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Apoptosis inducer 52

Apoptosis inducer 52 is a derivative of flutamide that induces apoptosis in prostate cancer cells. Apoptosis inducer 52 promotes apoptosis by activating both intrinsic and extrinsic apoptotic pathways, without generating reactive oxygen species (ROS) . Apoptosis inducer 52 triggers caspase 3/7 activity and the externalization of phosphatidylserine, leading to cell cycle arrest at the G0/G1 phase. Apoptosis inducer 52 can be used for the research of androgen receptor (AR) -dependent and -independent prostate cancers and leukemia[1].

Product Specifications

UNSPSC

12352005

Target

Apoptosis; Caspase

Related Pathways

Apoptosis

Applications

Cancer-programmed cell death

Field of Research

Cancer

Smiles

O=C(C1=CC=CN=C1NC2=CC=CC(C(F)(F)F)=C2)[Se]CC(NC3=CC=CC(C(F)(F)F)=C3)=O

Molecular Formula

C22H15F6N3O2Se

Molecular Weight

546.32

References & Citations

[1]Morán-Serradilla C, et al. Innovative Se-Flutamide Derivatives: Enhanced Activity Toward Androgen Receptor (AR) -Dependent and -Independent Prostate Cancer Cells. Arch Pharm (Weinheim) . 2025;358 (10) :e70119.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

Caspase 3; Caspase 7; Caspase 8; Caspase 9

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