A derivative of sorafenib
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CAY10773

Item No. 31806

Technical Information
Formal Name
N-(3,4-dichlorophenyl)-N′-[3-[(4-quinazolinylamino)methyl]phenyl]-urea
CAS Number
1648546-79-5
Molecular Formula
C22H17Cl2N5O
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 1 mg/mlDMSO: 1 mg/ml
λmax
264 nm
SMILES
O=C(NC1=CC=C(C(Cl)=C1)Cl)NC2=CC=CC(CNC3=C4C=CC=CC4=NC=N3)=C2O=C(NC1=CC=C(C(Cl)=C1)Cl)NC2=CC=CC(CNC3=C4C=CC=CC4=NC=N3)=C2
InChi Code
InChI=1S/C22H17Cl2N5O/c23-18-9-8-16(11-19(18)24)29-22(30)28-15-5-3-4-14(10-15)12-25-21-17-6-1-2-7-20(17)26-13-27-21/h1-11,13H,12H2,(H,25,26,27)(H2,28,29,30)
InChi Key
UFOVWAAXBJCADF-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    CAY10773 is a derivative of the ferroptosis inducer sorafenib (Item No. 10009644).1 It selectively inhibits proliferation of BEL-7402, MGC803, and T24 bladder cancer cells (IC50s = 5.77, 5.21 and 3.97 µM, respectively) over non-cancerous HCV-29 cells (IC50 = 23.19 µM). CAY10773 induces apoptosis in T24 cells when used at concentrations ranging from 2 to 6 µM but induces ferroptosis at concentrations greater than or equal to 6 µM with 10 hour or longer incubation times. It increases the production of reactive oxygen species (ROS) and decreases the mitochondrial membrane potential in T24 cells. CAY10773 (≥6 µM) also induces autophagy with incubation times longer than eight hours.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Chen, J.-N., Li, T., Cheng, L., et alSynthesis and in vitro anti-bladder cancer activity evaluation of quinazolinyl-arylurea derivatives. Eur. J. Med. Chem. 205, 112661 (2020).