Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H26N2O.ClH |
| Molecular Weight | 310.862 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCC(=O)N(C(C)CN1CCCCC1)C2=CC=CC=C2
InChI
InChIKey=AUEUUAMHKRZWEJ-UHFFFAOYSA-N
InChI=1S/C17H26N2O.ClH/c1-3-17(20)19(16-10-6-4-7-11-16)15(2)14-18-12-8-5-9-13-18;/h4,6-7,10-11,15H,3,5,8-9,12-14H2,1-2H3;1H
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C17H26N2O |
| Molecular Weight | 274.4011 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Phenampromide is an opioid analgesic, which is considered to be structurally similar to isomethadone. Phenampromide belongs to the ampromide family of drugs, which also include propiram and diampromide. According to the literature, (R)-phenampromide has greater analgesic potency than its (S)-enantiomer. Synthetic narcotic analgesic phenampromide is under international control according to the UN Single Convention 1961 and its amendments, Schedule I.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:28:11 GMT 2023
by
admin
on
Sat Dec 16 11:28:11 GMT 2023
|
| Record UNII |
7M3E9Q73VE
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID80913321
Created by
admin on Sat Dec 16 11:28:11 GMT 2023 , Edited by admin on Sat Dec 16 11:28:11 GMT 2023
|
PRIMARY | |||
|
7M3E9Q73VE
Created by
admin on Sat Dec 16 11:28:11 GMT 2023 , Edited by admin on Sat Dec 16 11:28:11 GMT 2023
|
PRIMARY | |||
|
98348-21-1
Created by
admin on Sat Dec 16 11:28:11 GMT 2023 , Edited by admin on Sat Dec 16 11:28:11 GMT 2023
|
PRIMARY | |||
|
3062539
Created by
admin on Sat Dec 16 11:28:11 GMT 2023 , Edited by admin on Sat Dec 16 11:28:11 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ACTIVE MOIETY |
|