Integral membrane proteins called serotonin transporters (SERTs) move serotonin from synaptic spaces into presynaptic neurons. Serotonin's function is effectively terminated and neuronal transmission is stopped by SERTs, which reabsorb it in the synaptic cleft. Reuptake of serotonin is essential for avoiding nerve overstimulation.
By delivering 5-hydroxytryptamine (5HT) to neurons and glial cells, the serotonin transporter (SERT) controls the extracellular levels of serotonin (5-hydroxytryptamine, 5HT) in the brain. Drugs used to treat emotional disorders, such as depression, primarily target the human SERT (hSERT). The bacterial leucine transporter (LeuT), for which a high resolution crystal structure is now available, is a member of the solute carrier 6 family, which also includes hSERT.
| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
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V121319 | (1R,4R)-4-(3,4-Dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride | 675126-09-7 | (1R,4R)-4-(3,4-Dichlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride is a metabolite of the selective serotonin reuptake inhibitor (SSRI) sertraline. |
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V87838 | (1S,4S)-N-Desmethyl Sertraline hydrochloride | 675126-10-0 | (1S,4S)-N-Desmethyl Sertraline (hydrochloride) is a metabolite of Sertraline. |
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V105612 | (R)-Duloxetine hydrochloride | 910138-96-4 | (R)-Duloxetine (LY248686) hydrochloride is a naphthoxy-substituted amine used in binding studies to human serum albumin and, unlike its enantiomer (S)-duloxetine, has limited efficacy as a dual serotonin and norepinephrine reuptake inhibitor (SNRI). |
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V70013 | (R)-Fluoxetine hydrochloride ((R)-Fluoxetine hydrochloride) | 114247-09-5 | (R)-Fluoxetine HCl, an antidepressant, is a serotonin reuptake inhibitor (SSRI). |
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V121947 | (R)-Norfluoxetine | 130194-43-3 | (R)-Norfluoxetine is the (R)-enantiomer of norfluoxetine. |
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V70010 | (S)-Fluoxetine hydrochloride (S-isomer of fluoxetine) | 114247-06-2 | (S)-Fluoxetine HCl is an antidepressant and serotonin reuptake inhibitor (SSRI). |
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V103032 | (S)-Norfluoxetine | 126924-38-7 | (S)-Norfluoxetine, the S enantiomer of norfluoxetine, is a selective serotonin reuptake inhibitor. |
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V70005 | (±)-cis-Sertraline-d3 hydrochloride ((±)-Sertraline d3 hydrochloride (hydrochloride)) | 1217741-83-7 | (±)-cis-Sertraline-d3 ( HCl) is the deuterated form of Sertraline HCl. |
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V70022 | (±)-Duloxetine hydrochloride ((Rac)-Duloxetine hydrochloride) | 947316-47-4 | (±)-Duloxetine ((Rac)-Duloxetine) HCl is the racemate of Duloxetine HCl. |
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V118462 | 2-(tert-Butylamino)-1-phenylpropan-1-one hydrochloride | 63199-74-6 | 2-(tert-butylamino)-1-phenylprop-1-one hydrochloride (compound Imp.1) is a non-selective monoamine transporter (DAT/NET/SERT) agonist. |
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V124483 | 2-Aminotetralin | 2954-50-9 | 2-Aminotetralin is a potent and selective 5-HT1 receptor agonist. |
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V125331 | 3-Chloroamphetamine hydrochloride | 35378-15-5 | 3-Chloroamphetamine hydrochloride is a derivative of amphetamine that acts as a central nervous system stimulant by releasing serotonin and dopamine. |
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V113667 | 6-Nitroquipazine | 77372-73-7 | 6-Nitroquinazine (DU24565) is a potent and selective 5-HT transporter inhibitor with a Ki value of 0.17 nM. |
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V102873 | 9β-Debilon | 9β-Debilon is a sesquiterpenoid found in Nardostachys grandiflora that may have SERT modulatory activity. | |
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V127989 | A6CDQ | 1005550-46-8 | A6CDQ is a human organic cation transporter (hOCT) inhibitor with antidepressant-like activity and the ability to cross the blood-brain barrier. |
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V70026 | Adoxosidic acid | 84375-46-2 | Adoxosidic acid is a SERT enhancer found in N. |
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V70016 | Ampreloxetine hydrochloride (TD-9855 hydrochloride) | 1227056-87-2 | Ampreloxetine (TD-9855) HCl is an orally bioactive and CNS-penetrating inhibitor of the norepinephrine transporter (NET) and the serotonin 5-HT uptake transporter (SERT), but not the dopamine transporter (DAT). |
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V129011 | Antidepressant agent 9 | 143899-90-5 | Antidepressant agent 9 is an orally effective NMDAR and SERT inhibitor that can cross the blood-brain barrier, with IC50 values of 3.50 μM and 1044 nM, respectively. |
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V130399 | BMS-570520 | 388101-58-4 | BMS-570520 is a highly bioavailable oral CCR3 antagonist with an IC50 of 1.9 nM for hCCR3 and 1300 nM for hCYP2D6. |
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V70003 | Bupropion-d9 hydrochloride (Amfebutamone-d9 (hydrochloride)) | 1189725-26-5 | Bupropion-d9 ( HCl) is the deuterated form of Bupropion HCl. |