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Sulfonyliminoimidazolidines. A new class of oral hypoglycemic agents. 1. 1-[[p-[2-(acylamino)ethyl]phenyl]sulfonyl]-2-iminoimidazolidines.

作者信息

Schweizer E H, Märki F, Lehmann C, Dietrich H

出版信息

J Med Chem. 1983 Jul;26(7):964-70. doi: 10.1021/jm00361a006.

DOI:10.1021/jm00361a006
PMID:6864736
Abstract

A series of 1-[[p-[2-(acylamino)ethyl]phenyl]sulfonyl]-2-iminoimidazolidines has been synthesized. Compounds from this new class of oral hypoglycemic agents lower blood glucose in normal and in streptozotocin-diabetic rats. Potent analogues were obtained by modification of the acyl residue. 1-[[p-[2-(Crotonylamino)ethyl]phenyl]-sulfonyl]-3-cyclohexyl-2-iminoimidazolidine (44) turned out to be the most potent compound in the normal rat (20 times tolbutamide), and 1-[[p-[2-(5-methylisoxazole-3-carboxamido)ethyl]phenyl]sulfonyl]-3-cyclohexyl-2-imino-imidazolidine (30) displayed the highest potency in the diabetic rat (similar to phenformin).

摘要

相似文献

1
Sulfonyliminoimidazolidines. A new class of oral hypoglycemic agents. 1. 1-[[p-[2-(acylamino)ethyl]phenyl]sulfonyl]-2-iminoimidazolidines.
J Med Chem. 1983 Jul;26(7):964-70. doi: 10.1021/jm00361a006.
2
Sulfonyliminoimidazolidines. A new class of oral hypoglycemic agents. 2. Mode of action and X-ray structure of 1-[[p-[2-(crotonylamino)ethyl]phenyl]sulfonyl]-3-cyclohexyl-2-iminoimidazolidine.磺酰亚氨基咪唑烷。一类新型口服降糖药。2. 1-[[对-[2-(巴豆酰氨基)乙基]苯基]磺酰基]-3-环己基-2-亚氨基咪唑烷的作用方式及X射线结构
J Med Chem. 1983 Jul;26(7):970-3. doi: 10.1021/jm00361a007.
3
Sulfonyliminoimidazolidines, a new class of oral hypoglycemic agents. 3. Hypoglycemic activity and mode of action of 1-[p-[2-(crotonylamino)-ethyl]-phenylsulfonyl]-3-cyclohexyl-2-imino- imidazolidine (CGP 11 112).磺酰亚氨基咪唑烷类,一类新型口服降糖药。3. 1-[对-[2-(巴豆酰氨基)-乙基]-苯磺酰基]-3-环己基-2-亚氨基咪唑烷(CGP 11 112)的降糖活性及作用方式
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Sulfonyliminoimidazolidines, a new class of oral hypoglycemic agents. 4. Toxicity and general pharmacology of 1-[p-[2-(crotonylamino)-ethyl]-phenylsulfonyl]-3-cyclohexy l-2-imino- imidazolidine (CGP 11 112).
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A novel series of non-carboxylic acid, non-hydantoin inhibitors of aldose reductase with potent oral activity in diabetic rat models: 6-(5-chloro-3-methylbenzofuran-2-sulfonyl)-2H-pyridazin-3-one and congeners.在糖尿病大鼠模型中具有强效口服活性的新型非羧酸、非乙内酰脲类醛糖还原酶抑制剂系列:6-(5-氯-3-甲基苯并呋喃-2-磺酰基)-2H-哒嗪-3-酮及其同系物。
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Effects of glucose and some oral hypoglycemic agents upon the plasma glucose and immuno-reactive insulin (IRI) in normal and streptozotocin induced diabetic rat.葡萄糖及某些口服降糖药对正常及链脲佐菌素诱导的糖尿病大鼠血糖和免疫反应性胰岛素(IRI)的影响。
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