- 영문명
- Receptor-Ligand Binding Characteristics of KR-31064
- 발행기관
- 대한약학회
- 저자명
- 이승호
- 간행물 정보
- 『약학회지』제58권 제1호 (2014년), 16~20쪽, 전체 5쪽
- 주제분류
- 의약학 > 기타의약학
- 파일형태
- 발행일자
- 2014.02.28

국문 초록
영문 초록
KR-31064 was developed for the strong angiotensin II receptor antagonist among the one of pyridyl imidazol
series compounds. To investigate the receptor-ligand binding characteristics of this nonpeptide antagonist, binding exper-iments were deployed in various conditions and ex vivo contractile responses were tested toward the standard compound,losartan. Receptor binding experiments with radiolabeled angiotensin II, the IC50 value for KR-31064 resulted 0.67 nM with-out any activities toward type 2 angiotensin II receptor. The comparative potency against losartan was more than 18 foldand the specific activity in type 1 angiotensin II receptor was more than 10,000 fold comparing to the type 2 receptor. Scat-chard analysis of saturation binding data showed KR-31064 acted on the receptor in a competitive mode. KR-31064 inhibited the contractile response derived by angiotensin II (pKB: 9.86) similar to that of losartan with decreased maximum signals. As a potent and specific type 1 angiotensin II receptor antagonist, KR-31064 may have possibilities for the development of diagnostic ligands that can be used as tools for various biochemical research experiments and non-invasive diagnostics.
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재료 및 실험방법
실험결과 및 고찰
결 론
감사의 말씀
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