메뉴 건너뛰기




Volumn 78, Issue 1, 2011, Pages 175-182

A three-dimensional pharmacophore model for IMPDH inhibitors

Author keywords

HypoRefine hypothes; Inosine 5' monophosphate dehydrogenase inhibitors; Molecular docking; Pharmacophore model

Indexed keywords

INOSINATE DEHYDROGENASE INHIBITOR;

EID: 79958795106     PISSN: 17470277     EISSN: 17470285     Source Type: Journal    
DOI: 10.1111/j.1747-0285.2011.01128.x     Document Type: Article
Times cited : (6)

References (38)
  • 1
    • 0016823448 scopus 로고
    • IMP dehydrogenase, an enzyme linked with proliferation and malignancy
    • Jackson R.C., Weber G., Morris H.P. (1975) IMP dehydrogenase, an enzyme linked with proliferation and malignancy. Nature;256:331-333.
    • (1975) Nature , vol.256 , pp. 331-333
    • Jackson, R.C.1    Weber, G.2    Morris, H.P.3
  • 2
    • 0032804406 scopus 로고    scopus 로고
    • IMP dehydrogenase: mechanism of action and inhibition
    • Hedstrom L. (1999) IMP dehydrogenase: mechanism of action and inhibition. Curr Med Chem;6:545-560.
    • (1999) Curr Med Chem , vol.6 , pp. 545-560
    • Hedstrom, L.1
  • 3
    • 0034121721 scopus 로고    scopus 로고
    • The structure of inosine 5'-monophosphate dehydrogenase and the design of novel inhibitors
    • Sintchak M.D., Nimmesgern E. (2000) The structure of inosine 5'-monophosphate dehydrogenase and the design of novel inhibitors. Immunopharmacology;47:163-184.
    • (2000) Immunopharmacology , vol.47 , pp. 163-184
    • Sintchak, M.D.1    Nimmesgern, E.2
  • 4
    • 0023697556 scopus 로고
    • Cloning and sequence analysis of the human and Chinese hamster inosine-5'-monophosphate dehydrogenase cDNAs
    • Collart F.R., Huberman E. (1988) Cloning and sequence analysis of the human and Chinese hamster inosine-5'-monophosphate dehydrogenase cDNAs. J Biol Chem;263:15769-15772.
    • (1988) J Biol Chem , vol.263 , pp. 15769-15772
    • Collart, F.R.1    Huberman, E.2
  • 7
    • 0027717956 scopus 로고
    • Characterization of human type I and type II IMP dehydrogenases
    • Carr S.F., Papp E., Wu J.C., Natsumeda Y. (1993) Characterization of human type I and type II IMP dehydrogenases. J Biol Chem;268:27286-27290.
    • (1993) J Biol Chem , vol.268 , pp. 27286-27290
    • Carr, S.F.1    Papp, E.2    Wu, J.C.3    Natsumeda, Y.4
  • 8
    • 0032775732 scopus 로고    scopus 로고
    • Consequences of IMP dehydrogenase inhibition, and its relationship to cancer and apoptosis
    • Jayaram H.N., Cooney D.A., Grusch M., Krupitza G. (1999) Consequences of IMP dehydrogenase inhibition, and its relationship to cancer and apoptosis. Curr Med Chem;6:561-574.
    • (1999) Curr Med Chem , vol.6 , pp. 561-574
    • Jayaram, H.N.1    Cooney, D.A.2    Grusch, M.3    Krupitza, G.4
  • 9
    • 0042190435 scopus 로고    scopus 로고
    • Targeted disruption of the inosine 5'-monophosphate dehydrogenase type I gene in mice
    • Gu J.J., Tolin A.K., Jain J., Huang H., Santiago L., Mitchell B.S. (2003) Targeted disruption of the inosine 5'-monophosphate dehydrogenase type I gene in mice. Mol Cell Biol;23:6702-6712.
    • (2003) Mol Cell Biol , vol.23 , pp. 6702-6712
    • Gu, J.J.1    Tolin, A.K.2    Jain, J.3    Huang, H.4    Santiago, L.5    Mitchell, B.S.6
  • 10
    • 0026687301 scopus 로고
    • New hypoxanthine nucleosides with RNA antiviral activity
    • Nair V., Ussery M.A. (1992) New hypoxanthine nucleosides with RNA antiviral activity. Antiviral Res;19:173-178.
    • (1992) Antiviral Res , vol.19 , pp. 173-178
    • Nair, V.1    Ussery, M.A.2
  • 11
    • 0029982866 scopus 로고    scopus 로고
    • IMP dehydrogenase as a target of antitumor and antiviral chemotherapy
    • Franchetti P., Cappellacci L., Grifantini M. (1996) IMP dehydrogenase as a target of antitumor and antiviral chemotherapy. Farmaco;51:457-469.
    • (1996) Farmaco , vol.51 , pp. 457-469
    • Franchetti, P.1    Cappellacci, L.2    Grifantini, M.3
  • 12
    • 0035040691 scopus 로고    scopus 로고
    • VX-497: a novel, selective IMPDH inhibitor and immunosuppressive agent
    • Jain J., Almquist S.J., Shlyakhter D., Harding M.W. (2001) VX-497: a novel, selective IMPDH inhibitor and immunosuppressive agent. J Pharm Sci;90:625-637.
    • (2001) J Pharm Sci , vol.90 , pp. 625-637
    • Jain, J.1    Almquist, S.J.2    Shlyakhter, D.3    Harding, M.W.4
  • 15
    • 33748604738 scopus 로고    scopus 로고
    • Inosine 5'-monophosphate dehydrogenase inhibitors for the treatment of autoimmune diseases
    • Ratcliffe A.J. (2006) Inosine 5'-monophosphate dehydrogenase inhibitors for the treatment of autoimmune diseases. Curr Opin Drug Discov Devel;9:595-605.
    • (2006) Curr Opin Drug Discov Devel , vol.9 , pp. 595-605
    • Ratcliffe, A.J.1
  • 16
    • 34447642328 scopus 로고    scopus 로고
    • Recent development of IMP dehydrogenase inhibitors for the treatment of cancer
    • Chen L., Pankiewicz K.W. (2007) Recent development of IMP dehydrogenase inhibitors for the treatment of cancer. Curr Opin Drug Discov Devel;10:403-412.
    • (2007) Curr Opin Drug Discov Devel , vol.10 , pp. 403-412
    • Chen, L.1    Pankiewicz, K.W.2
  • 17
    • 36849021519 scopus 로고    scopus 로고
    • Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery
    • Nair V., Shu Q. (2007) Inosine monophosphate dehydrogenase as a probe in antiviral drug discovery. Antivir Chem Chemother;18:245-258.
    • (2007) Antivir Chem Chemother , vol.18 , pp. 245-258
    • Nair, V.1    Shu, Q.2
  • 18
    • 39549088916 scopus 로고    scopus 로고
    • Inosine monophosphate dehydrogenase (IMPDH) as a target in drug discovery
    • Qingning S., Vasu N. (2008) Inosine monophosphate dehydrogenase (IMPDH) as a target in drug discovery. Med Res Rev;28:219-232.
    • (2008) Med Res Rev , vol.28 , pp. 219-232
    • Qingning, S.1    Vasu, N.2
  • 21
    • 0037161583 scopus 로고    scopus 로고
    • Discovery of N-[2-[2-[[3-Methoxy-4-(5-oxazolyl)phenyl]amino]-5-oxazolyl]phenyl]-N-methyl-4- morpholineacetamide as a novel and potent inhibitor of inosine monophosphate dehydrogenase with excellent in vivo activity
    • Dhar T.G., Shen Z., Guo J., Liu C., Watterson S.H., Gu H.H., Pitts W.J. (2002) Discovery of N-[2-[2-[[3-Methoxy-4-(5-oxazolyl)phenyl]amino]-5-oxazolyl]phenyl]-N-methyl-4- morpholineacetamide as a novel and potent inhibitor of inosine monophosphate dehydrogenase with excellent in vivo activity. Bioorg Med Chem Lett;45:2127-2130.
    • (2002) Bioorg Med Chem Lett , vol.45 , pp. 2127-2130
    • Dhar, T.G.1    Shen, Z.2    Guo, J.3    Liu, C.4    Watterson, S.H.5    Gu, H.H.6    Pitts, W.J.7
  • 28
    • 0037325577 scopus 로고    scopus 로고
    • Quinolone-based IMPDH inhibitors: introduction of basic residues on ring D and SAR of the corresponding mono, di and benzofused analogues
    • Dhar T.G., Watterson S.H., Chen P., Shen Z., Gu H.H., Norris D., Carlsen M. et al. (2003) Quinolone-based IMPDH inhibitors: introduction of basic residues on ring D and SAR of the corresponding mono, di and benzofused analogues. Bioorg Med Chem Lett;13:547-551.
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 547-551
    • Dhar, T.G.1    Watterson, S.H.2    Chen, P.3    Shen, Z.4    Gu, H.H.5    Norris, D.6    Carlsen, M.7
  • 37
    • 34547610513 scopus 로고    scopus 로고
    • Acridone-based inhibitors of inosine 5'-monophosphate dehydrogenase: discovery and SAR leading to the identification of N-(2-(6-(4-ethylpiperazin-1-yl)pyridin-3-yl)propan-2-yl)-2- fluoro-9-oxo-9,10-dihydroacridine-3-carboxamide (BMS-566419)
    • Watterson S.H., Chen P., Zhao Y., Gu H.H., Dhar T.G., Xiao Z., Ballentine S.K. (2007) Acridone-based inhibitors of inosine 5'-monophosphate dehydrogenase: discovery and SAR leading to the identification of N-(2-(6-(4-ethylpiperazin-1-yl)pyridin-3-yl)propan-2-yl)-2- fluoro-9-oxo-9, 10-dihydroacridine-3-carboxamide (BMS-566419). J Med Chem;50:3730-3742.
    • (2007) J Med Chem , vol.50 , pp. 3730-3742
    • Watterson, S.H.1    Chen, P.2    Zhao, Y.3    Gu, H.H.4    Dhar, T.G.5    Xiao, Z.6    Ballentine, S.K.7
  • 38
    • 84986522856 scopus 로고
    • Poling: promoting conformational variation
    • Smellie A., Teig S.L., Towbin P. (1995) Poling: promoting conformational variation. J Comput Chem;16:171-187.
    • (1995) J Comput Chem , vol.16 , pp. 171-187
    • Smellie, A.1    Teig, S.L.2    Towbin, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.