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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2056320생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2056320

반응식

참여 물질

역할이름HCID투입량
반응물Sodium FluorideHCID 5235—
반응물NADPHHCID 5884—
반응물Lacto-N-bioseHCID 440994—
반응물HCID 178434963HCID 178434963—
반응물HCID 178508932HCID 178508932—
용매IsopropanolHCID 3776—
생성물beta-D-Galp-(1->3)-(alpha-L-Fucp-(1->4))-D-GlcpNAcHCID 22806751—

반응 단계

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).]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07335500B2
출처 데이터셋uspto-grants-2008_02
ORD IDord-d3ce4051b17a4f8ebcc5a7fa5867c3d2
출처 메모uspto-grants-2008_02