The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 1-(Bis(4-chlorophenyl)methyl)piperazine( cas:27469-61-0 ) is researched.COA of Formula: C17H18Cl2N2.Eaton, John K.; Furst, Laura; Cai, Luke L.; Viswanathan, Vasanthi S.; Schreiber, Stuart L. published the article 《Structure-activity relationships of GPX4 inhibitor warheads》 about this compound( cas:27469-61-0 ) in Bioorganic & Medicinal Chemistry Letters. Keywords: structure preparation GPX4 inhibitor propiolamide NO warhead; Covalent inhibitors; Ferroptosis; GPX4; Masked electrophiles. Let’s learn more about this compound (cas:27469-61-0).
Direct inhibition of GPX4 requires covalent modification of the active-site selenocysteine. While phenotypic screening has revealed that activated alkyl chlorides and masked nitrile oxides can inhibit GPX4 covalently, a systematic assessment of potential electrophilic warheads with the capacity to inhibit cellular GPX4 has been lacking. Here, we survey more than 25 electrophilic warheads across several distinct GPX4-targeting scaffolds. We find that electrophiles with attenuated reactivity compared to chloroacetamides are unable to inhibit GPX4 despite the expected nucleophilicity of the selenocysteine residue. However, highly reactive propiolamides we uncover in this study can substitute for chloroacetamide and nitroisoxazole warheads in GPX4 inhibitors. Our observations suggest that electrophile masking strategies, including those we describe for propiolamide- and nitrile-oxide-based warheads, may be promising for the development of improved covalent GPX4 inhibitors.
There is still a lot of research devoted to this compound(SMILES:ClC1=CC=C(C=C1)C(N2CCNCC2)C3=CC=C(Cl)C=C3)COA of Formula: C17H18Cl2N2, and with the development of science, more effects of this compound(27469-61-0) can be discovered.
Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics