Coprostanone
Modify Date: 2024-01-02 17:44:17
Coprostanone structure
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Common Name | Coprostanone | ||
|---|---|---|---|---|
| CAS Number | 566-88-1 | Molecular Weight | 386.654 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 452.9±13.0 °C at 760 mmHg | |
| Molecular Formula | C27H46O | Melting Point | 127-131ºC | |
| MSDS | Chinese USA | Flash Point | 219.3±12.1 °C | |
Use of Coprostanone5alpha-Cholestan-3-one is a substrate of cholestenone 5alpha-reductase. |
| Name | 5α-cholestan-3-one |
|---|---|
| Synonym | More Synonyms |
| Density | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 452.9±13.0 °C at 760 mmHg |
| Melting Point | 127-131ºC |
| Molecular Formula | C27H46O |
| Molecular Weight | 386.654 |
| Flash Point | 219.3±12.1 °C |
| Exact Mass | 386.354858 |
| PSA | 17.07000 |
| LogP | 9.64 |
| Vapour Pressure | 0.0±1.1 mmHg at 25°C |
| Index of Refraction | 1.498 |
| Storage condition | -20℃ |
| Precursor 7 | |
|---|---|
| DownStream 8 | |
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In vitro modulation of rat adipocyte ghost membrane fluidity by cholesterol oxysterols.
Experientia 51(7) , 731-7, (1995) The effects of cholesterol and cholesterol-derived oxysterols (cholestanone, cholestenone, coprostanone and epicoprostanol) on adipocyte ghost membrane fluidity were studied using a fluorescence depol... |
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Diet, nutrition intake, and metabolism in populations at high and low risk for colon cancer. Metabolism of neutral sterols.
Am. J. Clin. Nutr. 40(4 Suppl) , 931-6, (1984) Cholesterol and its metabolites, together with bile acids, are implicated as risk factors in the genesis and progression of colon cancer. This study was designed to determine differences in the neutra... |
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Potentiation of beta-adrenoceptor agonist mediated-lipolysis by cholesterol-derived oxysterols.
Biochem. Mol. Biol. Int. 35(6) , 1349-58, (1995) Cholesterol-derived oxysterols such as cholestanol, cholestanone and coprostanone were able to potentiate epinephrine-induced lipolysis in intact rat adipocytes but not cholesterol. The relative poten... |
| 5alpha-Cholestanone |
| 5A-Cholestan-3-one |
| 5α-Cholestan-3-one |
| 5a-Cholestanone |
| 5α-Cholestane-3-one |
| 3-Keto-5alpha-cholestane |
| 5alpha-Coprostanone |
| (5α)-Cholestan-3-one |
| 5alpha-cholestan-3-one |
| (5S,8R,9S,10S,13R,14S,17R)-10,13-Dimethyl-17-[(2R)-6-methyl-2-heptanyl]hexadecahydro-3H-cyclopenta[a]phenanthren-3-one |
| Cholestan-3-one, (5α)- |
| 5α-Cholestan-3-one (8CI) |
| 5alpha-Cholestane-3-one |
| Coprostanone |
| (5S,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one |
| MFCD00065901 |