Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C23H30N2O |
| Molecular Weight | 350.4971 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(=O)N([C@H]1CCN(CCC2=CC=CC=C2)C[C@H]1C)C3=CC=CC=C3
InChI
InChIKey=MLQRZXNZHAOCHQ-KNQAVFIVSA-N
InChI=1S/C23H30N2O/c1-3-23(26)25(21-12-8-5-9-13-21)22-15-17-24(18-19(22)2)16-14-20-10-6-4-7-11-20/h4-13,19,22H,3,14-18H2,1-2H3/t19-,22+/m1/s1
| Molecular Formula | C23H30N2O |
| Molecular Weight | 350.4971 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:11:44 GMT 2025
by
admin
on
Mon Mar 31 23:11:44 GMT 2025
|
| Record UNII |
P57PR7Y64W
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Common Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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DTXSID50202032
Created by
admin on Mon Mar 31 23:11:44 GMT 2025 , Edited by admin on Mon Mar 31 23:11:44 GMT 2025
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PRIMARY | |||
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3041260
Created by
admin on Mon Mar 31 23:11:44 GMT 2025 , Edited by admin on Mon Mar 31 23:11:44 GMT 2025
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PRIMARY | |||
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53758-22-8
Created by
admin on Mon Mar 31 23:11:44 GMT 2025 , Edited by admin on Mon Mar 31 23:11:44 GMT 2025
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PRIMARY | |||
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P57PR7Y64W
Created by
admin on Mon Mar 31 23:11:44 GMT 2025 , Edited by admin on Mon Mar 31 23:11:44 GMT 2025
|
PRIMARY |
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TARGET -> AGONIST |
Mouse hot plate test. 2600 times more potent than morphine.
ED50
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PARENT -> METABOLITE INACTIVE |
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IMPURITY -> PARENT |
Immediate precursor
ED50
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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