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Cat.No. Product Name Information Area
T4518 Licochalcone D Licochalcone D may be a potential drug for human melanoma treatment by inhibiting pro...
T4092 AG 126 The tyrphostin AG-126 selectively inhibits the phosphorylation of ERK1 (p44) and ERK2... Other
T3378 17α-Estradiol Endogenous estrogen receptor ligand (Ki?values are 0.2 and 1.2 nM for ERα?and ERβ?rec...
T3714 SUN 11602 SUN11602, an aniline compound, mimics the neuroprotective mechanisms of basic fibrobl... Nervous system
T3668 Galangin Galangin is an agonist/antagonist of the arylhydrocarbon receptor, and also shows inh... Others
T3674 Hydroxysafflor yellow A Hydroxysafflor yellow A inhibited adipogenesis by increasing HSL promoter activities.... Others
T7005 Ulixertinib Ulixertinib (BVD-523, VRT752271) is an effective and reversible ERK1/ERK2 inhibitor. ... Others
T6948 Pluripotin Pluripotin (SC1), which keep embryonic stem cell (ESC) self-renewal, is a dual inhibi... Others
T6818 DEL-22379 DEL-22379 is a water-soluble ERK dimerization inhibitor with IC50 of ~0.5 μM. Others
T3166 VX-11e VX-11e is a potent, selective, and orally bioavailable ERK(Extracellular Signal-Regul... Cancer
T6511 Ravoxertinib GDC-0994 is an effective and orally available ERK1/2 inhibitor (IC50: 1.1/0.3 nM). Cancer
T6066 SCH772984 SCH 772984 is a potent inhibitor of ERK1/ERK2 (IC50: 4/1 nM) and has only weak inhibi... Cancer
T2961 Notoginsenoside R1 Notoginsenoside R1 has been shown to exhibit antioxidant, antiapoptotic, anti-inflamm... Cancer
T2416 BIX02189 BIX02189 is a selective inhibitor of MEK5 with IC50 of 1.5 nM. Other
T2356 Ro 3306 RO-3306 is a selectivity ATP-competitive CDK1 inhibitor (Ki: 20 nM). The selectivity ... Other
T1956 FR180204 FR180204 is a potent and selective ATP-competitive inhibitor of ERK1 and ERK2. Other
T1843 XMD8-92 XMD8-92 is an effective and specific BMK1/ERK5 inhibitor (Kd: 80 nM). Other
T1842 XMD17-109 XMD17-109 is a new selective ERK-5 inhibitor (EC50: 4.2 uM, HEK293 cells). Other