Abstract:
The invention describes novel nitrosated and/or nitrosylated cardiovascular compounds or pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated and/or nitrosylated cardiovascular compound, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides novel compositions and kits comprising at least one cardiovascular compound of the invention, that is optionally nitrosated and/or nitrosylated, and, optionally, at least one nitric oxide donor compound and/or at least one therapeutic agent. The invention also provides methods for (a) treating cardiovascular diseases; (b) treating renovascular diseases; (c) treating diabetes; (d) treating diseases resulting from oxidative stress; (e) treating endothelial dysfunctions; (f) treating diseases caused by endothelial dysfunctions; (g) treating cirrhosis; (h) treating pre-eclampsia; (j) treating osteoporosis; and (k) treating nephropathy. The nitrosated and/or nitrosylated cardiovascular compounds are preferably nitrosated and/or nitrosylated aldosterone antagonists, nitrosated and/or nitrosylated angiotensin II antagonists, nitrosated and/or nitrosylated calcium channel blockers, nitrosated and/or nitrosylated endothelin antagonists, nitrosated and/or nitrosylated hydralazine compounds, nitrosated and/or nitrosylated neutral endopeptidase inhibitors and nitrosated and/or nitrosylated renin inhibitors.
Abstract:
Neue heterocyclische Verbindungen der Formel (I) worin R 1 , D, W, T und T' die in Anspruch 1 angegebenen Bedeutungen haben, sind SGK-Inhibitoren und können zur Behandlung von SGK-bedingten Krankheiten und Leiden wie Diabetes, Fettsucht, metabolisches Syndrom (Dyslipidämie), systemische und pulmonale Hypertonie, Herzkreislauferkrankungen und Nierenerkrankungen, allgemein bei jeglicher Art von Fibrosen und entzündlichen Prozessen verwendet werden.
Abstract:
The present invention is directed at substituted heteroaryl- and phenylsulfamoyl compounds, pharmaceutical compositions containing such compounds and the use of such compounds as peroxisome proliferator activator receptor (PPAR) agonists. PPAR alpha activators, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and/or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases, in mammals, including humans. The compounds are also useful for the treatment of negative energy balance (NEB) and associated diseases in ruminants.
Abstract:
The invention relates to sulphonamide derivatives of formula (I), where R C is optionally substituted 4-6-membered heterocyclic ring containing one or more N atoms, or R C forms together with the phenyl ring to which it is attached a benzodioxolyl group, or R C is -NR 1 R 2 , R A is a group having the formula (A), (B) or (C) R B is hydrogen or alkyl. The invention also relates to the use of derivatives of formula (I) as inhibitors for collagen receptor integrins and a process for preparing sulphonamides of formula (I).
Abstract translation:本发明涉及式(I)的磺酰胺衍生物,其中RC是任选取代的含有一个或多个N原子的4-6元杂环,或与形成苯并二氧杂环戊烯基的苯环一起形成RC形式,或RC 是-NR 1 R 2,RA是具有式(A),(B)或(C)的基团,R b是氢或烷基。 本发明还涉及式(I)的衍生物作为胶原受体整联蛋白的抑制剂的用途和制备式(I)的磺酰胺的方法。
Abstract:
Biaryl substituted thiazole, oxazole and imidazole compounds are sodium channel blockers useful for the treatment of pain. Pharmaceutical compositions comprise an effective amount of the instant compounds, either alone, or in combination with one or more therapeutically active compounds, and a pharmaceutically acceptable carrier. Methods of treatment or prevention of conditions, including acute pain, chronic pain, visceral pain, inflammatory pain, and neuropathic pain comprise administering an effective amount of the present compounds, either alone, or in combination with one or more therapeutically active compounds.
Abstract:
The use of iodine as a primary oxidant for TEMPO provides a novel and selective method for oxidizing alcohols to their corresponding carbonyl compounds.
Abstract:
4-Aryl-1-difluoromethoxyimidazoles of formula (I) are disclosed, where the substituents R and R have the meanings given in the description. Compounds of formula (I) are effective herbicides and can be used for the treatment of undesired plant growth. Furthermore, compounds of formula (I) are suitable for the desiccation and/or defoliation of plants, in particular, of cotton. The invention further relates to herbicidal agents and agents for desiccation and/or defoliation of plants.
Abstract:
Disclosed are compounds of formula (I): or the pharmaceutically acceptable non-toxic salts thereof wherein Y, R1, R2, R3, R4, R5, R6, R7 R7' are variables defined herein, which compounds are modulators of Bradykinin B2 receptors. These compounds are therefore useful in the diagnosis and treatment of renal diseases, heart failure, hypertension, Meniere's disease, vaginal inflammation and pain, peripheral circulatory disorders, climacteric disturbance, retinochoroidal circulatory disorders, myocardial ischemia, myocardial infarction, postmyocardial infarction syndrome, angina pectoris, restenosis after percutaneous transluminal coronary angioplasty, hepatitis, liver cirrhosis, pancreatitis, ileus, diabetes, diabetic complications, male infertility, glaucoma, pain, asthma, and rhinitis, and for the increase of permeability of the blood-brain barrier or the blood-brain-tumor barrier.
Abstract:
4-Aryl-1-difluoromethoxyimidazoles of formula (I) are disclosed, where the substituents R and R have the meanings given in the description. Compounds of formula (I) are effective herbicides and can be used for the treatment of undesired plant growth. Furthermore, compounds of formula (I) are suitable for the desiccation and/or defoliation of plants, in particular, of cotton. The invention further relates to herbicidal agents and agents for desiccation and/or defoliation of plants.