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Details

Stereochemistry RACEMIC
Molecular Formula C19H22FN3O3.ClH
Molecular Weight 395.856
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GREPAFLOXACIN HYDROCHLORIDE

SMILES

Cl.CC1CN(CCN1)C2=C(F)C(C)=C3C(=O)C(=CN(C4CC4)C3=C2)C(O)=O

InChI

InChIKey=IEPMBYOIQGCVHO-UHFFFAOYSA-N
InChI=1S/C19H22FN3O3.ClH/c1-10-8-22(6-5-21-10)15-7-14-16(11(2)17(15)20)18(24)13(19(25)26)9-23(14)12-3-4-12;/h7,9-10,12,21H,3-6,8H2,1-2H3,(H,25,26);1H

HIDE SMILES / InChI

Molecular Formula C19H22FN3O3
Molecular Weight 359.3947
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
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 15:56:57 UTC 2023
Edited
by admin
on Fri Dec 15 15:56:57 UTC 2023
Record UNII
A4ER1Z8N9N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GREPAFLOXACIN HYDROCHLORIDE
JAN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN  
Official Name English
GREPAFLOXACIN HCL
Common Name English
GREPAFLOXACIN HYDROCHLORIDE [MART.]
Common Name English
GREPAFLOXACIN HYDROCHLORIDE [USAN]
Common Name English
(±)-1-CYCLOPROPYL-6-FLUORO-1,4-DIHYDRO-5-METHYL-7-(3-METHYL-1-PIPERAZINYL)-4-OXO-3-QUINOLINECARBOXYLIC ACID MONOHYDROCHLORIDE
Systematic Name English
Grepafloxacin hydrochloride [WHO-DD]
Common Name English
RAXAR
Brand Name English
GREPAFLOXACIN HYDROCHLORIDE [ORANGE BOOK]
Common Name English
3-QUINOLINECARBOXYLIC ACID, 1-CYCLOPROPYL-6-FLUORO-1,4-DIHYDRO-5-METHYL-7-(3-METHYL-1-PIPERAZINYL)-4-OXO-, MONOHYDROCHLORIDE, (±)-
Common Name English
GREPAFLOXACIN HYDROCHLORIDE [VANDF]
Common Name English
GREPAFLOXACIN HYDROCHLORIDE [MI]
Common Name English
OPC-17116
Code English
Classification Tree Code System Code
NCI_THESAURUS C795
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
Code System Code Type Description
RXCUI
236862
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY RxNorm
CAS
161967-81-3
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
SMS_ID
100000078442
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
PUBCHEM
656829
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
EPA CompTox
DTXSID0046692
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
ChEMBL
CHEMBL583
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
FDA UNII
A4ER1Z8N9N
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
MERCK INDEX
m5850
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY Merck Index
DRUG BANK
DBSALT000913
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
USAN
HH-58
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
NCI_THESAURUS
C65818
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
EVMPD
SUB14024MIG
Created by admin on Fri Dec 15 15:56:57 UTC 2023 , Edited by admin on Fri Dec 15 15:56:57 UTC 2023
PRIMARY
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ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
ENANTIOMER -> RACEMATE
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ACTIVE MOIETY