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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056320Generated: October 26, 2026

Sodium Fluoride → beta-D-Galp-(1->3)-(alpha-L-Fucp-(1->4))-D-GlcpNAc

https://huagongshe.com/reaction/2056320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium FluorideHCID 5235—
ReactantNADPHHCID 5884—
ReactantLacto-N-bioseHCID 440994—
ReactantHCID 178434963HCID 178434963—
ReactantHCID 178508932HCID 178508932—
SolventIsopropanolHCID 3776—
Productbeta-D-Galp-(1->3)-(alpha-L-Fucp-(1->4))-D-GlcpNAcHCID 22806751—

Reaction Steps

A mixture of GTP Na salt (6.0 mg, 10 μmol), Man-1-P K salt (3.5 mg, 10 μmol), Galβ1,3GlcNAc (3.8 mg, 10 μmol), NaF (0.42 mg, 10 μmol), NADPH (9.4 mg, 10 μmol), PEP K salt (4.1 mg, 20 μmol), MgCl2-6H2O (2.6 mg, 10 μmol), MnCl2-4H2O (2 mg, 10 μmol), 2-propanol (50 μL), ADH (12 U), PK (200 U), PPase (100 U), crude enzyme preparation of GDP-mannose pyrophosphorylase (1.0 mL), and crude enzyme preparation of GDP-Fuc producing enzyme (1.0 mL) in 100 mM tris buffer (pH 7.5) and diluted to 3 mL. α1,3/4-Fucosyltransferase (0.01 U) was added to the mixture and the resulting mixture was stirred under Ar for three days at room temperature. The mixture was filtered and the filtrate was applied to a column of Dowex 1-X8 (OH−) form followed with a column of Dowex 50W-X8 [H+] with water. The fractions were collected and lyophilized. The residual material was purified with a column of Sephadex G-25 (superfine) with water. The appropriate fractions were pooled and lyophilized to give Galβ1,3(Fucα1,4)GlcNAc. Its 1H-NMR spectrum was in good agreement with that reported. [Dumas et al., Biomed. Chem. Lett., 1:425 (1991).]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335500B2
Source datasetuspto-grants-2008_02
ORD IDord-d3ce4051b17a4f8ebcc5a7fa5867c3d2
Source noteuspto-grants-2008_02