Pramipexole hydrochloride hydrate

glutamate analogs as an inhibitor of glutamate decarboxylase.

Spherical, hydrophobic polystyrene-divinylbenzene resin for SPE Features Hydrophobic polystyrene-divinylbenzene copolymer pH stability 1&ndash14 High-purity material with highest reproducibility and lowest blank values due to an optimized manufactur

Spherical, hydrophobic polystyrene-divinylbenzene resin for SPE Features Hydrophobic polystyrene-divinylbenzene copolymer pH stability 1&ndash14 High-purity material with highest reproducibility and lowest blank values due to an optimized manufactur

Spherical, hydrophobic polystyrene-divinylbenzene resin for SPE Features Hydrophobic polystyrene-divinylbenzene copolymer pH stability 1&ndash14 High-purity material with highest reproducibility and lowest blank values due to an optimized manufactur

Biochem/physiol Actions CP-100263 is an NK-1 neurokinin receptor antagonist. Other Notes This compound was developed by Pfizer for Neuroscience research .

Biochem/physiol Actions CP-100263 is an NK-1 neurokinin receptor antagonist. Other Notes This compound was developed by Pfizer for Neuroscience research .

Application CP-31398 dihydrochloride hydrate has been used as a p53 stabilizer: to evaluate its effects on the upregulation of miRNA in human neuroblastoma cells to study its effects on arsenic trioxide (ATO) stabilization of p53 folding to

Application CP-31398 dihydrochloride hydrate has been used as a p53 stabilizer: to evaluate its effects on the upregulation of miRNA in human neuroblastoma cells to study its effects on arsenic trioxide (ATO) stabilization of p53 folding to

Biochem/physiol Actions CP-93129 is a potent and selective 5-HT 1B agonist. Other Notes This compound was developed by Pfizer for Neuroscience research .

Biochem/physiol Actions CP-93129 is a potent and selective 5-HT 1B agonist. Other Notes This compound was developed by Pfizer for Neuroscience research .

DL-3-Phenylserine hydrate

Application H-89 dihydrochloride hydrate has been used in the inhibition of protein kinase A in Leydig cells, primary calvarial osteoblasts (pOBs), rat granulosa cell line (LH-15 cells) and human umbilical vein endothelial cells (HUVECs).