A ferroptosis inducer
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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BCP-T.A.

Item No. 37659

Technical Information
Formal Name
[4-[bis(4-chlorophenyl)methyl]-1-piperazinyl](2-ethynyl-4-thiazolyl)-methanone
CAS Number
2786829-70-5
Purity
≥98%
A solid
DMF: 3 mg/mlDMSO: 10 mg/mlEthanol: 12 mg/ml
SMILES
O=C(N1CCN(C(C2=CC=C(C=C2)Cl)C3=CC=C(C=C3)Cl)CC1)C4=CSC(C#C)=N4
InChi Code
InChI=1S/C23H19Cl2N3OS/c1-2-21-26-20(15-30-21)23(29)28-13-11-27(12-14-28)22(16-3-7-18(24)8-4-16)17-5-9-19(25)10-6-17/h1,3-10,15,22H,11-14H2
InChi Key
XWHYWEHRTWXUFV-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    Product Description

    BCP-T.A. is a ferroptosis inducer.1 It induces ferroptosis in NCI H522 non-small cell lung cancer (NSCLC) cells (IC50 = 17 nM), an effect that can be blocked by the ferroptosis inhibitor liproxstatin-1 (Item No. 17730). BCP-T.A. binds to glutathione peroxidase (GPX4) and increases the accumulation of lipid peroxides in NCI H522 cells when used at a concentration of 0.5 µM. It is cytotoxic to WI38 human lung fibroblasts and mouse embryonic fibroblasts (MEFs; IC50s = 22 and 10 nM, respectively), as well as NCI H522, HT-1080 fibrosarcoma, MDA-MB-468 and MDA-MB-231 breast, and HeLa cervical cancer cells (IC50s = 17, 19, 84, 21, and 242 nM, respectively).

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Karaj, E., Sindi, S.H., Kuganesan, N., et alTunable cysteine-targeting electrophilic heteroaromatic warheads induce ferroptosis. J. Med. Chem. 65(17), 11788-11817 (2022).