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ARN-3236
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。
ARN-3236图片
CAS NO:1613710-01-2
包装与价格:
包装价格(元)
10mM (in 1mL DMSO)电议
2mg电议
5mg电议
10mg电议
50mg电议
100mg电议

产品介绍
ARN-3236是具有口服活性的盐诱导激酶2(SIK2)(IC50<1nM)的选择性抑制剂,具有抑制体内外卵巢癌细胞生长以及增加癌细胞对紫杉醇敏感度的活性。
Cas No.1613710-01-2
别名3-(2,4-二甲氧基苯基)-4-(3-噻吩基)-1H-吡咯并[2,3-B]吡啶
Canonical SMILESCOC1=CC=C(C2=CNC3=NC=CC(C4=CSC=C4)=C32)C(OC)=C1
分子式C19H16N2O2S
分子量336.41
溶解度DMSO : 130 mg/mL (386.43 mM)
储存条件Store at -20°C
General tipsFor obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.
Shipping ConditionEvaluation sample solution : ship with blue ice
All other available size: ship with RT , or blue ice upon request
产品描述

ARN-3236 is an oral active and selective inhibitor of salt-inducible kinase 2 (SIK2) (IC50<1 nM), with activity in inhibiting growth and enhancing paclitaxel sensitivity in cultures and xenografts of ovarian cancer cell lines[1][2].

[1]. Lombardi MS, et al. SIK inhibition in human myeloid cells modulates TLR and IL-1R signaling and induces an anti-inflammatory phenotype. J Leukoc Biol. 2016 May;99(5):711-21. [2]. Zhou J, et al. A Novel Compound ARN-3236 Inhibits Salt-Inducible Kinase 2 and Sensitizes Ovarian Cancer Cell Lines and Xenografts to Paclitaxel. Clin Cancer Res. 2017 Apr 15;23(8):1945-1954.