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Latrunculin A
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Latrunculin A图片
CAS NO:76343-93-6
包装:100 μg (237.2 μM * 1mL in Ethanol)
市场价:4300元

产品名称
LAT-A
产品介绍
Latrunculin A (LAT-A) 是一种 G-肌动蛋白聚合 (G-actin polymerization) 抑制剂,在红海海绵Latrunculia magnifica中发现的。Latrunculin A 能够与肌动蛋白 (actin) 单体结合,抑制其聚集,对 ATP-actin,ADP-Pi-actin,ADP-actin 和 G-actin 的Kd值分别为 0.1,0.4,4.7 μM 和 0.19 μM。Latrunculin A 具有有效的抗转移特性,可用于癌症的研究。Latrunculin A 抑制细胞迁移。
生物活性

Latrunculin A (LAT-A), found in the red seaspongeLatrunculia magnifica, is aG-actin polymerizationinhibitor. Latrunculin A binds to actin monomers and inhibits polymerization of actin withKds of 0.1, 0.4, 4.7 μM and 0.19 μM for ATP-actin, ADP-Pi-actin, ADP-actin and G-actin, respectively. Latrunculin A has effective anti-metastatic properties forcancerresearch. Latrunculin A blocks cell migration[1][2][3][4][5][6].

IC50& Target

Kd: 0.1 μM (ATP-actin), 0.4 μM (ADP-Pi-actin), 4.7 μM (ADP-actin), 0.19 μM (G-actin)[2]

体外研究
(In Vitro)

Latrunculin A (50-1000 nM) exhibits potent anti-invasive activity against human prostate cancer PC-3M cells, inhibits PC-3M-CT+ spheroids disaggregation and cell migration[3].
Latrunculin A (3-30 μM) inhibits hypoxia-induced HIF-1 activation with an IC50value of 6.7 μM in human breast carcinoma T47D cells[3].
Latrunculin A (0-0.2 μM, 4 hours) has a significant inhibitory effect on HuR levels at high concentrations such as 0.2 μM in human hepatoma HepG2 cells while inhibits HuR only at 0.02 μM but no inhibitory effect at high concentrations in human hepatoma Huh7 cells[4].
Latrunculin A (0.1 μM, 24 hours) can lead to a significant decrease in cell migration and has an inhibitory effect on cell proliferation in human hepatoma cell lines HepG2[4].

体内研究
(In Vivo)

Latrunculin A (intraperitoneal injection, 0.05 mg/kg, three doses in the first 20 days, 120 days) has strong antitumor effect in male BALB/c nude mice models infected with adenocarcinoma (MKN45) or carcinoma (NUGC-4)[5].

Animal Model:Male BALB/c nude mice models infected with adenocarcinoma (MKN45) or carcinoma (NUGC-4)[5]
Dosage:0.05 mg/kg
Administration:Intraperitoneal injection; three doses in the first 20 days; 120 days
Result:Extended the mean life expectancy to 23.5 days comparing to control of 16 days in adenocarcinoma (MKN45) mice and the mean survival time was 42 days comparing to untreated of 31 days in carcinoma (NUGC-4) mice.
Clinical Trial
分子量

421.55

性状

Liquid

Formula

C22H31NO5S

CAS 号

76343-93-6

结构分类
  • Antibiotics
  • Macrolide Antibiotics
来源

red sea sponge Latrunculia magnifica

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Solution, -20°C, 2 years