CS 137 radiography examination equipment

InformationUM-164 is a highly potent, dualc-Src/p38inhibitor ofc-Srcwith a binding constant Kd of 2.7 nM for c-Src and inhibits both p38α and p38β.Targetsp38α : p38β : c-Src (Cell-free assay) : 2.7 nM(Kd)In vitroUM-164 binds the inactive kinase

InformationUM-164 is a highly potent, dualc-Src/p38inhibitor ofc-Srcwith a binding constant Kd of 2.7 nM for c-Src and inhibits both p38α and p38β.Targetsp38α : p38β : c-Src (Cell-free assay) : 2.7 nM(Kd)In vitroUM-164 binds the inactive kinase

InformationT-26c T-26c is a highly potent and selective inhibitor of matrix metalloproteinase-13 (MMP-13) with IC50 of 6.9 pM, more than 2600-fold selectivity over other related metalloenzymes.TargetsMMP-13 (Cell-free assay) 6.9 pM.

Potent and highly selective ROCK inhibitor: orally active.

InformationT-26c T-26c is a highly potent and selective inhibitor of matrix metalloproteinase-13 (MMP-13) with IC50 of 6.9 pM, more than 2600-fold selectivity over other related metalloenzymes.TargetsMMP-13 (Cell-free assay) 6.9 pM.

InformationT-26c T-26c is a highly potent and selective inhibitor of matrix metalloproteinase-13 (MMP-13) with IC50 of 6.9 pM, more than 2600-fold selectivity over other related metalloenzymes.TargetsMMP-13 (Cell-free assay) 6.9 pM.

InformationT-26c T-26c is a highly potent and selective inhibitor of matrix metalloproteinase-13 (MMP-13) with IC50 of 6.9 pM, more than 2600-fold selectivity over other related metalloenzymes.TargetsMMP-13 (Cell-free assay) 6.9 pM.

InformationT-26c T-26c is a highly potent and selective inhibitor of matrix metalloproteinase-13 (MMP-13) with IC50 of 6.9 pM, more than 2600-fold selectivity over other related metalloenzymes.TargetsMMP-13 (Cell-free assay) 6.9 pM.

InformationT-26c T-26c is a highly potent and selective inhibitor of matrix metalloproteinase-13 (MMP-13) with IC50 of 6.9 pM, more than 2600-fold selectivity over other related metalloenzymes.TargetsMMP-13 (Cell-free assay) 6.9 pM.

Potent and highly selective ROCK inhibitor: orally active.

Potent and highly selective ROCK inhibitor: orally active.

Potent and highly selective ROCK inhibitor: orally active.