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Volumn 19, Issue 31, 2012, Pages 5364-5380

Structure-activity relationship studies on clinically relevant HIV-1 NNRTIs

Author keywords

AIDS; Delavirdine; DNA; Efavirenz; Etravirine; HIV; Nevirapine; NNRTIs; NRTIs; PIs; Rilpivirine; RNA

Indexed keywords

2 BENZYL 4 CYANOMETHYLENE 1,1,3 TRIOXO 2H,4H THIENO[3,4 E][1,2,4]THIADIAZINE; 3 [(4,7 DICHLORO 2 BENZOXAZOLYLMETHYL)AMINO] 5 ETHYL 6 METHYL 2(1H) PYRIDONE; 4 THIAZOLIDINONE DERIVATIVE; ABACAVIR; AMINO ACID; AMPRENAVIR; ATAZANAVIR; DAPIVIRINE; DARUNAVIR; DELAVIRDINE; DIDANOSINE; EFAVIRENZ; EMIVIRINE; EMTRICITABINE; ENFUVIRTIDE; ETRAVIRINE; FOSAMPRENAVIR; INDINAVIR; LAMIVUDINE; LOPINAVIR; LOPINAVIR PLUS RITONAVIR; MARAVIROC; N [4 CHLORO 3 (3 METHYL 2 BUTENYLOXY)PHENYL] 2 METHYL 3 FURANCARBOTHIOAMIDE; NELFINAVIR; NEVIRAPINE; NSC 287474; NSC 625487; PNU 14272; RALTEGRAVIR; RILPIVIRINE; RITONAVIR; SAQUINAVIR; STAVUDINE; TENOFOVIR DISOPROXIL; TIPRANAVIR; TIVIRAPINE; TROVIRDINE; UNCLASSIFIED DRUG; UNINDEXED DRUG; VIRUS RNA; ZALCITABINE; ZIDOVUDINE;

EID: 84870447919     PISSN: 09298673     EISSN: 1875533X     Source Type: Journal    
DOI: 10.2174/092986712803833326     Document Type: Article
Times cited : (36)

References (79)
  • 1
    • 0037195631 scopus 로고    scopus 로고
    • Historical essay: The early years of HIV/AIDS
    • Gallo, R., Historical essay: The early years of HIV/AIDS. Science, 2002, 298, (5599), 1728.
    • (2002) Science , vol.298 , Issue.5599 , pp. 1728
    • Gallo, R.1
  • 2
    • 77649202344 scopus 로고    scopus 로고
    • Highlights in the discovery of antiviral drugs: A personal retrospective
    • De Clercq, E., Highlights in the Discovery of Antiviral Drugs: A Personal Retrospective. J. Med. Chem., 2009, 53, (4), 1438-1450.
    • (2009) J. Med. Chem. , vol.53 , Issue.4 , pp. 1438-1450
    • De Clercq, E.1
  • 3
    • 84870463255 scopus 로고    scopus 로고
    • http://www.unaids.org/documents/20101123-GlobalReport-em.pdf
  • 4
    • 84870406429 scopus 로고    scopus 로고
    • http://www.who.int/hiv/data/fast-facts/en/.
  • 5
    • 0033927489 scopus 로고    scopus 로고
    • Novel compounds in preclinical/early clinical development for the treatment of HIV infections
    • De Clercq, E., Novel compounds in preclinical/early clinical development for the treatment of HIV infections. Rev. Med. Virol., 2000, 10, (4), 255-277.
    • (2000) Rev. Med. Virol. , vol.10 , Issue.4 , pp. 255-277
    • De Clercq, E.1
  • 6
    • 36749073433 scopus 로고    scopus 로고
    • The design of drugs for HIV and HCV
    • De Clercq, E., The design of drugs for HIV and HCV. Nat. Rev. Drug Discov., 2007, 6, (12), 1001-1018.
    • (2007) Nat. Rev. Drug Discov. , vol.6 , Issue.12 , pp. 1001-1018
    • De Clercq, E.1
  • 7
    • 0033534386 scopus 로고    scopus 로고
    • Structural biology of HIV
    • Turner, B.G.; Summers, M.F., Structural biology of HIV. J. Mol. Biol., 1999, 285, (1), 1-32.
    • (1999) J. Mol. Biol. , vol.285 , Issue.1 , pp. 1-32
    • Turner, B.G.1    Summers, M.F.2
  • 8
    • 73549089480 scopus 로고    scopus 로고
    • Current status and challenges of antiretroviral research and therapy
    • Esté, J.A.; Cihlar, T., Current status and challenges of antiretroviral research and therapy. Antiviral Res. 2010, 85, (1), 25-33.
    • (2010) Antiviral Res , vol.85 , Issue.1 , pp. 25-33
    • Esté, J.A.1    Cihlar, T.2
  • 9
    • 0026693137 scopus 로고
    • Crystal structure at 3.5 A resolution of HIV-1 reverse transcriptase complexed with an inhibitor
    • Kohlstaedt, L.; Wang, J.; Friedman, J.; Rice, P.; Steitz, T., Crystal structure at 3.5 A resolution of HIV-1 reverse transcriptase complexed with an inhibitor. Science, 1992, 256, (5065), 1783.
    • (1992) Science , vol.256 , Issue.5065 , pp. 1783
    • Kohlstaedt, L.1    Wang, J.2    Friedman, J.3    Rice, P.4    Steitz, T.5
  • 10
    • 0346855631 scopus 로고    scopus 로고
    • Structure and mechanism of action of nonnucleoside inhibitors of HIV-1 reverse transcriptase: Strategies to combat drug resistance
    • Smith, R.H.; J. Michejda, C.; Hughes, S.H.; Arnold, E.; Janssen, P.A.J.; Kroeger Smith, M.B., Structure and mechanism of action of nonnucleoside inhibitors of HIV-1 reverse transcriptase: strategies to combat drug resistance. J. Mol. Stru.: THEOCHEM, 1998, 423, (1-2), 67-77.
    • (1998) J. Mol. Stru.: THEOCHEM , vol.423 , Issue.1-2 , pp. 67-77
    • Smith, R.H.1    Michejda, J.C.2    Hughes, S.H.3    Arnold, E.4    Janssen, P.A.J.5    Kroeger Smith, M.B.6
  • 11
    • 14944344464 scopus 로고    scopus 로고
    • New approaches toward Anti-HIV chemotherapy
    • De Clercq, E., New Approaches toward Anti-HIV Chemotherapy. J. Med. Chem., 2005, 48, (5), 1297-1313.
    • (2005) J. Med. Chem. , vol.48 , Issue.5 , pp. 1297-1313
    • De Clercq, E.1
  • 12
    • 79958243009 scopus 로고    scopus 로고
    • Molecular and structural aspects of clinically relevant mutations related to the approved nonnucleoside inhibitors of HIV-1 reverse transcriptase
    • Alcaro, S.; Alteri, C.; Artese, A.; Ceccherini-Silberstein, F.; Costa, G.; Ortuso, F.; Parrotta, L.; Perno, C.F.; Svicher, V., Molecular and structural aspects of clinically relevant mutations related to the approved nonnucleoside inhibitors of HIV-1 reverse transcriptase. Drug Resist. Updates, 2011, 14, (3), 141-149.
    • (2011) Drug Resist. Updates , vol.14 , Issue.3 , pp. 141-149
    • Alcaro, S.1    Alteri, C.2    Artese, A.3    Ceccherini-Silberstein, F.4    Costa, G.5    Ortuso, F.6    Parrotta, L.7    Perno, C.F.8    Svicher, V.9
  • 13
    • 73549088708 scopus 로고    scopus 로고
    • Molecular basis of human immunodeficiency virus drug resistance: An update
    • Menéndez-Arias, L., Molecular basis of human immunodeficiency virus drug resistance: An update. Antiviral Res., 2010, 85, (1), 210-231.
    • (2010) Antiviral Res. , vol.85 , Issue.1 , pp. 210-231
    • Menéndez-Arias, L.1
  • 14
    • 43049144549 scopus 로고    scopus 로고
    • Structural basis for drug resistance mechanisms for non-nucleoside inhibitors of HIV reverse transcriptase
    • Ren, J.; Stammers, D.K., Structural basis for drug resistance mechanisms for non-nucleoside inhibitors of HIV reverse transcriptase. Virus Res., 2008, 134, (1-2), 157-170.
    • (2008) Virus Res. , vol.134 , Issue.1-2 , pp. 157-170
    • Ren, J.1    Stammers, D.K.2
  • 15
    • 35148845529 scopus 로고    scopus 로고
    • Characterization and structural analysis of novel mutations in human immunodeficiency virus type 1 reverse transcriptase involved in the regulation of resistance to nonnucleoside inhibitors
    • Ceccherini-Silberstein, F.; Svicher, V.; Sing, T.; Artese, A.; Santoro, M.M.; Forbici, F.; Bertoli, A.; Alcaro, S.; Palamara, G.; Monforte, A.A., Characterization and structural analysis of novel mutations in human immunodeficiency virus type 1 reverse transcriptase involved in the regulation of resistance to nonnucleoside inhibitors. J. Virol., 2007, 81, (20), 11507-11519.
    • (2007) J. Virol. , vol.81 , Issue.20 , pp. 11507-11519
    • Ceccherini-Silberstein, F.1    Svicher, V.2    Sing, T.3    Artese, A.4    Santoro, M.M.5    Forbici, F.6    Bertoli, A.7    Alcaro, S.8    Palamara, G.9    Monforte, A.A.10
  • 16
    • 77950654271 scopus 로고    scopus 로고
    • Computational Analysis of Human Immunodeficiency Virus (HIV) Type-1 Reverse Transcriptase Crystallographic Models Based on Significant Conserved Residues Found in Highly Active Antiretroviral Therapy (HAART)-Treated Patients (Supplementary Material)
    • Alcaro, S.; Artese, A.; Ceccherini-Silberstein, F.; Chiarella, V.; Dimonte, S.; Ortuso, F.; Perno, C.F., Computational Analysis of Human Immunodeficiency Virus (HIV) Type-1 Reverse Transcriptase Crystallographic Models Based on Significant Conserved Residues Found in Highly Active Antiretroviral Therapy (HAART)-Treated Patients (Supplementary Material). Curr. Med. Chem., 2010, 17, (4), 290-308.
    • (2010) Curr. Med. Chem. , vol.17 , Issue.4 , pp. 290-308
    • Alcaro, S.1    Artese, A.2    Ceccherini-Silberstein, F.3    Chiarella, V.4    Dimonte, S.5    Ortuso, F.6    Perno, C.F.7
  • 17
    • 82955197340 scopus 로고    scopus 로고
    • Docking analysis and resistance evaluation of clinically relevant mutations associated with the HIV-1 non-nucleoside reverse transcriptase inhibitors nevirapine, efavirenz and etravirine
    • Alcaro, S.; Alteri, C.; Artese, A.; Ceccherini-Silberstein, F.; Costa, G.; Ortuso, F.; Bertoli, A.; Forbici, F.; Santoro, M.M.; Parrotta, L., Docking Analysis and Resistance Evaluation of Clinically Relevant Mutations Associated with the HIV-1 Non-nucleoside Reverse Transcriptase Inhibitors Nevirapine, Efavirenz and Etravirine. ChemMedChem, 2011, 6, (12), 2203-2213.
    • (2011) ChemMedChem , vol.6 , Issue.12 , pp. 2203-2213
    • Alcaro, S.1    Alteri, C.2    Artese, A.3    Ceccherini-Silberstein, F.4    Costa, G.5    Ortuso, F.6    Bertoli, A.7    Forbici, F.8    Santoro, M.M.9    Parrotta, L.10
  • 18
    • 84863290357 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of 1-[(2-benzyloxyl/alkoxyl) methyl]-5-halo-6-aryluracils as potent HIV-1 nonnucleoside reverse transcriptase inhibitors with an improved drug resistance profile
    • Wang, X.; Zhang, J.; Huang, Y.; Wang, R.; Zhang, L.; Qiao, K.; Li, L.; Liu, C.; Ouyang, Y.; Xu, W.; Zhang, Z.; Zhang, L.; Shao, Y.; Jiang, S.; Ma, L.; Liu, J., Design, Synthesis, and Biological Evaluation of 1-[(2-Benzyloxyl/ alkoxyl)methyl]-5-halo-6-aryluracils as Potent HIV-1 Nonnucleoside Reverse Transcriptase Inhibitors with an Improved Drug Resistance Profile. J. Med. Chem, 2012, 55, (5), 2242-2250.
    • (2012) J. Med. Chem , vol.55 , Issue.5 , pp. 2242-2250
    • Wang, X.1    Zhang, J.2    Huang, Y.3    Wang, R.4    Zhang, L.5    Qiao, K.6    Li, L.7    Liu, C.8    Ouyang, Y.9    Xu, W.10    Zhang, Z.11    Zhang, L.12    Shao, Y.13    Jiang, S.14    Ma, L.15    Liu, J.16
  • 19
    • 84870434157 scopus 로고
    • 5, 11-dihydro-6H-dipyrido 3 2-B 2′ 3′-E)(1 4) diazepines and their use in the prevention or treatment of HIV infection
    • US Patent 5,366,972, November 22
    • Hargrave, K.D.; Proudfoot, J.R.; Adams, J.; Grozinger, K.G.; Schmidt, G.; Engel, W.; Trummlitz, G.; Eberlein, W. 5, 11-dihydro-6H-dipyrido (3, 2-B: 2′, 3′-E)(1, 4) diazepines and their use in the prevention or treatment of HIV infection. U.S. Patent 5,366,972, November 22, 1994.
    • (1994)
    • Hargrave, K.D.1    Proudfoot, J.R.2    Adams, J.3    Grozinger, K.G.4    Schmidt, G.5    Engel, W.6    Trummlitz, G.7    Eberlein, W.8
  • 20
    • 84870419990 scopus 로고    scopus 로고
    • Delavirdine high strength tablet formulation
    • U.S. Patent 5,563142, Jan 23
    • Martino, A.C.; Bates, A.H.; Morozowich, W.; Lee, E.J. Delavirdine high strength tablet formulation. U.S. Patent 5,563,142, Jan 23, 2001.
    • (2001)
    • Martino, A.C.1    Bates, A.H.2    Morozowich, W.3    Lee, E.J.4
  • 21
    • 2642608004 scopus 로고    scopus 로고
    • Benzoxazinones as inhibitors of HIV reverse transcriptase
    • U.S. Patent 5,519,021, May 21
    • Young, S.D.; Britcher, S.F.; Payne, L.S.; Tran, L.O.; Lumma Jr, W.C. Benzoxazinones as inhibitors of HIV reverse transcriptase. U.S. Patent 5,519,021, May 21, 1996.
    • (1996)
    • Young, S.D.1    Britcher, S.F.2    Payne, L.S.3    Tran, L.O.4    Lumma Jr., W.C.5
  • 22
    • 84863231119 scopus 로고    scopus 로고
    • Dihydro-alkoxyl-benzyl-oxopyrimidine Derivatives (DABOs) As Non-Nucleoside Reverse Transcriptase Inhibitors: An Update Review (2001-2011)
    • Yang, S.; Chen, F.E.; De Clercq, E., Dihydro-alkoxyl-benzyl-oxopyrimidine Derivatives (DABOs) As Non-Nucleoside Reverse Transcriptase Inhibitors: An Update Review (2001-2011). Curr. Med. Chem., 2012, 19, (2), 152-162.
    • (2012) Curr. Med. Chem. , vol.19 , Issue.2 , pp. 152-162
    • Yang, S.1    Chen, F.E.2    De Clercq, E.3
  • 23
    • 84864412506 scopus 로고    scopus 로고
    • HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design
    • Zhan, P.; Chen, X.; Li, D.; Fang, Z.; De Clercq, E.; Liu, X., HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design. Med. Res. Rev., 2011.
    • (2011) Med. Res. Rev.
    • Zhan, P.1    Chen, X.2    Li, D.3    Fang, Z.4    De Clercq, E.5    Liu, X.6
  • 24
    • 84870463657 scopus 로고    scopus 로고
    • Anti-AIDS agents 85. Design, synthesis, and evaluation of 1R, 2R-dicamphanoyl-3, 3-dimethyldihydropyrano-[2, 3-c] xanthen-7 (1H)-one (DCX derivatives as vel anti-HIV agents
    • Zhou, T.; Shi, Q.; Chen, C.H.; Huang, L.; Ho, P.; Morris-Natschke, S.L.; Lee, K.H., Anti-AIDS agents 85. Design, synthesis, and evaluation of 1R, 2R-dicamphanoyl-3, 3-dimethyldihydropyrano-[2, 3-c] xanthen-7 (1H)-one (DCX) derivatives as novel anti-HIV agents. Eur. J. Med. Chem., 2011.
    • (2011) Eur J Med Chem
    • Zhou, T.1    Shi, Q.2    Chen, C.H.3    Huang, L.4    Ho, P.5    Morris-Natschke, S.L.6    Lee, K.H.7
  • 27
    • 82555187418 scopus 로고    scopus 로고
    • Difluoromethylbenzoxazole pyrimidine thioether derivatives: A novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors
    • Boyer, J.; Arnoult, E.; Medebielle, M.; Guillemont, J.; Unge, J.; Jochmans, D., Difluoromethylbenzoxazole pyrimidine thioether derivatives: a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors. J. Med. Chem., 2011.
    • (2011) J. Med. Chem.
    • Boyer, J.1    Arnoult, E.2    Medebielle, M.3    Guillemont, J.4    Unge, J.5    Jochmans, D.6
  • 28
    • 84860289205 scopus 로고    scopus 로고
    • Strategies for the design of HIV-1 non-nucleoside reverse transcriptase inhibitors: Lessons from the development of seven representative Paradigms
    • Li, D.; Zhan, P.; De Clercq, E.; Liu, X., Strategies for the Design of HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors: Lessons from the Development of Seven Representative Paradigms. J. Med. Chem., 2012, 55, (8), 3595-3613.
    • (2012) J. Med. Chem. , vol.55 , Issue.8 , pp. 3595-3613
    • Li, D.1    Zhan, P.2    De Clercq, E.3    Liu, X.4
  • 30
    • 0031946993 scopus 로고    scopus 로고
    • In vitro blood-brain barrier permeability of nevirapine compared to other HIV antiretroviral agents
    • Glynn, S.; Yazdanian, M., In vitro blood-brain barrier permeability of nevirapine compared to other HIV antiretroviral agents. J. Pharmaceut. Sci., 1998, 87, (3), 306-310.
    • (1998) J. Pharmaceut. Sci. , vol.87 , Issue.3 , pp. 306-310
    • Glynn, S.1    Yazdanian, M.2
  • 31
    • 0028823979 scopus 로고
    • Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase. 4. 2-substituted dipyridodiazepinones as potent inhibitors of both wild-type and cysteine-181 HIV-1 reverse transcriptase enzymes
    • Proudfoot, J.R.; Hargrave, K.D.; Kapadia, S.R.; Patel, U.R.; Grozinger, K.G.; McNeil, D.W.; Cullen, E.; Cardozo, M.; Tong, L., Novel Non-nucleoside Inhibitors of Human Immunodeficiency Virus Type 1 (HIV-1) Reverse Transcriptase. 4. 2-Substituted Dipyridodiazepinones as Potent Inhibitors of Both Wild-Type and Cysteine-181 HIV-1 Reverse Transcriptase Enzymes. J. Med. Chem., 1995, 38, (24), 4830-4838.
    • (1995) J. Med. Chem. , vol.38 , Issue.24 , pp. 4830-4838
    • Proudfoot, J.R.1    Hargrave, K.D.2    Kapadia, S.R.3    Patel, U.R.4    Grozinger, K.G.5    McNeil, D.W.6    Cullen, E.7    Cardozo, M.8    Tong, L.9
  • 33
    • 0023251351 scopus 로고
    • Site-specific mutagenesis of AIDS virus reverse transcriptase
    • Larder, B.; DJM, P., Powell KL. and Darby G: Site-specific mutagenesis of AIDS virus reverse transcriptase. Nature, 1987, 327, 716-717.
    • (1987) Nature , vol.327 , pp. 716-717
    • Larder, B.1    Djm, P.2    Powell, K.L.3    Darby, G.4
  • 35
    • 0030814171 scopus 로고    scopus 로고
    • Novel non-nucleoside inhibitors of human immunodeficiency virus type 1 reverse transcriptase. 6. 2-indol-3-yl- and 2-azaindol-3-yldipyridodiazepinones1
    • Kelly, T.A.; McNeil, D.W.; Rose, J.M.; David, E.; Shih, C.-K.; Grob, P.M., Novel Non-Nucleoside Inhibitors of Human Immunodeficiency Virus Type 1 Reverse Transcriptase. 6. 2-Indol-3-yl- and 2-Azaindol-3- yldipyridodiazepinones1. J. Med. Chem., 1997, 40, (15), 2430-2433.
    • (1997) J. Med. Chem. , vol.40 , Issue.15 , pp. 2430-2433
    • Kelly, T.A.1    McNeil, D.W.2    Rose, J.M.3    David, E.4    Shih, C.-K.5    Grob, P.M.6
  • 39
    • 0030625248 scopus 로고    scopus 로고
    • Pyridazines 82[1]. Synthesis of pyridazino [3 4 b][1 5] benzodiazepin 5 ones and their biological evaluation as non nucleoside HIV reverse transcriptase inhibitors
    • Heinisch, G.; Huber, E.; Matuszczak, B.; Maurer, A.; Prillinger, U., Pyridazines 82 [1]. Synthesis of Pyridazino [3, 4 b][1, 5] benzodiazepin 5 ones and their Biological Evaluation as Non nucleoside HIV Reverse Transcriptase Inhibitors. Archiv der Pharm., 1997, 330, (1 2), 29-34.
    • (1997) Archiv der Pharm , vol.330 , Issue.1-2 , pp. 29-34
    • Heinisch, G.1    Huber, E.2    Matuszczak, B.3    Maurer, A.4    Prillinger, U.5
  • 40
  • 41
    • 0028273009 scopus 로고
    • Discovery, synthesis, and bioactivity of bis(heteroaryl)piperazines. 1. A novel class of non-nucleoside HIV-1 reverse transcriptase inhibitors
    • Romero, D.L.; Morge, R.A.; Biles, C.; Berrios-Pena, N.; May, P.D.; Palmer, J.R.; Johnson, P.D.; Smith, H.W.; Busso, M.; et, a., Discovery, Synthesis, and Bioactivity of Bis(heteroaryl)piperazines. 1. A Novel Class of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors. J. Med. Chem., 1994, 37, (7), 999-1014.
    • (1994) J. Med. Chem. , vol.37 , Issue.7 , pp. 999-1014
    • Romero, D.L.1    Morge, R.A.2    Biles, C.3    Berrios-Pena, N.4    May, P.D.5    Palmer, J.R.6    Johnson, P.D.7    Smith, H.W.8    Busso, M.9
  • 44
    • 0033533870 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of the (alkylamino)piperidine-containing BHAP Class of non-nucleoside reverse transcriptase inhibitors: Effect of 3-alkylpyridine ring substitution
    • Genin, M.J.; Poel, T.J.; May, P.D.; Kopta, L.A.; Yagi, Y.; Olmsted, R.A.; Friis, J.M.; Voorman, R.L.; Adams, W.J.; Thomas, R.C.; Romero, D.L., Synthesis and Structure-Activity Relationships of the (Alkylamino)piperidine-Containing BHAP Class of Non-Nucleoside Reverse Transcriptase Inhibitors: Effect of 3-Alkylpyridine Ring Substitution. J. Med. Chem., 1999, 42, (20), 4140-4149.
    • (1999) J. Med. Chem. , vol.42 , Issue.20 , pp. 4140-4149
    • Genin, M.J.1    Poel, T.J.2    May, P.D.3    Kopta, L.A.4    Yagi, Y.5    Olmsted, R.A.6    Friis, J.M.7    Voorman, R.L.8    Adams, W.J.9    Thomas, R.C.10    Romero, D.L.11
  • 45
  • 46
    • 0033571566 scopus 로고    scopus 로고
    • Synthesis and evaluation of benzoxazinones as HIV-1 reverse transcriptase inhibitors. Analogs of Efavirenz (SUSTIVA)
    • Patel, M.; McHugh, R.J.; Cordova, B.C.; Klabe, R.M.; Erickson-Viitanen, S.; Trainor, G.L.; Ko, S.S., Synthesis and evaluation of benzoxazinones as HIV-1 reverse transcriptase inhibitors. Analogs of Efavirenz (SUSTIVA). Bioorg. Med. Chem. Lett., 1999, 9, (22), 3221-3224.
    • (1999) Bioorg. Med. Chem. Lett. , vol.9 , Issue.22 , pp. 3221-3224
    • Patel, M.1    McHugh, R.J.2    Cordova, B.C.3    Klabe, R.M.4    Erickson-Viitanen, S.5    Trainor, G.L.6    Ko, S.S.7
  • 50
    • 1842779905 scopus 로고    scopus 로고
    • Structural and energetic analyses of the effects of the K103N mutation of HIV-1 reverse transcriptase on efavirenz analogs
    • Udier-Blagović, M.; Tirado-Rives, J.; Jorgensen, W.L., Structural and Energetic Analyses of the Effects of the K103N Mutation of HIV-1 Reverse Transcriptase on Efavirenz Analogs. J. Med. Chem., 2004, 47, (9), 2389-2392.
    • (2004) J. Med. Chem. , vol.47 , Issue.9 , pp. 2389-2392
    • Udier-Blagović, M.1    Tirado-Rives, J.2    Jorgensen, W.L.3
  • 51
    • 0035848389 scopus 로고    scopus 로고
    • Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor Efavirenz
    • Markwalder, J.A.; Christ, D.D.; Mutlib, A.; Cordova, B.C.; Klabe, R.M.; Seitz, S.P., Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor Efavirenz. Bioorg. Med. Chem. Lett., 2001, 11, (5), 619-622.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , Issue.5 , pp. 619-622
    • Markwalder, J.A.1    Christ, D.D.2    Mutlib, A.3    Cordova, B.C.4    Klabe, R.M.5    Seitz, S.P.6
  • 52
    • 0032786364 scopus 로고    scopus 로고
    • Expanded-spectrum nonnucleoside reverse transcriptase inhibitors inhibit clinically relevant mutant variants of human immunodeficiency virus type 1
    • Corbett, J.; Ko, S.; Rodgers, J.; Jeffrey, S.; Bacheler, L.; Klabe, R.; Diamond, S.; Lai, C.; Rabel, S.; Saye, J., Expanded-spectrum nonnucleoside reverse transcriptase inhibitors inhibit clinically relevant mutant variants of human immunodeficiency virus type 1. Antimicrob. Agents Chemother., 1999, 43, (12), 2893.
    • (1999) Antimicrob. Agents Chemother. , vol.43 , Issue.12 , pp. 2893
    • Corbett, J.1    Ko, S.2    Rodgers, J.3    Jeffrey, S.4    Bacheler, L.5    Klabe, R.6    Diamond, S.7    Lai, C.8    Rabel, S.9    Saye, J.10
  • 55
    • 44349131462 scopus 로고    scopus 로고
    • IV-1 reverse transcriptase inhibitors. Part 11: Structural modulations of diaryltriazines with potent anti-HIV activity
    • Xiong, Y.-Z.; Chen, F.-E.; Balzarini, J.; De Clercq, E.; Pannecouque, C., Non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 11: Structural modulations of diaryltriazines with potent anti-HIV activity. Eur. J. Med. Chem., 2008, 43, (6), 1230-1236.
    • (2008) Eur. J. Med. Chem. , vol.43 , Issue.6 , pp. 1230-1236
    • Xiong, Y.-Z.1    Chen, F.-E.2    Balzarini, J.3    De Clercq, E.4    Pannecouque, C.5    Non-Nucleoside, H.6
  • 62
    • 77950037962 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 4-(hydroxyimino)arylmethyl diarylpyrimidine analogs as potential nonnucleoside reverse transcriptase inhibitors against HIV
    • Feng, X.-Q.; Zeng, Z.-S.; Liang, Y.-H.; Chen, F.-E.; Pannecouque, C.; Balzarini, J.; Clercq, E.D., Synthesis and biological evaluation of 4-(hydroxyimino)arylmethyl diarylpyrimidine analogs as potential nonnucleoside reverse transcriptase inhibitors against HIV. Bioorg. Med. Chem., 2010, 18, (7), 2370-2374.
    • (2010) Bioorg. Med. Chem. , vol.18 , Issue.7 , pp. 2370-2374
    • Feng, X.-Q.1    Zeng, Z.-S.2    Liang, Y.-H.3    Chen, F.-E.4    Pannecouque, C.5    Balzarini, J.6    Clercq, E.D.7
  • 63
    • 77955316010 scopus 로고    scopus 로고
    • Hybrid diarylbenzopyrimidine nonnucleoside reverse transcriptase inhibitors as promising new leads for improved anti-HIV-1 chemotherapy
    • Zeng, Z.-S.; He, Q.-Q.; Liang, Y.-H.; Feng, X.-Q.; Chen, F.-E.; Clercq, E.D.; Balzarini, J.; Pannecouque, C., Hybrid diarylbenzopyrimidine nonnucleoside reverse transcriptase inhibitors as promising new leads for improved anti-HIV-1 chemotherapy. Bioorg. Med. Chem., 2010, 18, (14), 5039-5047.
    • (2010) Bioorg. Med. Chem. , vol.18 , Issue.14 , pp. 5039-5047
    • Zeng, Z.-S.1    He, Q.-Q.2    Liang, Y.-H.3    Feng, X.-Q.4    Chen, F.-E.5    Clercq, E.D.6    Balzarini, J.7    Pannecouque, C.8
  • 64
    • 68949110165 scopus 로고    scopus 로고
    • Discovery of diarylpyridine derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors
    • Tian, X.; Qin, B.; Lu, H.; Lai, W.; Jiang, S.; Lee, K.-H.; Chen, C.H.; Xie, L., Discovery of diarylpyridine derivatives as novel non-nucleoside HIV-1 reverse transcriptase inhibitors. Bioorg. Med. Chem. Lett., 2009, 19, (18), 5482-5485.
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , Issue.18 , pp. 5482-5485
    • Tian, X.1    Qin, B.2    Lu, H.3    Lai, W.4    Jiang, S.5    Lee, K.-H.6    Chen, C.H.7    Xie, L.8
  • 68
    • 33947580188 scopus 로고    scopus 로고
    • Synthesis and evaluation of 2-(2,6-dihalophenyl)-3-pyrimidinyl-1,3- thiazolidin-4-one analogs as anti-HIV-1 agents
    • Rawal, R.K.; Tripathi, R.; Katti, S.B.; Pannecouque, C.; De Clercq, E., Synthesis and evaluation of 2-(2,6-dihalophenyl)-3-pyrimidinyl-1,3-thiazolidin- 4-one analogs as anti-HIV-1 agents. Bioorg. Med. Chem., 2007, 15, (9), 3134-3142.
    • (2007) Bioorg. Med. Chem. , vol.15 , Issue.9 , pp. 3134-3142
    • Rawal, R.K.1    Tripathi, R.2    Katti, S.B.3    Pannecouque, C.4    De Clercq, E.5
  • 69
    • 27644537621 scopus 로고    scopus 로고
    • 2-(Aryl)-3-furan-2-ylmethyl-thiazolidin-4-ones as selective HIV-RT inhibitors
    • Rawal, R.K.; Prabhakar, Y.S.; Katti, S.B.; De Clercq, E., 2-(Aryl)-3-furan-2-ylmethyl-thiazolidin-4-ones as selective HIV-RT inhibitors. Bioorg. Med. Chem., 2005, 13, (24), 6771-6776.
    • (2005) Bioorg. Med. Chem. , vol.13 , Issue.24 , pp. 6771-6776
    • Rawal, R.K.1    Prabhakar, Y.S.2    Katti, S.B.3    De Clercq, E.4
  • 71
    • 33847781693 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of 2-aryl-3-heteroaryl-1,3-thiazolidin- 4-ones as anti-HIV agents
    • Rawal, R.K.; Tripathi, R.; Katti, S.B.; Pannecouque, C.; De Clercq, E., Design, synthesis, and evaluation of 2-aryl-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV agents. Bioorg. Med. Chem., 2007, 15, (4), 1725-1731.
    • (2007) Bioorg. Med. Chem. , vol.15 , Issue.4 , pp. 1725-1731
    • Rawal, R.K.1    Tripathi, R.2    Katti, S.B.3    Pannecouque, C.4    De Clercq, E.5
  • 72
    • 34447569299 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2,3-diaryl substituted-1,3- thiazolidin-4-ones as anti-HIV agents
    • Rawal, R.K.; Tripathi, R.; Katti, S.B.; Pannecouque, C.; De Clercq, E., Synthesis and biological evaluation of 2,3-diaryl substituted-1,3-thiazolidin-4- ones as anti-HIV agents. Med. Chem., 2007, 3, (4), 355-363.
    • (2007) Med. Chem. , vol.3 , Issue.4 , pp. 355-363
    • Rawal, R.K.1    Tripathi, R.2    Katti, S.B.3    Pannecouque, C.4    De Clercq, E.5
  • 74
    • 47949096992 scopus 로고    scopus 로고
    • Design and synthesis of 2-(2,6-dibromophenyl)-3-heteroaryl-1,3- thiazolidin-4-ones as anti-HIV agents
    • Rawal, R.K.; Tripathi, R.; Katti, S.B.; Pannecouque, C.; De Clercq, E., Design and synthesis of 2-(2,6-dibromophenyl)-3-heteroaryl-1,3-thiazolidin-4- ones as anti-HIV agents. Eur. J. Med. Chem., 2008, 43, (12), 2800-2806.
    • (2008) Eur. J. Med. Chem. , vol.43 , Issue.12 , pp. 2800-2806
    • Rawal, R.K.1    Tripathi, R.2    Katti, S.B.3    Pannecouque, C.4    De Clercq, E.5
  • 75
    • 34250186053 scopus 로고    scopus 로고
    • Synthesis and anti-HIV studies of 2-adamantyl-substituted thiazolidin-4-ones
    • Balzarini, J.; Orzeszko, B.; Maurin, J.K.; Orzeszko, A., Synthesis and anti-HIV studies of 2-adamantyl-substituted thiazolidin-4-ones. Eur. J. Med. Chem., 2007, 42, (7), 993-1003.
    • (2007) Eur. J. Med. Chem. , vol.42 , Issue.7 , pp. 993-1003
    • Balzarini, J.1    Orzeszko, B.2    Maurin, J.K.3    Orzeszko, A.4
  • 76
    • 22444444421 scopus 로고    scopus 로고
    • Topological descriptors in modeling the HIV inhibitory activity of 2-aryl-3-pyridyl-thiazolidin-4-ones
    • Prabhakar, Y.S.; Rawal, R.K.; Gupta, M.K.; Solomon, V.R.; Katti, S.B., Topological descriptors in modeling the HIV inhibitory activity of 2-aryl-3-pyridyl-thiazolidin-4-ones. Comb. Chem. High Throughput Scr., 2005, 8, (5), 431-437.
    • (2005) Comb. Chem. High Throughput Scr. , vol.8 , Issue.5 , pp. 431-437
    • Prabhakar, Y.S.1    Rawal, R.K.2    Gupta, M.K.3    Solomon, V.R.4    Katti, S.B.5
  • 77
    • 8544239371 scopus 로고    scopus 로고
    • CPMLR/ PLS Directed Structure-Activity Modeling of the HIV-1 RT Inhibitory Activity of 2,3-Diaryl-1,3-thiazolidin-4-ones
    • Prabhakar, Y.S.; Solomon, V.R.; Rawal, R.K.; Gupta, M.K.; Katti, S.B., CPMLR/ PLS Directed Structure-Activity Modeling of the HIV-1 RT Inhibitory Activity of 2,3-Diaryl-1,3-thiazolidin-4-ones. QSAR & Comb. Sci., 2004, 23, (4), 234-244.
    • (2004) QSAR & Comb. Sci. , vol.23 , Issue.4 , pp. 234-244
    • Prabhakar, Y.S.1    Solomon, V.R.2    Rawal, R.K.3    Gupta, M.K.4    Katti, S.B.5
  • 78
    • 34250676593 scopus 로고    scopus 로고
    • Molecular Surface Features in Modeling the HIV-1 RT Inhibitory Activity of 2-(2, 6-Disubstituted phenyl)-3-(substituted pyrimidin-2-yl)-thiazolidin-4- ones
    • Rawal, R.K.; Prabhakar, Y.S.; Katti, S.B., Molecular Surface Features in Modeling the HIV-1 RT Inhibitory Activity of 2-(2, 6-Disubstituted phenyl)-3-(substituted pyrimidin-2-yl)-thiazolidin-4-ones. QSAR & Comb. Sci., 2007, 26, (3), 398-406.
    • (2007) QSAR & Comb. Sci. , vol.26 , Issue.3 , pp. 398-406
    • Rawal, R.K.1    Prabhakar, Y.S.2    Katti, S.B.3


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