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Famitinib
SKU
HY-108713-10 mg
Category Reference compound
Tags Apoptosis;PDGFR;VEGFR, Apoptosis;Protein Tyrosine Kinase/RTK, Cancer
$590 – $4,900
Products Details
Product Description
– Famitinib (SHR1020), an orally active multi-targeted kinase inhibitor, inhibits the activity of c-kit, VEGFR-2 and PDGFRβ with IC50 values of 2.3 nM, 4.7 nM and 6.6 nM, respectively[1]. Famitinib exerts powerful antitumor activity in human gastric cancer cells and xenografts. Famitinib triggers apoptosis[2].
Web ID
– HY-108713
Storage Temperature
– -20°C, 3 years; 4°C, 2 years (Powder)
Shipping
– Room Temperature
Applications
– Cancer-Kinase/protease
Molecular Formula
– C23H27FN4O2
References
– [1]Liguang Lou, et al. Abstract 3604: Preclinical antitumor study of famitinib, an orally available multi-targeted kinase inhibitor of VEGFR/PDGFR/c-Kit in phase I clinical trials.|[2]Sai Ge, et al. Famitinib exerted powerful antitumor activity in human gastric cancer cells and xenografts. Oncol Lett. 2016 Sep;12(3):1763-1768.
CAS Number
– 1044040-56-3
Molecular Weight
– 410.48
Compound Purity
– 98.43
SMILES
– O=C1C2=C(NC(/C=C3C(NC4=C3C=C(F)C=C4)=O)=C2C)CCN1CCN(CC)CC
Clinical Information
– Phase 3
Research Area
– Cancer
Solubility
– DMSO : 4.17 mg/mL (ultrasonic;warming;heat to 60°C)
Target
– Apoptosis;PDGFR;VEGFR
Isoform
– PDGFRβ;VEGFR2/KDR/Flk-1
Pathway
– Apoptosis;Protein Tyrosine Kinase/RTK
Product type
– Reference compound
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