Avenasterol
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| Names | |
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| IUPAC name
(3β,24Z)-Stigmasta-7,24(28)-dien-3-ol
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| Systematic IUPAC name
(3S,5S,10S,13R)-10,13-Dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol | |
| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
PubChemCID
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| UNII | |
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| Properties | |
| C29H48O | |
| Molar mass | 412.702g·mol−1 |
| Melting point | 118–120 °C (244–248 °F; 391–393 K) |
Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).
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Avenasterol,orΔ-7-Avenasterolis a natural,stigmastane-typesterol.[1]
References
[edit]- ^Cederberg, H; Gylling, H; Miettinen, TA; Paananen, J; Vangipurapu, J; Pihlajamäki, J; Kuulasmaa, T; Stančáková, A; Smith, U; Kuusisto, J; Laakso, M (2013). Travis, Alexander J (ed.)."Non-cholesterol sterol levels predict hyperglycemia and conversion to type 2 diabetes in Finnish men".PLOS ONE.8(6): e67406.Bibcode:2013PLoSO...867406C.doi:10.1371/journal.pone.0067406.PMC3696087.PMID23840693.
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