1. Signaling Pathways
  2. GPCR/G Protein
  3. CaSR

CaSR (钙敏感受体)

Calcium-sensing receptor

The extracellular CaSR (calcium-sensing receptor is a unique G protein-coupled receptor (GPCR) activated by extracellular Ca2+ and by other physiological cations including Mg2+, amino acids, and polyamines. CaSR is the most important master controller of the extracellular Ca2+ homeostatic system being expressed at high levels in the parathyroid gland, kidney, gut, and bone, where it regulates parathyroid hormone (PTH) secretion, vitamin D synthesis, and Ca2+ absorption and resorption, respectively. Gain and loss of function mutations in the CaSR are responsible for severe disturbances in extracellular Ca2+ metabolism.

The CaSR stimulates two major signal transduction cascades. The first is the Gq/11-phospholipase C (PLC)-mediated generation of inositol 1,4,5-trisphosphate (IP3), which induces a rapid rise in intracellular calcium (Ca2+i) concentrations. The second is the mitogen-activated protein kinases (MAPKs), such as extracellular signal-regulated kinases 1 and 2 (ERK1/2), which phosphorylate proteins mediating cytosolic signaling and translocate into the nucleus to activate transcription factors involved in cellular proliferation and differentiation. The CaSR has been shown to activate MAPK signaling in a manner that depends on the G proteins Gq/11, and Gi/o, which inhibits cyclic adenosine monophosphate (cAMP) synthesis, and by a potentially G protein-independent mechanism involving β-arrestin types 1 and 2.

CaSR 相关产品 (33):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-107773
    GSK3004774 Agonist 98.11%
    GSK3004774 是一种有效的、不能吸收的 CaSR 激动剂,对人、小鼠和大鼠 CaSRpEC50 值分别为 7.3,6.6 和 6.5, 对人 CaSREC50 值为 50 nM。
    GSK3004774
  • HY-122819
    Calindol hydrochloride Agonist 99.88%
    Calindol hydrochloride 是拟钙钙敏感受体 (CaSR) 的正变构调节剂 (PAM),EC50 为 132 nM。
    Calindol hydrochloride
  • HY-P1955
    Etelcalcetide Activator
    Etelcalcetide (AMG 416) 是一种合成肽,有钙敏感受体 (CaSR) 活化剂的作用。Etelcalcetide 可有效降低接受血液透析的继发性甲状旁腺功能亢进患者的 甲状旁腺激素 (PTH) 浓度。
    Etelcalcetide
  • HY-109106
    Upacicalcet
    Upacicalcet 是一种静脉内拟钙剂。Upacicalcet 通过直接作用于甲状旁腺细胞膜钙敏感受体来抑制过量的甲状旁腺激素 (PTH) 分泌,从而降低血液中的 PTH 水平。Upacicalcet 可用于研究继发性甲状旁腺功能亢进症 (SHPT)。
    Upacicalcet
  • HY-P4376
    Gamma-Glu-Abu Agonist
    Gamma-Glu-Abu 是一种有效的钙敏感受体 (calcium sensing receptor (CaSR)) 激动剂。
    Gamma-Glu-Abu
  • HY-109106B
    (Rac)-Upacicalcet
    (Rac)-Upacicalcet 是 Upacicalcet 的消旋体。Upacicalcet 是一种静脉内拟钙剂。Upacicalcet 通过直接作用于甲状旁腺细胞膜钙敏感受体来抑制过量的甲状旁腺激素 (PTH) 分泌,从而降低血液中的 PTH 水平。Upacicalcet 可用于研究继发性甲状旁腺功能亢进症 (SHPT)。
    (Rac)-Upacicalcet
  • HY-153258
    CaSR antagonist-1 Antagonist
    CaSR antagonist-1是一种钙敏感受体(CaSR)拮抗剂,IC50值为50 nM。CaSR antagonist-1可用于骨质疏松等与骨或矿物质稳态异常相关的疾病的研究。
    CaSR antagonist-1
  • HY-70037S
    Cinacalcet-d3

    西那卡塞 d3

    Agonist
    Cinacalcet-d3 是 Cinacalcet 的氘代物。Cinacalcet (AMG 073) 是一种可口服的 Ca receptor (CaR) 激动剂,用于心血管疾病研究。
    Cinacalcet-d<sub>3</sub>
  • HY-117851
    AC-265347 Agonist 99.97%
    AC-265347 是一种钙敏感受体 (CaSR) 激动剂和正变构调节剂 (ago-PAM),功能亲和力 (pKB) 为 5.1。AC-265347 可用于甲状旁腺功能亢进及相关疾病的研究。
    AC-265347
  • HY-70037AS
    Cinacalcet-d3 hydrochloride

    盐酸西那卡塞 d3 (盐酸盐)

    Agonist
    Cinacalcet-d3 (hydrochloride) 是 Cinacalcet hydrochloride 的氘代物。Cinacalcet hydrochloride (AMG 073 hydrochloride) 是一种可口服的 Ca receptor (CaR) 激动剂,用于心血管疾病研究。
    Cinacalcet-d<sub>3</sub> hydrochloride
  • HY-15106
    SB-423557 Antagonist
    SB-423557 是口服活性钙敏感受体 (CaR) 拮抗剂 (IC50=520 nM),SB-423562 的前体 (IC50=73 nM)。SB-423557 在人体内耐受良好,可增加外源性甲状旁腺激素 (PTH) 的血浆浓度,刺激骨形成。
    SB-423557
  • HY-14752
    Ronacaleret Antagonist
    Ronacaleret (SB 751689) 是一种口服活性、高效、选择性的钙感应受体 (CaSR) 拮抗剂,能刺激甲状旁腺释放内源性甲状旁腺激素。Ronacaleret (SB 751689) 用于研究绝经后骨质疏松症.
    Ronacaleret
  • HY-161113
    Z8554052021 Activator
    Z8554052021 (compound 2021) 是一种有效的 CaSR 正变构调节剂 (PAM),实际上也是GPCR PAM,EC50 为 3.3 nM。Z8554052021 具有用于甲状旁腺功能亢进研究的潜力。
    Z8554052021