Abstract:
PROBLEM TO BE SOLVED: To obtain a new benzoylguanidine and its pharmaceutically permissible salt useful for cardiac infarction, arrhythmia, angina and shock states caused by ischemic states, and further useful in the fields of surgical operations, organ grafts, etc. SOLUTION: A benzoylguanidine of formula I [R(1) is R(13) -SOm , R(14) R(15) N-SO2 [(m) is 1, 2; R(13) is an alkyl, a perfluoroalkyl, an alkenyl, etc.; R(14) is H, an alkyl, a perfluoroalkyl, an alkenyl, etc.; R(15) is H, an alkyl, a perfluoroalkyl; R(14) and R(15) together form a methylene group]; one of R(2) and R(3) is H, and the other is CHR(30) R(31) [R(30) is a group of the formula II [R(32) is H, methyl; (q)-(i) are each 0-4; (k) is 1-4]; R(31) is H, an alkyl], etc.; R(4) is an alkyl, etc.,} or its salt, e.g. 2-chloro-3-(1'-hydroxy-2'-propyl'-5- methylsulfonylbenzoylguanidine. The compound of formula I is obtained by reacting a compound of formula III (L is a releasable group) with guanidine.
Abstract:
PROBLEM TO BE SOLVED: To obtain a new ortho-substituted benzoylguanidine or its pharmaceutically permissible salt useful as a medicine for treating and preventing cardiac infarction, arrhythmia, stenocardia, etc., caused by ischemic states. SOLUTION: An ortho-substituted benzoylguanidine of formula I [R(1) is H, F, Cl, Br, an alkyl, an alkoxy, a cycloalkyl, a cyclalkoxy, etc., or phenyl, naphthyl, biphenyl, a heteroaryl, or C[R(15) R(16) ]OH, etc., (R(15) , R(16) are each H, an alkyl, etc.); one of R(2) , R(3) is always R(1) ; R(4) , R(5) are each H, an alkyl, an alkoxy, F, Cl, Br, etc.,] or its salt, e.g. 4-acetyloxy-2-chloro-5- trifluoromethylbenzoylguanidine hydrochloride salt. The compound of formula I is obtained by reacting a compound of formula II (L is a releasable group capable of being easily nucleophilically substituted) with guanidine. The compound of formula I is active for antitheroselerotic arteriosclerosis, cancers, etc.
Abstract:
PROBLEM TO BE SOLVED: To produce the subject new compound, capable of manifesting excellent antiarrhythmic properties without causing unfavorable diuretic properties and useful as an antiarrhythymic agent having a cardiac protecting ingredient for preventing and treating infraction and treating angina pectoris. SOLUTION: This compound is represented by formula I [R(1) is CF3 ; either one of R(2) and R(3) is H and the other is C(OH)(CH3 )-CH2 OH, CH(CH3 )-CH2 OH or C(OH)(CH3 )2 ; R(4) is methyl, methoxy, Cl or CF3 ] or its salt, e.g. 4-(1'- hydroxy-2'-propyl)-2-methyl-5-trifluoromethylbenzoylguanidine hydrochloride. The compound represented by formula I is produced by reacting a compound represented by formula II (L is a readily nucleophilically substitutable residue and is methoxy, 1-imidazolyl, etc.) with guanidine.
Abstract:
PROBLEM TO BE SOLVED: To produce phenyl-substituted alkenylcarboxylic guanizid, which is a selective inhibitor of sodium/proton exchanger and can be used for treatment of arrhythmia, myocardial infarction, angina petoris, etc. SOLUTION: This phenyl-substituted alkenylcarboxylic guanizid of formula I [T is formula II [R(A) is H, a halogen, CN, etc.; R(B), R(C), and R(D) are each R(A); (x) and (y) are each 0-2; R(F) is H, a halogen, CN, etc.; R(E) is R(FF)], R(1) is T, H, a halogen, etc.; R(2)-R(5) are each R(1) or -CH-CH=CH- CH- in their combination, F, Cl, CF3 , etc.], for example, 1,2-bis(3-E-2- methylpropenic guanizid)]benzene dichloride, is obtained by a reaction of a compound of formula III (L is a nucleophilically replaceable eliminatory group with ganidine. This phenyl-substituted alkenylcarboxylic guanizid is effective for ischemic condition of heart, peripheral and central nerves, peripheral organs and extremities, shocks, etc.
Abstract:
PROBLEM TO BE SOLVED: To obtain the subject new pharmaceutical compound useful for the prevention and treatment of infarction, the treatment of stenocardia, etc., as an antiarrhythmic agent containing a heart-protecting component. SOLUTION: The objective compound is expressed by the formula I [R(1) to R(3) are each R(10)-SOa , etc., (R(10) is a 1-8C alkyl, etc.; (a) is 0-2); R(4) and R(5) are each a 1-4C alkyl, a 1-4C alkoxy, OH, etc.], e.g. 2,6- dichlorobenzoylguanidine hydrochlorice. The compound of the formula I can be produced by reacting a compound of the formula II (L is an eliminable group which may have nucleophilic substituent) with guanidine and optionally converting the product into a salt. The compound of the formula I is useful for the treatment and prophylayis of diseases caused by ischemic state, treatment of shock diseases, surgical operation and organ transplantation, the treatment for prostatic hyperplacia, etc. It is useful also as a diagnostic agent for hypertension, atherosclerosis, diabetes, proliferative diseases, etc.
Abstract:
Benzoylguanidine der Formel I worin bedeuten: R(1)R(13)-SOm oder R(14)R(15)N-SO2-; m1 oder 2; einer der Substituenten (R2) und R(3) Wasserstoff; und der jeweils andere Substituent R(2) und R(3) -CHR(30)R(31); R(30) -(CH2)g-(CHOH)h-(CH2)i-(CHOH)k-R(32) oder -(CH2)g-O-(CH2-CH2O)h-R(24); -C(OH)R(33)R(34); und R(4), R(13), R(14), R(15), R(24), R(31), R(32), g, h, i und k, die in den Ansprüchen gegebenen Bedeutungen haben, sind wertvolle antiarrhythmische Arzneimittel mit cardioprotektiver Komponente, auch zur Prävention ischämisch induzierter Schäden, insbesondere bei der Auslösung ischämisch induzierter Herzarrhythmien. Sie werden infolge Inhibition des zellulären Na /H -Austauschmechanismus zur Behandlung akuter oder chronischer durch Ischämie ausgelöster Schäden verwendet werden. Darüber hinaus zeichnen sie sich durch starke inhibierende Wirkung auf die Proliferationen von Zellen aus. Sie sind zur Verhinderung der Genese des Bluthochdrucks geeignet. Außerdem erniedrigen sie erhöhte Serum Konzentrationen an LDL und VLDL.
Abstract:
Ortho-substituierte Benzoylguanidine der Formel I worin R(1) bis R(4) die in den Ansprüchen angegebenen Bedeutungen haben, sind als antiarrhythmische Arzneimittel mit cardioprotektiver Komponente zur Infarktprophylaxe und der Infarktbehandlung sowie zur Behandlung der angina pectoris geeignet. Sie inhibieren auch präventiv die pathophysiologischen Vorgänge beim Entstehen ischämisch induzierter Schäden, insbesondere bei der Auslösung ischämisch induzierter Herzarrhythmien.
Abstract:
BENZOYLGUANIDINES OF FORMULA I IWITH R(1) TO R(4) AS DEFINED IN THE SPECIFICATION, ARE SUITABLE AS ANTIARRHYTHMIC PHARMACEUTICALS HAVING A CARDIOPROTECTIVE COMPONENT FOR INFARCT PROPHYLAXIS AND INFARCT TREATMENT AS WELL AS FOR THE TREATMENT OF ANGINA PECTORIS. THEY INHIBIT, IN A PREVENTIVE MANNER, THE PATHOPHYSIOLOGICAL PROCESSES IN THE FORMATION OF ISCHEMICALLY INDUCED DAMAGE, IN PARTICULAR IN THE ELICITATION OF ISCHEMICALLY INDUCED CARDIAC ARRHYTHMIAS.
Abstract:
In the present invention, there are disclosed ortho-substituted benzoylguanidines of the general formula I, wherein the meanings of symbols are specified in the descriptive section, and their pharmaceutically acceptable salts, medicaments and pharmaceutical compositions containing them. These compounds functioning as antiarrhythmic agents containing cardioprotective component are useful for prophylaxis and treatment of infarct and for the treatment of angina pectoris. They also inhibit in preventive way pathophysiological processes at occurrence of ischemically induced disorders, especially at occurrence of ischemically induced heart arrhythmias.