位置:首页 > 产品库 > AV-412 free base
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
AV-412 free base
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
AV-412 free base图片
CAS NO:451492-95-8

MP-412 free base
AV-412 free base (MP-412 free base) 是EGFR抑制剂,抑制EGFR,EGFRL858R,EGFRT790M,EGFRL858R/T790M和 ErbB2的IC50值分别为0.75,0.5,0.79,2.3,19 nM。
生物活性

AV-412 free base (MP-412 free base) is anEGFRinhibitor withIC50s of 0.75, 0.5, 0.79, 2.3, 19 nM forEGFR,EGFRL858R,EGFRT790M,EGFRL858R/T790Mand ErbB2, respectively.

IC50& Target[1]

EGFR

0.75 nM (IC50)

ErbB2

19 nM (IC50)

EGFRL858R

0.51 nM (IC50)

EGFRL858R/T790M

2.3 nM (IC50)

EGFRT790M

0.79 nM (IC50)

体外研究
(In Vitro)

AV-412 inhibits autophosphorylation of EGFR and ErbB2 with IC50of 43 and 282 nM, respectively. AV-412 also inhibits epidermal growth factor (EGF)-dependent cell proliferation with an IC50of 100 nM. AV-412 abrogates EGFR signaling in the gefitinib-resistant H1975 cell line, which harbors a double mutation of L858R and T790M in EGFR[1].

体内研究
(In Vivo)

In animal studies using cancer xenograft models, AV-412 (30 mg/kg) demonstrates complete inhibition of tumor growth of the A431 and BT-474 cell lines, which overexpress EGFR and ErbB2, respectively. AV-412 suppresses autophosphorylation of EGFR and ErbB2 at the dose corresponding to its antitumor efficacy. When various dosing schedules are applied, AV-412 shows significant effects with daily and every-other-day schedules, but not with a once-weekly schedule, suggesting that frequent dosing is preferable for this compound. Furthermore, AV-412 shows a significant antitumor effect on the ErbB2-overexpressing breast cancer KPL-4 cell line, which is resistant to gefitinib[1].

Clinical Trial
分子量

507.00

性状

Solid

Formula

C27H28ClFN6O

CAS 号

451492-95-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
溶解性数据
In Vitro: 

DMSO : 50 mg/mL(98.62 mM;Need ultrasonic)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM1.9724 mL9.8619 mL19.7239 mL
5 mM0.3945 mL1.9724 mL3.9448 mL
10 mM0.1972 mL0.9862 mL1.9724 mL
*

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℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂: 10% DMSO    40%PEG300   5%Tween-80   45% saline

    Solubility: ≥ 2.5 mg/mL (4.93 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (4.93 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH2O 中,得到澄清透明的生理盐水溶液
*以上所有助溶剂都可在本网站选购。
 
 
维奥蛋白资源库 - 中文蛋白资源 CopyRight © 2010-2024