UC2288 是一种新型的、具有细胞通透性和口服活性的 p21 衰减试剂 (对 p21 具有相对选择性活性),基于索拉非尼 (HY-10201) 的结构合成。UC2288 在不依赖 p53 的情况下下调 p21 mRNA 的表达,降低 p21 蛋白水平,对 p21 蛋白的稳定性影响很小。UC2288 对VEGFR2 和 Raf 激酶没有抑制作用,即使在 10 μM。 https://pubchem.ncbi.nlm.nih.gov/compound/60196635 生物活性: UC2288 is a novel, cell-permeable, and orally active p21 attenuator (relatively selective activity for p21), which is synthesized based Sorafenib (HY-10201). UC2288 decreases p21 mRNA expression independently of p53, and attenuates p21 protein levels with minimal effect on p21 protein stability. UC2288 has no inhibition of VEGFR2 and Raf kinases even at 10 μM Shipped at Room Temperature. Store at +4°C. Store In the Dark.
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UC2288
CAS number:1394011-91-6 molecular formula:C20H18ClF6N3O2
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| Chinese alias | 1-(4-氯-3-(三氟甲基)苯基)-3-((1r,4r)-4-(5-(三氟甲基)吡啶-2-基氧基)环己基)脲 | ||
| English alias | 1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-((1r,4r)-4-(5-(trifluoromethyl)pyridin-2-yloxy)cyclohexyl)urea | ||
| CAS number | 1394011-91-6 | molecular formula | C20H18ClF6N3O2 |
| molecular weight | 481.82 g/mol | Exact mass | ≥98% |
| PSA | 63.300 Ų | logp | 5.600 |
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