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|---|---|---|
| 100 mg | Get quote | |
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| 500 mg | Get quote | |
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| Cat. No. : | HY-15333 |
| M.Wt: | 443.50 |
| Formula: | C24H25N7O2 |
| Purity: | >98 % |
| Solubility: | 10 mM in DMSO |
ZK-261991 is an orally active VEGFR tyrosine kinase inhibitor with an IC50 of 5 nM for VEGFR2. IC50 & Target: IC50: 5 nM (VEGFR-2)[1] 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].
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