Dimetholizine phosphate

Rabbit anti Human Homer1 Antibody, Recombinant, could be used for WB and so on.Application:WB: 1/500-1/2000Protein Function:Postsynaptic density scaffolding protein. Binds and cross-links cytoplasmic regions of GRM1, GRM5, ITPR1, DNM3, RYR1, RYR2,

Rabbit anti Human Homer1 Antibody, Recombinant, could be used for WB and so on.Application:WB: 1/500-1/2000Protein Function:Postsynaptic density scaffolding protein. Binds and cross-links cytoplasmic regions of GRM1, GRM5, ITPR1, DNM3, RYR1, RYR2,

RIP2 kinase inhibitor 2 is a receptor interacting protein-2 ( RIP2 ) kinase inhibitor extracted from patent WO/2014043437 A1, compound example 9.In VitroRIP2 kinase inhibitor 2 is a novel prodrug of a quinazolyl amine that inhibits RIP2 kinase.

ROCK-IN-1 is a potent inhibitor of ROCK , with an IC 50 of 1.2 nM for ROCK2 .In VitroROCK-IN-1 shows potent cellular efficacy, with an EC 50 of 200 nM. MCE has not independently confirmed the accuracy of these methods. They are for reference

ROCK-IN-1 is a potent inhibitor of ROCK , with an IC 50 of 1.2 nM for ROCK2 .In VitroROCK-IN-1 shows potent cellular efficacy, with an EC 50 of 200 nM. MCE has not independently confirmed the accuracy of these methods. They are for reference

ROCK-IN-1 is a potent inhibitor of ROCK , with an IC 50 of 1.2 nM for ROCK2 .In VitroROCK-IN-1 shows potent cellular efficacy, with an EC 50 of 200 nM. MCE has not independently confirmed the accuracy of these methods. They are for reference

SAR407899 is a selective, potent and ATP-competitive ROCK inhibitor, with an IC 50 of 135 nM for ROCK-2 , and K i s of 36 nM and 41 nM for human and rat ROCK-2 , respectively. SAR407899 shows stable inhibition of migrasome formation.In

InformationSEL201 SEL-201 (SLV-2436, SEL201-88) is a highly potent and ATP-competitive inhibitor of MNK1 and MNK2 with IC50 of 10.8  nM and 5.4 nM, respectively.TargetsMNK2 (Cell-free assay): MNK1 (Cell-free assay) 5.4 nM: 10.8 nM.

InformationSEL201 SEL-201 (SLV-2436, SEL201-88) is a highly potent and ATP-competitive inhibitor of MNK1 and MNK2 with IC50 of 10.8  nM and 5.4 nM, respectively.TargetsMNK2 (Cell-free assay): MNK1 (Cell-free assay) 5.4 nM: 10.8 nM.

A cell-permeable 7-aza-8-hydroxyquinoline compound that acts as a potent, catalytic site-targeting inhibitor of SHP-1 and SHP-2 protein tyrosine phosphatases (IC 50 = 355 nM and 318 nM, respectively). It inhibits PTP1B and HePTP with less potency

SIRT-IN-2 is a potent inhibitor of SIRT1/2/3 , with IC 50 s of 4, 4, 7 μM, respectively.In VitroSIRT-IN-2 (compound 31) is one of the most potent truncated pan SIRT1/ 2/3 inhibitor, the IC 50 values are 4, 4, 7 μM, respectively. SIRT-IN-2 (SIRT1/2/3

Spherisorb Amino (NH2) Column, 80Å, 3 µm, 4.6 mm X 50 mm, 1/pk