Home>>Signaling Pathways>> Metabolism>> phosphatases>>L-690330

L-690330 Sale

目录号 : GC16451

L-690,330 是一种肌醇单磷酸酶 (IMPase) 的竞争性抑制剂,对重组人和牛 IMPase 的 Kis 分别为 0.27 和 0.19 μM,对人和牛额叶皮层 IMPase 的 Kis 分别为 0.30 和 0.42 μM。

L-690330 Chemical Structure

Cas No.:142523-38-4

规格 价格 库存 购买数量
10mg
¥2,426.00
现货
50mg
¥7,470.00
现货

电话:400-920-5774 Email: sales@glpbio.cn

Customer Reviews

Based on customer reviews.

Sample solution is provided at 25 µL, 10mM.

Description

L-690,330 is a competitive inhibitor of inositol monophosphatase (IMPase) with a Ki value of between 0.2 and 2 μM depending on the source of IMPase [1].

In the phosphatidylinositol (PI) cycle cell signalling pathway, IMPase is involved as a key enzyme. Inositol monophosphates, inositol(1)phosphate [Ins(l)P], inositol(3)phosphate [Ins(3)P], and inositol(4)phosphate [Ins(4)P] are hydrolyzed by IMPase and produce free inositol. Free inositol can then be used to synthesize PI [1].

In carbachol-stimulated m1 CHO cells, the treatment with L-690,330 alone did not increase the amount of [3H]InsP1. In the absence of L-690,330, the treatment with carbachol alone increased levels of [3H]InsP1, resulted in levels ranging from 20 to 100% above basal [3H]InsP1 levels. In the presence of carbachol, lithium at 10 mM increased the amount of [3H]InsP1 by approximate five folds (relative to [3H]InsP1 levels in carbachol-stimulated cells) and the EC50 value of this effect was about 1 mM. In carbachol-stimulated cells, L-690,330 at 10 mM resulted in only ~40% of the maximum response seen in the case with lithium treatment [1].

In mouse brains, in the absence of L-690,330, pilocarpine produced approximately doubled levels of Ins(1)P. In the absence of pilocarpine, L-690,330 did not affect Ins(1)P levels. Under pilocarpine-stimulated conditions, treatment with L-690,330 resulted in a pronounced accumulation of Ins(1)P, with the maximum level observed 1 h after injection. The maximum was of an approximate four-fold elevation [1].

Reference:
[1].  Atack JR, Cook SM, Watt AP, et al. In Vitro and In Vivo Inhibition of Inositol Monophosphatase by the Bisphosphonate L-690,330. Journal of neurochemistry, 1993, 60(2): 652-658.

实验参考方法

Cell experiment [1]:

Cell lines

M1 CHO cells

Preparation method

The solubility of this compound in sterile water is 100 mM. General tips for obtaining a higher concentration: Please warm the tube at 37 °C for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below - 20 °C for several months.

Reacting condition

0.1 ~ 10 mM

Applications

In Carbachol-stimulated m1 CHO cells, L-690,330 alone did not increase the amount of [3H]InsP1; lithium alone slightly elevated the amount of [3H]InsP1; Carbachol alone increased the amount of [3H]InsP1 ranging from 20 to 100%.

Animal experiment [1]:

Animal models

Pilocarpine-stimulated mice

Dosage form

0 ~ 1 mmol/kg; s.c.

Applications

In Pilocarpine-stimulated mice, L-690,330 dose-dependently increased brain Ins(1)P levels, with the ED50 values of 0.3 mmol/kg. L-690,330 induced a maximal increase in the Ins(1)P level (about 4-fold) 1 hr after injection.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Atack JR, Cook SM, Watt AP, et al. In Vitro and In Vivo Inhibition of Inositol Monophosphatase by the Bisphosphonate L-690,330. Journal of neurochemistry, 1993, 60(2): 652-658.

化学性质

Cas No. 142523-38-4 SDF
化学名 (1-(4-hydroxyphenoxy)ethane-1,1-diyl)diphosphonic acid
Canonical SMILES OP(O)(C(OC(C=C1)=CC=C1O)(C)P(O)(O)=O)=O
分子式 C8H12O8P2 分子量 298.13
溶解度 <29.81mg/ml in Water 储存条件 4°C, sealed storage, away from moisture
General tips 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。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

制备储备液
1 mg 5 mg 10 mg
1 mM 3.3542 mL 16.7712 mL 33.5424 mL
5 mM 0.6708 mL 3.3542 mL 6.7085 mL
10 mM 0.3354 mL 1.6771 mL 3.3542 mL
  • 摩尔浓度计算器

  • 稀释计算器

  • 分子量计算器

质量
=
浓度
x
体积
x
分子量
 
 
 
*在配置溶液时,请务必参考产品标签上、MSDS / COA(可在Glpbio的产品页面获得)批次特异的分子量使用本工具。

计算

动物体内配方计算器 (澄清溶液)

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)
给药剂量 mg/kg 动物平均体重 g 每只动物给药体积 ul 动物数量
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GLPBIO为您提供正确的澄清溶液配方)
% DMSO % % Tween 80 % saline
计算重置

产品文档

Quality Control & SDS

View current batch: