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
SMILES
CN(C(=O)CN(CCO)CCO)C1=CC=C(Cl)C=C1C(=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
| 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
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2119309
1, 3, 5, 8 or 12 mg/kg
Route of Administration:
Intraperitoneal
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:33:18 GMT 2025
by
admin
on
Mon Mar 31 18:33:18 GMT 2025
|
| Record UNII |
BK2633656Q
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C264
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
CHEMBL2104587
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
5813
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
BK2633656Q
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
DTXSID20226528
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
100000080477
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
71142
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
SUB06425MIG
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
C65497
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
75616-02-3
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY | |||
|
C065732
Created by
admin on Mon Mar 31 18:33:18 GMT 2025 , Edited by admin on Mon Mar 31 18:33:18 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |