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Pregnenolone
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Product Name Pregnenolone
Price: $31 / 20mg
Catalog No.: CN02584
CAS No.: 145-13-1
Molecular Formula: C21H32O2
Molecular Weight: 316.5 g/mol
Purity: >=98%
Type of Compound: Steroids
Physical Desc.: Cryst.
Source: The roots of Dictamnus dasycarpus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
SMILES: O[C@H]1CC[C@]2(C(=CC[C@@H]3[C@@H]2CC[C@]2([C@H]3CC[C@@H]2C(=O)C)C)C1)C
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Description Pregnenolone acts as a signaling-specific inhibitor of cannabinoid CB1 receptor, reduces several effects of tetrahydrocannabinol (THC).
Target CB1 Receptor Human Endogenous Metabolite
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].
Animal Admin Mice and Rats[1] Adult male Wistar rats (weighing 320-340g), Sprague Dawley male rats (weighing 330-350g), C57BL/6N mice (2-3 months) and CD1 mice (weighing 25-30 g at the beginning of the experiments) are used. Pregnenolone is injected subcutaneously (sc). The injection volumes are 1 mL/kg of body weight for rats and 10 mL/kg for mice[1].
Density1.1±0.1 g/cm3
Boiling Point443.3±45.0 °C at 760 mmHg
Flash Point188.9±21.3 °C
Exact Mass316.240234
PSA37.30000
LogP4.52
Vapour Pressure0.0±2.4 mmHg at 25°C
Storage condition2~8℃