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首页-小分子抑制剂&激动剂-NF-κB Pathway-MALT1-MLT-985
MLT-985

Chemical Structure : MLT-985

CAS No.: 1832576-25-6

MLT-985 (MLT985, MV088428)

货号: PC-49482Not For Human Use, Lab Use Only.

MLT-985 (MLT985) is a potent, highly selective allosteric MALT1 inhibitor with biochemical IC50 of 3 nM, and 20 nM in IL-2 reporter gene assay (Jurkat T cells).

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

MLT-985 (MLT985) is a potent, highly selective allosteric MALT1 inhibitor with biochemical IC50 of 3 nM, and 20 nM in IL-2 reporter gene assay (Jurkat T cells).
MLT-985 showed excellent selectivity against a panel of 23 human proteases (all IC50>10 uM), including cysteine proteases such as Caspase 3 and Cathepsin B, C, K, L and S.
MLT-985 inhibits human PBMC IL-2 release with IC50 of 0.5 uM.
MLT-985 demonstrated activity in cellular ABC-DLBCL models that is consistent with potent and selective inhibition of MALT1, suppresses growth and aberrant CARD11/BCL10/MALT1 complex signaling in ABC-DLBCL cells.
MLT-985 demonstrated tumor regression in the CARD11-mutant ABC-DLBCL xenograft model OCILy3.

物理化学性质&存储条件

分子量 448.27
分子式 C17H15Cl2N9O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(S)-1-(5-chloro-6-(2H-1,2,3-triazol-2-yl)pyridin-3-yl)-3-(2-chloro-7-(1-methoxyethyl)pyrazolo[1,5-a]pyrimidin-6-yl)urea

参考文献

1. Jean Quancard, et al. J Med Chem. 2020 Dec 10;63(23):14594-14608.

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