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Jayendra Z. Patel

University of Eastern Finland

21

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339

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Quinoline fumardiamides as novel quorum sensing inhibitors

2019
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Loratadine analogues as MAGL inhibitors

2015 Bioorganic & Medicinal Chemistry Letters
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Revisiting 1,3,4-Oxadiazol-2-ones: Utilization in the Development of ABHD6 Inhibitors.

2015 Bioorganic & Medicinal Chemistry
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Piperazine and piperidine carboxamides and carbamates as inhibitors of fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL).

2014 Bioorganic & Medicinal Chemistry
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Biochemical and pharmacological characterization of the human lymphocyte antigen B-associated transcript 5 (BAT5/ABHD16A).

2014 PLOS ONE
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Chiral 1,3,4-Oxadiazol-2-ones as Highly Selective FAAH Inhibitors

2013 Journal of Medicinal Chemistry
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New in Vitro Tools to Study Human Constitutive Androstane Receptor (CAR) Biology: Discovery and Comparison of Human CAR Inverse Agonists

2011 Molecular Pharmaceutics
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Bioisosteric replacement of dihydropyrazole of 4S-(−)-3-(4-chlorophenyl)-N-methyl-N′-[(4-chlorophenyl)-sulfonyl]-4-phenyl-4,5-dihydro-1H-pyrazole-1-caboxamidine (SLV-319) a potent CB1 receptor antagonist by imidazole and oxazole ☆

2008 Bioorganic & Medicinal Chemistry Letters
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Facile synthesis, ex-vivo and in vitro screening of 3-sulfonamide derivative of 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxylic acid piperidin-1-ylamide (SR141716) a potent CB1 receptor antagonist

2008 Bioorganic & Medicinal Chemistry Letters
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Diaryl Dihydropyrazole-3-carboxamides with Significant In Vivo Antiobesity Activity Related to CB1 Receptor Antagonism : Synthesis, Biological Evaluation, and Molecular Modeling in the Homology Model

2007 Journal of Medicinal Chemistry
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