Fluoroquinolone antibacterials: A review on chemistry, microbiology and therapeutic prospects
Sharma PC, Jain A, Jain S. Fluoroquinolone antibacterials: A review on chemistry, microbiology and therapeutic prospects. Acta Pol Pharm 2009;66:587-604
Therapeutic perspectives of fluoroquinolones: An update
November 28-30
Sharma PC, Jain A, Jain S. Therapeutic perspectives of fluoroquinolones: An update. In proceedings of the 1st Rashtriya Yuva Vagyanik Sammelan, Kurukshetra, November 28-30, 2008: Pp. 237-239
Fluoroquinolones in urinary tract infections: A study on perception analysis of prescribers
Sharma PC, Alawadhi N, Sharma A, Pahwa R, Rajak H. Fluoroquinolones in urinary tract infections: A study on perception analysis of prescribers. Der Chem Sinica 2010;1:84-90
Design Synthesis ntibacterial activity and physicochemical parameters of novel N-4-piperazinyl derivatives of norfloxacin
Abuo-Rahma Gel-D, Sarhan HA, Gad GF. Design, synthesis, antibacterial activity and physicochemical parameters of novel N-4-piperazinyl derivatives of norfloxacin. Bioorg Med Chem 2009;17:3879-3886
Synthesis and antibacterial activity of new fluoroquinolones containing a substituted N-(phenethyl)piperazine moiety
DOI 10.1016/j.bmcl.2006.03.103, PII S0960894X06004021
Foroumadi A, Ghodsi S, Emami S, Najjari S, Samadi N, Faramarzi MA et al. Synthesis and antibacterial activity of new fluoroquinolones containing a substituted N-(phenethyl)piperazine moiety. Bioorg Med Chem Lett 2006;16:3499-3503 (Pubitemid 43777121)
Synthesis and antibacterial activity of the 4-quinolone-3-carboxylic acid derivatives having a trifluoromethyl group as a novel n-1 substituent
DOI 10.1021/jm040204g
Asahina Y, Araya I, Iwase K, Iinuma F, Hosaka M, Ishizaki T. Synthesis and antibacterial activity of the 4-quinolone-3-carboxylic acid derivatives having a trifluoromethyl group as a novel N-1 substituent. J Med Chem 2005;48:3443-3446 (Pubitemid 40628062)
Synthesis and antibacterial activity of 1-(2-fluorovinyl)-7-substituted- 4- quinolone-3-carboxylic acid derivatives, conformationally restricted analogues of fleroxacin
DOI 10.1021/jm0402061
Asahina Y, Iwase K, Iinuma F, Hosaka M, Ishizaki T. Synthesis and antibacterial activity of 1-(2-fluorovinyl)-7-substituted-4-quinolone-3- carboxylic acid derivatives, conformationally restricted analogues of fleroxacin. J Med Chem 2005;48:3194-3202 (Pubitemid 40628039)
Gatifloxacin derivatives: Synthesis, antimycobacterial activities, and inhibition of Mycobacterium tuberculosis DNA gyrase
thesis
Sriram D, Aubry A, Yogeeswari P, Fisher LM. Gatifloxacin derivatives: Synthesis, antimycobacterial activities, and inhibition of Mycobacterium tuberculosis DNA gyrase. Bioorg Med Chem Lett 2006;16:2982-2985
Synthesis and antimycobacterial activities of novel 6-nitroquinolone-3- carboxylic acids
Senthilkumar P, Dinakaran M, Yogeeswari P, Sriram D, China A, Nagaraja V. Synthesis and antimycobacterial activities of novel 6-nitroquinolone-3- carboxylic acids. Eur J Med Chem 2009;44:345-358
Synthesis and anti-HIV activity of arylpiperazinyl fluoroquinolones: A new class of anti-HIV agents
DOI 10.1016/S0960-894X(99)00537-5, PII S0960894X99005375
Hagihara M, Kashiwase H, Katsube T, Kimura T, Komai T, Momota K et al. Synthesis and anti-HIV activity of arylpiperazinyl fluoroquinolones: A new class of anti-HIV agents. Bioorg Med Chem Lett 1999;9:3063-3068 (Pubitemid 29515383)
7-((4-Substituted)piperazin-1-yl) derivatives of ciprofloxacin: Synthesis and in vitro biological evaluation as potential antitumor agents
Azéma J, Guidetti B, Dewelle J, Le Calve B, Mijatovic T, Korolyov A et al. 7-((4-Substituted)piperazin-1-yl) derivatives of ciprofloxacin: Synthesis and in vitro biological evaluation as potential antitumor agents. Bioorg Med Chem 2009;17:5396-5407
Novel lipophilic 7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid derivatives as potential antitumor agents: Improved synthesis and in vitro evaluation
Korolyov A, Dorbes S, Azéma J, Guidetti B, Danel M, Lamoral-Theys D et al. Novel lipophilic 7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid derivatives as potential antitumor agents: Improved synthesis and in vitro evaluation. Bioorg Med Chem 2010;18:8537-8548
Thiazolidin-4-one and hydrazone derivatives of capric acid as possible anti-inflammatory, analgesic and hydrogen peroxide-scavenging agents
Sharma A, Kumar V, Jain S, Sharma PC. Thiazolidin-4-one and hydrazone derivatives of capric acid as possible anti-inflammatory, analgesic and hydrogen peroxide-scavenging agents. J Enzyme Inhib Med Chem 2011;26:546-552
Synthesis of some novel 2,5-disubstituted thiazolidinones from a long chain fatty acid as possible anti-inflammatory, analgesic and hydrogen peroxide scavenging agents
Kumar V, Sharma A, Sharma PC. Synthesis of some novel 2,5-disubstituted thiazolidinones from a long chain fatty acid as possible anti-inflammatory, analgesic and hydrogen peroxide scavenging agents. J Enzyme Inhib Med Chem 2011;26:198-203
Synthesis and biological evaluation of nonpeptide mimetics of ω-conotoxin GVIA
DOI 10.1016/j.bmc.2004.05.040, PII S0968089604004158
Baell JB, Duggan PJ, Forsyth SA, Lewis RJ, Lok YP, Schroeder CI. Synthesis and biological evaluation of nonpeptide mimetics of omega-conotoxin GVIA. Bioorg Med Chem 2004;12: 4025-4037 (Pubitemid 38891366)
Recent advances and future perspectives of triazole analogs as promising antiviral agents
Kharb R, Shahar Yar M, Sharma PC. Recent advances and future perspectives of triazole analogs as promising antiviral agents. Mini Rev Med Chem 2011;11:84-96
Synthesis and in-vitro antibacterial activity of some novel N-nicotinoyl-1-ethyl-6-fluoro-1,4-dihydro-7-piperazin-1-yl-4-oxoquinoline-3- carboxylates
Sharma PC, Jain S. Synthesis and in-vitro antibacterial activity of some novel N-nicotinoyl-1-ethyl-6-fluoro-1,4-dihydro-7-piperazin-1-yl-4-oxoquinoline- 3-carboxylates. Acta Pol Pharm 2008;65:551-556
Synthesis and in vitro anti-bacterial activity of certain novel N-nicotinoyl-1-ethyl-6-fluoro-1,4-dihydro-7-4-subsituted piperazin-1-yl-4- oxoquinoline 3-carboxylates
Sharma PC, Jain S. Synthesis and in vitro anti-bacterial activity of certain novel N-nicotinoyl-1-ethyl-6-fluoro-1,4-dihydro-7-4-subsituted piperazin-1-yl-4-oxoquinoline 3-carboxylates. Acta Pharm Sciencia 2008;50:35-40
Synthesis and anti-bacterial evaluation of fluoroquinolone derivatives
February 26-28
Sharma OP, Sharma PC, Jain S. Synthesis and anti-bacterial evaluation of fluoroquinolone derivatives In: Proceedings of the International Conference on Bioscience, Biochemistry and Bioinformatics, held at Singapore, February 26-28, 2011: Pp. 1-5
Synthesis and anti-bacterial evaluation of novel analogs of fluoroquinolones annulated with 6-subsituted 2-aminobenzothiazoles
Accepted manuscript 10.1016/j.arabjc.2011.04.008
Sharma PC, Jain A, ShaharYar M, Pahwa R, Singh J, Goel S. Synthesis and anti-bacterial evaluation of novel analogs of fluoroquinolones annulated with 6-subsituted 2-aminobenzothiazoles. Arabian J Chem 2011. Accepted manuscript doi: 10.1016/j.arabjc.2011.04.008
Relationships among antibacterial activity, inhibition of DNA gyrase, and intracellular accumulation of 11 fluoroquinolones
Bazile S, Moreau N, Bouzard D, Essiz M. Relationships among antibacterial activity, inhibition of DNA gyrase, and intracellular accumulation of 11 fluoroquinolones. Antimicrob Agents Chemother 1992;36:2622-2627
Effect of hydrophobicity and molecular mass on the accumulation of fluoroquinolones by Staphylococcus aureus
Piddock LJ, Jin YF, Griggs DJ. Effect of hydrophobicity and molecular mass on the accumulation of fluoroquinolones by Staphylococcus aureus. J Antimicrob Chemother 2001;47:261-270 (Pubitemid 32229567)
Investigation of the retention/pH profile of zwitterionic fluoroquinolones in reversed-phase and ion-interaction high performance liquid chromatography
DOI 10.1016/j.jpba.2005.03.032, PII S0731708505002657
Pistos C, Tsantili-Kakoulidou A, Koupparis M. Investigation of the retention/pH profile of zwitterionic fluoroquinolones in reversed-phase and ion-interaction high performance liquid chromatography. J Pharm Biomed Anal 2005;39:438-443 (Pubitemid 41196047)
Synthesis of a phenylalanine-rich peptide as potential anthelmintic and cytotoxic agent
Dahiya R. Synthesis of a phenylalanine-rich peptide as potential anthelmintic and cytotoxic agent. Acta Pol Pharm 2007;64:509-516 (Pubitemid 351360382)
The abdominal constriction response and its suppression by analgesic drugs in the mouse
Collier HO, Dinneen LC, Johnson CA, Schneider C. The abdominal constriction response and its suppression by analgesic drugs in the mouse. Br J Pharmacol Chemother 1968;32:295-310