14 Results for "

hOCT1

" in MedChemExpress (MCE) Product Catalog:
Products (14)

14 Results for "hOCT1" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-B1213
CAS No.: 521-78-8
Target:  

5-HT Receptor Bacterial

Research Areas:  

Neurological Disease

Trimipramine maleate is a 5-HT receptor antagonist, with blood-brain barrier permeability. Trimipramine maleate has pKi binding values of 6.39, 8.10, 4.66 for 5-HT1C, 5-HT2 and 5-HT1A, respectively. Trimipramine maleate is also a potent and selective inhibitor targeting human noradrenaline (hNAT), serotonin (hSERT) and organic cation transporters (hOCT1, hOCT2) with IC50 values of 4.99 μM, 2.11 μM, 3.72 μM, 8.00 μM, respectively. Trimipramine maleate has vascular activity and anxiolytic efficacy [1] .
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Cat. No.: HY-B1213A
CAS No.: 739-71-9
Target:  

5-HT Receptor Bacterial

Research Areas:  

Neurological Disease

Trimipramine is a 5-HT receptor antagonist, with pKi binding values of 6.39, 8.10, 4.66 for 5-HT1C, 5-HT2 and 5-HT1A, respectively. Trimipramine is also a potent and selective inhibitor targeting human noradrenaline (hNAT), serotonin (hSERT) and organic cation transporters (hOCT1, hOCT2) with IC50 values of 4.99 μM, 2.11 μM, 3.72 μM, 8.00 μM, respectively. Trimipramine has vascular activity and anxiolytic efficacy [1] .
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Cat. No.: HY-RS13061
Research Areas:  

Others

SLC22A1 Human Pre-designed siRNA Set A contains three designed siRNAs for SLC22A1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-147333
CAS No.: 14171-70-1
Target:  

Drug Metabolite

Research Areas:  

Neurological Disease

Trimipramine N-oxide is an active metabolite of the tricyclic antidepressant trimipramine. Trimipramine N-oxide inhibits the human monoamine transporters for noradrenaline (hNAT), serotonin (hSERT), dopamine (hDAT) and the human organic cation transporters (hOCT1 and hOCT2) with IC50s of 11.7, 3.59, 9.4, 9.35 and 27.4 nM, respectively. Trimipramine N-oxide can be used for the research of depression and anxiety [1].
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Cat. No.: HY-B1213AR
CAS No.: 739-71-9
Trimipramine (Standard) is the analytical standard of Trimipramine. This product is intended for research and analytical applications. Trimipramine is a 5-HT receptor antagonist, with pKi binding values of 6.39, 8.10, 4.66 for 5-HT1C, 5-HT2 and 5-HT1A, respectively. Trimipramine is also a potent and selective inhibitor targeting human noradrenaline (hNAT), serotonin (hSERT) and organic cation transporters (hOCT1, hOCT2) with IC50 values of 4.99 μM, 2.11 μM, 3.72 μM, 8.00 μM, respectively. Trimipramine has vascular activity and anxiolytic efficacy [1] .
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Cat. No.: HY-B1213R
CAS No.: 521-78-8
Trimipramine (maleate) (Standard) is the analytical standard of Trimipramine (maleate). This product is intended for research and analytical applications. Trimipramine maleate is a 5-HT receptor antagonist, with pKi binding values of 6.39, 8.10, 4.66 for 5-HT1C, 5-HT2 and 5-HT1A, respectively [1]. Trimipramine maleate is also a potent and selective inhibitor targeting human noradrenaline (hNAT), serotonin (hSERT) and organic cation transporters (hOCT1, hOCT2) with IC50 values of 4.99 μM, 2.11 μM, 3.72 μM, 8.00 μM, respectively . Trimipramine maleate has vascular activity and anxiolytic efficacy .
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Cat. No.: HY-N9418R
CAS No.: 561-56-8
Trimipramine (Standard) is the analytical standard of Trimipramine. This product is intended for research and analytical applications. Trimipramine is a 5-HT receptor antagonist, with pKi binding values of 6.39, 8.10, 4.66 for 5-HT1C, 5-HT2 and 5-HT1A, respectively. Trimipramine is also a potent and selective inhibitor targeting human noradrenaline (hNAT), serotonin (hSERT) and organic cation transporters (hOCT1, hOCT2) with IC50 values of 4.99 μM, 2.11 μM, 3.72 μM, 8.00 μM, respectively. Trimipramine has vascular activity and anxiolytic efficacy [1] .
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Cat. No.: HY-P83828
Synonyms: OCT1; hOCT1; oct1_cds; SLC22A1

Host:  

Mouse

Application:  

FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P83828A
Synonyms: OCT1; hOCT1; oct1_cds; SLC22A1

Host:  

Mouse

Application:  

FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P82681
Synonyms: hOCT1; OCT1; Slc22a1

Host:  

Rabbit

Application:  

WB, FC

Reactivity:  

Human

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Cat. No.: HY-182363
CAS No.: 1005550-46-8
Target:  

Serotonin Transporter

Research Areas:  

Neurological Disease

A6CDQ is a human organic cation transporter (hOCT) inhibitor with antidepressant-like activity that can cross the blood-brain barrier. A6CDQ potently inhibits the transport activities mediated by hOCT1, hOCT2 and hOCT3. A6CDQ exhibits significant antidepressant-like effects in the mouse tail suspension test. A6CDQ can be used in studies related to depression [1].
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Cat. No.: HY-P85379A
Synonyms: SLC22A1; OCT1; Solute carrier family 22 member 1; Organic cation transporter 1; hOCT1

Host:  

Mouse

Application:  

WB, ELISA

Reactivity:  

Human

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Cat. No.: HY-P85303
Synonyms: SLC22A1; OCT1; Solute carrier family 22 member 1; Organic cation transporter 1; hOCT1

Host:  

Rabbit

Application:  

WB, FC

Reactivity:  

Human

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Cat. No.: HY-P85379
Synonyms: SLC22A1; OCT1; Solute carrier family 22 member 1; Organic cation transporter 1; hOCT1

Host:  

Mouse

Application:  

WB, ELISA

Reactivity:  

Human

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