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E651740-5mg12-Ethyl-9-hydroxycamptothecin is a derivative of Camptothecin. Camptothecin (CPT), a kind of alkaloid, is a DNA topoisomerase I (Topo I) inhibitor with an IC 50 of 679 nM.In Vitro12-Ethyl-9-hydroxycamptothecin is a derivative of Camptothecin. MCE
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L647840-1mg15-LOX-1 inhibitor 1 is a potent inhibitor of 15-LOX-1 (15-lipoxygenase-1) with an IC 50 value of 0.19 μM. 15-LOX-1 inhibitor 1 protects macrophages from lipopolysaccharide-induced cytotoxicity. 15-LOX-1 inhibitor 1 inhibits NO formation and lipid
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A649457-100mg1A-116, a potent Rac1 inhibitor, is specific for W56 residues, can prevent EGF -induced Rac1 activation and block Rac1-P-Rex1 interaction. 1A-116 can induce apoptosis and inhibit cell proliferation, migration and cycle progression in a
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A649457-10mg1A-116, a potent Rac1 inhibitor, is specific for W56 residues, can prevent EGF -induced Rac1 activation and block Rac1-P-Rex1 interaction. 1A-116 can induce apoptosis and inhibit cell proliferation, migration and cycle progression in a
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A649457-25mg1A-116, a potent Rac1 inhibitor, is specific for W56 residues, can prevent EGF -induced Rac1 activation and block Rac1-P-Rex1 interaction. 1A-116 can induce apoptosis and inhibit cell proliferation, migration and cycle progression in a
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A649457-50mg1A-116, a potent Rac1 inhibitor, is specific for W56 residues, can prevent EGF -induced Rac1 activation and block Rac1-P-Rex1 interaction. 1A-116 can induce apoptosis and inhibit cell proliferation, migration and cycle progression in a
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A649457-5mg1A-116, a potent Rac1 inhibitor, is specific for W56 residues, can prevent EGF -induced Rac1 activation and block Rac1-P-Rex1 interaction. 1A-116 can induce apoptosis and inhibit cell proliferation, migration and cycle progression in a
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A655869-1ml1A-116, a potent Rac1 inhibitor, is specific for W56 residues, can prevent EGF -induced Rac1 activation and block Rac1-P-Rex1 interaction. 1A-116 can induce apoptosis and inhibit cell proliferation, migration and cycle progression in a
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G650263-100mg1G244 is a potent DPP8/9 inhibitor with IC 50 s of 12 nM and 84 nM, respectively. 1G244 does not inhibit DPPIV and DPPII. 1G244 induces apoptosis in multiple myeloma cells and has anti-myeloma effectsIn Vitro1G244 (0-100 μM: 72 hours: Delta47, U266
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G650263-10mg1G244 is a potent DPP8/9 inhibitor with IC 50 s of 12 nM and 84 nM, respectively. 1G244 does not inhibit DPPIV and DPPII. 1G244 induces apoptosis in multiple myeloma cells and has anti-myeloma effectsIn Vitro1G244 (0-100 μM: 72 hours: Delta47, U266
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G650263-25mg1G244 is a potent DPP8/9 inhibitor with IC 50 s of 12 nM and 84 nM, respectively. 1G244 does not inhibit DPPIV and DPPII. 1G244 induces apoptosis in multiple myeloma cells and has anti-myeloma effectsIn Vitro1G244 (0-100 μM: 72 hours: Delta47, U266
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G650263-50mg1G244 is a potent DPP8/9 inhibitor with IC 50 s of 12 nM and 84 nM, respectively. 1G244 does not inhibit DPPIV and DPPII. 1G244 induces apoptosis in multiple myeloma cells and has anti-myeloma effectsIn Vitro1G244 (0-100 μM: 72 hours: Delta47, U266