Vig R - Search Results

1

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. Among authors: vig r. 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.

2

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. Bioorg Med Chem. 1998 Oct;6(10):1789-97. doi: 10.1016/s0968-0896(98)00108-4. Bioorg Med Chem. 1998. PMID: 9839009

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. 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: vig r. 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

Aryl phosphate derivatives of 3'-deoxythymidine are not potent anti-human immunodeficiency virus agents.

Vig R, Venkatachalam TK, Jan ST, Uckun FM. Vig R, et al. Antivir Chem Chemother. 1998 Sep;9(5):439-43. Antivir Chem Chemother. 1998. PMID: 9875397

6

D4T-5'-[p-bromophenyl methoxyalaninyl phosphate] as a potent and non-toxic anti-human immunodeficiency virus agent.

Vig R, Venkatachalam TK, Uckun FM. Vig R, et al. Antivir Chem Chemother. 1998 Sep;9(5):445-8. Antivir Chem Chemother. 1998. PMID: 9875398

7

Enhancing effects of a mono-bromo substitution at the para position of the phenyl moiety on the metabolism and anti-HIV activity of d4T-phenyl methoxyalaninyl phosphate derivatives.

Venkatachalam TK, Tai HL, Vig R, Chen CL, Jan ST, Uckun FM. Venkatachalam TK, et al. Among authors: vig r. Bioorg Med Chem Lett. 1998 Nov 17;8(22):3121-6. doi: 10.1016/s0960-894x(98)00547-2. Bioorg Med Chem Lett. 1998. PMID: 9873688

8

Nucleoside conjugates. 15. Synthesis and biological activity of anti-HIV nucleoside conjugates of ether and thioether phospholipids.

Hong CI, Nechaev A, Kirisits AJ, Vig R, West CR, Manouilov KK, Chu CK. Hong CI, et al. Among authors: vig r. J Med Chem. 1996 Apr 26;39(9):1771-7. doi: 10.1021/jm950620o. J Med Chem. 1996. PMID: 8627600

9

Nucleoside conjugates. 13. Synthesis and antitumor activity of 1-beta-D-arabinofuranosylcytosine conjugates of thioether lipids with improved water solubility.

Hong CI, Nechaev A, Kirisits AJ, Vig R, West CR. Hong CI, et al. Among authors: vig r. J Med Chem. 1993 Jun 11;36(12):1785-90. doi: 10.1021/jm00064a012. J Med Chem. 1993. PMID: 8510106

10

Nucleoside conjugates. 14. Synthesis and antitumor activity of 1-beta-D-arabinofuranosylcytosine conjugates of ether lipids with improved water solubility.

Hong CI, Nechaev A, Kirisits AJ, Vig R, Hui SW, West CR. Hong CI, et al. Among authors: vig r. J Med Chem. 1995 May 12;38(10):1629-34. doi: 10.1021/jm00010a006. J Med Chem. 1995. PMID: 7752187

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