U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H20F2N2O4.CH4O3S.H2O
Molecular Weight 540.534
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GARENOXACIN MESYLATE

SMILES

O.CS(O)(=O)=O.C[C@H]1NCC2=CC(=CC=C12)C3=CC=C4C(=O)C(=CN(C5CC5)C4=C3OC(F)F)C(O)=O

InChI

InChIKey=IGTHEWGRXUAFKF-NVJADKKVSA-N
InChI=1S/C23H20F2N2O4.CH4O3S.H2O/c1-11-15-5-2-12(8-13(15)9-26-11)16-6-7-17-19(21(16)31-23(24)25)27(14-3-4-14)10-18(20(17)28)22(29)30;1-5(2,3)4;/h2,5-8,10-11,14,23,26H,3-4,9H2,1H3,(H,29,30);1H3,(H,2,3,4);1H2/t11-;;/m1../s1

HIDE SMILES / InChI

Molecular Formula C23H20F2N2O4
Molecular Weight 426.4127
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula CH4O3S
Molecular Weight 96.106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:25:55 UTC 2023
Edited
by admin
on Fri Dec 15 15:25:55 UTC 2023
Record UNII
OXI6EF55FR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GARENOXACIN MESYLATE
USAN  
USAN  
Official Name English
1-CYCLOPROPYL-8-(DIFLUOROMETHOXY)-7-((1R)-1-METHYL-2,3-DIHYDRO-1H-5-ISOINDOLYL)-4-OXO-1,4-DIHYDRO-3-QUINOLINECARBOXYLIC ACID MESYLATE MONOHYDRATE
Systematic Name English
1-CYCLOPROPYL-8-(DIFLUOROMETHOXY)-7-((1R)-1-METHYL-2,3-DIHYDRO-1H-ISOINDOL-5-YL)-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBOXYLIC ACID MONOMETHANESULPHONATE MONOHYDRATE
Systematic Name English
GARENOXACIN MESILATE HYDRATE [JAN]
Common Name English
Garenoxacin mesilate monohydrate [WHO-DD]
Common Name English
GARENOXACIN MESILATE MONOHYDRATE [MART.]
Common Name English
3-QUINOLINECARBOXYLIC ACID, 1-CYCLOPROPYL-8-(DIFLUOROMETHOXY)-7-((1R)-2,3-DIHYDRO-1-METHYL-1H-ISOINDOL-5-YL)-1,4-DIHYDRO-4-OXO-, MONOMETHANESULFONATE, MONOHYDRATE
Common Name English
1-CYCLOPROPYL-8-(DIFLUOROMETHOXY)-7-((1R)-1-METHYL-2,3-DIHYDRO-1H-5-ISOINDOLYL)-4-OXO-1,4-DIHYDRO-3-QUINOLINECARBOXYLIC ACID MESILATE MONOHYDRATE
Systematic Name English
GARENOXACIN MESILATE MONOHYDRATE
MART.   WHO-DD  
Common Name English
1-CYCLOPROPYL-8-(DIFLUOROMETHOXY)-7-((1R)-1-METHYL-2,3-DIHYDRO-1H-ISOINDOL-5-YL)-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBOXYLIC ACID METHANESULPHONATE HYDRATE
Systematic Name English
1-Cyclopropyl-8-(difluoromethoxy)-7-[(1R)-1-methyl-2,3-dihydro-1H-isoindol-5-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid monomethanesulfonate monohydrate
Systematic Name English
1-CYCLOPROPYL-8-(DIFLUOROMETHOXY)-7-((1R)-1-METHYL-2,3-DIHYDRO-1H-ISOINDOL-5-YL)-4-OXO-1,4-DIHYDROQUINOLINE-3-CARBOXYLIC ACID METHANESULFONATE HYDRATE
Systematic Name English
BMS-284756-01
Code English
GARENOXACIN MESILATE HYDRATE
JAN  
Common Name English
GARENOXACIN METHANESULFONATE MONOHYDRATE
MI  
Common Name English
GARENOXACIN MESYLATE [USAN]
Common Name English
3-QUINOLINECARBOXYLIC ACID, 1-CYCLOPROPYL-8-(DIFLUOROMETHOXY)-7-((1R)-2,3-DIHYDRO-1-METHYL-1H-ISOINDOL-5-YL)-1,4-DIHYDRO-4-OXO-, METHANESULFONATE, HYDRATE (1:1:1)
Common Name English
GENINAX
Brand Name English
GARENOXACIN METHANESULFONATE MONOHYDRATE [MI]
Common Name English
3-QUINOLINECARBOXYLIC ACID, 1-CYCLOPROPYL-8-(DIFLUOROMETHOXY)-7-((1R)-2,3-DIHYDRO-1-METHYL-1H-ISOINDOL-5-YL)-1,4-DIHYDRO-4-OXO-, METHANESULPHONATE, HYDRATE (1:1:1)
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C795
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
Code System Code Type Description
MERCK INDEX
m5672
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
USAN
MM-77
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
EPA CompTox
DTXSID4048644
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
JAPANESE REVIEW
GENINAX
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY APPROVED JULY 2007
PUBCHEM
157690
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
CAS
223652-90-2
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
SMS_ID
100000091589
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
EVMPD
SUB27012
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
FDA UNII
OXI6EF55FR
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
NCI_THESAURUS
C65801
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
DRUG BANK
DBSALT001994
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
ChEMBL
CHEMBL215303
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
EVMPD
SUB25395
Created by admin on Fri Dec 15 15:25:55 UTC 2023 , Edited by admin on Fri Dec 15 15:25:55 UTC 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY