Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Synthesis and Quantitative Structure-Activity Relationship of N-(3-Oxo-3, 4-dihydro-2H-benzo[1, 4]oxazine-5-carbonyl)guanidines as Na/H Exchange Inhibitors
Takeshi YAMAMOTOManabu HORIIkuo WATANABEHisayoshi TSUTSUIKengo HARADAShoji IKEDAJoji MARUOTominori MORITAHiroshi OHTAKA
Author information
JOURNAL FREE ACCESS

1998 Volume 46 Issue 11 Pages 1716-1723

Details
Abstract

N-(3-Oxo-3, 4-dihydro-2H-benzo[1, 4]oxazine-6-carbonyl)guanidines 4 were prepared and tested for Na/H exchange inhibitory activities in order to clarify the structure-activity relationship (SAR). Quantitative SAR (QSAR) analysis of 6-carbonylguanidines 4 indicated that the length of the 4-substituent was parabolically related to activity and that the calculated optimum 4-substituents were propyl, ethyl and isopropyl groups. This SAR was similar to the SAR of the 2- and 4-substituents of 7-carbonylguanidine derivatives 3, although the position relative to the essential guanidinocarbonyl group was different. Larger 2-substituents, such as a phenyl group were unfovorable. The most potent derivative in this series was N-(4-isopropyl-2, 2-dimethyl-3-oxo-3, 4-dihydro-2H-benzo[1, 4]oxazine-6-carbonyl)guanidine 4g, with an IC50 value of 0.12 μM. The methanesulfonate salt (KB-R9032) of 4g had excellent water-solubility and showed anti-arrhythmia activity against a rat acute myocardial infarction model. KB-R9032 was selected for further investigation as a therapy for ischemia-reperfusion induced injury.

Content from these authors
© The Pharmaceutical Society of Japan
Previous article Next article
feedback
Top