Fucosterol
Compound with free spectra: 4 NMR
| SpectraBase Compound ID | 10qQ4ddUoED |
|---|---|
| InChI | InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,10,19-20,23-27,30H,8-9,11-18H2,1-6H3/b21-7-/t20-,23+,24+,25-,26+,27+,28+,29-/m1/s1 |
| InChIKey | OSELKOCHBMDKEJ-WGMIZEQOSA-N |
| Mol Weight | 412.7 g/mol |
| Molecular Formula | C29H48O |
| Exact Mass | 412.370516 g/mol |
| Enantiomer InChIKey | OSELKOCHBMDKEJ-XHJXRJPQSA-N |
| Copyright | Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|
| Copyright | Copyright © 2016-2021 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- Isofucosterol
Isostelliferasterol
Cholest-5-en-3-ol, 24-propylidene-, (3.beta.)-
(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-yloct-5-en-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
E-28-Methylxestosterol
Z-28-Methylxestosterol
29-HYDROXYSTIGMASTA-5,24(28)-DIEN-3-BETA-OL
27-Norergosta-5,24-dien-3-ol, (3.beta.,24E)-
27-Norstigmasta-5,24-dien-3-ol, (3.beta.,24E)-
(6R)-6-[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-oxidanyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-heptan-3-one
| Title | Journal or Book | Year |
|---|---|---|
| Compositions of Royal Jelly II. Organic Acid Glycosides and Sterols of the Royal Jelly of Honeybees (Apis mellifera) | CHEMICAL & PHARMACEUTICAL BULLETIN | 2007 |
| 13C NMR Spectra of Δ24(28) Phytosterols | Organic Magnetic Resonance | 1980 |