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  • 化合物 MCC950|T3701|TargetMol

化合物 MCC950|T3701|TargetMol

MCC950
210826-40-7
369 2mg 起订
498 5mg 起订
790 10mg 起订
上海 更新日期:2024-09-29

TargetMol中国(陶术生物)

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邮箱:marketing@tsbiochem.com

产品详情:

中文名称:
化合物 MCC950
英文名称:
MCC950
CAS号:
210826-40-7
品牌:
TargetMol
产地:
美国
保存条件:
Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
纯度规格:
97%
产品类别:
抑制剂
货号:
T3701

Product Introduction

Bioactivity

名称MCC950
描述CP-456773 (MCC950 (CP-456773) and CRID3) is an effective and specific cytokine release inhibitor and NLRP3 inflammasome inhibitor. CP-456773 inhibits IL-1β secretion and caspase 1 processing. MCC950 blocked canonical and noncanonical NLRP3 activation at nanomolar concentrations. MCC950 specifically inhibited activation of NLRP3 but not the AIM2, NLRC4 or NLRP1 inflammasomes. MCC950 reduced IL-1β production in vivo and attenuated the severity of experimental autoimmune encephalomyelitis (EAE), a disease model of multiple sclerosis.
细胞实验MCC950 is dissolved in DMSO and stored, and then diluted with appropriate media before use[1]. BMDM are seeded at 5×105/mL or 1×106/mL, HMDM at 5×105/mL and PBMC at 2×106/mL or 5×106/mL in 96 well plates. The following day the overnight medium is replaced and cells are stimulated with 10 ng/mL LPS from Escherichia coli serotype EH100 (ra) TLRgrad for 3 h. Medium is removed and replaced with serum free medium (SFM) containing DMSO (1:1,000), MCC950 (0.001-10 μM), glyburide (200 μM), Parthenolide (10 μM) or Bayer cysteinyl leukotriene receptor antagonist 1-(5-carboxy-2{3-[4-(3-cyclohexylpropoxy)phenyl]propoxy}benzoyl)piperidine-4-carboxylic acid (40 μM) for 30 min. Cells are then stimulated with inflammasome activators: 5 mM adenosine 5'-triphosphate disodium salt hydrate (ATP) (1 h), 1 μg/mL Poly(deoxyadenylic-thymidylic) acid sodium salt (Poly dA:dT) transfected with Lipofectamine 200 (3-4 h), 200 μg/mL MSU (overnight) and 10 μM nigericin (1 h) or S. typhimurium UK-1 strain. Cells are also stimulated with 25 μg/mL Polyadenylic-polyuridylic acid (4 h). For non-canonical inflammasome activation cells are primed with 100 ng/mL Pam3CSK4 for 4 h, medium is removed and replaced with SFM containing DMSO or MCC950 and 2 μg/mL LPS is transfected using 0.25% FuGENE for 16 h. Supernatants are removed and analysed using ELISA kits. LDH release is measured using the CytoTox96 non-radioactive cytotoxicity assay[1].
激酶实验Disk diffusion is conducted, except that 10 μg of each antibiotic compound is used per filter. Growth in liquid medium in the presence of CHIR-090 is evaluated as follows: cells from overnight cultures are inoculated into 50 mL portions of LB broth at an A600 of 0.02 and grown with shaking at 30°C. When the A600 reaches 0.15, parallel cultures are treated with either 6 μL of 500 μg/mL CHIR-090 in DMSO or 6 μL of DMSO. To assess cumulative growth, cultures are maintained in log phase growth by 10-fold dilution into pre-warmed medium, containing the same concentrations of DMSO or DMSO/CHIR-090, whenever the A600 reaches 0.4. The minimal inhibitory concentration is defined as the lowest antibiotic concentration at which no measurable bacterial growth is observed in LB medium containing 1% DMSO (v/v), when inoculated at a starting density of A600=0.01. Cultures are incubated with shaking for 24 h at 30°C in the presence of CHIR-090. Experiments are performed in triplicate[1].
体外活性MCC950以纳摩尔浓度阻断NLRP3的典型与非典型激活,特异性地抑制NLRP3而不影响AIM2、NLRC4或NLRP1的激活。在小鼠骨髓来源的巨噬细胞(BMDM)和人源单核细胞衍生的巨噬细胞(HMDM)中测试了MCC950对NLRP3炎症体激活的影响,BMDM中MCC950的半抑制浓度(IC50)约为7.5 nM,而在HMDM中具有相似的抑制能力(IC50=8.1 nM)。MCC950还呈剂量依赖性地抑制IL-1β的分泌,但不抑制TNF-α的分泌。在非典型途径激活下,MCC950特异性阻断由caspase-11直接引起的NLRP3激活和IL-1β的分泌。即使在10 μM的浓度下,MCC950也不抑制由沙门氏菌(Salmonella typhimurium)激活的NLRC4刺激的IL-1β和TNF-α的分泌。在响应S. typhimurium时,MCC950不抑制caspase-1的激活或IL-1β的处理。MCC950处理对细胞裂解物中的pro-caspase-1和pro-IL-1β的表达没有显著影响[1]。
体内活性MCC950通过减少白介素-1β (IL-1β) 的产生和减轻实验性自身免疫性脑炎症(EAE) 的严重程度,来延缓多发性硬化症模型的发展。MCC950预处理能降低IL-1β和IL-6的血清浓度,但对TNF-α的数量影响不大。在小鼠身上应用MCC950能延缓EAE的发病时间并减轻症状。通过对第22天牺牲小鼠的脑部单核细胞进行细胞内细胞因子染色和流式细胞术(FACS)分析显示,与PBS处理的小鼠相比,MCC950处理的小鼠中IL-17和IFN-γ产生的CD3+ T细胞的频率有轻微降低。具体来说,IFN-γ和特别是IL-17产生的细胞数量在CD3+ T细胞的CD4+和γδ+亚群中也有所减少。
存储条件Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度DMSO : 83.33 mg/mL (206.02 mM), Sonication is recommended.
关键字CP 456773 | MCC 950 | Inhibitor | CRID-3 | NOD-like Receptor (NLR) | inhibit | MCC-950 | CRID3 | CP456773 | CRID 3 | MCC950
相关产品Bergenin | Selnoflast | NLRP3-IN-2 | NLRP3-IN-9 | Imperatorin | MCC950 sodium | INF39 | NLRP3-IN-10 | Nigericin sodium salt | Dapansutrile | NOD-IN-1 | CY-09
相关库抑制剂库 | 抗乳腺癌化合物库 | 经典已知活性库 | 已知活性化合物库 | 抗衰老化合物库 | 抗前列腺癌化合物库
CP-456773|TargetMol

公司简介

TargetMol Chemicals Inc. 总部位于马萨诸塞州波士顿,致力于为全球生化领域科学家的研究提供专业的产品和服务。TargetMol?品牌的客户群分布于40多个国家和地区,已发展成为全球知名的化合物库和小分子化合物研究供应商。 TargetMol?可提供160多种满足不同需求的化合物库,以及多种类型的生化试剂产品,包括12000多种抑制剂、16000多种天然产物和各类多肽、抗体、生命科学试剂盒等,此外,我们还建设有CADD(计算机辅助药物设计)研究中心、药理实验室、药化合成平台三大技术中心,全方位满足客户的定制需求。 凭借我们优质的产品和服务、快速高效的全球供应链和专业的技术支持,我们将有效帮助您缩短研发周期,取得更成功的结果。

成立日期 (12年)
注册资本 566.265100万人民币
员工人数 100-500人
年营业额 ¥ 1亿以上
经营模式 贸易,工厂,试剂,定制,服务
主营行业 天然产物,生化试剂,分子生物学,分子砌块,生物技术服务

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