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HRID 233545作成日:2026年10月24日

Potassium Chloride → GlyTouCan:G87605GW

https://huagongshe.com/ja/reaction/233545

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium ChlorideHCID 4873—
反応物5'-AtpHCID 5957—
反応物AcrylamideHCID 6579—
反応物4-(2-Hydroxyethyl)-1-piperazineethanesulfonic acidHCID 23831—
反応物N-Acetyl-Neuraminic AcidHCID 439197—
反応物beta-D-galactosyl-(1->4)-N-acetyl-D-glucosamineHCID 9800166—
反応物CMP-NeuAcHCID 23679065—
溶媒WaterHCID 962—
生成物GlyTouCan:G87605GWHCID 13171830897%

反応条件

温度25 °C

反応手順

NeuAc (0.92 g, 3 mmol), Galβ4GlcNAc (1.1 g, 3 mmol), CMP (0.1 g, 30 μmol), ATP (16 mg, 3 μmol), PEP (2.8 g, 6 mmol), MgCl2.6H2O (0.61 g, 3 mmol), MnCl2.4H2O (0.15 g, 0.8 mmol), KCl (0.22 g, 3 mmol), NMK or MK (450 U), PK (6,000 U), PPase (300 U), CMP-NeuAc synthetase (24 U), and Siaα2,6Gal sialyl transferase (4 U) were mixed with 150 ml of HEPES buffer (0.2M, pH 7.5) to form a reaction mixture and the reaction mixture maintained under argon at about 25° C. for about 48 hours. After the disappearance of NeuAc (determined by thin-layer chromatography) the reaction mixture was reduced in volume to 20 ml by lyophilization and the lyophilized reaction mixture applied to a Bio Gel P2 (200-400 mesh) column with water as the mobile phase. The trisaccharide-containing fractions were eluted, collected and lyophilized to give pure Neuα2,6Galβ1,4GlcNAc in 97 percent yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05593887
出典データセットuspto-grants-1997_01
ORD IDord-43871dab186d42b3850b75c2d43cf09b
出典メモuspto-grants-1997_01