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BR96 conjugates of highly potent anthracyclines.
Bioorg Med Chem Lett. 2003 Jul 7;13(13):2119-22. doi: 10.1016/s0960-894x(03)00375-5.
Bioorg Med Chem Lett. 2003.
PMID: 12798317
Triketoacid inhibitors of HIV-integrase: a new chemotype useful for probing the integrase pharmacophore.
Walker MA, Johnson T, Ma Z, Banville J, Remillard R, Kim O, Zhang Y, Staab A, Wong H, Torri A, Samanta H, Lin Z, Deminie C, Terry B, Krystal M, Meanwell N.
Walker MA, et al.
Bioorg Med Chem Lett. 2006 Jun 1;16(11):2920-4. doi: 10.1016/j.bmcl.2006.03.010. Epub 2006 Mar 20.
Bioorg Med Chem Lett. 2006.
PMID: 16546383
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Highly potent non-peptidic inhibitors of the HCV NS3/NS4A serine protease.
Sperandio D, Gangloff AR, Litvak J, Goldsmith R, Hataye JM, Wang VR, Shelton EJ, Elrod K, Janc JW, Clark JM, Rice K, Weinheimer S, Yeung KS, Meanwell NA, Hernandez D, Staab AJ, Venables BL, Spencer JR.
Sperandio D, et al. Among authors: staab aj.
Bioorg Med Chem Lett. 2002 Nov 4;12(21):3129-33. doi: 10.1016/s0960-894x(02)00680-7.
Bioorg Med Chem Lett. 2002.
PMID: 12372517
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Use of achiral/chiral SFC/MS for the profiling of isomeric cinnamonitrile/hydrocinnamonitrile products in chiral drug synthesis.
Alexander AJ, Staab A.
Alexander AJ, et al. Among authors: staab a.
Anal Chem. 2006 Jun 1;78(11):3835-8. doi: 10.1021/ac060326b.
Anal Chem. 2006.
PMID: 16737245
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