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Year | Number of Results |
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2002 | 2 |
2003 | 1 |
2004 | 1 |
2024 | 0 |
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Page 1
Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor.
Nat Struct Biol. 2002 Oct;9(10):745-9. doi: 10.1038/nsb842.
Nat Struct Biol. 2002.
PMID: 12244298
Probing the ATP ribose-binding domain of cyclin-dependent kinases 1 and 2 with O(6)-substituted guanine derivatives.
Gibson AE, Arris CE, Bentley J, Boyle FT, Curtin NJ, Davies TG, Endicott JA, Golding BT, Grant S, Griffin RJ, Jewsbury P, Johnson LN, Mesguiche V, Newell DR, Noble ME, Tucker JA, Whitfield HJ.
Gibson AE, et al. Among authors: whitfield hj.
J Med Chem. 2002 Aug 1;45(16):3381-93. doi: 10.1021/jm020056z.
J Med Chem. 2002.
PMID: 12139449
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N2-substituted O6-cyclohexylmethylguanine derivatives: potent inhibitors of cyclin-dependent kinases 1 and 2.
Hardcastle IR, Arris CE, Bentley J, Boyle FT, Chen Y, Curtin NJ, Endicott JA, Gibson AE, Golding BT, Griffin RJ, Jewsbury P, Menyerol J, Mesguiche V, Newell DR, Noble ME, Pratt DJ, Wang LZ, Whitfield HJ.
Hardcastle IR, et al. Among authors: whitfield hj.
J Med Chem. 2004 Jul 15;47(15):3710-22. doi: 10.1021/jm0311442.
J Med Chem. 2004.
PMID: 15239650
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Facilitation of addition-elimination reactions in pyrimidines and purines using trifluoroacetic acid in trifluoroethanol.
Whitfield HJ, Griffin RJ, Hardcastle IR, Henderson A, Meneyrol J, Mesguiche V, Sayle KL, Golding BT.
Whitfield HJ, et al.
Chem Commun (Camb). 2003 Nov 21;(22):2802-3. doi: 10.1039/b308948g.
Chem Commun (Camb). 2003.
PMID: 14651112
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