Home > Others & > Cytochalasin D Zygosporin A , NSC 209835

Cytochalasin D Zygosporin A , NSC 209835

Cytochalasin D (Zygosporin A, NSC 209835) 是一种源自真菌的有效肌动蛋白聚合抑制剂。 Cytochalasin D抑制细胞中肌动蛋白丝的动力学。它诱导 Yap磷酸化和细胞质滞留。

具体折扣请咨询客服

生物活性

Cytochalasin D (Zygosporin A) is a potent actin polymerization inhibitor, could be derived from fungus. Cytochalasin D has cell-permeable activity. Cytochalasin D inhibits the G-actin–cofilin interaction by binding to G-actin. Cytochalasin D also inhibits the binding of cofilin to F-actin and decreases the rate of both actin polymerization and depolymerization in living cells. Cytochalasin D can reduce exosome release, in turn reducing the amount of survivin present in the tumour environment. Cytochalasin D induces phosphorylation and cytoplasmic retention of Yap
体外研究

Western Blot Analysis

Cell Line: COS-7 cells[1]
Concentration: 3 and 10 μM
Incubation Time: 30 min
Result: Caused retraction and arborization of COS-7 cells and conversion of F-actin from long fibers to punctate structures.
体内研究
激酶实验
细胞实验
动物实验
不同实验动物依据体表面积的等效剂量转换表（数据来源于FDA指南）

动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数

例如，已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法：将88 mg/kg 乘以小鼠的Km系数（3），再除以大鼠的Km系数（6），得到该药物用于大鼠的等效剂量44 mg/kg。

参考文献

分子式 C30H37NO6	分子量 507.62	CAS号 22144-77-0	储存方式 -20°C
溶剂（常温）	DMSO	Water	Ethanol

体内溶解度

Clinical Trial Information ( data from http://clinicaltrials.gov )

注：以上所有数据均来自公开文献，并不保证对所有实验均有效，数据仅供参考。
相关化合物库
使用AMQUAR产品发表文献后请联系我们