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79953280504
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note
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3, THF, HOAc, rt, 16 h, 91% yield for two steps; (5) amide hydrolysis with 9N HCl, dioxane, reflux, 36 h, 73%.
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18
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0028099437
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J. Kitchin, R.C. Bethell, N. Cammack, S. Dolan, D.N. Evans, S. Holman, D.S. Holmes, P. McMeekin, C.L. Mo, N. Nieland, D.C. Orr, J. Saunders, B.E.V. Shenoy, I.D. Starkey, and R. Storert J. Med. Chem. 37 1994 3707
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41849092287
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For pyrrolo[2,3-d]pyrimidine Akt inhibitors with various PKA selectivity profiles see: J.J. Caldwell, T.G. Davies, A. Donald, T. McHardy, M.G. Rowlands, G.W. Aherne, L.K. Hunter, K. Taylor, R. Ruddle, F.I. Raynaud, M. Verdonk, P. Workman, M.D. Garrett, and I. Collins J. Med. Chem. 51 2008 2147
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B. Lippa, G. Pan, M. Corbett, C. Li, G.S. Kauffman, J. Pandit, S. Robinson, L. Wei, E. Kozina, E.S. Marr, G. Borzillo, E. Knauth, E.G. Barbacci-Tobin, P. Vincent, M. Troutman, D. Baker, F. Rajamohan, S. Kakar, T. Clark, and J. Morris Bioorg. Med. Chem. Lett. 18 2008 3359
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more..
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77949419584
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T. McHardy, J.J. Caldwell, K. Cheung, L.J. Hunter, K. Taylor, M. Rowlands, R. Ruddle, A. Henley, A. Brandon, H. De, M. Valenti, T.G. Davies, L. Fazal, L. Seavers, F.I. Raynaud, S.A. Eccles, G.W. Aherne, M.D. Garrett, and I. Collins J. Med. Chem. 53 2010 2239
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Eccles, S.A.16
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24
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77953758752
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K.D. Freeman-Cook, C. Autry, G. Borzillo, D. Gordon, E. Barbacci-Tobin, V. Bernardo, D. Briere, T. Clark, M. Corbett, J. Jakubczak, S. Kakar, E. Knauth, B. Lippa, M.J. Luzzio, M. Mansour, G. Martinelli, M. Marx, K. Nelson, J. Pandit, F. Rajamohan, S. Robinson, C. Subramanyam, L. Wei, M. Wythes, and J. Morris J. Med. Chem. 53 2010 4615
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Luzzio, M.J.14
Mansour, M.15
Martinelli, G.16
Marx, M.17
Nelson, K.18
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Rajamohan, F.20
Robinson, S.21
Subramanyam, C.22
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more..
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25
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79953285109
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Atomic co-ordinates of the structure 5 bound to Akt1 were deposited with the RCSB Protein Data Bank (PDB) under the accession code 3QKM
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Atomic co-ordinates of the structure 5 bound to Akt1 were deposited with the RCSB Protein Data Bank (PDB) under the accession code 3QKM.
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26
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79953291934
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Such a linkage was compatible with the conformation of compound 5 observed in the co-crystal structure with Akt1 (Fig. 3)
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Such a linkage was compatible with the conformation of compound 5 observed in the co-crystal structure with Akt1 (Fig. 3).
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