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
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
| Name | Type | Language | ||
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Official Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C1506
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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DEA NO. |
9638
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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204-967-1
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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PHENAMPROMIDE
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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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. | ||
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0600L2M6EZ
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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m8593
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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PRIMARY | Merck Index | ||
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CHEMBL2104589
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948
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SUB09750MIG
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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C66367
Created by
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129-83-9
Created by
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8523
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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DTXSID10911012
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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100000082209
Created by
admin on Fri Dec 15 16:22:48 GMT 2023 , Edited by admin on Fri Dec 15 16:22:48 GMT 2023
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PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)
SALT/SOLVATE (PARENT)
