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trans-3-cyclopropylcarbamoylpropenoic acid

中文名称
——
中文别名
——
英文名称
trans-3-cyclopropylcarbamoylpropenoic acid
英文别名
HOOC-CH=CHCONH-cyclopropyl;(Z)-3-Cyclopropylcarbamoyl-acrylic acid;(E)-4-(cyclopropylamino)-4-oxobut-2-enoic acid
trans-3-cyclopropylcarbamoylpropenoic acid化学式
CAS
——
化学式
C7H9NO3
mdl
——
分子量
155.153
InChiKey
JRJTUGAKFMYQEE-ONEGZZNKSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.1
  • 重原子数:
    11
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    66.4
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    trans-3-cyclopropylcarbamoylpropenoic acid 、 Mu-Ala-NH-NH-CH2CONH2 在 1-羟基苯并三唑N,N'-二环己基碳二亚胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以67%的产率得到N2-(N-piperidinylcarbonylalanyl)-N1-(carbamoylmethyl)-N1-trans-(3-cyclopropylcarbamoylpropenoyl)hydrazine
    参考文献:
    名称:
    Aza-Peptidyl Michael Acceptor and Epoxide Inhibitors—Potent and Selective Inhibitors of Schistosoma mansoni and Ixodes ricinus Legumains (Asparaginyl Endopeptidases)
    摘要:
    Aza-peptide Michael acceptors and epoxides with the general structure of YCO-Ala-Ala-AAsn-trans-CH=CHCOR and YCO-Ala-Ala-AAsn-EP-COR, respectively, are shown to be potent inhibitors of asparaginyl endopeptidases (legumains) from the bloodfluke, Schistosoma mansoni (SmAE), and the hard tick, Ixodes ricinus (IrAE). Structure-activity relationships (SARs) were determined for a set of 41 aza-peptide Michael acceptors and eight aza-peptide epoxides. Both enzymes prefer disubstituted amides to monosubstituted amides in the P1' position, and potency increased as we increased the hydrophobicity of the inhibitor in this position. Extending the inhibitor to P5 resulted in increased potency, especially against IrAE, and both enzymes prefer small over large hydrophobic residues at P2. Aza-peptide Michael acceptor inhibitors are more potent than aza-peptide epoxide inhibitors, and for some of these compounds, second-order inhibiton rate constants are the fastest yet discovered. Given the central functions of these enzymes in both parasites, the data presented here may facilitate the eventual design of selective antiparasitic drugs.
    DOI:
    10.1021/jm900849h
  • 作为产物:
    描述:
    trans-3-cyclopropylcarbamoylpropenoic acid ethyl ester 在 、 sodium hydroxide 作用下, 以 乙醇 为溶剂, 以91%的产率得到trans-3-cyclopropylcarbamoylpropenoic acid
    参考文献:
    名称:
    Aza-Peptidyl Michael Acceptor and Epoxide Inhibitors—Potent and Selective Inhibitors of Schistosoma mansoni and Ixodes ricinus Legumains (Asparaginyl Endopeptidases)
    摘要:
    Aza-peptide Michael acceptors and epoxides with the general structure of YCO-Ala-Ala-AAsn-trans-CH=CHCOR and YCO-Ala-Ala-AAsn-EP-COR, respectively, are shown to be potent inhibitors of asparaginyl endopeptidases (legumains) from the bloodfluke, Schistosoma mansoni (SmAE), and the hard tick, Ixodes ricinus (IrAE). Structure-activity relationships (SARs) were determined for a set of 41 aza-peptide Michael acceptors and eight aza-peptide epoxides. Both enzymes prefer disubstituted amides to monosubstituted amides in the P1' position, and potency increased as we increased the hydrophobicity of the inhibitor in this position. Extending the inhibitor to P5 resulted in increased potency, especially against IrAE, and both enzymes prefer small over large hydrophobic residues at P2. Aza-peptide Michael acceptor inhibitors are more potent than aza-peptide epoxide inhibitors, and for some of these compounds, second-order inhibiton rate constants are the fastest yet discovered. Given the central functions of these enzymes in both parasites, the data presented here may facilitate the eventual design of selective antiparasitic drugs.
    DOI:
    10.1021/jm900849h
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文献信息

  • CYCLOPROPYL COMPOUNDS AND COMPOSITIONS FOR DELIVERING ACTIVE AGENTS
    申请人:Tang Pingwah
    公开号:US20090220451A1
    公开(公告)日:2009-09-03
    Compounds and compositions for the delivery of active agents are provided. Methods of administration and preparation are provided as well.
    提供用于传递活性剂的化合物和组合物。同时提供了给药和制备方法。
  • US8541362B2
    申请人:——
    公开号:US8541362B2
    公开(公告)日:2013-09-24
  • [EN] CYCLOPROPYL COMPOUNDS AND COMPOSITIONS FOR DELIVERING ACTIVE AGENTS<br/>[FR] COMPOSES CYCLOPROPYLES ET COMPOSITIONS PERMETTANT DE LIBERER DES AGENTS ACTIFS
    申请人:EMISPHERE TECH INC
    公开号:WO2007022532A2
    公开(公告)日:2007-02-22
    [EN] Compounds and compositions for the delivery of active agents are provided. Methods of administration and preparation are provided as well.
    [FR] La présente invention concerne des composés et des compositions permettant de délibérer des agents actifs. Cette invention concerne également des procédés d'administration et de préparation correspondants.
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