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VEGFR-2-IN-30
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。
VEGFR-2-IN-30图片

VEGFR-2-IN-30 是一种 VEGFR-2 抑制剂 (IC50: 66 nM)。VEGFR-2-IN-30 还抑制 PDGFR、EGFR 和 FGFR1,IC50s 分别为 180、98、82 nM。VEGFR-2-IN-30 将癌细胞阻滞在 S 期并诱导早期和晚期细胞凋亡 (apoptosis)。
生物活性

VEGFR-2-IN-30 is aVEGFR-2inhibitor (IC50: 66 nM). VEGFR-2-IN-30 also inhibitsPDGFR,EGFRandFGFR1withIC50s of 180, 98, 82 nM respectively. VEGFR-2-IN-30 arrestscancercell at S-phase and induces early and lateapoptosis[1].

IC50& Target[1]

VEGFR2

66 nM (IC50)

体外研究
(In Vitro)

VEGFR-2-IN-30 (化合物 8f) (10 μM) 抑制 35% 的 UO-31 细胞生长[1]
VEGFR-2-IN-30 (10 μg/mL, 72 h) 抑制 HUVEC 细胞迁移[1].
VEGFR-2-IN-30 (5.29 μM, 24 h) 在阻滞 UO-31 细胞 在S 期[1]
VEGFR-2-IN-30 (5.29 μM, 24 h) 诱导 UO-31 细胞凋亡[1]
VEGFR-2-IN-30 (5.29 μM, 24 h) 在 UO-31 细胞中增加 Bax 水平并下调 Bcl-2 水平[1]

Cell Migration Assay[1]

Cell Line:NHUVEC
Concentration:10 μg/mL
Incubation Time:72 h
Result:Inhibited cell migration by 58.52%.

Apoptosis Analysis[1]

Cell Line:UO-31 cell
Concentration:5.29 μM
Incubation Time:24 h
Result:Increased early apoptotic cells from 0.61% to 23.51% and late apoptotic cells from 0.13% to 9.28%.
Increased the level of active caspase-3.
分子量

607.10

Formula

C28H23ClN6O4S2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

 
 
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