Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H25NS |
| Molecular Weight | 311.484 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CNCCCC1(SC(C)(C)C2=C1C=CC=C2)C3=CC=CC=C3
InChI
InChIKey=FKHYYOUFMJBLAF-UHFFFAOYSA-N
InChI=1S/C20H25NS/c1-19(2)17-12-7-8-13-18(17)20(22-19,14-9-15-21-3)16-10-5-4-6-11-16/h4-8,10-13,21H,9,14-15H2,1-3H3
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL222 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2999402 |
0.79 nM [IC50] | ||
Target ID: CHEMBL238 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2999402 |
9300.0 nM [IC50] | ||
Target ID: CHEMBL228 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2999402 |
850.0 nM [IC50] | ||
Target ID: CHEMBL222 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2999402 |
0.79 nM [IC50] |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Noradrenergic mechanisms in cocaine-induced reinstatement of drug seeking in squirrel monkeys. | 2007-08 |
|
| Synthesis and positron emission tomography evaluation of three norepinephrine transporter radioligands: [C-11]desipramine, [C-11]talopram and [C-11]talsupram. | 2005-12-03 |
|
| Synthesis and biological evaluation of [11C]talopram and [11C]talsupram: candidate PET ligands for the norepinephrine transporter. | 2004-08 |
| Name | Type | Language | ||
|---|---|---|---|---|
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Official Name | English | ||
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Preferred Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C265
Created by
admin on Mon Mar 31 19:15:33 GMT 2025 , Edited by admin on Mon Mar 31 19:15:33 GMT 2025
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| Code System | Code | Type | Description | ||
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C001750
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PRIMARY | |||
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C6Z73MW6CR
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PRIMARY | |||
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Talsupram
Created by
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PRIMARY | |||
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CHEMBL52247
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PRIMARY | |||
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DB09191
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PRIMARY | |||
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DTXSID50864992
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PRIMARY | |||
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100000083209
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PRIMARY | |||
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33014
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PRIMARY | |||
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SUB10815MIG
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PRIMARY | |||
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3076
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PRIMARY | |||
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21489-20-3
Created by
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PRIMARY | |||
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C75180
Created by
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PRIMARY |
ACTIVE MOIETY