Serotonin Transporter
Read More about this categoryShow Less
Serotonin Transporters (SERTs) are integral membrane proteins that transport serotonin from synaptic spaces into presynaptic neurons. SERTs function by reuptaking serotonin in the synaptic cleft, effectively terminating the function of serotonin and halting neuronal transmission. Serotonin reuptake is a critical process to prevent overstimulation of nerves.
Serotonin transporter (SERT) regulates extracellular levels of serotonin (5-hydroxytryptamine, 5HT) in the brain by transporting 5HT into neurons and glial cells. The human SERT (hSERT) is the primary target for drugs used in the treatment of emotional disorders, including depression. hSERT belongs to the solute carrier 6 family that includes a bacterial leucine transporter (LeuT), for which a high resolution crystal structure has become available.
Products Related to Serotonin Transporter(61)
- GC60394(±)-Duloxetine hydrochlorideCAS: 947316-47-4Purity: >99.50%
(±)-둘록세틴((Rac)-둘록세틴) 염산염은 둘록세틴 염산염의 라세미체입니다.
- GC60424(S)-VenlafaxineCAS: 93413-44-6Purity: >98%
(S)-Venlafaxine은 Venlafaxine의 (S)-구성입니다. 벤라팍신은 경구 활성, 강력한 세로토닌(5-HT)/노르에피네프린(NE) 재흡수 이중 억제제입니다. 벤라팍신은 항우울제입니다.
- GC60740Dapoxetine-D7 hydrochlorideCAS: 129938-20-1Purity: >99.50%
Dapoxetine-d7(LY-210448-d7) 염산염은 Dapoxetine 염산염으로 표지된 중수소입니다.
- GC70271Ampreloxetine hydrochlorideCAS: 1227056-87-2Purity: >99.00%
Ampreloxetine (TD-9855) hydrochloride is an orally active and CNS-penetrant inhibitor of Norepinephrine transporter (NET) and Serotonin 5-HT uptake transporter (SERT), but not Dopamine transporter (DAT).
- GC71618rel-Sertraline-d3 hydrochlorideCAS: 1330180-66-9
rel-Sertraline-d3 hydrochloride는 Sertraline 염산염으로 표기된 중수소입니다.
- GC79505RPI-GLYT2-82Purity: >99.00%
RPI-GLYT2-82 is a reversible, blood-brain barrier-permeable allosteric inhibitor of GlyT2 with an IC 50 value of 554 nM.
- GC79780SERT/5-HT-IN-1CAS: 3120534-54-2Purity: >99.00%
SERT/5-HT-IN-1 (compound D17) is an orally active and potent dual target inhibitor of SERT/5-HT3A ( SERT IC 50 = 1.5 nM, NET IC 50 = 49 nM, DAT IC 50 = 91 nM, 5-HT3A K i = 12 nM).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC60394 | (±)-Duloxetine hydrochloride | 947316-47-4 | >99.50% | |
(±)-둘록세틴((Rac)-둘록세틴) 염산염은 둘록세틴 염산염의 라세미체입니다. | ||||
| GC60424 | (S)-Venlafaxine | 93413-44-6 | >98% | |
(S)-Venlafaxine은 Venlafaxine의 (S)-구성입니다. 벤라팍신은 경구 활성, 강력한 세로토닌(5-HT)/노르에피네프린(NE) 재흡수 이중 억제제입니다. 벤라팍신은 항우울제입니다. | ||||
| GC60740 | Dapoxetine-D7 hydrochloride | 129938-20-1 | >99.50% | |
Dapoxetine-d7(LY-210448-d7) 염산염은 Dapoxetine 염산염으로 표지된 중수소입니다. | ||||
| GC65014 | DSP-1053 | 1176326-76-3 | >99.00% | |
벤질피페리딘 유도체인 DSP-1053은 Ki가 1.02nM인 강력한 세로토닌 운반체(SERT) 억제제입니다. | ||||
| GC65209 | Imipramine-d4 hydrochloride | 61361-33-9 | >99.50% | |
| GC69880 | SERT-IN-2 | 2055228-33-4 | >98.00% | |
SERT-IN-2는 강력한 SERT 억제제(IC50=0.58 nM)로, 항우울 활성을 가지고 있습니다. SERT-IN-2의 생체 이용도는 좋으며, 쥐에서 F(%)는 83.28%입니다. 또한 SERT-IN-2는 혈뇌 장벽을 통과할 수 있습니다. | ||||
| GC70178 | ZZL-7 | 99141-91-0 | >98.00% | |
ZZL-7는 빠른 효과를 가진 항우울제입니다. ZZL-7은 중심선반핵(DRN) 내의 세로토닌 수송체(SERT)와 신경원소 일산화질소 합성효소(nNOS) 간 상호작용을 파괴함으로써 작용합니다. ZZL-7은 혈뇌장벽을 쉽게 통과하여 중증우울증(MDD) 연구에 사용될 수 있습니다. | ||||
| GC70271 | Ampreloxetine hydrochloride | 1227056-87-2 | >99.00% | |
Ampreloxetine (TD-9855) hydrochloride is an orally active and CNS-penetrant inhibitor of Norepinephrine transporter (NET) and Serotonin 5-HT uptake transporter (SERT), but not Dopamine transporter (DAT). | ||||
| GC71618 | rel-Sertraline-d3 hydrochloride | 1330180-66-9 | - | |
rel-Sertraline-d3 hydrochloride는 Sertraline 염산염으로 표기된 중수소입니다. | ||||
| GC71620 | Venlafaxine-d6 | 1020720-02-8 | - | |
Venlafaxine-d6는 벤라팍신 (Venlafaxine)으로 표기된 중수소이다. | ||||
| GC79505 | RPI-GLYT2-82 | - | >99.00% | |
RPI-GLYT2-82 is a reversible, blood-brain barrier-permeable allosteric inhibitor of GlyT2 with an IC 50 value of 554 nM. | ||||
| GC79780 | SERT/5-HT-IN-1 | 3120534-54-2 | >99.00% | |
SERT/5-HT-IN-1 (compound D17) is an orally active and potent dual target inhibitor of SERT/5-HT3A ( SERT IC 50 = 1.5 nM, NET IC 50 = 49 nM, DAT IC 50 = 91 nM, 5-HT3A K i = 12 nM). | ||||
| GC79790 | A6CDQ | 1005550-46-8 | >98% | |
A6CDQ is a human organic cation transporter ( hOCT ) inhibitor with antidepressant-like activity that can cross the blood-brain barrier. | ||||
