| 产品详情 |
| Edit |   |
| Product Name | 10Z-Hymenialdisine |
| Description | MW: 324.13. Purity ≥97% by HPLC. Background: Isolated from sponge Axinella carteri. A potent inhibitor of mitogen-activated protein kinase kinase-1 (MEK-1) (IC?? = 6nM). Blocks the in vivo phosphorylation of the microtubule-binding protein tau at sites that are hyperphosphorylated by glycogen synthase kinase-beta (GSK-3beta) and CDK5/p35 in Alzheimer's disease. Inhibitor of DNA damage checkpoint at G2 phase (IC?? = 6 uM), cyclin-dependent kinases CDK1/cyclin B (IC?? = 22 nM), CDK2/cyclin A (I |
| Size | 0.25 mg, 1 mg |
| Concentration | n/a |
| Applications | n/a |
| Other Names | [4-(2-Amino-4-oxo-2-imidazolidin-5-ylidene)-2-bromo-4,5,6,7-tetrahydropyrrolo[2,3-c]azepin-8-one; Hymenialdisine] |
| Gene, Accession, CAS # | CAS: 82005-12-7 |
| Catalog # | MBS842939 |
| Price | |
| Order / More Info | 10Z-Hymenialdisine from MYBIOSOURCE INC. |
| Product Specific References | n/a |
| 产品资料 |
|
|