Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Serge Philibert Kuate"'
Autor:
Xavier Cheseto, Serge Philibert Kuate, David P Tchouassi, Mary Ndung'u, Peter E A Teal, Baldwyn Torto
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0127171 (2015)
Insects are increasingly being recognized not only as a source of food to feed the ever growing world population but also as potential sources of new products and therapeutic agents, among which are sterols. In this study, we sought to profile sterol
Externí odkaz:
https://doaj.org/article/80d753f3297148b0b0b03fed941f043a
Publikováno v:
Biofarmasi Journal of Natural Product Biochemistry. 16:83-98
Akumu AA, Nyambaka H, Kuate SP, Torto B.2018. Characterization of flavonoids from candidate striga grass in controlling diet legumes Cicer arietinum and Vigna radiata.Biofarmasi J Nat Prod Biochem 16: 83-98. In Africa, intercropping of some legumes w
Autor:
Renata Negrini, Raffaele Mezzenga, Serge Philibert Kuate, Ranajit Bandyopadhyay, Baldwyn Torto, Duncan O. Mbuge, W. M. Muiru, Livine O. Nyakundi
The ability of superabsorbent polymers (SAP) in drying maize and controlling aflatoxin contamination was studied under different temperatures, drying times and SAP-to-maize ratios. Temperature and drying time showed significant influence on the aflat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::897fc1d6a9028e56e3e3a468f6ce72db
https://europepmc.org/articles/PMC5055880/
https://europepmc.org/articles/PMC5055880/
Autor:
Baldwyn Torto, Ruth Sarah Rose, Serge Philibert Kuate, Melissa Brazier-Hicks, John A. Pickett, Mary L. Hamilton, Robert Edwards, Antony M. Hooper, John C. Caulfield
Publikováno v:
Phytochemistry. 84:169-176
Isoschaftoside, an allelopathic di-C-glycosylflavone from Desmodium spp. root exudates, is biosynthesised through sequential glucosylation and arabinosylation of 2-hydroxynaringenin with UDP-glucose and UDP-arabinose. Complete conversion to the flavo
Publikováno v:
Phytochemistry. 69:619-626
With respect to the cardenolide pathway and the characterization of enzymes involved in the formation of cardenolides, a malonyltransferase, termed malonyl-coenzyme A: 21-hydroxypregnane 21-O-malonyltransferase (Dp21MaT) has been purified. The enzyme
Autor:
Mary Ndungu, Baldwyn Torto, Xavier Cheseto, Peter E. A. Teal, David P. Tchouassi, Serge Philibert Kuate
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 5, p e0127171 (2015)
PLoS ONE, Vol 10, Iss 5, p e0127171 (2015)
Insects are increasingly being recognized not only as a source of food to feed the ever growing world population but also as potential sources of new products and therapeutic agents, among which are sterols. In this study, we sought to profile sterol
Publikováno v:
Journal of Ethnopharmacology. 103:160-165
The chemical composition of five column fractions of hexanic leaf extract of Cupressus lusitanica were analysed by gas chromatography and gas chromatography-mass spectrometry and then tested for their antidermatophytic activities using the agar dilut
Publikováno v:
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 860(2)
The butenolide ring is the main common characteristic of all cardenolides. Its formation is supposed to be initiated by the transfer of a malonyl moiety from malonyl-coenzyme A to an appropriate 21-hydroxypregnane. A new, reliable, fast and sensitive
Autor:
Wolfgang Kreis, Peter Gmeiner, Reiner Waibel, Stefanie Hahn, Serge Philibert Kuate, Rodrigo Maia de Pádua, Pia K. Schebitz
Publikováno v:
Steroids. 73(4)
A simple and versatile method for the chemical synthesis of 21-hydroxypregnane 21-O-malonyl hemiesters which may be important intermediates of cardenolide biosynthesis is described. Starting from commercial beta-methyldigitoxin, acid hydrolysis follo
Publikováno v:
East and Central African Journal of Pharmaceutical Sciences; Vol 7, No 1 (2004); 6-9
The antidermatophytic activity of nine essential oils from 7 plants against 6 fungi was investigated. Fungistatic effect was observed for the oil of Coreopsis bonariensis (2 mg/ml), Laggera alata var alata (1 mg/ml) against Microsporum audouinii and