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首页-小分子抑制剂&激动剂-Epigenetics-Histone Acetyltransferase (HAT)-C646
C646

Chemical Structure : C646

CAS No.: 328968-36-1

C646 (p300 inhibitor C646)

货号: PC-20778Not For Human Use, Lab Use Only.

C646 is a selective, competitive histone acetyltransferase (HAT) p300 inhibitor with Ki of 400 nM, less potent for other acetyltransferases.

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25 mg ¥1180 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

C646 is a selective, competitive histone acetyltransferase (HAT) p300 inhibitor with Ki of 400 nM, less potent for other acetyltransferases.
C646 blocks dynamic acetylation of H3K4me3 globally in mouse and fly cells, and locally across the promoter and start-site of inducible genes in the mouse, thereby disrupting RNA polymerase II association and the activation of genes.
C646 increses caspase-dependent apoptosis involving both extrinsic and intrinsic cell death pathways in androgen-dependent and castration-resistant prostate cancer cells.
C646 inhibits the growth of human melanoma and other tumor cells and promotes cellular senescence.

物理化学性质&存储条件

分子量 445.42
分子式 C24H19N3O6
外观性状 Solid
CAS No.
储存条件
固体粉末
-20°C 12 个月; 4°C 6 个月
配置液
-80°C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

4-[4-[[5-(4,5-Dimethyl-2-nitrophenyl)-2-furanyl]methylene]-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl]benzoic acid

参考文献

1. Bowers EM, et al. Chem Biol. 2010 May 28;17(5):471-82.

2. Yan G, et al. J Invest Dermatol. 2013 Oct;133(10):2444-2452.

3. Santer FR, et al. Mol Cancer Ther. 2011 Sep;10(9):1644-55.

4. Crump NT, et al. Proc Natl Acad Sci U S A. 2011 May 10;108(19):7814-9.

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