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有联系。

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

也抑制其他丝和半胱蛋白酶，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).

半胱所带有硫氢基（硫醇）决定了整个谷胱甘肽分子性质。

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竞争性抑制剂。也抑制鼠肝细胞中磷酯酶D和C活。

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蛋白酶，可能参与动脉粥样硬斑块演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白酶，如菠萝白酶、无花果白酶和木瓜白酶。

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.

组织白酶K，一种强有力的溶胶原半胱白酶，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）决定了整个胱子的化学性质。

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）决定了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）决定了整个谷分子的化学性。

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

醛。丝酸和半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.

也抑制其他的丝和蛋白，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).

所带有的硫氢（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.

也抑制其他的丝酸半胱酸蛋，如菠萝蛋、无花果蛋木瓜蛋。

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。丝酸半胱酸蛋可逆的竞争性抑制剂。也抑制鼠肝细胞中磷酸酯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.

组织蛋K，一种强有力的溶胶原半胱酸蛋，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。