
DRI-C21045
CAS No. 2101765-81-3
DRI-C21045 ( —— )
产品货号. M26176 CAS No. 2101765-81-3
Dri-c21045 对 B 细胞增殖诱导的 NF-kB 激活和所有 CD40L 表现出浓度依赖性抑制,IC50 分别为 17.1 μM 和 4.5 μM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥356 | 有现货 |
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5MG | ¥583 | 有现货 |
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10MG | ¥988 | 有现货 |
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25MG | ¥1879 | 有现货 |
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50MG | ¥3345 | 有现货 |
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100MG | ¥5006 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称DRI-C21045
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Dri-c21045 对 B 细胞增殖诱导的 NF-kB 激活和所有 CD40L 表现出浓度依赖性抑制,IC50 分别为 17.1 μM 和 4.5 μM。
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产品描述Dri-c21045 showed concentration-dependent inhibition of NF-kB activation and all CD40L induced by B cell proliferation with IC50 of 17.1 μM and 4.5 μM, respectively. Dri-c21045 is an effective selective inhibitor of CD40-CD40L synergistic stimulator protein-protein interaction (PPI) with IC50 of 0.17 μM.
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体外实验DRI-C21045 (3.2-100 μM; 18 h) concentration-dependently inhibits the CD40L-induced NF-κB activation in CD40 sensor cells.DRI-C21045 (0.6-50 μM; 48 h) blocks CD40L-induced functional activation of primary B cells.DRI-C21045 (0.4-50 μM; 48 h) inhibits CD40L-induced MHC-II upregulation in THP-1 cells.DRI-C21045 (2-100 μM; 48 h) inhibits CD40L-induced B cell proliferation.DRI-C21045 shows no signs of cytotoxicity for concentrations of up to 100 and 200 μM and has no genotoxic potential for concentrations of up to 500 μM.
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体内实验DRI-C21045 (30 mg/kg; daily, s.c.; in 20% HPβCD) prolongs graft survival in a murine allogeneic skin transplant model.DRI-C21045 (20-60 mg/kg; twice daily s.c.; in 20% HPβCD) inhibits alloantigen-induced T cell expansion in the draining lymph nodes (DLNs). Animal Model:Full-thickness ear skins from BALB/c were transplanted onto the dorsal thorax of C57BL/6 Dosage:30 mg/kg Administration:Daily s.c; administered in 20% w/v hydroxypropyl-β-cyclodextrin (HPβCD) solutionResult:Caused prolongation of skin allograft survival.
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同义词——
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通路Apoptosis
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靶点NF-κB
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受体anandamide cellular uptake
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研究领域——
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适应症——
化学信息
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CAS Number2101765-81-3
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分子量580.61
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分子式C32H24N2O7S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 2 mg/mL (3.44 mM)
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SMILESCOC(=O)c1ccc(cc1)C(=O)Nc1ccc(cc1)-c1ccc(cc1)C(=O)Nc1cccc2cccc(c12)S(O)(=O)=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Ortar G, et al. Novel selective and metabolically stable inhibitors of anandamide cellular uptake. Biochem Pharmacol. 2003 May 1;65(9):1473-81.
产品手册




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