Dinaciclib (SCH-727965) is an experimental drug that inhibits cyclin-dependent kinases (CDKs).[1] It is being evaluated in clinical trials for various cancer indications.[2]
Dinaciclib is being developed by Merck & Co. It was granted orphan drug status by the FDA in 2011.[3]
^Parry D, Guzi T, Shanahan F, Davis N, Prabhavalkar D, Wiswell D, et al. (August 2010). "Dinaciclib (SCH 727965), a novel and potent cyclin-dependent kinase inhibitor". Molecular Cancer Therapeutics. 9 (8): 2344–2353. doi:10.1158/1535-7163.MCT-10-0324. PMID 20663931.
^Bose P, Simmons GL, Grant S (June 2013). "Cyclin-dependent kinase inhibitor therapy for hematologic malignancies". Expert Opinion on Investigational Drugs. 22 (6): 723–738. doi:10.1517/13543784.2013.789859. PMC 4039040. PMID 23647051.
^"Dinaciclib". AdisInsight. Springer Nature Switzerland AG. Retrieved 31 January 2017.
Dinaciclib (SCH-727965) is an experimental drug that inhibits cyclin-dependent kinases (CDKs). It is being evaluated in clinical trials for various cancer...
currently being evaluated in phase II trials for hepatocellular carcinoma. Dinaciclib- a pan-CDK inhibitor against CDK1, CDK2, CDK5, and CDK9. As of December...
Nathanson, K.L., Smalley, K.S.M., Herlyn, M.: The anti-melanoma activity of dinaciclib, a cyclin-dependent kinase inhibitor, is dependent on p53 signaling. PLoS...
cells with the PKC-specific inhibitor Gö-6983 or the pan-CDK inhibitor dinaciclib. These findings indicate, that site-specific phosphorylation mediated...