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Dinaciclib information


Dinaciclib
Clinical data
Other namesSCH-727965
Legal status
Legal status
  • Investigational
Identifiers
IUPAC name
  • (S)-3-(((3-Ethyl-5-(2-(2-hydroxyethyl)piperidin-1-yl)pyrazolo[1,5-a]pyrimidin-7-yl)amino)methyl)pyridine 1-oxide
CAS Number
  • 779353-01-4
PubChem CID
  • 46926350
IUPHAR/BPS
  • 7379
ChemSpider
  • 25027387
UNII
  • 4V8ECV0NBQ
KEGG
  • D09604
ChEMBL
  • ChEMBL2103840
PDB ligand
  • 1QK (PDBe, RCSB PDB)
CompTox Dashboard (EPA)
  • DTXSID90999131 Edit this at Wikidata
ECHA InfoCard100.246.885 Edit this at Wikidata
Chemical and physical data
FormulaC21H28N6O2
Molar mass396.495 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • CCC1=C2N=C(C=C(N2N=C1)NCC3=C[N+](=CC=C3)[O-])N4CCCC[C@H]4CCO
InChI
  • InChI=1S/C21H28N6O2/c1-2-17-14-23-27-19(22-13-16-6-5-9-25(29)15-16)12-20(24-21(17)27)26-10-4-3-7-18(26)8-11-28/h5-6,9,12,14-15,18,22,28H,2-4,7-8,10-11,13H2,1H3/t18-/m0/s1
  • Key:PIMQWRZWLQKKBJ-SFHVURJKSA-N

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]

  1. ^ 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.
  2. ^ 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.
  3. ^ "Dinaciclib". AdisInsight. Springer Nature Switzerland AG. Retrieved 31 January 2017.

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