P9129

5-Pregnen-3β-ol-20-one

≥98%

• Sinónimos: 3β-Hydroxy-5-pregnen-20-one, Pregnenolone
• Fórmula empírica (notación de Hill): C₂₁H₃₂O₂
• Número de CAS: 145-13-1
• Peso molecular: 316.48
• Beilstein: 2059026
• Número CE: 205-647-4
• Número MDL: MFCD00003628
• Código UNSPSC: 12352211
• ID de la sustancia en PubChem: 24899008
• NACRES: NA.77

Propiedades

• origen biológico: synthetic (organic)
• Nivel de calidad: 200
• Análisis: ≥98%
• formulario: powder
• solubilidad: ethanol: soluble 10 mg/mL, clear, colorless to faintly yellow
• grupo funcional: ketone
• Condiciones de envío: ambient
• temp. de almacenamiento: room temp
• cadena SMILES: [H][C@@]12CC=C3C[C@@H](O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@H](CC[C@@]24[H])C(C)=O
• InChI: 1S/C21H32O2/c1-13(22)17-6-7-18-16-5-4-14-12-15(23)8-10-20(14,2)19(16)9-11-21(17,18)3/h4,15-19,23H,5-12H2,1-3H3/t15-,16-,17+,18-,19-,20-,21+/m0/s1
• Clave InChI: ORNBQBCIOKFOEO-QGVNFLHTSA-N
• Información sobre el gen: human ... SERPINA6(866) ; rat ... Ar(24208)

Descripción

Aplicación

5-Pregnen-3β-ol-20-one is suitable for use:

• as a substrate for 3β-HSD at a concentration of 1 μg/mL to study the time-dependent effect of reduced oxygen tension on 3β-hydroxysteroid dehydrogenase (3β-HSD) activity
• as a progestin precursor to study the effects of splenic macrophages on progestin secretion of luteal cells
• in the testicular interstitial cell culture medium at a concentration of 15mg/mL

Acciones bioquímicas o fisiológicas

One of a small number of "neurosteroids," steroids synthesized in the brain rather than peripheral sources. Decreased levels of these neurosteroids has been implicated in rodent cognitive decline with age, but studies in humans have been contradictory.

Testosterone production in rats occurs in Leydig cells of the testis via the Δ⁴ pathway. Cholesterol is first converted to pregnenolone, then to progesterone, and finally to testosterone. Pregnenolone is the key neurosteroid synthesized in steroidogenic glands. It is also present as a sulfate ester that serves as an antagonist of GABAergic neurons by interacting with γ-aminobutyric acid (GABA) receptor.

Información de seguridad

• Código de clase de almacenamiento: 13 - Non Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Gloves, type N95 (US)