Name |
5alpha-campestanol Campestanol Ergostanol (24S)24-Methylcholestan-3beta-ol |
Formula |
C28H50O |
Mw |
402.38616622 |
CAS RN |
474-60-2 |
C_ID |
C00007516
,
|
InChIKey |
ARYTXMNEANMLMU-JYZNDWCENA-N |
InChICode |
InChI=1S/C28H50O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h18-26,29H,7-17H2,1-6H3/t19-,20-,21+,22+,23-,24+,25+,26+,27-,28-/m1/s1 |
SMILES |
C1[C@@H](C[C@H]2[C@@](C1)([C@@H]1[C@H](CC2)[C@H]2[C@](CC1)([C@@H](CC2)[C@H](C)CC[C@H](C(C)C)C)C)C)O |
Start Substs in Alk. Biosynthesis (Prediction) |
|
Organism |
Kingdom |
Family |
Species |
Reference |
Amoebozoa | Physaridae | Physarum flavicomum | Ref. |
Amoebozoa | Physaridae | Physarum polycephalum | Ref. |
Plantae | Asteraceae | Calendula officinalis | Ref. |
Plantae | Cruciferae | Arabidopsis thaliana | Ref. |
Plantae | Poaceae | Oryza sativa | Ref. |
Plantae | Posidoniaceae | Posidonia oceanica | Ref. |
- | - | Caffea sp. | Ref. |
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zoom in
Organism | Physarum polycephalum | Reference | Lenfant,Phytochem.,9,(1970),2529-2535
Turner,Fungal Metabolites II,Academic Press,New York,NY,308 pp.(1983)
Bullock,J.Lipid Res.,17,(1976),565
Turner,Fungal Metabolites II,Academic Press, (1983),631 |
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