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ZK-261991
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。
ZK-261991图片
CAS NO:886563-25-3
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
ZK-261991 是一种可口服的VEGFR酪氨酸酶抑制剂,抑制 VEGFR-2 活性的IC50值为 5 nM。
生物活性

ZK-261991 is an orally activeVEGFRtyrosine kinase inhibitor with anIC50of 5 nM for VEGFR2.

IC50& Target[1]

VEGFR2

5 nM (IC50)

体外研究
(In Vitro)

ZK-261991 inhibits cellular receptor autophosphorylation in KDR-PAECs with an IC50of 2 nM. ZK991 inhibits VEGFR-3 autophosphorylation concentration dependently with an IC50of 20 nM[1].

体内研究
(In Vivo)

ZK991 results in a significantly reduced recruitment of CD11b+and LYVE-1+cells into the murine cornea. ZK991 significantly improves the graft survival rate after corneal transplantation[1].

分子量

443.50

Formula

C24H25N7O2

CAS 号

886563-25-3

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.