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

Details

Stereochemistry RACEMIC
Molecular Formula C11H11Cl2N3O
Molecular Weight 272.131
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MUZOLIMINE

SMILES

CC(N1N=C(N)CC1=O)C2=CC(Cl)=C(Cl)C=C2

InChI

InChIKey=RLWRMIYXDPXIEX-UHFFFAOYSA-N
InChI=1S/C11H11Cl2N3O/c1-6(16-11(17)5-10(14)15-16)7-2-3-8(12)9(13)4-7/h2-4,6H,5H2,1H3,(H2,14,15)

HIDE SMILES / InChI

Molecular Formula C11H11Cl2N3O
Molecular Weight 272.131
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

MUZOLIMINE, a dichlorobenzene derivative, is a loop diuretic with slow effect and long lasting action. It was used for the treatment of hypertension but was withdrawn from the market because of severe neurological effects.

Approval Year

PubMed

PubMed

TitleDatePubMed
Muzolimine and nitrendipine in the treatment of arterial hypertension.
1985
The diuretic effect of muzolimine.
1987 Dec
Muzolimine-induced severe neuromyeloencephalopathy: report of seven cases.
1991 Jan
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:18:58 GMT 2023
Edited
by admin
on Fri Dec 15 15:18:58 GMT 2023
Record UNII
07Z36289ZX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MUZOLIMINE
INN   MART.   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
3-Amino-1-(3,4-dichloro-α-methylbenzyl)-2-pyrazolin-5-one
Systematic Name English
muzolimine [INN]
Common Name English
MUZOLIMINE [USAN]
Common Name English
MUZOLIMINE [MI]
Common Name English
3H-PYRAZOL-3-ONE, 5-AMINO-2-(1-(3,4-DICHLOROPHENYL)ETHYL)-2,4-DIHYDRO-
Systematic Name English
3-AMINO-1-(3,4-DICHLORO-A-METHYLBENZYL)-2-PYRAZOLIN-5-ONE
Systematic Name English
MUZOLIMINE [MART.]
Common Name English
EDRUL
Brand Name English
BAY G 2821
Code English
BAY-G 2821
Code English
Muzolimine [WHO-DD]
Common Name English
BAY-G-2821
Code English
Classification Tree Code System Code
WHO-ATC C03CD01
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
WHO-VATC QC03CD01
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
Code System Code Type Description
SMS_ID
100000080603
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
PUBCHEM
41386
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
DRUG CENTRAL
1858
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
WIKIPEDIA
MUZOLIMINE
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
CAS
55294-15-0
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID50866476
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
NCI_THESAURUS
C175151
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
FDA UNII
07Z36289ZX
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
MERCK INDEX
m836
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB13801
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
ECHA (EC/EINECS)
259-573-2
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
ChEMBL
CHEMBL1697760
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
EVMPD
SUB09097MIG
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
INN
4119
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
MESH
D009156
Created by admin on Fri Dec 15 15:18:58 GMT 2023 , Edited by admin on Fri Dec 15 15:18:58 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY