Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他的丝酸和半胱酸蛋白酶，如菠萝蛋白酶、无花果蛋白酶和木瓜蛋白酶。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

半胱酸所带有的硫氢基（硫醇）决了整个谷胱甘肽分子的化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝酸和半胱酸蛋白酶可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酸酯酶D和C的活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织蛋白酶K，一种强有力的溶胶原半胱酸蛋白酶，可能参与动脉粥样硬化斑块的演化及与斑块不有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原子荧光光谱法,用L-半胱酸预还原法,对涂料中砷和锑进行了分析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他丝酸和半胱酸蛋白酶，如菠萝蛋白酶、无花果蛋白酶和木瓜蛋白酶。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

半胱酸所带有氢基（醇）决定了整个谷胱甘肽分子化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝酸和半胱酸蛋白酶可逆竞争性抑制剂。也抑制鼠肝细酸酯酶D和C活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织蛋白酶K，一种强有力溶胶原半胱酸蛋白酶，可能参与动脉粥样硬化斑块演化及与斑块不稳定有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原子荧光光谱法,用L-半胱酸预还原法,对涂料砷和锑进行了分析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他的丝胱蛋白酶，如菠萝蛋白酶、无花果蛋白酶木瓜蛋白酶。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

胱所带有的硫氢基（硫醇）决定了整个谷胱甘肽分子的化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝胱蛋白酶可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酯酶DC的活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织蛋白酶K，一种强有力的溶胶原胱蛋白酶，可能脉粥样硬化斑块的演化及斑块不稳定有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原子荧光光谱法,用L-胱预还原法,对涂料中砷锑进行了分析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他的丝酸和半胱酸，如菠萝、无花果和木瓜。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

半胱酸所带有的硫氢基（硫醇）决定了整个谷胱甘肽分子的化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝酸和半胱酸可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酸酯D和C的活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织K，有力的溶胶原半胱酸，可能参与动脉粥样硬化斑块的演化及与斑块不稳定有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原子荧光光谱法,用L-半胱酸预还原法,对涂料中砷和锑进行了分析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

制其他的丝酸和半胱酸蛋白酶，如菠萝蛋白酶、无花果蛋白酶和木瓜蛋白酶。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

半胱酸所带有的硫氢基（硫醇）整个谷胱甘肽分子的化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝酸和半胱酸蛋白酶可逆的竞争性制。制鼠肝细胞中磷酸酯酶D和C的活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织蛋白酶K，一种强有力的溶胶原半胱酸蛋白酶，可能参与动脉粥样硬化斑块的演化及与斑块不稳有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原子荧光光谱法,用L-半胱酸预还原法,对涂料中砷和锑进行分析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他丝酸和半胱酸蛋白酶，如菠萝蛋白酶、无花果蛋白酶和木瓜蛋白酶。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

半胱酸所带有基（醇）决定了整个谷胱甘肽分子化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝酸和半胱酸蛋白酶可逆竞争性抑制剂。也抑制鼠肝磷酸酯酶D和C活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织蛋白酶K，一种强有力溶胶原半胱酸蛋白酶，可能参与动脉粥样硬化斑块演化及与斑块不稳定有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用化物发生-原子荧光光谱法,用L-半胱酸预还原法,对涂料砷和锑进行了分析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他的丝胱蛋白酶，如菠萝蛋白酶、无花果蛋白酶木瓜蛋白酶。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

胱所带有的硫氢基（硫醇）决定了整个谷胱甘肽分子的化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝胱蛋白酶可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酯酶DC的活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织蛋白酶K，一种强有力的溶胶原胱蛋白酶，可能脉粥样硬化斑块的演化及斑块不稳定有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原子荧光光谱法,用L-胱预还原法,对涂料中砷锑进行了分析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他丝酸和半胱酸蛋白，如菠萝蛋白、无花果蛋白和木瓜蛋白。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

半胱酸所带有硫氢基（硫醇）决定了整个谷胱甘肽化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝酸和半胱酸蛋白竞争性抑制剂。也抑制鼠肝细胞中磷酸酯D和C活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织蛋白K，一种强有力溶胶原半胱酸蛋白，能参与动脉粥样硬化斑块演化及与斑块不稳定有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原荧光光谱法,用L-半胱酸预还原法,对涂料中砷和锑进行了析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他的丝和半胱，菠萝、无花果和木瓜。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

半胱所带有的硫氢基（硫醇）决定了整个谷胱甘肽分子的化学性质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝和半胱可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酯D和C的活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织K，一种强有力的溶胶原半胱，可能参与动脉粥样硬化斑块的演化及与斑块不稳定有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原子荧光光谱法,用L-半胱预还原法,对涂料中砷和锑进行了分析。

Inhibits also some other serine and cysteine proteases like bromelain, ficin and papain.

也抑制其他的丝酸和半酸蛋白酶，如菠萝蛋白酶、无花果蛋白酶和木瓜蛋白酶。

The sulfhydryl (thiol) group (SH) of cysteine is responsible for the chemical properties of the whole GSH molecule (L-gamma-glutamyl-Lcysteinylglycine).

半酸所带有的硫氢基（硫醇）决定了整个肽分子的化学质。

Tripeptide aldehyde. Reversible competitive inhibitor of serine and cysteine proteases. Inhibits also phospholipase D and C activation in rat hepatocytes.

三肽醛。丝酸和半酸蛋白酶可逆的抑制剂。也抑制鼠肝细胞中磷酸酯酶D和C的活化。

Background— Cathepsin K (CatK), a potent elastinolytic and collagenolytic cysteine protease, likely participates in the evolution and destabilization of atherosclerotic plaques.

组织蛋白酶K，一种强有力的溶胶原半酸蛋白酶，可能参与动脉粥样硬化斑块的演化及与斑块不稳定有联系。

The content of As and Sb in paints are analyzed by hydride generat io n atomic fluorescence spectrometry (HG-AFS) and L-cysteine prereduction proces s.

采用氢化物发生-原子荧光光谱法,用L-半酸预还原法,对涂料中砷和锑进行了分析。