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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (2) Show 2 proteins XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-09-14 15:40:03 UTC

HMDB ID

HMDB0001265

Secondary Accession Numbers

HMDB0062489
HMDB01265
HMDB62489

Metabolite Identification

Common Name

Fucose 1-phosphate

Description

Fucose 1-phosphate (CAS: 16562-58-6) belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphate group linked to the carbohydrate unit. Fucose 1-phosphate is an intermediate in the reversible synthesis of GDP-L-fucose catalyzed by the enzyme guanosine triphosphate fucose pyrophosphorylase (GFPP, EC 2.7.7.30). The reversible reaction is magnesium-dependent, although the enzyme is partially active when cobalt or manganese is substituted. The reaction is unusual in that, of the four canonical nucleoside triphosphates, only guanosine can be utilized efficiently to form a nucleotide-sugar. Free cytosolic fucose is phosphorylated by L-fucokinase (EC 2.7.1.52) to form fucose-1-phosphate in the salvage pathway of GDP-L-fucose (PMID: 16185085 , 14686921 ).

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652306192020162D          

 15 15  0  0  0  0            999 V2000
10000.903110000.2956    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.903110001.1207    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10000.903110001.9457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.078110001.1206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.728110001.1207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.9031 9998.6457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.4741 9997.8207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9998.045210000.2957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.0452 9998.6456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.1886 9999.8831    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.1886 9999.0582    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9999.4741 9998.6457    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9998.7597 9999.0581    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9998.7597 9999.8832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9999.474210000.2957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 10 15  1  0  0  0  0
 14 15  1  0  0  0  0
 10  1  1  6  0  0  0
 11  6  1  1  0  0  0
 12  7  1  6  0  0  0
 14  8  1  6  0  0  0
 13  9  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0001265

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@@H]1O[C@H](OP(O)(O)=O)[C@@H](O)[C@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C6H13O8P/c1-2-3(7)4(8)5(9)6(13-2)14-15(10,11)12/h2-9H,1H3,(H2,10,11,12)/t2-,3+,4+,5-,6+/m0/s1

> <INCHI_KEY>
PTVXQARCLQPGIR-SXUWKVJYSA-N

> <FORMULA>
C6H13O8P

> <MOLECULAR_WEIGHT>
244.136

> <EXACT_MASS>
244.034804377

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
19.998868940614585

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phosphonic acid

> <ALOGPS_LOGP>
-1.53

> <JCHEM_LOGP>
-2.009195282666666

> <ALOGPS_LOGS>
-0.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.219259191809283

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.1557140415655103

> <JCHEM_PKA_STRONGEST_BASIC>
-3.612214176029089

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
45.2526

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.42e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
fucose 1-phosphate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-JUN-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-20         0                                  
HETATM    1  O   UNK     0    8668.3528667.218   0.000  0.00  0.00           O+0
HETATM    2  P   UNK     0    8668.3528668.759   0.000  0.00  0.00           P+0
HETATM    3  O   UNK     0    8668.3528670.299   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0    8666.8128668.758   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0    8669.8928668.759   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    8668.3528664.139   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0    8665.6858662.599   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0    8663.0188667.219   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0    8663.0188664.138   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0    8667.0198666.448   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8667.0198664.909   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8665.6858664.139   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8664.3518664.908   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8664.3518666.449   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0    8665.6858667.219   0.000  0.00  0.00           O+0
CONECT    1    2   10                                                       
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2                                                            
CONECT    6   11                                                            
CONECT    7   12                                                            
CONECT    8   14                                                            
CONECT    9   13                                                            
CONECT   10   11   15    1                                                  
CONECT   11   10   12    6                                                  
CONECT   12   11   13    7                                                  
CONECT   13   12   14    9                                                  
CONECT   14   13   15    8                                                  
CONECT   15   10   14                                                       
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

COMPND    HMDB0001265
HETATM    1  C1  UNL     1      -2.440   1.047  -1.339  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.241   0.990  -0.381  1.00  0.00           C  
HETATM    3  O1  UNL     1      -0.247   0.314  -1.036  1.00  0.00           O  
HETATM    4  C3  UNL     1       0.744  -0.197  -0.245  1.00  0.00           C  
HETATM    5  O2  UNL     1       1.566  -0.991  -1.078  1.00  0.00           O  
HETATM    6  P1  UNL     1       3.156  -0.429  -1.066  1.00  0.00           P  
HETATM    7  O3  UNL     1       3.943  -1.265  -2.036  1.00  0.00           O  
HETATM    8  O4  UNL     1       3.176   1.181  -1.530  1.00  0.00           O  
HETATM    9  O5  UNL     1       3.774  -0.660   0.487  1.00  0.00           O  
HETATM   10  C4  UNL     1       0.243  -1.120   0.842  1.00  0.00           C  
HETATM   11  O6  UNL     1       0.616  -0.602   2.101  1.00  0.00           O  
HETATM   12  C5  UNL     1      -1.273  -1.123   0.825  1.00  0.00           C  
HETATM   13  O7  UNL     1      -1.681  -1.686  -0.373  1.00  0.00           O  
HETATM   14  C6  UNL     1      -1.679   0.354   0.907  1.00  0.00           C  
HETATM   15  O8  UNL     1      -3.011   0.516   1.189  1.00  0.00           O  
HETATM   16  H1  UNL     1      -3.275   1.618  -0.916  1.00  0.00           H  
HETATM   17  H2  UNL     1      -2.031   1.481  -2.280  1.00  0.00           H  
HETATM   18  H3  UNL     1      -2.765   0.019  -1.596  1.00  0.00           H  
HETATM   19  H4  UNL     1      -0.995   2.053  -0.158  1.00  0.00           H  
HETATM   20  H5  UNL     1       1.382   0.597   0.199  1.00  0.00           H  
HETATM   21  H6  UNL     1       3.672   1.757  -0.898  1.00  0.00           H  
HETATM   22  H7  UNL     1       3.499   0.041   1.114  1.00  0.00           H  
HETATM   23  H8  UNL     1       0.660  -2.133   0.786  1.00  0.00           H  
HETATM   24  H9  UNL     1       1.164   0.234   1.991  1.00  0.00           H  
HETATM   25  H10 UNL     1      -1.688  -1.700   1.659  1.00  0.00           H  
HETATM   26  H11 UNL     1      -1.120  -2.472  -0.554  1.00  0.00           H  
HETATM   27  H12 UNL     1      -1.039   0.781   1.724  1.00  0.00           H  
HETATM   28  H13 UNL     1      -3.113   1.393   1.666  1.00  0.00           H  
CONECT    1    2   16   17   18
CONECT    2    3   14   19
CONECT    3    4
CONECT    4    5   10   20
CONECT    5    6
CONECT    6    7    7    8    9
CONECT    8   21
CONECT    9   22
CONECT   10   11   12   23
CONECT   11   24
CONECT   12   13   14   25
CONECT   13   26
CONECT   14   15   27
CONECT   15   28
END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
6-Deoxy-1-O-phosphono-beta-L-galactopyranose	ChEBI
6-Deoxy-L-galactose 1-phosphate	ChEBI
Fucopyranosyl phosphate	ChEBI
Fucose 1-phosphate	ChEBI
6-Deoxy-1-O-phosphono-b-L-galactopyranose	Generator
6-Deoxy-1-O-phosphono-β-L-galactopyranose	Generator
6-Deoxy-L-galactose 1-phosphoric acid	Generator
Fucopyranosyl phosphoric acid	Generator
Fucose 1-phosphoric acid	Generator
b-L-Fucose 1-phosphate	Generator
b-L-Fucose 1-phosphoric acid	Generator
beta-L-Fucose 1-phosphoric acid	Generator
Β-L-fucose 1-phosphate	Generator
Β-L-fucose 1-phosphoric acid	Generator
beta-L-Fucopyranosyl dicyclohexylammonium phosphate	MeSH
beta-L-Fucose 1-phosphate	KEGG
L-Fucopyranose 1-(dihydrogen phosphate)	HMDB
L-Fucose 1-phosphate	HMDB
L-Fucose-1-phosphate	HMDB
beta-L-Fucopyranosyl phosphate	HMDB
β-L-Fucopyranosyl phosphate	HMDB

Chemical Formula

C₆H₁₃O₈P

Average Molecular Weight

244.136

Monoisotopic Molecular Weight

244.034804377

IUPAC Name

{[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}phosphonic acid

Traditional Name

fucose 1-phosphate

CAS Registry Number

16562-59-7

SMILES

C[C@@H]1O[C@H](OP(O)(O)=O)[C@@H](O)[C@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C6H13O8P/c1-2-3(7)4(8)5(9)6(13-2)14-15(10,11)12/h2-9H,1H3,(H2,10,11,12)/t2-,3+,4+,5-,6+/m0/s1

InChI Key

PTVXQARCLQPGIR-SXUWKVJYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphated group linked to the carbohydrate unit.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Monosaccharide phosphates

Alternative Parents

Substituents

Hexose monosaccharide
Monosaccharide phosphate
Monoalkyl phosphate
Alkyl phosphate
Phosphoric acid ester
Oxane
Organic phosphoric acid derivative
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxide
Hydrocarbon derivative
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

L-fucopyranose 1-phosphate (CHEBI:12387 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Cytoplasm (HMDB: HMDB0001265)

Source

Endogenous

Endogenous (HMDB: HMDB0001265)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Fructose and Mannose Degradation (HMDB: HMDB0001265)
Fructose and Mannose Degradation (PathBank: SMP0087296)

Disease pathway

Fructose Intolerance, Hereditary (HMDB: HMDB0001265)
Fructose Intolerance, Hereditary (PathBank: SMP0120657)
Fructosuria (PathBank: SMP0120625)

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	34.2 g/L	ALOGPS
logP	-1.5	ALOGPS
logP	-2	ChemAxon
logS	-0.85	ALOGPS
pKa (Strongest Acidic)	1.16	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	45.25 m³·mol⁻¹	ChemAxon
Polarizability	20 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	140.579	30932474
DeepCCS	[M-H]-	138.184	30932474
DeepCCS	[M-2H]-	172.696	30932474
DeepCCS	[M+Na]+	147.129	30932474
AllCCS	[M+H]+	154.2	32859911
AllCCS	[M+H-H2O]+	150.5	32859911
AllCCS	[M+NH4]+	157.7	32859911
AllCCS	[M+Na]+	158.7	32859911
AllCCS	[M-H]-	144.8	32859911
AllCCS	[M+Na-2H]-	145.4	32859911
AllCCS	[M+HCOO]-	146.1	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	1.78 minutes	32390414
Predicted by Siyang on May 30, 2022	9.6811 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	8.31 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	431.7 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	493.4 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	293.2 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	26.9 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	177.4 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	72.5 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	307.4 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	232.9 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	757.6 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	582.0 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	41.3 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	629.6 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	181.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	292.6 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	832.5 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	479.3 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	420.5 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Fucose 1-phosphate	C[C@@H]1O[C@H](OP(O)(O)=O)[C@@H](O)[C@H](O)[C@@H]1O	3218.7	Standard polar	33892256
Fucose 1-phosphate	C[C@@H]1O[C@H](OP(O)(O)=O)[C@@H](O)[C@H](O)[C@@H]1O	1906.2	Standard non polar	33892256
Fucose 1-phosphate	C[C@@H]1O[C@H](OP(O)(O)=O)[C@@H](O)[C@H](O)[C@@H]1O	2050.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Fucose 1-phosphate,1TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O	1906.1	Semi standard non polar	33892256
Fucose 1-phosphate,1TMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O	1906.7	Semi standard non polar	33892256
Fucose 1-phosphate,1TMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C	1936.5	Semi standard non polar	33892256
Fucose 1-phosphate,1TMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O	1949.6	Semi standard non polar	33892256
Fucose 1-phosphate,2TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	1925.7	Semi standard non polar	33892256
Fucose 1-phosphate,2TMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	1914.3	Semi standard non polar	33892256
Fucose 1-phosphate,2TMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O	1958.9	Semi standard non polar	33892256
Fucose 1-phosphate,2TMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	1929.8	Semi standard non polar	33892256
Fucose 1-phosphate,2TMS,isomer #5	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O	1963.5	Semi standard non polar	33892256
Fucose 1-phosphate,2TMS,isomer #6	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C	1971.8	Semi standard non polar	33892256
Fucose 1-phosphate,2TMS,isomer #7	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O	1981.5	Semi standard non polar	33892256
Fucose 1-phosphate,3TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	1946.7	Semi standard non polar	33892256
Fucose 1-phosphate,3TMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	1957.0	Semi standard non polar	33892256
Fucose 1-phosphate,3TMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	1970.3	Semi standard non polar	33892256
Fucose 1-phosphate,3TMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O	1949.6	Semi standard non polar	33892256
Fucose 1-phosphate,3TMS,isomer #5	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	1977.4	Semi standard non polar	33892256
Fucose 1-phosphate,3TMS,isomer #6	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O	1979.7	Semi standard non polar	33892256
Fucose 1-phosphate,3TMS,isomer #7	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C	1942.5	Semi standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2015.1	Semi standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2032.4	Standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2366.2	Standard polar	33892256
Fucose 1-phosphate,4TMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	2018.6	Semi standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	2070.9	Standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O	2350.1	Standard polar	33892256
Fucose 1-phosphate,4TMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	2033.4	Semi standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	2083.0	Standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C	2258.9	Standard polar	33892256
Fucose 1-phosphate,4TMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2036.6	Semi standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2083.5	Standard non polar	33892256
Fucose 1-phosphate,4TMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2267.1	Standard polar	33892256
Fucose 1-phosphate,5TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2072.3	Semi standard non polar	33892256
Fucose 1-phosphate,5TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2105.7	Standard non polar	33892256
Fucose 1-phosphate,5TMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	2211.4	Standard polar	33892256
Fucose 1-phosphate,1TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	2172.1	Semi standard non polar	33892256
Fucose 1-phosphate,1TBDMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2177.3	Semi standard non polar	33892256
Fucose 1-phosphate,1TBDMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2197.9	Semi standard non polar	33892256
Fucose 1-phosphate,1TBDMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O	2194.7	Semi standard non polar	33892256
Fucose 1-phosphate,2TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2382.8	Semi standard non polar	33892256
Fucose 1-phosphate,2TBDMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2377.8	Semi standard non polar	33892256
Fucose 1-phosphate,2TBDMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	2394.6	Semi standard non polar	33892256
Fucose 1-phosphate,2TBDMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2388.4	Semi standard non polar	33892256
Fucose 1-phosphate,2TBDMS,isomer #5	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2398.4	Semi standard non polar	33892256
Fucose 1-phosphate,2TBDMS,isomer #6	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2413.8	Semi standard non polar	33892256
Fucose 1-phosphate,2TBDMS,isomer #7	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O	2407.2	Semi standard non polar	33892256
Fucose 1-phosphate,3TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2603.8	Semi standard non polar	33892256
Fucose 1-phosphate,3TBDMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2598.3	Semi standard non polar	33892256
Fucose 1-phosphate,3TBDMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2617.1	Semi standard non polar	33892256
Fucose 1-phosphate,3TBDMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O	2592.5	Semi standard non polar	33892256
Fucose 1-phosphate,3TBDMS,isomer #5	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2610.5	Semi standard non polar	33892256
Fucose 1-phosphate,3TBDMS,isomer #6	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2583.2	Semi standard non polar	33892256
Fucose 1-phosphate,3TBDMS,isomer #7	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2587.8	Semi standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2818.3	Semi standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2802.6	Standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2764.2	Standard polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2800.0	Semi standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2799.8	Standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #2	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	2760.5	Standard polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2819.0	Semi standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2824.9	Standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #3	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	2678.3	Standard polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2806.7	Semi standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2819.5	Standard non polar	33892256
Fucose 1-phosphate,4TBDMS,isomer #4	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2689.0	Standard polar	33892256
Fucose 1-phosphate,5TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	3013.8	Semi standard non polar	33892256
Fucose 1-phosphate,5TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2980.7	Standard non polar	33892256
Fucose 1-phosphate,5TBDMS,isomer #1	C[C@@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	2727.2	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Fucose 1-phosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Fucose 1-phosphate GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 10V, Positive-QTOF	splash10-0002-9130000000-7b4a4232dd7a0bd8dbac	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 20V, Positive-QTOF	splash10-0002-9230000000-2ee74b8ac83ba7b48ef3	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 40V, Positive-QTOF	splash10-0002-9000000000-3bc59b08305310a3654f	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 10V, Negative-QTOF	splash10-002g-9170000000-875253e07281671ff694	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 20V, Negative-QTOF	splash10-004i-9000000000-a8e79a6083cde3a1b0d1	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 40V, Negative-QTOF	splash10-004i-9000000000-ef5dc3379a78dd68ac33	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 10V, Negative-QTOF	splash10-0006-3090000000-87959ec9e9952d6c1e7e	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 20V, Negative-QTOF	splash10-004i-9000000000-c08a47f59e790b5f91b9	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 40V, Negative-QTOF	splash10-004i-9000000000-a5e502a2627af2048a1f	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 10V, Positive-QTOF	splash10-0002-0390000000-8f9f4139490c8a36f799	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 20V, Positive-QTOF	splash10-002b-4900000000-cc61be796553b9786469	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Fucose 1-phosphate 40V, Positive-QTOF	splash10-052g-9000000000-a31cfa738e614a05eb5d	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Name	SMPDB/PathBank	KEGG
Fructose and mannose metabolism	Not Available
Fructosuria		Not Available
Fructose intolerance, hereditary		Not Available

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022520

KNApSAcK ID

Not Available

Chemspider ID

58841

KEGG Compound ID

C02985

BioCyc ID

CPD-488

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

6120

PubChem Compound

65369

PDB ID

Not Available

ChEBI ID

12387

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Quirk S, Seley KL: Identification of catalytic amino acids in the human GTP fucose pyrophosphorylase active site. Biochemistry. 2005 Oct 4;44(39):13172-8. [PubMed:16185085 ]
Niittymaki J, Mattila P, Roos C, Huopaniemi L, Sjoblom S, Renkonen R: Cloning and expression of murine enzymes involved in the salvage pathway of GDP-L-fucose. Eur J Biochem. 2004 Jan;271(1):78-86. [PubMed:14686921 ]

Enzymes

Enzyme Details

1. Fucose-1-phosphate guanylyltransferase

General function:: Involved in fucose-1-phosphate guanylyltransferase acti
Specific function:: Catalyzes the formation of GDP-L-fucose from GTP and L-fucose-1-phosphate. Functions as a salvage pathway to reutilize L-fucose arising from the turnover of glycoproteins and glycolipids.
Gene Name:: FPGT
Uniprot ID:: O14772
Molecular weight:: 37630.405

Reactions

Guanosine triphosphate + Fucose 1-phosphate → Pyrophosphate + GDP-L-fucose	details

Enzyme Details

2. L-fucose kinase

General function:: Involved in ATP binding
Specific function:: Takes part in the salvage pathway for reutilization of fucose from the degradation of oligosaccharides.
Gene Name:: FUK
Uniprot ID:: Q8N0W3
Molecular weight:: 117621.795

Reactions

Adenosine triphosphate + L-Fucose → ADP + Fucose 1-phosphate	details

Showing metabocard for Fucose 1-phosphate (HMDB0001265)

MOL for HMDB0001265 (Fucose 1-phosphate)

3D MOL for HMDB0001265 (Fucose 1-phosphate)

3D SDF for HMDB0001265 (Fucose 1-phosphate)

3D-SDF for HMDB0001265 (Fucose 1-phosphate)

PDB for HMDB0001265 (Fucose 1-phosphate)

3D PDB for HMDB0001265 (Fucose 1-phosphate)

SMILES for HMDB0001265 (Fucose 1-phosphate)

INCHI for HMDB0001265 (Fucose 1-phosphate)

Structure for HMDB0001265 (Fucose 1-phosphate)

3D Structure for HMDB0001265 (Fucose 1-phosphate)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions

Reactions