%0 Journal Article %T Chemical Constituents from Ethyl Acetate Extract of Graptophyllum glandulosum Turrill and New Semi-Synthetic Derivative with Antimicrobial Activities %A Cyrille Ngoufack Tagousop %A Donald Lé %A onel Feugap Tsamo %A Arnaud Joseph Nguetse Dongmo %A Dominique Harakat %A Laurence Voutquenne-Nazabadioko %A Jean-de-Dieu Tamokou %A David Ngnokam %J Advances in Biological Chemistry %P 18-30 %@ 2162-2191 %D 2025 %I Scientific Research Publishing %R 10.4236/abc.2025.151002 %X From the ethyl acetate extract of the medicinal plant Graptophyllum glandulosum Turrill, five known compounds: Lupeol (1), Oleanolic acid (2), Chrysoeriol (3), N-methyl-isonicotinamide (4) and β-sitosterol 3-O-β-D-glucopyranoside (5) were isolated. In addition, oxidation reactions carried out on lupeol (1) yielded two semi-synthetic compounds, including a previously unreported: (20R)-formyloxy-29-nor-lupan-3-one (1b) and one other well-known Lupenone (1a). The structures of natural and semi-synthetic compounds were determined by analysis of 1D-(1H, 13C), 2D-(COSY, HSQC and HMBC) NMR data in conjunction with mass spectrometry (TOFESIMS and HR-TOFESIMS) and by comparison with the reported data. The evaluation of antimicrobial activities of substrate (1) as well as semi-synthetic derivatives (1a and 1b) using broth microdilution method showed that compound 1b was the most active (16 ≤ MIC ≤ 32 μg/mL) against Escherichia coli, Staphylococcus aureus and Candida albicans compared to the starting material 1 (16 ≤ MIC ≤ 64 μg/mL) and derivative 1a (32 ≤ MIC ≤ 64 μg/mL). %K Graptophyllum glandulosum Turrill %K Lupeol %K Oxidation Reaction %K Antimicrobial Activities %U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=140640