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Submit ReviewA 939572 is a potent stearoyl-CoA desaturase 1 (SCD1) inhibitor (IC50 = 0.4 nM). Selective for SCD1 over a range of kinases and hERG channels. Inhibits proliferation of squamous cell carcinoma FaDu cells in vitro. Also induces cell death of undifferentiated human embryonic stem cells (ESCs). Orally bioavailable.
A 939572 is also offered as part of the Tocriscreen 2.0 Max and Tocriscreen Stem Cell Library. 了解 Tocris 化合物库的更多信息。
分子量 | 387.86 |
公式 | C20H22ClN3O3 |
储存 | Store at +4°C |
纯度 | ≥99% (HPLC) |
CAS Number | 1032229-33-6 |
PubChem ID | 24905400 |
InChI Key | DPYTYQFYDLYWHZ-UHFFFAOYSA-N |
Smiles | O=C(NC3=CC(C(NC)=O)=CC=C3)N1CCC(OC2=C(Cl)C=CC=C2)CC1 |
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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 38.79 | 100 |
以下数据基于产品分子量 387.86。 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.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 2.58 mL | 12.89 mL | 25.78 mL |
5 mM | 0.52 mL | 2.58 mL | 5.16 mL |
10 mM | 0.26 mL | 1.29 mL | 2.58 mL |
50 mM | 0.05 mL | 0.26 mL | 0.52 mL |
参考文献是支持产品生物活性的出版物。
Ben-David et al (2013) Selective elimination of human pluripotent stem cells by an oleate synthesis inhibitor discovered in a high-throughput screen. Cell Stem Cell 12 167 PMID: 23318055
Xin et al (2008) Discovery of piperidine-aryl urea-based stearoyl-CoA desaturase 1 inhibitors. Bioorg.Med.Chem.Lett. 18 4298 PMID: 18632269
If you know of a relevant reference for A 939572, please let us know.
关键词: A 939572, A 939572 supplier, A939572, potent, stearoyl-co1, desaturase, inhibitors, inhibits, SCD1, stem, cells, lipid, metabolism, Stearoyl-CoA, 9-desaturase, ESCs, and, iPSC, 4845, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 A 939572 的部分引用包括:
Lien et al (2021) Low glycaemic diets alter lipid metabolism to influence tumour growth Nature 599 302 PMID: 34671163
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