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经验配方 CAS号 C₂₅H₂₃N₇OS 925434-55-5 描述 概述 A cell-permeable quinolinecarboxamide compound that is shown to inhibit the mitochondrial SIRT3 in a substrate AceCS2-competitive (Ki = 0.56 µM; Km = 2.44 µM), but NAD+-uncompetitive (Ki = 0.34 µM; Km = 280 µM), manner. Also reported to decrease cellular p53 Lys382 acetylation (Effective conc. = 10 µM in U2OS and MEF cultures) and inhibit p300 HAT activity (IC50 = 9 µM) in vitro, as well as offer therapeutic benefits in several murine and rodent type 2 diabetes models (100 mg/kg/dayl p.o.) in vivo. Whether and how SRT1720 activates SIRT1 activity remains uncertain. Also available as a 25 mM solution in DMSO (Cat. No. 530748). 产品目录编号 567860 品牌系列 Calbiochem®
同义词 N-(2-(3-(1-Piperazinylmethyl)imidazo[2,1-b]thiazol-6-yl)phenyl)-2-quinolinecarboxamide, Sirtuin-3 Inhibitor, SRT1720, SIRT3 Inhibitor II, HAT Inhibitor XI, Histone Acetyltransferase Inhibitor XI, p300/CBP Inhibitor IX 参考 参考 Baur, J.A., et al. 2012. Nat. Rev. Drug Discov. 11, 443.
Minor, R.K., et al. 2011. Sci. Rep. 1, 70.
Huber, J.L., et al. 2010. Future Med. Chem. 2, 1751
Pacholec, M., et al. 2010. J. Biol. Chem. 285, 8340
Jin, L., et al. 2009. Protein Sci. 18, 514
Feige, J.N., et al. 2008. Cell Metab. 8, 347
Milne, J.C., et al. 2007. Nature 450, 712.产品信息 CAS号 925434-55-5 形式 Yellow solid Hill配方 C₂₅H₂₃N₇OS 化学配方 C₂₅H₂₃N₇OS Molar Mass 469.6 结构配方图像 生物信息 纯度 ≥97% by HPLC 理化信息 溶解度 DMSO 储存和货运信息 货运代码 Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
毒性 Regulatory Review
储存 -20°C
避光 Protect from light
无需冷冻 No
特殊指南 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C. 包装信息 惰性气体下包装 Packaged under inert gas
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