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Organic compounds useful for the treatment of a disease mediated by the inhibition of aldosterone synthase
专利权人:
NOVARTIS AG
发明人:
ADAMS, CHRISTOPHER,HU, QI-YING,MCQUIRE, LESLIE WIGHTON,PAPILLON, JULIEN
申请号:
NZ58966609
公开号:
NZ589666A
申请日:
2009.06.25
申请国别(地区):
NZ
年份:
2012
代理人:
摘要:
Disclosed are indole-pyridine compounds represented by general formula (II). Examples of the compounds of formula (II) are: N-Methyl-N-[5-(1-methyl-3-cyano-1H-indol-2-yl)-pyridin-3-ylmethyl]-methanesulfonamide; N-[5-(6-Chloro-3-cyano-1-methyl-1H-indol-2-yl)-pyridin-3-ylmethyl]-N-methylmethanesulfonamide; and 2,2,2-Trifluoro-ethanesulfonic acid [5-(6-chloro-3-cyano-1-methyl-1H-indol-2-yl)-pyridin-3-ylmethyl]-amide. The compounds are used to treat heart failure, congestive heart failure, arrhythmia, diastolic dysfunction, left ventricular diastolic dysfunction, diastolic heart failure, impaired diastolic filling, systolic dysfunction, ischemia, hypertropic cardiomyopathy, sudden cardiac death, myocardial and vascular fibrosis, impaired arterial compliance, myocardial necrotic lesions, vascular damage, myocardial infarction, left ventricular hypertrophy, decreased ejection fraction, cardiac lesions, vascular wall hypertrophy, endothelial thickening, fibrinoid necrosis of coronary arteries, renal dysfunction, liver diseases, cerebrovascular diseases, vascular diseases, retinopathy, neuropathy, insulinopathy, edema, endothelial dysfunction, baroreceptor dysfunction, migraine headaches, and hypertension. These are diseases or disorders all mediated by the inhibition of aldosterone synthase.
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