中文名称: 诺考达唑 促销
英文名称: Nocodazole
CAS No: 31430-18-9
分子式: C14H11N3O3S
分子量: 301.32
EINEC: 250-626-5
N80005 诺考达唑 ≥99% (psaitong)
熔点:
300°C
包装规格:
2mg 10mg 50mg in glass bottle
溶解性:
溶于DMSO(10mg/ml 加热)和水
产品描述:

基本信息

产品编号:N80005

产品名称:Nocodazole

CAS:

31430-18-9

 

储存条件

粉末

2-8℃

四年

 

 

分子式:

C14H11N3O3S

溶于液体

-80℃

六个月

分子量

301.32

-20℃

一个月

化学名: 

 

 

Solubility (25°C)

 

体外

DMSO

7.5mg/mL (24.89mM)

Ethanol

Insoluble

Water

Insoluble

体内(现配现用)

2% DMSO+30% PEG 300+2% Tween 80+ddH2O

1mg/mL

1mg/ml表示微溶或不溶。

普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;⼀旦配成溶液,请分装保存,避免反复冻融造成的产品失效。

 

制备储备液

 

浓度

 

溶液体积

质量

 

1mg

 

5mg

 

10mg

1mM

3.3187mL

16.5937mL

33.1873mL

5mM

0.6637mL

3.3187mL

6.6375mL

10mM

0.3319mL

1.6594mL

3.3187mL

 

生物活性

产品描述

快速可逆的微管聚合抑制剂,也可有效抑制ABL,ABL(E255K) 和 ABL(T315I) 的活性,IC50 值分别为 0.21?μM,0.53?μM 和 0.64?μM。

靶点/IC50

Abl 91nM (Kd)

ABL(T315I) 170nM (Kd)

EGFR (WT)
(Cell-free assay)

BRAF 1.8μM (Kd)

BRAF(V600E) 1.μM (Kd)

c-KIT 1.6μM (Kd)

MEK1 1.7μM (Kd)

MEK2 1.6μM (Kd)

MET 1.7μM (Kd)

PI3Kγ 1.5μM (Kd)

Microtubule/Tubulin (Kd)

CRISPR/Cas9 (Kd)

 

体外研究

Nocodazole exhibits good affinity toward c-KIT, with a Kd value of 1.6 μM in highly malignant human cancer cells. Nocodazole displays good binding affinity toward the components of the mitogen-activated protein kinase (MAPK) pathway, such as BRAF (Kd=1.8μM), BRAF(V600E) (Kd=1.1μM), MEK1 (Kd=1.7μM), and MEK2 (Kd=1.6μM). Nocodazole has the highest affinity for αβIV and the lowest affinity for αβIII. Nocodazole (1nM) induces apoptosis of COLO 205 cancer cells. Nocodazole (≥ 30µg/mL) significantly increases the percentage of annexin-V-binding cells without significantly modifying average forward scatter of human erythrocytes.

 

体内研究

Nocodazole (5 mg/kg/three times per week, i.p.)has antitumor effects in athymic mice bearing COLO 205 tumor xenografts.Nocodazole (1nM) + R-41400 dramatically increase the levels of p21/CIP1 and p27/KIP1 protein in the tumor tissues.

 

推荐实验方法(仅供参考)

细胞实验:

Proteins are loaded at 50μg/lane and separated by 12% (w:v) sodium dodecyl sulfate-polyacrylamide gel electrophoresis, blotted, and probed with antibodies for cyclin E, p53, p21/CIP1, p27/KIP1, glyceraldehyde 3-phosphate dehydrogenase (GAPDH), cyclin A, cyclin D1, cyclin D3, cyclin B, CDK2, CDK4, and cytochrome C. Immunoreactive bands are visualized by incubating with the colorigenic substrates nitroblue tetrazolium and 5-bromo-4-chloro-3-indolyl-phosphate. The expression of GAPDH is used as the control for equal protein loading.

 

动物实验:

 

COLO 205 cells are grown in RPMI 1640 supplemented with 10% FCS. Cells are harvested through two consecutive trypsinizations, centrifuged at 300×g; for 5 min, washed twice, and resuspended in sterile phosphate-buffered saline (PBS). Cells (5×105 ) in 0.1mL are injected subcutaneously between the scapulae of each nude mouse. After transplantation, tumor size is measured with calipers, and the tumor volume is estimated. Once tumors reach a mean size of 200 mm3 , animals receive intraperitoneal injections of DMSO (25μL), R-41400 (50mg/kg), nocodazole (5mg/kg), or R-41400 + nocodazole three times per week for 6 wk.

保存条件:
2-8℃
UN码:
HazardClass:
危害声明:
安全说明:
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参考文献 & 客户发表文献

本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:
质量 (g) = 浓度 (mol/L) x 体积 (L) x 分子量 (g/mol)

摩尔浓度计算公式

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    *
    *选择对应的单位 *空出希望得到的变量,填写另外两个变量

用本工具协助配置特定浓度的溶液,使用的计算公式为:
开始浓度 x 开始体积 = 最终浓度 x 最终体积

稀释公式

稀释公式一般简略地表示为:C1V1 = C2V2 ( 输入 输出 )

  • * = *

连续稀释计算器方程

  • 连续稀释

  • 初始浓度:
  • 稀释倍数:
  • 计算结果

  • C1=C0/X C1: LOG(C1):
    C2=C1/X C2: LOG(C2):
    C3=C2/X C3: LOG(C3):
    C4=C3/X C4: LOG(C4):
    C5=C4/X C5: LOG(C5):
    C6=C5/X C6: LOG(C6):
    C7=C6/X C7: LOG(C7):
    C8=C7/X C8: LOG(C8):