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Volumn 47, Issue 15, 2004, Pages 3710-3722

N2-substituted O6-cyclohexylmethylguanine derivatives: Potent inhibitors of cyclin-dependent kinases 1 and 2

Author keywords

[No Author keywords available]

Indexed keywords

4 (6 CYCLOHEXYLMETHOXY 2 YLAMINO) N METHYLBENZENESULFONAMIDE; 4 (6 CYCLOHEXYLMETHOXY 9H PURIN 2 YLAMINO)BENZAMIDE; 6 CYCLOHEXYLMETHOXY 2 (4 SULFAMOYLANILINO)PURINE; 6 CYCLOHEXYLMETHOXY 2 (4' HYDROXYANILINO)PURINE; 6 CYCLOHEXYLMETHOXY 2 (4' SULFAMOYLANILINO)PURINE; 6 O CYCLOHEXYLMETHYLGUANINE; 6 O CYCLOHEXYLMETHYLGUANINE DERIVATIVE; 6 O METHYLGUANINE; ADENOSINE TRIPHOSPHATE; AMIDE; CYCLIN A; CYCLIN A3; CYCLIN B; CYCLIN DEPENDENT KINASE 1; CYCLIN DEPENDENT KINASE 1 INHIBITOR; CYCLIN DEPENDENT KINASE 2; CYCLIN DEPENDENT KINASE 2 INHIBITOR; CYCLIN DEPENDENT KINASE INHIBITOR; SULFONAMIDE; UNCLASSIFIED DRUG; CDK2 PROTEIN, HUMAN; CYCLIN DEPENDENT KINASE; CYCLOHEXANE DERIVATIVE; DRUG DERIVATIVE; GUANINE; PURINE DERIVATIVE;

EID: 3142580855     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm0311442     Document Type: Article
Times cited : (120)

References (55)
  • 1
    • 0026693966 scopus 로고
    • Animal cell-cycles and their control
    • Norbury, C.; Nurse, P. A. Animal cell-cycles and their control. Annu. Rev. Biochem. 1992, 61, 441-470.
    • (1992) Annu. Rev. Biochem. , vol.61 , pp. 441-470
    • Norbury, C.1    Nurse, P.A.2
  • 2
    • 0028931265 scopus 로고
    • Principles of CDK regulation
    • Morgan, D. O. Principles of CDK regulation. Nature 1995, 374, 131-134.
    • (1995) Nature , vol.374 , pp. 131-134
    • Morgan, D.O.1
  • 3
    • 0033564697 scopus 로고    scopus 로고
    • CDK inhibitors: Positive and negative regulators of G1-phase progression
    • Sherr, C. J.; Roberts, J. M. CDK inhibitors: positive and negative regulators of G1-phase progression. Genes Dev. 1999, 13, 1501-1512.
    • (1999) Genes Dev. , vol.13 , pp. 1501-1512
    • Sherr, C.J.1    Roberts, J.M.2
  • 4
    • 0029921317 scopus 로고    scopus 로고
    • Genetic alterations of cyclins, cyclin-dependent kinases, and CDK inhibitors in human cancer
    • Hall, M.; Peters, G. Genetic alterations of cyclins, cyclin-dependent kinases, and CDK inhibitors in human cancer. Adv. Cancer Res. 68, 1996, 67-108.
    • (1996) Adv. Cancer Res. , vol.68 , pp. 67-108
    • Hall, M.1    Peters, G.2
  • 6
    • 0034642532 scopus 로고    scopus 로고
    • Cyclin-dependent Kinase inhibitors: Useful targets in cell cycle regulation
    • Sielecki, T. M.; Boylan, J. F.; Benfield, P. A.; Trainor, G. L. Cyclin-dependent Kinase inhibitors: Useful targets in cell cycle regulation. J. Med. Chem. 2000, 43, 1-18.
    • (2000) J. Med. Chem. , vol.43 , pp. 1-18
    • Sielecki, T.M.1    Boylan, J.F.2    Benfield, P.A.3    Trainor, G.L.4
  • 8
    • 0036710767 scopus 로고    scopus 로고
    • Pharmacological inhibitors of cyclin-dependent kinases
    • Knockaert, M.; Greegard, P.; Meijer, L. Pharmacological inhibitors of cyclin-dependent kinases. Trends Pharmacol. Sci. 2002, 23, 417-425.
    • (2002) Trends Pharmacol. Sci. , vol.23 , pp. 417-425
    • Knockaert, M.1    Greegard, P.2    Meijer, L.3
  • 9
    • 0036679627 scopus 로고    scopus 로고
    • Progress toward the development of agents to modulate the cell cycle
    • Toogood, P. L. Progress toward the development of agents to modulate the cell cycle. Curr. Opin. Chem. Biol. 2002, 6, 472-478.
    • (2002) Curr. Opin. Chem. Biol. , vol.6 , pp. 472-478
    • Toogood, P.L.1
  • 10
    • 0034040974 scopus 로고    scopus 로고
    • UCN-01 (7-hydroxystaurosporine) and other indolocarbazole compounds: A new generation of anti-cancer agents for the new century?
    • Akinaga, S.; Sugiyama, K.; Akiyama, T. UCN-01 (7-hydroxystaurosporine) and other indolocarbazole compounds: a new generation of anti-cancer agents for the new century? Anti-Cancer Drug Des. 2000, 15, 43-52.
    • (2000) Anti-Cancer Drug Des. , vol.15 , pp. 43-52
    • Akinaga, S.1    Sugiyama, K.2    Akiyama, T.3
  • 15
    • 0037665145 scopus 로고    scopus 로고
    • Roscovitine and other purines as kinase inhibitors. From starfish oocytes to clinical trials
    • in press
    • Meijer, L.; Raymond, E. Roscovitine and other purines as kinase inhibitors. From starfish oocytes to clinical trials. Acc. Chem. Res. 2003, in press.
    • (2003) Acc. Chem. Res.
    • Meijer, L.1    Raymond, E.2
  • 17
  • 18
    • 0034611620 scopus 로고    scopus 로고
    • Cyclin-dependent kinase inhibition by new C-2 alkynylated purine derivatives and molecular structure of a CDK2-inhibitor complex
    • Legraverend, M.; Tunnah, P.; Noble, M.; Ducrot, M.; Ludwig, O.; Grierson, D. S.; Leost, M.; Meijer, L.; Endicott, J. Cyclin-dependent kinase inhibition by new C-2 alkynylated purine derivatives and molecular structure of a CDK2-inhibitor complex. J. Med. Chem. 2000, 43, 1282-1292.
    • (2000) J. Med. Chem. , vol.43 , pp. 1282-1292
    • Legraverend, M.1    Tunnah, P.2    Noble, M.3    Ducrot, M.4    Ludwig, O.5    Grierson, D.S.6    Leost, M.7    Meijer, L.8    Endicott, J.9
  • 22
    • 0034434429 scopus 로고    scopus 로고
    • Imidazo 2,1-b thiazolylmethylene- and indolylmethylene-2-indolinones: A new class of cyclin-dependent kinase inhibitors. Design, synthesis, and CDK1/cyclin B inhibition
    • Andreani, A.; Cavalli, A.; Granaiola, M.; Leoni, A.; Locatelli, A.; Morigi, R.; Rambaldi, M.; Recanatini, M.; Garnier, M.; Meijer, L. Imidazo 2,1-b thiazolylmethylene- and indolylmethylene-2-indolinones: a new class of cyclin-dependent kinase inhibitors. Design, synthesis, and CDK1/cyclin B inhibition. Anti-Cancer Drug Des. 2000, 15, 447-452.
    • (2000) Anti-Cancer Drug Des. , vol.15 , pp. 447-452
    • Andreani, A.1    Cavalli, A.2    Granaiola, M.3    Leoni, A.4    Locatelli, A.5    Morigi, R.6    Rambaldi, M.7    Recanatini, M.8    Garnier, M.9    Meijer, L.10
  • 25
    • 0034642482 scopus 로고    scopus 로고
    • Binding mode of the 4-anilinoquinazoline class of protein kinase inhibitors: X-ray crystallographic studies of 4-anilinoquinazolinones bound to cyclin-dependent kinase 2 and p38 kinase
    • Shewchuk, L.; Hassell, A.; Wisely, B.; Rocque, W.; Holmes, W.; Veal, J.; Kuyper, L. F. Binding mode of the 4-anilinoquinazoline class of protein kinase inhibitors: X-ray crystallographic studies of 4-anilinoquinazolinones bound to cyclin-dependent kinase 2 and p38 kinase. J. Med. Chem. 2000, 43, 133-138.
    • (2000) J. Med. Chem. , vol.43 , pp. 133-138
    • Shewchuk, L.1    Hassell, A.2    Wisely, B.3    Rocque, W.4    Holmes, W.5    Veal, J.6    Kuyper, L.F.7
  • 28
    • 3142565941 scopus 로고    scopus 로고
    • Structure-based design and protein X-ray analysis of a protein kinase inhibitor
    • Furet, P.; Meyer, T.; Strauss, A.; Raccuglia, S.; Rondeau, J. M. Structure-based design and protein X-ray analysis of a protein kinase inhibitor. Bioorg. Med. Chem. Lett. 2001, 11, 1157-1160.
    • (2001) Bioorg. Med. Chem. Lett. , vol.11 , pp. 1157-1160
    • Furet, P.1    Meyer, T.2    Strauss, A.3    Raccuglia, S.4    Rondeau, J.M.5
  • 33
    • 0037194619 scopus 로고    scopus 로고
    • Discovery of aminothiazole inhibitors of cyclin-dependent kinase 2: Synthesis, X-ray crystallographic analysis, and biological activities
    • Kim, K. S.; Kimball, S. D.; Misra, R. N.; Rawlins, D. B.; Hunt, J. T. et al. Discovery of aminothiazole inhibitors of cyclin-dependent kinase 2: Synthesis, X-ray crystallographic analysis, and biological activities. J. Med. Chem. 2002, 45, 3905-3927.
    • (2002) J. Med. Chem. , vol.45 , pp. 3905-3927
    • Kim, K.S.1    Kimball, S.D.2    Misra, R.N.3    Rawlins, D.B.4    Hunt, J.T.5
  • 35
    • 0037468466 scopus 로고    scopus 로고
    • Evaluation of the first cytostatically active 1-aza-9-oxofluorenes as novel selective CDK1 inhibitors with P-glycoprotein modulating properties
    • Brachwitz, K.; Voigt, B.; Meijer, L.; Lozach, O.; Schachtele, C.; Molnar, J.; Hilgeroth, A. Evaluation of the first cytostatically active 1-aza-9-oxofluorenes as novel selective CDK1 inhibitors with P-glycoprotein modulating properties. J. Med. Chem. 2003, 46, 876-879.
    • (2003) J. Med. Chem. , vol.46 , pp. 876-879
    • Brachwitz, K.1    Voigt, B.2    Meijer, L.3    Lozach, O.4    Schachtele, C.5    Molnar, J.6    Hilgeroth, A.7
  • 39
    • 0034089542 scopus 로고    scopus 로고
    • Structure-based design modifications of the paullone molecular scaffold for cyclin-dependent kinase inhibition
    • Gussio, R. Structure-based design modifications of the paullone molecular scaffold for cyclin-dependent kinase inhibition. Anti-cancer Drug. Des. 2000, 15, 53-66.
    • (2000) Anti-Cancer Drug. Des. , vol.15 , pp. 53-66
    • Gussio, R.1
  • 40
    • 0034162636 scopus 로고    scopus 로고
    • Preclinical and clinical development of cyclin-dependent kinase modulators
    • Senderowicz, A. M.; Sausville, E. A. Preclinical and clinical development of cyclin-dependent kinase modulators. J. Natl. Cancer Inst. 2000, 92, 376-387.
    • (2000) J. Natl. Cancer Inst. , vol.92 , pp. 376-387
    • Senderowicz, A.M.1    Sausville, E.A.2
  • 41
    • 0036220822 scopus 로고    scopus 로고
    • Complexities in the development of cyclin-dependent kinase inhibitor drugs
    • Sausville, E. A. Complexities in the development of cyclin-dependent kinase inhibitor drugs. Trends Mol. Med. 2002, 8 (Suppl. 4), S32-S37.
    • (2002) Trends Mol. Med. , vol.8 , Issue.SUPPL. 4
    • Sausville, E.A.1
  • 44
    • 3142614563 scopus 로고
    • Anomalous halogen to dimethylamino replacement with N,N-dimethylformamide catalyzed by ethylenediamine or 2-aminoethanol
    • Yamamoto, H. Anomalous halogen to dimethylamino replacement with N,N-dimethylformamide catalyzed by ethylenediamine or 2-aminoethanol. Bull. Chem. Soc. Jpn. 1982, 55, 2685-2686.
    • (1982) Bull. Chem. Soc. Jpn. , vol.55 , pp. 2685-2686
    • Yamamoto, H.1
  • 50
    • 0002454081 scopus 로고
    • Science and Engineering Research Council UK: Daresbury Laboratory, Warrington
    • Evans, P. R. Data Reduction; Science and Engineering Research Council UK: Daresbury Laboratory, Warrington, 1993; pp 114-122.
    • (1993) Data Reduction , pp. 114-122
    • Evans, P.R.1
  • 51
    • 0028103275 scopus 로고
    • CCP4 the CCP4 Suite: Programs for Protein Crystallography
    • CCP4 The CCP4 Suite: Programs for Protein Crystallography. Acta Crystallogr., Sect. D: Biol. Crystallogr. 1994, 50, 760-763.
    • (1994) Acta Crystallogr., Sect. D: Biol. Crystallogr. , vol.50 , pp. 760-763
  • 54
    • 84889120137 scopus 로고
    • Kjeldgaard Improved methods for binding protein models in electron density maps and the location of errors in these models
    • Jones, T. A.; Zou, J. Y.; Cowan, S. W. Kjeldgaard Improved methods for binding protein models in electron density maps and the location of errors in these models. Acta Crystallogr., Sect. A: Found. Crystallogr. 1991, 47, 110-119.
    • (1991) Acta Crystallogr., Sect. A: Found. Crystallogr. , vol.47 , pp. 110-119
    • Jones, T.A.1    Zou, J.Y.2    Cowan, S.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.