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Synthesis and evaluation of 2-(1H-indol-3-yl)-4-phenylquinolines as inhibitors of cholesterol esterase
(Elsevier, 2014-03)
A series of 2-(substituted) phenyl and 2-indolyl quinoline derivatives (10a–l) was synthesized by an efficient microwave-assisted, trifluoroacetic acid-catalyzed, solvent-free method. Evaluation of the inhibitory activity ...
Synthesis of oseltamivir conjugates with lactose analogs for inhibition studies on Trypanosoma cruzi trans-sialidase
(Arkat USA, 2011-03)
Trypanosoma cruzi, the agent of Chagas disease, expresses a unique enzyme, the trans-sialidase (TcTS) involved in the transfer of sialic acid from host glycoconjugates to mucins of the parasite. Crystallographic studies ...
Synthesis of PEGylated lactose analogs for inhibition studies on T.cruzi trans-sialidase
(Springer, 2010-07)
Trypanosoma cruzi, the agent of Chagas disease, expresses a unique enzyme, the trans-sialidase (TcTS) involved in the transfer of sialic acid from host glycoconjugates to mucins of the parasite. The enzyme is shed to the ...
Central inhibition of nitric oxide synthesis blocks the cardiovascular responses induced by moxonidine in anesthetized rats
(Federation Amer Soc Exp Biol, 2014)
CALCIUM INHIBITION OF THE ATP REVERSIBLE-[P-32]PI EXCHANGE AND OF NET ATP SYNTHESIS CATALYZED BY BOVINE SUBMITOCHONDRIAL PARTICLES
(Elsevier Science BvAmsterdamHolanda, 1990)