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Chromenone derivatives as a versatile scaffold with dual mode of inhibition of HIV-1 reverse transcriptase-associated Ribonuclease H function and integrase activity

European journal of medicinal chemistry, 2019-11, Vol.182, p.111617, Article 111617

2019

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A Stability Indicating UPLC Method for the Determination of Levofloxacin Hemihydrate in Pharmaceutical Dosage Form : Application to Pharmaceutical Analysis

Chromatography research international, 2013-12, Vol.2013 (2013), p.1-5

2013

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Synthesis Characterization and Biological Evaluation of Some Novel Amino Pyrazole Derivatives

Asian journal of chemistry, 2018, Vol.30 (12), p.2647-2651

2018

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Sensitive and Rapid determination of Trientine and N1-Acetyl Trientine in Human Plasma by LC-MS/MS for bioequivalence study

Journal of drug delivery and therapeutics, 2019-05, Vol.9 (3), p.310-318

2019

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Synthesis and Antimicrobial Activity of Novel Series of Diversely Substituted Acetyl Pyrazoline Bearing Biphenyl Carbonitrile Motif

International letters of chemistry, physics and astronomy, 2016-08, Vol.69, p.42-48

2016

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Synthesis and Antimicrobial Activity of Novel Series of Diversely Substituted Acetyl Pyrazoline Bearing Biphenyl Carbonitrile Motif

International letters of chemistry, physics and astronomy, 2016-08, Vol.69, p.42-48

2016

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Development and Validation of High Performance LCMS Methods for Estimation of Silodosin and Silodosin β-D-Glucuronide in Human Plasma

Pharmaceutical Analytical Chemistry, 2017, Vol.3 (1)

2017

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Synthesis and Bio-Evaluation of Novel N-(4-(8-Methoxy-2-Oxo-2H-Chromen-3-Yl) Thiazol-2-Yl) Amide Derivatives

International letters of chemistry, physics and astronomy, 2016-11, Vol.71, p.19-28

2016

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Synthesis and Bio-Evaluation of Novel N-(4-(8-Methoxy-2-Oxo-2H-Chromen-3-Yl) Thiazol-2-Yl) Amide Derivatives

International letters of chemistry, physics and astronomy, 2016-11, Vol.71, p.19-28

2016

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Development and Validation of High Performance LCMS Methods for Estimation of Ebastine and Carebastine in Human Plasma

International journal of pharmaceutical sciences and drug research, 2018-09, p.426-432

2018

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Screening for In Vitro Antimycobacterial Activity and Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) Study of 4-(arylamino)coumarin Derivatives

Chemical biology & drug design, 2010-11, Vol.76 (5), p.412-424

2010

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Method Development and Validation of a Stability-Indicating RP-HPLC Method for the Quantitative Analysis of Dronedarone Hydrochloride in Pharmaceutical Tablets

Scientia pharmaceutica, 2013, Vol.81 (1), p.115-122

2013

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Synthesis of some novel imidazolinones as potent anticonvulsant agents

European journal of medicinal chemistry, 2003-09, Vol.38 (9), p.837-840

2003

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Synthesis of 1-(2,6-dichlorophenyl)-3-methylene-1,3-dihydro-indol-2-one derivatives and in vitro anticancer evaluation against SW620 colon cancer cell line

European journal of medicinal chemistry, 2009-03, Vol.44 (3), p.1355-1362

2009

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Fast Stability Indicating UPLC Method for Quantitative Analysis of Dronedarone in Pharmaceutical Dosage Form: Force Degradation Study

ISRN Chromatography, 2014-01, Vol.2014, p.1-7

2014

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Synthesis, Characterization, Crystal and Molecular Structure Analysis of 2,6-Dimethyl-3-acetyl-5-carbomethoxy-4-(3-nitrophenyl)-1,4-dihydropyridine

Journal of chemical crystallography, 2009-06, Vol.39 (6), p.389-394

2009

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Synthesis and Crystal Structure of a novel substituted 1,4-dihydropyridine

Molecular crystals and liquid crystals (Philadelphia, Pa. : 2003), 2007-11, Vol.474 (1), p.55-65

2007

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Synthesis of Monomethylated Dimeric Benzopyrans as HIV-1 and HIV-2 Inhibitors. Part 1

ChemInform, 2003-03, Vol.34 (9), p.no-no

2003

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Synthesis of Some Novel Imidazolinones as Potent Anticonvulsant Agents

ChemInform, 2004-02, Vol.35 (7), p.no-no

2004

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Chromenone derivatives as a versatile scaffold with dual mode of inhibition of HIV-1 reverse transcriptase-associated Ribonuclease H function and integrase activity

A Stability Indicating UPLC Method for the Determination of Levofloxacin Hemihydrate in Pharmaceutical Dosage Form : Application to Pharmaceutical Analysis

Synthesis Characterization and Biological Evaluation of Some Novel Amino Pyrazole Derivatives

Sensitive and Rapid determination of Trientine and N1-Acetyl Trientine in Human Plasma by LC-MS/MS for bioequivalence study

Synthesis and Antimicrobial Activity of Novel Series of Diversely Substituted Acetyl Pyrazoline Bearing Biphenyl Carbonitrile Motif

Synthesis and Antimicrobial Activity of Novel Series of Diversely Substituted Acetyl Pyrazoline Bearing Biphenyl Carbonitrile Motif

Development and Validation of High Performance LCMS Methods for Estimation of Silodosin and Silodosin β-D-Glucuronide in Human Plasma

Synthesis and Bio-Evaluation of Novel N-(4-(8-Methoxy-2-Oxo-2H-Chromen-3-Yl) Thiazol-2-Yl) Amide Derivatives

Synthesis and Bio-Evaluation of Novel N-(4-(8-Methoxy-2-Oxo-2H-Chromen-3-Yl) Thiazol-2-Yl) Amide Derivatives

Development and Validation of High Performance LCMS Methods for Estimation of Ebastine and Carebastine in Human Plasma

Screening for In Vitro Antimycobacterial Activity and Three-Dimensional Quantitative Structure-Activity Relationship (3D-QSAR) Study of 4-(arylamino)coumarin Derivatives

Method Development and Validation of a Stability-Indicating RP-HPLC Method for the Quantitative Analysis of Dronedarone Hydrochloride in Pharmaceutical Tablets

Synthesis of some novel imidazolinones as potent anticonvulsant agents

Synthesis of 1-(2,6-dichlorophenyl)-3-methylene-1,3-dihydro-indol-2-one derivatives and in vitro anticancer evaluation against SW620 colon cancer cell line

Fast Stability Indicating UPLC Method for Quantitative Analysis of Dronedarone in Pharmaceutical Dosage Form: Force Degradation Study

Synthesis, Characterization, Crystal and Molecular Structure Analysis of 2,6-Dimethyl-3-acetyl-5-carbomethoxy-4-(3-nitrophenyl)-1,4-dihydropyridine

Synthesis and Crystal Structure of a novel substituted 1,4-dihydropyridine

Synthesis of Monomethylated Dimeric Benzopyrans as HIV-1 and HIV-2 Inhibitors. Part 1

Synthesis of Some Novel Imidazolinones as Potent Anticonvulsant Agents

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