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. 2003 Oct;47(10):3123-9.
doi: 10.1128/AAC.47.10.3123-3129.2003.

Novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI) UIC-94017 (TMC114) with potent activity against multi-PI-resistant human immunodeficiency virus in vitro

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Novel bis-tetrahydrofuranylurethane-containing nonpeptidic protease inhibitor (PI) UIC-94017 (TMC114) with potent activity against multi-PI-resistant human immunodeficiency virus in vitro

Yasuhiro Koh et al. Antimicrob Agents Chemother. 2003 Oct.

Abstract

We designed, synthesized, and identified UIC-94017 (TMC114), a novel nonpeptidic human immunodeficiency virus type 1 (HIV-1) protease inhibitor (PI) containing a 3(R),3a(S),6a(R)-bis-tetrahydrofuranylurethane (bis-THF) and a sulfonamide isostere which is extremely potent against laboratory HIV-1 strains and primary clinical isolates (50% inhibitory concentration [IC(50)], approximately 0.003 micro M; IC(90), approximately 0.009 micro M) with minimal cytotoxicity (50% cytotoxic concentration for CD4(+) MT-2 cells, 74 micro M). UIC-94017 blocked the infectivity and replication of each of HIV-1(NL4-3) variants exposed to and selected for resistance to saquinavir, indinavir, nelfinavir, or ritonavir at concentrations up to 5 micro M (IC(50)s, 0.003 to 0.029 micro M), although it was less active against HIV-1(NL4-3) variants selected for resistance to amprenavir (IC(50), 0.22 micro M). UIC-94017 was also potent against multi-PI-resistant clinical HIV-1 variants isolated from patients who had no response to existing antiviral regimens after having received a variety of antiviral agents. Structural analyses revealed that the close contact of UIC-94017 with the main chains of the protease active-site amino acids (Asp-29 and Asp-30) is important for its potency and wide spectrum of activity against multi-PI-resistant HIV-1 variants. Considering the favorable pharmacokinetics of UIC-94017 when administered with ritonavir, the present data warrant that UIC-94017 be further developed as a potential therapeutic agent for the treatment of primary and multi-PI-resistant HIV-1 infections.

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Figures

FIG. 1.
FIG. 1.
Structures of UIC-94017 and amprenavir.
FIG. 2.
FIG. 2.
Stereoview of X-ray crystal structure of HIV-1 protease complexed with UIC-94017. UIC-94017 is depicted in purple, and significant HIV-1 protease residues are shown in green with the corresponding three-letter amino acid codes and sequence numbers. Nitrogen and oxygen atoms are shown in blue and red, respectively. Hydrogen bonds between UIC-94017 and each amino acid and those between UIC-94017 and the water molecule are indicated by green dashed lines.

References

    1. Carrillo, A., K. Stewart, H. Sham, D. Norbeck, W. Kohlbrenner, J. Leonard, D. Kempf, and A. Molla. 1998. In vitro selection and characterization of human immunodeficiency virus type 1 variants with increased resistance to ABT-378, a novel protease inhibitor. J. Virol. 72:7532-7541. - PMC - PubMed
    1. Colonno, R. J., A. Thiry, K. Limoli, and N. Parkin. 2003. Activities of atazanavir (BMS-232632) against a large panel of human immunodeficiency virus type 1 clinical isolates resistant to one or more approved protease inhibitors. Antimicrob. Agents Chemother. 47:1324-1333. - PMC - PubMed
    1. De Clercq, E. 2002. Strategies in the design of antiviral drugs. Nat. Rev. Drug Discovery 1:13-25. - PubMed
    1. Erickson, J. W., and S. K. Burt. 1996. Structural mechanisms of HIV drug resistance. Annu. Rev. Pharmacol. Toxicol. 36:545-571. - PubMed
    1. Ferrer, E., D. Podzamczer, M. Arnedo, E. Fumero, P. McKenna, A. Rinehart, J. L. Perez, M. J. Barbera, T. Pumarola, J. M. Gatell, and F. Gudiol. 2003. Genotype and phenotype at baseline and at failure in human immunodeficiency virus-infected antiretroviral-naive patients in a randomized trial comparing zidovudine and lamivudine plus nelfinavir or nevirapine. J. Infect. Dis. 187:687-690. - PubMed

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