Adams J - Search Results

1

Novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 7. 8-Arylethyldipyridodiazepinones as potent broad-spectrum inhibitors of wild-type and mutant enzymes.

Klunder JM, Hoermann M, Cywin CL, David E, Brickwood JR, Schwartz R, Barringer KJ, Pauletti D, Shih CK, Erickson DA, Sorge CL, Joseph DP, Hattox SE, Adams J, Grob PM. Klunder JM, et al. Among authors: adams j. J Med Chem. 1998 Jul 30;41(16):2960-71. doi: 10.1021/jm9707028. J Med Chem. 1998. PMID: 9685235

2

Inhibition of HIV-1 replication by a nonnucleoside reverse transcriptase inhibitor.

Merluzzi VJ, Hargrave KD, Labadia M, Grozinger K, Skoog M, Wu JC, Shih CK, Eckner K, Hattox S, Adams J, et al. Merluzzi VJ, et al. Among authors: adams j. Science. 1990 Dec 7;250(4986):1411-3. doi: 10.1126/science.1701568. Science. 1990. PMID: 1701568

3

Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. 5. 4-Substituted and 2,4-disubstituted analogs of nevirapine.

Kelly TA, Proudfoot JR, McNeil DW, Patel UR, David E, Hargrave KD, Grob PM, Cardozo M, Agarwal A, Adams J. Kelly TA, et al. Among authors: adams j. J Med Chem. 1995 Nov 24;38(24):4839-47. doi: 10.1021/jm00024a011. J Med Chem. 1995. PMID: 7490733

4

Prophylaxis against HIV-1 infection in chimpanzees by nevirapine, a nonnucleoside inhibitor of reverse transcriptase.

Grob PM, Cao Y, Muchmore E, Ho DD, Norris S, Pav JW, Shih CK, Adams J. Grob PM, et al. Among authors: adams j. Nat Med. 1997 Jun;3(6):665-70. doi: 10.1038/nm0697-665. Nat Med. 1997. PMID: 9176494

5

A novel dipyridodiazepinone inhibitor of HIV-1 reverse transcriptase acts through a nonsubstrate binding site.

Wu JC, Warren TC, Adams J, Proudfoot J, Skiles J, Raghavan P, Perry C, Potocki I, Farina PR, Grob PM. Wu JC, et al. Among authors: adams j. Biochemistry. 1991 Feb 26;30(8):2022-6. doi: 10.1021/bi00222a003. Biochemistry. 1991. PMID: 1705436

6

Potent and selective inhibitors of the proteasome: dipeptidyl boronic acids.

Adams J, Behnke M, Chen S, Cruickshank AA, Dick LR, Grenier L, Klunder JM, Ma YT, Plamondon L, Stein RL. Adams J, et al. Bioorg Med Chem Lett. 1998 Feb 17;8(4):333-8. doi: 10.1016/s0960-894x(98)00029-8. Bioorg Med Chem Lett. 1998. PMID: 9871680

7

Crystal structure of nevirapine, a non-nucleoside inhibitor of HIV-1 reverse transcriptase, and computational alignment with a structurally diverse inhibitor.

Mui PW, Jacober SP, Hargrave KD, Adams J. Mui PW, et al. Among authors: adams j. J Med Chem. 1992 Jan;35(1):201-2. doi: 10.1021/jm00079a029. J Med Chem. 1992. PMID: 1370694 No abstract available.

8

Characterization of the binding site for nevirapine (BI-RG-587), a nonnucleoside inhibitor of human immunodeficiency virus type-1 reverse transcriptase.

Cohen KA, Hopkins J, Ingraham RH, Pargellis C, Wu JC, Palladino DE, Kinkade P, Warren TC, Rogers S, Adams J, et al. Cohen KA, et al. Among authors: adams j. J Biol Chem. 1991 Aug 5;266(22):14670-4. J Biol Chem. 1991. PMID: 1713587 Free article.

9

Structure-activity relationships of boronic acid inhibitors of dipeptidyl peptidase IV. 1. Variation of the P2 position of Xaa-boroPro dipeptides.

Coutts SJ, Kelly TA, Snow RJ, Kennedy CA, Barton RW, Adams J, Krolikowski DA, Freeman DM, Campbell SJ, Ksiazek JF, Bachovchin WW. Coutts SJ, et al. Among authors: adams j. J Med Chem. 1996 May 10;39(10):2087-94. doi: 10.1021/jm950732f. J Med Chem. 1996. PMID: 8642568

10

Inhibition of herpes simplex virus type 1 ribonucleotide reductase by substituted tetrapeptide derivatives.

Moss N, Déziel R, Adams J, Aubry N, Bailey M, Baillet M, Beaulieu P, DiMaio J, Duceppe JS, Ferland JM, et al. Moss N, et al. Among authors: adams j. J Med Chem. 1993 Oct 1;36(20):3005-9. doi: 10.1021/jm00072a021. J Med Chem. 1993. PMID: 8411018

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