Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C14H22N2O2 |
| Molecular Weight | 250.3367 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCNC(=O)C(C)NC1=CC=C(OCC)C=C1
InChI
InChIKey=VVUMWAHNKOLVSN-UHFFFAOYSA-N
InChI=1S/C14H22N2O2/c1-4-10-15-14(17)11(3)16-12-6-8-13(9-7-12)18-5-2/h6-9,11,16H,4-5,10H2,1-3H3,(H,15,17)
| Molecular Formula | C14H22N2O2 |
| Molecular Weight | 250.3367 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Propetamide (also known as FC 379) is a propionamide derivative patented by All-Union Scientific Research Chemical-Pharmaceutical Institute as an analgesic compound. In mice, Propetamide produced both a depression of spontaneous motility and relaxation of muscular tone. However, Propetamide was less active than meprobamate. Propetamide at 400 mg/kg reduced muscular relaxation in 70% of the animals, while the same effect was obtained in 100% of the animals with meprobamate at 200 mg/kg.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:27:59 GMT 2023
by
admin
on
Sat Dec 16 10:27:59 GMT 2023
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| Record UNII |
HS697V67GJ
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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68937
Created by
admin on Sat Dec 16 10:27:59 GMT 2023 , Edited by admin on Sat Dec 16 10:27:59 GMT 2023
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35188-06-8
Created by
admin on Sat Dec 16 10:27:59 GMT 2023 , Edited by admin on Sat Dec 16 10:27:59 GMT 2023
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HS697V67GJ
Created by
admin on Sat Dec 16 10:27:59 GMT 2023 , Edited by admin on Sat Dec 16 10:27:59 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> ENANTIOMER |
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RACEMATE -> ENANTIOMER |
