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两种新型柳氮磺胺吡啶类似物——依沙拉嗪和巴柳氮的研究。

Studies of two novel sulfasalazine analogs, ipsalazide and balsalazide.

作者信息

Chan R P, Pope D J, Gilbert A P, Sacra P J, Baron J H, Lennard-Jones J E

出版信息

Dig Dis Sci. 1983 Jul;28(7):609-15. doi: 10.1007/BF01299921.

Abstract

Sulfasalazine appears to exert its beneficial effect in colitis by releasing 5-aminosalicylic acid in the colon, but its use can be limited by side effects. Ipsalazide and balsalazide are novel sulfasalazine analogs designed to release 5-aminosalicylic acid and a nontoxic carrier molecule in the gastrointestinal tract. They have a low oral toxicity following single or repeat administration to mouse, rat, and ferret, and balsalazide is not mutagenic in the Ames test. Ipsalazide and balsalazide are split in rat and man, and the urinary and fecal excretion pattern of the 5-aminosalicylic acid released is similar to that of sulfasalazine; the carrier molecules are absorbed to a lesser extent than the sulfapyridine derived from sulfasalazine. These two analogs deserve therapeutic trial.

摘要

柳氮磺胺吡啶似乎通过在结肠中释放5-氨基水杨酸而在结肠炎中发挥有益作用,但其使用可能受到副作用的限制。伊泼拉嗪和巴柳氮是新型柳氮磺胺吡啶类似物,设计用于在胃肠道中释放5-氨基水杨酸和一种无毒载体分子。对小鼠、大鼠和雪貂单次或重复给药后,它们的口服毒性较低,并且巴柳氮在艾姆斯试验中无致突变性。伊泼拉嗪和巴柳氮在大鼠和人体中会分解,释放出的5-氨基水杨酸的尿排泄和粪排泄模式与柳氮磺胺吡啶相似;载体分子的吸收程度低于柳氮磺胺吡啶衍生的磺胺吡啶。这两种类似物值得进行治疗试验。

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