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Molecular and Cellular Endocrinology
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September 22, 2006
Manipulation of small-molecule inhibitory kinetics modulates MCH-R1 function
David A Schwarz, Molly M Allen, Robert E Petroski, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 14, 2005
Synthesis and structure-activity relationships of biarylcarboxamide bis-aminopyrrolidine urea derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1)
Martin W Rowbottom, Troy D Vickers, Brian Dyck, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 14, 2007
Synthesis and structure-activity relationships of spirohydantoin-derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1)
Martin W Rowbottom, Troy D Vickers, Junko Tamiya, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 11, 2006
Synthesis and structure-activity relationships of retro bis-aminopyrrolidine urea (rAPU) derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1). Part 2
Sarah Hudson, Mehrak Kiankarimi, Martin W Rowbottom, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 4, 2006
Synthesis and structure-activity relationships of retro bis-aminopyrrolidine urea (rAPU) derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1). Part 1
Martin W Rowbottom, Troy D Vickers, Brian Dyck, et al.
Journal of Medicinal Chemistry
|
June 23, 2006
A thienopyridazinone-based melanin-concentrating hormone receptor 1 antagonist with potent in vivo anorectic properties
Brian Dyck, Stacy Markison, Liren Zhao, et al.
Journal of Medicinal Chemistry
|
June 2, 2015
Structure-Guided Design of Group I Selective p21-Activated Kinase Inhibitors
James J Crawford, Wendy Lee, Ignacio Aliagas, et al.
The Journal of Biological Chemistry
|
July 31, 2013
Histone deacetylase (HDAC) inhibitor kinetic rate constants correlate with cellular histone acetylation but not transcription and cell viability
Benjamin E L Lauffer, Robert Mintzer, Rina Fong, et al.
ACS Medicinal Chemistry Letters
|
November 17, 2023
Lipid Tales: Optimizing Arylomycin Membrane Anchors
Michael F T Koehler, Yi-Chen Chen, Yongsheng Chen, et al.
Science Translational Medicine
|
May 27, 2011
A therapeutic antibody targeting BACE1 inhibits amyloid-β production in vivo
Jasvinder K Atwal, Yongmei Chen, Cecilia Chiu, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 67) with videos related to
Sort By:
Page
of 7
Molecular and Cellular Endocrinology
|
September 22, 2006
Manipulation of small-molecule inhibitory kinetics modulates MCH-R1 function
David A Schwarz, Molly M Allen, Robert E Petroski, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 14, 2005
Synthesis and structure-activity relationships of biarylcarboxamide bis-aminopyrrolidine urea derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1)
Martin W Rowbottom, Troy D Vickers, Brian Dyck, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 14, 2007
Synthesis and structure-activity relationships of spirohydantoin-derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1)
Martin W Rowbottom, Troy D Vickers, Junko Tamiya, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 11, 2006
Synthesis and structure-activity relationships of retro bis-aminopyrrolidine urea (rAPU) derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1). Part 2
Sarah Hudson, Mehrak Kiankarimi, Martin W Rowbottom, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 4, 2006
Synthesis and structure-activity relationships of retro bis-aminopyrrolidine urea (rAPU) derived small-molecule antagonists of the melanin-concentrating hormone receptor-1 (MCH-R1). Part 1
Martin W Rowbottom, Troy D Vickers, Brian Dyck, et al.
Journal of Medicinal Chemistry
|
June 23, 2006
A thienopyridazinone-based melanin-concentrating hormone receptor 1 antagonist with potent in vivo anorectic properties
Brian Dyck, Stacy Markison, Liren Zhao, et al.
Journal of Medicinal Chemistry
|
June 2, 2015
Structure-Guided Design of Group I Selective p21-Activated Kinase Inhibitors
James J Crawford, Wendy Lee, Ignacio Aliagas, et al.
The Journal of Biological Chemistry
|
July 31, 2013
Histone deacetylase (HDAC) inhibitor kinetic rate constants correlate with cellular histone acetylation but not transcription and cell viability
Benjamin E L Lauffer, Robert Mintzer, Rina Fong, et al.
ACS Medicinal Chemistry Letters
|
November 17, 2023
Lipid Tales: Optimizing Arylomycin Membrane Anchors
Michael F T Koehler, Yi-Chen Chen, Yongsheng Chen, et al.
Science Translational Medicine
|
May 27, 2011
A therapeutic antibody targeting BACE1 inhibits amyloid-β production in vivo
Jasvinder K Atwal, Yongmei Chen, Cecilia Chiu, et al.
Page
of 7