SR 8278

Pricing Availability   Qty
说明: Rev-Erbα antagonist
化学名: 1,2,3,4-Tetrahydro-2-[[5-(methylthio)-2-thienyl]carbonyl]-3-isoquinolinecarboxylic acid ethyl ester
纯度: ≥99% (HPLC)
说明书
引用文献 (4)
评论

生物活性 for SR 8278

SR 8278 is a Rev-Erbα antagonist; inhibits Rev-Erbα transcriptional repression (EC50 = 0.47 μM). Blocks activity of Rev-Erbα agonist GSK 4112 (Cat. No. 3663) in HEK293 cells. Increases expression of glucose-regulating genes, G6Pase and PEPCK in HepG2 cells.

化合物库 for SR 8278

SR 8278 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for SR 8278

分子量 361.48
公式 C18H19NO3S2
储存 Store at +4°C
纯度 ≥99% (HPLC)
CAS Number 1254944-66-5
PubChem ID 53393127
InChI Key UIEBLUZPSFAFOC-UHFFFAOYSA-N
Smiles CCOC(=O)C1CC2=CC=CC=C2CN1C(=O)C1=CC=C(SC)S1

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.

溶解性数据 for SR 8278

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 36.15 100
ethanol 18.07 50

制备储备液 for SR 8278

以下数据基于产品分子量 361.48。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 2.77 mL 13.83 mL 27.66 mL
5 mM 0.55 mL 2.77 mL 5.53 mL
10 mM 0.28 mL 1.38 mL 2.77 mL
50 mM 0.06 mL 0.28 mL 0.55 mL

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产品说明书 for SR 8278

分析证书/产品说明书
选择另一批次:

参考文献 for SR 8278

参考文献是支持产品生物活性的出版物。

Kojetin et al (2011) Identification of SR8278, a synthetic antagonist of the nuclear heme receptor REV-ERB. ACS Chem. Biol. 6 131 PMID: 21043485


If you know of a relevant reference for SR 8278, please let us know.

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关键词: SR 8278, SR 8278 supplier, SR8278, REV-ERB, heme, nuclear, receptors, antagonists, inhibits, glucose, regulation, circadian, Rev-Erb, Receptors, 4463, Tocris Bioscience

4 篇 SR 8278 的引用文献

引用文献是使用了 Tocris 产品的出版物。 SR 8278 的部分引用包括:

Ning et al (2023) Nuclear receptor modulators inhibit osteosarcoma cell proliferation and tumour growth by regulating the mTOR signaling pathway. Cell Death Dis 14 51 PMID: 36681687

Parker et al (2017) Ligand and Target Discovery by Fragment-Based Screening in Human Cells. Cell 168 527 PMID: 28111073

Hyun Ok et al (2022) Sinapic Acid Ameliorates REV-ERB α Modulated Mitochondrial Fission against MPTP-Induced Parkinson's Disease Model. Biomol Ther (Seoul) 30 409-417 PMID: 35611585

Hanne M et al (2022) Co-alterations of circadian clock gene transcripts in human placenta in preeclampsia. Sci Rep 12 17856 PMID: 36284122


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