Molecular structure of Lumisterol, CAS Number: 474-69-1
Lumisterol (CAS 474-69-1)
Alternate Names:
(3β,9β,10α,22E)-Ergosta-5,7,22-trien-3-ol; 9.beta.,10α-Ergosta-5,7,22-trien-3-ol; 9β,10α-Ergosta-5,7,22-trien-3.beta.-ol; 9β,10α-Ergosterol
CAS Number:
474-69-1
Molecular Weight:
396.65
Molecular Formula:
C28H44O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
Lumisterol is a steroid hormone that occurs naturally in the human body, where it originates from cholesterol and is synthesized in the adrenal glands, ovaries, and testes. It has been observed to participate in the maintenance of salt and water levels, the timing of biological cycles, and the functioning of immune responses. Additionally, it is thought to act through binding to specific receptors, initiating a series of biochemical events that culminate in the observed effects on bodily functions.
Lumisterol (CAS 474-69-1) References
- Ergosterol from the soilborne fungus Ganoderma boninense. | Toh Choon, RL., et al. 2012. J Basic Microbiol. 52: 608-12. PMID: 22143962
- Generation of potentially bioactive ergosterol-derived products following pulsed ultraviolet light exposure of mushrooms (Agaricus bisporus). | Kalaras, MD., et al. 2012. Food Chem. 135: 396-401. PMID: 22868105
- Lumisterol to Tachysterol Photoisomerization in EPA Glass at 77 K. A Comparative Study. | Bayda, M., et al. 2017. J Phys Chem A. 121: 2331-2342. PMID: 28234492
- A new xanthone from the fungus Apiospora montagnei. | Arthan, S., et al. 2017. Nat Prod Res. 31: 1766-1771. PMID: 28278634
- Two approaches to 14,15-secoergostane intermediates for the synthesis of strophasterols. | Fukuda, Y., et al. 2018. Biosci Biotechnol Biochem. 82: 986-992. PMID: 29587618
- Oral Intake of Lumisterol Affects the Metabolism of Vitamin D. | Kotwan, J., et al. 2021. Mol Nutr Food Res. 65: e2001165. PMID: 34061442
- Selective ability of rat 7-Dehydrocholesterol reductase (DHCR7) to act on some 7-Dehydrocholesterol metabolites but not on lumisterol metabolites. | Tuckey, RC., et al. 2021. J Steroid Biochem Mol Biol. 212: 105929. PMID: 34098080
- A new look at edible and medicinal mushrooms as a source of ergosterol and ergosterol peroxide - UHPLC-MS/MS analysis. | Nowak, R., et al. 2022. Food Chem. 369: 130927. PMID: 34461517
- Ergosterol analogs as inhibitors of cyclin dependent kinase 8. | Siapkaras, PD. and Solum, EJ. 2022. Steroids. 178: 108965. PMID: 35065996
- Ergosterol isolated from cloud ear mushroom (Auricularia polytricha) attenuates bisphenol A-induced BV2 microglial cell inflammation. | Sillapachaiyaporn, C., et al. 2022. Food Res Int. 157: 111433. PMID: 35761673
- Modulation of yeast Erg1 expression and terbinafine susceptibility by iron bioavailability. | Jordá, T., et al. 2022. Microb Biotechnol. 15: 2705-2716. PMID: 35837730
- Neuroprotective effects of ergosterol against TNF-α-induced HT-22 hippocampal cell injury. | Sillapachaiyaporn, C., et al. 2022. Biomed Pharmacother. 154: 113596. PMID: 36030584
- Optimization of ultrasound-assisted production of ergosterol from Penicillium brevicompactum by Taguchi statistical method. | Vali, N., et al. 2022. Biotechnol Lett. 44: 1217-1230. PMID: 36057882
- Prevention of hospital pathogen biofilm formation by antimicrobial peptide KWI18. | Lima, LS., et al. 2022. Microb Pathog. 172: 105791. PMID: 36150557
- Hepatoprotective Constituents of Macrocybe gigantea (Agaricomycetes) from India. | Kumar, SN., et al. 2022. Int J Med Mushrooms. 24: 35-47. PMID: 36374947
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Lumisterol, 2.5 mg | sc-489325 | 2.5 mg | $627.00 |