Splitomicin

Discontinued Product

1542 has been discontinued.

View all Class III HDACs (Sirtuins) products.
说明: Sir2p inhibitor
化学名: 1,2-Dihydro-3H-naphtho[2,1-b]pyran-3-one
纯度: ≥97% (HPLC)
说明书
引用文献 (2)
评论
文献 (1)

生物活性 for Splitomicin

Splitomicin is a inhibitor of Sir2p (IC50 = 60 μM), an NAD+-dependent Sir2 family deacetylase required for chromatin-dependent silencing in yeast.

技术数据 for Splitomicin

分子量 198.22
公式 C13H10O2
储存 Store at -20°C
纯度 ≥97% (HPLC)
CAS Number 5690-03-9
PubChem ID 5269
InChI Key ISFPDBUKMJDAJH-UHFFFAOYSA-N
Smiles O=C1CCC2=C(O1)C=CC1=CC=CC=C21

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.

产品说明书 for Splitomicin

分析证书/产品说明书
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参考文献 for Splitomicin

参考文献是支持产品生物活性的出版物。

Bedalov et al (2001) Identification of a small molecule inhibitor of Sir2p. Proc.Natl.Acad.Sci.U.S.A. 98 15113 PMID: 11752457

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关键词: Splitomicin, Splitomicin supplier, Sir2p, inhibitors, inhibits, Sirtuin, Sir2-like, Family, Deacetylases, Class, III, HDACs, (Sirtuins), 1542, Tocris Bioscience

2 篇 Splitomicin 的引用文献

引用文献是使用了 Tocris 产品的出版物。 Splitomicin 的部分引用包括:

Kumari and Usdin (2014) Polycomb group complexes are recruited to reactivated FMR1 alleles in Fragile X syndrome in response to FMR1 transcription. Hum Mol Genet 23 6575 PMID: 25055869

Stavrou et al (2015) Reduced thrombosis in Klkb1-/- mice is mediated by increased Mas receptor, prostacyclin, Sirt1, and KLF4 and decreased tissue factor. J Neurosci 125 710 PMID: 25339356


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该领域的文献

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

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Rheumatoid Arthritis Poster

Rheumatoid Arthritis Poster

Rheumatoid arthritis (RA) is a chronic destructive inflammatory autoimmune disease that results from a breakdown in immune tolerance, for reasons that are as yet unknown. This poster summarizes the pathology of RA and the inflammatory processes involved, as well as describing some of the epigenetic modifications associated with the disease and the potential for targeting these changes in the discovery of new treatments.