Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H26N2O |
| Molecular Weight | 274.4011 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N(C(C)CN1CCCCC1)C2=CC=CC=C2
InChI
InChIKey=DHTRHEVNFFZCNU-UHFFFAOYSA-N
InChI=1S/C17H26N2O/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
| 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 | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:22:48 UTC 2023
by
admin
on
Fri Dec 15 16:22:48 UTC 2023
|
| Record UNII |
0600L2M6EZ
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C1506
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
||
|
DEA NO. |
9638
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
204-967-1
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
PHENAMPROMIDE
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | Phenampromide is an opioid analgesic from the ampromide family of drugs, related to other drugs such as propiram and diampromide. It was invented in the 1960s[1] by American Cyanamid Co.[2] Although never given a general release, it was trialled and 50mg codeine ≈ 60mg phenampromide. Tests on the 2 isomers showed that all of the analgesic effects were caused by the (S) isomer. | ||
|
0600L2M6EZ
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
m8593
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | Merck Index | ||
|
CHEMBL2104589
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
948
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
SUB09750MIG
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
C66367
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
129-83-9
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
8523
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
DTXSID10911012
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY | |||
|
100000082209
Created by
admin on Fri Dec 15 16:22:48 UTC 2023 , Edited by admin on Fri Dec 15 16:22:48 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
SALT/SOLVATE -> PARENT |
APPROXIMATE PURE ANHYDROUS DRUG CONTENT (IN PERCENT)
|
||
|
SALT/SOLVATE -> PARENT |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
