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Merck
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文件

5.38120

Sigma-Aldrich

类端粒沉默干扰体1(NLRP3)抑制剂,MCC950

别名:

类端粒沉默干扰体1(NLRP3)抑制剂,MCC950

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About This Item

经验公式(希尔记法):
C20H23N2O5S · Na
分子量:
426.46
分類程式碼代碼:
51111800
NACRES:
NA.77

化驗

≥97% (HPLC)

品質等級

形狀

powder

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
desiccated (hygroscopic)
protect from light

顏色

white

溶解度

water: 1 mg/mL
DMSO: 50 mg/mL

儲存溫度

−20°C

InChI

1S/C20H24N2O5S.Na/c1-20(2,24)14-10-17(27-11-14)28(25,26)22-19(23)21-18-15-7-3-5-12(15)9-13-6-4-8-16(13)18;/h9-11,24H,3-8H2,1-2H3,(H2,21,22,23);/q;+1/p-1

InChI 密鑰

LFQQNXFKPNZRFT-UHFFFAOYSA-M

一般說明

MCC950 is an antagonist ofInterleukin-1 beta (IL-1β). It interacts with both the inactive as well as active forms of NOD-like receptor protein 3 (NLRP3) and targets the Walker B motif within the NLRP3 NACHT domain. A cell-permeable, bioavailable, non-toxic sulfonylurea-derived compound that selectively interacts with the NLRP3 inflammasome and prevents its activation in a reversible manner with no effect on NLRC4 and NLRP1. Dose-dependently reduces IL-1β production (IC50 = 7.5 & 8.1 nM in LPS & ATP-treated BMDMs & HMDMs, respectively) with minimal effect on IL-1α & TNF-α. Specifically, it blocks NLRP3-dependent pyroptotic cell death by inhibiting caspase-1 &-11 activation, IL-1β processing, and ASC oligomerization. Does neither block K+ efflux, Ca2+ flux, or NLRP3-ASC interactions nor inhibits NLRC4, AIM2, TLR signaling, or NLRP3 priming. Effectively suppresses T cell responses and IL-1β& IL-6 secretion, reduces the severity of EAE, and rescues neonatal lethality in a mouse model of CAPS (10 mg/kg, i.p., q.d., & 20 mg/kg, i.p., every other day, respectively). Displays an attractive PK profile with desirable microsomal stability and minimal liability towards CYP450 isozymes (<15% inhibition at 10 µM) & hERG (IC50 >30 µM). It has demonstrated effectiveness against metabolic diseases, autoimmune diseases, cardiovascular diseases, and other conditions.

應用

MCC950 has been used in:

  • hemolysis-affected mice to study the involvement of the NLRP3 inflammasome in kidney function injury.
  • MCC950-mediated inflammasome inhibition assays.
  • testing synergistic effect of pharmacologic inhibition of NLRP3 inflammasome in combination with immune checkpoint inhibitors (ICI) immunotherapy in tumor-bearing animals.
  • studying the role of NLRP3 inflammasome in the development of endothelial dysfunction in early sepsis in mice.

生化/生理作用

主要靶标
NLRP3
可逆性:是
细胞可渗透性:具有

包裝

用惰性气体包装

警告

毒性:标准处理(A)

外觀

以钠盐供应。

重構

复溶后,等分并冷冻保存(-20°C)。贮备液在-20°C下可稳定保存至多3个月。

其他說明

Pleasenote that the molecular weight for this compound is batch-specific due tovariable water content. Please refer to the vial label or the certificate ofanalysis for the batch-specific molecular weight. The molecular weight providedrepresents the baseline molecular weight without water.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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访问文档库

Role of the Nucleotide-Binding Domain-Like Receptor Protein 3 Inflammasome in the Endothelial Dysfunction of Early Sepsis
Luo M, et al.
Inflammation, 43, 1561?1571-1561?1571 (2020)
Therapeutic potential of MCC950, a specific inhibitor of NLRP3 inflammasome
Hao Li, et al.
European Journal of Pharmacology, 928, 175091-175091 (2022)
Ablation of NLRP3 inflammasome rewires MDSC function and promotes tumor regression
Iosif Papafragkos, et al.
Journal of Separation Science, 13 (2022)
NLRP3 inflammasome of renal tubular epithelial cells induces kidney injury in acute hemolytic transfusion reactions
Zhixin Liu, et al.
Clinical and Translational Medicine, 11(3), e373-e373 (2021)

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