tcsc1970 Pregnenolone

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Product Description

Pregnenolone acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, reduces several effects of tetrahydrocannabinol (THC).

IC50 & Target: Cannabinoid CB1 receptor[1]

In Vitro: The effect of THC is significantly attenuated when slices are pre-treated with Pregnenolone 100 nM (15.1±1.8 % of inhibition). These effects are likely due to a pre-synaptic action of Pregnenolone. Thus, Pregnenolone blocks the increase in paired-pulse ratio (PPR) induced by THC but does not modify either the amplitude or the decay time of miniature EPSC (mEPSC)[1].

In Vivo: Pregnenolone administration (2-6 mg/kg) blocks THC-induced food-intake in Wistar rats and in C57BL/6N mice, and blunts the memory impairment induced by THC in mice, but it does not modify these behaviors per se. Injections of Pregnenolone (2 and 4mg/kg) before each self-administration session reduce the intake of WIN 55,212-2 and reduce the break-point in a progressive ratio schedule[1].

Information

CAS No145-13-1
FormulaC21H32O2
Clinical Informationclinicalinformation
PathwayAutophagy
GPCR/G Protein
Metabolic Enzyme/Protease
TargetAutophagy
Cannabinoid Receptor
Endogenous Metabolite

Specifications

Purity / Grade>98%
SolubilityDMSO : 12.5 mg/mL (39.50 mM; Need ultrasonic); H2O : < 0.1 mg/mL (insoluble)
Smilessmiles

Misc Information

Alternative NamesArthenolone;3β-Hydroxy-5-pregnen-20-one
Observed Molecular Weight316.48
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