1. GPCR/G Protein
    Neuronal Signaling
  2. 5-HT Receptor

5-HT Receptor

5-HT receptors (Serotonin receptors) are a group of G protein-coupled receptors (GPCRs) and ligand-gated ion channels (LGICs) found in the central and peripheral nervous systems. Type: 5-HT1, 5-HT2, 5-HT3, 5-HT4, 5-HT5, 5-HT6, 5-HT7. They mediate both excitatory and inhibitory neurotransmission. The serotonin receptors are activated by the neurotransmitter serotonin, which acts as their natural ligand. The serotonin receptors modulate the release of many neurotransmitters, including glutamate, GABA, dopamine, epinephrine / norepinephrine, and acetylcholine, as well as many hormones, including oxytocin, prolactin, vasopressin, cortisol, corticotropin, and substance P, among others. The serotonin receptors influence various biological and neurological processes such as aggression, anxiety, appetite, cognition, learning, memory, mood, nausea, sleep, andthermoregulation. The serotonin receptors are the target of a variety of pharmaceutical drugs, including many antidepressants, antipsychotics, anorectics,antiemetics, gastroprokinetic agents, antimigraine agents, hallucinogens, and entactogens.

5-HT Receptor 相关产品 (226):

Cat. No. Product Name Effect Purity
  • HY-17366
    Clozapine N-oxide Antagonist 99.63%
    Clozapine N-oxide (CNO) 是抗精神病药物氯氮平的主要代谢产物。 Clozapine N-oxide是 DREADD 系统的激动剂。
  • HY-B0407A
    Chlorpromazine hydrochloride Antagonist 99.83%
    Chlorpromazine Hydrochloride 是一种有效的 dopamine D2 受体,5-HT2A 受体,potassium channelsodium channel 的拮抗剂,抑制 D2 受体和 serotonin 5-HT2A 受体的活性,Ki 值分别为 363 nM 和 8.3 nM。
  • HY-N0737A
    Harmine Inhibitor 99.58%
    Harmine是一种具有抗癌和抗炎活性的天然双特异性酪氨酸磷酸化调节激酶 ((DYRK)) 抑制剂。
  • HY-N0296A
    Scopolamine hydrobromide Inhibitor >98.0%
    Scopolamine hydrobromide 是高亲和力的 (nM 级别) 毒蕈碱 (muscarinic) 拮抗剂。Scopolamine 可逆抑制 5-HT3 受体反应,IC50 为 2.09 μM。
  • HY-14557
    Pimavanserin Inhibitor 99.73%
    Pimavanserin是选择性的 5-HT2A 受体反向激动剂,pIC50pKd 分别为8.73 and 9.3。
  • HY-N0066
    Eucalyptol Inhibitor >98.0%
    Eucalyptol 是 5-HT3 受体, 钾通道, TNF-αIL-1β 的抑制剂。
  • HY-14940
    Volinanserin Antagonist 99.71%
    Volinanserin 是一种有效的,选择性的 5-HT2 受体拮抗剂,Ki 值为 0.36 nM,对其选择性是对 5-HT1c,alpha-1 和 DA D2 受体的 300 倍,可用于精神疾病的研究。
  • HY-101331
    Phenylbiguanide Agonist >98.0%
    Phenylbiguanide 是一种选择性的 5-HT3 受体激动剂,EC50 为 3.0±0.1 μM。
  • HY-15780
    Brexpiprazole Modulator 99.38%
    Brexpiprazole是人 5-HT1A多巴胺受体的部分激动剂,Ki分别为0.12 nM 和 0.3 nM。 Brexpiprazole也是 5-HT2A 受体的拮抗剂,Ki 为0.47 nM。
  • HY-14546
    Aripiprazole Agonist 99.98%
    Aripiprazole(Abilify)是人5-HT1A受体部分激动剂,Ki为4.2 nM。
  • HY-N0060A
    Ferulic acid sodium Activator 99.74%
    Ferulic acid (sodium) 是一种酚类化合物,能够抑制由氧化应激和炎症产生的机体紊乱。
  • HY-B0965
    Thioridazine hydrochloride Antagonist 99.93%
    Thioridazine是一种治疗精神类疾病的药物, 如精神分裂症, 具有多巴胺D4受体选择性和5-羟色胺拮抗作用。
  • HY-B1272
    Desipramine hydrochloride Inhibitor 99.68%
    Desipramine hydrochloride 是去甲肾上腺素转运蛋白 (NET), 5-羟色胺转运体 (SERT) 和多巴胺转运 (DAT) 的抑制剂,其 Ki 值分别为 4, 61 和 78,720 nM。
  • HY-B1473
    Serotonin hydrochloride Agonist 99.97%
    Serotonin hydrochloride 是 CNS 中的单胺神经递质和内源性 5-HT 受体激动剂。Serotonin hydrochloride 也是儿茶酚 O-甲基转移酶 (COMT) 的抑制剂其 Ki 值为 44 μM。
  • HY-11018
    Risperidone Inhibitor 99.16%
    Risperidone是 5-HT2 受体的阻断剂,P-糖蛋白 (P-Glycoprotein) 的抑制剂 和 dopamine D2 受体的拮抗剂,其对 5-HT2A 和 dopamine D2 受体的 Ki 值分别为 4.8,5.9 nM。
  • HY-14763A
    Cariprazine hydrochloride Modulator 99.89%
    Cariprazine(RGH188)盐酸盐有抗精神病活性,对D3和D2受体有较高亲和力,Ki分别为0.09 nM和0.5 nM,对5-HT(1A)受体有一定亲和力。
  • HY-14763
    Cariprazine Modulator 98.01%
    Cariprazine是一种新型抗精神病候选药物,结合D3, D25-HT1AKi 为0.085 nM,0.49 nM,2.6 nM。
  • HY-14541
    Olanzapine Antagonist 99.94%
    Olanzapine(LY170053)是5-HT2和D2受体高亲和性拮抗剂。
  • HY-14544
    Quetiapine Antagonist 99.83%
    Quetiapine(Ketipinor)是非典型的抗精神病化合物,可作用于精神分裂,狂躁和抑郁症。
  • HY-16978
    TG6-10-1 Antagonist 99.28%
    TG6-10-1是一种EP2拮抗剂, 低nM时只有效作用于EP2, 比作用于人EP3, EP4和IP受体选择性高300, EP1受体选择性高100倍的。
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