ZK-261991

Modify Date: 2024-01-20 10:10:30

ZK-261991 Structure
ZK-261991 structure
Common Name ZK-261991
CAS Number 886563-25-3 Molecular Weight 443.501
Density 1.3±0.1 g/cm3 Boiling Point 682.1±55.0 °C at 760 mmHg
Molecular Formula C24H25N7O2 Melting Point N/A
MSDS N/A Flash Point 366.3±31.5 °C

 Use of ZK-261991


ZK-261991 is an orally active VEGFR tyrosine kinase inhibitor with an IC50 of 5 nM for VEGFR2.

 Names

Name ZK-261991
Synonym More Synonyms

 ZK-261991 Biological Activity

Description ZK-261991 is an orally active VEGFR tyrosine kinase inhibitor with an IC50 of 5 nM for VEGFR2.
Related Catalog
Target

VEGFR2:5 nM (IC50)

In Vitro ZK-261991 inhibits cellular receptor autophosphorylation in KDR-PAECs with an IC50 of 2 nM. ZK991 inhibits VEGFR-3 autophosphorylation concentration dependently with an IC50 of 20 nM[1].
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].
Cell Assay HLMVECs are cultured in EGM 2-MV medium. For the cytotoxicity assay, cells are seeded in 96-well plates in EGM 2-MV medium at a density of 5×103 cells/well. Medium is changed every second day, and cells are cultured until reaching confluence. Then the medium is replaced with serum-free medium containing a tyrosine kinase inhibitor (PTK/ZK or ZK991; concentration 20 nM) and left overnight. Control cells receive the substance vehicle. The next day, cytotoxicity assay (WST-1 based) is performed according to the manufacturer's instructions. Colorimetric analysis is performed with an ELISA reader. Subsequent statistical analysis is performed, and graphs are drawn. The number of wells per group is as follows: PTK/ZK control group, n = 30; PTK/ZK 20 nM, n = 30; ZK991 control group, n = 30; ZK991 20 nM, n = 30.
Animal Admin Before corneal neovascularization, each animal is deeply anesthetized. Three 11-0 nylon sutures are placed intrastromally with two stromal incursions extending over 120°C of corneal circumference each. The outer point of suture placement is chosen near the limbus, and the inner suture point is chosen near the corneal center equidistant from the limbus to obtain standardized angiogenic responses. Sutures are left in place for 14 days. The first treatment group receive the tyrosine kinase inhibitor PTK/ZK (75 mg/kg, orally, twice daily), the second treatment group receive the tyrosine kinase inhibitor ZK991 (50 mg/kg, orally, twice daily), and control mice receive equal amounts of the substance vehicle. After 2 weeks, mice are killed and corneas are prepared. The corneal neovascularization assay includes 22 mice in the control group, 11 mice in the PTK/ZK treatment group, and 11 mice in the ZK991 treatment group.
References

[1]. Deniz Hos, et al. Inflammatory Corneal (Lymph)angiogenesis Is Blocked by VEGFR-Tyrosine Kinase Inhibitor ZK 261991, Resulting in Improved Graft Survival after Corneal Transplantation. Investigative Ophthalmology & Visual Science May 2008, Vol.49, 1836-1842.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 682.1±55.0 °C at 760 mmHg
Molecular Formula C24H25N7O2
Molecular Weight 443.501
Flash Point 366.3±31.5 °C
Exact Mass 443.206970
LogP 1.65
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.668

 Synonyms

2-[({2-[(Dimethylcarbamoyl)amino]-4-pyridinyl}methyl)amino]-N-(2-methyl-2H-indazol-6-yl)benzamide
Benzamide, 2-[[[2-[[(dimethylamino)carbonyl]amino]-4-pyridinyl]methyl]amino]-N-(2-methyl-2H-indazol-6-yl)-
Top Suppliers:I want be here



Get all suppliers and price by the below link:

ZK-261991 suppliers


Price: $1200/1mg

Reference only. check more ZK-261991 price