CAS NO: | 159109-11-2 |
包装 | 价格(元) |
10mg | 电议 |
50mg | 电议 |
Cas No. | 159109-11-2 |
化学名 | 5-ethyl-1-hydroxy-7,8-dimethoxy-3H-pyrrolo[3,4-c]isoquinolin-3-one |
Canonical SMILES | CCC1=NC2=C(C(O)=NC2=O)C3=CC(OC)=C(OC)C=C31 |
分子式 | C15H14N2O4 |
分子量 | 286.28 |
溶解度 | Soluble in DMSO |
储存条件 | Store at -20℃ |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
产品描述 | IC50: 34 and 304 nM in the presence of 10 and 100 μM ATP, respectively. 3F8 is a potent and selective GSK-3β (Glycogen Synthase Kinase 3) inhibitor GSK3 was identified as a serine/threonine protein kinase for the first time in the late 1970s and is highly conserved in all animals examined. GSK3 can regulate cell differentiation and apoptosis, and is an important component of the canonical Wnt pathway as well as the hedgehog pathway In vitro: 3F8 specifically abolishes eye and forebrain formation in zebrafish embryos with the similar as a typical Wnt overexpression phenotype. Cell reporter assays, chemical informatics analysis and in vitro kinase experiments exhibited that 3F8 is a selective GSK3 inhibitor with more potent than SB216763 (a commonly used GSK3 inhibitor). Together, 3F8 and its derivatives could be useful as new agents and potential therapeutic candidates for GSK3 related diseases [1]. The interaction of 3F8 with its binding site were studied. To this end, first computational analysis conducted, and the results suggested that maleimide moiety of 3F8 might interact with the ATP binding site of GSK-3β, and the N-4 and C-5 positions were solvent-exposed, indicating the less key role of this region to the binding affinity. [2]. In vivo: The lowest ratio (CE/IC50 = 221) of 3F8 implied that 3F8 was more efficient in vivo, likely according to better absorption and/or stability [1]. By injection of a sub-lethal amount of morpholino antisense oligonucleotides, individual knockdown of gsk3a and gsk3b translations in zebrafish caused cardiac defect [1]. Clinical trial: Clinical study has been conducted. References: |