Cytochalasin D (Synonyms: 细胞松弛素D; Zygosporin A; NSC 209835)
目录号: PC61658 纯度: ≥99%

Cytochalasin D (Zygosporin A) 是一种有效的肌动蛋白聚合抑制剂,可以来源于真菌。Cytochalasin D 具有细胞渗透活性。Cytochalasin D 通过结合 G-actin 抑制 G-actin–cofilin 的相互作用。Cytochalasin D 还能抑制 cofilin 与 F-actin 的结合,降低了活细胞中肌动蛋白聚合和解聚的速率。Cytochalasin D 可以减少外泌体的释放,进而减少肿瘤环境中 survivin 的量。 Cytochalasin D 诱导 Yap 磷酸化,阻止其核易位保留在胞质中。

CAS No. :22144-77-0
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中文名称
Cytochalasin D
中文别名
细胞松驰素D;细胞松弛素 D;胞松弛素D;松胞素 D(RG);松胞素D;松胞菌素C;松胞菌素D;松胞素C;细胞分裂抑素C;细胞松驰素C;细胞松驰素 D;细胞松弛素D
英文名称
Cytochalasin D
英文别名
1H-Cycloundec[d]isoindole-1,11(2H)-dione,15-(acetyloxy)-3,3a,4,5,6,6a,9,10,12,15-decahydro-6,12-dihydroxy-4,10,12-trimethyl-5-methylene-3-(phenylmethyl)-,(3S,3aR,4S,6S,6aR,7E,10S,12R,13E,15R,15aR)-;Cytochalasin D;1H-Cycloundec[d]isoindole-1,11(2H)-dione,15-(acetyloxy)-3,3a,4,5,6,6a,9,10,12,15-decahydro-6,1...;1H-Cycloundec[d]isoindole-1,11(2H)-dione,15-(acetyloxy)-3,3a,4,5,6,6a,9,10,12,15-decahydro-6,12-dihydroxy-4,10,12-trimethyl-5;Cytochalasin D (NSC 209835, Zygosporin A);13C-Cytochalasin D;19-trien-17-one;CYTOCHALACIND;Cytochalasin D,Zygosporin A;CYTOCHALICIND;Cytohalasin d;Lygosporin a;Methylmalonate;Zygosporin A;[ "Zygosporin A" ];[(1R,2R,5R,7S,11R,12S,14S,15R,16S)-16-Benzyl-5,12-dihydroxy-5,7,14-trimethyl-13-methylidene-6,18-dio
Cas No.
22144-77-0
分子式
C30H37NO6
分子量
507.62
包装储存
Powder; -20°C; 3 years;In solvent; -80°C; 6 months;
产品详情
Cytochalasin D (Zygosporin A) 是一种有效的肌动蛋白聚合抑制剂,可以来源于真菌。Cytochalasin D 具有细胞渗透活性。Cytochalasin D 通过结合 G-actin 抑制 G-actin–cofilin 的相互作用。Cytochalasin D 还能抑制 cofilin 与 F-actin 的结合,降低了活细胞中肌动蛋白聚合和解聚的速率。Cytochalasin D 可以减少外泌体的释放,进而减少肿瘤环境中 survivin 的量。 Cytochalasin D 诱导 Yap 磷酸化,阻止其核易位保留在胞质中。
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.
性状
Solid
体外研究(In Vitro)
Cytochalasin D (3 and 10 μM; 30 min) causes retraction and arborization of COS-7 cells and conversion of F-actin from long fibers to punctate structures.
Cytochalasin D (0.3, 1, 3 and 10 μM; 30 min) concentration-dependently decreases the rate of actin depolymerization in COS-7 cells.
Cytochalasin D (1 μM; NIH3T3 cells) disrupts stress fibers, induces phosphorylation of Yap, while cells maintains original area and lost nuclear Yap localization.Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
ass="cpd-vitro-
运输条件
Room temperature or refrigerated transport.
储存方式
Powder; -20°C; 3 years;In solvent; -80°C; 6 months;
ClinicalTrial
结构分类
Others
来源
molds
溶解度数据
体外研究:
DMSO : 25 mg/mL(49.25 mM;ultrasonic and warming and heat to 60°C)
配制储存液<
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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