Synthesis, characterization and anti-microbial studies of some novel 2,4-disubstituted thiazoles.

[1]  T. Govender,et al.  Design, synthesis, characterization, and antibacterial activity of {5-chloro-2-[(3-substitutedphenyl-1,2,4-oxadiazol-5-yl)-methoxy]-phenyl}-(phenyl)-methanones. , 2010, European journal of medicinal chemistry.

[2]  A. M. Vijesh,et al.  Novel chromeno [2,3-b]-pyrimidine derivatives as potential anti-microbial agents. , 2010, European journal of medicinal chemistry.

[3]  P. Shetty,et al.  Synthesis, characterization and biological activity of some new 1,3,4-oxadiazole bearing 2-flouro-4-methoxy phenyl moiety. , 2010, European journal of medicinal chemistry.

[4]  A. Isloor,et al.  Synthesis, characterization and biological activities of some new benzo[b]thiophene derivatives. , 2010, European journal of medicinal chemistry.

[5]  Balakrishna Kalluraya,et al.  Regioselective reaction: synthesis, characterization and pharmacological studies of some new Mannich bases derived from 1,2,4-triazoles. , 2009, European journal of medicinal chemistry.

[6]  S. Bondock,et al.  Synthesis and antimicrobial evaluation of some new thiazole, thiazolidinone and thiazoline derivatives starting from 1-chloro-3,4-dihydronaphthalene-2-carboxaldehyde. , 2007, European journal of medicinal chemistry.

[7]  J. Rudolph,et al.  seco-Cyclothialidines: new concise synthesis, inhibitory activity toward bacterial and human DNA topoisomerases, and antibacterial properties. , 2001, Journal of medicinal chemistry.

[8]  G. Çapan,et al.  Synthesis and Hypnotic Activity of New 4‐Thiazolidinone and 2‐Thioxo‐4,5‐imidazolidinedione Derivatives , 1999, Archiv der Pharmazie.

[9]  C. Koboldt,et al.  Synthesis and activity of sulfonamide-substituted 4,5-diaryl thiazoles as selective cyclooxygenase-2 inhibitors. , 1999, Bioorganic & medicinal chemistry letters.

[10]  J. Herbert,et al.  New orally active non-peptide fibrinogen receptor (GpIIb-IIIa) antagonists: identification of ethyl 3-[N-[4-[4-[amino[(ethoxycarbonyl) imino]methyl]phenyl]-1,3-thiazol-2-yl]-N-[1-[(ethoxycarbonyl)methyl]pip erid -4-yl]amino]propionate (SR 121787) as a potent and long-acting antithrombotic agent. , 1997, Journal of medicinal chemistry.

[11]  J M Morin,et al.  Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogs. , 1995, Journal of medicinal chemistry.

[12]  H. Ishikawa,et al.  Synthesis and anti-pseudomonal activity of new 2-isocephems with a dihydroxypyridone moiety at C-7 , 1994 .

[13]  A. Doherty,et al.  Structure-activity relationships of a series of 2-amino-4-thiazole-containing renin inhibitors. , 1992, Journal of medicinal chemistry.

[14]  T. Heffner,et al.  4-(1,2,5,6-Tetrahydro-1-alkyl-3-pyridinyl)-2-thiazolamines: a novel class of compounds with central dopamine agonist properties. , 1990, Journal of medicinal chemistry.

[15]  K. D. Hargrave,et al.  N-(4-substituted-thiazolyl)oxamic acid derivatives, a new series of potent, orally active antiallergy agents. , 1983, Journal of medicinal chemistry.