150651-39-1
Chemical Structure
iFSP1
- CAS No.: 150651-39-1
- Formula:C20H13N5
- Molecular Weight:323.35
IUPAC Name: 1-amino-3-(p-tolyl)benzo[4,5]imidazo[1,2-a]pyridine-2,4-dicarbonitrile
InChIKey: FNESYDFRCQEEKA-UHFFFAOYSA-N
SMILES: N#CC1=C(N)N2C3=CC=CC=C3N=C2C(C#N)=C1C4=CC=C(C)C=C4
Biological Activity: iFSP1 is a potent, selective and glutathione-independent inhibitor of ferroptosis suppressor protein 1 (FSP1) (AIFM2) with an EC50 of 103 nM. iFSP1 selectively induces ferroptosis in GPX4-knockout cells which overexpressed FSP1. iFSP1 is able to sensitize a variety of human cancer cell lines to the ferroptosis inducer, such as (1S,3R)-RSL3 (HY-100218A)[1].
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iFSP1 | 99.88% | iFSP1 is a potent, selective and glutathione-independent inhibitor of ferroptosis suppressor protein 1 (FSP1) (AIFM2) with an EC50 of 103 nM. iFSP1 selectively induces ferroptosis in GPX4-knockout cells which overexpressed FSP1. iFSP1 is able to sensitize a variety of human cancer cell lines to the ferroptosis inducer, such as (1S,3R)-RSL3 (HY-100218A). | ||||||||||||||||||||
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iFSP1 (Standard) | ≥98% | iFSP1 (Standard) is the analytical standard of iFSP1 (HY-136057). This product is intended for research and analytical applications. iFSP1 is a potent, selective and glutathione-independent inhibitor of ferroptosis suppressor protein 1 (FSP1) (AIFM2) with an EC50 of 103 nM. iFSP1 selectively induces ferroptosis in GPX4-knockout cells which overexpressed FSP1. iFSP1 is able to sensitize a variety of human cancer cell lines to the ferroptosis inducer, such as (1S,3R)-RSL3 (HY-100218A). | ||||||||||||||||||||
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Similarity Score 0.54
HY-147964α-Glucosidase-IN-9 -
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HY-123562GNF7686 -
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HY-187161IL-4-IN-3 -
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