CAS: 2495-96-7; N-((2R,3R,4R,5S,6R)-2-Ethoxy-4,5-Dihydroxy-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-3-yl)Acetamide

该化合物是N-eterylglucosamine的胶质衍生物,通常用于血液生物学和碳水化合物化学研究,其乙基甘基边联系与免费减少糖相比增强了稳定性,使其适合用于酶和合成研究.β配置确保与生物系统兼容,特别是在研究甘油和甘油酶转移酶活动方面.该化合物是合成寡醇酸盐和甘醇基甲的有价值的中间体,对立体化学进行精确控制.其在极地有机溶剂和水中的溶性促进了多种实验应用.研究人员在对碳水化合物加工酶的机械性研究中支持其明确的结构和可靠性.

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相似化合物

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上下游产品

CAS号76155-50-5 乙基-2-乙酰氨基-3,4,6... | CAS号64-17-5 乙醇 | CAS号7512-17-6 N-乙酰-D-氨基葡萄糖 | CAS号3068-34-6 2-乙酰氨基-3,4,6-三-... | CAS号10034-19-2 (2R,3R,4R,5S,6R... | CAS号51533-00-7 trans-1-methoxy... | CAS号3006-60-8 2-(乙酰氨基)-2-脱氧-B...

合成工艺路线路线简述

  • 合成目标产物 Ethyl 2-Acetamido-2-Deoxy-Beta-D-Glucopyranoside 主要起始原料 Ethyl 2-Acetamido-3,4,6-Tri-O-Acetyl-2-Deoxy-Beta-D-Glucopyranoside
  • (文献来源)合成步骤主要原料 Ethyl 2-Acetamido-3,4,6-Tri-O-Acetyl-2-Deoxy-Beta-D-Glucopyranoside
📜2-乙酰氨基-3,4,6-三-O-乙酰-2-脱氧-α-D-吡喃葡萄糖酰基氯置于甲醇,Sodium Methylate,氰化汞体系中,化学反应 27.0H,反应生成乙基-2-乙酰氨基-2-脱氧-β-D-吡喃葡萄糖苷
参考文献:Discovery Of The Chemical Function Of Glycosidases: Design,Synthesis,And Evaluation Of Mass-Differentiated Carbohydrate Libraries
标题:Discovery Of The Chemical Function Of Glycosidases: Design,Synthesis,And Evaluation Of Mass-Differentiated Carbohydrate Libraries
摘要:Discovery Of The Catalytic Chemical Function Of The Many Putative Glycosidases Coded In Genomes Currently Relies On Individual Testing Of Possible Substrates,Usually As Their P-Nitrophenol Conjugate. Herein,We Present An Alternative Chemical Proteomics Approach Using A Synthetic Mass-Differentiated Heat-Stable Substrate Library With Mass Spectrometry Readout. Library Components Do Not Serve As Reaction Inhibitors And Both Primary And Secondary Enzyme Substrates Can Be Delineated.
Doi:10.1021/ol049389B

海关参考信息

专利信息


专利号:US-8816050-B2
优先权日:2006-03-22
标题:Method of preparing glycopeptides
发明人:WONG CHI-HUEY; BRIK ASHRAF; YANG YU-YING; FICHT SIMON; PAYNE RICHARD
权利人:WONG CHI-HUEY; BRIK ASHRAF; YANG YU-YING; FICHT SIMON; PAYNE RICHARD; SCRIPPS RESEARCH INST
摘要:A method is provided for the synthesis of glycopeptides using a sugar assisted ligation strategy, wherein an N-terminal peptide portion in the form of a thioester is coopled with a C-terminal peptide portion bearing a carbohydrate moiety comprising a thiol group.

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✅ COA系统入驻 | 共享模式

合成参考文献

合成方法参考DOI号:10.1021/ol049389b
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