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Volumn 5, Issue 11, 2014, Pages 1259-1262

Picomolar inhibitors of HIV-1 reverse transcriptase: Design and crystallography of naphthyl phenyl ethers

Author keywords

Anti HIV agents; NNRTIs; protein crystallography

Indexed keywords

ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; DIPHENYL ETHER DERIVATIVE; EFAVIRENZ; ETRAVIRINE; NAPHTHALENE DERIVATIVE; NAPHTHYL PHENYL ETHER DERIVATIVE; NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR; PIROXICAM; RILPIVIRINE; UNCLASSIFIED DRUG;

EID: 84925946409     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml5003713     Document Type: Article
Times cited : (34)

References (18)
  • 1
    • 84880579842 scopus 로고    scopus 로고
    • The Nucleoside Reverse Transcriptase Inhibitors, Nonnucleoside Reverse Transcriptase Inhibitors, and Protease Inhibitors in the Treatment of HIV Infections (AIDS)
    • De Clercq, E. The Nucleoside Reverse Transcriptase Inhibitors, Nonnucleoside Reverse Transcriptase Inhibitors, and Protease Inhibitors in the Treatment of HIV Infections (AIDS) Adv. Pharmacol. 2013, 67, 317-358
    • (2013) Adv. Pharmacol. , vol.67 , pp. 317-358
    • De Clercq, E.1
  • 2
    • 84862580827 scopus 로고    scopus 로고
    • In Search of a Treatment for HIV: Current Therapies and the Role of Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs)
    • Reynolds, C.; de Koning, C. B.; Pelly, S. C.; van Otterlo, W. A. L.; Bode, M. L. In Search of a Treatment for HIV: Current Therapies and the Role of Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) Chem. Soc. Rev. 2012, 41, 4657-4670
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 4657-4670
    • Reynolds, C.1    De Koning, C.B.2    Pelly, S.C.3    Van Otterlo, W.A.L.4    Bode, M.L.5
  • 3
    • 84876852661 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. 2013, 33, E1-E72
    • (2013) Med. Res. Rev. , vol.33 , pp. 1-E72
    • Zhan, P.1    Chen, X.2    Li, D.3    Fang, Z.4    De Clercq, E.5    Liu, X.6
  • 6
    • 73549115378 scopus 로고    scopus 로고
    • Non-nucleoside Reverse Transcriptase Inhibitors (NNRTIs), Their Discovery, Development, and Use in the Treatment of HIV-1 Infection: A Review of the Last 20 Years (1989-2009)
    • de Béthune, M.-P. Non-nucleoside Reverse Transcriptase Inhibitors (NNRTIs), Their Discovery, Development, and Use in the Treatment of HIV-1 Infection: A Review of the Last 20 Years (1989-2009) Antiviral Res. 2010, 85, 75-90
    • (2010) Antiviral Res. , vol.85 , pp. 75-90
    • De Béthune, M.-P.1
  • 9
    • 37849048981 scopus 로고    scopus 로고
    • Study of Equilibrium Solubility Measurement by Saturation Shake-Flask Method Using Hydrochlorothiaide as Model Compound
    • Baka, E.; Comer, J. E. A; Takács-Novák, K. Study of Equilibrium Solubility Measurement by Saturation Shake-Flask Method Using Hydrochlorothiaide as Model Compound J. Pharm. Biomed. Anal. 2008, 46, 335-341
    • (2008) J. Pharm. Biomed. Anal. , vol.46 , pp. 335-341
    • Baka, E.1    Comer, J.E.A.2    Takács-Novák, K.3
  • 10
    • 0028047132 scopus 로고
    • Antiviral Activity of 2′,3′-Dideoxy-β- l -5-fluorocytidine (β- l -EddC) and 2′,3′-Dideoxy-β- l -cytidine (β- l -ddC) against Hepatitis B Virus and Human Immunodeficiency Virus Type 1 in Vitro
    • Lin, T. S.; Luo, M. Z.; Liu, M. C.; Pai, S. B.; Dutschman, G. E.; Cheng, Y. C. Antiviral Activity of 2′,3′-Dideoxy-β- l -5-fluorocytidine (β- l -EddC) and 2′,3′-Dideoxy-β- l -cytidine (β- l -ddC) against Hepatitis B Virus and Human Immunodeficiency Virus Type 1 in Vitro Biochem. Pharmacol. 1994, 47, 171-174
    • (1994) Biochem. Pharmacol. , vol.47 , pp. 171-174
    • Lin, T.S.1    Luo, M.Z.2    Liu, M.C.3    Pai, S.B.4    Dutschman, G.E.5    Cheng, Y.C.6
  • 11
    • 0036172840 scopus 로고    scopus 로고
    • Novel Use of a Guanosine Prodrug Approach to Convert 2′,3′-Didehydro-2′,3′-dideoxyguanosine into a Viable Antiviral Agent
    • Ray, A. S.; Yang, Z.; Chu, C. K.; Anderson, K. S. Novel Use of a Guanosine Prodrug Approach to Convert 2′,3′-Didehydro-2′,3′-dideoxyguanosine into a Viable Antiviral Agent Antimicrob. Agents Chemother. 2002, 46, 887-891
    • (2002) Antimicrob. Agents Chemother. , vol.46 , pp. 887-891
    • Ray, A.S.1    Yang, Z.2    Chu, C.K.3    Anderson, K.S.4
  • 12
    • 0028340366 scopus 로고
    • Estimation and Correlation of Drug Water Solubility with Pharmacological Parameters Required for Biological Activity
    • Morelock, M. M.; Choi, L. L.; Bell, G. L.; Wright, J. L. Estimation and Correlation of Drug Water Solubility with Pharmacological Parameters Required for Biological Activity J. Pharm. Sci. 1994, 83, 948-952
    • (1994) J. Pharm. Sci. , vol.83 , pp. 948-952
    • Morelock, M.M.1    Choi, L.L.2    Bell, G.L.3    Wright, J.L.4
  • 15
    • 84862820228 scopus 로고    scopus 로고
    • Optimization of 2,4-Diarylanilines As Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors
    • Sun, L.-Q.; Qin, B.; Huang, L.; Qian, K.; Chen, C.-H.; Lee, K.-H.; Xie, L. Optimization of 2,4-Diarylanilines As Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors Bioorg. Med. Chem. Lett. 2012, 22, 2376-2379
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 2376-2379
    • Sun, L.-Q.1    Qin, B.2    Huang, L.3    Qian, K.4    Chen, C.-H.5    Lee, K.-H.6    Xie, L.7
  • 16
    • 0037204544 scopus 로고    scopus 로고
    • Prediction of Drug Solubility from Structure
    • Jorgensen, W. L.; Duffy, E. M. Prediction of Drug Solubility from Structure Adv. Drug Delivery Rev. 2002, 54, 355-366
    • (2002) Adv. Drug Delivery Rev. , vol.54 , pp. 355-366
    • Jorgensen, W.L.1    Duffy, E.M.2
  • 18
    • 67649225348 scopus 로고    scopus 로고
    • Efficient Drug Lead Discovery and Optimization
    • Jorgensen, W. L. Efficient Drug Lead Discovery and Optimization Acc. Chem. Res. 2009, 42, 724-733
    • (2009) Acc. Chem. Res. , vol.42 , pp. 724-733
    • Jorgensen, W.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.