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Novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 7. 8-Arylethyldipyridodiazepinones as potent broad-spectrum inhibitors of wild-type and mutant enzymes.
J Med Chem. 1998 Jul 30;41(16):2960-71. doi: 10.1021/jm9707028.
J Med Chem. 1998.
PMID: 9685235
Novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 8. 8-Aryloxymethyl- and 8-arylthiomethyldipyridodiazepinones.
Cywin CL, Klunder JM, Hoermann M, Brickwood JR, David E, Grob PM, Schwartz R, Pauletti D, Barringer KJ, Shih CK, Sorge CL, Erickson DA, Joseph DP, Hattox SE.
Cywin CL, et al. Among authors: klunder jm.
J Med Chem. 1998 Jul 30;41(16):2972-84. doi: 10.1021/jm9707030.
J Med Chem. 1998.
PMID: 9685236
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Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 2. Tricyclic pyridobenzoxazepinones and dibenzoxazepinones.
Klunder JM, Hargrave KD, West M, Cullen E, Pal K, Behnke ML, Kapadia SR, McNeil DW, Wu JC, Chow GC, et al.
Klunder JM, et al.
J Med Chem. 1992 May 15;35(10):1887-97. doi: 10.1021/jm00088a027.
J Med Chem. 1992.
PMID: 1375293
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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. Among authors: klunder jm.
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
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