Mohamed, M. (2018). ANTIMICROBIAL & ANTI-DIABETIC EFFECT OF TRITERPENE BARRINGOTOGENOL C GLYCOSIDES ISOLATED FROM AERIAL PART OF MEDICAGOSATIVA L.(ALFALFA) (FAMILY FABACEAE) CULTIVATED IN EGYPT.. Al-Azhar Journal of Pharmaceutical Sciences, 57(1), 70-88. doi: 10.21608/ajps.2018.46628
Maie Mohamed. "ANTIMICROBIAL & ANTI-DIABETIC EFFECT OF TRITERPENE BARRINGOTOGENOL C GLYCOSIDES ISOLATED FROM AERIAL PART OF MEDICAGOSATIVA L.(ALFALFA) (FAMILY FABACEAE) CULTIVATED IN EGYPT.". Al-Azhar Journal of Pharmaceutical Sciences, 57, 1, 2018, 70-88. doi: 10.21608/ajps.2018.46628
Mohamed, M. (2018). 'ANTIMICROBIAL & ANTI-DIABETIC EFFECT OF TRITERPENE BARRINGOTOGENOL C GLYCOSIDES ISOLATED FROM AERIAL PART OF MEDICAGOSATIVA L.(ALFALFA) (FAMILY FABACEAE) CULTIVATED IN EGYPT.', Al-Azhar Journal of Pharmaceutical Sciences, 57(1), pp. 70-88. doi: 10.21608/ajps.2018.46628
Mohamed, M. ANTIMICROBIAL & ANTI-DIABETIC EFFECT OF TRITERPENE BARRINGOTOGENOL C GLYCOSIDES ISOLATED FROM AERIAL PART OF MEDICAGOSATIVA L.(ALFALFA) (FAMILY FABACEAE) CULTIVATED IN EGYPT.. Al-Azhar Journal of Pharmaceutical Sciences, 2018; 57(1): 70-88. doi: 10.21608/ajps.2018.46628
ANTIMICROBIAL & ANTI-DIABETIC EFFECT OF TRITERPENE BARRINGOTOGENOL C GLYCOSIDES ISOLATED FROM AERIAL PART OF MEDICAGOSATIVA L.(ALFALFA) (FAMILY FABACEAE) CULTIVATED IN EGYPT.
Four triterpene barringotogenol C glycosidesnamely; 3-O-[α-L-rhamnopyranosyl (1-4)β-D-glucopyranosyl(1-4)-β-D-glucouronopyranoside]-21-O-α-L-rhamnopyranoside barringotogenolC(I), 3-O-[α-L-rhamnopyranosyl(1-4) β-glucopyranosyl(1-4)β-D-galactopyranosyl]21-O-α-L- rhamnopyranosidebarringotogenolC(II),3-O-[β-D-glucopyranosyl(1-4) β-D-glucopyranosyl (1-4) β-D glucuronopyranoside] 21-O-α-L-rhamnopyranosidebarringotogenolC(III),3-O-[β-D-glucopyranosyl(1-6)β-D-glucopyranosyl]21-O-β-D-glucopyranosidebarringotogenol C(IV),Were isolated for the first time from the aerial part of Medicago sativa L.All compounds (I-IV) were identified by combination of spectroscopic methods (ID & 2DNMR) and compared with literature data.The extracts (Methanol & Dichloromethane) & isolated pure compounds were evaluated in vitro for their antimicrobial activity against Streptococcus pneumoniae (RCMB010010), Staphylococcus aureus (RCMB010028) (Gram+vestrain bacteria), Pseudomonas aeuroginosa (RCMB010043), Escherichia coli (RCMB010052) (Gram -vestrainbacteria) and Antifungal activity against Aspergillus fumigatus (RCMB02568) and Candida albicans (RCMB05036). Furthermore, theywere evaluated for their in vitro Anti-diabetic activity using α-Amylase inhibition method.
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