Compound ID | 2210
Synonym(s): TXY6129
Class: FtsZ inhibitor
Spectrum of activity: | Gram-negative |
Details of activity: | Inhibits Escherichia coli FtsZ polymerization |
Description: | Synthetic compound from TAXIS Pharmaceuticals Inc (FtsZ-targeting molecules for Gram-positive FtsZ); compounds have lipophilic aromatic groups and halogens at the C-4 and C-5 positions of the oxazole ring which are necessary for Gram-negative activity; induced morphological changes in Escherichia coli and Klebsiella pneumoniae indicative of cell division inhibition |
Year first mentioned: | 2022 |
Development status: | Experimental |
Chemical structure(s): | |
Canonical SMILES: | C1=C(C=CC(=C1)C(F)(F)F)C2=C(Br)OC(=N2)COC3=CC=C(C(=C3F)C(=O)N)F |
Isomeric SMILES: | C1=CC(=CC=C1C2=C(OC(=N2)COC3=C(C(=C(C=C3)F)C(=O)N)F)Br)C(F)(F)F |
InChI: | InChI=1S/C18H10BrF5N2O3/c19-16-15(8-1-3-9(4-2-8)18(22,23)24)26-12(29-16)7-28-11-6-5-10(20)13(14(11)21)17(25)27/h1-6H,7H2,(H2,25,27) |
InChI Key: | ONGPJYSSZQHFBU-UHFFFAOYSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/72947301 |
External links: | |
Guide to Pharmacology: | TXA6101 |
Main Source: | https://www.nature.com/articles/s41429-022-00531-9#Abs1 |