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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=CC=CC=C2Cl)C3=CC(=CC=C3NC1=O)[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
Meclonazepam analogues as potential new antihelmintic agents.
2008 Apr 1
Praziquantel and the benzodiazepine Ro 11-3128 do not compete for the same binding sites in schistosomes.
2008 Jan
The effects of 3-methylclonazepam on Schistosoma mansoni musculature are not mediated by benzodiazepine receptors.
2009 Mar 15
Comparison of microscopy and Alamar blue reduction in a larval based assay for schistosome drug screening.
2010 Aug 10
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 Fri Dec 15 16:59:19 GMT 2023
Edited
by admin
on Fri Dec 15 16:59:19 GMT 2023
Record UNII
RN43209SMA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MECLONAZEPAM
INN  
INN  
Official 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
(+)-(S)-5-(O-CHLOROPHENYL)-1,3-DIHYDRO-3-METHYL-7-NITRO-2H-1,4-BENZODIAZEPIN-2-ONE
Common Name English
Meclonazepam [NFLIS-DRUG]
Common Name English
Classification Tree Code System Code
WIKIPEDIA Designer-drugs-Meclonazepam
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
NCI_THESAURUS C1012
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
Code System Code Type Description
INN
4912
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
NCI_THESAURUS
C83911
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID10207366
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
EVMPD
SUB08680MIG
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
ChEMBL
CHEMBL1908326
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
SMS_ID
100000081758
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
FDA UNII
RN43209SMA
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
CAS
58662-84-3
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
PUBCHEM
3033985
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
MESH
C020602
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
PRIMARY
WIKIPEDIA
MECLONAZEPAM
Created by admin on Fri Dec 15 16:59:19 GMT 2023 , Edited by admin on Fri Dec 15 16:59:19 GMT 2023
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