CAS 64744-50-9
:2-Azaspiro[4.5]decan-3-ona
- 2-Azaspiro[4.5]decan-3-one
- 3,3-Pentamethylene-4-butyrolactam
- Gabapentin-lactams
- Gabapentin-lactam
4,4-Pentamethylene-2-pyrrolidone
CAS:Fórmula:C9H15NOPureza:>98.0%(GC)Cor e Forma:White to Almost white powder to crystalPeso molecular:153.23Gabapentin Related Compound A (2-Azaspiro[4.5]decan-3-one)
CAS:Lactams not elsewhere specified or includedFórmula:C9H15NOCor e Forma:Off-White PowderPeso molecular:153.115364,4-Pentamethylene-2-pyrrolidinone
CAS:4,4-Pentamethylene-2-pyrrolidinoneFórmula:C9H15NOPureza:98%Cor e Forma: white solidPeso molecular:153.22g/molGabapentin EP Impurity A (Gabapentin USP Related Compound A)
CAS:Fórmula:C9H15NOCor e Forma:White To Off-White SolidPeso molecular:153.23Gabapentin-lactam 100 µg/mL in Acetonitrile
CAS:Fórmula:C9H15NOCor e Forma:Single SolutionPeso molecular:153.22Gabapentin Lactam-d6
CAS:Produto ControladoApplications Gabapentin Lactam-d6, is the labeled analogue of Gabapentin Lactam (G117275), that reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington’s disease. It opens mitochondrial ATP-dependent potassium channels.
References Zucker, B.,et al.: Naunyn Schmiedebergs Arch. Pharmacol., 370, 131 (2004)Fórmula:C9H9D6NOCor e Forma:Off White SolidPeso molecular:159.26Gabapentin Related Compound A
CAS:Produto ControladoImpurity Gabapentin EP Impurity A; Gabapentin USP Related Compound A
Applications Gabapentin Lactam (Gabapentin EP Impurity A; Gabapentin USP Related Compound A) reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington’s disease. It opens mitochondrial ATP-dependent potassium channels.
References Zucker, B.,et al.: Naunyn Schmiedebergs Arch. Pharmacol., 370, 131 (2004)Fórmula:C9H15NOCor e Forma:WhitePeso molecular:153.22Gabapentin related compound A
CAS:Gabapentin related compound A is a gamma-aminobutyric acid analogue that has been shown to reduce diabetic neuropathy in vivo. It binds to the GABA-B receptor, which is a ligand-gated chloride channel. Gabapentin related compound A produces a rapid increase in chloride ion conductance and hyperpolarization of neurons, leading to its neuroprotective effect. The chemical stability of this drug has been investigated by hydrolysis with hydrochloric acid under various conditions. The reaction mechanism for gabapentin related compound A is similar to that of gabapentin, but it has an analog structure that confers additional stability.
Fórmula:C9H15NOPureza:Min. 95%Cor e Forma:White To Off-White SolidPeso molecular:153.22 g/mol












