1. Signaling Pathways
  2. GPCR/G Protein
  3. Trace Amine-associated Receptor (TAAR)

Trace Amine-associated Receptor (TAAR) (痕量胺相关受体)

Trace amine associated-receptors (TAARs) are a class of G protein-coupled receptors that were discovered in 2001. Humans possess six functional isoforms (TAAR1, TAAR2, TAAR5, TAAR6, TAAR8, and TAAR9), whereas some fish species express over 100. It acts as an endogenous receptor for the trace amines. Trace amines are endogenous compounds classically regarded as comprising β-phenylethyalmine, p-tyramine, tryptamine, p-octopamine, and some of their metabolites.

Although all other TAARs serve predominantly or exclusively as chemosensory receptors in the main olfactory system, TAAR 1 has been demonstrated to be a novel modulator of dopaminergic, serotonergic and glutamatergic activity in the brain. And TAAR 1 has been identified as a novel therapeutic target for schizophrenia, depression, and addiction. In the periphery, TAAR1 regulates nutrient-induced hormone secretion, suggesting its potential as a novel therapeutic target for diabetes and obesity. TAAR1 may also regulate immune responses by regulating leukocyte differentiation and activation.

Trace Amine-associated Receptor (TAAR) 相关产品 (9):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-110098
    Ro 5212773 99.70%
    Ro 5212773 (EPPTB) 是一种有效和选择性的 (TAAR1) 拮抗剂(对于小鼠 TAAR1 的 Ki 值为 0.9 nM),对其他 TAARs 没有显著影响。TAAR1 是一种 G 蛋白偶联受体 (GPCR),由内源性氨基酸代谢产物非选择性激活。
    Ro 5212773
  • HY-109157
    Ralmitaront Agonist 99.92%
    Ralmitaront (RO6889450) 是一种具有口服活性的微量胺相关受体 1 (TAAR1) 的激动剂,EC50 值为 110.4 nM。Ralmitaront 在啮齿动物中具有抗精神病、认知改善和抗抑郁的活性。Ralmitaront 可作为一种神经抑制剂,用于神经相关疾病的研究,如精神分裂症 (SCZ)、分裂情感性障碍。
    Ralmitaront
  • HY-12700
    RO5256390 98.75%
    RO5256390 是微量胺相关受体 1 (TAAR1) 的激动剂,是一种内源性微量胺结合的高度保守的 G 蛋白偶联受体 (GPCR)。RO5256390 可通过活性分子对中脑皮质系统的作用,减少活性分子滥用的多种行为效应。RO5256390 是一种单胺,能调节神经传递,可以阻止精神刺激剂引起的亢奋,并产生类似抗精神病活性分子奥氮平的大脑激活模式,显示出类似抗精神病活性分子的特性。
    RO5256390
  • HY-12699
    RO5166017 99.48%
    RO5166017 是具有口服活性的、跨物种的 TAAR1 的激动剂,其对小鼠、大鼠、人和食蟹猴的 Ki 值分别为1.9 nM、2.7 nM、31 nM 和 24 nM。
    RO5166017
  • HY-108015
    RO5263397 99.26%
    RO5263397 是一种有效的,选择性的和口服的 TAAR1 激动剂,对人TAAR1 和大鼠 TAAR1 的 EC50 分别为 17 和 35 nM。RO5263397调节清醒度和 EEG 频谱组成。
    RO5263397
  • HY-42346
    ZH8651

    4-溴苯乙胺 1G

    Agonist 99.71%
    ZH8651 是 TAAR1 的激动剂,可同时激活 Gs 和 Gq 信号通路。ZH8651 可用于研究精神分裂症。
    ZH8651
  • HY-161317
    Gαq/11 protein-IN-1 Agonist
    Gαq/11 protein-IN-1 (compound F33) 是一种 Gαq/11 蛋白抑制剂,IC50 值为 9.4 μM。 Gαq/11 protein-IN-1 具有抗肿瘤活性。
    Gαq/11 protein-IN-1
  • HY-157955
    TAAR1 agonist 1 Agonist
    TAAR1 agonist 1 (compound 6E) 是一种有效的 TAAR1 激动剂,具有有效的 TAAR1-Gs/Gq 双通路激活特性。TAAR1 agonist 1 显着缓解 MK-801 诱导的精神分裂症样认知表型。
    TAAR1 agonist 1
  • HY-157955A
    TAAR1 agonist 1 hydrochloride Agonist
    TAAR1 agonist 1 hydrochloride (6e·HCl) 是一种新型的 G 蛋白偶联受体 TAAR1 激动剂。TAAR1 agonist 1 hydrochloride 可用于精神分裂症的研究。
    TAAR1 agonist 1 hydrochloride