Meena V Patel

发表

Discovery of ABBV-3373, an Anti-TNF Glucocorticoid Receptor Modulator Immunology Antibody Drug Conjugate.

Christian Goess, A. Hobson, S. Mathieu, 2022, Journal of medicinal chemistry.

Discovery of Potent and Selective A2A Antagonists with Efficacy in Animal Models of Parkinson's Disease and Depression.

A. Chugh, S. Chaudhary, D. Barawkar, 2017, ACS medicinal chemistry letters.

Discovery of 3-methyl-N-(1-oxy-3',4',5',6'-tetrahydro-2'H-[2,4'-bipyridine]-1'-ylmethyl)benzamide (ABT-670), an orally bioavailable dopamine D4 agonist for the treatment of erectile dysfunction.

D. Donnelly-roberts, Jill M. Wetter, G. Gintant, 2006, Journal of medicinal chemistry.

Structure-activity relationship of triazafluorenone derivatives as potent and selective mGluR1 antagonists.

Meena Patel, M. Nakane, J. Brioni, 2005, Journal of medicinal chemistry.

An efficient one-pot synthesis of substituted 2-arylbenzo[b]thiophene derivatives

V. Gracias, T. Kolasa, Meena V. Patel, 2003 .

Synthesis of 4,5-diaryl-1H-pyrazole-3-ol derivatives as potential COX-2 inhibitors.

R. Henry, R. Bell, T. Kolasa, 2004, The Journal of organic chemistry.

A-412997 is a selective dopamine D4 receptor agonist in rats

Jill M. Wetter, J. Brioni, R. Moreland, 2005, Pharmacology Biochemistry and Behavior.

Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as off-targets

J. Brioni, A. Saraf, J. Rogers, 2007, Neuropharmacology.

A2B adenosine receptor antagonists: Design, synthesis and biological evaluation of novel xanthine derivatives.

G. Bedse, S. Menon, A. Chugh, 2017, European journal of medicinal chemistry.

Correlation between brain/plasma ratios and efficacy in neuropathic pain models of selective metabotropic glutamate receptor 1 antagonists.

Jill M. Wetter, J. Brioni, S. Baker, 2006, Bioorganic & medicinal chemistry letters.

Discovery of novel and potent heterocyclic carboxylic acid derivatives as protein tyrosine phosphatase 1B inhibitors.

S. Menon, D. Barawkar, Vishal V Pathade, 2012, Bioorganic & medicinal chemistry letters.

Design, Synthesis of Novel, Potent, Selective, Orally Bioavailable Adenosine A2A Receptor Antagonists and Their Biological Evaluation.

S. Menon, S. Chaudhary, D. Barawkar, 2017, Journal of medicinal chemistry.

Discovery of 2-(4-pyridin-2-ylpiperazin-1-ylmethyl)-1H-benzimidazole (ABT-724), a dopaminergic agent with a novel mode of action for the potential treatment of erectile dysfunction.

D. Donnelly-roberts, J. Sullivan, M. Nakane, 2004, Journal of medicinal chemistry.

Design and synthesis of novel xanthine derivatives as potent and selective A2B adenosine receptor antagonists for the treatment of chronic inflammatory airway diseases.

S. Menon, A. Chugh, V. Karande, 2017, European journal of medicinal chemistry.

An Efficient One‐Pot Synthesis of Substituted 2‐Arylbenzo[b]thiophene Derivatives.

V. Gracias, T. Kolasa, Meena V Patel, 2003 .

Rational design, synthesis, and structure-activity relationships of 5-amino-1H-pyrazole-4-carboxylic acid derivatives as protein tyrosine phosphatase 1B inhibitors.

P. Prathipati, V. Jain, Ramana R Jinugu, 2017, Bioorganic & medicinal chemistry.

Discovery of (R)-(3-fluoropyrrolidin-1-yl)(6-((5-(trifluoromethyl)pyridin-2-yl)oxy)quinolin-2-yl)methanone (ABBV-318) and analogs as small molecule Nav1.7/ Nav1.8 blockers for the treatment of pain.

G. Gintant, R. Gum, T. Neelands, 2022, Bioorganic & medicinal chemistry.

Synthesis and structure-activity studies on N-[5-(1H-imidazol-4-yl)-5,6,7,8-tetrahydro-1-naphthalenyl]methanesulfonamide, an imidazole-containing alpha(1A)-adrenoceptor agonist.

J. Sullivan, M. Nakane, J. Kuk, 2004, Journal of medicinal chemistry.