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Volumn 56, Issue 4, 2013, Pages 1573-1582

Optimization of non-ATP competitive CDK/cyclin groove inhibitors through REPLACE-mediated fragment assembly

Author keywords

[No Author keywords available]

Indexed keywords

1 (3,5 DICHLOROPHENYL) 5 METHYL 1H 1,2,4 TRIAZOLE 3 CARBOXYLIC ACID; 1 (3,5 DICHLOROPHENYL) 5 METHYL 1H PYRAZOLE 3 CARBOXYLIC ACID; 1 (4 CHLOROPHENYL) 1H PYRROLE 3 CARBALDEHYDE; 1 (4 CHLOROPHENYL) 1H PYRROLE 3 CARBOXYLIC ACID; 2 (3 FLUOROPHENYL) 1H IMIDAZOLE 4 CARBOXYLIC ACID; 5 (3,5 DICHLOROPHENYL)FURAN 2 CARBOXYLIC ACID; CARBOXYLIC ACID DERIVATIVE; CYCLIN DEPENDENT KINASE 2; CYCLIN DEPENDENT KINASE 2 INHIBITOR; ETHYL 1 (3,5 DICHLOROPHENYL) 5 METHYL 1H 1,2,4 TRIAZOLE 3 CARBOXYLATE; ETHYL 1 (3,5 DICHLOROPHENYL) 5 METHYL 1H PYRAZOLE 3 CARBOXYLATE; ETHYL 2 (3 FLUOROPHENYL) 1H IMIDAZOLE 4 CARBOXYLATE; UNCLASSIFIED DRUG; [4 (3 CHLOROPHENOXY)PYRIDIN 2 YL]METHANAMINE;

EID: 84874607678     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm3013882     Document Type: Article
Times cited : (19)

References (24)
  • 1
    • 0029849620 scopus 로고    scopus 로고
    • Cancer cell cycles
    • Sherr, C. J. Cancer cell cycles Science 1996, 274, 1672-1677
    • (1996) Science , vol.274 , pp. 1672-1677
    • Sherr, C.J.1
  • 2
    • 0035754080 scopus 로고    scopus 로고
    • To cycle or not to cycle: A critical decision in cancer
    • Malumbres, M.; Barbacid, M. To cycle or not to cycle: a critical decision in cancer Nat. Rev. Cancer 2001, 1, 222-231 (Pubitemid 33741897)
    • (2001) Nature Reviews Cancer , vol.1 , Issue.3 , pp. 222-231
    • Malumbres, M.1    Barbacid, M.2
  • 4
    • 0036136668 scopus 로고    scopus 로고
    • Regulation of RNA polymerase II activity by CTD phosphorylation and cell cycle control
    • DOI 10.1002/jcp.10058
    • Oelgeschlager, T. Regulation of RNA polymerase II activity by CTD phosphorylation and cell cycle control J. Cell. Physiol. 2002, 190, 160-169 (Pubitemid 34027819)
    • (2002) Journal of Cellular Physiology , vol.190 , Issue.2 , pp. 160-169
    • Oelgeschlager, T.1
  • 5
    • 0036830109 scopus 로고    scopus 로고
    • WAF1-derived peptide inhibitors of CDK-mediated pRb phosphorylation: Delineation and structural insight into their interactions with cyclin A
    • DOI 10.1034/j.1399-3011.2002.21014.x
    • WAF1 derived peptide inhibitors of CDK-mediated pRb phosphorylation: delineation and structural insight into their interactions with cyclin A J. Pept. Res. 2002, 60, 257-270 (Pubitemid 35246787)
    • (2002) Journal of Peptide Research , vol.60 , Issue.5 , pp. 257-270
    • Zheleva, D.I.1    McInnes, C.2    Gavine, A.-L.3    Zhelev, N.Z.4    Fischer, P.M.5    Lane, D.P.6
  • 8
    • 0031025385 scopus 로고    scopus 로고
    • Cell-cycle arrest and inhibition of Cdk4 activity by small peptides based on the carboxy-terminal domain of p21(WAF1)
    • Ball, K. L.; Lain, S.; FaÌŠhraeus, R.; Smythe, C.; Lane, D. P. Cell-cycle arrest and inhibition of Cdk4 activity by small peptides based on the carboxy-terminal domain of p21WAF1 Curr. Biol. 1996, 7, 71-80 (Pubitemid 27058942)
    • (1997) Current Biology , vol.7 , Issue.1 , pp. 71-80
    • Ball, K.L.1    Lain, S.2    Fahraeus, R.3    Smythe, C.4    Lane, D.P.5
  • 9
    • 0037374549 scopus 로고    scopus 로고
    • Selective cyclin-dependent kinase 2/cyclin A antagonists that differ from ATP site inhibitors block tumor growth
    • Mendoza, N.; Fong, S.; Marsters, J.; Koeppen, H.; Schwall, R.; Wickramasinghe, D. Selective cyclin-dependent kinase 2/cyclin A antagonists that differ from ATP site inhibitors block tumor growth Cancer Res. 2003, 63, 1020-1024 (Pubitemid 36278433)
    • (2003) Cancer Research , vol.63 , Issue.5 , pp. 1020-1024
    • Mendoza, N.1    Fong, S.2    Marsters, J.3    Koeppen, H.4    Schwall, R.5    Wickramasinghe, D.6
  • 13
    • 84864871913 scopus 로고    scopus 로고
    • Targeting sub-cellular localization through the Polo-Box domain: Non-ATP competitive inhibitors recapitulate a PLK1phenotype
    • McInnes, C.; Estes, K.; Yang, Z.; Farag, D. B.; Johnson, P.; Lazo, J.; Michael, D. W. Targeting sub-cellular localization through the Polo-Box domain: non-ATP competitive inhibitors recapitulate a PLK1phenotype Mol. Cancer Ther. 2012, 8, 1683-1692
    • (2012) Mol. Cancer Ther. , vol.8 , pp. 1683-1692
    • McInnes, C.1    Estes, K.2    Yang, Z.3    Farag, D.B.4    Johnson, P.5    Lazo, J.6    Michael, D.W.7
  • 15
    • 80955177192 scopus 로고    scopus 로고
    • An effective nitrilimine cycloaddition for the synthesis of 1,3,5-trisubstituted 1,2,4-triazoles from oximes with hydrazonoyl hydrochlorides
    • Wang, L.-Y.; Tseng, W.-C.; Lin, H-Y.; Wong, F. F. An effective nitrilimine cycloaddition for the synthesis of 1,3,5-trisubstituted 1,2,4-triazoles from oximes with hydrazonoyl hydrochlorides Synlett 2011, 10, 1467-1471
    • (2011) Synlett , vol.10 , pp. 1467-1471
    • Wang, L.-Y.1    Tseng, W.-C.2    Lin, H.-Y.3    Wong, F.F.4
  • 18
    • 1542284725 scopus 로고    scopus 로고
    • Synthesis and in vitro antimycobacterial activity of novel 3-(1H-pyrrol-1-yl)-2-oxazolidinone analogues of PNU-100480
    • DOI 10.1016/j.bmcl.2004.01.010, PII S0960894X04000435
    • Sbardella, G.; Mai, A.; Artico, M.; Loddo, R.; Setzu, M. G.; La Colla, P. Synthesis and in vitro antimycobacterial activity of novel 3-(1 H -pyrrol-1-yl)-2-oxazolidinone analogues of PNU-100480 Bioorg. Med. Chem. Lett. 2004, 14, 1537-1541 (Pubitemid 38299445)
    • (2004) Bioorganic and Medicinal Chemistry Letters , vol.14 , Issue.6 , pp. 1537-1541
    • Sbardella, G.1    Mai, A.2    Artico, M.3    Loddo, R.4    Setzu, M.G.5    La Colla, P.6
  • 19
    • 0022379946 scopus 로고
    • Imidazo[1,5-d][1,2,4]triazines as potential antiasthma agents
    • DOI 10.1021/jm00149a029
    • Paul, R.; Brockman, J. A.; Hallett, W. A.; Hanifin, J. W.; Tarrant, M. E.; Torley, L. W.; Callahan, F. M.; Fabio, P. F.; Johnson, B. D.; Lenhard, R. H.; Schaub, R. E.; Wissner, A. Imidazo[ 1,5-d][ 1,2,4]triazines as Potential Antiasthma Agents J. Med. Chem. 1985, 28, 1704-1716 (Pubitemid 16204842)
    • (1985) Journal of Medicinal Chemistry , vol.28 , Issue.11 , pp. 1704-1716
    • Paul, R.1    Brockman, J.A.2    Hallett, W.A.3
  • 20
    • 78650562602 scopus 로고    scopus 로고
    • Structural and functional analysis of cyclin D1 reveals p27 and substrate inhibitor binding requirements
    • Liu, S.; Bolger, J. K.; Kirkland, L. O.; Premnath, P. N.; McInnes, C. Structural and functional analysis of cyclin D1 reveals p27 and substrate inhibitor binding requirements ACS Chem. Biol. 2010, 5, 1169-1182
    • (2010) ACS Chem. Biol. , vol.5 , pp. 1169-1182
    • Liu, S.1    Bolger, J.K.2    Kirkland, L.O.3    Premnath, P.N.4    McInnes, C.5
  • 21
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • DOI 10.1016/S0169-409X(96)00423-1, PII S0169409X96004231
    • Lipinski, C. A.; Lombardo, F.; Dominy, B. W.; Feeney, P. J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv. Drug Delivery Rev. 1997, 23, 3-25 (Pubitemid 27046991)
    • (1997) Advanced Drug Delivery Reviews , vol.23 , Issue.1-3 , pp. 3-25
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 22
    • 0032600640 scopus 로고    scopus 로고
    • A knowledge-based approach in designing combinatorial or medicinal chemistry libraries for drug discovery. 1. A qualitative and quantitative characterization of known drug databases
    • Ghose, A. K.; Viswanadhan, V. N.; Wendoloski, J. J. A knowledge-based approach in designing combinatorial or medicinal chemistry libraries for drug discovery. 1. A qualitative and quantitative characterization of known drug databases J. Comb. Chem. 1999, 1, 55-68
    • (1999) J. Comb. Chem. , vol.1 , pp. 55-68
    • Ghose, A.K.1    Viswanadhan, V.N.2    Wendoloski, J.J.3
  • 23
    • 67749106463 scopus 로고    scopus 로고
    • Truncation and optimization of peptide inhibitors of cyclin-dependent kinase 2-cyclin a through structure-guided design
    • Kontopidis, G.; Andrews, M. J.; McInnes, C.; Plater, A.; Innes, L.; Renachowski, S.; Cowan, A.; Fischer, P. M. Truncation and optimization of peptide inhibitors of cyclin-dependent kinase 2-cyclin a through structure-guided design ChemMedChem 2009, 4, 1120-1128
    • (2009) ChemMedChem , vol.4 , pp. 1120-1128
    • Kontopidis, G.1    Andrews, M.J.2    McInnes, C.3    Plater, A.4    Innes, L.5    Renachowski, S.6    Cowan, A.7    Fischer, P.M.8
  • 24
    • 6344240541 scopus 로고    scopus 로고
    • Design, synthesis, biological activity and structural analysis of cyclic peptide inhibitors targeting the substrate recruitment site of cyclin-dependent kinase complexes
    • Andrews, M. J.; McInnes, C.; Kontopidis, G.; Innes, L.; Cowan, A.; Plater, A.; Fischer, P. M. Design, synthesis, biological activity and structural analysis of cyclic peptide inhibitors targeting the substrate recruitment site of cyclin-dependent kinase complexes Org. Biomol. Chem. 2004, 2, 2735-2741
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 2735-2741
    • Andrews, M.J.1    McInnes, C.2    Kontopidis, G.3    Innes, L.4    Cowan, A.5    Plater, A.6    Fischer, P.M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.