FIELD: chemistry; pharmaceutics.
SUBSTANCE: invention relates to chemistry and pharmaceutics, specifically to a compound of formula (I-2), specific compounds specified below, pharmaceutically acceptable salts thereof, a pharmaceutical composition based thereon and their use for preparing a drug for preventing and treating a disease caused by gram-negative bacteria, which are E. coli, Klebsiella, Enterobacter, Pseudomonas aeruginosa and Acinetobacter. In general formula (I-2), X is CH; T is S; E is where each of R1 and R2 is independently selected from the group consisting of C1-C6 alkyl; F is a single bond; A is C1-C6 alkylene;
is a quaternary ammonium group containing one or more N atoms and selected from the group consisting of a heterocyclyl containing from 5 ring atoms, where one ring atom is a heteroatom selected from nitrogen; G2 is C1-C6 alkylene; C2 is -NR31-C(=O)-, where each R31 is independently selected from the group consisting of C1-C6 alkyl and C1-C6 alkoxy, where each of alkyl and alkoxy is independently substituted with one or more substitutes selected from
; ring D1 is phenyl; Rm is selected from phenyl, where phenyl is substituted with three substitutes selected from the group consisting of halogen and hydroxy, each R4 is independently selected from halogen; n is 1; Ri is hydrogen.
,
.
EFFECT: cephalosporin antibacterial compound and its pharmaceutical use are disclosed.
6 cl, 1 tbl, 14 ex
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Authors
Dates
2024-11-28—Published
2021-01-22—Filed