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Cl-amidine TFA_1043444-18-3_Absin

产品信息
抗原名称
PAD1 ,PAD4 ,PAD3
商品描述

Cl-amidine is a cell-permeable compound that acts as a pan PAD inhibitor (IC50 = 0.8 μM, 6.2 μM and 5.9 μM for PAD1, PAD3, and PAD4, respectively) in enzymatic assays.

分子量
424.8
纯度

>98%

可溶性
DMSO :84 mg/mL warmed (197.74 mM)
Ethanol :84 mg/mL warmed (197.74 mM)
Water :70 mg/mL warmed (164.78 mM)
外观
Powder
In vitro(体外研究)
Cl-amidine antagonizes the PAD4-mediated enhancement of the the p300GBD-GRIP1 interaction in a dose-dependent manner. The inhibitory effect of this compound is not a nonspecific one but is targeted at the active PAD4 enzyme. Cl-amidine increases p53 expression in CD45 positive immune cells. It triggers the differentiation and apoptosis of multiple cancer cell lines that are p53+/+ and p53−/− (e.g., HL60, HT29, TK6, and U2-OS cells). Cl-amidine induces the expression of p53 and several downstream target genes including the cyclin dependent kinase inhibitor p21, GADD45, and the proapoptotic protein PUMA in U2-OS osteosarcoma cells.
In vivo(体内研究)
Cl-amidine treatment inhibits NZM(New Zealand mixed 2328) NET(neutrophil extracellular trap) formation in vivo and significantly alters circulating autoantibody profiles and complement levels while reducing glomerular IgG deposition. Further, Cl-amidine increases the differentiation capacity of bone marrow endothelial progenitor cells, improves endothelium-dependent vasorelaxation, and markedly delays time to arterial thrombosis induced by photochemical injury. Cl-amidine delays thrombosis development in NZM mice. It inhibits PADs in mice without significant toxicity and improves disease phenotypes in animal models of inflammatory arthritis and inflammatory bowel disease. And It is shown to reduce disease severity in mouse models of ulcerative colitis and RA.
背景
别名
Cl-Amidine (trifluoroacetate salt)
分子式
C14H19ClN4O2 • CF3CO2H
CAS号
1043444-18-3
制备和贮存
保存方式
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.

参考图片

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