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AttributesValues
rdf:type
rdfs:label
  • Crizotinib
rdfs:subClassOf
Concept_In_Subset
Semantic_Type
  • Pharmacologic Substance
Preferred_Name
  • Crizotinib
UMLS_CUI
  • C1957666
CAS_Registry
  • 877399-52-5
Accepted_Therapeutic_Use_For
  • Non-Small Cell Lung Cancer
FDA_UNII_Code
  • 53AH36668S
Contributing_Source
  • FDA
ALT_DEFINITION
  • A substance being studied in the treatment of some types of cancer. It blocks enzymes that cancer cells need to grow and spread. It may also prevent the growth of new blood vessels that tumors need to grow. It is a type of tyrosine kinase inhibitor and a type of antiangiogenesis agent.NCI-GLOSS
PDQ_Open_Trial_Search_ID
  • 586080
PDQ_Closed_Trial_Search_ID
  • 586080
Chemical_Formula
  • C21H22Cl2FN5O
Legacy_Concept_Name
  • MET_Tyrosine_Kinase_Inhibitor_PF-02341066
CHEBI_ID
  • CHEBI:64310
FULL_SYN
  • (R)-3-(1-(2,6-Dichloro-3-Fluorophenyl)Ethoxy)-5-(1-(Piperidin-4-Yl)-1h-Pyrazol-4-Yl)Pyridin-2-AmineSNNCI
  • MET tyrosine kinase inhibitor PF-02341066PTNCI-GLOSSCDR0000658849
  • 2-Pyridinamine, 3-((1R)-1-(2,6-Dichloro-3-Fluorophenyl)Ethoxy)-5-(1-(4-Piperidinyl)-1H-Pyrazol-4-yl)-SNNCI
  • XalkoriBRNCI
  • CRIZOTINIBPTFDA53AH36668S
  • MET Tyrosine Kinase Inhibitor PF-02341066SYNCI
  • PF-2341066CNNCI
  • PF-02341066PTNCI-GLOSSCDR0000658850
  • CrizotinibPTNCI
DEFINITION
  • An orally available aminopyridine-based inhibitor of the receptor tyrosine kinase anaplastic lymphoma kinase (ALK) and the c-Met/hepatocyte growth factor receptor (HGFR) with antineoplastic activity. Crizotinib, in an ATP-competitive manner, binds to and inhibits ALK kinase and ALK fusion proteins. In addition, crizotinib inhibits c-Met kinase, and disrupts the c-Met signaling pathway. Altogether, this agent inhibits tumor cell growth. ALK belongs to the insulin receptor superfamily and plays an important role in nervous system development. ALK dysregulation and gene rearrangements are associated with a series of tumors.NCI
code
  • C74061
sameAs
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