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Submit Review7rh is a potent and selective DDR1 inhibitor (IC50 = 6.8 nM). Exhibits selectivity for DDR1 over DDR2, Bcr-Abl and c-Kit (IC50 values are 101.4 and 355 nM and > 10 μM, respectively) and a range of other kinases. Inhibits proliferation of cancer cell lines expressing high levels of DDR1 in vitro and suppresses cancer cell invasion, adhesion and tumorigenicity. Orally bioavailable.
分子量 | 546.59 |
公式 | C30H29F3N6O |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 1429617-90-2 |
PubChem ID | 71550931 |
InChI Key | DDLPXZXBWGJRGK-UHFFFAOYSA-N |
Smiles | O=C(NC1=CC(CN2CCN(C)CC2)=CC(C(F)(F)F)=C1)C3=CC(C#CC(C=N4)=CN5C4=CC=N5)=C(CC)C=C3 |
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 | 54.66 | 100 |
以下数据基于产品分子量 546.59。 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 | 1.83 mL | 9.15 mL | 18.3 mL |
5 mM | 0.37 mL | 1.83 mL | 3.66 mL |
10 mM | 0.18 mL | 0.91 mL | 1.83 mL |
50 mM | 0.04 mL | 0.18 mL | 0.37 mL |
参考文献是支持产品生物活性的出版物。
Gao et al (2013) Discovery and optimization of 3-(2-(pyrazolo[1,5-a]pyrimidin-6-yl)ethynyl)benzamides as novel selective and orally bioavailable discoidin domain receptor 1 (DDR1) inhibitors. J.Med.Chem. 56 3281 PMID: 23521020
If you know of a relevant reference for 7rh, please let us know.
关键词: 7rh, 7rh supplier, Discoidin, domain, receptors, 1, inhibitors, inhibits, potent, selective, DDR1, orally, bioavailable, Other, RTKs, 5860, Tocris Bioscience
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