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Journal of Pharmacokinetics and Pharmacodynamics
|
October 8, 2014
Modeling and simulation for medical product development and evaluation: highlights from the FDA-C-Path-ISOP 2013 workshop
Klaus Romero, Vikram Sinha, Sandra Allerheiligen, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 13, 2010
Design and synthesis of disubstituted thiophene and thiazole based inhibitors of JNK
Roy K Hom, Simeon Bowers, Jennifer M Sealy, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 3, 2011
Design, synthesis and structure-activity relationship of novel [3.3.1] bicyclic sulfonamide-pyrazoles as potent γ-secretase inhibitors
Danielle L Aubele, Anh P Truong, Darren B Dressen, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 15, 2011
Design and synthesis of a novel, orally active, brain penetrant, tri-substituted thiophene based JNK inhibitor
Simeon Bowers, Anh P Truong, R Jeffrey Neitz, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 9, 2009
Design and synthesis of cell potent BACE-1 inhibitors: structure-activity relationship of P1' substituents
Jennifer M Sealy, Anh P Truong, Luke Tso, et al.
Hepatology (Baltimore, Md.)
|
January 23, 2018
Candidate biomarkers for the diagnosis and prognosis of drug-induced liver injury: An international collaborative effort
Rachel J Church, Gerd A Kullak-Ublick, Jiri Aubrecht, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 15, 2013
Discovery of a novel [3.2.1] benzo fused bicyclic sulfonamide-pyrazoles as potent, selective and efficacious γ-secretase inhibitors
Xiaocong M Ye, Andrei W Konradi, Minghua Sun, et al.
G3 (Bethesda, Md.)
|
October 23, 2020
Slow Growth and Increased Spontaneous Mutation Frequency in Respiratory Deficient <i>afo1</i><sup>-</sup> Yeast Suppressed by a Dominant Mutation in <i>ATP3</i>
Jing Li, Mark Rinnerthaler, Johannes Hartl, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 17, 2010
Improving the permeability of the hydroxyethylamine BACE-1 inhibitors: structure-activity relationship of P2' substituents
Anh P Truong, Gary D Probst, Jose Aquino, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 17, 2013
Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: prime side chromane-containing inhibitors
Raymond A Ng, Minghua Sun, Simeon Bowers, et al.
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Search research articles
Search
Showing results (181-190 of 199) with videos related to
Sort By:
Page
of 20
Journal of Pharmacokinetics and Pharmacodynamics
|
October 8, 2014
Modeling and simulation for medical product development and evaluation: highlights from the FDA-C-Path-ISOP 2013 workshop
Klaus Romero, Vikram Sinha, Sandra Allerheiligen, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 13, 2010
Design and synthesis of disubstituted thiophene and thiazole based inhibitors of JNK
Roy K Hom, Simeon Bowers, Jennifer M Sealy, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 3, 2011
Design, synthesis and structure-activity relationship of novel [3.3.1] bicyclic sulfonamide-pyrazoles as potent γ-secretase inhibitors
Danielle L Aubele, Anh P Truong, Darren B Dressen, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 15, 2011
Design and synthesis of a novel, orally active, brain penetrant, tri-substituted thiophene based JNK inhibitor
Simeon Bowers, Anh P Truong, R Jeffrey Neitz, et al.
Bioorganic & Medicinal Chemistry Letters
|
October 9, 2009
Design and synthesis of cell potent BACE-1 inhibitors: structure-activity relationship of P1' substituents
Jennifer M Sealy, Anh P Truong, Luke Tso, et al.
Hepatology (Baltimore, Md.)
|
January 23, 2018
Candidate biomarkers for the diagnosis and prognosis of drug-induced liver injury: An international collaborative effort
Rachel J Church, Gerd A Kullak-Ublick, Jiri Aubrecht, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 15, 2013
Discovery of a novel [3.2.1] benzo fused bicyclic sulfonamide-pyrazoles as potent, selective and efficacious γ-secretase inhibitors
Xiaocong M Ye, Andrei W Konradi, Minghua Sun, et al.
G3 (Bethesda, Md.)
|
October 23, 2020
Slow Growth and Increased Spontaneous Mutation Frequency in Respiratory Deficient <i>afo1</i><sup>-</sup> Yeast Suppressed by a Dominant Mutation in <i>ATP3</i>
Jing Li, Mark Rinnerthaler, Johannes Hartl, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 17, 2010
Improving the permeability of the hydroxyethylamine BACE-1 inhibitors: structure-activity relationship of P2' substituents
Anh P Truong, Gary D Probst, Jose Aquino, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 17, 2013
Design and synthesis of hydroxyethylamine (HEA) BACE-1 inhibitors: prime side chromane-containing inhibitors
Raymond A Ng, Minghua Sun, Simeon Bowers, et al.
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of 20