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dc.contributor.authorOchieng, Charles O
dc.contributor.authorMang'uro, Lawrence AO
dc.contributor.authorOwuor, P Okinda
dc.contributor.authorAkala, Hosea
dc.contributor.authorIshola, Ismail O
dc.date.accessioned2018-01-25T10:28:23Z
dc.date.available2018-01-25T10:28:23Z
dc.date.issued2012-01-01
dc.identifier.urihttps://repository.maseno.ac.ke/handle/123456789/263
dc.description.abstractThe chloroform and ethyl acetate extract (100mg/kg) of Caesalpinia volkensii H. exhibited significant (P≤ 0.05) antinociceptive activities using hot plate and writhing tests in mice while the later showed antiplasmodial activity (IC50 0.23±0.07 and 4.39±2.49 μg/ml) against chloroquine sensitive (D6) and chloroquine-resistant (W2), respectively. Two new furanoditerpenes [rel. 1β, 5α-dihydroxyvoucapane (1) and rel. 1β, 6β-dihydroxyvoucapane; 19β-methyl ester (2)] together with seven known compounds [voucapane (3), voucapan-5-ol (4), deoxycaesaldekarin C (5), caesaldekarin C (6), 5-hydroxyvinhaticoic acid (7), triacontanyl-(E)-ferulate (8), triacontanyl-(E)-caffaete (9) and 30′-hydroxytriacontanyl-(E)- ferulate (10)] were isolated from the two extracts. The administration of 3, 4, 5 and 6 (100mg/kg ip) caused a significant (P≤ 0.05) reduction in the number of writhing …en_US
dc.publisherElsevieren_US
dc.titleAntinociceptive and antiplasmodial activities of cassane furanoditerpenes from Caesalpinia volkensii H. root barken_US
dc.typeArticleen_US


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