D-(-)-Fructose (C6H12O6)
BMRB entry bmse000010
Entry DOI: doi:10.13018/BMSE000010
Data source: Madison Metabolomics Consortium - Francisca Jofre, Mark E. Anderson, John L. Markley
NMR-STAR file:
bmse000010.strNMR-STAR
interactive viewerStructure file (mol/sdf):
bmse000010.molAll files for
bmse000010Time Domain Data:
bmse000010.zipSample and instrument details are given with the spectrum
Assigned chemical shifts
Set 1
Sample: multiple; see NMR-STAR file
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
| Atom ID | Author Nomenclature | Value | Ambiguity Code |
|---|---|---|---|
| C6 | C1 | 104.234 | 1 |
| C6 | C1 | 100.824 | 1 |
| C5 | C2 | 83.400 | 4 |
| C5 | C2 | 78.032 | 4 |
| C5 | C2 | 77.122 | 4 |
| C5 | C2 | 72.393 | 4 |
| C5 | C2 | 71.926 | 4 |
| C5 | C2 | 70.232 | 4 |
| C2 | C4 | 66.572 | 4 |
| C2 | C4 | 66.093 | 4 |
| C2 | C4 | 65.322 | 4 |
| C2 | C4 | 65.105 | 4 |
| C4 | C6 | 83.400 | 4 |
| C4 | C6 | 78.032 | 4 |
| C4 | C6 | 77.122 | 4 |
| C4 | C6 | 72.393 | 4 |
| C4 | C6 | 71.926 | 4 |
| C4 | C6 | 70.232 | 4 |
| C3 | C8 | 83.400 | 4 |
| C3 | C8 | 78.032 | 4 |
| C3 | C8 | 77.122 | 4 |
| C3 | C8 | 72.393 | 4 |
| C3 | C8 | 71.926 | 4 |
| C3 | C8 | 70.232 | 4 |
| C1 | C11 | 66.572 | 4 |
| C1 | C11 | 66.093 | 4 |
| C1 | C11 | 65.322 | 4 |
| C1 | C11 | 65.105 | 4 |
| H19 | H13 | 4.106 | 4 |
| H19 | H13 | 3.986 | 4 |
| H19 | H13 | 3.886 | 4 |
| H19 | H13 | 3.806 | 4 |
| H15 | H14 | 4.030 | 4 |
| H15 | H14 | 4.005 | 4 |
| H15 | H14 | 3.806 | 4 |
| H15 | H14 | 3.683 | 4 |
| H15 | H14 | 3.550 | 4 |
| H16 | H15 | 4.030 | 4 |
| H16 | H15 | 4.005 | 4 |
| H16 | H15 | 3.806 | 4 |
| H16 | H15 | 3.683 | 4 |
| H16 | H15 | 3.550 | 4 |
| H18 | H17 | 4.106 | 4 |
| H18 | H17 | 3.986 | 4 |
| H18 | H17 | 3.886 | 4 |
| H18 | H17 | 3.806 | 4 |
| H17 | H19 | 4.106 | 4 |
| H17 | H19 | 3.986 | 4 |
| H17 | H19 | 3.886 | 4 |
| H17 | H19 | 3.806 | 4 |
| H13 | H22 | 4.030 | 4 |
| H13 | H22 | 4.005 | 4 |
| H13 | H22 | 3.806 | 4 |
| H13 | H22 | 3.683 | 4 |
| H13 | H22 | 3.550 | 4 |
| H14 | H23 | 4.030 | 4 |
| H14 | H23 | 4.005 | 4 |
| H14 | H23 | 3.806 | 4 |
| H14 | H23 | 3.683 | 4 |
| H14 | H23 | 3.550 | 4 |
NMR experiments
1: 1D 1H, 0.5 mM
Sample: 0.5mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
2: 1D 1H, 2.0 mM
Sample: 2.0mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
3: 1D 1H
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
4: 2D [1H,1H]-TOCSY
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
![Spectrum for experiment #4: 2D [1H,1H]-TOCSY](/ftp/pub/bmrb/metabolomics/entry_directories/bmse000010/nmr/set01/spectra/HH_TOCSY/00.png)
5: 1D 13C
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
6: 1D DEPT90
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
7: 1D DEPT135
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
8: 2D [1H,13C]-HSQC
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
![Spectrum for experiment #8: 2D [1H,13C]-HSQC](/ftp/pub/bmrb/metabolomics/entry_directories/bmse000010/nmr/set01/spectra/1H_13C_HSQC/00.png)
9: 2D [1H,13C]-HMBC
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
![Spectrum for experiment #9: 2D [1H,13C]-HMBC](/ftp/pub/bmrb/metabolomics/entry_directories/bmse000010/nmr/set01/spectra/1H_13C_HMBC/00.png)
10: 2D [1H,1H]-COSY
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 500MHz
![Spectrum for experiment #10: 2D [1H,1H]-COSY](/ftp/pub/bmrb/metabolomics/entry_directories/bmse000010/nmr/set01/spectra/HH_COSY/00.png)
11: 2D [1H,13C]-HSQC SW small
Sample: 100mM in D2O, ref: DSS
Conditions: temperature: 298K, pH: 7.4
Spectrometer: Bruker DMX - 400MHz