Activin and Inhibin

Empagliflozin-d 4 is deuterium labeled Empagliflozin. Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2.In VitroStable heavy isotopes of hydrogen, carbon, and other

Empagliflozin-d 4 is deuterium labeled Empagliflozin. Empagliflozin (BI 107730 is a selective sodium glucose cotransporter-2 (SGLT-2) inhibitor with an IC50 of 3.1 nM for human SGLT-2.In VitroStable heavy isotopes of hydrogen, carbon, and other

Emprumapimod (PF-07265803) hydrochloride is an orally active and selective inhibitor of p38α MAPK . Emprumapimod hydrochloride can be used for the research of dilated cardiomyopathy and acute inflammatory pain.Appearance:SolidIC50&amp: Target:p38αIn

EN40 is a potent, selective aldehyde dehydrogenase 3A1 (ALDH3A1) inhibitor as a covalent ligand, exhibits an IC 50 value of 2 uMIn VitroEN40 (10-1000 μM: 48 hours) shows inhibitory effecton ALDH3A1 activity and impairs A549 cell survival. MCE has

EN40 is a potent, selective aldehyde dehydrogenase 3A1 (ALDH3A1) inhibitor as a covalent ligand, exhibits an IC 50 value of 2 uMIn VitroEN40 (10-1000 μM: 48 hours) shows inhibitory effecton ALDH3A1 activity and impairs A549 cell survival. MCE has

EN40 is a potent, selective aldehyde dehydrogenase 3A1 (ALDH3A1) inhibitor as a covalent ligand, exhibits an IC 50 value of 2 uMIn VitroEN40 (10-1000 μM: 48 hours) shows inhibitory effecton ALDH3A1 activity and impairs A549 cell survival. MCE has

EN40 is a potent, selective aldehyde dehydrogenase 3A1 (ALDH3A1) inhibitor as a covalent ligand, exhibits an IC 50 value of 2 uMIn VitroEN40 (10-1000 μM: 48 hours) shows inhibitory effecton ALDH3A1 activity and impairs A549 cell survival. MCE has

EN40 is a potent, selective aldehyde dehydrogenase 3A1 (ALDH3A1) inhibitor as a covalent ligand, exhibits an IC 50 value of 2 uMIn VitroEN40 (10-1000 μM: 48 hours) shows inhibitory effecton ALDH3A1 activity and impairs A549 cell survival. MCE has

Endomorphin 1 acetate, a high affinity, highly selective agonist of the μ-opioid receptor ( K i : 1.11 nM), displays reasonable affinities for kappa 3 binding sites, with K i value between 20 and 30 nM. Endomorphin 1 acetate has antinociceptive

Endomorphin 1 acetate, a high affinity, highly selective agonist of the μ-opioid receptor ( K i : 1.11 nM), displays reasonable affinities for kappa 3 binding sites, with K i value between 20 and 30 nM. Endomorphin 1 acetate has antinociceptive

Endomorphin 1 acetate, a high affinity, highly selective agonist of the μ-opioid receptor ( K i : 1.11 nM), displays reasonable affinities for kappa 3 binding sites, with K i value between 20 and 30 nM. Endomorphin 1 acetate has antinociceptive

Endomorphin 2 TFA, a high affinity, highly selective agonist of the μ-opioid receptor , displays reasonable affinities for kappa 3 binding sites, with K i value between 20 and 30 nMForm:SolidIC50&amp: Target:Ki: 20-30 nM (kappa 3 opioid receptor).