메뉴 건너뛰기




Volumn 43, Issue 15, 2000, Pages 2797-2804

Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles

Author keywords

[No Author keywords available]

Indexed keywords

2,6 DIAMINO 4 CYCLOHEXYLMETHOXY 5 NITROSOPYRIMIDINE; 2,6 DIAMINO 4 CYCLOHEXYLMETHYLOXY 5 NITROSOPYRIMIDINE; 6 O CYCLOHEXYLMETHYLGUANINE; CYCLIN DEPENDENT KINASE INHIBITOR; CYCLINE; FLAVOPIRIDOL; GUANINE; OLOMOUCINE; PROTEIN SERINE THREONINE KINASE; PURINE; PYRIMIDINE ANTAGONIST; UNCLASSIFIED DRUG;

EID: 0034721195     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm990628o     Document Type: Article
Times cited : (215)

References (46)
  • 1
    • 0029000579 scopus 로고
    • Cyclins and cyclin-dependent kinases: A biochemical view
    • Pines, J. Cyclins and cyclin-dependent kinases: A biochemical view. Biochem. J. 1995, 308, 697-711.
    • (1995) Biochem. J. , vol.308 , pp. 697-711
    • Pines, J.1
  • 2
    • 0030561285 scopus 로고    scopus 로고
    • Cell cycle control of replication initiation in eukaryotes
    • Chevalier, S.; Blow, J. J. Cell cycle control of replication initiation in eukaryotes. Curr. Opin. Cell Biol. 1996, 8, 815-821.
    • (1996) Curr. Opin. Cell Biol. , vol.8 , pp. 815-821
    • Chevalier, S.1    Blow, J.J.2
  • 3
    • 0031722249 scopus 로고    scopus 로고
    • Understanding the cell cycle
    • Nurse, P.; Masui, Y.; Hartwell, L. Understanding the cell cycle. Nature Med. 1998, 4, 1103-1106.
    • (1998) Nature Med. , vol.4 , pp. 1103-1106
    • Nurse, P.1    Masui, Y.2    Hartwell, L.3
  • 4
    • 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
  • 5
    • 0031466305 scopus 로고    scopus 로고
    • Cyclin-dependent kinases: Engines, clocks and microprocessors
    • Morgan, D. O. Cyclin-dependent kinases: Engines, Clocks and Microprocessors. Annu. Rev. Cell Dev. Biol. 1997, 13, 261-291.
    • (1997) Annu. Rev. Cell Dev. Biol. , vol.13 , pp. 261-291
    • Morgan, D.O.1
  • 6
    • 0029921317 scopus 로고    scopus 로고
    • Genetics alterations of cyclins, cyclin-dependent dependent kinases, and Cdk inhibitors in human cancer
    • Hall, M.; Peters, G. Genetics alterations of cyclins, cyclin-dependent dependent kinases, and Cdk inhibitors in human cancer. Adv. Cancer Res. 1996, 68, 67-108.
    • (1996) Adv. Cancer Res. , vol.68 , pp. 67-108
    • Hall, M.1    Peters, G.2
  • 8
    • 0031436243 scopus 로고    scopus 로고
    • Small-molecule inhibitors of cyclin-dependent kinases: Molecular tools and potential therapeutics
    • Walker, D. H. Small-molecule inhibitors of cyclin-dependent kinases: Molecular tools and potential therapeutics. Curr. Top. Microbiol. Immunol. 1998, 227, 149-165.
    • (1998) Curr. Top. Microbiol. Immunol. , vol.227 , pp. 149-165
    • Walker, D.H.1
  • 15
    • 0031725137 scopus 로고    scopus 로고
    • Flavopiridol mediates cell cycle arrest and apoptosis in esophageal cancer cells
    • Schrump, D. S.; Matthews, W.; Che, G. A.; Mixon, A.; Altorki, N. K. Flavopiridol mediates cell cycle arrest and apoptosis in esophageal cancer cells. Clin. Cancer. Res. 1998, 4, 2885-2890.
    • (1998) Clin. Cancer. Res. , vol.4 , pp. 2885-2890
    • Schrump, D.S.1    Matthews, W.2    Che, G.A.3    Mixon, A.4    Altorki, N.K.5
  • 22
    • 0032492705 scopus 로고    scopus 로고
    • Synthesis of C2 alkynylated purines, a new family of potent inhibitors of cyclin-dependent kinases
    • LeGraverend, M.; Ludwig, O.; Bisagni, E.; LeClerc, S.; Meijer, L. Synthesis of C2 alkynylated purines, a new family of potent inhibitors of cyclin-dependent kinases. Bioorg. Med. Chem. Lett. 1998, 8, 793-798.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 793-798
    • LeGraverend, M.1    Ludwig, O.2    Bisagni, E.3    LeClerc, S.4    Meijer, L.5
  • 23
  • 25
    • 0029090514 scopus 로고
    • Multiple modes of ligand recognition: Crystal structure of cyclin-dependent protein kinase 2 in complex with ATP and two inhibitors, olomoucine and isopentenyladenine
    • Schulze-Gahmen, U.; Brandsen, J.; Jones, H. D.; Morgan, D. O.; Meijer, L.; Vesely, J.; Kim, S.-H. Multiple modes of ligand recognition: Crystal structure of cyclin-dependent protein kinase 2 in complex with ATP and two inhibitors, olomoucine and isopentenyladenine. Proteins 1995, 22, 378-391.
    • (1995) Proteins , vol.22 , pp. 378-391
    • Schulze-Gahmen, U.1    Brandsen, J.2    Jones, H.D.3    Morgan, D.O.4    Meijer, L.5    Vesely, J.6    Kim, S.-H.7
  • 26
    • 0031028163 scopus 로고    scopus 로고
    • Inhibition of cyclin-dependent kinases by purine analogues. Crystal structure of human cdk2 complexed with roscovitine
    • de Azevedo, W. F., Jr.; LeClerc, S.; Meijer, L.; Havlicek, L.; Strnad, M.; Kim, S.-H. Inhibition of cyclin-dependent kinases by purine analogues. Crystal structure of human cdk2 complexed with roscovitine. Eur. J. Biochem. 1997, 243, 518-526.
    • (1997) Eur. J. Biochem. , vol.243 , pp. 518-526
    • De Azevedo W.F., Jr.1    LeClerc, S.2    Meijer, L.3    Havlicek, L.4    Strnad, M.5    Kim, S.-H.6
  • 28
    • 33748529352 scopus 로고    scopus 로고
    • Facilitation of displacements at the 6-position of purines by the use of 1,4-diazabicyclo[2,2,2]octane as leaving group
    • Lembicz, N. K.; Grant, S.; Clegg, W.; Griffin, R. J.; Heath, S. L.; Golding, B. T. Facilitation of displacements at the 6-position of purines by the use of 1,4-diazabicyclo[2,2,2]octane as leaving group. J. Chem. Soc., Perkin Trans, 1 1997, 185-186.
    • (1997) J. Chem. Soc., Perkin Trans, 1 , pp. 185-186
    • Lembicz, N.K.1    Grant, S.2    Clegg, W.3    Griffin, R.J.4    Heath, S.L.5    Golding, B.T.6
  • 29
    • 67649642917 scopus 로고
    • Synthesis of 2-amino-4-alkoxypteridine
    • Pfleiderer, W.; Lohrmann, R. Synthesis of 2-amino-4-alkoxypteridine. Chem. Ber. 1961, 94, 12-18.
    • (1961) Chem. Ber. , vol.94 , pp. 12-18
    • Pfleiderer, W.1    Lohrmann, R.2
  • 31
    • 0031253655 scopus 로고    scopus 로고
    • Protein kinase inhibition by staurosporine: Details of the molecular interaction determined by the X-ray crystallographic analysis of a CDK2-staurosporine complex
    • Lawrie, A. M.; Noble, M. E. M.; Tunnah, P.; Brown, N. R.; Johnson, L. N.; Endicott, J. A. Protein kinase inhibition by staurosporine: Details of the molecular interaction determined by the X-ray crystallographic analysis of a CDK2-staurosporine complex. Nature Struct. Biol. 1997, 4, 796-802.
    • (1997) Nature Struct. Biol. , vol.4 , pp. 796-802
    • Lawrie, A.M.1    Noble, M.E.M.2    Tunnah, P.3    Brown, N.R.4    Johnson, L.N.5    Endicott, J.A.6
  • 32
    • 0002452464 scopus 로고
    • Oscillation data reduction program
    • Sawyer, L., Isaacs, N., Bailey, S., Eds.; SERC Laboratory: Daresbury, Warrington, U.K.
    • Otwinowski, Z. Oscillation data reduction program. In DL/SC1/R34; Sawyer, L., Isaacs, N., Bailey, S., Eds.; SERC Laboratory: Daresbury, Warrington, U.K., 1993; pp 56-62.
    • (1993) DL/SC1/R34 , pp. 56-62
    • Otwinowski, Z.1
  • 33
    • 84889120137 scopus 로고
    • Improved method for building models in electron density maps and the location of errors in these models
    • Jones, T. A.; Zou, J. Y.; Cowan, S. W.; Kjeldgaard, M. Improved method for building models in electron density maps and the location of errors in these models. Acta Crystallogr. 1991, A47, 110-119.
    • (1991) Acta Crystallogr. , vol.A47 , pp. 110-119
    • Jones, T.A.1    Zou, J.Y.2    Cowan, S.W.3    Kjeldgaard, M.4
  • 34
  • 35
    • 0030924992 scopus 로고    scopus 로고
    • Refinement of macromolecular structures by the maximum-likelihood method
    • Murshudov, G. N.; Vagen, A. A.; Dodson, E. J. Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallogr. 1997, D53, 240-255.
    • (1997) Acta Crystallogr. , vol.D53 , pp. 240-255
    • Murshudov, G.N.1    Vagen, A.A.2    Dodson, E.J.3
  • 36
    • 0028103275 scopus 로고
    • The CCP4 suite: Programs for protein crystallography
    • Collaborative Computational Project, Number 4. The CCP4 suite: programs for protein crystallography. Acta Crystallogr. 1994, D50, 760-763.
    • (1994) Acta Crystallogr. , vol.D50 , pp. 760-763
  • 37
    • 0000127585 scopus 로고
    • Automated refinement of protein models
    • Lamzin, V. S.; Wilson, K. S. Automated refinement of protein models. Acta Crystallogr. 1993, D49, 129-147.
    • (1993) Acta Crystallogr. , vol.D49 , pp. 129-147
    • Lamzin, V.S.1    Wilson, K.S.2
  • 39
    • 0024312538 scopus 로고
    • Display and analysis of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm
    • Paull, K. D.; Shoemaker, R. H.; Hodes, L.; Monks, A.; Scudiero, D. A.; Rubinstein, L.; Plowman, J.; Boyd, M. R. Display and analysis of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm. JNCI, J. Natl. Cancer Inst. 1989, 81, 1088-1092.
    • (1989) JNCI, J. Natl. Cancer Inst. , vol.81 , pp. 1088-1092
    • Paull, K.D.1    Shoemaker, R.H.2    Hodes, L.3    Monks, A.4    Scudiero, D.A.5    Rubinstein, L.6    Plowman, J.7    Boyd, M.R.8
  • 43
    • 0029767016 scopus 로고    scopus 로고
    • Structural basis of cyclin-dependent kinase activation by phosphorylation
    • Russo, A.; Jeffrey, P. D.; Pavletich, N. P. Structural basis of cyclin-dependent kinase activation by phosphorylation. Nature Struct. Biol. 1996, 3, 696-700.
    • (1996) Nature Struct. Biol. , vol.3 , pp. 696-700
    • Russo, A.1    Jeffrey, P.D.2    Pavletich, N.P.3
  • 44
    • 0029116545 scopus 로고
    • Inactivation of Cdc2 increases the level of apoptosis induced by DNA damage
    • Ongkeko, W.; Ferguson, D. J. P.; Harris, A. L.; Norbury, C. Inactivation of Cdc2 increases the level of apoptosis induced by DNA damage. J. Cell Sci. 1995, 108, 2897-2904.
    • (1995) J. Cell Sci. , vol.108 , pp. 2897-2904
    • Ongkeko, W.1    Ferguson, D.J.P.2    Harris, A.L.3    Norbury, C.4
  • 45
    • 0001309005 scopus 로고
    • Molecular surface triangulation
    • Connolly, M. Molecular surface triangulation. J. Appl. Crystallogr. 1985, 18, 499-505.
    • (1985) J. Appl. Crystallogr. , vol.18 , pp. 499-505
    • Connolly, M.1
  • 46
    • 0000746745 scopus 로고    scopus 로고
    • Multivariate characterization of molecules for QSAR
    • Goodford, P. Multivariate characterization of molecules for QSAR. J. Chemom. 1996, 10, 107-117.
    • (1996) J. Chemom. , vol.10 , pp. 107-117
    • Goodford, P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.