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Details

Stereochemistry ABSOLUTE
Molecular Formula C6H12O5
Molecular Weight 164.1565
Optical Activity ( - )
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Elfucose

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

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Studies on the plasma membrane of normal and psoriatic keratinocytes. 6. Cell surface and shed glycoproteins.
1983 Jan
Fucosyltransferases: differential plasma and tissue alterations in hepatocellular carcinoma and cirrhosis.
1991 Apr
Monoclonal antibody FW6 defines an epitope on alpha 3/4-monofucosylated polylactosaminoglycans expressed by fetal and colon carcinoma-associated mucins.
1993 Sep 15
O-linked L-fucose is present in Desmodus rotundus salivary plasminogen activator.
1996 Mar 29
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 Apr 17
The metabolism of 6-deoxyhexoses in bacterial and animal cells.
1998 Nov
[Role of cytokines in the metabolism of the extracellular matrix carbohydrate-protein components in patients of various ages with gastroduodenal ulcer].
2001 Jul-Aug
The oligosaccharidic content of the glycoconjugates of the prepubertal descended and undescended testis: lectin histochemical study.
2004 Apr-Jun
Polysaccharides of Ganoderma lucidum alter cell immunophenotypic expression and enhance CD56+ NK-cell cytotoxicity in cord blood.
2004 Nov 1
Substrate discrimination by the human GTP fucose pyrophosphorylase.
2005 Aug 16
Patents
Name Type Language
Elfucose
USAN   INN  
Official Name English
FUCOSE
INCI  
INCI  
Preferred Name English
L-FUCOSE
MI   USP-RS  
Common Name English
6-deoxy-L-galactose
Systematic Name English
elfucose [INN]
Common Name English
ELFUCOSE [USAN]
Common Name English
(-)-FUCOSE
Common Name English
DEOXYGALACTOSE-CERECOR
Common Name English
FUCOSE, L-
Common Name English
6-deoxy-L-galactopyranose
Common Name English
L-FUCOSE [MI]
Common Name English
FUCOSE-CERECOR
Common Name English
FUCOSE [INCI]
Common Name English
L-(-)-FUCOSE
Common Name English
L-FUCOSE [USP-RS]
Common Name English
NSC-1219
Code English
L-GALACTOMETHYLOSE
Common Name English
L-fucopyranose
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 667018
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
NCI_THESAURUS C68479
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
FDA ORPHAN DRUG 753120
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
Code System Code Type Description
CHEBI
18287
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
CHEBI
33984
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
USAN
JK-273
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
CAS
87-96-7
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
ALTERNATIVE
RXCUI
2466731
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
ECHA (EC/EINECS)
201-785-4
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
ALTERNATIVE
DAILYMED
28RYY2IV3F
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
EPA CompTox
DTXSID50883845
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
CAS
2438-80-4
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
INN
12611
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
FDA UNII
28RYY2IV3F
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
NSC
1219
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
NCI_THESAURUS
C68481
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY NCIT
DRUG BANK
DB15236
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
MESH
D005643
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
PUBCHEM
3034656
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
SMS_ID
300000041011
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
MERCK INDEX
m5578
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY Merck Index
RS_ITEM_NUM
1286606
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
WIKIPEDIA
FUCOSE
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
ECHA (EC/EINECS)
219-452-7
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY
CHEBI
2181
Created by admin on Fri Dec 15 16:41:26 UTC 2023 , Edited by admin on Fri Dec 15 16:41:26 UTC 2023
PRIMARY