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

也抑制其他的丝和半胱蛋白，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).

半胱所有的硫氢基（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。丝和半胱蛋白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.

组织蛋白K，一种强有力的溶胶原半胱蛋白，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。

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).

半胱酸所带有基（醇）决定了整个谷胱甘分子化学性质。

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

三醛。丝酸和半胱酸蛋白可逆竞争性抑制剂。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，可能参与动脉粥样硬化斑块演化及与斑块不稳定有联系。

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).

半胱酸所有硫氢基（硫醇）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。也抑制鼠肝细胞中磷酸酯酶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。

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

也抑制其他的丝胱，如菠萝、无花果木瓜。

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。丝胱可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酯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K，一种强有力的溶胶原胱，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。

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

其他的丝酸和半胱酸蛋白，如菠萝蛋白、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。丝酸和半胱酸蛋白可逆的竞争性剂。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.

组织蛋白K，一种强有力的溶胶原半胱酸蛋白，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。

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

也抑制其他的酸和半胱酸蛋白酶，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）决定了整个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。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稳定有联系。

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

也抑制其他的丝和半蛋白酶，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).

半所带有的硫氢基（硫醇）决定了整个谷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。丝和半蛋白酶可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酯酶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。

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

也抑制其他的丝和半胱蛋白酶，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).

半胱所带有的硫氢基（硫醇）决定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。丝和半胱蛋白酶可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酶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。

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

也抑制其他的丝酶，如菠萝酶、无花果酶木瓜酶。

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

所带有的硫氢基（硫醇）决定了整个谷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.

组织酶K，一种强有力的溶胶原酶，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。