FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Chemical: axitinib
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General Information
Name
axitinib
FlyBase ID
FBch0000413
ChEBI Name
axitinib
ChEBI ID
PubChem Name
Axitinib
PubChem ID
Chemical Structure
Chemical structure of axitinib
axitinib
InChIKey

RITAVMQDGBJQJZ-FMIVXFBMSA-N

Definition (ChEBI)

ChEBI: Axitinib is an indazole substituted at position 3 by a 2-(pyridin-2-yl)vinyl group and at position 6 by a 2-(N-methylaminocarboxy)phenylsulfanyl group. Used for the treatment of advanced renal cell carcinoma after failure of a first line systemic treatment. It has a role as an antineoplastic agent, a tyrosine kinase inhibitor and a vascular endothelial growth factor receptor antagonist. It is a member of indazoles, a member of pyridines, an aryl sulfide and a member of benzamides.NCI Thesaurus (NCIt): Axitinib is an orally bioavailable tyrosine kinase inhibitor. Axitinib inhibits the proangiogenic cytokines vascular endothelial growth factor (VEGF) and platelet-derived growth factor receptor (PDGF), thereby exerting an anti-angiogenic effect.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (24)
Synonyms
(E)-N-Methyl-2-((3-(2-(pyridin-2-yl)vinyl)-1H-indazol-6-yl)thio)benzamide
(e)-n-methyl-2-((3-(2-(pyridin-2-yl)vinyl)-1h-indazol-6-yl)thio)benzamide
319460-85-0
AG 013736
AG-13736
AG013736
C9LVQ0YUXG
N-methyl-2-({3-[(E)-2-(pyridin-2-yl)ethenyl]-1H-indazol-6-yl}sulfanyl)benzamide
N-methyl-2-({3-[(E)-2-(pyridin-2-yl)vinyl]-1H-indazol-6-yl}sulfanyl)benzamide
PubChem:6450551
UNII-C9LVQ0YUXG
ag 013736
ag-013736
ag-13736
ag013736
axitinibum
c9lvq0yuxg
pubchem:6450551
unii-c9lvq0yuxg
Secondary FlyBase IDs
    References (4)