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Rational design and synthesis of novel 2-(substituted-2H-chromen-3-yl)-5-aryl-1H-imidazole derivatives as an anti-angiogenesis and anti-cancer agent

RSC advances, 2014-01, Vol.4 (99), p.56489-56501

2014

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Molecular modeling studies of phenoxypyrimidinyl imidazoles as p38 kinase inhibitors using QSAR and docking

European journal of medicinal chemistry, 2008-04, Vol.43 (4), p.830-838

2008

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Novel targets for antiinflammatory and antiarthritic agents

Current pharmaceutical design, 2006-07, Vol.12 (19), p.2437

2006

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Multidrug Resistance Reversal Activity of Some New Dihydropyridines Studied by IN SITU Single-Pass Intestinal Perfusion (SPIP) Method in Rat

Pharmaceutical chemistry journal, 2018-04, Vol.52 (1), p.8-14

2018

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Design, synthesis and evaluation of new 2,6-dihydroimidazo[1,2-c]pyrimido[5,4-e]-pyrimidine-5(3H)-thiones as possible antihistaminic/antiasthmatic agents

Indian journal of pharmaceutical sciences, 2014-11, Vol.76 (6), p.519-528

2014

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Synthesis and Pharmacological Evaluation of (6-Substituted 4-Oxo-4H-chromene-3 yl) methyl N-substituted Aminoacetates

Indian journal of pharmaceutical sciences, 2008-01, Vol.70 (1), p.118-120

2008

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Quaternary salts of 4,3′ and 4,4′ bis-pyridinium monooximes. Part 2: Synthesis and biological activity

Bioorganic & medicinal chemistry letters, 2006-04, Vol.16 (8), p.2134-2138

2006

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Rational design and synthesis of novel 2-(substituted-2H-chromen-3-yl)-5-aryl-1H-imidazole derivatives as an anti-angiogenesis and anti-cancer agentElectronic supplementary information (ESI) available. See DOI: 10.1039/c4ra09945a

2014-10

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ChemInform Abstract: Synthesis, Characterization and Antiinflammatory Activity of Novel Pyrazolyl Ketoamides

ChemInform, 2014-02, Vol.45 (6), p.no-no

2014

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ChemInform Abstract: Synthesis of 6‐Alkyl/Aralkyl‐5a,11‐dihydro‐9‐nitro(1)benzopyrano‐(2,3‐b)(1,5)benzodiazepin‐13‐ones as Possible Antipsychotic Agents

ChemInform, 1989-02, Vol.20 (7), p.no-no

1989

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Clinical relevance of non-tuberculous mycobacteria isolated from respiratory specimens: seven year experience in a UK hospital

Scientific reports, 2019-02, Vol.9 (1), p.1730, Article 1730

2019

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S41Clinical relevance of pulmonary non-tuberculous mycobacteria isolated over 7 years at a single uk centre

Thorax, 2016-12, Vol.71 (Suppl 3), p.A26-A26

2016

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S41 Clinical relevance of pulmonary non-tuberculous mycobacteria isolated over 7 years at a single uk centre

Thorax, 2016-12, Vol.71 (Suppl 3), p.A26-A26

2016

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Pyrazole derivatives as potent inhibitors of c-Jun N-terminal kinase: Synthesis and SAR studies

Bioorganic & medicinal chemistry, 2014-11, Vol.22 (21), p.6209-6219

2014

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Design, synthesis and characterization of N', N"-diaryl ureas as p38 kinase inhibitors

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2013-03, Vol.9 (2), p.213

2013

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Synthesis, p38 kinase inhibitory and anti-inflammatory activity of new substituted benzimidazole derivatives

Medicinal chemistry (Shp-sariqah, United Arab Emirates), 2013-02, Vol.9 (1), p.91

2013

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Strategies to design pyrazolyl urea derivatives for p38 kinase inhibition: a molecular modeling study

Journal of computer-aided molecular design, 2007-04, Vol.21 (4), p.155-166

2007

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Rational design and synthesis of novel 2-(substituted-2H-chromen-3-yl)-5-aryl-1H-imidazole derivatives as an anti-angiogenesis and anti-cancer agent

Molecular modeling studies of phenoxypyrimidinyl imidazoles as p38 kinase inhibitors using QSAR and docking

Novel targets for antiinflammatory and antiarthritic agents

Multidrug Resistance Reversal Activity of Some New Dihydropyridines Studied by IN SITU Single-Pass Intestinal Perfusion (SPIP) Method in Rat

Design, synthesis and evaluation of new 2,6-dihydroimidazo[1,2-c]pyrimido[5,4-e]-pyrimidine-5(3H)-thiones as possible antihistaminic/antiasthmatic agents

Synthesis and Pharmacological Evaluation of (6-Substituted 4-Oxo-4H-chromene-3 yl) methyl N-substituted Aminoacetates

Quaternary salts of 4,3′ and 4,4′ bis-pyridinium monooximes. Part 2: Synthesis and biological activity

Rational design and synthesis of novel 2-(substituted-2H-chromen-3-yl)-5-aryl-1H-imidazole derivatives as an anti-angiogenesis and anti-cancer agentElectronic supplementary information (ESI) available. See DOI: 10.1039/c4ra09945a

ChemInform Abstract: Synthesis, Characterization and Antiinflammatory Activity of Novel Pyrazolyl Ketoamides

ChemInform Abstract: Synthesis of 6‐Alkyl/Aralkyl‐5a,11‐dihydro‐9‐nitro(1)benzopyrano‐(2,3‐b)(1,5)benzodiazepin‐13‐ones as Possible Antipsychotic Agents

Clinical relevance of non-tuberculous mycobacteria isolated from respiratory specimens: seven year experience in a UK hospital

S41Clinical relevance of pulmonary non-tuberculous mycobacteria isolated over 7 years at a single uk centre

S41 Clinical relevance of pulmonary non-tuberculous mycobacteria isolated over 7 years at a single uk centre

Pyrazole derivatives as potent inhibitors of c-Jun N-terminal kinase: Synthesis and SAR studies

Design, synthesis and characterization of N', N"-diaryl ureas as p38 kinase inhibitors

Synthesis, p38 kinase inhibitory and anti-inflammatory activity of new substituted benzimidazole derivatives

Strategies to design pyrazolyl urea derivatives for p38 kinase inhibition: a molecular modeling study

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