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ACS Medicinal Chemistry Letters
|
February 16, 2023
Pyrazole Ureas as Low Dose, CNS Penetrant Glucosylceramide Synthase Inhibitors for the Treatment of Parkinson's Disease
Anthony J Roecker, Kathy M Schirripa, H Marie Loughran, 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.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 2017
Structural characterization of nonactive site, TrkA-selective kinase inhibitors
Hua-Poo Su, Keith Rickert, Christine Burlein, 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.
Viruses
|
July 27, 2024
Novel Pan-Coronavirus 3CL Protease Inhibitor MK-7845: Biological and Pharmacological Profiling
Nadine Alvarez, Gregory C Adam, John A Howe, 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
|
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.
Journal of Medicinal Chemistry
|
February 16, 2024
Invention of MK-7845, a SARS-CoV-2 3CL Protease Inhibitor Employing a Novel Difluorinated Glutamine Mimic
Valerie W Shurtleff, Mark E Layton, Craig A Parish, et al.
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Search research articles
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Showing results (71-80 of 78) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 78 results.
ACS Medicinal Chemistry Letters
|
February 16, 2023
Pyrazole Ureas as Low Dose, CNS Penetrant Glucosylceramide Synthase Inhibitors for the Treatment of Parkinson's Disease
Anthony J Roecker, Kathy M Schirripa, H Marie Loughran, 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.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 2017
Structural characterization of nonactive site, TrkA-selective kinase inhibitors
Hua-Poo Su, Keith Rickert, Christine Burlein, 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.
Viruses
|
July 27, 2024
Novel Pan-Coronavirus 3CL Protease Inhibitor MK-7845: Biological and Pharmacological Profiling
Nadine Alvarez, Gregory C Adam, John A Howe, 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
|
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.
Journal of Medicinal Chemistry
|
February 16, 2024
Invention of MK-7845, a SARS-CoV-2 3CL Protease Inhibitor Employing a Novel Difluorinated Glutamine Mimic
Valerie W Shurtleff, Mark E Layton, Craig A Parish, et al.
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