Fengxiang Yan

发表

Serine 331 is major site of phosphorylation and desensitization induced by protein kinase C in thromboxane receptor alpha.

H. Tai, Huiping Zhou, D. Liao, 2002, Acta pharmacologica Sinica.

Prostaglandin catabolizing enzymes.

H. Tai, Huiping Zhou, M. Tong, 2002, Prostaglandins & other lipid mediators.

Identification of the Molecular Mechanisms by Which the Diterpenoid Salvinorin A Binds to κ-Opioid Receptors†

Bryan L Roth, Philip D Mosier, B. Roth, 2005 .

Convenient synthesis and in vitro pharmacological activity of 2-thioanalogs of salvinorins A and B.

B. Roth, J. Zjawiony, R. Bikbulatov, 2007, Bioorganic & medicinal chemistry letters.

Structure-based design, synthesis, and biochemical and pharmacological characterization of novel salvinorin A analogues as active state probes of the kappa-opioid receptor.

Bryan L Roth, Philip D Mosier, Carol E Parker, 2009, Biochemistry.

Studies toward the pharmacophore of salvinorin A, a potent kappa opioid receptor agonist.

Bryan L Roth, B. Roth, M. Rizzacasa, 2005, Journal of medicinal chemistry.

Design, synthesis, and biological evaluation of novel urolithins derivatives as potential phosphodiesterase II inhibitors

Xianfeng Huang, Guoqiang Song, Hecheng Wang, 2021, Scientific Reports.

TransductionGPCRs as Tools to Modulate Signal

B. Roth, Sarah C. Rogan, Fengxiang Yan, 2016 .

Engineered GPCRs as tools to modulate signal transduction.

B. Roth, Ying Pei, Sarah C. Rogan, 2008, Physiology.

Molecular mechanisms by which salvinorin A binds to and activates the κ-opioid receptor.

F. Yan, Fengxiang Yan, 2008 .

List of Tables vi List of Figures viii List of Abbreviations ix

B. Roth, K. Palczewski, V. Anderson, 2008 .

Structure-based Design, Synthesis, Biochemical and Pharmacological Characterization of Novel Salvinorin A Analogues as Active State Probes of the κ -Opioid Receptor

W. Wetsel, B. Roth, R. Westkaemper, 2009 .

Structure and function of human NAD(+)-linked 15-hydroxyprostaglandin dehydrogenase.

H. Tai, Huiping Zhou, F. Yan, 2002, Advances in experimental medicine and biology.

Agents that elevate cyclic AMP induce receptor phosphorylation primarily at serine 331 in HEK 293 cells overexpressing human thromboxane receptor alpha.

H. Tai, Huiping Zhou, Fengxiang Yan, 2002, Biochemical pharmacology.

Bioisosteric Modification of Salvinorin A, a Potent and Selective Kappa-Opioid Receptor Agonist

B. Roth, H. Fahmy, D. Stewart, 2006, Arzneimittelforschung.

Salvinorin A: a novel and highly selective kappa-opioid receptor agonist.

Bryan L. Roth, B. Roth, Feng Yan, 2004, Life sciences.

Engineered GPCRs as tools to modulate signal transduction.

B. Roth, Ying Pei, Sarah C. Rogan, 2008, Physiology.

Galpha-subunits differentially alter the conformation and agonist affinity of kappa-opioid receptors.

Bryan L Roth, Philip D Mosier, B. Roth, 2008, Biochemistry.