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9
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more..
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10
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34248176943
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For a related series of selective erbB2 inhibitors, see also
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For a related series of selective erbB2 inhibitors, see also. Lippa B., Kauffman G.S., Arcari J., Kwan T., Chen J., Hungerford W., Bhattacharya S., Zhao X., Williams C., Xiao J., Pustilnik L., Su C., Moyer J.D., Ma L., Campbell M., and Steyn S. Bioorg. Med. Chem. Lett. 17 (2007) 3081
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11
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23944476133
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Ballard P., Bradbury R.H., Hennequin L.F.A., Hickinson D.M., Johnson P.D., Kettle J.G., Klinowska T., Morgentin R., Ogilvie D.J., and Olivier A. Bioorg. Med. Chem. Lett. 15 (2005) 4226
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9844235351
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16
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0034721142
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For a similar transformation, see:
-
For a similar transformation, see:. Ugarkar B.G., Castellino A.J., DaRe J.M., Kopcho J.J., Wiesner J.B., Schanzer J.M., and Erion M.D. J. Med. Chem. 43 (2000) 2894
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Schanzer, J.M.6
Erion, M.D.7
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17
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38849125669
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For experimental procedures and description of kinase and clone 24 assays, see: Barlaam, B.C., Ducray, R., Kettle, J.G. PCT Int. Appl. WO2006064196.
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For experimental procedures and description of kinase and clone 24 assays, see: Barlaam, B.C., Ducray, R., Kettle, J.G. PCT Int. Appl. WO2006064196.
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19
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38849169012
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note
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Replacement of the 2-pyridyl group in compound 12k by a 3-fluorophenyl led to a significant decrease of the unbound fraction in rat plasma (from 10% to 0.9% free drug).
-
-
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20
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38849086001
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note
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50 values of 5 in erbB2 and EGFR kinase inhibition assays are, respectively, 0.002 and 0.14 μM (see Ref. 8).
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