Details
| Stereochemistry | MIXED |
| Molecular Formula | C21H25NO2.ClH |
| Molecular Weight | 359.89 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC1N(CC(=O)C2=CC=CC=C2)CCCC1(C)C3=CC=CC(O)=C3
InChI
InChIKey=ARCUFWKZXDWDIH-UHFFFAOYSA-N
InChI=1S/C21H25NO2.ClH/c1-16-21(2,18-10-6-11-19(23)14-18)12-7-13-22(16)15-20(24)17-8-4-3-5-9-17;/h3-6,8-11,14,16,23H,7,12-13,15H2,1-2H3;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 | C21H25NO2 |
| Molecular Weight | 323.4287 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Myfadol is a phenacylpiperidine derivative patented by Tanabe Seiyaku Co., Ltd as low molecular weight non-peptide analgesic. Myfadol produces hot-plate analgesia in rodents with minimal side-effects, and when given parenterally in humans produces analgesia to experimentally-produced and postoperative pain.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:33:07 GMT 2025
by
admin
on
Mon Mar 31 17:33:07 GMT 2025
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| Record UNII |
6HX7RST519
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| Record Status |
Validated (UNII)
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| Record Version |
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4370-33-6
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DTXSID60963102
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6HX7RST519
Created by
admin on Mon Mar 31 17:33:07 GMT 2025 , Edited by admin on Mon Mar 31 17:33:07 GMT 2025
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20384
Created by
admin on Mon Mar 31 17:33:07 GMT 2025 , Edited by admin on Mon Mar 31 17:33:07 GMT 2025
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
