Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C16H25NO2 |
| Molecular Weight | 263.3752 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=CC(=C1)[C@@]2(O)CCCC[C@@H]2CN(C)C
InChI
InChIKey=TVYLLZQTGLZFBW-ZBFHGGJFSA-N
InChI=1S/C16H25NO2/c1-17(2)12-14-7-4-5-10-16(14,18)13-8-6-9-15(11-13)19-3/h6,8-9,11,14,18H,4-5,7,10,12H2,1-3H3/t14-,16+/m1/s1
| Molecular Formula | C16H25NO2 |
| Molecular Weight | 263.3752 |
| 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
Sat Dec 16 10:19:24 UTC 2023
by
admin
on
Sat Dec 16 10:19:24 UTC 2023
|
| Record UNII |
0NG5TTM63P
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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| Code System | Code | Type | Description | ||
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DTXSID401167150
Created by
admin on Sat Dec 16 10:19:24 UTC 2023 , Edited by admin on Sat Dec 16 10:19:24 UTC 2023
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33741
Created by
admin on Sat Dec 16 10:19:24 UTC 2023 , Edited by admin on Sat Dec 16 10:19:24 UTC 2023
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75725
Created by
admin on Sat Dec 16 10:19:24 UTC 2023 , Edited by admin on Sat Dec 16 10:19:24 UTC 2023
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123154-38-1
Created by
admin on Sat Dec 16 10:19:24 UTC 2023 , Edited by admin on Sat Dec 16 10:19:24 UTC 2023
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0NG5TTM63P
Created by
admin on Sat Dec 16 10:19:24 UTC 2023 , Edited by admin on Sat Dec 16 10:19:24 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST | |||
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TARGET -> INHIBITOR | |||
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ENANTIOMER -> ENANTIOMER |
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RACEMATE -> ENANTIOMER |
Agonist of the μ. opioid receptor and inhibits serotonin reuptake.
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