20ALPHA-HYDROXYCHOLESTEROL
- Product Name
- 20ALPHA-HYDROXYCHOLESTEROL
- CAS No.
- 516-72-3
- Chemical Name
- 20ALPHA-HYDROXYCHOLESTEROL
- Synonyms
- C05500;20-hydroxycholesterol;20A-HYDROXYCHOLESTEROL;20α-Hydroxy Cholesterol;Cholesterol Impurity 32;5-Cholestene-3B,20a-diol;5-cholestene-3β,20α-diol;Cholest-5-ene-3,20a-diol;Cholest-5-ene-3β,20-diol;20[S]-HYDROXYCHOLESTEROL
- CBNumber
- CB2372501
- Molecular Formula
- C27H46O2
- Formula Weight
- 402.65
- MOL File
- 516-72-3.mol
20ALPHA-HYDROXYCHOLESTEROL Property
- Melting point:
- 136-137°C
- Boiling point:
- 512.3±23.0 °C(Predicted)
- Density
- 1.03±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,2-8°C
- solubility
- Soluble in DMSO or in Ethanol.
- form
- Solid
- pka
- 15.04±0.70(Predicted)
- color
- White
- Stability:
- Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months.
Safety
- WGK Germany
- 3
N-Bromosuccinimide Price
- Product number
- H6378
- Product name
- 20α-Hydroxycholesterol
- Purity
- analytical standard
- Packaging
- 5mg
- Price
- $187.15
- Updated
- 2025/07/31
- Product number
- 20103
- Product name
- 20(S)-hydroxy Cholesterol
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $50
- Updated
- 2024/03/01
- Product number
- 20103
- Product name
- 20(S)-hydroxy Cholesterol
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $111
- Updated
- 2024/03/01
- Product number
- 20103
- Product name
- 20(S)-hydroxy Cholesterol
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $195
- Updated
- 2024/03/01
- Product number
- 4474
- Product name
- 20(S)-Hydroxycholesterol
- Purity
- ≥95%(HPLC)
- Packaging
- 10
- Price
- $184
- Updated
- 2021/12/16
20ALPHA-HYDROXYCHOLESTEROL Chemical Properties,Usage,Production
Description
20(S)-hydroxy Cholesterol is an allosteric agonist of the smoothened (Smo) receptor that activates the hedgehog (Hh) signaling pathway with an EC50 value of approxiately 3 μM in a gene transcription reporter assay using NIH3T3 cells. 20(S)-hydroxy Cholesterol is necessary for normal Hh signaling. It induces Smo accumulation in primary cilia, an early event in signaling, and binds to the extracellular, cysteine-rich domain of Smo. 20(S)-hydroxy Cholesterol also stimulates osteogenic differentiation of pluripotent bone marrow stromal cells, a process mediated via Hh and Notch signaling.
Chemical Properties
White Solid
Uses
A metabolite of Cholesterol. Cholesterol oxidation product having cytotoxicity effects
Uses
A metabolite of Cholesterol (C432501). Cholesterol oxidation product having cytotoxicity effects.
Definition
ChEBI: An oxysterol that is cholesterol substituted by a hydroxy group at position 20.
storage
Store at -20°C
References
[1] An oxysterol signaling pathway mediated by the nuclear receptor LXR7alpha
[2] HOA TON KHA. Oxysterols Regulate Differentiation of Mesenchymal Stem Cells: Pro-Bone and Anti-Fat†[J]. Journal of Bone and Mineral Research, 2009, 19 5: 830-840. DOI:10.1359/jbmr.040115
[3] WOO-KYUN KIM. Osteogenic oxysterol, 20(S)-hydroxycholesterol, induces notch target gene expression in bone marrow stromal cells[J]. Journal of Bone and Mineral Research, 2010, 25 4: 782-795. DOI:10.1359/jbmr.091024
[4] JENNIFER R DWYER. Oxysterols are novel activators of the hedgehog signaling pathway in pluripotent mesenchymal cells.[J]. The Journal of Biological Chemistry, 2007, 282 12: 8959-8968. DOI:10.1074/jbc.m611741200
[5] DANIEL NEDELCU. Oxysterol binding to the extracellular domain of Smoothened in Hedgehog signaling[J]. Nature chemical biology, 2013, 9 9: 557-564. DOI:10.1038/nchembio.1290
[6] YU-SHIUAN CHENG. A proteome-wide map of 20(S)-hydroxycholesterol interactors in cell membranes[J]. Nature chemical biology, 2021, 17 12: 1271-1280. DOI:10.1038/s41589-021-00907-2
20ALPHA-HYDROXYCHOLESTEROL Preparation Products And Raw materials
Raw materials
Preparation Products
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