Drug Synergism: Studies of Combination of RK-52 and Curcumin against Rhodesain of Trypanosoma brucei rhodesiense

ACS medicinal chemistry letters(2020)

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摘要
Rhodesain is an enzyme essential for the life of a parasite causing a rapid-onset form of Human African Trypanosomiasis. is a synthetic inhibitor of rhodesain, characterized by an impressive value ( = 67000 × 10 M min) and by a picomolar affinity toward the trypanosomal protease ( = 38 pM). Differently, curcumin, the golden multitarget nutraceutical obtained from L., was proven to inhibit rhodesain noncompetitively with an IC of 7.75 μM. In the present study, we carried out studies of a combination of RK-52 and curcumin toward rhodesain, by applying the Chou and Talalay approach, which led us to obtain a combination index <1 for the most relevant f values, which means a potent synergistic effect for the reduction of rhodesain activity from 40% to 99%.
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Rhodesain,Trypanosoma,drug combination studies,curcumin,synthetic inhibitor,synergism
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