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Category:natural substances and extractives
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
| Assay: | 95.00 to 100.00
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| Food Chemicals Codex Listed: | No |
| Soluble in: |
| | water, 0.000181 mg/L @ 25 °C (est) |
Organoleptic Properties:
| Odor and/or flavor descriptions from others (if found). |
Cosmetic Information:
Suppliers:
Safety Information:
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| Hazards identification |
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| Classification of the substance or mixture |
| GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
| None found. |
| GHS Label elements, including precautionary statements |
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| Pictogram | |
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| Hazard statement(s) |
| None found. |
| Precautionary statement(s) |
| None found. |
| Oral/Parenteral Toxicity: |
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Not determined
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| Dermal Toxicity: |
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Not determined
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| Inhalation Toxicity: |
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Not determined
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Safety in Use Information:
| Category: | | natural substances and extractives |
| Recommendation for 22,23-dihydroergosterol usage levels up to: | | | not for fragrance use.
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| Recommendation for 22,23-dihydroergosterol flavor usage levels up to: |
| | not for flavor use.
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Safety References:
| EPI System: View |
| AIDS Citations:Search |
| Cancer Citations:Search |
| Toxicology Citations:Search |
| EPA ACToR:Toxicology Data |
| EPA Substance Registry Services (SRS):Registry |
| Laboratory Chemical Safety Summary :5326970 |
| National Institute of Allergy and Infectious Diseases:Data |
| (3S,9S,10R,13R,14R,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol |
| Chemidplus:0000516790 |
References:
| | (3S,9S,10R,13R,14R,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol |
| NIST Chemistry WebBook: | Search Inchi |
| Pubchem (cid): | 5326970 |
| Pubchem (cas): | 516-79-0 |
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
| (3S,9S,10R,13R,14R,17R)-17-[(2R,5S)-5,6- | dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol |
Articles:
| PubMed:Simultaneous HPLC determination of ergosterol and 22,23-dihydroergosterol in Flammulina velutipes sterol-loaded microemulsion. |
| PubMed:Enhanced oral bioavailability and tissue distribution of a new potential anticancer agent, Flammulina velutipes sterols, through liposomal encapsulation. |
| PubMed:Cytotoxic effect of novel Flammulina velutipes sterols and its oral bioavailability via mixed micellar nanoformulation. |
| PubMed:Enhanced oral bioavailability of a sterol-loaded microemulsion formulation of Flammulina velutipes, a potential antitumor drug. |
| PubMed:Vitamin D4 in mushrooms. |
| PubMed:Human cytochrome P450scc (CYP11A1) catalyzes epoxide formation with ergosterol. |
| PubMed:Vitamin D and sterol composition of 10 types of mushrooms from retail suppliers in the United States. |
| PubMed:[Search for and structural elucidation of medicinal products from the vegetable kingdom (crude drugs and plant materials)]. |
| PubMed:Identification of a sterol Delta7 reductase gene involved in desmosterol biosynthesis in Mortierella alpina 1S-4. |
| PubMed:Characterization of Saccharomyces cerevisiae CYP61, sterol delta22-desaturase, and inhibition by azole antifungal agents. |
| PubMed:[Substrate specificity of the biotransformation enzymes in a Nocardia erythropolis culture]. |
| PubMed:[Effect of a subinhibitory dose of amphotericin B on cellular fatty acid and sterol composition of Candida albicans]. |
| PubMed:Critical role of ring structure in the differential uptake of cholesterol and plant sterols by membrane preparations in vitro. |
| PubMed:Characterization of a Saccharomyces cerevisiae mutant, N22, defective in ergosterol synthesis and preparation of [28-14C]ergosta-5,7-dien-3 beta-ol with the mutant. |
| PubMed:Uptake of 7-dehydro derivatives of cholesterol, campesterol, and beta-sitosterol by rat erythrocytes, jejunal villus cells, and brush border membranes. |
| PubMed:Involvement of cytochrome P-450 in delta 22-desaturation in ergosterol biosynthesis of yeast. |
| PubMed:Unsaturated steroids. Part 7. A simple synthesis of 22,23-dihydroergosterol. |
| PubMed:Unsaturated steroids. Part I. Synthesis of 22,23-dihydroergosterol. |
| PubMed:Synthetic use of steroidal ring B diene protection: 22,23-dihydroergosterol. |
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3D/inchi