您好,欢迎来到试剂信息网! [登录] [免费注册]
试剂信息网
位置:首页 > 产品库 > WM-1119
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
WM-1119
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
WM-1119图片
CAS NO:2055397-28-7
规格:≥98%
包装与价格:
包装价格(元)
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW) 389.38
Formula C18H13F2N3O3S
CAS No. 2055397-28-7
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: ≥ 150 mg/mL (385 mM)
Water: NA
Ethanol: NA
SynonymsWM1119; WM 1119; WM-1119
实验参考方法
In Vitro

In vitro activity: WM-1119 can induce cell cycle exit and cellular senescence without causing DNA damage. WM-1119 is 1,100-fold and 250-fold more active against KAT6A than against KAT5 or KAT7, respectively, and so shows greater specificity for KAT6A than does WM-8014. The testing of WM-1119 at 1 μM and 10 μM against a pharmacological panel of 159 diverse biological targets reveal no affinity. Treatment of MEFs with WM-1119 results in cell cycle arrest in G1 and a senescence phenotype similar to that seen upon treatment with WM-8014. Notably, the activity of WM-1119 in this cell-based assay is an order of magnitude greater than WM-8014 and WM-1119 is able to induce cell cycle arrest at 1 μM. Treatment with WM-8014 or WM-1119 inhibits the proliferation of the EMRK1184 lymphoma cells in vitro, WM-1119 (IC50=0.25 μM) is ninefold more active than WM-8014 (IC50=2.3 μM), as expected on the basis of reduced protein binding.


Kinase Assay: WM-1119 is a novel, highly potent, and selective inhibitor of KAT6A/B (lysine acetyltransferase) with an IC50 value of of 0.25 μM for KAT6A, KD value of 2 nM for KAT6A, KD value of 2.2 μM for KAT5, and KD value of 0.5 μM for KAT7.


Cell Assay: Treatment of MEFs with WM-1119 resulted in cell cycle arrest in G1 and a senescence phenotype similar to that seen upon treatment with WM-8014 (Extended Data Fig. 8). Notably, the activity of WM-1119 in this cell-based assay is an order of magnitude greater than WM-8014 and WM-1119 is able to induce cell cycle arrest at 1 μM.

In VivoThe cohorts that are treated four times per day with WM-1119 have arrested tumour growth By day 14, with the exception of one mouse that does not respond. Spleen weights in the WM-1119-treatment group (treated four times per day) are substantially lower than spleen weights in the vehicle-treated group, and not significantly different from those of tumour-free eight-weekold mice. Treatment with WM-1119 three times per day leads to a significant reduction in tumour burden and spleen weight, but is not as effective as treatment four times per day. WM-1119 is well-tolerated; mice show no generalized ill effects and weight loss is not observed. WM-1119 treatment has no effect on haematocrit, erythrocytes or platelet numbers, but there is overall leukopenia. The proportion and overall number of tumour cells is substantially reduced by WM-1119 treatment (four times per day).
Animal model Mouse tumor models
Formulation & Dosage
References Nature. 2018 Aug;560(7717):253-257.