N-Methyl Gatifloxacin

COC1=C(N2CCN(C)C(C)C2)C(F)=CC3=C1N(C=C(C(O)=O)C3=O)C4CC4

InChIKey=YDBVQXCJOKMPST-UHFFFAOYSA-N

InChI=1S/C20H24FN3O4/c1-11-9-23(7-6-22(11)2)17-15(21)8-13-16(19(17)28-3)24(12-4-5-12)10-14(18(13)25)20(26)27/h8,10-12H,4-7,9H2,1-3H3,(H,26,27)

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Substance Class	Chemical Created by `admin` on `Wed Apr 02 17:39:26 GMT 2025` Edited by `admin` on `Wed Apr 02 17:39:26 GMT 2025`
Record UNII	JAX323Q55Y
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

1-Cyclopropyl-7-(3,4-dimethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acid

Preferred Name

English

N-Methyl Gatifloxacin

Common Name

English

3-Quinolinecarboxylic acid, 1-cyclopropyl-7-(3,4-dimethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-8-methoxy-4-oxo-

Systematic Name

English

Code System Code Type Description

FDA UNII

JAX323Q55Y

Created by admin on Wed Apr 02 17:39:26 GMT 2025 , Edited by admin on Wed Apr 02 17:39:26 GMT 2025

PRIMARY

EPA CompTox

DTXSID20560570

Created by admin on Wed Apr 02 17:39:26 GMT 2025 , Edited by admin on Wed Apr 02 17:39:26 GMT 2025

PRIMARY

CAS

114213-69-3

Created by admin on Wed Apr 02 17:39:26 GMT 2025 , Edited by admin on Wed Apr 02 17:39:26 GMT 2025

PRIMARY

PUBCHEM

14457270

Created by admin on Wed Apr 02 17:39:26 GMT 2025 , Edited by admin on Wed Apr 02 17:39:26 GMT 2025

PRIMARY

Related Record Type Details


					2YA8GN9A6A

SALT/SOLVATE -> PARENT

Amount: