1. Signaling Pathways
  2. GPCR/G Protein
    Neuronal Signaling
  3. MCHR1 (GPR24)

MCHR1 (GPR24) (黑色素浓缩激素受体1)

Melanin concentrating hormone receptor 1

MCHR1 (GPR24), also known as Melanin concentrating hormone receptor 1, is a class A G-protein-coupled receptor (GPCR). MCHR1 has received considerable attention, as potent and selective antagonists acting at that receptor display anxiolytic, antidepressant and/or anorectic properties. MCHR1 is the sole receptor expressed in rodents and couples to Gi and Gq proteins.

MCH is a ubiquitous vertebrate neuropeptide predominantly synthesized by neurons of the diencephalon that can act through two G protein-coupled receptors, called MCHR1 and MCHR2. MCHR1 can inhibit cAMP accumulation and stimulate intracellular calcium flux, and is probably involved in the neuronal regulation of food consumption. Although structurally similar to somatostatin receptors, this protein does not seem to bind somatostatin.

MCHR1 (GPR24) 相关产品 (28):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-107625
    SNAP 94847 Antagonist
    SNAP 94847 是一种新型的,高亲和力的选择性黑色素浓缩激素受体 1 (MCHR1) 拮抗剂,其 (Ki= 2.2 nM, Kd=530 pM),它对 MCHα1AMCHD2 受体分别显示出 >80 倍和 >500 倍的选择性。 SNAP 94847 以高亲和力与小鼠和大鼠 MCHR1 结合,与其他 GPCR,离子通道,酶和转运蛋白的交叉反应性很小。
    SNAP 94847
  • HY-P3155
    Ac-hMCH(6-16)-NH2 Agonist
    Ac-hMCH(6-16)-NH2 是人脑中 MCH 的非选择性肽类激动剂,其对MCH-1R 和MCH-2R 的 IC50 值分别为 0.16 nM 和2.7 nM。
    Ac-hMCH(6-16)-NH2
  • HY-136152
    MCHR1 antagonist 3 Antagonist
    MCHR1 antagonist 3 是一种有效的黑色素浓缩激素受体 1 (MCHR1) 拮抗剂。MCHR1 antagonist 3 用于调节能量代谢。
    MCHR1 antagonist 3
  • HY-P4745
    hMCH-1R antagonist 1 Antagonist
    hMCH-1R antagonist 1 (Compound 30) 是一种有效的和选择性的人黑色素聚集激素受体 1 (hMCHR1) 拮抗剂,KB 值为 3.6 nM。hMCH-1R antagonist 1 能与 hMCHR1hMCHR2 结合,IC50 值分别为 65 nM 和 49 nM。hMCH-1R antagonist 1 可用于代谢研究。
    hMCH-1R antagonist 1
  • HY-12433
    BMS-819881 Antagonist
    BMS-819881 是一种黑色素浓缩激素受体1 (MCHR1) 拮抗剂,结合大鼠 MCHR1,Ki 值为 7 nM。BMS-819881 还有效且选择性地作用于 CYP3A4EC50 为 13 μM。
    BMS-819881
  • HY-100318
    NGD-4715 Antagonist
    NGD-4715是选择性,有口服活性的黑色素浓缩激素受体1 (melanin-concentrating hormone receptor 1 (MCHR1)) 的拮抗剂。
    NGD-4715
  • HY-100308
    SB-568849 Antagonist
    SB-568849 是一种黑色素浓缩激素受体 1 (MCH R1) 拮抗剂,pKi 值为 7.7。
    SB-568849
  • HY-U00353
    MCHR1 antagonist 1 Antagonist
    MCHR1 antagonist 1 是一种选择性的黑色素浓集激素 1 型受体 (melanin concentrating hormone-1 receptor) 拮抗剂,对人 MCH1 受体的 KbKi 值分别为 1 nM 和 4 nM,在降低体重方面可能起作用。
    MCHR1 antagonist 1