Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C19H27NO |
| Molecular Weight | 285.4238 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC(N1CCCC1)C(=O)C2=CC3=C(CCCC3)C=C2
InChI
InChIKey=MMIKQWIZKBYLKZ-UHFFFAOYSA-N
InChI=1S/C19H27NO/c1-2-7-18(20-12-5-6-13-20)19(21)17-11-10-15-8-3-4-9-16(15)14-17/h10-11,14,18H,2-9,12-13H2,1H3
| Molecular Formula | C19H27NO |
| Molecular Weight | 285.4238 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:16:59 GMT 2023
by
admin
on
Sat Dec 16 10:16:59 GMT 2023
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| Record UNII |
S5MU9GV87C
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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WIKIPEDIA |
Designer-drugs-TH-PVP
Created by
admin on Sat Dec 16 10:16:59 GMT 2023 , Edited by admin on Sat Dec 16 10:16:59 GMT 2023
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| Code System | Code | Type | Description | ||
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DTXSID201337111
Created by
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CYCLOHEXANE-.ALPHA.-PVP
Created by
admin on Sat Dec 16 10:16:59 GMT 2023 , Edited by admin on Sat Dec 16 10:16:59 GMT 2023
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TH-PVP
Created by
admin on Sat Dec 16 10:16:59 GMT 2023 , Edited by admin on Sat Dec 16 10:16:59 GMT 2023
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132989549
Created by
admin on Sat Dec 16 10:16:59 GMT 2023 , Edited by admin on Sat Dec 16 10:16:59 GMT 2023
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S5MU9GV87C
Created by
admin on Sat Dec 16 10:16:59 GMT 2023 , Edited by admin on Sat Dec 16 10:16:59 GMT 2023
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TH-PVP
Created by
admin on Sat Dec 16 10:16:59 GMT 2023 , Edited by admin on Sat Dec 16 10:16:59 GMT 2023
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2304915-07-7
Created by
admin on Sat Dec 16 10:16:59 GMT 2023 , Edited by admin on Sat Dec 16 10:16:59 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> INHIBITOR |
Inhibition of [125I]RTI-55 binding Ki ± sem (μΜ) (n)
Ki
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TARGET -> INHIBITOR |
nhibition of [3H]neurotransmitter uptake IC50 ± sem (μΜ).
IC50
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
Pharmacological studies in vitro showed it to inhibit reuptake and promote the release of monoamine neurotransmitters with some selectivity for serotonin,
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