11-alpha-hydroxyprogesterone (C21H30O3)
BMRB entry bmse000529
Entry DOI: doi:10.13018/BMSE000529
Data source: Madison Metabolomics Consortium - Francisca Jofre, Isabelle Jeacomine, Mark E. Anderson, John L. Markley
NMR-STAR file:
bmse000529.strNMR-STAR
interactive viewerStructure file (mol/sdf):
bmse000529.molAll files for
bmse000529Time Domain Data:
bmse000529.zipSample and instrument details are given with the spectrum
Assigned chemical shifts
Set 1
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
| Atom ID | Author Nomenclature | Value | Ambiguity Code |
|---|---|---|---|
| C17 | C4 | 55.817 | 1 |
| C21 | C5 | 44.608 | 1 |
| C15 | C6 | 35.416 | 1 |
| C19 | C7 | 59.426 | 1 |
| C20 | C8 | 40.412 | 1 |
| C11 | C9 | 50.876 | 1 |
| C16 | C10 | 63.595 | 1 |
| C18 | C11 | 69.294 | 1 |
| C7 | C12 | 24.711 | 1 |
| C5 | C13 | 34.065 | 1 |
| C6 | C14 | 23.412 | 1 |
| C13 | C15 | 171.479 | 1 |
| C3 | C16 | 14.978 | 1 |
| C4 | C17 | 32.009 | 1 |
| C9 | C18 | 37.973 | 1 |
| C2 | C19 | 18.773 | 1 |
| C12 | C20 | 209.323 | 1 |
| C8 | C21 | 34.658 | 1 |
| C10 | C22 | 125.015 | 1 |
| C14 | C23 | 200.734 | 1 |
| C1 | C24 | 31.846 | 1 |
| H51 | H25 | 1.261 | 4 |
| H49 | H26 | 2.376 | 4 |
| H53 | H27 | 1.139 | 4 |
| H47 | H28 | 2.190 | 4 |
| H48 | H29 | 1.729 | 4 |
| H50 | H30 | 2.569 | 1 |
| H52 | H31 | 4.040 | 1 |
| H40 | H32 | 1.534 | 4 |
| H41 | H33 | 2.376 | 4 |
| H36 | H34 | 2.190 | 4 |
| H37 | H35 | 1.729 | 4 |
| H38 | H36 | 1.534 | 4 |
| H39 | H37 | 2.376 | 4 |
| H31 | H38 | 0.703 | 1 |
| H33 | H39 | 0.703 | 1 |
| H32 | H40 | 0.703 | 1 |
| H34 | H41 | 1.854 | 4 |
| H35 | H42 | 1.139 | 4 |
| H44 | H43 | 2.683 | 2 |
| H45 | H44 | 2.026 | 2 |
| H28 | H45 | 1.326 | 1 |
| H30 | H46 | 1.326 | 1 |
| H29 | H47 | 1.326 | 1 |
| H42 | H48 | 2.190 | 4 |
| H43 | H49 | 1.729 | 4 |
| H54 | H50 | 1.534 | 4 |
| H46 | H51 | 5.739 | 1 |
| H26 | H52 | 2.142 | 1 |
| H25 | H53 | 2.142 | 1 |
| H27 | H54 | 2.142 | 1 |
NMR experiments
1: 1D 1H
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
2: 2D [1H,1H]-TOCSY
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
![Spectrum for experiment #2: 2D [1H,1H]-TOCSY](/ftp/pub/bmrb/metabolomics/entry_directories/bmse000529/nmr/set01/spectra/HH_TOCSY.png)
3: 1D 13C
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
4: 1D DEPT90
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
5: 1D DEPT135
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
6: 2D [1H,13C]-HSQC
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
![Spectrum for experiment #6: 2D [1H,13C]-HSQC](/ftp/pub/bmrb/metabolomics/entry_directories/bmse000529/nmr/set01/spectra/1H_13C_HSQC.png)
7: 2D [1H,13C]-HMBC
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
![Spectrum for experiment #7: 2D [1H,13C]-HMBC](/ftp/pub/bmrb/metabolomics/entry_directories/bmse000529/nmr/set01/spectra/1H_13C_HMBC.png)
8: 2D [1H,1H]-COSY
Sample: Saturated1 in CDCl3, ref: TMS
Conditions: temperature: 298K, pH: n/a
Spectrometer: Bruker DMX - 500MHz
![Spectrum for experiment #8: 2D [1H,1H]-COSY](/ftp/pub/bmrb/metabolomics/entry_directories/bmse000529/nmr/set01/spectra/HH_COSY.png)