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Cyclacel Limited

Contact Details:
Address:James Lindsay Place
Dundee Scotland
Postcode:DD1 5JJ
Country:UK

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Recent Publications by Cyclacel Limited:

Discovery and characterization of 2-anilino-4- (thiazol-5-yl)pyrimidine transcriptional CDK inhibitors as anticancer agents.
The main difficulty in the development of ATP antagonist kinase inhibitors...
Cyclacel Limited, Dundee DD15JJ, Scotland, UK. Chem Biol. 2010 Oct 29;17(10):1111-21.
DOI Direct Link
REPLACE: a strategy for iterative design of cyclin-binding groove inhibitors.
We describe a drug-design strategy termed REPLACE (REplacement with...
Cyclacel Limited, James Lindsay Place, Dundee, DD1 5JJ, UK. Chembiochem. 2006 Dec;7(12):1909-15.
DOI Direct Link
Recent progress in the discovery and development of cyclin-dependent kinase inhibitors.
Cyclin-dependent kinases (CDKs) have long been known to be the main...
Cyclacel Limited, James Lindsay Place, Dundee DD1 5JJ, Scotland, UK. Expert Opin Investig Drugs. 2005 Apr;14(4):457-77.
DOI Direct Link
Synthesis and biological activity of conjugates between paclitaxel and the cell delivery vector penetratin.
Synthesis of paclitaxel-penetratin (pAntp) constructs, in which the 2'- or...
Cyclacel Limited, James Lindsay Place, Dundee DD1 5JJ, Scotland, UK. Bioorg Med Chem Lett. 2006 May 15;16(10):2628-31. Epub 2006 Mar 2.
DOI Direct Link
Design, synthesis, biological activity and structural analysis of cyclic peptide inhibitors targeting the substrate recruitment site of cyclin-dependent kinase complexes.
Inhibition of cyclin A- and cyclin E-associated cyclin-dependent kinase-2...
Cyclacel Limited, James Lindsay Place, Dundee, Scotland, UK. Org Biomol Chem. 2004 Oct 7;2(19):2735-41. Epub 2004 Sep 9.
DOI Direct Link

Cyclacel Limited Patents:

US Patent No.Title
7902361 Pyrimidin-4-yl-3, 4-thione compounds and their use in therapy
6992169 Carrier based drug delivery system
6972198 Methods and compositions using protein binding partners
6972182 Methods and compositions using coiled binding partners
6962792 Methods and means for inhibition of Cdk4 activity