Latrunculin A (Synonyms:LAT-A)
目录号 : KM16530 CAS No. : 76343-93-6 纯度 : ≥97%

Latrunculin A (LAT-A) 是从红海海绵 Latrunculia magnifica 中得到的一种毒素,能够与肌动蛋白 (actin) 单体结合,抑制肌动蛋白聚集,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。

规格 价格 是否有货 数量
100µg
In-stock
1mg
In-stock

Other Forms of Rapamycin:

KKL Med 的所有产品和服务仅用于科学研究,不能被用于人体,兽医,我们也不向个人提供产品和服务。
生物活性

Latrunculin A (LAT-A) is a toxin isolated from the red sea sponge Latrunculia magnifica, binds to actin monomers, inhibits polymerization of actin, with Kds of 0.1, 0.4, 4.7 μM and 0.19 μM for ATP-actin, ADP-Pi-actin, ADP-actin and G-actin, respectively.

IC50&Target

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

体外研究

LatruncuLin A (50-1000 nM) exhibits potent anti invasive activity against human prostate cancer PC-3M cells, inhibiting PC-3M-CT+sphere depolymerization and cell migration.

LauncuLin A (3-30 μM) inhibited hypoxia induced HIF-1 activation, and the IC50 value in human breast cancer T47D cells was 6.7 μM [1].

LatruncuLin A (0-0.2 μM, 4 hours) has a significant inhibitory effect on HuR levels in human liver cancer HepG2 cells at high concentrations (e.g. 0.2 μM), while only inhibiting HuR at 0.02 μM, but has no inhibitory effect on human liver cancer Huh7 cells at high concentrations [2].

LatruncuLin A (0.1 μM, 24 hours) can significantly reduce cell migration and inhibit cell proliferation in the human liver cancer cell line HepG2 [2].

体内研究

LatruncuLin A (intraperitoneal injection, 0.05 mg/kg, administered three times in the first 20 days, 120 days) has strong anti-tumor effects on male BALB/c nude mouse models infected with adenocarcinoma (MKN45) or cancer (NugC-4).

 

Animal Model: Male BALB/c nude mice models infected with adenocarcinoma (MKN45) or carcinoma (NUGC-4)
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.
 
分子式
C22H31NO5S
分子量
421.55
CAS号
76343-93-6
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

 -20°C, 2 years

临床试验
The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2
动物实验计算换算器
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量)
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系客服为您提供正确的澄清溶液配方)
+
+
+

计算结果:

工作液浓度 mg/ml;

DMSO母液配制方法 mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,

体内配方配制方法μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL ddH2O,混匀澄清。

配置后的溶液总体积

1. 首先保证母液是澄清的;
           2. 一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。