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C649590-10mg123C4 is a potent, selective and competitive agonist of the receptor tyrosine kinase EPHA4 , with a K i value of 0.65 μMForm:SolidIC50& Target:Ki: 0.65 μM (EPHA4)
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C649590-1mg123C4 is a potent, selective and competitive agonist of the receptor tyrosine kinase EPHA4 , with a K i value of 0.65 μMForm:SolidIC50& Target:Ki: 0.65 μM (EPHA4)
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C649590-5mg123C4 is a potent, selective and competitive agonist of the receptor tyrosine kinase EPHA4 , with a K i value of 0.65 μMForm:SolidIC50& Target:Ki: 0.65 μM (EPHA4)
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A650669-100mgALW-II-49-7 is a selective EphB2 kinase inhibitor with an EC 50 value of 40 nM in cellIn VitroALW-II-49-7 (compound 9) exhibits selectivity profile of binding to a set of kinases including b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2,
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A650669-10mgALW-II-49-7 is a selective EphB2 kinase inhibitor with an EC 50 value of 40 nM in cellIn VitroALW-II-49-7 (compound 9) exhibits selectivity profile of binding to a set of kinases including b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2,
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A650669-1mgALW-II-49-7 is a selective EphB2 kinase inhibitor with an EC 50 value of 40 nM in cellIn VitroALW-II-49-7 (compound 9) exhibits selectivity profile of binding to a set of kinases including b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2,
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A650669-25mgALW-II-49-7 is a selective EphB2 kinase inhibitor with an EC 50 value of 40 nM in cellIn VitroALW-II-49-7 (compound 9) exhibits selectivity profile of binding to a set of kinases including b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2,
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A650669-50mgALW-II-49-7 is a selective EphB2 kinase inhibitor with an EC 50 value of 40 nM in cellIn VitroALW-II-49-7 (compound 9) exhibits selectivity profile of binding to a set of kinases including b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2,
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A650669-5mgALW-II-49-7 is a selective EphB2 kinase inhibitor with an EC 50 value of 40 nM in cellIn VitroALW-II-49-7 (compound 9) exhibits selectivity profile of binding to a set of kinases including b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2,
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A656369-1mlALW-II-49-7 is a selective EphB2 kinase inhibitor with an EC 50 value of 40 nM in cellIn VitroALW-II-49-7 (compound 9) exhibits selectivity profile of binding to a set of kinases including b-raf, CSF1R, DDR1, DDR2, EphA2, EphA5, EphA8, EphB1, EphB2,
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B648638-1mgBT5528 is a bicyclic peptide toxin conjugate, an EphA2 activator. BT5528, made up of a bicyclic peptide and Auristatin E ( HY-15582 ), is derivated from BCY6099. BT5528 shows potent anti-tumor activity without bleeding or coagulation toxicity in
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E650963-10mgEph inhibitor 1 is a potent Eph inhibitor. Eph inhibitor 1 has the potential for the research of neurological disorders.Form:Solid