GSK 2801

Discontinued Product

5635 has been discontinued.

View all Bromodomains products.
说明: Selective BAZ2A and BAZ2B inhibitor
化学名: 1-[1-[2-(Methylsulfonyl)phenyl]-7-propoxy-3-indolizinyl]ethanone
纯度: ≥98% (HPLC)
说明书
引用文献
评论
文献 (4)

生物活性 for GSK 2801

GSK 2801 is a selective BAZ2A and BAZ2B inhibitor (IC50 values are 0.40 and 0.43 μM, respectively). Selective for BAZ2A/B over TAF1L and BRD9. Cell permeable and orally available.

许可信息

This probe is supplied in conjunction with the Structural Genomics Consortium. For further characterization details, please visit the GSK 2801 probe summary on the SGC website.

External Portal Information for GSK 2801

Chemicalprobes.org is a portal that offers independent guidance on the selection and/or application of small molecules for research. The use of GSK2801 is reviewed on the chemical probes website.

技术数据 for GSK 2801

分子量 371.45
公式 C20H21NO4S
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 1619994-68-1
PubChem ID 73010930
InChI Key KHWCPNJRJCNVRI-UHFFFAOYSA-N
Smiles CCCOC1=CC2=C(C3=C(S(C)(=O)=O)C=CC=C3)C=C(C(C)=O)N2C=C1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

参考文献 for GSK 2801

参考文献是支持产品生物活性的出版物。

Chen et al (2015) Discovery and characterization of GSK2801, a selective chemical probe for the bromodomains BAZ2A and BAZ2B. J.Med.Chem PMID: 25799074

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关键词: GSK 2801, GSK 2801 supplier, selective, bromodomain, inhibitors, inhibits, cell, permeable, orally, bioavailable, BAZ2A, BAZ2B, structural, genomics, consortium, SGC, GSK2801, Bromodomains, 5635, Tocris Bioscience

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