1032265-57-8

1032265-57-8 structure
1032265-57-8 structure
  • Name: tafetinib
  • Chemical Name: tafetinib
  • CAS Number: 1032265-57-8
  • Molecular Formula: C24H29FN4O2
  • Molecular Weight: 424.51
  • Catalog: Signaling Pathways Protein Tyrosine Kinase/RTK c-Kit
  • Create Date: 2023-11-25 22:25:38
  • Modify Date: 2024-01-27 14:55:38
  • Tafetinib (SIM010603) is an oral multi-targets receptor tyrosine kinases inhibitor. Tafetinib inhibitsstem cell factor receptor (Kit),vascular endothelial growth factor receptor-2 (VEGFR-2),platelet-derived growth factor receptor-β (PDGFR-β),glial cell line-derived neurotrophic factor receptor (Rearranged during Transfection; RET), andFms-like tyrosine kinase-3 (FLT3)withIC50values between 5.0 and 68.1 nmol/l. Tafetinib inhibits the phosphorylation ofPDGFR-βandVEGFR-2. Tafetinib inhibits endothelial cell proliferation, endothelial cells chemotaxis, and corneal angiogenesis[1].

Name tafetinib
Synonyms SIM-010603
SIM010603
Description Tafetinib (SIM010603) is an oral multi-targets receptor tyrosine kinases inhibitor. Tafetinib inhibitsstem cell factor receptor (Kit),vascular endothelial growth factor receptor-2 (VEGFR-2),platelet-derived growth factor receptor-β (PDGFR-β),glial cell line-derived neurotrophic factor receptor (Rearranged during Transfection; RET), andFms-like tyrosine kinase-3 (FLT3)withIC50values between 5.0 and 68.1 nmol/l. Tafetinib inhibits the phosphorylation ofPDGFR-βandVEGFR-2. Tafetinib inhibits endothelial cell proliferation, endothelial cells chemotaxis, and corneal angiogenesis[1].
Related Catalog
References

[1]. Wang D, et al. Preclinical anti-angiogenesis and anti-tumor activity of SIM010603, an oral, multi-targets receptor tyrosine kinases inhibitor. Cancer Chemother Pharmacol. 2012;69(1):173-183.  

Density 1.251±0.06 g/cm3(Predicted)
Boiling Point 618.2±55.0 °C(Predicted)
Molecular Formula C24H29FN4O2
Molecular Weight 424.51
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