Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Michael D. Serby"'
Publikováno v:
Expert Opinion on Therapeutic Patents. 18:989-998
Background: Ghrelin is an endogenous ligand of the growth hormone secretagogue receptor (GHS-R) that functions as a short-term meal initiator and a long-term energy balance regulator. Antagonizing GHS-R could be a method to treat obesity. Objective:
Autor:
Christine A. Collins, Mei Liu, Hongyu Zhao, Rich S. Janis, Heidi S. Camp, Teresa K. Surowy, Gang Liu, Bo Liu, Nelson Lissa T, Harriet T. Smith, Ning Cao, Tom S. Suhar, Michael D. Serby, Zhili Xin, Hing L. Sham, Bruce G. Szczepankiewicz
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:4298-4302
A series of structurally novel stearoyl-CoA desaturase1 (SCD1) inhibitors has been identified via molecular scaffold manipulation. Preliminary structure-activity relationship (SAR) studies led to the discovery of potent, and orally bioavailable piper
Autor:
Teresa K. Surowy, Hing L. Sham, Tom S. Suhar, Ning Cao, Michael D. Serby, Heidi S. Camp, Christine A. Collins, Hongyu Zhao, Gang Liu, Harriet T. Smith
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:3388-3391
A series of novel stearoyl-CoA desaturase 1 (SCD1) inhibitors were identified by scaffold design based on known SCD1 inhibitors. Large structural changes were made leading to multiple analogs with comparable or improved potency. This approach is valu
Autor:
Ning Cao, Zhili Xin, Jennifer L. Freeman, Bo Liu, Teresa K. Surowy, Rich S. Janis, Hongyu Zhao, Christine A. Collins, Ruojing Yang, Michael D. Serby, Heidi S. Camp, Tom S. Suhar, Philip R. Kym, David W A Beno, Lynch John K, Gang Liu, Steven P Cepa, Harriet T. Smith, Hing L. Sham, Joel A. Krauser
Publikováno v:
Journal of Medicinal Chemistry. 50:3086-3100
Stearoyl-CoA desaturase 1 (SCD1) catalyzes the committed step in the biosynthesis of monounsaturated fatty acids from saturated, long-chain fatty acids. Studies with SCD1 knockout mice have established that these animals are lean and protected from l
Autor:
David W A Beno, Gang Liu, Zhili Xin, James S. Polakowski, Nathan L. Lubbers, Bo Liu, Mei Liu, James M. Trevillyan, Hongyu Zhao, Michael D. Serby, Hing L. Sham, D. L. Widomski
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:495-500
The hemodynamic effects of a series of potent and selective 4-aminopyridine carboxamide-based pan-JNK inhibitors were assessed in an anesthetized rat model. The effects of these agents on mean arterial pressure, heart rate, cardiac contractility, and
Autor:
Hing L. Sham, Zhili Xin, Christi Kosogof, Terry Pederson, Hongyu Zhao, Cele Abad-Zapatero, Bo Liu, Michael D. Serby, Bruce G. Szczepankiewicz, Gang Liu, Cristina M. Rondinone, Nelson Lissa T, Deanna L. Haasch, Jill E. Clampit, Sanyi Wang, Rebecca J. Gum, James M. Trevillyan, Elizabeth H. Fry, Eric F. Johnson, Mei Liu
Publikováno v:
Journal of Medicinal Chemistry. 49:4455-4458
C-Jun NH2 terminal kinases (JNKs) are important cell signaling enzymes. JNK1 plays a central role in linking obesity and insulin resistance. JNK2 and JNK3 may be involved in inflammatory and neurological disorders, respectively. Small-molecule JNK in
Autor:
James M. Trevillyan, Elizabeth H. Fry, Eric F. Johnson, Chaohong Sun, Hing L. Sham, Charles W. Hutchins, Thomas H. Lubben, Bruce G. Szczepankiewicz, Edward T. Olejniczak, Michael A. Stashko, Cele Abad-Zapatero, Michael D. Serby, Rebecca J. Gum, Hongyu Zhao, Kristi Haskins, Zhili Xin, Bo Liu, Sarah A Dorwin, Jill E. Clampit, Nelson Lissa T, Gang Liu, Mei Liu, Christi Kosogof, Cristina M. Rondinone, Sanyi Wang, Deanna L. Haasch
Publikováno v:
Journal of Medicinal Chemistry. 49:3563-3580
The c-Jun N-terminal kinases (JNK-1, -2, and -3) are members of the mitogen activated protein (MAP) kinase family of enzymes. They are activated in response to certain cytokines, as well as by cellular stresses including chemotoxins, peroxides, and i
Autor:
Verlyn G. Schaefer, Michael D. Serby, Bo Liu, Christine A. Collins, H. Douglas Falls, Hongyu Zhao, Eugene N. Bush, Victoria Knourek-Segel, Theresa M Turner, Michael E. Brune, Gang Liu, Thomas A. Fey, Wiweka Kaszubska, Brian A. Droz, Christi Kosogof, Zhili Xin, David W A Beno, Robin Shapiro, Peer B. Jacobson, Bruce G. Szczepankiewicz, Mei Liu, Nelson Lissa T, Hing L. Sham
Publikováno v:
Journal of Medicinal Chemistry. 49:2568-2578
Ghrelin, a gut-derived orexigenic hormone, is an endogenous ligand of the growth hormone secretagogue receptor (GHS-R). Centrally administered ghrelin has been shown to cause hunger and increase food intake in rodents. Inhibition of ghrelin actions w
Autor:
Thomas A. Fey, Brian A. Droz, Hing L. Sham, Christi Kosogof, Zhili Xin, Michael D. Serby, Kathy Sarris, H. Douglas Falls, Robin Shapiro, Hongyu Zhao, Michael E. Brune, Bo Liu, Ethan D. Hoff, Gang Liu, Charles W. Hutchins, Mei Liu, David W A Beno, Christopher A. Ogiela, Chun W. Lin, Eugene N. Bush, Bruce G. Szczepankiewicz, Peer B. Jacobson, Christine A. Collins, Victoria Knourek-Segel, Teresa M. Turner
Publikováno v:
Journal of medicinal chemistry. 49(15)
The discovery and pharmacological evaluation of potent, selective, and orally bioavailable growth hormone secretagogue receptor (GHS-R) antagonists are reported. Previously, 2,4-diaminopyrimidine-based GHS-R antagonists reported from our laboratories
Autor:
Bo Liu, Zhili Xin, Michael D. Serby, Sanyi Wang, James M. Trevillyan, Michael A. Stashko, Jill E. Clampit, Gang Liu, Chaohong Sun, Thomas H. Lubben
Publikováno v:
The FASEB Journal. 20