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Current Opinion in Drug Discovery & Development
|
August 29, 2002
Using X-ray crystallography in drug discovery
R Scott Rowland
Frontiers in Neuroscience
|
February 23, 2024
Methylone is a rapid-acting neuroplastogen with less off-target activity than MDMA
Jennifer Warner-Schmidt, Martin Stogniew, Blake Mandell, et al.
Journal of Medicinal Chemistry
|
August 23, 2013
Potent histone deacetylase inhibitors derived from 4-(aminomethyl)-N-hydroxybenzamide with high selectivity for the HDAC6 isoform
Christopher Blackburn, Cynthia Barrett, Janice Chin, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 3, 2014
Histone deacetylase inhibitors derived from 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine and related heterocycles selective for the HDAC6 isoform
Christopher Blackburn, Cynthia Barrett, Mable Brunson, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 17, 2010
Discovery and optimization of pyrazoline compounds as B-Raf inhibitors
Matthew O Duffey, Ruth Adams, Christopher Blackburn, et al.
Journal of Medicinal Chemistry
|
February 24, 2011
Design and optimization of potent and orally bioavailable tetrahydronaphthalene Raf inhibitors
Alexandra E Gould, Ruth Adams, Sharmila Adhikari, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Current Opinion in Drug Discovery & Development
|
August 29, 2002
Using X-ray crystallography in drug discovery
R Scott Rowland
Frontiers in Neuroscience
|
February 23, 2024
Methylone is a rapid-acting neuroplastogen with less off-target activity than MDMA
Jennifer Warner-Schmidt, Martin Stogniew, Blake Mandell, et al.
Journal of Medicinal Chemistry
|
August 23, 2013
Potent histone deacetylase inhibitors derived from 4-(aminomethyl)-N-hydroxybenzamide with high selectivity for the HDAC6 isoform
Christopher Blackburn, Cynthia Barrett, Janice Chin, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 3, 2014
Histone deacetylase inhibitors derived from 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine and related heterocycles selective for the HDAC6 isoform
Christopher Blackburn, Cynthia Barrett, Mable Brunson, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 17, 2010
Discovery and optimization of pyrazoline compounds as B-Raf inhibitors
Matthew O Duffey, Ruth Adams, Christopher Blackburn, et al.
Journal of Medicinal Chemistry
|
February 24, 2011
Design and optimization of potent and orally bioavailable tetrahydronaphthalene Raf inhibitors
Alexandra E Gould, Ruth Adams, Sharmila Adhikari, et al.
Page
of 1