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S V Gulnik

Showing results (11-20 of 17) with videos related to

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AIDS Research and Human Retroviruses|January 1, 1996
Design, synthesis, and resistance patterns of MP-134 and MP-167, two novel inhibitors of HIV type 1 proteaseH Mo, M Markowitz, P Majer, et al.
Bioorganic & Medicinal Chemistry Letters|February 6, 1999
Unsymmetric nonpeptidic HIV protease inhibitors containing anthranilamide as a P2' ligandR S Randad, L Lubkowska, M A Eissenstat, et al.
Biochemistry|December 23, 1998
Functional characterization of the protease of human endogenous retrovirus, K10: can it complement HIV-1 protease?E M Towler, S V Gulnik, T N Bhat, et al.
Journal of Medicinal Chemistry|May 30, 1998
Cyclopropane-derived peptidomimetics. Design, synthesis, evaluation, and structure of novel HIV-1 protease inhibitorsS F Martin, G O Dorsey, T Gane, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 1996
Structure and inhibition of plasmepsin II, a hemoglobin-degrading enzyme from Plasmodium falciparumA M Silva, A Y Lee, S V Gulnik, et al.
Journal of Medicinal Chemistry|November 26, 1997
4-hydroxy-5,6-dihydropyrones. 2. Potent non-peptide inhibitors of HIV proteaseB D Tait, S Hagen, J Domagala, et al.
Journal of Medicinal Chemistry|March 15, 2000
5,6-Dihydropyran-2-ones possessing various sulfonyl functionalities: potent nonpeptidic inhibitors of HIV proteaseF E Boyer, J V Vara Prasad, J M Domagala, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
AIDS Research and Human Retroviruses|January 1, 1996
Design, synthesis, and resistance patterns of MP-134 and MP-167, two novel inhibitors of HIV type 1 proteaseH Mo, M Markowitz, P Majer, et al.
Bioorganic & Medicinal Chemistry Letters|February 6, 1999
Unsymmetric nonpeptidic HIV protease inhibitors containing anthranilamide as a P2' ligandR S Randad, L Lubkowska, M A Eissenstat, et al.
Biochemistry|December 23, 1998
Functional characterization of the protease of human endogenous retrovirus, K10: can it complement HIV-1 protease?E M Towler, S V Gulnik, T N Bhat, et al.
Journal of Medicinal Chemistry|May 30, 1998
Cyclopropane-derived peptidomimetics. Design, synthesis, evaluation, and structure of novel HIV-1 protease inhibitorsS F Martin, G O Dorsey, T Gane, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 17, 1996
Structure and inhibition of plasmepsin II, a hemoglobin-degrading enzyme from Plasmodium falciparumA M Silva, A Y Lee, S V Gulnik, et al.
Journal of Medicinal Chemistry|November 26, 1997
4-hydroxy-5,6-dihydropyrones. 2. Potent non-peptide inhibitors of HIV proteaseB D Tait, S Hagen, J Domagala, et al.
Journal of Medicinal Chemistry|March 15, 2000
5,6-Dihydropyran-2-ones possessing various sulfonyl functionalities: potent nonpeptidic inhibitors of HIV proteaseF E Boyer, J V Vara Prasad, J M Domagala, et al.
Pageof 2