Sunitinib Malate

SKU: orb1310676

Description

Sunitinib Malate

Research Area

Cardiovascular Research, Cell Biology, Signal Transduction

Key Properties

• CAS Number: 341031-54-7
• MW: 532.56
• Purity: 99.26%
• Formula: C₂₆H₃₃FN₄O₇
• SMILES: O[C@@H](CC(O)=O)C(O)=O.CCN(CC)CCNC(=O)c1c(C)[nH]c(\C=C2/C(=O)Nc3ccc(F)cc23)c1C
• Target: IRE1,FLT,VEGFR,Mitophagy,PDGFR,Apoptosis,Autophagy,c-Kit
• Solubility: DMSO:15.47 mg/mL (29.05 mM);H2O:10 mg/mL (18.78 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:1 mg/mL (1.88 mM)

Bioactivity

• Target IC50:
  VEGFR2:80 nM (cell free)|PDGFRβ:2 nM (cell free)
• In Vivo:
  Sunitinib (80 mg/kg/day) inhibits the growth of established SF763T and Colo205 tumor xenografts in athymic mice. Sunitinib treatment effectively inhibits the growth of established tumor xenografts. Sunitinib malate is an inhibitor of VEGFR, PDGFR, FGFR, and is used in the treatment of advanced renal cell carcinoma and gastrointestinal stromal tumors. Sunitinib malate-treated rats display much lower levels of tumor growth than untreated rats, and their tumors have much smaller necrotic areas and lower vascular density
• In Vitro:
  Sunitinib is also a good inhibitor of KIT and FLT-3 . In biochemical assays, Sunitinib exhibits competitive inhibition (with regard to ATP) against Flk-1 and PDGFRβ with Ki values of 9 nM and 8 nM, respectively. Sunitinib is also a competitive, albeit less potent, an inhibitor of FGFR1 tyrosine kinase activity, with a Ki value of 0.83 μM. In these biochemical assays, the IC50 values for Sunitinib are generally at least 10-fold higher than those for Flk-1 and PDGFR (e.g., IC50s: >10 μM for EGFR and Cdk2; 4 μM for Met; 2.4 μM for IGFR-1; 0.8 μM for Abl; 0.6 μM for Src) . In RS4;11 cells (FLT3-WT), treatment with Sunitinib inhibits FLT3-WT phosphorylation in a dose-dependent manner with IC50 of approximately 250 nM. In MV4;11 cells that express FLT3-ITD, Sunitinib inhibits FLT3-ITD phosphorylation in a dose-dependent manner with an IC50 of 50 nM following a 2-hour treatment .
• Cell Research:
  RS4;11 and MV4;11 cell lines are starved overnight in medium containing 0.1% FBS prior to addition of Sunitinib (1-500 nM) and FL (50 ng/mL; FLT3-WT cells only). Proliferation is measured after 48 hours of culture using the Alamar Blue assay in triplicate for each condition, as described by the manufacturer. Trypan blue cell viability assays are performed in parallel and yielded similar results .
• Animal Research:
  Female nu/nu mice (8-12 weeks old, 25 g) are used. Briefly, 3-5×106 tumor cells are implanted s.c. into the hind flank region of mice on day 0. Daily treatment of tumor-bearing mice with oral administration of SU11248 as a carboxymethyl cellulose suspension or as citrate buffered (pH 3.5) solution is initiated once the tumors reached the indicated average size. Tumor growth is evaluated based on the twice-weekly measurement of tumor volume. Typically, studies are terminated when tumors in vehicle-treated animals reach an average size of 1000 mm3 or when the tumors are judged to adversely affect the well being of the animals .

Storage & Handling

• Storage: Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
• Expiration Date: 12 months from date of receipt.
• Disclaimer: For research use only

Alternative Names

cKit, Autophagy, Apoptosis, inhibit, Kit, IRE1, Mitophagy, Mitochondrial Autophagy, Platelet-derived growth factor receptor, FLT3, Inhibitor, Inositol requiring enzyme 1, SU 11248, SU 11248 (Malate), SU11248, SU-11248, Sunitinib, Sunitinib Malate, Sutent, PDGFRβ, PDGFR, VEGFR2, Vascular endothelial growth factor receptor, VEGFR

Compound Identifiers

PubChem CID

6456015