Compounds 7h, 7i, 7j and 7k exhibited potential antimycobacterial

Compounds 7h, 7i, 7j and 7k exhibited potential antimycobacterial activity. Among the compounds reported here in, compound (7j) is arguably the most potent because it contain 4-fluro phenyl ring at 4th-position of dihydropyrimidines

it enhance the antimycobacterial activity. A series of novel Biginelli dihydropyrimidines of biological interest were synthesized and analyzed for their structures. The Biginelli compounds were prepared by using laboratory made PTSA as an efficient catalyst. SB203580 price The importance of substitutions at the fourth and fifth positions of dihydropyrimidines was studied toward the antimycobacterial activity. The antitubercular data revealed that the all synthesized Biginelli dihydropyrimidines proved to be active against the test organism M. tuberculosis CIP and H37RVstrain. Almost all of the titled compounds exhibited weak, moderate, or high antimycobacterial activity. Compounds, such as 7h, 7i, 7j and 7k, exhibited potential antimycobacterial activity. Some of new derivatives showed an in vitro activity

against M. tuberculosis better than that of antitubercular drug pyrazinamide. Among the compounds reported here in, compound (7j) is arguably Selleck ABT737 the most potent, our present study makes it an interesting compound when compared to the current therapeutic agents and are considered the candidates to investigate further for the same. All authors have none to declare. This research was supported by the Jayamukhi Institute of Pharmaceutical Sciences and

we thank the Tuberculosis Research Center, Chennai, India. “
“Ceftiofur hydrochloride1 and 2 ((6R–7R)-7-[[(2-amino-4-thiazolyl)-Z-(methoxyimino) acetyl] amino]-3-[[(2furanylcarbonyl) thiomethyl]-8-oxo-5-thia-1-aza bicycle [4.2.0] oct-2-ene-2-carboxylicacid, monohydrochloride]) (Fig. 1) is a third generation cephalosporin antibiotic. Ceftiofur Hydrochloride is indicated for treatment of bovine respiratory Levetiracetam disease (shipping fever, pneumonia) associated with Pasturella hemolytica, Pasturella multocida and Haemophilus somnus in lactating or non-lactating cattle and ceftiofur hydrochloride is indicated in horses for respiratory disease associated with Streptococcus zooepidemicus. Ceftiofur HCl is also approved for foot rot in cattle. Ceftiofur inhibits cell wall synthesis (at stage three) of susceptible multiplying bacteria. Ceftiofur exhibits a spectrum of activity similar to that of Cefotaxime. It has a broad range of in vitro activity against a variety of pathogens, including many species of Pasturella, Streptococcus, Staphylococcus, Salmonella, and Escherichia coli. Ceftiofur hydrochloride is not an official drug in any pharmacopoeia. Several spectrophotometric and HPLC methods3, 4, 5, 6, 7, 8, 9, 10, 11, 12 and 13 were published for the estimation of ceftiofur hydrochloride in biological fluids and in pure form.

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