Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Noha H. Amin"'
Publikováno v:
Analytical Methods. 15:1016-1027
Two rapid, accurate and ecofriendly chromatographic methods were developed for simultaneous determination of bendamustine, gemcitabine and vinorelbine for the purpose of an in vivo pharmacokinetics study in rats.
Publikováno v:
Chromatographia. 86:109-123
Combination therapy of gemcitabine and sorafenib is synergistically effective and well tolerated in patients with non-small cell lung cancer (NSCLC). In this study, the pharmacokinetic parameters of both gemcitabine and sorafenib were estimated after
Publikováno v:
Journal of AOAC International.
Background Gemcitabine (GEM), a pyrimidine nucleoside, has been used as a first line treatment in non-small cell lung cancer (NSCLC). Sorafenib (SOR), a non-selective multi kinase inhibitor, is used as a chemotherapeutic agent in different types of c
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 299:122836
Publikováno v:
Bioanalysis. 13:969-983
Aim: Green, accurate and rapid methods, namely LC–MS/MS and thin layer chromatography-densitometric methods, were developed for determination of amlodipine besylate and celecoxib in presence of its process-related impurities, 4-methylacetophenone i
Publikováno v:
International Journal of Modelling and Simulation. 42:415-425
HCV is an RNA virus, which affects millions of people worldwide and it has no available vaccine so far. Because of genetic differences between the six HCV genotypes, the development of a pan-genoty...
Publikováno v:
Bioorganic Chemistry. 135:106496
Publikováno v:
Journal of Molecular Structure. 1274:134583
Publikováno v:
Bioorganic chemistry. 121
A series of 1,2,4-triazolo[1,5-a]pyrimidine derivatives have been designed and synthesized as combretastatin CA-4 analogs. They were screened for anticancer and tubulin polymerization inhibition activities. The trimethoxyphenyl 1,2,4-triazolo[1,5-a]p
Publikováno v:
Bioorganic Chemistry. 128:106042
Herein, the design, synthesis and mechanistic study of five series of imidazo[1,2-a]pyridines 8a-d, 9a-f, 11a-c, 12a-d and 14a-d as anticancer agents were discussed. The cytotoxicity of imidazo[1,2-a]pyridine derivatives was screened against NCI 60 c