Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C6H12O5 |
| Molecular Weight | 164.1567 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)C=O
InChI
InChIKey=PNNNRSAQSRJVSB-KCDKBNATSA-N
InChI=1S/C6H12O5/c1-3(8)5(10)6(11)4(9)2-7/h2-6,8-11H,1H3/t3-,4+,5+,6-/m0/s1
| Molecular Formula | C6H12O5 |
| Molecular Weight | 164.1567 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Molecular cloning and characterization of a novel human beta1,3-glucosyltransferase, which is localized at the endoplasmic reticulum and glucosylates O-linked fucosylglycan on thrombospondin type 1 repeat domain. | 2006-12 |
|
| Substrate discrimination by the human GTP fucose pyrophosphorylase. | 2005-08-16 |
|
| Human symbionts use a host-like pathway for surface fucosylation. | 2005-03-18 |
|
| Polysaccharides of Ganoderma lucidum alter cell immunophenotypic expression and enhance CD56+ NK-cell cytotoxicity in cord blood. | 2004-11-01 |
|
| The oligosaccharidic content of the glycoconjugates of the prepubertal descended and undescended testis: lectin histochemical study. | 2004-10-16 |
|
| Pharmacology of skin aging. Stimulation of glycosaminoglycan biosynthesis by L-fucose and fucose-rich polysaccharides, effect of in vitro aging of fibroblasts. | 2004-04 |
|
| [Role of cytokines in the metabolism of the extracellular matrix carbohydrate-protein components in patients of various ages with gastroduodenal ulcer]. | 2001-11-06 |
|
| Evaluation of glycoproteins as prognosticators in head and neck malignancy. | 2001-10-23 |
|
| GDP-4-keto-6-deoxy-D-mannose epimerase/reductase from Escherichia coli, a key enzyme in the biosynthesis of GDP-L-fucose, displays the structural characteristics of the RED protein homology superfamily. | 1998-11-15 |
|
| The metabolism of 6-deoxyhexoses in bacterial and animal cells. | 1998-11 |
|
| Human epidermal Langerhans cells express the mannose-fucose binding receptor. | 1998-11 |
|
| Sialyl Lewis(x) epitopes do not occur on acute phase proteins in mice: relationship to the absence of alpha3-fucosyltransferase in the liver. | 1998-04 |
|
| [Adhesins of Acinetobacter strains]. | 1998 |
|
| Effect of L-fucose and D-glucose concentration on L-fucoprotein metabolism in human Hep G2 cells and changes in fucosyltransferase and alpha-L-fucosidase activity in liver of diabetic rats. | 1997-04-17 |
|
| O-linked L-fucose is present in Desmodus rotundus salivary plasminogen activator. | 1996-03-29 |
|
| 750 MHz 1H and 1H-13C NMR spectroscopy of human blood plasma. | 1995-03-01 |
|
| Monoclonal antibody FW6 defines an epitope on alpha 3/4-monofucosylated polylactosaminoglycans expressed by fetal and colon carcinoma-associated mucins. | 1993-09-15 |
|
| A monoclonal IgM kappa from a blood group B individual with specificity for alpha-galactosyl epitopes on partially hydrolyzed blood group B substance. | 1993-05-07 |
|
| Fucosyltransferases: differential plasma and tissue alterations in hepatocellular carcinoma and cirrhosis. | 1991-04 |
|
| Lectin cytochemical evaluation of somatosensory neurons and their peripheral and central processes in rat and man. | 1986 |
|
| Studies on the plasma membrane of normal and psoriatic keratinocytes. 6. Cell surface and shed glycoproteins. | 1983-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:34:34 GMT 2025
by
admin
on
Mon Mar 31 18:34:34 GMT 2025
|
| Record UNII |
28RYY2IV3F
|
| Record Status |
FAILED
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
FDA ORPHAN DRUG |
667018
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
||
|
NCI_THESAURUS |
C68479
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
||
|
FDA ORPHAN DRUG |
753120
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
18287
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
33984
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
JK-273
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
87-96-7
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
ALTERNATIVE | |||
|
2466731
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
201-785-4
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
ALTERNATIVE | |||
|
28RYY2IV3F
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
DTXSID50883845
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
2438-80-4
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
12611
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
28RYY2IV3F
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
1219
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
C68481
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | NCIT | ||
|
DB15236
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
D005643
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
3034656
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
300000041011
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
m5578
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | Merck Index | ||
|
1286606
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
FUCOSE
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
219-452-7
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY | |||
|
2181
Created by
admin on Mon Mar 31 18:34:34 GMT 2025 , Edited by admin on Mon Mar 31 18:34:34 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ACTIVE MOIETY |
Fucose replacements
|