CAS NO: | 944547-46-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | Mycro 3 is an orally active, potent and selective inhibitor ofMyc-associated factor X (MAX) dimerization. Mycro 3 also inhibit DNA binding ofc-Myc[1]. Mycro 3 could be used for the research of pancreaticcancer[2]. | ||||||||||||||||
IC50& Target | Myc-MAX dimerization[1] | ||||||||||||||||
体外研究 (In Vitro) | Mycro 3 is a potent and selective c-Myc inhibitor in whole cell assays, with weak inhibitory activity against Activator protein 1 (AP-1). Mycro 3 has a superior specificity profile to its predecessors. Mycro 3 inhibits the interaction between c-Myc and Max. Mycro 3 has high selectivity and inhibits c-Myc/Max dimerization and conjugation with DNA[1]. Mycro 3 exhibits an excellent specificity with IC50s of 0.25 and 9.0 μM for cells with intact Myc alleles and Myc-null cells, respectively[2]. | ||||||||||||||||
体内研究 (In Vivo) | Mycro 3 (100 mg/kg; oral administration; daily for two months) induces marked shrinkage of pancreatic ductal adenocarcinoma (PDA), increases cancer cell apoptosis, and reduces cell proliferation. Tumor growth is also drastically attenuated in Mycro 3-treated NOD/SCID mice carrying orthotopic or heterotopic xenografts of human pancreatic cancer cells[2].
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分子量 | 526.88 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C24H17ClF2N6O4 | ||||||||||||||||
CAS 号 | 944547-46-0 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : ≥ 100 mg/mL(189.80 mM) *"≥" means soluble, but saturation unknown. 配制储备液
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