Abstract:
PROBLEM TO BE SOLVED: To provide a medicine useful for the treatment of a disease or a pathological state which is known that the disorder of endothelial function is the cause of the disease and/or the mechanism of worsening the disease because the medicine can limit the disorder of the endothelial function or the reduction of ability for utilizing the blood vessel. SOLUTION: The compound represented by formula (I) [wherein, V is a single bond or the like; M is a single bond or the like; A and E are each a nitrogen atom or the like; R3 is an aryl or a heteroaryl A group which may be substituted as necessary; Y is an aryloxy which may be substituted as necessary or the like], the isomer, the hydrate, the solvate or the addition salt with a pharmaceutically acceptable acid are provided. The pharmaceutical composition containing the compound is also provided.
Abstract:
PROBLEM TO BE SOLVED: To provide a compound which can restrain endothelium malfunction and the drop in possible use of NO by blood vessels, and is useful for the treatment of the crisis and expansion of the legion of atherosclerosis, the prevention of diseases complicated with it, the prevention of a blood vessel complication after blood vessel bypass, vasodilation, blood vessel re-circulation and heart transplantation, the treatment of cardiac muscle or peripheral ischemia, cardiac incompetence and pulmonary hypertension. SOLUTION: The compound represented by formula (1) [X is a 5 to 12-membered heterocyclic group or the like; n is 0 or 1; R1 is hydrogen atom or the like; Ra is single bond or the like; A is nitrogen atom or the like; E is nitrogen atom or the like; Rb is single bond or the like; W is an aryl or the like] and its optical isomer, its hydrate, its solvate and its addition salt with a pharmaceutically acceptable acid are included.
Abstract:
Compounds of formula (I), of trans relative configuration: in which: X is an oxygen atom or an NR 2 group, Y is a group selected from -CH 2 -, -(CH 2 ) 2 - and -CH=CH-, R 1 and R 2 , which may be identical or different, are each a hydrogen atom or a group selected from alkyl, cycloalkyl and cycloalkylalkyl, in racemic form or in the form of optical isomers, and also addition salts thereof with a pharmaceutically acceptable acid and hydrates thereof. Said compounds are useful as dopaminergic receptor ligands for the treatment of central nervous system diseases.
Abstract:
Medicinal products containing the same which are useful in treating or preventing pathologies which are the result of activation of the RhoA/ROCK pathway and phosphorylation of the myosin light chain.
Abstract:
The invention relates to novel isoquinoline derivatives of formula (I), to the synthesis thereof, and to the use of same in the prevention and/or treatment of pathologies resulting from the activation of the RhoA/ROCK pathway and the phosphorylation of the light chain of myosin. X represents a group -C(=0)-, -CH(OH)- or -CH
Abstract:
Compuestos de fórmula I, con configuración relativa trans: en la que: X representa un átomo de oxígeno o un grupo NR2, Y representa un grupo seleccionado de entre -CH2-, -(CH2)2- y -CH=CH-, R1 y R2, idénticos o diferentes, representan cada uno un átomo de hidrógeno o un grupo seleccionado de entre alquilo(C1-C6) lineal o ramificado, cicloalquilo(C3-C8) y cicloalquilalquilo donde la parte alquilo tiene de 1 a 6 átomos de carbono y es lineal o ramificada y la parte cicloalquilo tiene de 3 a 8 átomos de carbono, en su forma racémica o isómeros ópticos, así como sus sales de adición de un ácido farmacéuticamente aceptable y sus hidratos.