Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C15H21NO2.ClH |
| Molecular Weight | 283.794 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCC(=O)OC1(CCN(C)C1C)C2=CC=CC=C2
InChI
InChIKey=RBBBYDOGRKOESS-UHFFFAOYSA-N
InChI=1S/C15H21NO2.ClH/c1-4-14(17)18-15(10-11-16(3)12(15)2)13-8-6-5-7-9-13;/h5-9,12H,4,10-11H2,1-3H3;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 | C15H21NO2 |
| Molecular Weight | 247.3327 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Prodilidine is an arylpyrrolidine derivative patented by Mead Johnson & Co.as moderately potent analgesic. By comparison with other drugs, including morphine, Prodilidine has a prompt and unusually sustained antinociceptive action in rodents by all routes. Prodilidine substantially lacks antipyretic, anti-inflammatory, antitussive, constipating, respiratory depressant, and cardiovascular effects. Prodilidine resembles meperidine in excitatory properties and body-temperature lowering action at high dosage. The d-isomer is about twice as potent and toxic as the l-isomer parenterally; by the gastric route, the difference is markedly less.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:45:14 GMT 2025
by
admin
on
Mon Mar 31 17:45:14 GMT 2025
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| Record UNII |
8I871CD421
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| Record Status |
Validated (UNII)
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| Record Version |
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223-094-7
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C171685
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CHEMBL2110974
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8I871CD421
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DTXSID00958451
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172119
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3734-16-5
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300000055019
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3032452
Created by
admin on Mon Mar 31 17:45:14 GMT 2025 , Edited by admin on Mon Mar 31 17:45:14 GMT 2025
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| Related Record | Type | Details | ||
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