Cyrille Ngoufack Tagousop, J. Tamokou, Léonel Donald Tsamo Feugap, D. Harakat, L. Voutquenne-Nazabadioko, D. Ngnokam
{"title":"New Hemisynthetic Oleanane Saponin with Antimicrobial Activities","authors":"Cyrille Ngoufack Tagousop, J. Tamokou, Léonel Donald Tsamo Feugap, D. Harakat, L. Voutquenne-Nazabadioko, D. Ngnokam","doi":"10.4236/ABC.2021.111001","DOIUrl":null,"url":null,"abstract":"A new hemisynthetic oleanane saponin: 4',2\",3\",4\",6\"-penta-O-acetyl-6'-O- methyl-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucuronopyranosyl \noleanolic acid (2) was obtained after acetylation and methylation reaction on 3-O-β-D- glucopyranosyl-(1→2)-β-D-glucuronopyranosyl oleanolic acid (1). Its structure was established by extensive analysis of 1D-(1H, 13C), \n2D-(COSY, HSQC and HMBC) NMR data in conjunction with mass spectrometry (HR- TOFESIMS). \nThe evaluation of antimicrobial activities using microdilution method showed \nthat, reaction product (2) presented \nthe lowest values of MIC against E. coli (MIC = 16 μg/mL), S. aureus (MIC = 8 μg/mL), C. tropicalis (MIC = 16 μg/mL) C. albicans (MIC = 8 μg/mL) compare to the substrate (1) against the same microbial \nstrains: E. coli (MIC = 32 μg/mL), S. aureus (MIC = 16 μg/mL), C. tropicalis (MIC = 32 μg/mL), C. albicans (MIC = 16 μg/mL). These results indicate that, acetylation \nand methylation reactions of compound 1 increase its antimicrobial \nactivities against the tested microorganisms.","PeriodicalId":59114,"journal":{"name":"生物化学进展(英文)","volume":"11 1","pages":"1-11"},"PeriodicalIF":0.0000,"publicationDate":"2021-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"生物化学进展(英文)","FirstCategoryId":"1089","ListUrlMain":"https://doi.org/10.4236/ABC.2021.111001","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
A new hemisynthetic oleanane saponin: 4',2",3",4",6"-penta-O-acetyl-6'-O- methyl-3-O-β-D-glucopyranosyl-(1→2)-β-D-glucuronopyranosyl
oleanolic acid (2) was obtained after acetylation and methylation reaction on 3-O-β-D- glucopyranosyl-(1→2)-β-D-glucuronopyranosyl oleanolic acid (1). Its structure was established by extensive analysis of 1D-(1H, 13C),
2D-(COSY, HSQC and HMBC) NMR data in conjunction with mass spectrometry (HR- TOFESIMS).
The evaluation of antimicrobial activities using microdilution method showed
that, reaction product (2) presented
the lowest values of MIC against E. coli (MIC = 16 μg/mL), S. aureus (MIC = 8 μg/mL), C. tropicalis (MIC = 16 μg/mL) C. albicans (MIC = 8 μg/mL) compare to the substrate (1) against the same microbial
strains: E. coli (MIC = 32 μg/mL), S. aureus (MIC = 16 μg/mL), C. tropicalis (MIC = 32 μg/mL), C. albicans (MIC = 16 μg/mL). These results indicate that, acetylation
and methylation reactions of compound 1 increase its antimicrobial
activities against the tested microorganisms.