Details
Stereochemistry | RACEMIC |
Molecular Formula | C21H28N2O |
Molecular Weight | 324.4598 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N(CC(C)N(C)CCC1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=RXTHKWVSXOIHJS-UHFFFAOYSA-N
InChI=1S/C21H28N2O/c1-4-21(24)23(20-13-9-6-10-14-20)17-18(2)22(3)16-15-19-11-7-5-8-12-19/h5-14,18H,4,15-17H2,1-3H3
Diampromide is a synthetic narcotic analgesic. It was designed as a methadone analog and hence with a chiral center similar to that of the parent. Diampromide approximates to the potency of pethidine and morphine in mice and rats, respectively. It has been evaluated in postoperative pain. Diampromide is not found in any pharmaceutical preparations sold in the United States. It is under international control according to the UN Single Convention 1961 and its amendments, Schedule I.
Approval Year
Name | Type | Language | ||
---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
DEA NO. |
9615
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
||
|
NCI_THESAURUS |
C67413
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
950
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
850
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
552-25-0
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
26G7YC77BU
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
C77286
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
DTXSID70862177
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
DB01502
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
SUB07065MIG
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
62370
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
CHEMBL2106220
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
DIAMPROMIDE
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
100000082904
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | |||
|
m1110
Created by
admin on Mon Mar 31 18:19:32 GMT 2025 , Edited by admin on Mon Mar 31 18:19:32 GMT 2025
|
PRIMARY | Merck Index |
ACTIVE MOIETY