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Nature products
Antibodies
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Intermediate
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- Heterocyclic Series
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Raw Materials
Ephrin Receptor
Chemical Structure | Cat. No. | Product Name | CAS No. |
---|
BCP44969 | 123C4 New | 2034159-30-1 | |
123C4 is a novel, potent, and selective agonist of the tyrosine kinase EphA4 receptor.
|
BCP43510 | NVP-BHG712 isomer New | 2245892-85-5 | |
NVP-BHG712 isomer, a regioisomer of NVP-BHG712, shows conserved non-bonded binding to EPHA2 and EPHB4.
|
BCP16892 | JI-101 | 900573-88-8 | |
JI-101 is a n orally active inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2), platelet-derived growth factor receptor beta (PDGFRb), and the ephrin B4 receptor B4 (EphB4) with potential antiangiogenic and antineoplastic activities.
|
BCP02362 | NVP-BHG712 | 940310-85-0 | |
NVP-BHG712 is a small molecule specific EphB4, VEGFR2, c-raf, c-src and c-Abl kinase inhibitor with ED50 of 25 nM, 4.2, 0.4, 1.3 and 1.7μM, respectively.
|
BCP23438 | Tesevatinib New | 781613-23-8 | |
XL-647 (Tesevatinib, EXEL-7647, KD-019) is a novel spectrum-selective kinase inhibitor that potently inhibits the EGFR, ErbB2, KDR and EphB4 with IC50 of 0.3, 16, 1.5 and 1.4 nM, respectively.
|
BCP02839 | XL647(Racemate) | 874286-84-7 | |
XL-647 (Tesevatinib;XL-647;KD-019) is an orally available, multi-target tyrosine kinase inhibitor; inhibits EGFR, ErbB2, KDR, Flt4 and EphB4 kinase with IC50s of 0.3, 16, 1.5, 8.7, and 1.4 nM.
|
BCP26205 | ALW-II-41-27 | 1186206-79-0 | |
ALW-II-41-27 is a Eph receptor tyrosine kinase inhibitor.
|