Sudbeck EA - Search Results

1

Rational design and synthesis of phenethyl-5-bromopyridyl thiourea derivatives as potent non-nucleoside inhibitors of HIV reserve transcriptase.

Vig R, Mao C, Venkatachalam TK, Tuel-Ahlgren L, Sudbeck EA, Uckun FM. Vig R, et al. Among authors: sudbeck ea. Bioorg Med Chem. 1998 Oct;6(10):1789-97. doi: 10.1016/s0968-0896(98)00108-4. Bioorg Med Chem. 1998. PMID: 9839009

2

Structure-based design of novel dihydroalkoxybenzyloxopyrimidine derivatives as potent nonnucleoside inhibitors of the human immunodeficiency virus reverse transcriptase.

Sudbeck EA, Mao C, Vig R, Venkatachalam TK, Tuel-Ahlgren L, Uckun FM. Sudbeck EA, et al. Antimicrob Agents Chemother. 1998 Dec;42(12):3225-33. doi: 10.1128/AAC.42.12.3225. Antimicrob Agents Chemother. 1998. PMID: 9835518 Free PMC article.

3

5-Alkyl-2-[(methylthiomethyl)thio]-6-(benzyl)-pyrimidin-4-(1H)-ones as potent non-nucleoside reverse transcriptase inhibitors of S-DABO series.

Vig R, Mao C, Venkatachalam TK, Tuel-Ahlgren L, Sudbeck EA, Uckun FM. Vig R, et al. Among authors: sudbeck ea. Bioorg Med Chem Lett. 1998 Jun 16;8(12):1461-6. doi: 10.1016/s0960-894x(98)00250-9. Bioorg Med Chem Lett. 1998. PMID: 9873370

4

Structure-based design of N-[2-(1-piperidinylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea and N-[2-(1-piperazinylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea as potent non-nucleoside inhibitors of HIV-1 reverse transcriptase.

Mao C, Vig R, Venkatachalam TK, Sudbeck EA, Uckun FM. Mao C, et al. Among authors: sudbeck ea. Bioorg Med Chem Lett. 1998 Aug 18;8(16):2213-8. doi: 10.1016/s0960-894x(98)00384-9. Bioorg Med Chem Lett. 1998. PMID: 9873515

5

Rational design and synthesis of a novel anti-leukemic agent targeting Bruton's tyrosine kinase (BTK), LFM-A13 [alpha-cyano-beta-hydroxy-beta-methyl-N-(2, 5-dibromophenyl)propenamide].

Mahajan S, Ghosh S, Sudbeck EA, Zheng Y, Downs S, Hupke M, Uckun FM. Mahajan S, et al. Among authors: sudbeck ea. J Biol Chem. 1999 Apr 2;274(14):9587-99. doi: 10.1074/jbc.274.14.9587. J Biol Chem. 1999. PMID: 10092645 Free article.

6

Rational design of N-[2-(2,5-dimethoxyphenylethyl)]-N'-[2-(5-bromopyridyl)]-thiourea (HI-236) as a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus.

Mao C, Sudbeck EA, Venkatachalam TK, Uckun FM. Mao C, et al. Among authors: sudbeck ea. Bioorg Med Chem Lett. 1999 Jun 7;9(11):1593-8. doi: 10.1016/s0960-894x(99)00235-8. Bioorg Med Chem Lett. 1999. PMID: 10386942

7

Structure-based design of non-nucleoside reverse transcriptase inhibitors of drug-resistant human immunodeficiency virus.

Mao C, Sudbeck EA, Venkatachalam TK, Uckun FM. Mao C, et al. Among authors: sudbeck ea. Antivir Chem Chemother. 1999 Sep;10(5):233-40. doi: 10.1177/095632029901000502. Antivir Chem Chemother. 1999. PMID: 10574178 Free article.

8

Antioxidant function of phenethyl-5-bromo-pyridyl thiourea compounds with potent anti-HIV activity.

Dong Y, Venkatachalam TK, Narla RK, Trieu VN, Sudbeck EA, Uckun FM. Dong Y, et al. Among authors: sudbeck ea. Bioorg Med Chem Lett. 2000 Jan 3;10(1):87-90. doi: 10.1016/s0960-894x(99)00581-8. Bioorg Med Chem Lett. 2000. PMID: 10636251

9

Inhibitor of HIV-1 reverse transcriptase: N'-(5-bromo-2-pyridyl)-N-[2-(2,5-dimethoxyphenyl)ethyl]thiourea.

Sudbeck EA, Jennissen JD, Venkatachalam TK, Uckun FM. Sudbeck EA, et al. Acta Crystallogr C. 1999 Dec 15;55 ( Pt 12):2122-4. doi: 10.1107/s0108270199012044. Acta Crystallogr C. 1999. PMID: 10641283

10

Structure-based design of potent inhibitors of EGF-receptor tyrosine kinase as anti-cancer agents.

Ghosh S, Narla RK, Zheng Y, Liu XP, Jun X, Mao C, Sudbeck EA, Uckun FM. Ghosh S, et al. Among authors: sudbeck ea. Anticancer Drug Des. 1999 Oct;14(5):403-10. Anticancer Drug Des. 1999. PMID: 10766295

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