1oit: Difference between revisions

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==Overview==
==Overview==
High-throughput screening identified the imidazo[1,2-a]pyridine and, bisanilinopyrimidine series as inhibitors of the cyclin-dependent kinase, CDK4. Comparison of their experimentally-determined binding modes and, emerging structure-activity trends led to the development of potent and, selective imidazo[1,2-a]pyridine inhibitors for CDK4 and in particular, CDK2.
High-throughput screening identified the imidazo[1,2-a]pyridine and bisanilinopyrimidine series as inhibitors of the cyclin-dependent kinase CDK4. Comparison of their experimentally-determined binding modes and emerging structure-activity trends led to the development of potent and selective imidazo[1,2-a]pyridine inhibitors for CDK4 and in particular CDK2.


==About this Structure==
==About this Structure==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Transferred entry: 2.7.11.1]]
[[Category: Transferred entry: 2 7.11 1]]
[[Category: Beattie, J.F.]]
[[Category: Beattie, J F.]]
[[Category: Breault, G.A.]]
[[Category: Breault, G A.]]
[[Category: Byth, K.F.]]
[[Category: Byth, K F.]]
[[Category: Culshaw, J.D.]]
[[Category: Culshaw, J D.]]
[[Category: Ellston, R.P.A.]]
[[Category: Ellston, R P.A.]]
[[Category: Green, S.]]
[[Category: Green, S.]]
[[Category: Jewsbury, P.J.]]
[[Category: Jewsbury, P J.]]
[[Category: Minshull, C.A.]]
[[Category: Minshull, C A.]]
[[Category: Norman, R.A.]]
[[Category: Norman, R A.]]
[[Category: Pauptit, R.A.]]
[[Category: Pauptit, R A.]]
[[Category: Thomas, A.P.]]
[[Category: Thomas, A P.]]
[[Category: HDT]]
[[Category: HDT]]
[[Category: protein kinase]]
[[Category: protein kinase]]


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