1-ALPHA,25-DIHYDROXYVITAMIN-D3
Compound with spectra: 5 NMR, and 1 MS (GC)
| SpectraBase Compound ID | GqazjACbOg0 |
|---|---|
| InChI | InChI=1S/C27H44O3/c1-18(8-6-14-26(3,4)30)23-12-13-24-20(9-7-15-27(23,24)5)10-11-21-16-22(28)17-25(29)19(21)2/h10-11,18,22-25,28-30H,2,6-9,12-17H2,1,3-5H3/b20-10+,21-11-/t18-,22-,23-,24+,25+,27-/m1/s1 |
| InChIKey | GMRQFYUYWCNGIN-NKMMMXOESA-N |
| Mol Weight | 416.6 g/mol |
| Molecular Formula | C27H44O3 |
| Exact Mass | 416.329045 g/mol |
| Enantiomer InChIKey | GMRQFYUYWCNGIN-FAUDWNASSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | F-70-8521-2 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 1-ALPHA,25-DIHYDROXY-CHOLECALCIFEROL;VITAMIN-D-DERIVATIVE
- 1-ALPHA,25-DIHYDROXY-20-EPI-VITAMIN-D3;1-ALPHA,25(OH)-20-EPI-D3
- (1R,3S,5Z)-5-[(2E)-2-[(1R,3aS,7aR)-1-[(1R)-5-hydroxy-1,5-dimethyl-hexyl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylene-cyclohexane-1,3-diol
(5E)-5-[(2Z)-2-[1-(5-hydroxy-1,5-dimethyl-hexyl)-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylene-cyclohexane-1,3-diol
1.alpha.-18O-1,25-dihydroxycholecalciferol
1a,25-Dihydroxy-cholecalciferol
1.beta.,25-Diydroxy-3-epivitamin D3
1.alpha.,25-Diydroxy-3-epivitamin D3
(5E)-5-[(2Z)-2-[1-(5-hydroxy-1,5-dimethyl-hexyl)-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylene-cyclohexane-1,3-diol
9,10-Secocholesta-5,7,10(19)-triene-1,3,25-triol, (1.alpha.,3.beta.,5Z,7E)-
5,6-TRANS-1-ALPHA,25-DIHYDROXYVITAMIN-D3
1-Hydroxy-25-fluorovitamin D3
9,10-Secocholesta-5,7,10(19)-triene-1,3-diol, 25-[(trimethylsilyl)oxy]-, (3.beta.,5Z,7E)-
1a-Hydroxy-cholecalciferol
1-ALPHA-HYDROXY-CHOLECALCIFEROL;VITAMIN-D-DERIVATIVE
1,3-Cyclohexanediol, 4-methylene-5-((octahydro-1-(7-hydroxy-1,7-dimethyloctyl)-7a-methyl-4H-inden-4-ylidene)ethylidene)-, (1R-(1alpha(R*),3abeta,4e(1R*,3S*,5Z),7aalpha))-
| Title | Journal or Book | Year |
|---|---|---|
| An efficient synthesis of 1α,25-dihydroxy-20-epi-vitamin D3 | The Journal of Steroid Biochemistry and Molecular Biology | 2013 |
| Pd-Catalyzed Carbocyclization−Negishi Cross-Coupling Cascade: A Novel Approach to 1α,25-Dihydroxyvitamin D3 and Analogues | Organic Letters | 2005 |
| Synthesis and NMR Studies of 13C-Labeled Vitamin D Metabolites1 | The Journal of Organic Chemistry | 2002 |
| Natural Abundance13C-NMR. of Vitamin D3Metabolites | Helvetica Chimica Acta | 1980 |
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