Selisistat (EX 527)

製品コードS1541 バッチS154103

印刷

化学情報

Chemical Structure Synonyms SEN0014196 Storage
(From the date of receipt)		 3 years -20°C powder
1 years -80°C in solvent
化学式

C13H13ClN2O
分子量 248.71 CAS No. 49843-98-3
Solubility (25°C)* 体外 DMSO 50 mg/mL (201.03 mM)
Ethanol 18 mg/mL (72.37 mM)
Water Insoluble
* <1 mg/ml means slightly soluble or insoluble.
* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

溶剤液（一定の濃度）を調合する

生物活性

製品説明 Selisistat (EX 527, SEN0014196) is a potent and selective SIRT1 inhibitor with IC50 of 38 nM in a cell-free assay, exhibits >200-fold selectivity against SIRT2 and SIRT3. Phase 2.
in vitro EX 527 exhibits potently inhibitory effect against SIRT1 deacetylase activity in a concentration-dependent manner with an IC50 of 38 nM, displays much lower activity against SIRT2 and SIRT3 with IC50 values of 19.6 μM and 48.7 μM, respectively. EX 527 does not inhibit SIRT4-7 and class I/II HDAC activity at concentrations up to 100 μM. EX-527 alone (1 μM) has no detectable effect on the acetylation of p53 lysine 382 in NCI-H460 cells. EX-527 significantly increases the amount of acetylated p53 in NCI-H460 cells, human mammary epithelial cells, U-2 OS and MCF-7 cells subjected to genotoxic agents such as Etoposide, Doxorubicin, Hydroxyurea, and Hydrogen peroxide, which is more effective than that caused by Nicotinamide (5 mM). But surprisingly EX 527 does not result in detectable effects on p53-controled gene expression, cell survival, or cell proliferation. [1] EX 527 causes a 90% increase in cell number of HCT116 cells after 7 days in the condition of 0.1% serum but not 10% serum, suggesting that SIRT1 is a significant regulator of cell proliferation during growth factor deprivation conditions. [2] EX 527 abrogates resveratrol effects on glucose responses, and prevents resveratrol-induced up-regulation of Glut2, glucokinase, Pdx-1, and Tfam in INS-1E Cells, due to the opposite effect of EX 527 and resveratrol on SIRT1 deacetylase activity. [3]
in vivo Administration of EX 527 (~10 μg) to rats increases hypothalamic acetyl-p53 levels by inhibiting hypothalamic SIRT1 activity. Co-administration of EX 527 with ghrelin markedly blunts the orexigenic action of ghrelin by decreasing the pAMPK levels, increasing the ACC levels, and abolishing the higher expression of the transcription factors FoxO1, pCREB, and Bsx and the neuropeptides NPY and AgRP in the hypothalamic arcuate nucleus. [4]
特徴 Greater potency, specificity, stability, and lower toxicity than other inhibitors of SIRT1 catalytic activity identified to date.

プロトコル(参考用のみ)

キナーゼアッセイ Inhibition of GST-SIRT1 deacetylase activity
293T cells are transiently transfected with GST-tagged human SIRT1 in the pDEST27 Gateway vector using FuGENE-6. After 48 hours, the cells are lysed with 50 mM Tris, pH 8.0, 120 mM NaCl, 1 mM EDTA, and 0.5% Nonidet P-40, supplemented with Complete Mini protease inhibitor cocktail tablets. GST-SIRT1 is purified from lysates using glutathione-Sepharose beads and washed extensively in the above buffer. The deacetylation assay is performed with approximately 30 ng of GST-SIRT1 in the presence of EX 527 (48 pM to 100 μM). Deacetylation is measured using the Fluor de Lys kit using a fluorogenic peptide encompassing residues 379 to 382 of p53, acetylated on lysine 382. The acetylated lysine residue is coupled to an aminomethylcoumarin moiety. The peptide is deacetylated by SIRT1, followed by the addition of a proteolytic developer that releases the fluorescent aminomethylcoumarin. Briefly, enzyme preparations are incubated with 170 μM NAD+ and 100 μM p53 fluorogenic peptide for 45 minutes at 37 °C followed by incubation in developer for 15 minutes at 37 °C. Fluorescence is measured by excitation at 360 nm and emission at 460 nm and enzymatic activity is expressed in relative fluorescence units.
細胞アッセイ 細胞株 NCI-H460, MCF-7, U-2 OS and HMEC
濃度 Dissolved in DMSO, final concentration 1 μM
反応時間 48 or 72 hours
実験の流れ For viability assays, cells are treated with EX 527 for 48 hours. Cell viability is then determined using the Cell Titer-Glo luminescent assay, which measures total ATP level as an index of cell number. Luminescence is measured on a Luminoskan Ascent. For the proliferation assay, 0.5 μCi/mL of [14C]thymidine is added to the medium immediately after EX 527. Plates are counted at 48 hours (HMEC) or 72 hours (NCI-H460, MCF-7, and U-2 OS cells) in a Microbeta liquid scintillation counter. Thymidine incorporated by the cells is detected by proximity to the scintillant in the base of the Cytostar-T tissue culture plate.
動物実験 動物モデル Male Sprague-Dawley rats
投薬量 ~5 μg/rat
投与方法 Intracerebroventricular injection

カスタマーフィードバック

Data from [Data independently produced by J Pineal Res, 2014, 57(2), 228-38]

Data from [Cancer Res, 2014, 74(1), 298-308]

Data from [Data independently produced by J Trauma Acute Care Surg, 2014, 10.1097/TA.0347]

Selleckの高級品が、幾つかの出版された研究調査結果（以下を含む）で使われた：

Genetic determinants of micronucleus formation in vivo [ Nature, 2024, 10.1038/s41586-023-07009-0] PubMed: 38355793
Single-cell NAD(H) levels predict clonal lymphocyte expansion dynamics [ Sci Immunol, 2024, 9(93):eadj7238] PubMed: 38489349
α-Ketoglutarate improves cardiac insufficiency through NAD+-SIRT1 signaling-mediated mitophagy and ferroptosis in pressure overload-induced mice [ Mol Med, 2024, 30(1):15] PubMed: 38254035
Human cytomegalovirus modulates mTORC1 to redirect mRNA translation within quiescently infected monocytes [ J Virol, 2024, 98(2):e0188823] PubMed: 38289104
MicroRNA-141-3p reduces pulmonary hypoxia/reoxygenation injury through suppression of Beclin-1-dependent autophagy [ Aging (Albany NY), 2024, 16(2):1352-1373] PubMed: 38261732
Protective role of forsythoside B in Kawasaki disease-induced cardiac injury: Inhibition of pyroptosis via the SIRT1-NF-κB-p65 signaling pathway [ Chem Biol Interact, 2024, 392:110953] PubMed: 38471628
Cath-KP, a novel peptide derived from frog skin, prevents oxidative stress damage in a Parkinson's disease model [ Zool Res, 2024, 45(1):108-124] PubMed: 38114437
NAD-Dependent Protein Deacetylase Sirtuin-1 Mediated Mitophagy Regulates Early Brain Injury After Subarachnoid Hemorrhage [ J Inflamm Res, 2024, 17:1971-1981] PubMed: 38562659
Protectin D1 ameliorates non-compressive lumbar disc herniation through SIRT1-mediated CGRP signaling [ Mol Pain, 2024, 20:17448069241232349] PubMed: 38288478
NAD+ regulates nucleotide metabolism and genomic DNA replication [ Nat Cell Biol, 2023, 10.1038/s41556-023-01280-z] PubMed: 37957325

長期の保管のために-20°Cの下で製品を保ってください。

人間や獣医の診断であるか治療的な使用のためにでない。

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