Ebrotidine, a unique H-2-receptor antagonist, with gastroprotective activity against acid-dependent and acid-independent ulcerogens.

被引：0

作者：

Brzozowski, T

Konturek, SJ

Konturek, PC

Hahn, EG

机构：

[1] KRAKOW TECH UNIV, SCH MED, EG HAHN INST PHYSIOL, PL-31155 KRAKOW, POLAND

[2] UNIV ERLANGEN NURNBERG, DEPT MED, D-8520 ERLANGEN, GERMANY

来源：

GASTROENTEROLOGY | 1997年 / 112卷 / 04期

关键词：

D O I：

暂无

中图分类号：

R57 [消化系及腹部疾病];

学科分类号：

摘要：

引用

页码：A351 / A351

页数：1

共 48 条

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[45] HEALING-PROMOTING ACTION OF THE NEW HISTAMINE H-2-RECEPTOR ANTAGONIST N-ETHYL-N'-[3-[3-(PIPERIDINOMETHYL)PHENOXY]PROPYL]UREA WITH DUAL ACTION ON CHRONIC GASTRIC AND DUODENAL-ULCERS INDUCED BY ACETIC-ACID IN RATS
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[46] Structure-activity characterization of an H-2-receptor antagonist, 3-amino-4-[4-[4-(1-piperidinomethyl)-2-pyridyloxy]-cis-2-butenylamino]-3-cyclobutene-1,2-dione hydrochloride (IT-066), involved in the insurmountable antagonism against histamine-induced positive chronotropic action in guinea pig atria
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[47] Discovery of 6-oxo-3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-1(6H)pyridazinebutanoic acid (FK838):: A novel non-xanthine adenosine A1 receptor antagonist with potent diuretic activity
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Kato, T
Kinoshita, T
Kita, Y
Kusunoki, T
Terai, T
Yoshida, K
Shiokawa, Y
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (05) : 779 - 783
[48] Structure-activity relationships of a novel class of endothelin-A receptor antagonists and discovery of potent and selective receptor antagonist, 2-(benzo[1,3]dioxol-5-yl)-6-isopropyloxy-4-(4-methoxyphenyl)-2H-chromene-3-carboxylic acid (S-1255).: 1.: Study on structure-activity relationships and basic structure crucial for ETA antagonism
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JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (10) : 2041 - 2055

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