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D-(+)-Fucose (6-Deoxy-D-galactose)

$195.00

Catalog Number: B2010461 (50 mg)
D-(+)-Fucose (6-Deoxy-D-galactose) is a highly pure (> 98%) substrate with various biochemical and enzymatic applications. Custom bulk orders of this product are available upon request.
Live Enquiry about this product via Text/SMS: 1-858-900-3210.

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SKU: B2010461 Categories: , ,

Description

D-(+)-Fucose (6-Deoxy-D-galactose)
Catalog number: B2010461
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 50 mg
Molecular Weight or Concentration: 164.16
Supplied as: Powder
Appearance: Powder
Applications: highly pure (> 98%) substrate with various biochemical and enzymatic applications.
Storage: RT
Keywords: Rhodeose, 6-Deoxy-D-galactose, D-Fucose
Grade: Biotechnology grade. All solid components are highly pure (minimum 95%). All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: He Y, Zhang L, Wang H. The biological activities of the antitumor drug
Grifola frondosa polysaccharide. Prog Mol Biol Transl Sci. 2019;163:221-261.

2: Stefan-van Staden RI, Nejem RM, van Staden JF, Aboul-Enein HY. Determination
of L- and D-fucose using amperometric electrodes based on diamond paste.
Analyst. 2012 Feb 21;137(4):903-9.

3: Mukhopadhyay C, Rao VS. Computer modelling approach to study the modes of
binding of alpha- and beta-anomers of D-galactose, D-fucose and D-glucose to
L-arabinose-binding protein. Int J Biol Macromol. 1989 Aug;11(4):194-200.

4: Beverin S, Sheppard DE, Park SS. D-Fucose as a gratuitous inducer of the
L-arabinose operon in strains of Escherichia coli B-r mutant in gene araC. J
Bacteriol. 1971 Jul;107(1):79-86.

5: Ko Y, Lin GM, Ruszczycky MW, Liu HW. Mechanistic Implications of the
Deamination of TDP-4-amino-4-deoxy-d-fucose Catalyzed by the Radical SAM Enzyme
DesII. Biochemistry. 2018 Jun 5;57(22):3130-3133.

6: Yoshida Y, Nakano Y, Nezu T, Yamashita Y, Koga T. A novel
NDP-6-deoxyhexosyl-4-ulose reductase in the pathway for the synthesis of
thymidine diphosphate-D-fucose. J Biol Chem. 1999 Jun 11;274(24):16933-9.

7: Cortezano-Arellano O, Meléndez-Becerra CA, Cortés F, Sartillo-Piscil F,
Cordero-Vargas A. Stereoselective C-glycosidation of D-fu_cose derivatives
directed by the protective groups. Carbohydr Res. 2014 Jul 1;393:51-9.

8: Bylsma M, Bennett CS. Stereospecific Synthesis of the Saccharosamine-
Rhamnose-Fu_cose Fragment Present in Saccharomicin B. Org Lett. 2018 Aug
3;20(15):4695-4698.
9: Shafer CM, Molinski TF. Practical synthesis of 2,6-dideoxy-D-lyxo-hexose
(“2-deoxy-D-fucose”) from D-galactose. Carbohydr Res. 1998 Aug;310(4):223-8.

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