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Details

Stereochemistry ACHIRAL
Molecular Formula C19H20FN5O4.ClH
Molecular Weight 437.853
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ZABOFLOXACIN HYDROCHLORIDE

SMILES

Cl.CO\N=C1/CN(CC12CNC2)C3=C(F)C=C4C(=O)C(=CN(C5CC5)C4=N3)C(O)=O

InChI

InChIKey=IFPBSRFVNPCZMK-MHVDTSALSA-N
InChI=1S/C19H20FN5O4.ClH/c1-29-23-14-6-24(9-19(14)7-21-8-19)17-13(20)4-11-15(26)12(18(27)28)5-25(10-2-3-10)16(11)22-17;/h4-5,10,21H,2-3,6-9H2,1H3,(H,27,28);1H/b23-14+;

HIDE SMILES / InChI

Molecular Formula C19H20FN5O4
Molecular Weight 401.3916
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

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 Sat Dec 16 08:58:30 UTC 2023
Edited
by admin
on Sat Dec 16 08:58:30 UTC 2023
Record UNII
O889MR47PQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZABOFLOXACIN HYDROCHLORIDE
WHO-DD  
Common Name English
1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID, 1-CYCLOPROPYL-6-FLUORO-1,4-DIHYDRO-7-(8-(METHOXYIMINO)-2,6-DIAZASPIRO(3.4)OCT-6-YL)-4-OXO-, MONOHYDROCHLORIDE
Systematic Name English
ZABOFLOXACIN MONOHYDROCHLORIDE
Common Name English
Zabofloxacin hydrochloride [WHO-DD]
Common Name English
DW-224A
Common Name English
1,8-NAPHTHYRIDINE-3-CARBOXYLIC ACID, 1-CYCLOPROPYL-6-FLUORO-1,4-DIHYDRO-7-(8-(METHOXYIMINO)-2,6-DIAZASPIRO(3.4)OCT-6-YL)-4-OXO-, HYDROCHLORIDE (1:1)
Systematic Name English
Code System Code Type Description
SMS_ID
100000182644
Created by admin on Sat Dec 16 08:58:30 UTC 2023 , Edited by admin on Sat Dec 16 08:58:30 UTC 2023
PRIMARY
PUBCHEM
10388395
Created by admin on Sat Dec 16 08:58:30 UTC 2023 , Edited by admin on Sat Dec 16 08:58:30 UTC 2023
PRIMARY
FDA UNII
O889MR47PQ
Created by admin on Sat Dec 16 08:58:30 UTC 2023 , Edited by admin on Sat Dec 16 08:58:30 UTC 2023
PRIMARY
CAS
623574-00-5
Created by admin on Sat Dec 16 08:58:30 UTC 2023 , Edited by admin on Sat Dec 16 08:58:30 UTC 2023
PRIMARY
EVMPD
SUB196893
Created by admin on Sat Dec 16 08:58:30 UTC 2023 , Edited by admin on Sat Dec 16 08:58:30 UTC 2023
PRIMARY
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