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

Details

Stereochemistry ABSOLUTE
Molecular Formula C16H12ClN3O3
Molecular Weight 329.738
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MECLONAZEPAM

SMILES

C[C@@H]1N=C(C2=C(Cl)C=CC=C2)C3=C(NC1=O)C=CC(=C3)[N+]([O-])=O

InChI

InChIKey=LMUVYJCAFWGNSY-VIFPVBQESA-N
InChI=1S/C16H12ClN3O3/c1-9-16(21)19-14-7-6-10(20(22)23)8-12(14)15(18-9)11-4-2-3-5-13(11)17/h2-9H,1H3,(H,19,21)/t9-/m0/s1

HIDE SMILES / InChI

Molecular Formula C16H12ClN3O3
Molecular Weight 329.738
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Meclonazepam (Ro11-3128 or 3-methylclonazepam) is a benzodiazepine derivative. It exerts anxiolytic activity. Meclonazepam demonstrated anti-schistosomal action, it causes spastic paralysis, calcium influx and tegumental disruption in the parasites. Contracturant effect of meclonazepam is not a result of its binding to the worm benzodiazepine binding sites.

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparison of microscopy and Alamar blue reduction in a larval based assay for schistosome drug screening.
2010-08-10
The effects of 3-methylclonazepam on Schistosoma mansoni musculature are not mediated by benzodiazepine receptors.
2009-03-15
Schistosoma mansoni: lack of correlation between praziquantel-induced intra-worm calcium influx and parasite death.
2008-07
Meclonazepam analogues as potential new antihelmintic agents.
2008-04-01
Praziquantel and the benzodiazepine Ro 11-3128 do not compete for the same binding sites in schistosomes.
2008-01
The anti-schistosomal drug praziquantel is an adenosine antagonist.
2007-08
Patents

Patents

Sample Use Guides

Initial study of meclonazepam in generalized anxiety disorder. Daily dosage was flexible, from three to six tablets of meclonazepam 1 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:38:56 GMT 2025
Edited
by admin
on Mon Mar 31 18:38:56 GMT 2025
Record UNII
RN43209SMA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MECLONAZEPAM
INN  
INN  
Official Name English
(+)-(S)-5-(O-CHLOROPHENYL)-1,3-DIHYDRO-3-METHYL-7-NITRO-2H-1,4-BENZODIAZEPIN-2-ONE
Preferred Name English
5-(2-chlorophenyl)-3-methyl-7-nitro-2,3-dihydro-1H-1,4-benzodiazepin-2-one
Systematic Name English
RO 11-3128/002
Common Name English
meclonazepam [INN]
Common Name English
2H-1,4-BENZODIAZEPIN-2-ONE, 5-(2-CHLOROPHENYL)-1,3-DIHYDRO-3-METHYL-7-NITRO-, (3S)-
Systematic Name English
Ro 11-3128
Common Name English
Meclonazepam [NFLIS-DRUG]
Common Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-Meclonazepam
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
NCI_THESAURUS C1012
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
Code System Code Type Description
INN
4912
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
NCI_THESAURUS
C83911
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
EPA CompTox
DTXSID10207366
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
EVMPD
SUB08680MIG
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
ChEMBL
CHEMBL1908326
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
SMS_ID
100000081758
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
FDA UNII
RN43209SMA
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
CAS
58662-84-3
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
PUBCHEM
3033985
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
MESH
C020602
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
WIKIPEDIA
MECLONAZEPAM
Created by admin on Mon Mar 31 18:38:56 GMT 2025 , Edited by admin on Mon Mar 31 18:38:56 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
TARGET ORGANISM->INHIBITOR
Meclonazepam was never marketed because of sedative effects.
Related Record Type Details
METABOLITE -> PARENT
MAJOR
URINE
Related Record Type Details
ACTIVE MOIETY