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HDAC-IN-43
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。
HDAC-IN-43图片
CAS NO:1809163-24-3
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
HDAC-IN-43是一种强效的HDAC 1/3/6抑制剂,IC50值分别为82、45和24 nM。HDAC-IN-43是一种弱的PI3K/mTOR抑制剂,IC50值分别为3.6 和 3.7 μM。HDAC-IN-43具有广谱的抗增殖活性。
生物活性

HDAC-IN-43 is a potentHDAC1/3/6inhibitor withIC50values of 82, 45, and 24 nM, respectively. HDAC-IN-43 is a weakPI3K/mTORinhibitors withIC50values of 3.6 and 3.7 μM, respectively. HDAC-IN-43 shows broad anti-proliferative activity[1].

IC50& Target

HDAC1

82 nM (IC50)

HDAC2

358 nM (IC50)

HDAC3

45 nM (IC50)

HDAC6

24 nM (IC50)

HDAC8

1441 nM (IC50)

HDAC10

182 nM (IC50)

HDAC11

9061 nM (IC50)

体外研究
(In Vitro)

HDAC-IN-43 demonstrats broad anti-cancer activities against 38 cancer cell lines at 72 hours[1].

Cell Viability Assay

Cell Line:K562, MOLT4, MV4-11, Raji, Ramos, SU-DHL-6, HepG2, HuH-7, PLC/PRF/5, SK-HEP1, SNU-387, SNU-398, MCF7 and PC-2[1]
Concentration:0.22-1.42 μM
Incubation Time:72 h
Result:showed anti-cancer activities, the IC50values of K562, MOLT4, MV4-11, Raji, Ramos, SU-DHL-6, HepG2, HuH-7, PLC/PRF/5, SK-HEP1, SNU-387, SNU-398, MCF7 and PC-2 are 0.22-1.42 μM[1].
分子量

440.50

Formula

C22H28N6O4

CAS 号

1809163-24-3

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.