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Bioorganic & Medicinal Chemistry
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June 27, 2001
Arylisothiocyanate-containing esters of caffeic acid designed as affinity ligands for HIV-1 integrase
X Zhang, N Neamati, Y K Lee, et al.
Journal of Medicinal Chemistry
|
January 17, 1997
Coumarin-based inhibitors of HIV integrase
H Zhao, N Neamati, H Hong, et al.
Journal of Medicinal Chemistry
|
March 14, 1997
Depsides and depsidones as inhibitors of HIV-1 integrase: discovery of novel inhibitors through 3D database searching
N Neamati, H Hong, A Mazumder, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 16, 1998
Identification of a nucleotide binding site in HIV-1 integrase
R R Drake, N Neamati, H Hong, et al.
Journal of Medicinal Chemistry
|
March 14, 1997
Discovery of HIV-1 integrase inhibitors by pharmacophore searching
H Hong, N Neamati, S Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 6, 1998
Structure of the catalytic domain of avian sarcoma virus integrase with a bound HIV-1 integrase-targeted inhibitor
J Lubkowski, F Yang, J Alexandratos, et al.
Bioorganic & Medicinal Chemistry
|
November 1, 2000
Identification of HIV-1 integrase inhibitors via three-dimensional database searching using ASV and HIV-1 integrases as targets
I J Chen, N Neamati, M C Nicklaus, et al.
Journal of Medicinal Chemistry
|
June 21, 1996
Antiretroviral agents as inhibitors of both human immunodeficiency virus type 1 integrase and protease
A Mazumder, S Wang, N Neamati, et al.
Molecular Pharmacology
|
August 23, 2000
Viral entry as the primary target for the anti-HIV activity of chicoric acid and its tetra-acetyl esters
W Pluymers, N Neamati, C Pannecouque, et al.
Journal of Medicinal Chemistry
|
August 14, 1998
Salicylhydrazine-containing inhibitors of HIV-1 integrase: implication for a selective chelation in the integrase active site
N Neamati, H Hong, J M Owen, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Bioorganic & Medicinal Chemistry
|
June 27, 2001
Arylisothiocyanate-containing esters of caffeic acid designed as affinity ligands for HIV-1 integrase
X Zhang, N Neamati, Y K Lee, et al.
Journal of Medicinal Chemistry
|
January 17, 1997
Coumarin-based inhibitors of HIV integrase
H Zhao, N Neamati, H Hong, et al.
Journal of Medicinal Chemistry
|
March 14, 1997
Depsides and depsidones as inhibitors of HIV-1 integrase: discovery of novel inhibitors through 3D database searching
N Neamati, H Hong, A Mazumder, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 16, 1998
Identification of a nucleotide binding site in HIV-1 integrase
R R Drake, N Neamati, H Hong, et al.
Journal of Medicinal Chemistry
|
March 14, 1997
Discovery of HIV-1 integrase inhibitors by pharmacophore searching
H Hong, N Neamati, S Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 6, 1998
Structure of the catalytic domain of avian sarcoma virus integrase with a bound HIV-1 integrase-targeted inhibitor
J Lubkowski, F Yang, J Alexandratos, et al.
Bioorganic & Medicinal Chemistry
|
November 1, 2000
Identification of HIV-1 integrase inhibitors via three-dimensional database searching using ASV and HIV-1 integrases as targets
I J Chen, N Neamati, M C Nicklaus, et al.
Journal of Medicinal Chemistry
|
June 21, 1996
Antiretroviral agents as inhibitors of both human immunodeficiency virus type 1 integrase and protease
A Mazumder, S Wang, N Neamati, et al.
Molecular Pharmacology
|
August 23, 2000
Viral entry as the primary target for the anti-HIV activity of chicoric acid and its tetra-acetyl esters
W Pluymers, N Neamati, C Pannecouque, et al.
Journal of Medicinal Chemistry
|
August 14, 1998
Salicylhydrazine-containing inhibitors of HIV-1 integrase: implication for a selective chelation in the integrase active site
N Neamati, H Hong, J M Owen, et al.
Page
of 5