H1015

25-Hydroxycholesterol

≥98%

• Sinónimos: 5-Cholestene-3β,25-diol
• Fórmula empírica (notación de Hill): C₂₇H₄₆O₂
• Número de CAS: 2140-46-7
• Peso molecular: 402.65
• Beilstein: 3161259
• Número MDL: MFCD00057815
• Código UNSPSC: 41141804
• eCl@ss: 39023139
• ID de la sustancia en PubChem: 329815150
• NACRES: NA.77

Propiedades

• origen biológico: synthetic (organic)
• Ensayo: ≥98%
• Formulario: powder
• Condiciones de envío: ambient
• temp. de almacenamiento: room temp
• cadena SMILES: [H][C@@]12[C@]([C@](CC[C@H](O)C3)(C)C3=CC2)([H])CC[C@@]4(C)[C@@]1([H])CC[C@]4([H])[C@]([H])(C)CCCC(C)(O)C
• InChI: 1S/C27H46O2/c1-18(7-6-14-25(2,3)29)22-10-11-23-21-9-8-19-17-20(28)12-15-26(19,4)24(21)13-16-27(22,23)5/h8,18,20-24,28-29H,6-7,9-17H2,1-5H3/t18-,20+,21+,22-,23+,24+,26+,27-/m1/s1
• Clave InChI: INBGSXNNRGWLJU-ZHHJOTBYSA-N

Descripción

Aplicación

25-Hydroxycholesterol was used to treat mouse neuroblastoma cells to activate the ABCA1 signaling and in studies related to fatty acid metabolism.

Acciones bioquímicas o fisiológicas

25-Hydroxycholesterol is a side-chain oxysterol that reportedly triggers activation of a number of cholesterol molecules. This triggers their movement from cell membrane to the endoplasmic reticulum (ER). 25-Hydroxycholesterol affects the immune system and has a key role in the pathogenesis of atherosclerosis.

Suppresses the cleavage of sterol regulatory element binding proteins (SREBPs). 25-Hydroxycholesterol induces apoptosis through down-regulation of Bcl-2 expression and activation of caspases.

Nota de preparación

A stock solution of 25-Hydroxycholesterol may be prepared in ethanol and dissolved in cell culture medium to give a final concentration of 1 mg/ml.

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable