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  1. GPCR/G Protein
    Neuronal Signaling
  2. Opioid Receptor

Opioid Receptor

Opioid receptors are a group of G protein-coupled receptors with opioids as ligands. The endogenous opioids are dynorphins, enkephalins, endorphins, endomorphins and nociceptin. Opioid receptors are distributed widely in the brain, and are found in the spinal cord and digestive tract. Opioid receptors are molecules, or sites, within the body that are activated by opioid substances. Opioid receptors inhibit the transmission of impulse in excitatory pathways within the human body system. These pathways include the serotonin, catecholamine, and substance P pathways, which are all implicated in pain perception and feelings of well-being. Opioid receptors are further subclassified into mu, delta, and kappa receptors. All the classes, while exhibiting differing modes of action, share some basic similarities. They all are driven by the potassium pump mechanism, which is found on the plasma membrane of the majority of cells.

Opioid Receptor 相关产品 (60):

Cat. No.Product NameEffectPurity
  • HY-101386
    PZM21Agonist 99.45%
    PZM21是高效选择性的μ opioid receptor受体激动剂,EC50值为1.8 nM。
  • HY-B0418A
    Loperamide hydrochlorideAgonist 99.69%
    Loperamide (hydrochloride) (R-18553 (hydrochloride)) 是用于治疗腹泻的阿片受体 (opioid receptor) 激动剂。
  • HY-13044
    ADL-5859Agonist 99.65%
    ADL5859是δ-阿片受体选择性激动剂,Ki为0.8 nM,对hERG有弱抑制性。
  • HY-16655A
    Oliceridine hydrochlorideAgonist 98.70%
    Oliceridine hydrochloride (TRV130 hydrochloride) 是新颖的 MOR 激动剂,能够优先激活 G-protein 信号通路,而对 β-arrestin 的作用稍弱。
  • HY-10487
    JDTic dihydrochlorideAntagonist 99.79%
    JDTic dihydrochloride 是一种有效的 kappa-opioid receptors (KOR) 的拮抗剂,常用于神经系统疾病的研究。
  • HY-A0118A
    Naloxegol oxalateAntagonist 99.90%
    Naloxegol oxalate (NKTR-118 oxalate; AZ-13337019 oxalate) 是阿片受体拮抗剂。
  • HY-P1594A
    Dynorphin A (1-10) TFAAgonist
    Dynorphin A (1-10) (TFA) 是一种内源性的阿片样神经肽,与 κ 阿片受体 (κ-opioid receptor) 结合。Dynorphin A (1-10) (TFA) 也阻断 NMDA激活的电流,IC50 为 42.0 μM。
  • HY-A0118
    NaloxegolAntagonist
    Naloxegol (NKTR-118; AZ-13337019) 是阿片受体拮抗剂。
  • HY-G0021
    N-DesmethylclozapineAgonist 98.66%
    N-Desmethylclozapine 是登革病毒抑制剂,同时为 δ-opioid 受体的激动剂。
  • HY-N0164
    MatrineAgonist >98.0%
    Matrine (Matridin-15-one) 是来源于植物的生物碱,有抗肿瘤活性,是kappa阿片受体激动剂。
  • HY-101177
    Naltrindole hydrochlorideAntagonist 99.68%
    Naltrindole hydrochloride是高效,选择性的非多肽类 δ opioid受体拮抗剂,Ki值为0.02 nM。
  • HY-101718
    AticaprantAntagonist 99.24%
    Aticaprant (CERC-501) 是一种有效地可渗透中枢神经的kappa opioid受体拮抗剂,Ki值为0.807 nM。
  • HY-P0210
    DAMGOAgonist 98.10%
    DAMGO 是 一种选择性的 μ-阿片受体 (μ-OPR) 激动剂。
  • HY-15536
    CebranopadolAgonist 98.76%
    Cebranopadol 是NOPopioid receptor 激动剂,作用于人NOP,MOP,KOP 和δ-阿片肽(DOP)受体,Ki/EC50 分别为 0.9 nM/13 nM,0.7 nM/1.2 nM,2.6 nM/17 nM,18 nM/110 nM。
  • HY-13274
    JTC-801Antagonist 99.20%
    JTC-801 是一种具有选择性的 opioid receptor-like1 (ORL1) receptor抑制剂,其Ki 值为 8.2 nM。
  • HY-15122A
    Sinomenine hydrochlorideActivator >98.0%
    Sinomenine hydrochloride 是 NF-κB 活化的阻断剂,也是 μ 阿片受体 (μ-opioid receptor) 的激活剂。
  • HY-P0073
    Tyr-Gly-Gly-Phe-Met-OHActivator 99.81%
    Tyr-Gly-Gly-Phe-Met-OH 通过结合阿片样物质受体 (opioid receptor),可调控人类免疫功能,抑制肿瘤生长。
  • HY-P0183
    NociceptinAgonist 99.79%
    Nociceptin 是一种十七肽,为 nociceptin 受体的内源性配体,具有镇痛作用。
  • HY-P0288
    [Leu5]-EnkephalinAgonist 99.72%
    [Leu5]-Enkephalin 是一种具有吗啡药性的五肽。作为阿片受体 (opioid receptors) 激动剂。
  • HY-111454
    SR17018Agonist >98.0%
    SR17018 是一种 mu 型阿片受体 (mu-opioid-receptor) 激动剂,能够与 GTPγS 结合,EC50 值为 97 nM。
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