메뉴 건너뛰기




Volumn 42, Issue 2, 2008, Pages 133-140

QSAR analysis of 6-aryl-2,4-dioxo-5-hexenoic acids as HIV-1 integrase inhibitors

Author keywords

Hexenoic acid; Human immunodeficiency virus; Inhibition; Integrase; Quantitative structure activity relationship

Indexed keywords

6 ARYL 2,4 DIOXO 5 HEXENOIC ACID DERIVATIVE; INTEGRASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 67650622420     PISSN: 00195464     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (6)

References (21)
  • 1
    • 0029011730 scopus 로고
    • Toward improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections
    • De Clercq E. Toward improved anti-HIV chemotherapy: therapeutic strategies for intervention with HIV infections. J Med Chem 1995;38:2491-517.
    • (1995) J Med Chem , vol.38 , pp. 2491-2517
    • de Clercq, E.1
  • 2
    • 0025031786 scopus 로고
    • The IN protein of Moloney murine leukemia virus processes the DNA viral ends and accomplishes their integration in vitro
    • Craigie R, Fujiwara T, Bushman F. The IN protein of Moloney murine leukemia virus processes the DNA viral ends and accomplishes their integration in vitro. Cell 1990; 62:829-35.
    • (1990) Cell , vol.62 , pp. 829-835
    • Craigie, R.1    Fujiwara, T.2    Bushman, F.3
  • 3
    • 0025011051 scopus 로고
    • The avian retroviral IN protein protein is both necessary and sufficient for integrative recombination in vitro
    • Katz RA, Merkel G, Kulkosk T, Leis J, Salka AM. The avian retroviral IN protein is both necessary and sufficient for integrative recombination in vitro. Cell 1990;63:87-91.
    • (1990) Cell , vol.63 , pp. 87-91
    • Katz, R.A.1    Merkel, G.2    Kulkosk, T.3    Leis, J.4    Salka, A.M.5
  • 4
    • 0033821651 scopus 로고    scopus 로고
    • Identification of HIV-1 integrase inhibitors via three-dimensional database searching using ASV and HIV-1 integrases as targets
    • Chen IJ, Neamati N, Nicklaus MC et al. Identification of HIV-1 integrase inhibitors via three-dimensional database searching using ASV and HIV-1 integrases as targets. Bioorg Med Chem 2000;8: 2385-90.
    • (2000) Bioorg Med Chem , vol.8 , pp. 2385-2390
    • Chen, I.J.1    Neamati, N.2    Nicklaus, M.C.3
  • 5
    • 0036107683 scopus 로고    scopus 로고
    • Patented small molecule inhibitors of HIV-1 integrase: A 10-year saga
    • Neamati N. Patented small molecule inhibitors of HIV-1 integrase: a 10-year saga. Expert Opin Ther Patents 2002;12:709.
    • (2002) Expert Opin Ther Patents , vol.12 , pp. 709
    • Neamati, N.1
  • 6
    • 0042423354 scopus 로고    scopus 로고
    • HIV-1 integrase inhibition: Binding sites, structure activity relationships and future perspectives
    • Parril AL. HIV-1 integrase inhibition: binding sites, structure activity relationships and future perspectives. Curr Med Chem 2003;10:1811-15.
    • (2003) Curr Med Chem , vol.10 , pp. 1811-1815
    • Parril, A.L.1
  • 10
    • 0030041593 scopus 로고    scopus 로고
    • Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase
    • Eich E, Pertz H, Kaloga M, Schulz J, Fesen MR, Mazumder A, Pommier Y. Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase. J Med Chem 1996;39:86-92.
    • (1996) J Med Chem , vol.39 , pp. 86-92
    • Eich, E.1    Pertz, H.2    Kaloga, M.3    Schulz, J.4    Fesen, M.R.5    Mazumder, A.6    Pommier, Y.7
  • 12
    • 0026659014 scopus 로고
    • Inhibition of HIV-1 integration protein by aurintricarboxylic acid monomers, monomer analogs, and polymer fractions
    • Cushman M, Sherman P. Inhibition of HIV-1 integration protein by aurintricarboxylic acid monomers, monomer analogs, and polymer fractions. Biochem Biophys Res Commun 1992;185:58-63.
    • (1992) Biochem Biophys Res Commun , vol.185 , pp. 58-63
    • Cushman, M.1    Sherman, P.2
  • 13
    • 10244260392 scopus 로고    scopus 로고
    • Dicaffeoylguinic acid inhibitors of human immunodeficiency virus integrase: Inhibition of the core catalytic domain of human immunodeficiency virus integrase
    • Robinson WE Jr, Cordeiro M, Abdel-Malek S et al. Dicaffeoylguinic acid inhibitors of human immunodeficiency virus integrase: inhibition of the core catalytic domain of human immunodeficiency virus integrase. Mol Pharmacol 1996;50:846-50.
    • (1996) Mol Pharmacol , vol.50 , pp. 846-850
    • Robinson Jr., W.E.1    Cordeiro, M.2    Abdel-Malek, S.3
  • 16
    • 0242677271 scopus 로고
    • A quantitative approach to biochemical structure-activity relationships
    • Hansch C. A quantitative approach to biochemical structure-activity relationships. Acc Chem Res 1969;2:232-8.
    • (1969) Acc Chem Res , vol.2 , pp. 232-238
    • Hansch, C.1
  • 17
    • 0034463939 scopus 로고    scopus 로고
    • Three-dimensional quantitative structure-activity relationships study on HIV-1 reverse transcriptase inhibitors in the class of dipyridodiazepinone derivatives, using comparative molecular field analysis
    • Pungpo P, Hannongbua S. Three-dimensional quantitative structure-activity relationships study on HIV-1 reverse transcriptase inhibitors in the class of dipyridodiazepinone derivatives, using comparative molecular field analysis. J Mol Graphics & Model 2000;18:581-90.
    • (2000) J Mol Graphics & Model , vol.18 , pp. 581-590
    • Pungpo, P.1    Hannongbua, S.2
  • 18
    • 33947607163 scopus 로고    scopus 로고
    • Predicting anti-HIV activity of PETT derivatives: CoMFA approach
    • Ravichandran V, Agrawal RK. Predicting anti-HIV activity of PETT derivatives: CoMFA approach. Bioorg Med Chem Lett 2007;17:2197-02.
    • (2007) Bioorg Med Chem Lett , vol.17 , pp. 2197-2102
    • Ravichandran, V.1    Agrawal, R.K.2
  • 19
    • 0033491040 scopus 로고    scopus 로고
    • Comparative molecular field analysis (CoMFA) and docking studies of nonnucleoside HIV-1 RT inhibitors (NNIS)
    • Barreca ML, Carotti A, Chimirri A, Monforte AM. Comparative molecular field analysis (CoMFA) and docking studies of nonnucleoside HIV-1 RT inhibitors (NNIS), Bioorg Med Chem 1999;7:2283-92.
    • (1999) Bioorg Med Chem , vol.7 , pp. 2283-2292
    • Barreca, M.L.1    Carotti, A.2    Chimirri, A.3    Monforte, A.M.4
  • 20
    • 34548456464 scopus 로고    scopus 로고
    • QSAR study of novel 1, 1, 3 - trioxo [1, 2, 4] -thiadiazine (TTDs) analogues as potent anti-HIV agents
    • Ravichandran V, Mourya VK, Agrawal RK. QSAR study of novel 1, 1, 3 - trioxo [1, 2, 4] -thiadiazine (TTDs) analogues as potent anti-HIV agents. Arkivoc 2007;XIV:204-12.
    • (2007) Arkivoc , vol.14 , pp. 204-212
    • Ravichandran, V.1    Mourya, V.K.2    Agrawal, R.K.3
  • 21
    • 12144288755 scopus 로고    scopus 로고
    • Artico M et al. 6-Aryl-2,4-dioxo-5-hexenoic acids, novel integrase inhibitors active against HIV-1 multiplication in cell-based assays
    • Costi R, Santo RD, Artico M et al. 6-Aryl-2,4-dioxo-5-hexenoic acids, novel integrase inhibitors active against HIV-1 multiplication in cell-based assays. Bioorg Med Chem Lett 2004;14:1745-9.
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 1745-1749
    • Costi, R.1    Santo, R.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.