| S2202 |
NVP-BHG712
|
NVP-BHG712 is a specific EphB4 inhibitor with ED50 of 25 nM that discriminates between VEGFR and EphB4 inhibition; this compound also shows activity against c-Raf, c-Src and c-Abl with IC50 of 0.395 μM, 1.266 μM and 1.667 μM, respectively.
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BMC Oral Health, 2025, 25(1):118
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Nat Commun, 2024, 15(1):5894
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Apoptosis, 2024, 10.1007/s10495-024-02042-4
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| S6515 |
ALW II-41-27
|
ALW II-41-27 (compound 7) is a potent inhibitor of Eph receptor tyrosine kinase with Kd of 12 nM for EphA2.
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Cell Death Differ, 2025, 10.1038/s41418-025-01536-1
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Sci Rep, 2025, 15(1):24245
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Biol Pharm Bull, 2025, 48(2):172-176
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| S0256 |
Ehp-inhibitor-1
|
Ehp-inhibitor-1 (Ehp inhibitor 2) is an Eph family tyrosine kinase inhibitor that targets Eph receptors.
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King's College London, 2023,
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| E2835 |
NVP-BHG712 isomer
|
NVP-BHG712 isomer, a regioisomer of NVP-BHG712, shows conserved non-bonded binding to EphA2 and EphB4.
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| E0614 |
AWL-II-38.3
|
AWL-II-38.3 is a potent Ephrin type-A receptor 3 (EphA3) kinase inhibitor.
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| S8573 |
Sitravatinib (MGCD516)
|
Sitravatinib (MGCD516, MG-516) is a novel small molecule inhibitor targeting multiple RTKs involved in driving sarcoma cell growth, including c-Kit, PDGFRβ, PDGFRα, c-Met, and Axl.
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Commun Biol, 2025, 8(1):1185
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Res Sq, 2025, rs.3.rs-6431257
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JCI Insight, 2022, e148717
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