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)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥562 | 有现货 |
|
| 10MG | ¥946 | 有现货 |
|
| 25MG | ¥1628 | 有现货 |
|
| 50MG | ¥2409 | 有现货 |
|
| 100MG | ¥3339 | 有现货 |
|
| 200MG | ¥4473 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称DRI-C21045
-
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
-
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。
-
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.
-
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.
-
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.
-
同义词——
-
通路Apoptosis
-
靶点NF-κB
-
受体anandamide cellular uptake
-
研究领域——
-
适应症——
化学信息
-
CAS Number2101765-81-3
-
分子量580.61
-
分子式C32H24N2O7S
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 2 mg/mL (3.44 mM)
-
SMILESCOC(=O)c1ccc(cc1)C(=O)Nc1ccc(cc1)-c1ccc(cc1)C(=O)Nc1cccc2cccc(c12)S(O)(=O)=O
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
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
关联产品
-
Hentriacontane
三十烷是一种天然产物,具有多种药理作用,包括抗炎、抗肿瘤和抗菌活性。
-
Didox
核糖核苷酸还原酶抑制剂;克服 PC-3 细胞中 Bcl-2 介导的辐射抗性。
-
Antiproliferative ag...
Antiproliferative agent-22 (compound 2) 是一种抗癌剂。Antiproliferative agent-22 对 MCF-7、MDA-MB-231 和 MDA-MB-468 细胞具有抗增殖活性,IC50 值分别为 6.2 μM、3.3 μM 和 3.3 μM。
021-51111890
购物车()
sales@molnova.cn

