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Bioorganic & Medicinal Chemistry Letters
|
March 11, 2006
Non-peptide calcitonin gene-related peptide receptor antagonists from a benzodiazepinone lead
Theresa M Williams, Craig A Stump, Diem N Nguyen, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Discovery of MK-3207: A Highly Potent, Orally Bioavailable CGRP Receptor Antagonist
Ian M Bell, Steven N Gallicchio, Michael R Wood, et al.
Journal of Medicinal Chemistry
|
October 2, 2008
Discovery of 3-{5-[(6-amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5-chlorobenzonitrile (MK-4965): a potent, orally bioavailable HIV-1 non-nucleoside reverse transcriptase inhibitor with improved potency against key mutant viruses
Thomas J Tucker, John T Sisko, Robert M Tynebor, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 18, 2007
Novel indole-3-sulfonamides as potent HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs)
Zhijian Zhao, Scott E Wolkenberg, Philip E J Sanderson, et al.
ACS Infectious Diseases
|
February 21, 2017
Identification of Highly Specific Diversity-Oriented Synthesis-Derived Inhibitors of Clostridium difficile
Jeremy R Duvall, Leanne Bedard, Adel M Naylor-Olsen, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 8, 2007
Dihydroxypyridopyrazine-1,6-dione HIV-1 integrase inhibitors
John S Wai, Boyoung Kim, Thorsten E Fisher, et al.
Journal of Medicinal Chemistry
|
December 8, 2006
Discovery of oxadiazoyl tertiary carbinamine inhibitors of beta-secretase (BACE-1)
Hemaka A Rajapakse, Philippe G Nantermet, Harold G Selnick, et al.
Journal of Medicinal Chemistry
|
June 23, 2007
Discovery of isonicotinamide derived beta-secretase inhibitors: in vivo reduction of beta-amyloid
Matthew G Stanton, Shaun R Stauffer, Alison R Gregro, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 18, 2008
The discovery of highly potent CGRP receptor antagonists
Craig A Stump, Ian M Bell, Rodney A Bednar, et al.
Journal of Medicinal Chemistry
|
February 7, 2003
Design and synthesis of 8-hydroxy-[1,6]naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells
Linghang Zhuang, John S Wai, Mark W Embrey, et al.
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of 9
Search research articles
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Showing results (41-50 of 84) with videos related to
Sort By:
Page
of 9
Bioorganic & Medicinal Chemistry Letters
|
March 11, 2006
Non-peptide calcitonin gene-related peptide receptor antagonists from a benzodiazepinone lead
Theresa M Williams, Craig A Stump, Diem N Nguyen, et al.
ACS Medicinal Chemistry Letters
|
June 6, 2014
Discovery of MK-3207: A Highly Potent, Orally Bioavailable CGRP Receptor Antagonist
Ian M Bell, Steven N Gallicchio, Michael R Wood, et al.
Journal of Medicinal Chemistry
|
October 2, 2008
Discovery of 3-{5-[(6-amino-1H-pyrazolo[3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5-chlorobenzonitrile (MK-4965): a potent, orally bioavailable HIV-1 non-nucleoside reverse transcriptase inhibitor with improved potency against key mutant viruses
Thomas J Tucker, John T Sisko, Robert M Tynebor, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 18, 2007
Novel indole-3-sulfonamides as potent HIV non-nucleoside reverse transcriptase inhibitors (NNRTIs)
Zhijian Zhao, Scott E Wolkenberg, Philip E J Sanderson, et al.
ACS Infectious Diseases
|
February 21, 2017
Identification of Highly Specific Diversity-Oriented Synthesis-Derived Inhibitors of Clostridium difficile
Jeremy R Duvall, Leanne Bedard, Adel M Naylor-Olsen, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 8, 2007
Dihydroxypyridopyrazine-1,6-dione HIV-1 integrase inhibitors
John S Wai, Boyoung Kim, Thorsten E Fisher, et al.
Journal of Medicinal Chemistry
|
December 8, 2006
Discovery of oxadiazoyl tertiary carbinamine inhibitors of beta-secretase (BACE-1)
Hemaka A Rajapakse, Philippe G Nantermet, Harold G Selnick, et al.
Journal of Medicinal Chemistry
|
June 23, 2007
Discovery of isonicotinamide derived beta-secretase inhibitors: in vivo reduction of beta-amyloid
Matthew G Stanton, Shaun R Stauffer, Alison R Gregro, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 18, 2008
The discovery of highly potent CGRP receptor antagonists
Craig A Stump, Ian M Bell, Rodney A Bednar, et al.
Journal of Medicinal Chemistry
|
February 7, 2003
Design and synthesis of 8-hydroxy-[1,6]naphthyridines as novel inhibitors of HIV-1 integrase in vitro and in infected cells
Linghang Zhuang, John S Wai, Mark W Embrey, et al.
Page
of 9