Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H26N2O.C4H6O6 |
| Molecular Weight | 424.488 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@H]([C@@H](O)C(O)=O)C(O)=O.CCC(=O)N(C(C)CN1CCCCC1)C2=CC=CC=C2
InChI
InChIKey=NBTYMRMHKVEMHS-LREBCSMRSA-N
InChI=1S/C17H26N2O.C4H6O6/c1-3-17(20)19(16-10-6-4-7-11-16)15(2)14-18-12-8-5-9-13-18;5-1(3(7)8)2(6)4(9)10/h4,6-7,10-11,15H,3,5,8-9,12-14H2,1-2H3;1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1
| 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 | ( + / - ) |
| Molecular Formula | C4H6O6 |
| Molecular Weight | 150.0868 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
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
Mon Mar 31 17:53:20 GMT 2025
by
admin
on
Mon Mar 31 17:53:20 GMT 2025
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| Record UNII |
JVM97L26U3
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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Common Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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155801572
Created by
admin on Mon Mar 31 17:53:20 GMT 2025 , Edited by admin on Mon Mar 31 17:53:20 GMT 2025
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PRIMARY | PUBCHEM | ||
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7645-04-7
Created by
admin on Mon Mar 31 17:53:20 GMT 2025 , Edited by admin on Mon Mar 31 17:53:20 GMT 2025
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PRIMARY | |||
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JVM97L26U3
Created by
admin on Mon Mar 31 17:53:20 GMT 2025 , Edited by admin on Mon Mar 31 17:53:20 GMT 2025
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PRIMARY |