Synthetic organic

Impentamine dihydrobromide is a selective H|3|receptor antagonist. This compound displays &gt:30000-fold selectivity over H|1|and H|2|receptors. In SK-N-MC cells expressing human H|3|receptors, this can act as a partial agonist. Impentamine

Impentamine dihydrobromide is a selective H|3|receptor antagonist. This compound displays &gt:30000-fold selectivity over H|1|and H|2|receptors. In SK-N-MC cells expressing human H|3|receptors, this can act as a partial agonist. Impentamine

improgan.

improgan.

impromidine.

impromidine.

InformationIMR-1 IMR-1 is a novel class of Notch inhibitors targeting the transcriptional activation with IC50 of 26 μM.TargetsNotch (Cell-free assay) 26 μMCell Research(from reference)Cell lines：OE33 and 786-0 cells Concentrations：5, 10, 15, 25 μM.

InformationIMR-1 IMR-1 is a novel class of Notch inhibitors targeting the transcriptional activation with IC50 of 26 μM.TargetsNotch (Cell-free assay) 26 μMCell Research(from reference)Cell lines：OE33 and 786-0 cells Concentrations：5, 10, 15, 25 μM.

InformationIMR-1 IMR-1 is a novel class of Notch inhibitors targeting the transcriptional activation with IC50 of 26 μM.TargetsNotch (Cell-free assay) 26 μMCell Research(from reference)Cell lines：OE33 and 786-0 cells Concentrations：5, 10, 15, 25 μM.

InformationIMR-1 IMR-1 is a novel class of Notch inhibitors targeting the transcriptional activation with IC50 of 26 μM.TargetsNotch (Cell-free assay) 26 μMCell Research(from reference)Cell lines：OE33 and 786-0 cells Concentrations：5, 10, 15, 25 μM.

InformationIMR-1 IMR-1 is a novel class of Notch inhibitors targeting the transcriptional activation with IC50 of 26 μM.TargetsNotch (Cell-free assay) 26 μMCell Research(from reference)Cell lines：OE33 and 786-0 cells Concentrations：5, 10, 15, 25 μM.

IMR-1.