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CAS: 75541-83-2
分子式: C15H12FNO3
分子量: 273.26
中文名称: 
2-(4-氟苯甲酰基氨基)甲基苯甲酸酯
2-(4-氟苯甲酰基氨基)苯甲酸甲酯
英文名称: 
exo 1
2-(4-fluorobenzoylamino)methylbenzoate
2-(4-fluorobenzoylamino)benzoic acid methyl ester
用途: Exo1 是 exocytic pathway 的抑制剂。
推荐供应商
货号品牌产品名称规格包装、参考价格
E877521MACKLINExo1 99%450元/10mg;   1576元/50mg;   4208元/250mg;   咨询
储存:2-8℃
状态:白色到灰白色固体
E792547MACKLINExo110mM in DMSO583元/1ml;   咨询
储存:-20°C
E8280Sigma-AldrichExo 1≥98% (HPLC), solid730.08元/5 MG;   2457.91元/25 MG;   咨询

产品说明

应用

Exo 1 已被用作 BRB80 缓冲液的组成成分,以被用于研究外壳蛋白 1 (COPI) 介导的膜运输。它也被用作高尔基体抑制剂来研究其对长散布的核元件 1 (L1) 逆转录转座的影响。

包装

5, 25 mg in glass bottle

生化/生理作用

Exo 1 是一种可渗透细胞的邻氨基苯甲酸甲酯类似物,可促进二磷酸腺苷 (ADP)-核糖基化因子 (ARF) 1 从高尔基体膜释放。它还可抑制内质网 (ER) 和高尔基体之间的膜运输。
可逆的胞吐抑制剂; 高尔基体ARF 1(ADP-核糖基化因子)GTPase激活剂。

基本信息

经验(实验)分子式C15H12NFO3
分子量273.26
MDL编号MFCD00028104
PubChem化学物质编号24724477
NACRESNA.77

产品性质

质量水平100
测定≥98% (HPLC)
形式solid
溶解性DMSO: soluble 19 mg/mL
SMILES stringCOC(=O)c1ccccc1NC(=O)c2ccc(F)cc2
InChI1S/C15H12FNO3/c1-20-15(19)12-4-2-3-5-13(12)17-14(18)10-6-8-11(16)9-7-10/h2-9H,1H3,(H,17,18)
InChI keyKIAPWMKFHIKQOZ-UHFFFAOYSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
个人防护装备Eyeshields, Gloves, type N95 (US)
341220Sigma-AldrichExo1-CAS 75541-83-2-CalbiochemA cell-permeable methylanthranilate analog that reversibly inhibits vesicular traffic from ER to Golgi in mammalian cells by inducing tubulation and collapsing of the Golgi membrane.2118.65元/25 MG;   咨询

产品说明

一般描述

A cell-permeable methylanthranilate analog that reversibly blocks vesicular traffic from the ER to the Golgi in mammalian cells (IC50 = 20 µM in BSC1 cells) by inducing tubulation and collapsing of the Golgi membrane and re-directing the traffic back to the ER. Acts as a potent and selective modifier of Golgi ARF1 GTPase activity. Unlike another membrane traffic inhibitor, Brefeldin A (BFA) (Cat. No. 203729), the effects appear to be limited to the Golgi, as no effects are detected on endocytic organelles, such as endosomes and trans-Golgi network (TGN). The inhibitory mechanism and target(s) appear to be different from those of BFA, thus making it a valuable alternative that complements BFA in membrane trafficking studies.
A cell-permeable methylanthranilate analog that reversibly inhibits vesicular traffic from ER to Golgi in mammalian cells (IC50 = 20 µM in BSC1 cells) by inducing tubulation and collapsing of the Golgi membrane and redirecting the traffic back to ER. Acts as a potent and selective modifier of Golgi ARF1 GTPase activity. Unlike another membrane traffic inhibitor Brefeldin A (BFA; Cat. No. 203729), its effect seems to be limited to Golgi, as no effect can be detected on endocytic organelles, such as endosomes and TGN (trans-Golgi network). Its inhibitory mechanism and target(s) appear to be quite different from those of BFA and thus serves as a valuable alternative that complements BFA in membrane traffic studies.

包装

25 mg in Plastic ampoule
Packaged under inert gas

生化/生理作用

Cell permeable: yes
Target IC50: 20 µM inhibiting vesicular traffic from ER to Golgi in BSC1 cells
Product does not compete with ATP.
Primary Target
Golgi ARF1 GTPase
Reversible: yes

警告

Toxicity: Harmful (C)

重悬

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

其他说明

Feng. Y., et al. 2003. Proc. Natl. Acad. Sci. USA100, 6469.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

基本信息

经验(实验)分子式C15H12FNO3
分子量273.26
MDL编号MFCD00028104

产品性质

质量水平100
测定≥95% (HPLC)
形式solid
manufacturer/tradenameCalbiochem®
储存条件OK to freeze
protect from light
颜色 white
溶解性DMF: 25 mg/mL
DMSO: 25 mg/mL
ethanol: 5 mg/mL
methanol: 5 mg/mL
运输ambient
储存温度2-8℃
InChI1S/C15H12FNO3/c1-20-15(19)12-4-2-3-5-13(12)17-14(18)10-6-8-11(16)9-7-10/h2-9H,1H3,(H,17,18)
InChI keyKIAPWMKFHIKQOZ-UHFFFAOYSA-N

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
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