328265-32-3

PGP/FSP1-IN-1 Chemical Structure
328265-32-3

Chemical Structure

PGP/FSP1-IN-1

  • CAS No.: 328265-32-3
  • Formula:C28H20N2O7
  • Molecular Weight:496.47

InChIKey: UIRNMCRFFYWCBB-UHFFFAOYSA-N

SMILES: O=C(C1=CC=CC=C1NC(C2=CC=C(C=C2)OC3=CC=C(C=C3)C(NC4=C(C=CC=C4)C(O)=O)=O)=O)O

Biological Activity: PGP/FSP1-IN-1 is a dual PGP and FSP1 inhibitor and ferroptosis inducer that inhibits the oxidoreductase activity of FSP1. PGP/FSP1-IN-1 competes with NAD (P) H for binding to the pocket of FSP1 and induces FSP1 self-assembly, thereby directly blocking the catalytic function of the relevant enzyme. PGP/FSP1-IN-1 promotes lipid peroxidation and significantly enhances cellular sensitivity to ferroptosis when GPX4 activity is impaired or glutathione synthesis is inhibited. PGP/FSP1-IN-1 can be used in cancer research[1].

Cat. No. Product Name Purity Description Pricing
HY-184489
PGP/FSP1-IN-1 PGP/FSP1-IN-1 is a dual PGP and FSP1 inhibitor and ferroptosis inducer that inhibits the oxidoreductase activity of FSP1. PGP/FSP1-IN-1 competes with NAD (P) H for binding to the pocket of FSP1 and induces FSP1 self-assembly, thereby directly blocking the catalytic function of the relevant enzyme. PGP/FSP1-IN-1 promotes lipid peroxidation and significantly enhances cellular sensitivity to ferroptosis when GPX4 activity is impaired or glutathione synthesis is inhibited. PGP/FSP1-IN-1 can be used in cancer research.
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