Arthur Gomtsyan
AbbVie (United States)(US)
Publications by Year
Research Areas
Ion Channels and Receptors, Pain Mechanisms and Treatments, Asymmetric Synthesis and Catalysis, Quinazolinone synthesis and applications, Herbal Medicine Research Studies
Most-Cited Works
- → Heterocycles in drugs and drug discovery(2012)585 cited
- → TRPV1 Receptors in the CNS Play a Key Role in Broad-Spectrum Analgesia of TRPV1 Antagonists(2006)311 cited
- → A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a Novel Transient Receptor Potential Type V1 Receptor Antagonist, Relieves Pathophysiological Pain Associated with Inflammation and Tissue Injury in Rats(2005)254 cited
- → Novel Transient Receptor Potential Vanilloid 1 Receptor Antagonists for the Treatment of Pain: Structure−Activity Relationships for Ureas with Quinoline, Isoquinoline, Quinazoline, Phthalazine, Quinoxaline, and Cinnoline Moieties(2005)163 cited
- → Repeated dosing of ABT-102, a potent and selective TRPV1 antagonist, enhances TRPV1-mediated analgesic activity in rodents, but attenuates antagonist-induced hyperthermia(2009)145 cited
- → A-425619 [1-Isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a Novel and Selective Transient Receptor Potential Type V1 Receptor Antagonist, Blocks Channel Activation by Vanilloids, Heat, and Acid(2005)110 cited
- → Molecular Recognition and Self-Assembly by Weak Hydrogen Bonding: Unprecedented Supramolecular Helicate Structures from Diamine/Diol Motifs(1994)107 cited
- → Asymmetric synthesis of enantiomerically pure and diversely functionalized cyclopropanes.(1995)105 cited
- → ABT-702 (4-Amino-5-(3-bromophenyl)-7-(6-morpholino-pyridin- 3-yl)pyrido[2,3-d]pyrimidine), a Novel Orally Effective Adenosine Kinase Inhibitor with Analgesic and Anti-Inflammatory Properties. II. In Vivo Characterization in the Rat(2000)104 cited
- → TRPV1 antagonists that cause hypothermia, instead of hyperthermia, in rodents: Compounds’ pharmacological profiles, in vivo targets, thermoeffectors recruited and implications for drug development(2018)87 cited