نتایج جستجو برای: hydroxypropyl

تعداد نتایج: 2411  

2015
Ashish Pandey Ravda Ramesh

treatment, biologically. Levobunolol HCl occuserts were prepared using hydroxypropyl methylcellulose (HPMC, 3% & 4%), poly vinyl pyrrolidone (PVP, 1%), methyl cellulose (MC, 1% & 2%) as polymers by solvent casting technique with objectives of increasing contact time, achieving controlled release, reduction in frequency of administration and greater therapeutic efficacy. Based on their physioche...

Journal: :IOP Conference Series: Materials Science and Engineering 2020

Journal: :The Journal of antibiotics 1994
S Negi M Sasho M Yamanaka I Sugiyama Y Komatsu A Tsuruoka A Kamada I Tsukada R Hiruma K Katsu

In an effort to find a new oral cephalosporin with well-balanced antibacterial spectrum, good oral absorbability and long plasma half-life, a series of oxyimino aminothiazolyl 3-[(E)- or (Z)-N-substituted carbamoyloxy]propenyl cephems was synthesized and evaluated for antibacterial activity and oral absorbability. The substituents of the carbamoyloxy group affected their in vitro activity and b...

Journal: :International journal of pharmaceutics 2003
Madaisy Cueto M Jesús Dorta Obdulia Munguía Matías Llabrés

A central composite rotate second order design was used to evaluate chicken egg-white lysozyme (lysozyme) thermal stability at different pH, and lysozyme, sucrose and 2-hydroxypropyl-beta-cyclodextrin (HPbetaCD) concentrations, by means of differential scanning calorimetry (DSC). Four measurements were used to characterize the thermogram: the calorimetric enthalpy (DeltaH(cal)), the temperature...

2014
Evelyn Winter Gustavo Jabor Gozzi Louise Domeneghini Chiaradia-Delatorre Nathalia Daflon-Yunes Raphael Terreux Charlotte Gauthier Alessandra Mascarello Paulo César Leal Silvia M Cadena Rosendo Augusto Yunes Ricardo José Nunes Tania Beatriz Creczynski-Pasa Attilio Di Pietro

A series of chalcones substituted by a quinoxaline unit at the B-ring were synthesized and tested as inhibitors of breast cancer resistance protein-mediated mitoxantrone efflux. These compounds appeared more efficient than analogs containing other B-ring substituents such as 2-naphthyl or 3,4-methylenedioxyphenyl while an intermediate inhibitory activity was obtained with a 1-naphthyl group. In...

Journal: :Journal of the American Chemical Society 2008
Kido Nwe Christopher M Andolina Janet R Morrow

Dinuclear europium(III) complexes of the macrocycles 1,3-bis[1-(4,7,10-tris(carbamoylmethyl)-1,4,7,10-tetraazacyclododecane]-m-xylene (1), 1,4-bis[1-(4,7,10-tris(carbamoylmethyl)-1,4,7,10-tetraazacyclododecane]-p-xylene (2), and mononuclear europium(III) complexes of macrocycles 1-methyl-,4,7,10-tris(carbamoylmethyl)-1,4,7,10-tetraazacyclododecane (3), 1-[3'-(N,N-diethylaminomethyl)benzyl]-4,7,...

Journal: :Antimicrobial agents and chemotherapy 1980
J R Martin P Johnson J Tadanier A Goldstein

Treatment of fortimicin B with lithium in ethylamine gave 3-O-demethylfortimicin B. The latter was converted by methodology developed with fortimicin B to 3-O-demethylfortimicin A, 4-N-sarcosyl-3-O-demethylfortimicin B, 4-N-beta-alanyl-3-O-demethylfortimicin B, and 4-N-(beta-aminoethyl)-3-O-demethylfortimicin B. 3-O-demethylfortimicin A and the 4-N-acyl-3-O-demethylfortimicins B had appreciably...

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