Ruxolitinib US FDA Label

  • Compound: (3R)-3-cyclopentyl-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)pyrazol-1-yl]propanenitrile
  • Description: Ruxolitinib is a pyrazole substituted at position 1 by a 2-cyano-1-cyclopentylethyl group and at position 3 by a pyrrolo[2,3-d]pyrimidin-4-yl group. Used as the phosphate salt for the treatment of patients with intermediate or high-risk myelofibrosis, including primary myelofibrosis, post-polycythemia vera myelofibrosis and post-essential thrombocythemia myelofibrosis. It has a role as an antineoplastic agent and an EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor. It is a nitrile, a pyrrolopyrimidine and a member of pyrazoles.

Identifiers (4)

  • International Nonproprietary Name: Ruxolitinib [INN] (Source: PubChem)
  • KEGG Drug ID: D09959 (Source: PubChem)
  • USFDA Precision ID: UNII-82S8X8XX8H (Source: PubChem)
  • US Adopted Name: RUXOLITINIB [USAN] (Source: PubChem)