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Submit ReviewCeefourin 1 is a selective MRP (multidrug resistance-associated protein) 4 inhibitor (IC50 = 2.6 μM). Selective for MRP4 over P-gp, MRP1 and ABCG2. Sensitizes MRP4 over-expressing cells to SN 38 (Cat. No. 2684). Ceefourin 1 inhibits cAMP efflux from acute myeloid leukemia cells (AML) and promotes apoptosis in combination with Histamine (Cat. No. 3545).
分子量 | 294.42 |
公式 | C11H10N4S3 |
储存 | Store at +4°C |
纯度 | ≥98% (HPLC) |
CAS Number | 315702-40-0 |
PubChem ID | 704306 |
InChI Key | KVNBVHCJAUXKPJ-UHFFFAOYSA-N |
Smiles | CN1C(NN=C1CSC2=NC3=CC=CC=C3S2)=S |
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 | 29.44 | 100 |
以下数据基于产品分子量 294.42。 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 | 3.4 mL | 16.98 mL | 33.97 mL |
5 mM | 0.68 mL | 3.4 mL | 6.79 mL |
10 mM | 0.34 mL | 1.7 mL | 3.4 mL |
50 mM | 0.07 mL | 0.34 mL | 0.68 mL |
参考文献是支持产品生物活性的出版物。
Cheung et al (2014) High-throughput screening identifies Ceefourin 1 and Ceefourin 2 as highly selective inhibitors of multidrug resistance protein 4 (MRP4). Biochem.Pharmacol. 91 97 PMID: 24973542
Sahores et al (2023) Ceefourin-1, a MRP4/ABCC4 inhibitor, induces apoptosis in AML cells enhanced by histamine. Biochim.Biophys.Acta 1867 130322 PMID: 36773726
If you know of a relevant reference for Ceefourin 1, please let us know.
关键词: Ceefourin 1, Ceefourin 1 supplier, multidrug, resistance-associated, protein, 4, MRP4, inhibitors, inhibits, transporters, ABCC4, AML, acute, myeloid, leukemia, apoptosis, Multidrug, Transporters, Other, Apoptosis, 5867, Tocris Bioscience
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There are two currently recognized forms of programmed cell death: apoptosis and necroptosis. This poster summarizes the signaling pathways involved in apoptosis, necroptosis and cell survival following death receptor activation, and highlights the influence of the molecular switch, cFLIP, on cell fate.