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M C Nicklaus

Showing results (21-30 of 27) with videos related to

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Journal of Medicinal Chemistry|March 14, 1997
Discovery of HIV-1 integrase inhibitors by pharmacophore searchingH Hong, N Neamati, S Wang, et al.
Nucleosides, Nucleotides & Nucleic Acids|September 21, 2001
Inhibition of (cytosine C5)-methyltransferase by oligonucleotides containing flexible (cyclopentane) and conformationally constrained (bicyclo[3.1.0]hexane) abasic sitesV E Marquez, P Wang, M C Nicklaus, et al.
Nucleosides & Nucleotides|August 5, 1999
Conformationally restricted nucleosides. The reaction of adenosine deaminase with substrates built on a bicyclo[3.1.0]hexane templateV E Marquez, P Russ, R Alonso, 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 targetsI J Chen, N Neamati, M C Nicklaus, et al.
Journal of Medicinal Chemistry|June 1, 2001
An optimized protein kinase C activating diacylglycerol combining high binding affinity (Ki) with reduced lipophilicity (log P)K Nacro, D M Sigano, S Yan, et al.
Journal of Medicinal Chemistry|December 1, 2001
Conformationally constrained analogues of diacylglycerol. 18. The incorporation of a hydroxamate moiety into diacylglycerol-lactones reduces lipophilicity and helps discriminate between sn-1 and sn-2 binding modes to protein kinase C (PK-C). Implications for isozyme specificityJ Lee, K C Han, J H Kang, et al.
Biochemistry|September 14, 2000
Interactions of conformationally biased north and south 2'-fluoro-2', 3'-dideoxynucleoside 5'-triphosphates with the active site of HIV-1 reverse transcriptaseL Mu, S G Sarafianos, M C Nicklaus, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Journal of Medicinal Chemistry|March 14, 1997
Discovery of HIV-1 integrase inhibitors by pharmacophore searchingH Hong, N Neamati, S Wang, et al.
Nucleosides, Nucleotides & Nucleic Acids|September 21, 2001
Inhibition of (cytosine C5)-methyltransferase by oligonucleotides containing flexible (cyclopentane) and conformationally constrained (bicyclo[3.1.0]hexane) abasic sitesV E Marquez, P Wang, M C Nicklaus, et al.
Nucleosides & Nucleotides|August 5, 1999
Conformationally restricted nucleosides. The reaction of adenosine deaminase with substrates built on a bicyclo[3.1.0]hexane templateV E Marquez, P Russ, R Alonso, 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 targetsI J Chen, N Neamati, M C Nicklaus, et al.
Journal of Medicinal Chemistry|June 1, 2001
An optimized protein kinase C activating diacylglycerol combining high binding affinity (Ki) with reduced lipophilicity (log P)K Nacro, D M Sigano, S Yan, et al.
Journal of Medicinal Chemistry|December 1, 2001
Conformationally constrained analogues of diacylglycerol. 18. The incorporation of a hydroxamate moiety into diacylglycerol-lactones reduces lipophilicity and helps discriminate between sn-1 and sn-2 binding modes to protein kinase C (PK-C). Implications for isozyme specificityJ Lee, K C Han, J H Kang, et al.
Biochemistry|September 14, 2000
Interactions of conformationally biased north and south 2'-fluoro-2', 3'-dideoxynucleoside 5'-triphosphates with the active site of HIV-1 reverse transcriptaseL Mu, S G Sarafianos, M C Nicklaus, et al.
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