monopeptide bond
单肽键
monopeptide synthesis
单肽合成
containing monopeptides
含有单肽
monopeptide sequence
单肽序列
monopeptide structure
单肽结构
monopeptides form
单肽形成
monopeptide chain
单肽链
monopeptide cleavage
单肽裂解
monopeptide analysis
单肽分析
monopeptide fragments
单肽片段
the monopeptide exhibited strong binding affinity to the receptor.
该单肽表现出对受体的强结合亲和力。
synthesis of the monopeptide was achieved using solid-phase peptide synthesis.
单肽的合成使用固相肽合成法实现。
we designed a monopeptide to mimic a natural protein sequence.
我们设计了一种单肽来模仿天然蛋白质序列。
the monopeptide's structure was analyzed by nmr spectroscopy.
单肽的结构通过核磁共振波谱法进行分析。
the monopeptide demonstrated selective inhibition of the enzyme.
该单肽表现出对酶的选择性抑制作用。
modifications to the monopeptide improved its stability in solution.
对单肽的改性提高了其在溶液中的稳定性。
the monopeptide was conjugated to a carrier protein for enhanced immunogenicity.
单肽与载体蛋白结合以增强免疫原性。
we screened a library of monopeptides for potential drug candidates.
我们筛选了一组单肽库以寻找潜在的药物候选者。
the monopeptide's biological activity was evaluated in vitro.
单肽的生物活性在体外进行评估。
a cyclic monopeptide was synthesized to enhance proteolytic stability.
合成了一种环状单肽以增强蛋白水解稳定性。
the monopeptide's sequence was optimized for improved cell permeability.
优化了单肽序列以提高细胞渗透性。
monopeptide bond
单肽键
monopeptide synthesis
单肽合成
containing monopeptides
含有单肽
monopeptide sequence
单肽序列
monopeptide structure
单肽结构
monopeptides form
单肽形成
monopeptide chain
单肽链
monopeptide cleavage
单肽裂解
monopeptide analysis
单肽分析
monopeptide fragments
单肽片段
the monopeptide exhibited strong binding affinity to the receptor.
该单肽表现出对受体的强结合亲和力。
synthesis of the monopeptide was achieved using solid-phase peptide synthesis.
单肽的合成使用固相肽合成法实现。
we designed a monopeptide to mimic a natural protein sequence.
我们设计了一种单肽来模仿天然蛋白质序列。
the monopeptide's structure was analyzed by nmr spectroscopy.
单肽的结构通过核磁共振波谱法进行分析。
the monopeptide demonstrated selective inhibition of the enzyme.
该单肽表现出对酶的选择性抑制作用。
modifications to the monopeptide improved its stability in solution.
对单肽的改性提高了其在溶液中的稳定性。
the monopeptide was conjugated to a carrier protein for enhanced immunogenicity.
单肽与载体蛋白结合以增强免疫原性。
we screened a library of monopeptides for potential drug candidates.
我们筛选了一组单肽库以寻找潜在的药物候选者。
the monopeptide's biological activity was evaluated in vitro.
单肽的生物活性在体外进行评估。
a cyclic monopeptide was synthesized to enhance proteolytic stability.
合成了一种环状单肽以增强蛋白水解稳定性。
the monopeptide's sequence was optimized for improved cell permeability.
优化了单肽序列以提高细胞渗透性。
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