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CAS号 | 146062-49-9 | 货号 | BCP16099 |
中文名 | MSDC-0160 | ||
英文名 | MSDC-0160 | ||
中文别名 | |||
英文别名 | MSDC0160;MSDC 0160;Mitoglitazone;CAY10415; CAY-10415; CAY 10415;PNU-91325; | ||
SMILES | CCC1=CN=C(C=C1)C(=O)COC2=CC=C(C=C2)CC3C(=O)NC(=O)S3 | ||
化学名称 | |||
分子式 | C19H18N2O4S | 分子量 | 370.42 |
纯度 | 98% | 配送 | 惯例下常温包邮 |
产品描述 | MSDC-0160 reduces resistance in the insulin/IGF-1 signaling pathway and restores IGF-1-induced Akt and GSK-3 phosphorylation. MSDC-0160 in combination with IGF-1 and 8 mM glucose increases β-cell specific gene expression of insulin, pdx1, nkx6.1, and nkx2.2, and maintains insulin content without altering glucose-stimulated insulin secretion. Furthermore, MSDC-0160 promotes human β-cell differentiation and reduces the expression of markers of apoptosis.CAY10415 is a novel peroxisome proliferator-activated receptor (PPAR)γ ligand. CAY10415 induced cell death and ROS generation in a PPARγ-independent manner. CAY10415 enhanced γ-radiation-induced apoptosis and caspase-3-mediated poly (ADP-ribose) polymerase (PARP) cleavage in vitro. The combined CAY10415 / γ-radiation treatment triggered caspase-8 activation, and this initiator caspase played an important role in the combination-induced apoptosis. The combined treatment of CAY10415 and γ-radiation synergistically induced DNA damage and apoptosis, which was regulated by ROS. |
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