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. 2011 Nov 23;3(4):4170–4190. doi: 10.3390/cancers3044170

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© 2011 by the authors; licensee MDPI, Basel, Switzerland.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).

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Figure 4. — CDK inhibitors. Structures of (a) DRB, (b) flavopiridol, (c) seliciclib (d) SNS-032, (e) dinaciclib, (f) R547, (g) AT8319, (h) P276-00, (i) ARC, and (j) RGB 286638.