메뉴 건너뛰기




Volumn 98, Issue 3, 2013, Pages 365-372

A novel anti-HIV active integrase inhibitor with a favorable in vitro cytochrome P450 and uridine 5'-diphospho-glucuronosyltransferase metabolism profile

Author keywords

Anti HIV; CYP UGT profiles; Drug drug interactions; Integrase; Resistance

Indexed keywords

ANTI HUMAN IMMUNODEFICIENCY VIRUS INTEGRASE INHIBITOR; CYTOCHROME P450; GLUCURONOSYLTRANSFERASE; INTEGRASE INHIBITOR; UNCLASSIFIED DRUG; URIDINE 5' DIPHOSPHO GLUCURONOSYLTRANSFERASE;

EID: 84877244757     PISSN: 01663542     EISSN: 18729096     Source Type: Journal    
DOI: 10.1016/j.antiviral.2013.04.005     Document Type: Article
Times cited : (4)

References (46)
  • 2
    • 0022495870 scopus 로고
    • Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone
    • Adachi A., Gendelman H.E., Koenig S., Folks T., Willey R., Rabson A., Martin M.A. Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone. J. Virol. 1986, 59:284-291.
    • (1986) J. Virol. , vol.59 , pp. 284-291
    • Adachi, A.1    Gendelman, H.E.2    Koenig, S.3    Folks, T.4    Willey, R.5    Rabson, A.6    Martin, M.A.7
  • 3
    • 0025810128 scopus 로고
    • Characterization of an HIV-1 isolate displaying an apparent absence of virion-associated reverse-transcriptase activity
    • Buckheit R.W., Swanstrom R. Characterization of an HIV-1 isolate displaying an apparent absence of virion-associated reverse-transcriptase activity. AIDS Res. Hum. Retroviruses. 1991, 7:295-303.
    • (1991) AIDS Res. Hum. Retroviruses. , vol.7 , pp. 295-303
    • Buckheit, R.W.1    Swanstrom, R.2
  • 6
    • 77952326903 scopus 로고    scopus 로고
    • The population dynamics and control of tuberculosis
    • Dye C., Williams B.G. The population dynamics and control of tuberculosis. Science 2010, 328:856-861.
    • (2010) Science , vol.328 , pp. 856-861
    • Dye, C.1    Williams, B.G.2
  • 11
    • 77949365510 scopus 로고    scopus 로고
    • Retroviral intasome assembly and inhibition of DNA strand transfer
    • Hare S., Gupta S.S., Valkov E., Engelman A., Cherepanov P. Retroviral intasome assembly and inhibition of DNA strand transfer. Nature 2010, 464:232-236.
    • (2010) Nature , vol.464 , pp. 232-236
    • Hare, S.1    Gupta, S.S.2    Valkov, E.3    Engelman, A.4    Cherepanov, P.5
  • 12
    • 0032723359 scopus 로고    scopus 로고
    • Integrating DNA: transposases and retroviral integrases
    • Haren L., Ton-Hoang B., Chandler M. Integrating DNA: transposases and retroviral integrases. Annu. Rev. Microbiol. 1999, 53:245-281.
    • (1999) Annu. Rev. Microbiol. , vol.53 , pp. 245-281
    • Haren, L.1    Ton-Hoang, B.2    Chandler, M.3
  • 13
    • 0034005970 scopus 로고    scopus 로고
    • Use of calibrated viral load standards for group m subtypes of human immunodeficiency virus type 1 to assess the performance of viral RNA quantitation tests
    • Jagodzinski L.L., Wiggins D.L., McManis J.L., Emery S., Overbaugh J., Robb M., Bodrug S., Michael N.L. Use of calibrated viral load standards for group m subtypes of human immunodeficiency virus type 1 to assess the performance of viral RNA quantitation tests. J. Clin. Microbiol. 2000, 38:1247-1249.
    • (2000) J. Clin. Microbiol. , vol.38 , pp. 1247-1249
    • Jagodzinski, L.L.1    Wiggins, D.L.2    McManis, J.L.3    Emery, S.4    Overbaugh, J.5    Robb, M.6    Bodrug, S.7    Michael, N.L.8
  • 14
    • 78649482869 scopus 로고    scopus 로고
    • Drug-drug interactions in the treatment of HIV infection: focus on pharmacokinetic enhancement through CYP3A inhibition
    • Josephson F. Drug-drug interactions in the treatment of HIV infection: focus on pharmacokinetic enhancement through CYP3A inhibition. J. Intern. Med. 2010, 268:530-539.
    • (2010) J. Intern. Med. , vol.268 , pp. 530-539
    • Josephson, F.1
  • 17
    • 15244342411 scopus 로고    scopus 로고
    • UDP-glucuronosyltransferases and clinical drug-drug interactions
    • Kiang T.K.L., Ensom M.H.H., Chang T.K.H. UDP-glucuronosyltransferases and clinical drug-drug interactions. Pharmacol. Ther. 2005, 106:97-132.
    • (2005) Pharmacol. Ther. , vol.106 , pp. 97-132
    • Kiang, T.K.L.1    Ensom, M.H.H.2    Chang, T.K.H.3
  • 18
    • 0026562720 scopus 로고
    • Detection of replication-competent and pseudotyped human-immunodeficiency-virus with a sensitive cell-line on the basis of activation of an integrated beta-galactosidase gene
    • Kimpton J., Emerman M. Detection of replication-competent and pseudotyped human-immunodeficiency-virus with a sensitive cell-line on the basis of activation of an integrated beta-galactosidase gene. J. Virol. 1992, 66:2232-2239.
    • (1992) J. Virol. , vol.66 , pp. 2232-2239
    • Kimpton, J.1    Emerman, M.2
  • 21
    • 84870324937 scopus 로고    scopus 로고
    • Retroviral integrase proteins and HIV-1 DNA integration
    • Krishnan L., Engleman A. Retroviral integrase proteins and HIV-1 DNA integration. J. Biol. Chem. 2012, 287:40858-40866.
    • (2012) J. Biol. Chem. , vol.287 , pp. 40858-40866
    • Krishnan, L.1    Engleman, A.2
  • 22
    • 57749197592 scopus 로고    scopus 로고
    • Dose-response of ritonavir on hepatic CYP3A activity and elvitegravir oral exposure
    • Mathias A.A., West S., Hui J., Kearney B.P. Dose-response of ritonavir on hepatic CYP3A activity and elvitegravir oral exposure. Clin. Pharmacol. Ther. 2009, 85:64-70.
    • (2009) Clin. Pharmacol. Ther. , vol.85 , pp. 64-70
    • Mathias, A.A.1    West, S.2    Hui, J.3    Kearney, B.P.4
  • 25
    • 0344610168 scopus 로고    scopus 로고
    • Predicting human drug glucuronidation parameters: application of in vitro and in silico modeling approaches
    • Miners J.O., Smith P.A., Sorich M.J., McKinnon R.A., Mackenzie P.I. Predicting human drug glucuronidation parameters: application of in vitro and in silico modeling approaches. Annu. Rev. Pharmacol. 2004, 44:1-25.
    • (2004) Annu. Rev. Pharmacol. , vol.44 , pp. 1-25
    • Miners, J.O.1    Smith, P.A.2    Sorich, M.J.3    McKinnon, R.A.4    Mackenzie, P.I.5
  • 26
    • 31544474642 scopus 로고    scopus 로고
    • HIV integrase inhibitors with nucleobase scaffolds: discovery of a highly potent anti-HIV agent
    • Nair V., Chi G., Ptak R., Neamati N. HIV integrase inhibitors with nucleobase scaffolds: discovery of a highly potent anti-HIV agent. J. Med. Chem. 2006, 49:445-447.
    • (2006) J. Med. Chem. , vol.49 , pp. 445-447
    • Nair, V.1    Chi, G.2    Ptak, R.3    Neamati, N.4
  • 27
    • 34447548922 scopus 로고    scopus 로고
    • HIV integrase inhibitors as therapeutic agents in AIDS
    • Nair V., Chi G. HIV integrase inhibitors as therapeutic agents in AIDS. Rev. Med. Virol. 2007, 17:277-295.
    • (2007) Rev. Med. Virol. , vol.17 , pp. 277-295
    • Nair, V.1    Chi, G.2
  • 32
    • 75749130650 scopus 로고    scopus 로고
    • Panel of prototypical raltegravir-resistant infectious molecular clones in a novel integrase-deleted cloning vector
    • Reuman E.C., Bachmann M.H., Varghese V., Fessel W.J., Shafer R.W. Panel of prototypical raltegravir-resistant infectious molecular clones in a novel integrase-deleted cloning vector. Antimicrob. Agents Chemother. 2010, 54:934-936.
    • (2010) Antimicrob. Agents Chemother. , vol.54 , pp. 934-936
    • Reuman, E.C.1    Bachmann, M.H.2    Varghese, V.3    Fessel, W.J.4    Shafer, R.W.5
  • 33
    • 77952356637 scopus 로고    scopus 로고
    • Tuberculosis: what we don't know can, and does, hurt us
    • Russell D.G., Barry C.E., Flynn J.L. Tuberculosis: what we don't know can, and does, hurt us. Science 2010, 328:852-856.
    • (2010) Science , vol.328 , pp. 852-856
    • Russell, D.G.1    Barry, C.E.2    Flynn, J.L.3
  • 36
    • 0021719086 scopus 로고
    • Monoclonal-antibody and enzymatic profiles of human-malignant lymphoid-T cells and derived cell-lines
    • Smith S.D., Shatsky M., Cohen P.S., Warnke R., Link M.P., Glader B.E. Monoclonal-antibody and enzymatic profiles of human-malignant lymphoid-T cells and derived cell-lines. Cancer Res. 1984, 44:5657-5660.
    • (1984) Cancer Res. , vol.44 , pp. 5657-5660
    • Smith, S.D.1    Shatsky, M.2    Cohen, P.S.3    Warnke, R.4    Link, M.P.5    Glader, B.E.6
  • 37
    • 0036150897 scopus 로고    scopus 로고
    • Developmental aspects of human hepatic drug glucuronidation in young children and adults
    • Strassburg C.P., Strassburg A., Kneip S., Barut A., Tukey R.H., Rodeck B., Manns M.P. Developmental aspects of human hepatic drug glucuronidation in young children and adults. Gut 2002, 50:259-265.
    • (2002) Gut , vol.50 , pp. 259-265
    • Strassburg, C.P.1    Strassburg, A.2    Kneip, S.3    Barut, A.4    Tukey, R.H.5    Rodeck, B.6    Manns, M.P.7
  • 40
    • 77954633050 scopus 로고    scopus 로고
    • HIV persistence and the prospect of long-term drug-free remissions for HIV-infected individuals
    • Trono D., Van Lint C., Rouzioux C., Verdin E., Barre-Sinoussi F., Chun T.W., Chomont N. HIV persistence and the prospect of long-term drug-free remissions for HIV-infected individuals. Science 2010, 329:174-180.
    • (2010) Science , vol.329 , pp. 174-180
    • Trono, D.1    Van Lint, C.2    Rouzioux, C.3    Verdin, E.4    Barre-Sinoussi, F.5    Chun, T.W.6    Chomont, N.7
  • 41
    • 0034128936 scopus 로고    scopus 로고
    • Human UDP-glucuronosyltransferases: metabolism, expression, and disease
    • Tukey R.H., Strassburg C.P. Human UDP-glucuronosyltransferases: metabolism, expression, and disease. Annu. Rev. Pharmacol. 2000, 40:581-616.
    • (2000) Annu. Rev. Pharmacol. , vol.40 , pp. 581-616
    • Tukey, R.H.1    Strassburg, C.P.2
  • 42
    • 33344473930 scopus 로고    scopus 로고
    • Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) "probes" for human UDP-glucuronosyltransferases
    • Uchaipichat V., Mackenzie P.I., Elliot D.J., Miners J.O. Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) "probes" for human UDP-glucuronosyltransferases. Drug Metab. Dispos. 2006, 34:449-456.
    • (2006) Drug Metab. Dispos. , vol.34 , pp. 449-456
    • Uchaipichat, V.1    Mackenzie, P.I.2    Elliot, D.J.3    Miners, J.O.4
  • 43
    • 1842536833 scopus 로고    scopus 로고
    • Human UDP-glucuronosyltransferases: isoform selectivity and kinetics of 4-methylumbelliferone and 1-naphthol glucuronidation, effects of organic solvents, and inhibition by diclofenac and probenecid
    • Uchaipichat V., Mackenzie P.I., Guo X.H., Gardner-Stephen D., Galetin A., Houston J.B., Miners J.O. Human UDP-glucuronosyltransferases: isoform selectivity and kinetics of 4-methylumbelliferone and 1-naphthol glucuronidation, effects of organic solvents, and inhibition by diclofenac and probenecid. Drug Metab. Dispos. 2004, 32:413-423.
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 413-423
    • Uchaipichat, V.1    Mackenzie, P.I.2    Guo, X.H.3    Gardner-Stephen, D.4    Galetin, A.5    Houston, J.B.6    Miners, J.O.7
  • 44
    • 0032804249 scopus 로고    scopus 로고
    • Performance of the Affymetrix GeneChip HIV PRT 440 platform for antiretroviral drug resistance genotyping of human immunodeficiency virus type 1 clades and viral isolates with length polymorphisms
    • Vahey M., Nau M.E., Barrick S., Cooley J.D., Sawyer R., Sleeker A.A., Vickerman P., Bloor S., Larder B., Michael N.L., Wegner S.A. Performance of the Affymetrix GeneChip HIV PRT 440 platform for antiretroviral drug resistance genotyping of human immunodeficiency virus type 1 clades and viral isolates with length polymorphisms. J. Clin. Microbiol. 1999, 37:2533-2537.
    • (1999) J. Clin. Microbiol. , vol.37 , pp. 2533-2537
    • Vahey, M.1    Nau, M.E.2    Barrick, S.3    Cooley, J.D.4    Sawyer, R.5    Sleeker, A.A.6    Vickerman, P.7    Bloor, S.8    Larder, B.9    Michael, N.L.10    Wegner, S.A.11
  • 45
    • 27644596457 scopus 로고    scopus 로고
    • Predicting in vivo drug interactions from in vitro drug discovery data
    • Wienkers L.C., Heath T.G. Predicting in vivo drug interactions from in vitro drug discovery data. Nat. Rev. Drug Discov. 2005, 4:825-833.
    • (2005) Nat. Rev. Drug Discov. , vol.4 , pp. 825-833
    • Wienkers, L.C.1    Heath, T.G.2
  • 46
    • 6944221357 scopus 로고    scopus 로고
    • Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUC(i)/AUC) ratios
    • Williams J.A., Hyland R., Jones B.C., Smith D.A., Hurst S., Goosen T.C., Peterkin V., Koup J.R., Ball S.E. Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUC(i)/AUC) ratios. Drug Metab. Dispos. 2004, 32:1201-1208.
    • (2004) Drug Metab. Dispos. , vol.32 , pp. 1201-1208
    • Williams, J.A.1    Hyland, R.2    Jones, B.C.3    Smith, D.A.4    Hurst, S.5    Goosen, T.C.6    Peterkin, V.7    Koup, J.R.8    Ball, S.E.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.