Rangan (Ronnie) Maitra

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Functionalized 6-(piperidin-1-yl)-8,9-diphenyl purines as inverse agonists of the CB1 receptor - SAR efforts towards selectivity and peripheralization

The monoacylglycerol lipase inhibitor ABX-1431 does not improve alcoholic liver disease

Apelin receptor (APJ) agonists and uses thereof

Dual-acting cholinesterase-human cannabinoid receptor 2 ligands show pronounced neuroprotection in vitro and overadditive and disease-modifying neuroprotective effects in vivo

Pyrazole agonist of the apelin receptor improves symptoms of metabolic syndrome in mice

A disease-relevant high-content screening assay to identify anti-inflammatory compounds for use in cystic fibrosis

Peripherally selective CB1 receptor antagonist improves symptoms of metabolic syndrome in mice

Metabolic profiling of CB1 neutral antagonists: (Chapter 9)

Peripherally Selective Diphenyl Purine Antagonist of the CB1 Receptor

Development of a peripherally restricted cb1 receptor antagonist for alcoholic steatosis

Discovery of a potent, selective, and brain-penetrant small molecule that activates the orphan receptor GPR88 and reduces alcohol intake

Design, Synthesis, and Biological Evaluation of (3R)-1,2,3,4-Tetrahydro-7-hydroxy-N-[(1S)-1-[[(3R,4R)-4-(3-hydroxyphenyl)-3,4-dim ethyl-1-piperidinyl]methyl]-2-methylpropyl]-3-isoquinolinecarboxamide (JDTic) Analogues: In Vitro Pharmacology and ADME Profi

Discovery of a novel small molecule agonist scaffold for the APJ receptor

Evaluation of amide bioisosteres leading to 1,2,3-triazole containing compounds as GPR88 agonists: Design, synthesis, and structure-activity relationship studies

Design, synthesis, and pharmacological evaluation of JDTic analogs to examine the significance of the 3-and 4-methyl substituents

"Photo-Rimonabant": Synthesis and biological evaluation of novel photoswitchable molecules derived from Rimonabant lead to a highly selective and nanomolar "Cis-On" CB1R antagonist

Structural analogs of pyrazole and sulfonamide cannabinoids: Effects on acute food intake in mice

Altered Biogenesis of DeltaF508-CFTR Following Treatment with Doxorubicin

Increased functional cell surface expression of CFTR and Delta F508-CFTR by the anthracycline doxorubicin

Diaryl purine derivatives with improved bioavailability