메뉴 건너뛰기




Volumn 6, Issue 2, 2010, Pages 100-108

QSAR analysis of HIV-1 reverse transcriptase inhibitory 5-alkyl-2- [(aryl and alkyloxylcarbonylmethyl) thio]-6- (1-napthylmethyl) pyrimidin-4 (3H)-ones

Author keywords

HIV 1 reverse transcriptase inhibitors; MOE; NNRTIS; QSAR; S DABO

Indexed keywords

5 ALKYL 2 [(ARYL AND ALKYLOXYCARBONYLMETHYL)THIO] 6 (1 NAPHTHYLMETHYL)PYRIMIDIN 4 (3H)ONE DERIVATIVE; PYRIMIDINE DERIVATIVE; RNA DIRECTED DNA POLYMERASE; RNA DIRECTED DNA POLYMERASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 79959228504     PISSN: 18164900     EISSN: None     Source Type: Journal    
DOI: 10.3923/ijv.2007.19.27     Document Type: Article
Times cited : (1)

References (34)
  • 1
    • 0033081564 scopus 로고    scopus 로고
    • Resistance to non-nucleoside inhibitors of HIV-1 reverse transcriptase
    • Bacheler, L.T., 1999. Resistance to non-nucleoside inhibitors of HIV-1 reverse transcriptase. Drug Resist. Updates, 2: 56-67.
    • (1999) Drug Resist. Updates , vol.2 , pp. 56-67
    • Bacheler, L.T.1
  • 2
    • 8844285333 scopus 로고    scopus 로고
    • QSAR modelling of HIV-1 reverse transcriptase inhibition by benzoxazinones using a combination of P_VSA and pharmacophore feature descriptors
    • Balaji, S., C. Karthikeyan, N.S. Hari Narayan Moorthy and P. Trivedi, 2004. QSAR modelling of HIV-1 reverse transcriptase inhibition by benzoxazinones using a combination of P_VSA and pharmacophore feature descriptors. Bioorg. Med. Chem. Lett., 14: 6089-6094.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 6089-6094
    • Balaji, S.1    Karthikeyan, C.2    Hari, N.M.N.S.3    Trivedi, P.4
  • 4
    • 0343831900 scopus 로고    scopus 로고
    • Quantitative Structure-Activity Relationship (QSAR) study of new fiuorovinyloxyacetamides
    • Cho, D.H., S.K. Lee, B.T. Kim and K.T. No, 2001. Quantitative Structure-Activity Relationship (QSAR) study of new fiuorovinyloxyacetamides. Bull. Korean Chem. Soc, 22: 388-394.
    • (2001) Bull. Korean Chem. Soc , vol.22 , pp. 388-394
    • Cho, D.H.1    Lee, S.K.2    Kim, B.T.3    No, K.T.4
  • 5
    • 0028248489 scopus 로고
    • Augest, J., M.W. Ander, F. Murad (Eds.), San Diego, Academic
    • Darke, P.L. and J.R. Huff, 1994. Advances in Pharamacology. Augest, J., M.W. Ander, F. Murad (Eds.), San Diego, Academic, pp: 399-415.
    • (1994) Advances In Pharamacology , pp. 399-415
    • Darke, P.L.1    Huff, J.R.2
  • 6
    • 0029011730 scopus 로고
    • Toward improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections
    • De Clercq, E., 1995. Toward improved anti-HIV chemotherapy: Therapeutic strategies for intervention with HIV infections. J. Med. Chem., 38: 2491-2517.
    • (1995) J. Med. Chem , vol.38 , pp. 2491-2517
    • de Clercq, E.1
  • 7
    • 0032437454 scopus 로고    scopus 로고
    • The role of non-nucleoside reverses transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection
    • De Clercq, E., 1998. The role of non-nucleoside reverses transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection. Antiviral Res., 38: 153-179.
    • (1998) Antiviral Res , vol.38 , pp. 153-179
    • de Clercq, E.1
  • 8
    • 0033927489 scopus 로고    scopus 로고
    • Novel compounds in preclinical/early clinical development for the treatment of HIV infections
    • De Clercq, E., 2000. Novel compounds in preclinical/early clinical development for the treatment of HIV infections. Rev. Med. Virol, 10: 255-277.
    • (2000) Rev. Med. Virol , vol.10 , pp. 255-277
    • de Clercq, E.1
  • 9
    • 0035271620 scopus 로고    scopus 로고
    • New developments in anti-HIV chemotherapy
    • De Clercq, E., 2001. New developments in anti-HIV chemotherapy. II Farmaco, 56: 3-12.
    • (2001) II Farmaco , vol.56 , pp. 3-12
    • de Clercq, E.1
  • 10
    • 0036846898 scopus 로고    scopus 로고
    • New anti-HIV agents and targets
    • De Clercq, E., 2002a. New anti-HIV agents and targets. Med. Res. Rev., 22: 531-565.
    • (2002) Med. Res. Rev , vol.22 , pp. 531-565
    • de Clercq, E.1
  • 11
    • 0037130296 scopus 로고    scopus 로고
    • New developments in anti-HIV chemotherapy
    • De Clercq, E., 2002b. New developments in anti-HIV chemotherapy. Biochim. Biophys. Acta, 1587:258-275.
    • (2002) Biochim. Biophys. Acta , vol.1587 , pp. 258-275
    • de Clercq, E.1
  • 12
    • 0031805095 scopus 로고    scopus 로고
    • S-1153 inhibits replication of known drug-resistant strains of human immunodeficiency virus type 1
    • Fujiwara, T., A. Sato, M. El-Farrash, S. Miki and K. Abe et al., 1998. S-1153 inhibits replication of known drug-resistant strains of human immunodeficiency virus type 1. Antimicrob. Agents Chemother., 42: 1340-1345.
    • (1998) Antimicrob. Agents Chemother , vol.42 , pp. 1340-1345
    • Fujiwara, T.1    Sato, A.2    El-Farrash, M.3    Miki, S.4    Abe, K.5
  • 13
    • 1542301644 scopus 로고    scopus 로고
    • QSAR study on some anti-HIV HEPT analogues using physicochemical and topological parameters
    • Gayen, S., B. Debnath, S. Samantha and T. Jha, 2004. QSAR study on some anti-HIV HEPT analogues using physicochemical and topological parameters. Biorg. Med. Chem., 12: 1493-1503.
    • (2004) Biorg. Med. Chem , vol.12 , pp. 1493-1503
    • Gayen, S.1    Debnath, B.2    Samantha, S.3    Jha, T.4
  • 14
    • 0026003110 scopus 로고
    • Pyridone derivatives: Specific human immunodeficiency virus type 1 reverse transcriptase inhibitors with antiviral activity
    • Goldman, M.E., J.H. Nunberg, J.A. O'Brien, J.C. Quintero and W.A. Schleif et al., 1991. Pyridone derivatives: Specific human immunodeficiency virus type 1 reverse transcriptase inhibitors with antiviral activity. Proc. Natl. Acad. Sci. USA., 88: 6863-6867.
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 6863-6867
    • Goldman, M.E.1    Nunberg, J.H.2    O'Brien, J.A.3    Quintero, J.C.4    Schleif, W.A.5
  • 15
    • 0000805679 scopus 로고
    • The molecular connectivity chi indices and kappa shape indices in structure-property modeling
    • Hall, L.H. and L.B. Kier, 1991. The molecular connectivity chi indices and kappa shape indices in structure-property modeling. Rev. Comput. Chem., Vol. 2.
    • (1991) Rev. Comput. Chem , vol.2
    • Hall, L.H.1    Kier, L.B.2
  • 16
    • 2442610540 scopus 로고    scopus 로고
    • 5-Alkyl-2-[(aryl and alkyloxylcarbonylmethyl)thio]-6- (1-naphthylmethyl) pyrimidin-4(3H)-ones as an unique HIV reverse transcriptase inhibitors of S-DABO series
    • He, Y., C. Fener, S. Guangfu, W. Yueping, E. De Clercq, J. Balzarini and C. Pannecouque, 2004. 5-Alkyl-2-[(aryl and alkyloxylcarbonylmethyl)thio]-6- (1-naphthylmethyl) pyrimidin-4(3H)-ones as an unique HIV reverse transcriptase inhibitors of S-DABO series. Bioorg. Med. Chem. Lett., 14: 3173-3176.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , pp. 3173-3176
    • He, Y.1    Fener, C.2    Guangfu, S.3    Yueping, W.4    de Clercq, E.5    Balzarini, J.6    Pannecouque, C.7
  • 17
    • 0034059835 scopus 로고    scopus 로고
    • The HIV-1 reverse transcription (RT) process as target for RT inhibitors
    • Jonckheere, H., J. Anne and E. De Clercq, 2000. The HIV-1 reverse transcription (RT) process as target for RT inhibitors. Med. Res. Rev., 20: 129-154.
    • (2000) Med. Res. Rev , vol.20 , pp. 129-154
    • Jonckheere, H.1    Anne, J.2    de Clercq, E.3
  • 18
    • 0017754506 scopus 로고
    • Structure-activity studies on hallucinogenic amphetamines using molecular connectivity
    • Kier, L.B. and L.H. Hall, 1977. Structure-activity studies on hallucinogenic amphetamines using molecular connectivity. J. Med. Chem., 20: 1631-1636.
    • (1977) J. Med. Chem , vol.20 , pp. 1631-1636
    • Kier, L.B.1    Hall, L.H.2
  • 19
    • 2942550228 scopus 로고    scopus 로고
    • Classical QSAR Modeling of HIV-1 Reverse Transcriptase Inhibitor 2-Amino-6-arylsulfonylbenzonitriles and Congeners
    • Leonard, J. and K. Roy, 2004. Classical QSAR Modeling of HIV-1 Reverse Transcriptase Inhibitor 2-Amino-6-arylsulfonylbenzonitriles and Congeners. QSAR Combi. Sci., 23: 23-35.
    • (2004) QSAR Combi. Sci , vol.23 , pp. 23-35
    • Leonard, J.1    Roy, K.2
  • 21
    • 17944376896 scopus 로고    scopus 로고
    • Evolution of anti-HIV drug candidates. Part 1: From R-Anilinophenylacetamide (RAPA) to imidazolyl thiourea (ITU)
    • Ludovici, D.W., M.J. Kukla, P.G. Grous, S. Krishnan and K. Andries et al., 2001. Evolution of anti-HIV drug candidates. Part 1: From R-Anilinophenylacetamide (RAPA) to imidazolyl thiourea (ITU). Bioorg. Med. Chem. Lett., 11: 2225-2228.
    • (2001) Bioorg. Med. Chem. Lett , vol.11 , pp. 2225-2228
    • Ludovici, D.W.1    Kukla, M.J.2    Grous, P.G.3    Krishnan, S.4    Andries, K.5
  • 22
    • 0001728908 scopus 로고    scopus 로고
    • Quantum-chemical descriptors in QSAR/QSPR studies
    • Mati, K. and V.S. Lobanov, 1996. Quantum-chemical descriptors in QSAR/QSPR studies. Chem. Rev., 96: 1027-1043.
    • (1996) Chem. Rev , vol.96 , pp. 1027-1043
    • Mati, K.1    Lobanov, V.S.2
  • 24
    • 2642709177 scopus 로고    scopus 로고
    • For the HIV outpatient study investigators. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection
    • Palella, F.J., K.M. Delaney, A.C. Moorman, M.O. Loveless, J. Fuhrer, G.A. Satten, D.J. Aschman and S.D. Holmberg, 1998. For the HIV outpatient study investigators. Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. N. Eng. J. Med., 338: 853-860.
    • (1998) N. Eng. J. Med , vol.338 , pp. 853-860
    • Palella, F.J.1    Delaney, K.M.2    Moorman, A.C.3    Loveless, M.O.4    Fuhrer, J.5    Satten, G.A.6    Aschman, D.J.7    Holmberg, S.D.8
  • 25
    • 0025014499 scopus 로고
    • Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives
    • Pauwels, R., K. Andries, J. Desmijter, D. Schols and M.J. Kukla et al., 1990. Potent and selective inhibition of HIV-1 replication in vitro by a novel series of TIBO derivatives. Nature, 343: 470-474.
    • (1990) Nature , vol.343 , pp. 470-474
    • Pauwels, R.1    Andries, K.2    Desmijter, J.3    Schols, D.4    Kukla, M.J.5
  • 26
    • 0027407551 scopus 로고
    • Potent and highly selective human immunodeficiency virus type 1 (HIV-1) inhibition by a series of R-anilinophenylacetamide derivatives targeted at HIV-1 reverse transcriptase
    • Pauwels, R., K. Andries, Z. Debryser, P. Van Daele and D. Schols et al., 1993. Potent and highly selective human immunodeficiency virus type 1 (HIV-1) inhibition by a series of R-anilinophenylacetamide derivatives targeted at HIV-1 reverse transcriptase. Proc. Natl. Acad. Sci. USA., 90: 1711-1715.
    • (1993) Proc. Natl. Acad. Sci. USA , vol.90 , pp. 1711-1715
    • Pauwels, R.1    Andries, K.2    Debryser, Z.3    van Daele, P.4    Schols, D.5
  • 27
    • 0000697995 scopus 로고
    • Applications of the radius-diameter diagram to the classification of topological and geometrical shapes of chemical compounds
    • Petitjean, M., 1992. Applications of the radius-diameter diagram to the classification of topological and geometrical shapes of chemical compounds. J. Chem. Inf. Comput. Sci., 32: 331-337.
    • (1992) J. Chem. Inf. Comput. Sci , vol.32 , pp. 331-337
    • Petitjean, M.1
  • 29
    • 8544239371 scopus 로고    scopus 로고
    • CP-MLR/PLS Directed structure-activity modeling of the HIV-1 RT inhibitory activity of 2,3-Diaryl-l,3-thiazolidin-4-ones
    • Prabhakar, Y.S., V.R Soloman, RK. Rawal, M.K. Gupta and S.B. Katti, 2004. CP-MLR/PLS Directed structure-activity modeling of the HIV-1 RT inhibitory activity of 2,3-Diaryl-l,3-thiazolidin-4-ones. QSAR Combi. Sci., 23:234-244.
    • (2004) QSAR Combi. Sci , vol.23 , pp. 234-244
    • Prabhakar, Y.S.1    Soloman, V.R.2    Rawal, R.K.3    Gupta, M.K.4    Katti, S.B.5
  • 32
  • 34
    • 8544254107 scopus 로고
    • Structural determination of paraffin boiling points
    • Wiener, H., 1947. Structural determination of paraffin boiling points. J. Am. Chem. Soc, 69: 17-20.
    • (1947) J. Am. Chem. Soc , vol.69 , pp. 17-20
    • Wiener, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.