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目錄:MedChemExpress LLC>>生化試劑>> MCC950 sodium | MCE

MCC950 sodium | MCE
  • MCC950 sodium | MCE
參考價 600
具體成交價以合同協議為準
參考價 600
具體成交價以合同協議為準
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更新時間:2023-06-20 09:34:00瀏覽次數:300評價

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CAS 256373-96-3 純度 99.61%
分子量 426.46 分子式 C??H??N?NaO?S
供貨周期 現貨 規格 5 mg
貨號 HY-12815A 應用領域 醫療衛生,化工,生物產業,制藥/生物制藥
MCC950 sodium | MCEMCC950 sodium (CP-456773 sodium; CRID3 sodium salt) is a potent, selective <b>NLRP3</b> inhibitor with <b>IC<sub>50</sub></b>s of 7.5 and 8.1 nM in BMDMs and HMDMs, respectively.

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MCC950 sodium

CAS No. : 256373-96-3

產品活性:MCC950 sodium (CP-456773 sodium; CRID3 sodium salt) is a potent, selective NLRP3 inhibitor with IC50s of 7.5 and 8.1 nM in BMDMs and HMDMs, respectively.

研究領域:Immunology/Inflammation

作用靶點:NOD-like Receptor (NLR)

In Vitro: MCC950 blocks canonical and non-canonical NLRP3 activation at nanomolar concentrations. MCC950 specifically inhibits NLRP3 but not AIM2, NLRC4 or NLRP1 activation. The effect of MCC950 on NLRP3 inflammasome activation is tested in mouse bone marrow derived macrophages (BMDM) and human monocyte derived macrophages (HMDM). The IC50 of MCC950 in BMDM is approximately 7.5 nM, while in HMDM it has a similar inhibitory capacity (IC50=8.1 nM). MCC950 also dose dependently inhibit IL-1β but not TNF-α secretion.MCC950 specifically blocks caspase-11-directed NLRP3 activation and IL-1β secretion upon stimulation of the non-canonical pathway. NLRC4-stimulated IL-1β and TNF-α secretion (as activated by Salmonella typhimurium) are not inhibited by MCC950 even at a concentration of 10 µM. MCC950 does not inhibit caspase-1 activation or IL-1β processing in response to S. typhimurium. The expression of pro-caspase-1 and pro-IL-1β in cell lysates is not substantially affected by MCC950 treatment.

In Vivo: MCC950 reduces Interleukin-1p (IL-1β) production and attenuates the severity of experimental autoimmune encephalomyelitis (EAE), a disease model of multiple sclerosis. Pre-treatment with MCC950 reduces serum concentrations of IL-1β and IL-6 while it does not considerably decrease the amount of TNF-α. Treatment of mice with MCC950 delays the onset and reduced the severity of EAE. Intracellular cytokine staining and FACS analysis of brain mononuclear cells from mice sacrificed on day 22 shows modestly reduced frequencies of IL-17 and IFN-γ producing CD3+ T cells in MCC950 treated mice in comparison with PBS-treated mice. IFN-γ and particularly IL-17 producing cell numbers are also reduced in both the CD4+ and γδ+ sub-populations of CD3+ T cells.

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