloiden_US
dc.subjectimidazoleen_US
dc.subjectantileishmanialsen_US
dc.subjectleishmaniasisen_US
dc.subjectantitrypanosomalsen_US
dc.subjecttrypanosomiasisen_US
dc.titlePaenidigyamycin G: 1-Acetyl-2,4-dimethyl-3-phenethyl-1H-imidazol-3-iumen_US
dc.typeArticleen_US

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