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| | CEREVISTEROL Basic information |
| Product Name: | CEREVISTEROL | | Synonyms: | (22E)-5α-Ergosta-7,22-diene-3β,5,6β-triol;(22E)-Ergosta-7,22-diene-3β,5α,6β-triol;(22E,24R)-24-Methyl-5α-cholesta-7,22-diene-3β,5,6β-triol;(22E,24R)-5α-Ergosta-7,22-diene-3β,5,6β-triol;(22E,24R)-Ergosta-7,22-diene-3β,5α,6β-triol;CEREVISTEROL;Beer sterol;Ergosta-7,22-diene-3,5,6-triol,(3b,5a,6b,22E)- | | CAS: | 516-37-0 | | MF: | C28H46O3 | | MW: | 430.66 | | EINECS: | | | Product Categories: | | | Mol File: | 516-37-0.mol |  |
| | CEREVISTEROL Chemical Properties |
| Melting point | >240 °C | | Boiling point | 535.0±50.0 °C(Predicted) | | density | 1.08±0.1 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | pka | 13.52±0.70(Predicted) | | form | Powder | | color | White to off-white |
| | CEREVISTEROL Usage And Synthesis |
| Uses | Cerevisterin is a metabolite from endophytic fungus Mollisia. | | Definition | ChEBI: An ergostanoid that is (22E)-ergosta-7,22-diene substituted by hydroxy groups at positions 3, 5 and 6 (the 3beta,5alpha,6beta stereoisomer). It has been isolated from the fungus, Xyl
ria species. | | target | DNA/RNA Synthesis |
| | CEREVISTEROL Preparation Products And Raw materials |
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