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Cbz-Lys-N-ε-Boc-Lys-N-ε-Boc-PABC-AMC | 1616957-66-4

中文名称
——
中文别名
——
英文名称
Cbz-Lys-N-ε-Boc-Lys-N-ε-Boc-PABC-AMC
英文别名
benzyloxycarbonyl-Lys-N-ε-(tert-butoxycarbonyl)-Lys-N-ε-(tert-butoxycarbonyl)-PABC-(7-amino-4-methylcoumarin);[4-[[(2S)-6-[(2-methylpropan-2-yl)oxycarbonylamino]-2-[[(2S)-6-[(2-methylpropan-2-yl)oxycarbonylamino]-2-(phenylmethoxycarbonylamino)hexanoyl]amino]hexanoyl]amino]phenyl]methyl N-(4-methyl-2-oxochromen-7-yl)carbamate
Cbz-Lys-N-ε-Boc-Lys-N-ε-Boc-PABC-AMC化学式
CAS
1616957-66-4
化学式
C48H62N6O12
mdl
——
分子量
915.053
InChiKey
MIGBROSZHBNPPY-UWXQCODUSA-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):
    6.3
  • 重原子数:
    66
  • 可旋转键数:
    26
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    238
  • 氢给体数:
    6
  • 氢受体数:
    12

反应信息

  • 作为反应物:
    描述:
    Cbz-Lys-N-ε-Boc-Lys-N-ε-Boc-PABC-AMC三氟乙酸二氯甲烷 为溶剂, 反应 0.25h, 以47%的产率得到Cbz-Lys-Lys-PABC-AMC*2TFA
    参考文献:
    名称:
    Prodrug-Inspired Probes Selective to Cathepsin B over Other Cysteine Cathepsins
    摘要:
    Cathepsin B (CTB) is a cysteine protease believed to be an important therapeutic target or biomarker for several diseases including aggressive cancer, arthritis, and parasitic infections. The development of probes capable of assessing CTB activity in cell lysates, living cells, and animal models of disease are needed to understand its role in disease progression. However, discovering probes selective to cathepsin B over other cysteine cathepsins is a significant challenge due to overlap of preferred substrates and binding site homology in this family of proteases. Herein we report the synthesis and detailed evaluation of two prodrug-inspired fluorogenic peptides designed to be efficient and selective substrate-based probes for CTB. Through cell lysate and cell assays, a promising lead candidate was identified that is efficiently processed and has high specificity for CTB over other cysteine cathepsins. This work represents a key step toward the design of rapid release prodrugs or substrate-based molecular imaging probes specific to CTB.
    DOI:
    10.1021/jm500544p
  • 作为产物:
    参考文献:
    名称:
    Prodrug-Inspired Probes Selective to Cathepsin B over Other Cysteine Cathepsins
    摘要:
    Cathepsin B (CTB) is a cysteine protease believed to be an important therapeutic target or biomarker for several diseases including aggressive cancer, arthritis, and parasitic infections. The development of probes capable of assessing CTB activity in cell lysates, living cells, and animal models of disease are needed to understand its role in disease progression. However, discovering probes selective to cathepsin B over other cysteine cathepsins is a significant challenge due to overlap of preferred substrates and binding site homology in this family of proteases. Herein we report the synthesis and detailed evaluation of two prodrug-inspired fluorogenic peptides designed to be efficient and selective substrate-based probes for CTB. Through cell lysate and cell assays, a promising lead candidate was identified that is efficiently processed and has high specificity for CTB over other cysteine cathepsins. This work represents a key step toward the design of rapid release prodrugs or substrate-based molecular imaging probes specific to CTB.
    DOI:
    10.1021/jm500544p
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文献信息

  • [EN] CATHEPSIN B-TARGETING PROBES<br/>[FR] SONDES DE CIBLAGE DE LA CATHEPSINE B
    申请人:THUNDER BAY REGIONAL RES INST
    公开号:WO2015123783A1
    公开(公告)日:2015-08-27
    Compounds that are cathepsin B substrates and that are useful as imaging probes, for example in positron emission tomography (PET) or fluorescence imaging are described.
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