메뉴 건너뛰기




Volumn 3, Issue 1, 2009, Pages 63-77

Efficacy and resistance of recently developed non-nucleoside reverse transcriptase inhibitors for HIV-1

Author keywords

Drug resistance; Genetic barrier; HIV 1; Non nucleoside reverse transcriptase inhibitor; Viral evolution

Indexed keywords

5 [3,5 DIETHYL 1 (2 HYDROXYETHYL) 4 PYRAZOLYLOXY] 1,3 BENZENEDINITRILE; ATAZANAVIR; BENZOPHENONE DERIVATIVE; BILR 355BS; DARUNAVIR PLUS RITONAVIR; EFAVIRENZ; ENFUVIRTIDE; ETRAVIRINE; GW 4511; GW 678248; GW 678284; GW 695634; IDX 899; INDAZOLE DERIVATIVE; MK 1107; MK 4965; NEVIRAPINE; PLACEBO; PROTEINASE INHIBITOR; RDEA 806; RILPIVIRINE; RITONAVIR; RNA DIRECTED DNA POLYMERASE INHIBITOR; RO 5028; UNCLASSIFIED DRUG; ZIDOVUDINE;

EID: 67149086037     PISSN: 17584310     EISSN: None     Source Type: Journal    
DOI: 10.2217/17584310.3.1.63     Document Type: Review
Times cited : (9)

References (80)
  • 1
    • 0025186450 scopus 로고
    • Molecular target for AIDS therapy
    • Mitsuya H, Yarchoan R, Broder S: Molecular target for AIDS therapy. Science 249, 1533-1544 (1990).
    • (1990) Science , vol.249 , pp. 1533-1544
    • Mitsuya, H.1    Yarchoan, R.2    Broder, S.3
  • 2
    • 0025014499 scopus 로고
    • Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives
    • Pauwels R, Andries K, Desmyter J et al.: Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives. Nature 343, 470-474 (1990).
    • (1990) Nature , vol.343 , pp. 470-474
    • Pauwels, R.1    Andries, K.2    Desmyter, J.3
  • 3
    • 0032573488 scopus 로고    scopus 로고
    • Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: Implications for drug resistance
    • Huang H, Chopra R, Verdine GL et al.: Structure of a covalently trapped catalytic complex of HIV-1 reverse transcriptase: implications for drug resistance. Science 282, 1669-1675 (1998).
    • (1998) Science , vol.282 , pp. 1669-1675
    • Huang, H.1    Chopra, R.2    Verdine, G.L.3
  • 4
    • 0026693137 scopus 로고
    • Crystal structure at 35 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor
    • Kohlstaedt LA, Wang J, Friedman JM et al.: Crystal structure at 35 Å resolution of HIV-1 reverse transcriptase complexed with an inhibitor. Science 256, 1783-1790 (1992).
    • (1992) Science , vol.256 , pp. 1783-1790
    • Kohlstaedt, L.A.1    Wang, J.2    Friedman, J.M.3
  • 5
    • 43049144549 scopus 로고    scopus 로고
    • Ren J, Stammers DK: Structural basis for drug resistance mechanisms for non-nucleoside inhibitors of HIV reverse transcriptase. Virus Res. 134, 157-170 (2008). ■■ Describes the mechanisms of non-nucleoside reverse transcriptase inhibitor (NNRTI) resistance, including updated crystallographic and other biochemical analyses.
    • Ren J, Stammers DK: Structural basis for drug resistance mechanisms for non-nucleoside inhibitors of HIV reverse transcriptase. Virus Res. 134, 157-170 (2008). ■■ Describes the mechanisms of non-nucleoside reverse transcriptase inhibitor (NNRTI) resistance, including updated crystallographic and other biochemical analyses.
  • 6
    • 0035160478 scopus 로고    scopus 로고
    • New developments in anti-HIV chemotherapy
    • De Clercq E: New developments in anti-HIV chemotherapy. Curr. Med. Chem. 8, 1543-1572 (2001).
    • (2001) Curr. Med. Chem , vol.8 , pp. 1543-1572
    • De Clercq, E.1
  • 7
    • 46349092759 scopus 로고    scopus 로고
    • Update of the drug resistance mutations in HIV-1: Spring 2008
    • Johnson VA, Brun-Vezinet F, Clotet B et al.: Update of the drug resistance mutations in HIV-1: Spring 2008. Top. HIV Med. 16, 62-68 (2008).
    • (2008) Top. HIV Med , vol.16 , pp. 62-68
    • Johnson, V.A.1    Brun-Vezinet, F.2    Clotet, B.3
  • 8
    • 0028924567 scopus 로고
    • Mechanism of inhibition of HIV-1 reverse transcriptase by non-nucleoside inhibitors
    • Esnouf R, Ren J, Ross C et al.: Mechanism of inhibition of HIV-1 reverse transcriptase by non-nucleoside inhibitors. Nat. Struct. Biol. 2, 303-308 (1995).
    • (1995) Nat. Struct. Biol , vol.2 , pp. 303-308
    • Esnouf, R.1    Ren, J.2    Ross, C.3
  • 9
    • 0028120730 scopus 로고    scopus 로고
    • De Clercq: E HIV resistance to reverse transcriptase inhibitors. Biochem. Pharmacol. 47, 155-169 (1994).
    • De Clercq: E HIV resistance to reverse transcriptase inhibitors. Biochem. Pharmacol. 47, 155-169 (1994).
  • 10
    • 0031578901 scopus 로고    scopus 로고
    • Resistance to nevirapine of HIV-1 reverse transcriptase mutants: Loss of stabilizing interactions and thermodynamic or steric barriers are induced by different single amino acid substitutions
    • Maga G, Amacker M, Ruel N et al.: Resistance to nevirapine of HIV-1 reverse transcriptase mutants: loss of stabilizing interactions and thermodynamic or steric barriers are induced by different single amino acid substitutions. J. Mol. Biol. 274, 738-747 (1997).
    • (1997) J. Mol. Biol , vol.274 , pp. 738-747
    • Maga, G.1    Amacker, M.2    Ruel, N.3
  • 11
    • 9644290714 scopus 로고    scopus 로고
    • Understanding the basis of resistance in the irksome Lys103Asn HIV-1 reverse transcriptase mutant through targeted molecular dynamics simulations
    • Rodriguez-Barrios F, Gago F: Understanding the basis of resistance in the irksome Lys103Asn HIV-1 reverse transcriptase mutant through targeted molecular dynamics simulations. J. Am. Chem. Soc. 126, 15386-15387 (2004).
    • (2004) J. Am. Chem. Soc , vol.126 , pp. 15386-15387
    • Rodriguez-Barrios, F.1    Gago, F.2
  • 12
    • 2342620790 scopus 로고    scopus 로고
    • Roles of conformational and positional adaptability in structure based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants
    • Das K, Clark AD Jr, Lewi PJ et al.: Roles of conformational and positional adaptability in structure based design of TMC125-R165335 (etravirine) and related non-nucleoside reverse transcriptase inhibitors that are highly potent and effective against wild-type and drug-resistant HIV-1 variants. J. Med. Chem. 47, 2550-2560 (2004).
    • (2004) J. Med. Chem , vol.47 , pp. 2550-2560
    • Das, K.1    Clark Jr, A.D.2    Lewi, P.J.3
  • 13
    • 10744228247 scopus 로고    scopus 로고
    • Novel benzophenones as non-nucleoside reverse transcriptase inhibitors of HIV-1
    • Chan JH, Freeman GA, Tidwell JH et al.: Novel benzophenones as non-nucleoside reverse transcriptase inhibitors of HIV-1. J. Med. Chem. 47, 1175-1182 (2004).
    • (2004) J. Med. Chem , vol.47 , pp. 1175-1182
    • Chan, J.H.1    Freeman, G.A.2    Tidwell, J.H.3
  • 14
    • 11144245802 scopus 로고    scopus 로고
    • Structural studies of benzophenone/HIV-1 RT complexes: Insights into the potency of the next generation NNRTIs against WT and mutant HIV-1
    • S
    • Stammers DK, Stuart DI, Ren J et al.: Structural studies of benzophenone/HIV-1 RT complexes: insights into the potency of the next generation NNRTIs against WT and mutant HIV-1. Antivir. Ther. 9, S36 (2004).
    • (2004) Antivir. Ther , vol.9 , pp. 36
    • Stammers, D.K.1    Stuart, D.I.2    Ren, J.3
  • 15
    • 0842289678 scopus 로고    scopus 로고
    • Crystal structures of HIV-1 reverse transcriptase mutated at codons 100, 106 and 108 and mechanisms of resistance to non-nucleoside inhibitors
    • Ren J, Nichols CE, Chamberlain PP et al.: Crystal structures of HIV-1 reverse transcriptase mutated at codons 100, 106 and 108 and mechanisms of resistance to non-nucleoside inhibitors. J. Mol. Biol. 336, 569-578 (2004).
    • (2004) J. Mol. Biol , vol.336 , pp. 569-578
    • Ren, J.1    Nichols, C.E.2    Chamberlain, P.P.3
  • 16
    • 0037159928 scopus 로고    scopus 로고
    • Emergence of drug-resistant HIV-1 variants in patients undergoing structured treatment interruptions
    • Schweighardt B, Ortiz GM, Grant RM et al.: Emergence of drug-resistant HIV-1 variants in patients undergoing structured treatment interruptions. AIDS 16, 2342-2344 (2002).
    • (2002) AIDS , vol.16 , pp. 2342-2344
    • Schweighardt, B.1    Ortiz, G.M.2    Grant, R.M.3
  • 17
    • 2942565660 scopus 로고    scopus 로고
    • Structural and biochemical effects of human immunodeficiency virus mutants resistant to non-nucleoside reverse transcriptase inhibitors
    • Interesting review describes the in vivo and in vitro effects of mutations selected by first-generation NNRTIs, ■
    • Domaoal RA, Demeter LM: Structural and biochemical effects of human immunodeficiency virus mutants resistant to non-nucleoside reverse transcriptase inhibitors. Int. J. Biochem. Cell Biol. 36, 1735-1751 (2004). ■ Interesting review describes the in vivo and in vitro effects of mutations selected by first-generation NNRTIs.
    • (2004) Int. J. Biochem. Cell Biol , vol.36 , pp. 1735-1751
    • Domaoal, R.A.1    Demeter, L.M.2
  • 18
    • 0033840455 scopus 로고    scopus 로고
    • Human immunodeficiency virus type-1 mutations selected in patients failing efavirenz combination therapy
    • Bacheler LT, Anton ED, Kudish P et al.: Human immunodeficiency virus type-1 mutations selected in patients failing efavirenz combination therapy. Antimicrob. Agents Chemother. 44, 2475-2484 (2000).
    • (2000) Antimicrob. Agents Chemother , vol.44 , pp. 2475-2484
    • Bacheler, L.T.1    Anton, E.D.2    Kudish, P.3
  • 19
    • 0027957791 scopus 로고
    • Nevirapine resistance mutations of human immunodeficiency virus type 1 selected during therapy
    • Richman DD, Havlir D, Corbeil J et al.: Nevirapine resistance mutations of human immunodeficiency virus type 1 selected during therapy. J. Virol. 68, 1660-1666 (1994).
    • (1994) J. Virol , vol.68 , pp. 1660-1666
    • Richman, D.D.1    Havlir, D.2    Corbeil, J.3
  • 20
    • 0029897567 scopus 로고    scopus 로고
    • (Alkylamino) piperidine bis(heteroaryl) piperizine analogs are potent, broad-spectrum non nucleoside reverse transcriptase inhibitors of drug resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes
    • Olmsted RA, Slade DE, Kopta LA et al.: (Alkylamino) piperidine bis(heteroaryl) piperizine analogs are potent, broad-spectrum non nucleoside reverse transcriptase inhibitors of drug resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes. J. Virol. 70, 3698-3705 (1996).
    • (1996) J. Virol , vol.70 , pp. 3698-3705
    • Olmsted, R.A.1    Slade, D.E.2    Kopta, L.A.3
  • 21
    • 0027273015 scopus 로고
    • Activity of a novel quinoxaline derivative against human immunodeficiency virus type 1 reverse transcriptase and viral replication
    • Kleim JP, Bender R, Bilhardt UM et al.: Activity of a novel quinoxaline derivative against human immunodeficiency virus type 1 reverse transcriptase and viral replication. Antimicrob. Agents Chemother. 37, 1659-1664 (1993).
    • (1993) Antimicrob. Agents Chemother , vol.37 , pp. 1659-1664
    • Kleim, J.P.1    Bender, R.2    Bilhardt, U.M.3
  • 22
    • 13144282707 scopus 로고    scopus 로고
    • Structures of Tyr188Leu mutant and wild-type HIV-1 reverse transcriptase complexed with the non-nucleoside inhibitor HBY 097: Inhibitor flexibility is a useful design feature for reducing drug resistance
    • Hsiu Y, Das K, Ding J et al.: Structures of Tyr188Leu mutant and wild-type HIV-1 reverse transcriptase complexed with the non-nucleoside inhibitor HBY 097: inhibitor flexibility is a useful design feature for reducing drug resistance. J. Mol. Biol. 284, 313-323 (1998).
    • (1998) J. Mol. Biol , vol.284 , pp. 313-323
    • Hsiu, Y.1    Das, K.2    Ding, J.3
  • 23
    • 41249088246 scopus 로고    scopus 로고
    • Impact of residues in the nonnucleoside reverse transcriptase inhibitor binding pocket on HIV-1 reverse transcriptase heterodimer stability
    • Figueiredo A, Zelina S, Sluis-Cremer N et al.: Impact of residues in the nonnucleoside reverse transcriptase inhibitor binding pocket on HIV-1 reverse transcriptase heterodimer stability. Curr. HIV Res. 6(2), 130-137 (2008).
    • (2008) Curr. HIV Res , vol.6 , Issue.2 , pp. 130-137
    • Figueiredo, A.1    Zelina, S.2    Sluis-Cremer, N.3
  • 24
    • 0025831249 scopus 로고
    • Catalytic properties of the reverse transcriptases of human immunodeficiency viruses type 1 and type 2
    • Hizi A, Tal R, Shaharabany M et al.: Catalytic properties of the reverse transcriptases of human immunodeficiency viruses type 1 and type 2. J. Biol. Chem. 266, 6230-6239 (1991).
    • (1991) J. Biol. Chem , vol.266 , pp. 6230-6239
    • Hizi, A.1    Tal, R.2    Shaharabany, M.3
  • 25
    • 0037195081 scopus 로고    scopus 로고
    • Structure of HIV-2 reverse transcriptase at 2.35-Å resolution and the mechanism of resistance to non-nucleoside inhibitors
    • Few data are available regarding the HIV-2 molecular structure and its diversity compared with HIV-1. This paper, although not so recent, provides some interesting insights into the crystallographic structure of HIV-2 reverse transcriptase, ■
    • Ren J, Bird LE, Chamberlain PP et al.: Structure of HIV-2 reverse transcriptase at 2.35-Å resolution and the mechanism of resistance to non-nucleoside inhibitors. Proc. Natl Acad. Sci. USA 99(22), 14410-14415 (2002). ■ Few data are available regarding the HIV-2 molecular structure and its diversity compared with HIV-1. This paper, although not so recent, provides some interesting insights into the crystallographic structure of HIV-2 reverse transcriptase.
    • (2002) Proc. Natl Acad. Sci. USA , vol.99 , Issue.22 , pp. 14410-14415
    • Ren, J.1    Bird, L.E.2    Chamberlain, P.P.3
  • 26
    • 0034053131 scopus 로고    scopus 로고
    • Phenylethylthiazolylthiourea (PETT) non-nucleoside inhibitors of HIV-1 and HIV-2 reverse transcriptases. Structural and biochemical analyses
    • Ren J, Diprose J, Warren RM et al.: Phenylethylthiazolylthiourea (PETT) non-nucleoside inhibitors of HIV-1 and HIV-2 reverse transcriptases. Structural and biochemical analyses. J. Biol. Chem. 275, 5633-5639 (2000).
    • (2000) J. Biol. Chem , vol.275 , pp. 5633-5639
    • Ren, J.1    Diprose, J.2    Warren, R.M.3
  • 27
    • 3142698606 scopus 로고    scopus 로고
    • The phenylethylthiazolylthiourea nonnucleoside reverse transcriptase (RT) inhibitor MSK-076 selects for a resistance mutation in the active site of human immunodeficiency virus type-2 RT
    • Auwerx J, Stevens M, Van Rompay AR et al.: The phenylethylthiazolylthiourea nonnucleoside reverse transcriptase (RT) inhibitor MSK-076 selects for a resistance mutation in the active site of human immunodeficiency virus type-2 RT. J. Virol. 78 (14), 7427-7437 (2004).
    • (2004) J. Virol , vol.78 , Issue.14 , pp. 7427-7437
    • Auwerx, J.1    Stevens, M.2    Van Rompay, A.R.3
  • 28
    • 2942704146 scopus 로고    scopus 로고
    • Clinical utility of current NNRTIs and perspectives of new agents in this class under development
    • Zhang Z, Hamatake R, Hong Z: Clinical utility of current NNRTIs and perspectives of new agents in this class under development. Antivir. Chem. Chemother. 15, 121-134 (2004).
    • (2004) Antivir. Chem. Chemother , vol.15 , pp. 121-134
    • Zhang, Z.1    Hamatake, R.2    Hong, Z.3
  • 29
    • 0036782103 scopus 로고    scopus 로고
    • Inhibitor binding alters the directions of domain motions in HIV-1 reverse transcriptase
    • Temiz NA, Bahar I: Inhibitor binding alters the directions of domain motions in HIV-1 reverse transcriptase. Proteins 49, 61-70 (2002).
    • (2002) Proteins , vol.49 , pp. 61-70
    • Temiz, N.A.1    Bahar, I.2
  • 30
    • 0037613579 scopus 로고    scopus 로고
    • Validation of a model for the complex of HIV-1 reverse transcriptase with nonnucleoside inhibitor TMC125
    • Udier-Blagovic M, Tirado-Rives J, Jorgensen WL: Validation of a model for the complex of HIV-1 reverse transcriptase with nonnucleoside inhibitor TMC125. J. Am. Chem. Soc. 125, 6016-6017 (2003).
    • (2003) J. Am. Chem. Soc , vol.125 , pp. 6016-6017
    • Udier-Blagovic, M.1    Tirado-Rives, J.2    Jorgensen, W.L.3
  • 31
    • 0034435564 scopus 로고    scopus 로고
    • Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase
    • Ren J, Milton J, Weaver KL et al.: Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase. Struct. Fold Des. 8, 1089-1094 (2000).
    • (2000) Struct. Fold Des , vol.8 , pp. 1089-1094
    • Ren, J.1    Milton, J.2    Weaver, K.L.3
  • 33
    • 12144287763 scopus 로고    scopus 로고
    • An open-label assessment of TMC125: A new, next-generation NNRTI, for 7 days in HIV-1 infected individuals with NNRTI resistance
    • Gazzard BG, Pozniak AL, Rosenbaum W et al.: An open-label assessment of TMC125: a new, next-generation NNRTI, for 7 days in HIV-1 infected individuals with NNRTI resistance. AIDS 17, F49-F54 (2003).
    • (2003) AIDS , vol.17
    • Gazzard, B.G.1    Pozniak, A.L.2    Rosenbaum, W.3
  • 34
    • 34147134958 scopus 로고    scopus 로고
    • efficacy and safety of etravirine (TMC125) in patients with highly resistant HIV-1: Primary 24 week analysis
    • The TMC125-C223 Writing Group
    • The TMC125-C223 Writing Group: efficacy and safety of etravirine (TMC125) in patients with highly resistant HIV-1: primary 24 week analysis. AIDS 21, F1-F10 (2007).
    • (2007) AIDS , vol.21
  • 35
    • 34347327010 scopus 로고    scopus 로고
    • Madruga JV, Cahn P, Grinzstejn B et al.: Efficacy and safety of TMC125 (etravirine) in treatment-experienced HIV-1-infected patients in DUET-1, 24-week results from a randomized, double-blind, placebo-controlled trial. Lancet 370, 29-38 (2007). ■ Along with [36], describes the most important studies that led to the US FDA approval of etravirine and provide useful information about several aspects of TMC125.
    • Madruga JV, Cahn P, Grinzstejn B et al.: Efficacy and safety of TMC125 (etravirine) in treatment-experienced HIV-1-infected patients in DUET-1, 24-week results from a randomized, double-blind, placebo-controlled trial. Lancet 370, 29-38 (2007). ■ Along with [36], describes the most important studies that led to the US FDA approval of etravirine and provide useful information about several aspects of TMC125.
  • 36
    • 34347354196 scopus 로고    scopus 로고
    • Lazzarin A, Campbell T, Clotet B et al.: Efficacy and safety of TMC125 (etravirine) in treatment-experienced HIV-1-infected patients in DUET-2, 24-week results from a randomized, double-blind, placebo-controlled trial. Lancet 370, 39-48 (2007). ■ Along with [35], describes the most important studies that led to the FDA approval of etravirine and provide useful information about several aspects of TMC125.
    • Lazzarin A, Campbell T, Clotet B et al.: Efficacy and safety of TMC125 (etravirine) in treatment-experienced HIV-1-infected patients in DUET-2, 24-week results from a randomized, double-blind, placebo-controlled trial. Lancet 370, 39-48 (2007). ■ Along with [35], describes the most important studies that led to the FDA approval of etravirine and provide useful information about several aspects of TMC125.
  • 37
    • 43749121302 scopus 로고    scopus 로고
    • DUET-1: Week 48 results of a Phase III randomized double-blind trial to evaluate the efficacy and safety of TMC125 versus placebo in 612 treatment-experienced HIV-1-infected patients
    • Presented at:, Boston, MA, USA, 3-6 February
    • Haubrich R, Cahn P, Grinsztejn B et al.: DUET-1: week 48 results of a Phase III randomized double-blind trial to evaluate the efficacy and safety of TMC125 versus placebo in 612 treatment-experienced HIV-1-infected patients. Presented at: 15th conference on retroviruses and opportunistic infections. Boston, MA, USA, 3-6 February 2008.
    • (2008) 15th conference on retroviruses and opportunistic infections
    • Haubrich, R.1    Cahn, P.2    Grinsztejn, B.3
  • 38
    • 43749103048 scopus 로고    scopus 로고
    • DUET-2: Week 48 results of a Phase III randomized double-blind trial to evaluate the efficacy and safety of tmc125 vs placebo in 591 treatment-experienced HIV-1-infected patients
    • Presented at:, Boston, MA, USA, 3-6 February
    • Johnson M, Campbell T, Clotet B et al.: DUET-2: week 48 results of a Phase III randomized double-blind trial to evaluate the efficacy and safety of tmc125 vs placebo in 591 treatment-experienced HIV-1-infected patients. Presented at: 15th Conference on Retroviruses and Opportunistic Infections. Boston, MA, USA, 3-6 February 2008.
    • (2008) 15th Conference on Retroviruses and Opportunistic Infections
    • Johnson, M.1    Campbell, T.2    Clotet, B.3
  • 39
    • 55749085253 scopus 로고    scopus 로고
    • Impact of reverse transcriptase resistance on the efficacy of TMC125 (etravirine) with two nucleoside reverse transcriptase inhibitors in protease inhibitor-naive, nonnucleoside reverse transcriptase inhibitor-experienced patients: Study TMC125-C227
    • Ruxrungtham K, Pedro RJ, Latiff GH et al.: Impact of reverse transcriptase resistance on the efficacy of TMC125 (etravirine) with two nucleoside reverse transcriptase inhibitors in protease inhibitor-naive, nonnucleoside reverse transcriptase inhibitor-experienced patients: study TMC125-C227. HIV Med. 9, 883-896 (2008).
    • (2008) HIV Med , vol.9 , pp. 883-896
    • Ruxrungtham, K.1    Pedro, R.J.2    Latiff, G.H.3
  • 40
    • 67149130842 scopus 로고    scopus 로고
    • Pooled 24-week results of DUET-1 and -2: TMC125 (etravirine; ETR) versus placebo in 1203 treatment-experienced HIV-1-infected patients
    • Presented at:, Chicago, IL, USA, 17-20 September
    • Cahn P, Haubrich R, Leider J et al.: Pooled 24-week results of DUET-1 and -2: TMC125 (etravirine; ETR) versus placebo in 1203 treatment-experienced HIV-1-infected patients. Presented at: 47th Interscience Conference on Antimicrobial Agents and Chemotherapy. Chicago, IL, USA, 17-20 September 2007.
    • (2007) 47th Interscience Conference on Antimicrobial Agents and Chemotherapy
    • Cahn, P.1    Haubrich, R.2    Leider, J.3
  • 41
    • 63349101361 scopus 로고    scopus 로고
    • An update of the list of NNRTI mutations associated with decreased virological response to etravirine: Multivariate analyses on the pooled DUET-1 and DUET-2 clinical trial data
    • Represents the most up-to-date study on etravirine resistance-associated mutations, ■
    • Vingerhoets J, Peters M, Azijn H et al.: An update of the list of NNRTI mutations associated with decreased virological response to etravirine: multivariate analyses on the pooled DUET-1 and DUET-2 clinical trial data. Antivir. Ther. 13(Suppl. 3), A26 (2008). ■ Represents the most up-to-date study on etravirine resistance-associated mutations.
    • (2008) Antivir. Ther , vol.13 , Issue.SUPPL. 3
    • Vingerhoets, J.1    Peters, M.2    Azijn, H.3
  • 42
    • 58149515307 scopus 로고    scopus 로고
    • Biological and clinical cut-off analyses for etravirine in the Phenosense™ HIV assay
    • Coakley E, Chappey C, Benhamida J et al.: Biological and clinical cut-off analyses for etravirine in the Phenosense™ HIV assay. Antivir. Ther. 13(Suppl. 3), A134 (2008).
    • (2008) Antivir. Ther , vol.13 , Issue.SUPPL. 3
    • Coakley, E.1    Chappey, C.2    Benhamida, J.3
  • 43
    • 63349101361 scopus 로고    scopus 로고
    • Determination of phenotypic clinical cut-offs for etravirine: Pooled week 24 results of the DUET-1 and DUET-2 trials
    • Peeters M, Nijs S, Vingerhoets J et al.: Determination of phenotypic clinical cut-offs for etravirine: pooled week 24 results of the DUET-1 and DUET-2 trials. Antivir. Ther. 13(Suppl. 3), A133 (2008).
    • (2008) Antivir. Ther , vol.13 , Issue.SUPPL. 3
    • Peeters, M.1    Nijs, S.2    Vingerhoets, J.3
  • 44
    • 58149505548 scopus 로고    scopus 로고
    • HIV-1 genotype algorithms for prediction of etravirine susceptibility: Novel mutations and weighting factors identified through correlations to phenotype
    • Benhamida J, Chappey C, Coakley E et al.: HIV-1 genotype algorithms for prediction of etravirine susceptibility: novel mutations and weighting factors identified through correlations to phenotype. Antivir. Ther. 13(Suppl. 3), A142 (2008).
    • (2008) Antivir. Ther , vol.13 , Issue.SUPPL. 3
    • Benhamida, J.1    Chappey, C.2    Coakley, E.3
  • 45
    • 0033840455 scopus 로고    scopus 로고
    • Human immunodeficiency virus type 1 mutations selected in patients failing efavirenz combination therapy
    • Bacheler LT, Anton ED, Kudosh P et al.: Human immunodeficiency virus type 1 mutations selected in patients failing efavirenz combination therapy. Antimicrob. Agents Chemother. 44(9), 2475-2484 (2008).
    • (2008) Antimicrob. Agents Chemother , vol.44 , Issue.9 , pp. 2475-2484
    • Bacheler, L.T.1    Anton, E.D.2    Kudosh, P.3
  • 46
    • 0003206350 scopus 로고    scopus 로고
    • The presence or absence of zidovudine in a nevirapine-containing antiviral regimen determines which of two nevirapine-mutations occurs on virologic failure
    • Presented at:, San Francisco, CA, USA, 26-29 September
    • MacArthur RD, Kosmyna JM, Crane LR et al.: The presence or absence of zidovudine in a nevirapine-containing antiviral regimen determines which of two nevirapine-mutations occurs on virologic failure. Presented at: 39th Interscience Conference on Antimicrobial Agents and Chemotherapy. San Francisco, CA, USA, 26-29 September 1999.
    • (1999) 39th Interscience Conference on Antimicrobial Agents and Chemotherapy
    • MacArthur, R.D.1    Kosmyna, J.M.2    Crane, L.R.3
  • 47
    • 67149083588 scopus 로고    scopus 로고
    • Failing therapy with efavirenz results in significantly fewer mutations limiting to etravirine than failing therapy with nevirapine: On-treatment analyses from the CPCRA first study
    • Presented at:, Sitges, Spain 10-14 June
    • MacArthur RD, Huppler Hullsiek K, Peng G et al.: Failing therapy with efavirenz results in significantly fewer mutations limiting to etravirine than failing therapy with nevirapine: on-treatment analyses from the CPCRA first study. Presented at: XVII International HIV Drug Resistance Workshop. Sitges, Spain 10-14 June 2008.
    • (2008) XVII International HIV Drug Resistance Workshop
    • MacArthur, R.D.1    Huppler Hullsiek, K.2    Peng, G.3
  • 48
    • 73849145850 scopus 로고    scopus 로고
    • Prevalence of mutations and determinants of genotypic resistance to etravirine (TMC125) in a large Italian resistance database (ARCA)
    • Presented at:, Budapest, Hungary, 26-28 March
    • Di Vincenzo P, Rusconi S, Adorni F et al.: Prevalence of mutations and determinants of genotypic resistance to etravirine (TMC125) in a large Italian resistance database (ARCA). Presented at: 6th European HIV Drug Resistance Workshop. Budapest, Hungary, 26-28 March 2008.
    • (2008) 6th European HIV Drug Resistance Workshop
    • Di Vincenzo, P.1    Rusconi, S.2    Adorni, F.3
  • 49
    • 47649094086 scopus 로고    scopus 로고
    • Prevalence and risk factors for etravirine resistance among patients failing to non-nucleoside reverse transcriptase inhibitors
    • Lapadula G, Calabrese A, Castelnuovo F et al.: Prevalence and risk factors for etravirine resistance among patients failing to non-nucleoside reverse transcriptase inhibitors. Antivir. Ther. 13(4), 601-605 (2008).
    • (2008) Antivir. Ther , vol.13 , Issue.4 , pp. 601-605
    • Lapadula, G.1    Calabrese, A.2    Castelnuovo, F.3
  • 50
    • 20144366006 scopus 로고    scopus 로고
    • Synthesis of novel diarylpyrimidine analogues and their antiviral activity against human immunodeficiency virus type 1
    • Guillemont J, Pasquier E, Palandjian P et al.: Synthesis of novel diarylpyrimidine analogues and their antiviral activity against human immunodeficiency virus type 1. J. Med. Chem. 48, 2072-2079 (2005).
    • (2005) J. Med. Chem , vol.48 , pp. 2072-2079
    • Guillemont, J.1    Pasquier, E.2    Palandjian, P.3
  • 51
    • 20144372481 scopus 로고    scopus 로고
    • In search of a novel anti-HIV drug: Multidisciplinary coordination in the discovery of 4-[[4-[[4-[(1E)-2-cyanoethenyl] 2,6-dimethylphenyl]amino]-2-pyrimidinyl] amino]benzonitrile (R278474, Rilpivirine)
    • Janssen PA, Lewi PJ, Arnold E et al.: In search of a novel anti-HIV drug: multidisciplinary coordination in the discovery of 4-[[4-[[4-[(1E)-2-cyanoethenyl] 2,6-dimethylphenyl]amino]-2-pyrimidinyl] amino]benzonitrile (R278474, Rilpivirine). J. Med. Chem. 48, 1901-1909 (2005).
    • (2005) J. Med. Chem , vol.48 , pp. 1901-1909
    • Janssen, P.A.1    Lewi, P.J.2    Arnold, E.3
  • 52
    • 10744233372 scopus 로고    scopus 로고
    • On the detection of multiple-binding modes of ligands to proteins, from biological, structural and modeling data
    • Lewi PJ, de Jonge M, Daeyaert F et al.: On the detection of multiple-binding modes of ligands to proteins, from biological, structural and modeling data. J. Comput. Aided Mol. Des. 17, 129-134 (2003).
    • (2003) J. Comput. Aided Mol. Des , vol.17 , pp. 129-134
    • Lewi, P.J.1    de Jonge, M.2    Daeyaert, F.3
  • 53
    • 40349091258 scopus 로고    scopus 로고
    • High-resolution structures of HIV-1 reverse transcriptase/TMC278 complexes: Strategic flexibility explains potency against resistance mutations
    • Das K, Bauman JD, Clark AD Jr et al.: High-resolution structures of HIV-1 reverse transcriptase/TMC278 complexes: strategic flexibility explains potency against resistance mutations. Proc. Natl Acad. Sci. USA 105(5), 1466-1471 (2008).
    • (2008) Proc. Natl Acad. Sci. USA , vol.105 , Issue.5 , pp. 1466-1471
    • Das, K.1    Bauman, J.D.2    Clark Jr, A.D.3
  • 54
    • 4344683266 scopus 로고    scopus 로고
    • which HIV-1 drug resistance mutations are common in clinical practice?
    • Cheung PK, Wynhoven B, Harrigan PR: which HIV-1 drug resistance mutations are common in clinical practice? AIDS Rev. 6, 107-116 (2004).
    • (2004) AIDS Rev , vol.6 , pp. 107-116
    • Cheung, P.K.1    Wynhoven, B.2    Harrigan, P.R.3
  • 55
    • 33748036988 scopus 로고    scopus 로고
    • Short-term antiviral activity of TMC278: A novel NNRTI - in treatment-naive HIV-1 infected subjects
    • Goebel F, Yakovlev A, Pozniak AL et al.: Short-term antiviral activity of TMC278: a novel NNRTI - in treatment-naive HIV-1 infected subjects. AIDS 20, 1721-1726 (2006).
    • (2006) AIDS , vol.20 , pp. 1721-1726
    • Goebel, F.1    Yakovlev, A.2    Pozniak, A.L.3
  • 56
    • 65149102179 scopus 로고    scopus 로고
    • TMC278 (rilpivirine), a next-generation NNRTI, demonstrates long-term efficacy and tolerability in ARV-naive patients: 96 weeks results of study C204
    • Presented at:, Mexico City, Mexico, 3-8 August, ■ is a highly promising antiretroviral owing to its strong potency and high genetic barrier to resistance. This paper highlights some of the latest available data on this drug
    • Santoscoy M, Cahn P, Gonsalez C et al.: TMC278 (rilpivirine), a next-generation NNRTI, demonstrates long-term efficacy and tolerability in ARV-naive patients: 96 weeks results of study C204. Presented at: 17th International AIDS Conference. Mexico City, Mexico, 3-8 August 2008. ■ TMC278 is a highly promising antiretroviral owing to its strong potency and high genetic barrier to resistance. This paper highlights some of the latest available data on this drug.
    • (2008) 17th International AIDS Conference
    • Santoscoy, M.1    Cahn, P.2    Gonsalez, C.3
  • 57
    • 84883167976 scopus 로고    scopus 로고
    • The pharmacokinetic (PK) interaction between rifabutin and TMC278, an investigational non-nucleoside reverse transcriptase inhibitor (NNRTI)
    • Presented at:, Mexico City, Mexico, 3-8 August
    • Crauwels H, van Heeswijk R, Kestens D et al.: The pharmacokinetic (PK) interaction between rifabutin and TMC278, an investigational non-nucleoside reverse transcriptase inhibitor (NNRTI). Presented at: 17th International AIDS Conference. Mexico City, Mexico, 3-8 August 2008.
    • (2008) 17th International AIDS Conference
    • Crauwels, H.1    van Heeswijk, R.2    Kestens, D.3
  • 58
    • 35548930054 scopus 로고    scopus 로고
    • IDX12899 anti-HIV-1 activity and resistance profile is superior to efavirenz
    • S
    • Jakubik J, Seifer M, Gray L et al.: IDX12899 anti-HIV-1 activity and resistance profile is superior to efavirenz. Antivir. Ther. 12(Suppl. 1), S32 (2007).
    • (2007) Antivir. Ther , vol.12 , Issue.SUPPL. 1 , pp. 32
    • Jakubik, J.1    Seifer, M.2    Gray, L.3
  • 59
    • 67149115786 scopus 로고    scopus 로고
    • In vitro cross-resistance profile for a next-generation non-nucleoside reverse transcriptase inhibitor: IDX899
    • Although only in vitro data are presented here, the paper describes the cross-resistance mutations among currently available, in-development NNRTIs and this new molecule, IDX899, ■
    • Jakubik JJ, Chapron C, Hubbard L et al.: In vitro cross-resistance profile for a next-generation non-nucleoside reverse transcriptase inhibitor: IDX899. Antivir. Ther. 13(Suppl. 3), A28 (2008). ■ Although only in vitro data are presented here, the paper describes the cross-resistance mutations among currently available, in-development NNRTIs and this new molecule, IDX899.
    • (2008) Antivir. Ther , vol.13 , Issue.SUPPL. 3
    • Jakubik, J.J.1    Chapron, C.2    Hubbard, L.3
  • 60
    • 63849309660 scopus 로고    scopus 로고
    • IDX899, a novel HIV-1 NNRTI with high barrier to resistance, provides suppression of HIV viral load in treatment-naive HIV-1-infected subjects
    • Presented at:, Mexico City, Mexico, 3-8 August
    • Zala C, Murphy R, Zhou XJ et al.: IDX899, a novel HIV-1 NNRTI with high barrier to resistance, provides suppression of HIV viral load in treatment-naive HIV-1-infected subjects. Presented at: 17th International AIDS Conference. Mexico City, Mexico, 3-8 August 2008.
    • (2008) 17th International AIDS Conference
    • Zala, C.1    Murphy, R.2    Zhou, X.J.3
  • 61
    • 67149108993 scopus 로고    scopus 로고
    • Pharmacokinetic drug-drug interaction between IDX899 and Atazanavir
    • Presented at:, Mexico City, Mexico, 3-8 August
    • Zhou XJ, Pietropaolo K, Belanger B et al.: Pharmacokinetic drug-drug interaction between IDX899 and Atazanavir. Presented at: 17th International AIDS Conference. Mexico City, Mexico, 3-8 August 2008.
    • (2008) 17th International AIDS Conference
    • Zhou, X.J.1    Pietropaolo, K.2    Belanger, B.3
  • 62
    • 33746233238 scopus 로고    scopus 로고
    • Tri-substituted triazoles as potent non-nucleoside inhibitors of the HIV-1 reverse transcriptase
    • De La Rosa M, Kim HW, Gunic E et al.: Tri-substituted triazoles as potent non-nucleoside inhibitors of the HIV-1 reverse transcriptase. Bioorg. Med. Chem. Lett. 16 (17), 4444-4449 (2006).
    • (2006) Bioorg. Med. Chem. Lett , vol.16 , Issue.17 , pp. 4444-4449
    • De La Rosa, M.1    Kim, H.W.2    Gunic, E.3
  • 65
    • 67149114131 scopus 로고    scopus 로고
    • In vitro selection and characterization of viruses resistant to RO-5028, a novel non-nucleoside reverse transcriptase inhibitor
    • Javanbakht H, Li Y, Sweeney Z et al.: In vitro selection and characterization of viruses resistant to RO-5028, a novel non-nucleoside reverse transcriptase inhibitor. Antivir. Ther. 13(Suppl. 3), A23 (2008).
    • (2008) Antivir. Ther , vol.13 , Issue.SUPPL. 3
    • Javanbakht, H.1    Li, Y.2    Sweeney, Z.3
  • 66
    • 67149117383 scopus 로고    scopus 로고
    • Preclinical profile of R7180, a prodrug of the novel NNRTI RO-5028, with high antiviral potency against wild-type and NNRTI-resistant viruses
    • Few data are available on this drug. This paper covers the development of the molecule so far, ■
    • Klumpp K, Dunn J, Su G et al.: Preclinical profile of R7180, a prodrug of the novel NNRTI RO-5028, with high antiviral potency against wild-type and NNRTI-resistant viruses. Antivir. Ther. 13(Suppl. 3), A29 (2008). ■ Few data are available on this drug. This paper covers the development of the molecule so far.
    • (2008) Antivir. Ther , vol.13 , Issue.SUPPL. 3
    • Klumpp, K.1    Dunn, J.2    Su, G.3
  • 68
    • 46749084403 scopus 로고    scopus 로고
    • UK-453,061: A non-nucleoside reverse transcriptase inhibitor for the treatment of drug-resistant HIV infections
    • Presented at:, Chicago, IL, USA, 17-20 September
    • Corbau R, Allan G, Burt C et al.: UK-453,061: a non-nucleoside reverse transcriptase inhibitor for the treatment of drug-resistant HIV infections. Presented at: 47th Interscience Conference on Antimicrobial Agents and Chemotherapy. Chicago, IL, USA, 17-20 September 2007.
    • (2007) 47th Interscience Conference on Antimicrobial Agents and Chemotherapy
    • Corbau, R.1    Allan, G.2    Burt, C.3
  • 69
    • 73849130055 scopus 로고    scopus 로고
    • Fatkenheuer G, Staszewski S, Plettenburg A et al.: Short-term monotherapy with UK-453,061, a novel NNRTI, reduces viral load in HIV-infected patients. Presented at: 3rd International AIDS Society Conference. Sydney, Australia, 22-25 July 2007. ■ This work shows the first, though limited, clinical data on in vivo use of UK-453,061.
    • Fatkenheuer G, Staszewski S, Plettenburg A et al.: Short-term monotherapy with UK-453,061, a novel NNRTI, reduces viral load in HIV-infected patients. Presented at: 3rd International AIDS Society Conference. Sydney, Australia, 22-25 July 2007. ■ This work shows the first, though limited, clinical data on in vivo use of UK-453,061.
  • 70
    • 32544437940 scopus 로고    scopus 로고
    • Crystallographic study with BILR 355 BS, a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) with a broad anti HIV-1 profile
    • Presented at:, Rio de Janeiro, Brazil, 24-27 July
    • Coulombe R, Fink D, Landry S et al.: Crystallographic study with BILR 355 BS, a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) with a broad anti HIV-1 profile. Presented at: 3rd International AIDS Society Conference. Rio de Janeiro, Brazil, 24-27 July 2005.
    • (2005) 3rd International AIDS Society Conference
    • Coulombe, R.1    Fink, D.2    Landry, S.3
  • 71
    • 33646545948 scopus 로고    scopus 로고
    • Antiviral characterization and human experience with BILR 355 BS, a novel next-generation non-nucleoside reverse transcriptase inhibitor with a broad anti HIV-1 profile
    • Presented at:, Boston, MA, USA, 22-25 February
    • Bonneau P, Robinson P, Duan J et al.: Antiviral characterization and human experience with BILR 355 BS, a novel next-generation non-nucleoside reverse transcriptase inhibitor with a broad anti HIV-1 profile. Presented at: 12th Conference on Retroviruses and Opportunistic Infections. Boston, MA, USA, 22-25 February 2005.
    • (2005) 12th Conference on Retroviruses and Opportunistic Infections
    • Bonneau, P.1    Robinson, P.2    Duan, J.3
  • 72
    • 57049116193 scopus 로고    scopus 로고
    • Huang F, Koenen-Bergmann M, MacGregor TR et al.: Pharmacokinetic and safety evaluation of BILR355, a second generation non-nucleoside reverse transcriptase inhibitor, in healthy volunteers. Antimicrob. Agents Chemother. 52(12), 4300-4307 (2008). ■ This paper represents the most recent data about BILR 355 BS; since pharmacokinetic characteristics of BILR 355 BS appear to be its main drawback factor; the paper provides comprehensive information on this matter.
    • Huang F, Koenen-Bergmann M, MacGregor TR et al.: Pharmacokinetic and safety evaluation of BILR355, a second generation non-nucleoside reverse transcriptase inhibitor, in healthy volunteers. Antimicrob. Agents Chemother. 52(12), 4300-4307 (2008). ■ This paper represents the most recent data about BILR 355 BS; since pharmacokinetic characteristics of BILR 355 BS appear to be its main drawback factor; the paper provides comprehensive information on this matter.
  • 73
    • 33750946415 scopus 로고    scopus 로고
    • Sex differences in CYP3A activity using intravenous and oral midazolam
    • Chen M, Ma L, Drusano GL et al.: Sex differences in CYP3A activity using intravenous and oral midazolam. Clin. Pharmacol. Ther. 80, 531-538 (2006).
    • (2006) Clin. Pharmacol. Ther , vol.80 , pp. 531-538
    • Chen, M.1    Ma, L.2    Drusano, G.L.3
  • 75
    • 54549125887 scopus 로고    scopus 로고
    • Discovery of 3-{5-[(6-amino-1Hpyrazolo [3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5- chlorobenzonitrile (MK-4965): A potent, orally bioavailable HIV-1 non-nucleoside reverse transcriptase inhibitor with improved potency against key mutant viruses
    • Tucker TJ, Sisko JT, Tynebor RM et al.: Discovery of 3-{5-[(6-amino-1Hpyrazolo [3,4-b]pyridine-3-yl)methoxy]-2-chlorophenoxy}-5- chlorobenzonitrile (MK-4965): a potent, orally bioavailable HIV-1 non-nucleoside reverse transcriptase inhibitor with improved potency against key mutant viruses. J. Med. Chem. 51, 6503-6511 (2008).
    • (2008) J. Med. Chem , vol.51 , pp. 6503-6511
    • Tucker, T.J.1    Sisko, J.T.2    Tynebor, R.M.3
  • 76
    • 67149145103 scopus 로고    scopus 로고
    • Y188H, which is a potential intermediate between wild-type (WT) and Y188L, has markedly reduced replication efficiency
    • Presented at:, Los Angeles, CA, USA, 25-28 February
    • Dykes C, Demeter LM: Y188H, which is a potential intermediate between wild-type (WT) and Y188L, has markedly reduced replication efficiency. Presented at: 14th Conference on Retroviruses and Opportunistic Infections. Los Angeles, CA, USA, 25-28 February 2007.
    • (2007) 14th Conference on Retroviruses and Opportunistic Infections
    • Dykes, C.1    Demeter, L.M.2
  • 77
    • 10744228247 scopus 로고    scopus 로고
    • Novel benzophenones as non-nucleoside reverse transcriptase inhibitors of HIV-1
    • Chan JH, Freeman GA, Tidwell JH et al.: Novel benzophenones as non-nucleoside reverse transcriptase inhibitors of HIV-1. J. Med. Chem. 47 (5), 1175-1182 (2004).
    • (2004) J. Med. Chem , vol.47 , Issue.5 , pp. 1175-1182
    • Chan, J.H.1    Freeman, G.A.2    Tidwell, J.H.3
  • 78
    • 31544435514 scopus 로고    scopus 로고
    • Structure-activity relationship studies of novel benzophenones leading to the discovery of a potent, next generation HIV nonnucleoside reverse transcriptase inhibitor
    • Romines KR, Freeman GA, Schaller LT et al.: Structure-activity relationship studies of novel benzophenones leading to the discovery of a potent, next generation HIV nonnucleoside reverse transcriptase inhibitor. J. Med. Chem. 79 (2), 727-739 (2006).
    • (2006) J. Med. Chem , vol.79 , Issue.2 , pp. 727-739
    • Romines, K.R.1    Freeman, G.A.2    Schaller, L.T.3
  • 79
    • 25844436257 scopus 로고    scopus 로고
    • Antiviral activity of GW678248, a novel benzophenone nonucleoside reverse transcriptase inhibitor
    • Ferris RG, Hazen RJ, Roberts GB et al.: Antiviral activity of GW678248, a novel benzophenone nonucleoside reverse transcriptase inhibitor. Antimicrob. Agents Chemother. 49 (10), 4046-4051 (2005).
    • (2005) Antimicrob. Agents Chemother , vol.49 , Issue.10 , pp. 4046-4051
    • Ferris, R.G.1    Hazen, R.J.2    Roberts, G.B.3
  • 80
    • 47749109429 scopus 로고    scopus 로고
    • Discovery and optimization of pyridazinone non-nucleoside inhibitors of HIV-1 reverse transcriptase
    • Sweeney ZK, Dunn JP, Li Y et al.: Discovery and optimization of pyridazinone non-nucleoside inhibitors of HIV-1 reverse transcriptase. Bioorg. Med. Chem. Lett. 18, 4352-4354 (2008).
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , pp. 4352-4354
    • Sweeney, Z.K.1    Dunn, J.P.2    Li, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.