Cas No.: | 347174-05-4 |
Chemical Name: | Ethyl 3-amino-4-(cyclohexylamino)benzoate |
Synonyms: | Ethyl 3-amino-4-(cyclohexylamino)benzoate;Ferrostatin-1 (Fer-1);ethyl 3-amino-4-cyclohexylaminobenzoate;Ferrostatin 1;Ferrostatin-1;3-amino-4-cyan-1-phenyl-pyrrol-2-carbonsaeureethylester;3-Amino-4-cyclohexylamino benzoic acid ethyl ester;3-amino-4-cyclohexylamino-benzoic acid ethyl ester;AC1LDIR8;AG-G-09537;CTK1E8332;ethyl 3-amino-4-cyano-1-phenyl-1H-pyrrole-2-carboxylate;HMS2445A21;Fer-1;Benzoic acid, 3-amino-4-(cyclohexylamino)-, ethyl ester;ferrostatin-1-fer-1;UJHBVMHOBZBWMX-UHFFFAOYSA-N;HMS3653M21;BCP17366;s7243;SB19587;SEL10496268;SEL10496253;ST45002378;SW2 |
SMILES: | O(C([H])([H])C([H])([H])[H])C(C1C([H])=C([H])C(=C(C=1[H])N([H])[H])N([H])C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H])=O |
Formula: | C15H22N2O2 |
M.Wt: | 262.3474 |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | Ferrostatin-1 is a potent inhibitor of ferroptosis with an EC50 of 60 nM. |
In Vitro: | Ferrostatin-1 is the most potent inhibitor of erastin-induced ferroptosis in HT-1080 cells (EC50=60 nM). Ferrostatin-1 does not inhibit ERK phosphorylation or arrest the proliferation of HT-1080 cells. Ferrostatin-1 does, however, prevent erastin-induced accumulation of cytosolic and lipid ROS[1]. Cells pretreated with 0.4 μM Ferrostatin-1 displays significantly reduce intracellular reactive oxygen species (ROS) and nitrogen species (RNS) below basal levels. Additionally, increased intracellular ROS levels are also significantly lowered below basal levels by a 0.4 µM Ferrostatin-1 pretreatment. Ferrostatin-1 treatment for 24 h does not change the expression level of i-NOS in SHSY-5Y cell when compare with vehicle (0.02 % DMSO) treated cells[2]. |