Cas No.: | 1354745-52-0 |
Chemical Name: | 6-Chloro-7-methoxy-2-methyl-3-[4-[4-(trifluoromethoxy)phenoxy]phenyl]-1H-quinolin-4-one |
Synonyms: | ELQ300;6-chloro-7-methoxy-2-methyl-3-[4-[4-(trifluoromethoxy)phenoxy]phenyl]-1H-quinolin-4-one;WZDNKHCQIZRDKW-UHFFFAOYSA-N;GTPL10021;BCP30856;ELQ300; ELQ 300;SB17071;Q15410945;6-chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)phenoxy)phenyl)quinolin-4(1H)-one;6-chloro-7-methoxy-2-methyl-3-(4-(4-(trifluoromethoxy)phenoxy) phenyl) quinolin-4(1H)-one;6-Chloro-2-methyl-3-[4-[4-(trifluoromethoxy)phenoxy]phenyl]-7-methoxyquinol;ELQ-300 |
SMILES: | ClC1=C(C([H])=C2C(=C1[H])C(C(C1C([H])=C([H])C(=C([H])C=1[H])OC1C([H])=C([H])C(=C([H])C=1[H])OC(F)(F)F)=C(C([H])([H])[H])N2[H])=O)OC([H])([H])[H] |
Formula: | C24H17ClF3NO4 |
M.Wt: | 475.8443 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | ELQ-300 is a potent antimalarial agent, acts as an inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1)[1]. |
References: | [1]. Stickles AM, et al. Subtle changes in endochin-like quinolone structure alter the site of inhibition within the cytochrome bc1 complex of Plasmodium falciparum. Antimicrob Agents Chemother. 2015 Apr;59(4):1977-82. |