N-phenethyl(1'-(benzyloxy)-3',4'-epoxy-1'-oxophosphol-2'-yl)acetamide | 163929-72-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-phenethyl(1'-(benzyloxy)-3',4'-epoxy-1'-oxophosphol-2'-yl)acetamide
• CAS: 163929-72-4
• 化学式: C₂₁H₂₄NO₄P
• 分子量: 385.4
• InChiKey: IKBAQPGZPRPNBU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.38
• 重原子数：
  27.0
• 可旋转键数：
  8.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  67.93
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  N-phenethyl(1'-(benzyloxy)-3',4'-epoxy-1'-oxophosphol-2'-yl)acetamide 在 叠氮基三甲基硅烷 、 水 、 aluminum isopropoxide 、 三苯基膦 作用下， 生成 N-phenethyl(1'-(benzyloxy)-3'-hydroxy-4'-amino-1'-oxophosphol-2'-yl)acetamide
  参考文献：
  名称：

  Antibody-Catalyzed Rearrangement of a Peptide Bond: Mechanistic and Kinetic Investigations

  摘要：

  Catalysis of the deamidation of asparagine residues may provide a powerful method for the deactivation of proteins. Catalytic antibodies (Gibbs et al. Science 1992, 258, 803) have been induced that catalyze the deamidation of a model dipeptide through an intermediate succinimide. Investigations of the mechanistic characteristics of two such antibodies, RG2-23C7 and RG2-2E4, revealed their ability to accelerate the hydrolysis of either the R- or S-enantiomers of the succinimide by factors of 10-500-fold to yield differing ratios of the aspartate and isoaspartate products. The mixed product ratios imply that two tetrahedral binding sites of unequal effectiveness were induced in response to the tetrahedral mimics (a phosphinate or secondary hydroxyl) within the hapten structure. The antibody RG2-2E4 also catalyzes the deamidation of either the D- or L-asparagine within the dipeptide through the intermediate cyclic imide, resulting in a multistep reaction sequence featuring a series of tetrahedral transition states. pH-rate profiles do not implicate functional groups within the antibodies' combining sites for either the deamidation or hydrolytic reactions. The strategy of bifunctional or higher order transition state mimics should provide a route to developing catalytic antibodies for reactions requiring multistep processing.

  DOI：

  10.1021/ja00122a001
• 作为产物：
  描述：

  N-phenethyl(1'-(benzyloxy)-1'-oxophosphol-3'-en-2'-yl)acetamide 在 间氯过氧苯甲酸 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 以57%的产率得到N-phenethyl(1'-(benzyloxy)-3',4'-epoxy-1'-oxophosphol-2'-yl)acetamide
  参考文献：
  名称：

  Antibody-Catalyzed Rearrangement of a Peptide Bond: Mechanistic and Kinetic Investigations

  摘要：

  Catalysis of the deamidation of asparagine residues may provide a powerful method for the deactivation of proteins. Catalytic antibodies (Gibbs et al. Science 1992, 258, 803) have been induced that catalyze the deamidation of a model dipeptide through an intermediate succinimide. Investigations of the mechanistic characteristics of two such antibodies, RG2-23C7 and RG2-2E4, revealed their ability to accelerate the hydrolysis of either the R- or S-enantiomers of the succinimide by factors of 10-500-fold to yield differing ratios of the aspartate and isoaspartate products. The mixed product ratios imply that two tetrahedral binding sites of unequal effectiveness were induced in response to the tetrahedral mimics (a phosphinate or secondary hydroxyl) within the hapten structure. The antibody RG2-2E4 also catalyzes the deamidation of either the D- or L-asparagine within the dipeptide through the intermediate cyclic imide, resulting in a multistep reaction sequence featuring a series of tetrahedral transition states. pH-rate profiles do not implicate functional groups within the antibodies' combining sites for either the deamidation or hydrolytic reactions. The strategy of bifunctional or higher order transition state mimics should provide a route to developing catalytic antibodies for reactions requiring multistep processing.

  DOI：

  10.1021/ja00122a001

文献信息

• Antibody-Catalyzed Rearrangement of a Peptide Bond: Mechanistic and Kinetic Investigations
  作者：Louis J. Liotta、Richard A. Gibbs、Scott D. Taylor、Patricia A. Benkovic、Stephen J. Benkovic

  DOI：10.1021/ja00122a001

  日期：1995.5

  Catalysis of the deamidation of asparagine residues may provide a powerful method for the deactivation of proteins. Catalytic antibodies (Gibbs et al. Science 1992, 258, 803) have been induced that catalyze the deamidation of a model dipeptide through an intermediate succinimide. Investigations of the mechanistic characteristics of two such antibodies, RG2-23C7 and RG2-2E4, revealed their ability to accelerate the hydrolysis of either the R- or S-enantiomers of the succinimide by factors of 10-500-fold to yield differing ratios of the aspartate and isoaspartate products. The mixed product ratios imply that two tetrahedral binding sites of unequal effectiveness were induced in response to the tetrahedral mimics (a phosphinate or secondary hydroxyl) within the hapten structure. The antibody RG2-2E4 also catalyzes the deamidation of either the D- or L-asparagine within the dipeptide through the intermediate cyclic imide, resulting in a multistep reaction sequence featuring a series of tetrahedral transition states. pH-rate profiles do not implicate functional groups within the antibodies' combining sites for either the deamidation or hydrolytic reactions. The strategy of bifunctional or higher order transition state mimics should provide a route to developing catalytic antibodies for reactions requiring multistep processing.