GC Mass Selective Detectors

1-Methylpiperazine is a heterocyclic diamine used as a versatile building block and intermediate in organic synthesis. Application 1-Methylpiperazine was used as mimic template in the preparation of molecularly imprinted microspheres (MIMs) .

Otenabant (CP-945598) HCl is a potent and selective cannabinoid receptor CB1 antagonist with Ki of 0.7 nM, exhibits 10,000-fold greater selectivity against human CB2 receptorA selective and high affinity CB1 antagonist.

Escitalopram is an inhibitor of SR-2A.

Escitalopram is an inhibitor of SR-2A.

InformationG150 G150 is a potent and highly selective human cyclic GMP-AMP synthase (cGAS) inhibitor with IC50 of 10.2 nM.Targetsh-cGAS (Cell-free assay) 10.2 nMIn vitroThe most potent h-cGAS-specific derivative with 2-amino pyridine (G150) shows

InformationG150 G150 is a potent and highly selective human cyclic GMP-AMP synthase (cGAS) inhibitor with IC50 of 10.2 nM.Targetsh-cGAS (Cell-free assay) 10.2 nMIn vitroThe most potent h-cGAS-specific derivative with 2-amino pyridine (G150) shows

InformationG150 G150 is a potent and highly selective human cyclic GMP-AMP synthase (cGAS) inhibitor with IC50 of 10.2 nM.Targetsh-cGAS (Cell-free assay) 10.2 nMIn vitroThe most potent h-cGAS-specific derivative with 2-amino pyridine (G150) shows

InformationG150 G150 is a potent and highly selective human cyclic GMP-AMP synthase (cGAS) inhibitor with IC50 of 10.2 nM.Targetsh-cGAS (Cell-free assay) 10.2 nMIn vitroThe most potent h-cGAS-specific derivative with 2-amino pyridine (G150) shows

InformationG150 G150 is a potent and highly selective human cyclic GMP-AMP synthase (cGAS) inhibitor with IC50 of 10.2 nM.Targetsh-cGAS (Cell-free assay) 10.2 nMIn vitroThe most potent h-cGAS-specific derivative with 2-amino pyridine (G150) shows

InformationG150 G150 is a potent and highly selective human cyclic GMP-AMP synthase (cGAS) inhibitor with IC50 of 10.2 nM.Targetsh-cGAS (Cell-free assay) 10.2 nMIn vitroThe most potent h-cGAS-specific derivative with 2-amino pyridine (G150) shows

InformationGK921 GK921 is a transglutaminase 2 (TGase 2) inhibitor with an IC50 of 8.93 μM under a modified assay condition.TargetsTGase 2 8.93 μM.

GlyT1 Inhibitor 1 is a potent and selective GlyT1 inhibitor with an IC 50 of 38 nM for rGlyT1 Antipsychotic activityIn VivoGlyT1 Inhibitor 1 (Compound 46) demonstrates in vivo efficacy in a rat novel object recognition (NOR) assay after oral dosing