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- A-83-01 909910-43-6

- A-83-01 909910-43-6
A-83-01 909910-43-6
产品描述 描述 A-83-01 is a selective inhibitor of TGF-β type I receptor ALK5 kinase, type I activin/nodal receptor ALK4 and type I nodal receptor ALK7 with IC50 values of 12 nM, 45 nM and 7.5 nM, respectively.
纯度 ≥98%储存/保存方法 Store at -20℃ for three years(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.注意事项 该产品在溶液状态不稳定,建议您现用现配,即刻使用。基本信息 别名 A83-01;A 83-01外观 white to beige powder可溶性/溶解性 DMSO : 30 mg/mL (71.17 mM; Need ultrasonic)生物活性 靶点 ALK4;ALK5;ALK7In vitro(体外研究) A-83-01 (4 µM) treatment increases myotube formation, the expression of MyHC and the expression of Myf5 and MyoD in C2C12 cells. Expression of pSmad3 is increased by the addition of TGF-β1, and the effects of TGF-β1 are inhibited in ovarian cancer cells by A-83-01. TGF-β1 increases cell motility, adhesion and invasion, while A-83-01 decreases these behaviors in HM-1 cells. A-83-01 treatment significantly increases these parameters within 24 h that is positively related to pericyte coverage and tumor cell proliferation. Apparent diffusion coefficient (ADC) determined by diffusion-weighed imaging is decreased by A-83-01 treatment, suggesting the decrease of tumor interstitial fluid pressure.In vivo(体内研究) A-83-01 (50, 150 and 500 μg/mouse, i.p.) significantly improves survival of the mice without body weight or neurobehavioral appearances. A-83-01 (0.5 mg/kg, i.p.) shows a significantly stronger antitumor effect in mice bearing M109 cells.研究领域 研究领域 CancerCancer MetabolismResponse to hypoxiaMetabolismPathways and ProcessesMetabolism processesHypoxiaNeuroscienceDevelopmentStem CellsSignaling PathwaysTGF betaSurface MoleculesDrug DiscoverySmall Molecule DrugLead Compound DiscoveryA-83-01 909910-43-6温馨提示:本产品仅作科研实验使用,不支持临床等研究
