MiMeDB: Showing metabocard for beta-D-fructofuranosyl alpha-D-mannopyranoside 6(F)-phosphate (MMDBc0054363)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-05 23:08:39 UTC

Update Date

2022-09-01 02:28:41 UTC

Metabolite ID

MMDBc0054363

Metabolite Identification

Common Name

beta-D-fructofuranosyl alpha-D-mannopyranoside 6(F)-phosphate

Description

Structure

MOL SDF PDB SMILES InChI

 
  Mrv1533006051511202D          
 
 27 28  0  0  1  0            999 V2000
   14.4244  -13.3307    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7132  -13.7490    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0021  -13.3307    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7132  -14.5438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.2910  -13.7490    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0021  -14.9621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.4244  -14.9621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2910  -14.5438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5799  -13.3307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0021  -15.7987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5799  -14.9621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9943  -13.8745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1355  -12.8706    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.8047  -12.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3864  -13.6654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.5916  -12.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4740  -12.9124    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.2230  -13.6654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.9263  -14.3765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7250  -14.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9391  -12.3436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6502  -12.3436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4868  -12.3436    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   19.3234  -12.3436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4868  -11.5070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4868  -13.3036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7550  -12.3268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  4  7  1  1  0  0  0
  5  8  1  0  0  0  0
  5  9  1  1  0  0  0
  6 10  1  1  0  0  0
  8 11  1  6  0  0  0
  9 12  1  0  0  0  0
  6  8  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  1  0  0  0
 14 17  1  0  0  0  0
 15 18  1  0  0  0  0
 15 19  1  6  0  0  0
 18 20  1  1  0  0  0
 17 18  1  0  0  0  0
 17 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  2  0  0  0  0
 13  1  1  6  0  0  0
 16 27  1  0  0  0  0
M  END

 
  Mrv1533006051511202D          
 
 27 28  0  0  1  0            999 V2000
   14.4244  -13.3307    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7132  -13.7490    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0021  -13.3307    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7132  -14.5438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.2910  -13.7490    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0021  -14.9621    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.4244  -14.9621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2910  -14.5438    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5799  -13.3307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0021  -15.7987    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5799  -14.9621    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.9943  -13.8745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1355  -12.8706    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.8047  -12.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3864  -13.6654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.5916  -12.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4740  -12.9124    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.2230  -13.6654    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.9263  -14.3765    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7250  -14.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9391  -12.3436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6502  -12.3436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4868  -12.3436    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   19.3234  -12.3436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4868  -11.5070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.4868  -13.3036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7550  -12.3268    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  4  7  1  1  0  0  0
  5  8  1  0  0  0  0
  5  9  1  1  0  0  0
  6 10  1  1  0  0  0
  8 11  1  6  0  0  0
  9 12  1  0  0  0  0
  6  8  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  1  0  0  0
 14 17  1  0  0  0  0
 15 18  1  0  0  0  0
 15 19  1  6  0  0  0
 18 20  1  1  0  0  0
 17 18  1  0  0  0  0
 17 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  2  0  0  0  0
 13  1  1  6  0  0  0
 16 27  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0054363

> <DATABASE_NAME>
MIME

> <SMILES>
OC[C@H]1O[C@H](O[C@]2(CO)O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C12H23O14P/c13-1-4-6(15)8(17)9(18)11(24-4)26-12(3-14)10(19)7(16)5(25-12)2-23-27(20,21)22/h4-11,13-19H,1-3H2,(H2,20,21,22)/t4-,5-,6-,7-,8+,9+,10+,11-,12+/m1/s1

> <INCHI_KEY>
PJTTXANTBQDXME-VJRJJCRKSA-N

> <FORMULA>
C12H23O14P

> <MOLECULAR_WEIGHT>
422.276

> <EXACT_MASS>
422.082542419

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
35.71081494064795

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)-5-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-yl]methoxy}phosphonic acid

> <ALOGPS_LOGP>
-2.76

> <JCHEM_LOGP>
-4.652400995000001

> <ALOGPS_LOGS>
-1.04

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.247474860332638

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2216535541317723

> <JCHEM_PKA_STRONGEST_BASIC>
-3.455826384437903

> <JCHEM_POLAR_SURFACE_AREA>
236.05999999999995

> <JCHEM_REFRACTIVITY>
79.64699999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.85e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
mannosucrose 6(F)-phosphate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-JUN-15   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-JUN-15         0                                  
HETATM    1  O   UNK     0      26.925 -24.884   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      25.598 -25.665   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      24.271 -24.884   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      25.598 -27.148   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      22.943 -25.665   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      24.271 -27.929   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      26.925 -27.929   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      22.943 -27.148   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.616 -24.884   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      24.271 -29.491   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      21.616 -27.929   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      20.523 -25.899   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      28.253 -24.025   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      29.502 -23.166   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      28.721 -25.509   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      27.238 -23.010   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      30.751 -24.103   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      30.283 -25.509   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      27.862 -26.836   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      31.220 -26.758   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      31.620 -23.041   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      32.947 -23.041   0.000  0.00  0.00           O+0
HETATM   23  P   UNK     0      34.509 -23.041   0.000  0.00  0.00           P+0
HETATM   24  O   UNK     0      36.070 -23.041   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      34.509 -21.480   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      34.509 -24.833   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      25.676 -23.010   0.000  0.00  0.00           O+0
CONECT    1    2   13                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2    5                                                       
CONECT    4    2    6    7                                                  
CONECT    5    3    8    9                                                  
CONECT    6    4   10    8                                                  
CONECT    7    4                                                            
CONECT    8    5   11    6                                                  
CONECT    9    5   12                                                       
CONECT   10    6                                                            
CONECT   11    8                                                            
CONECT   12    9                                                            
CONECT   13   14   15   16    1                                             
CONECT   14   13   17                                                       
CONECT   15   13   18   19                                                  
CONECT   16   13   27                                                       
CONECT   17   14   18   21                                                  
CONECT   18   15   20   17                                                  
CONECT   19   15                                                            
CONECT   20   18                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23                                                            
CONECT   27   16                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   56    0
END

Synonyms

Value	Source
beta-D-Fructofuranosyl-alpha-D-mannopyranoside 6(F)-phosphate	ChEBI
Mannosucrose 6(F)-phosphate	ChEBI
Mannosylfructose 6-phosphate	ChEBI
Mannosylfructose 6(F)-phosphate	ChEBI
b-D-Fructofuranosyl-a-D-mannopyranoside 6(F)-phosphate	Generator
b-D-Fructofuranosyl-a-D-mannopyranoside 6(F)-phosphoric acid	Generator
beta-D-Fructofuranosyl-alpha-D-mannopyranoside 6(F)-phosphoric acid	Generator
Β-D-fructofuranosyl-α-D-mannopyranoside 6(F)-phosphate	Generator
Β-D-fructofuranosyl-α-D-mannopyranoside 6(F)-phosphoric acid	Generator
Mannosucrose 6(F)-phosphoric acid	Generator
Mannosylfructose 6-phosphoric acid	Generator
Mannosylfructose 6(F)-phosphoric acid	Generator
b-D-Fructofuranosyl a-D-mannopyranoside 6(F)-phosphate	Generator
b-D-Fructofuranosyl a-D-mannopyranoside 6(F)-phosphoric acid	Generator
beta-D-Fructofuranosyl alpha-D-mannopyranoside 6(F)-phosphoric acid	Generator
Β-D-fructofuranosyl α-D-mannopyranoside 6(F)-phosphate	Generator
Β-D-fructofuranosyl α-D-mannopyranoside 6(F)-phosphoric acid	Generator

Molecular Formula

C₁₂H₂₃O₁₄P

Average Mass

422.276

Monoisotopic Mass

422.082542419

IUPAC Name

{[(2R,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)-5-{[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-yl]methoxy}phosphonic acid

Traditional Name

mannosucrose 6(F)-phosphate

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@H](O[C@]2(CO)O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C12H23O14P/c13-1-4-6(15)8(17)9(18)11(24-4)26-12(3-14)10(19)7(16)5(25-12)2-23-27(20,21)22/h4-11,13-19H,1-3H2,(H2,20,21,22)/t4-,5-,6-,7-,8+,9+,10+,11-,12+/m1/s1

InChI Key

PJTTXANTBQDXME-VJRJJCRKSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as disaccharide phosphates. These are disaccharides carrying one or more phosphate group on a sugar unit.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Disaccharide phosphates

Alternative Parents

Substituents

Disaccharide phosphate
C-glycosyl compound
Glycosyl compound
O-glycosyl compound
Ketal
Monoalkyl phosphate
Alkyl phosphate
Phosphoric acid ester
Oxane
Organic phosphoric acid derivative
Tetrahydrofuran
Secondary alcohol
Polyol
Oxacycle
Acetal
Organoheterocyclic compound
Primary alcohol
Hydrocarbon derivative
Organic oxide
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

disaccharide phosphate (CHEBI:51834 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	38.5 g/L	ALOGPS
logP	-2.8	ALOGPS
logP	-4.7	ChemAxon
logS	-1	ALOGPS
pKa (Strongest Acidic)	1.22	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	236.06 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	79.65 m³·mol⁻¹	ChemAxon
Polarizability	35.71 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_3_9) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-03di-0490000000-bd38095ef92f86cc6030	2019-02-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-03di-1930000000-202dfd8bd9314dd5b998	2019-02-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-03di-1910000000-315b33a342bf4b74323f	2019-02-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-054o-7190100000-3400aa0f94adc20bebaf	2019-02-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004i-9150000000-39aa07f49b1df09ec63b	2019-02-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9000000000-a9f521b20fd8274a2938	2019-02-23	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Proteobacteria	1

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C18050

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

46174043

PDB ID

Not Available

ChEBI ID

51834

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for beta-D-fructofuranosyl alpha-D-mannopyranoside 6(F)-phosphate (MMDBc0054363)

MOL for #<Metabolite:0x00007fecab0e2e88>

3D MOL for #<Metabolite:0x00007fecab0e2e88>

3D SDF for #<Metabolite:0x00007fecab0e2e88>

3D-SDF for #<Metabolite:0x00007fecab0e2e88>

PDB for #<Metabolite:0x00007fecab0e2e88>

3D PDB for #<Metabolite:0x00007fecab0e2e88>

SMILES for #<Metabolite:0x00007fecab0e2e88>

INCHI for #<Metabolite:0x00007fecab0e2e88>

Structure for #<Metabolite:0x00007fecab0e2e88>

3D Structure for #<Metabolite:0x00007fecab0e2e88>