| Common Name |
D-Fucose
| Description |
Not Available
| Structure |
MOLSDF3D-SDFPDBSMILESInChI View 3D Structure
Structure for HMDB29196 (D-Fucose)
| Synonyms |
| Value |
Source |
alpha-D-FucChEBI
alpha-D-FucpChEBI
a-D-FucGenerator
α-D-fucGenerator
a-D-FucpGenerator
α-D-fucpGenerator
6-Deoxy-D-galactopyranoseHMDB
6-Deoxy-D-galactoseHMDB
D-FucopyranoseHMDB
| Chemical Formlia |
C6H12O5
| Average Molecliar Weight |
164.1565
| Monoisotopic Molecliar Weight |
164.068473494
| IUPAC Name |
(2S,3R,4S,5R,6R)-6-methyloxane-2,3,4,5-tetrol
| Traditional Name |
α-d-fucose
| CAS Registry Number |
Not Available
| SMILES |
C[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O
| InChI Identifier |
InChI=1S/C6H12O5/c1-2-3(7)4(8)5(9)6(10)11-2/h2-10H,1H3/t2-,3+,4+,5-,6+/m1/s1
| InChI Key |
SHZGCJCMOBCMKK-PHYPRBDBSA-N
| Chemical Taxonomy |
| Description |
This compound belongs to the class of chemical entities known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.
| Kingdom |
Chemical entities
| Super Class |
Organic compounds
| Class |
Organic oxygen compounds
| Sub Class |
Organooxygen compounds
| Direct Parent |
Hexoses
| Alternative Parents |
Oxanes
Secondary alcohols
Hemiacetals
Polyols
Oxacyclic compounds
Hydrocarbon derivatives
| Substituents |
Hexose monosaccharide
Oxane
Secondary alcohol
Hemiacetal
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Alcohol
Aliphatic heteromonocyclic compound
| Molecliar Framework |
Aliphatic heteromonocyclic compounds
| External Descriptors |
D-fucopyranose (CHEBI:42564 )
| Ontology |
| Status |
Detected but not Quantified
| Origin |
Not Available
| Biofunction |
Nutrient
| Application |
Not Available
| Cellliar locations |
Not Available
| Physical Properties |
| State |
Solid
| Experimental Properties |
| Property |
Value |
Reference |
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
| Predicted Properties |
| Property |
Value |
Source |
Water Solubility827.0 mg/mLALOGPS
logP-2.4ALOGPS
logP-1.9ChemAxon
logS0.7ALOGPS
pKa (Strongest Acidic)11.3ChemAxon
pKa (Strongest Basic)-3.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area90.15 Å2ChemAxon
Rotatable Bond Count0ChemAxon
Refractivity34.38 m3·mol-1ChemAxon
Polarizability15.18 Å3ChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rlie of FiveYesChemAxon
Ghose FilterYesChemAxon
Vebers RlieYesChemAxon
MDDR-like RlieYesChemAxon
| Spectra |
| Spectra |
Not Available
| Biological Properties |
| Cellliar Locations |
Not Available
| Biofluid Locations |
Feces
| Tissue Location |
Not Available
| Pathways |
Not Available
| Normal Concentrations |
FecesDetected but not Quantified Adlit (>18 years old)Both
Normal
24029555
details
|
| Abnormal Concentrations |
|
Not Available
| Associated Disorders and Diseases |
| Disease References |
None
| Associated OMIM IDs |
None
| External Links |
| DrugBank ID |
Not Available
| DrugBank Metabolite ID |
Not Available
| Phenol Explorer Compound ID |
Not Available
| Phenol Explorer Metabolite ID |
Not Available
| FoodDB ID |
Not Available
| KNApSAcK ID |
Not Available
| Chemspider ID |
392189
| KEGG Compound ID |
C01018
| BioCyc ID |
Not Available
| BiGG ID |
Not Available
| Wikipedia Link |
Not Available
| NuGOwiki Link |
HMDB29196
| Metagene Link |
HMDB29196
| METLIN ID |
Not Available
| PubChem Compound |
444200
| PDB ID |
FCA
| ChEBI ID |
42564
Product: BLU-554
References |
| Synthesis Reference |
Not Available |
| Material Safety Data Sheet (MSDS) |
Not Available |
| General References |
Not Available |
PMID: 25938462
