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ACS Medicinal Chemistry Letters
|
June 6, 2014
Novel Quinoline-Based P2-P4 Macrocyclic Derivatives As Pan-Genotypic HCV NS3/4a Protease Inhibitors
Unmesh Shah, Charles Jayne, Samuel Chackalamannil, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 23, 2012
Development of macrocyclic inhibitors of HCV NS3/4A protease with cyclic constrained P2-P4 linkers
Michael T Rudd, Charles J McIntyre, Joseph J Romano, et al.
Journal of Medicinal Chemistry
|
March 25, 2016
Identification and in Vivo Evaluation of Liver X Receptor β-Selective Agonists for the Potential Treatment of Alzheimer's Disease
Shawn J Stachel, Celina Zerbinatti, Michael T Rudd, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 2, 2012
Development of potent macrocyclic inhibitors of genotype 3a HCV NS3/4A protease
Michael T Rudd, John A McCauley, Joseph J Romano, et al.
Chemmedchem
|
March 12, 2015
P2-quinazolinones and bis-macrocycles as new templates for next-generation hepatitis C virus NS3/4a protease inhibitors: discovery of MK-2748 and MK-6325
Michael T Rudd, John W Butcher, Kevin T Nguyen, et al.
ACS Medicinal Chemistry Letters
|
August 16, 2023
Discovery of MK-8768, a Potent and Selective mGluR2 Negative Allosteric Modulator
Michael T Rudd, Peter J Manley, Barbara Hanney, et al.
Science Translational Medicine
|
January 12, 2022
The PET tracer [<sup>11</sup>C]MK-6884 quantifies M4 muscarinic receptor in rhesus monkeys and patients with Alzheimer's disease
Wenping Li, Yuchuan Wang, Talakad G Lohith, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Discovery of MK-5172, a Macrocyclic Hepatitis C Virus NS3/4a Protease Inhibitor
Steven Harper, John A McCauley, Michael T Rudd, et al.
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of 14
Search research articles
Search
Showing results (131-140 of 138) with videos related to
Sort By:
Page
of 14
You have reached the last page of results.
This site can display upto 138 results.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Novel Quinoline-Based P2-P4 Macrocyclic Derivatives As Pan-Genotypic HCV NS3/4a Protease Inhibitors
Unmesh Shah, Charles Jayne, Samuel Chackalamannil, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 23, 2012
Development of macrocyclic inhibitors of HCV NS3/4A protease with cyclic constrained P2-P4 linkers
Michael T Rudd, Charles J McIntyre, Joseph J Romano, et al.
Journal of Medicinal Chemistry
|
March 25, 2016
Identification and in Vivo Evaluation of Liver X Receptor β-Selective Agonists for the Potential Treatment of Alzheimer's Disease
Shawn J Stachel, Celina Zerbinatti, Michael T Rudd, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 2, 2012
Development of potent macrocyclic inhibitors of genotype 3a HCV NS3/4A protease
Michael T Rudd, John A McCauley, Joseph J Romano, et al.
Chemmedchem
|
March 12, 2015
P2-quinazolinones and bis-macrocycles as new templates for next-generation hepatitis C virus NS3/4a protease inhibitors: discovery of MK-2748 and MK-6325
Michael T Rudd, John W Butcher, Kevin T Nguyen, et al.
ACS Medicinal Chemistry Letters
|
August 16, 2023
Discovery of MK-8768, a Potent and Selective mGluR2 Negative Allosteric Modulator
Michael T Rudd, Peter J Manley, Barbara Hanney, et al.
Science Translational Medicine
|
January 12, 2022
The PET tracer [<sup>11</sup>C]MK-6884 quantifies M4 muscarinic receptor in rhesus monkeys and patients with Alzheimer's disease
Wenping Li, Yuchuan Wang, Talakad G Lohith, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Discovery of MK-5172, a Macrocyclic Hepatitis C Virus NS3/4a Protease Inhibitor
Steven Harper, John A McCauley, Michael T Rudd, et al.
Page
of 14