Cediranib

FOB Price
USD $280.00 / Piece
Place Of Origin
Hubei, China
Minimum Order
100
Packaging
Aluminum Foil Bags or Fiber Drum.
Delivery
15 Days
Top Quality Small Molecular API Cediranib
(CAS: 288383-20-0)

Chemical Information:
Product Name Cediranib
Molecular Formula C25H27FN4O3
Molecular Weight 450.51
Storage Store at -20°C
Targets VEGFR2/KDR c-Kit VEGFR3/FLT4 VEGFR1/FLT1 PDGFRβ
IC50 0.5 nM 2 nM ≤3 nM ≤3 nM 5 nM
Dosage 5 mg/kg
Stability
3 years - 20 ºC powder
6 months -80 ºC dissolved in a solvent
Solubility Soluble in DMSO > 10 mM
General tips For obtaining a higher solubility , please warm the tube at 37 ºC and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20ºC for several months.
Shipping Condition
Evaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request

Details:
Synonyms:Cediranib;4-(4-Fluoro-2-methylindol-5-yloxy)-6-methoxy-7-[3-(pyrrolidin-1-yl)propoxy]quinazoline;Cadiranib(AZD2171);Cediranib(AZD2171);AZD2171;Recentin;Cadiranib;Cediranib R
Description:Cediranib is a highly potent inhibitor of VEGFR with IC50 value of <1 nM.

Application:
Cediranib inhibition of bFGF and EGF when an IC50 of 0.5 and 0.11 μM. In the MG63 cell lines, Cediranib inhibiting PDGF-AA, IC50 of 0.04 μM. Cediranib Flt-1 associated kinase inhibition, IC50 of 5 nM, Cediranib inhibition of VEGF-C and VEGF-D receptor Flt-4, IC50 of less than 3 nM. [1] In addition, cediranib inhibition of c-Kit and PDGFR-β tyrosine kinase, IC50 were 2 and 5 nM. In vitro, micromolar concentrations cediranib can directly inhibit the proliferation of tumor cells. Sub nanomolar Cediranib blocking tubules produced, and inhibits VEGF-induced angiogenesis in vivo.
COA:
Item Specification
Specific rotation +39.5 to +41.5°
State of solution(transmittance) Clear 98.0% min.
Chloride[cl] 0.020% max.
Ammonium [NH4] 0.02% max.
Sulfate[SO4] 0.020% max
Iron[Fe] 10ppm max.
Heavy metals [Pb] 10ppm max
Arsenic[As2O3] 1ppm max
Other amino acids Chromatographically not detectable
Loss on drying 0.20% max.
Residue on ignition[sulfated] 0.10% max.
Assay 99.0% min
Notification:This compound is used only for research and not for human trials!
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FEATURED PRODUCT:
Wuhan Newbio Pharm-tech Co., Ltd.
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Cediranib (Cas No.288383-20-0)
Cediranib (Cas No.288383-20-0)

Cediranib (AZD2171) is a highly potent VEGFR(KDR) inhibitor with IC50 of <1 nM, also inhibits Flt1/4 with IC50 of 5 nM/≤3 nM, similar activity against c-Kit and PDGFRβ, 36-, 110-fold and >1000-fold selective more for VEGFR than PDGFR-α, CSF-1R and Flt3. ...

Shanghai Sun-shine bio-technology Co., Ltd