Details
| Stereochemistry | MIXED |
| Molecular Formula | C28H35ClN2O3 |
| Molecular Weight | 483.042 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(C)N(CC(OC(=O)C1=CC=C(O)C=C1)C2=CC=CN2CC3=C(Cl)C=CC=C3)C(C)CC
InChI
InChIKey=HZTHPJGBPGLHIS-UHFFFAOYSA-N
InChI=1S/C28H35ClN2O3/c1-5-20(3)31(21(4)6-2)19-27(34-28(33)22-13-15-24(32)16-14-22)26-12-9-17-30(26)18-23-10-7-8-11-25(23)29/h7-17,20-21,27,32H,5-6,18-19H2,1-4H3
| Molecular Formula | C28H35ClN2O3 |
| Molecular Weight | 483.042 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Viminol is an opioid analgesic developed by the company Zambon. It is marketed under tradename Dividol for the treatment of pain due to various causes, including the treatment of pain due to osteoarthritis, neuritic pain, vascular pain, visceral pain, neoplastic pain, and pain due to other sources. In vivo studies demonstrated that the analgesic effects of viminol depend on the stereo configuration: the R,R-enantiomer exhibit agonistic activity, while the S,S-enantiomer produce the opposite effect.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:54:59 GMT 2025
by
admin
on
Mon Mar 31 21:54:59 GMT 2025
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| Record UNII |
PLI450958N
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| Record Status |
Validated (UNII)
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| Record Version |
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SUB05097MIG
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DTXSID10944067
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PLI450958N
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177158
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21466-60-4
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |