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Details

Stereochemistry ACHIRAL
Molecular Formula C20H22Cl2N2O4
Molecular Weight 425.306
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DULOZAFONE

SMILES

CN(C(=O)CN(CCO)CCO)C1=C(C=C(Cl)C=C1)C(=O)C2=C(Cl)C=CC=C2

InChI

InChIKey=BYWMOMBWRFUAMC-UHFFFAOYSA-N
InChI=1S/C20H22Cl2N2O4/c1-23(19(27)13-24(8-10-25)9-11-26)18-7-6-14(21)12-16(18)20(28)15-4-2-3-5-17(15)22/h2-7,12,25-26H,8-11,13H2,1H3

HIDE SMILES / InChI

Molecular Formula C20H22Cl2N2O4
Molecular Weight 425.306
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Dulozafone is an anticonvulsant and anxiolytic agent. Dulozafone was derived from glycine. Neuro-pharmacological experiments had demonstrated that dulozafone shows the same pharmacological activity as benzodiazepines and a good in vivo affinity for the benzodiazepine receptor. Dulozafone is a pro-drug, metabolized in vivo to an active form. One of its putative metabolites could be ortho-chloro-diazepam, which is pharmacologically active. Dulozafone had the same anticonvulsant effect on kindled seizures as diazepam. It is potent inhibitor of convulsions and epileptic discharges of fully kindled rats. Dulozafone exerts their anticonvulsant properties in inhibiting the propagation of the epileptic discharge from amygdala to other cerebral structures, particularly those implicated in the motor generalization, such as the substantia nigra.

Approval Year

PubMed

PubMed

TitleDatePubMed
Anticonvulsive properties of F1933 (dulozafone) on kindled seizures in the rat.
1990 Jun 21

Sample Use Guides

1, 3, 5, 8 or 12 mg/kg
Route of Administration: Intraperitoneal
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:38:21 GMT 2023
Edited
by admin
on Fri Dec 15 16:38:21 GMT 2023
Record UNII
BK2633656Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DULOZAFONE
INN  
INN  
Official Name English
2-(BIS(2-HYDROXYETHYL)AMINO)-4'-CHLORO-2'-(O-CHLOROBENZOYL)-N-METHYLACETANILIDE
Common Name English
dulozafone [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2104587
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
INN
5813
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
FDA UNII
BK2633656Q
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
EPA CompTox
DTXSID20226528
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
SMS_ID
100000080477
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
PUBCHEM
71142
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
EVMPD
SUB06425MIG
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
NCI_THESAURUS
C65497
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
CAS
75616-02-3
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
MESH
C065732
Created by admin on Fri Dec 15 16:38:21 GMT 2023 , Edited by admin on Fri Dec 15 16:38:21 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY