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Submit ReviewAZ 6102 is a potent TNKS2 and TNKS1 inhibitor (IC50 values are 1 and 3 nM, respectively). Exhibits >100-fold selectivity for TNKS1/2 over PARP-1, PARP-2 and PARP-6. Inhibits Wnt signaling in DLD-1 cells (IC50 = 5 nM). Exhibits moderate oral bioavailability.
Chemicalprobes.org is a portal that offers independent guidance on the selection and/or application of small molecules for research. The use of AZ6102 is reviewed on the chemical probes website.
AZ 6102 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。
分子量 | 428.53 |
公式 | C25H28N6O |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 1645286-75-4 |
PubChem ID | 91663328 |
InChI Key | WCPTUQOMNJBIET-CALCHBBNSA-N |
Smiles | CC1=CC(N2C[C@H](C)N[C@H](C)C2)=NC=C1C3=CC=C(C(N4)=NC5=C(C=CN5C)C4=O)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 | 21.43 | 50 |
以下数据基于产品分子量 428.53。 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 |
---|---|---|---|
0.5 mM | 4.67 mL | 23.34 mL | 46.67 mL |
2.5 mM | 0.93 mL | 4.67 mL | 9.33 mL |
5 mM | 0.47 mL | 2.33 mL | 4.67 mL |
25 mM | 0.09 mL | 0.47 mL | 0.93 mL |
参考文献是支持产品生物活性的出版物。
Johannes et al (2015) Pyrimidinone nicotinamide mimetics as selective tankyrase and wnt pathway inhibitors suitable for in vivo pharmacology. ACS Med.Chem.Lett. 13 254 PMID: 25815142
If you know of a relevant reference for AZ 6102, please let us know.
关键词: AZ 6102, AZ 6102 supplier, AZ6102, potent, selective, TNKS1, TNKS2, inhibitors, inhibits, tankyrases, Wnt, signaling, Tankyrase, 5775, Tocris Bioscience
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