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L-硫代瓜氨酸、L-高硫代瓜氨酸和S-甲基-L-硫代瓜氨酸的合成:一类新型强效一氧化氮合酶抑制剂。

Synthesis of L-thiocitrulline, L-homothiocitrulline, and S-methyl-L-thiocitrulline: a new class of potent nitric oxide synthase inhibitors.

作者信息

Narayanan K, Griffith O W

机构信息

Department of Biochemistry, Medical College of Wisconsin, Milwaukee 53226.

出版信息

J Med Chem. 1994 Apr 1;37(7):885-7. doi: 10.1021/jm00033a004.

Abstract

Nitric oxide synthase catalyzes the NADPH- and O2-dependent conversion of L-arginine to L-citrulline and nitric oxide. L-Thiocitrulline, L-homothiocitrulline, and S-methyl-L-thiocitrulline, novel citrulline analogs, have been synthesized and are shown to be potent inhibitors of both the constitutive brain and the inducible smooth muscle isoforms of nitric oxide synthase. Although many N omega-monosubstituted arginine derivatives inhibit nitric oxide synthase, inhibitory citrulline derivatives have not previously been reported. S-Methyl-L-thiocitrulline is significantly more potent than N omega-methyl-L-arginine, the prototypic nitric oxide synthase inhibitor.

摘要

一氧化氮合酶催化L-精氨酸在依赖烟酰胺腺嘌呤二核苷酸磷酸(NADPH)和氧气的条件下转化为L-瓜氨酸和一氧化氮。L-硫代瓜氨酸、L-高硫代瓜氨酸和S-甲基-L-硫代瓜氨酸是新型瓜氨酸类似物,已被合成出来,并且被证明是一氧化氮合酶组成型脑亚型和诱导型平滑肌亚型的有效抑制剂。尽管许多Nω-单取代精氨酸衍生物可抑制一氧化氮合酶,但此前尚未有抑制性瓜氨酸衍生物的报道。S-甲基-L-硫代瓜氨酸的效力明显高于一氧化氮合酶的原型抑制剂Nω-甲基-L-精氨酸。

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