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CAS: 42494-73-5
分子式: C12H8KN2O5V  
分子量: 350.24 (anhydrous basis)
中文名称: 
双过氧(1,10-菲咯啉)氧钒酸钾(v)水合物
英文名称: 
bpv(phen)
potassium bisperoxo(1,10-phenanthroline)oxovanadate (v) hydrate
推荐供应商
货号品牌产品名称规格包装、参考价格
V920856MACKLINBisperoxo(1,10-菲咯啉)氧钒酸钾(V)三水合物95% V basis854元/5mg;   咨询
储存:-20 °C,密封,干燥
状态:微黄色到暗黄色到橙色固体
SML0889Sigma-AldrichbpV(phen)≥95% V basis921.1元/5 MG;   3342.43元/25 MG;   咨询

产品说明

包装

5, 25 mg in glass bottle

生化/生理作用

bpV(phen)(双过氧双(二吡啶)氧钒酸钾)可通过介导NO依赖性杀微生物作用而对利什曼病的疾病进展显示出保护作用。
bpV(phen)是一种胰岛素受体激酶(IRK)激活剂和蛋白质磷酸酪氨酸磷酸酶抑制剂,具有对PTEN、磷酸酶和张力蛋白同源物的选择性,而后者是一种参与细胞周期调节的肿瘤抑制磷酸酶。bpV(phen)对PTEN的IC50值为38 nM,而PTPβ为343 nM、PTP-1β为920 nM。bpV(phen)在氧化应激中具有抗炎作用,包括对氧化应激诱导的心肌细胞损伤的抑制作用,可以通过ROS对PTEN的作用部分调节。它也可能参与分化。

其他说明

光敏性

基本信息

经验(实验)分子式KVO5C12H8N2 · xH2O
分子量350.24 (anhydrous basis)
NACRESNA.77

产品性质

质量水平100
测定≥95% V basis
形式powder
储存条件protect from light
颜色faintly yellow to dark yellow
溶解性H2O: 20 mg/mL, clear
储存温度−20℃
SMILES stringO=[V]123([N]4=CC=CC5=C4C6=C(C=CC=[N]62)C=C5)(OO3)OO1.[K]

安全信息

象形图GHS07
警示用语:Warning
危险声明H315 - H319 - H335
预防措施声明P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
危险分类Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官Respiratory system
储存分类代码11 - Combustible Solids
WGKWGK 3
闪点(F)Not applicable
闪点(C)Not applicable
203695Sigma-AldrichbpV(phen)-CAS 42494-73-5-CalbiochemA potent protein phosphotyrosine phosphatase inhibitor and insulin receptor kinase (IRK) activator.3124.36元/10 MG;   咨询

产品说明

一般描述

The water content varies from lot to lot and is supplied on the label along with the lot-specific molecular weight.
A potent protein phosphotyrosine phosphatase inhibitor and insulin receptor kinase (IRK) activator. Excellent insulin mimetic at 15 µg/kg in vitro and in vivo for use. Inhibits the in situ dephosphorylation of autophosphorylated insulin receptors with over 1000-fold greater potency than sodium orthovanadate. Arrests proliferation of neuroblastoma NB 41 and glioma C6 cells at the G2/M transition of the cell cycle. Also reported to potently inhibit PTEN (IC50 = 38 nM).
A potent insulin receptor kinase (IRK) activator and protein phosphotyrosine phosphatase inhibitor. Excellent insulin mimetic for in vitro and in vivo use (15 µg/kg). Inhibits in situ dephosphorylation of autophosphorylated insulin receptors with greater than 1000-fold potency over sodium orthovanadate. Arrests proliferation of neuroblastoma NB 41 and glioma C6 cells at the G2/M transition of the cell cycle. Also reported to potently inhibit PTEN (IC50 = 38 nM). The water content varies from lot to lot and is supplied on the label along with the lot-specific molecular weight.

包装

10 mg in Plastic ampoule
Packaged under inert gas

生化/生理作用

Product does not compete with ATP.
Reversible: no
Cell permeable: no
Primary Target
PTEN

警告

Toxicity: Standard Handling (A)

重悬

Unstable in solution; reconstitute just prior to use.

其他说明

Schmid, A.C., et al. 2004. FEBS Lett.566, 35.
Muzyamba, M.C., et al. 1999. J. Physiol. 517, 421.
Drake, P.G., et al. 1996. Endocrinology137, 4960.
Bevan, A.P., et al. 1995. Am. J. Physiol.268, E60.
Bevan, A.P., et al. 1995. J. Biol. Chem. 270, 10784.
Yale, J.F., et al. 1995. Diabetes 44, 1274.
Posner, B.I., et al. 1994. J. Biol. Chem. 269, 4596.

法律信息

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

基本信息

线性分子式K[VO(O2)2C12H8N2]

产品性质

质量水平100
测定≥99% (51V-NMR)
形式solid
效能38 nM IC50
manufacturer/tradenameCalbiochem®
储存条件OK to freeze
protect from light
颜色 yellow
溶解性water: 5 mg/mL
运输ambient
储存温度−20℃

安全信息

储存分类代码11 - Combustible Solids
WGKWGK 1
闪点(F)Not applicable
闪点(C)Not applicable
CAS号首数字顺序排列: 1 2 3 4 5 6 7 8 9
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