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Molecular Pharmacology|November 3, 2016
Discovery and Characterization of Novel GPR39 Agonists Allosterically Modulated by ZincSeiji Sato, Xi-Ping Huang, Wesley K Kroeze, et al.
Bioorganic & Medicinal Chemistry Letters|July 11, 2003
Ring substituted analogues of 5-aminomethyl-10,11-dihydro-dibenzo[a,d]cycloheptene (AMDH): potential modes of binding to the 5-HT(2A) receptorSrinivas Peddi, Bryan L Roth, Richard A Glennon, et al.
Biochemistry|January 22, 2008
Galpha-subunits differentially alter the conformation and agonist affinity of kappa-opioid receptorsFeng Yan, Philip D Mosier, Richard B Westkaemper, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 2007
Convenient synthesis and in vitro pharmacological activity of 2-thioanalogs of salvinorins A and BRuslan V Bikbulatov, Feng Yan, Bryan L Roth, et al.
Science Signaling|April 7, 2021
Biased ligands at opioid receptors: Current status and future directionsTao Che, Hemlata Dwivedi-Agnihotri, Arun K Shukla, et al.
Drug Discovery Today|December 5, 2023
Illuminating the understudied GPCR-omeSreeparna Majumdar, Yi-Ting Chiu, Julie E Pickett, et al.
Pharmacology & Therapeutics|March 29, 2011
Serotonin receptors and heart valve disease--it was meant 2BJoshua D Hutcheson, Vincent Setola, Bryan L Roth, et al.
European Journal of Pharmacology|December 9, 2003
Spiro[9,10-dihydroanthracene]-9,3'-pyrrolidine-a structurally unique tetracyclic 5-HT2A receptor antagonistSrinivas Peddi, Bryan L Roth, Richard A Glennon, et al.
Nature Methods|January 8, 2013
A pharmacological organization of G protein-coupled receptorsHenry Lin, Maria F Sassano, Bryan L Roth, et al.
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