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CAY10603
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。
CAY10603图片
CAS NO:1045792-66-2
包装与价格:
包装价格(元)
1 mg询价
5 mg询价
10 mg询价
25 mg询价
50 mg询价
100 mg询价
1 mL*10 mM(in DMSO)询价

HDAC6 Inhibitor
BML-281
CAY10603 是一种选择性HDAC6抑制剂,IC50值为 2 pM。它也可抑制 HDAC1、HDAC2、HDAC3、HDAC8 和 HDAC10,IC50值分别为 271、252、0.42、6851和90.7 nM。

产品描述

CAY10603 is a potent and selective inhibitor of HDAC6.

体内活性

CAY10603通过抑制HDAC6,表现出对胰腺癌细胞系有效的抗增殖活性,IC50<1 μM。

激酶实验

HDAC Inhibition Assays: Purified HDACs are incubated with 1 mM carboxyfluorescein (FAM)-labeled acetylated peptide substrate and test compound for 17 h at 25 °C in HDAC assay buffer containing 100 mM HEPES (pH 7.5), 25 mM KCl, 0.1% BSA, and 0.01% Triton X-100. Reactions are terminated by the addition of buffer containing 0.078% SDS for a final SDS concentration of 0.05%. Substrate and product are separated electrophoretically using a Caliper LabChip 3000 system with blue laser excitation and green fluorescence detection (CCD2). The fluorescence intensity in the substrate and product peaks is determined using the Well Analyzer software on the Caliper system. The reactions are performed in duplicate for each sample. IC50 values are automatically calculated using the IDBS XLFit version 4.2.1 plug-in for Microsoft Excel and the XLFit 4-Parameter Logistic Model: ((A+((B_A)/1+((C/x)D)))), in which x is compound concentration, A and B are respectively the estimated minimum and maximum of percent inhibition, C is the inflection point, and D is the Hill slope of the sigmoidal curve. The standard errors of the IC50 values are automatically calculated using the IDBS XLFit version 4.2.1 plug-in for Microsoft Excel and the formula xf4_FitResultStdError.

细胞实验

The pancreatic cancer cell lines BxPc-3, HupT3, Mia Paca-2, Panc 04.03, and SU 86.86 are grown in medium (DMEM or RPMI) containing 10% fetal calf serum and l-glutamine. Pancreatic cancer cells are plated out in duplicate into 6 wells of a 96-well microtiter plate. Four hours post plating, individual wells are treated with diluent (DMSO) or varying concentrations of SAHA or the indicated HDACIs from a concentration of 1 nM to 50 mM. Cytotoxicity is measured at time "0", and 72 h post treatment using the colorimetric MTT assay according to the manufacturer's suggestions. The IC50 values are calculated using XLfit.(Only for Reference)

Cas No.

1045792-66-2

分子式

C22H30N4O6

分子量

446.504

别名

HDAC6 Inhibitor;BML-281

储存和溶解度

H2O:<1 mgml
Ethanol:5 mg/mL (11.19 mM),warmed
DMSO:82 mg/mL (183.7 mM)
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
 
 
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