摘要:
Compounds shown by the above formula or salt thereof show a strong angiotensin II antagonistic activity and hypotensive action and CNS activity, and are useful as therapeutic agents of circulatory diseases such as hypertensive diseases and heart diseases (e.g. hypercardia, heart failure, cardiac infarction), strokes, cerebral apoplexy, nephritis, atherosclerosis, Alzheimer's disease, senile dementia, etc.
摘要翻译:上述式表示的化合物或其盐显示强烈的血管紧张素II拮抗作用和降血压作用和CNS活性,并且可用作循环系统疾病如高血压疾病和心脏病(例如高血压,心力衰竭,心肌梗塞)的治疗剂, 脑卒中,脑中风,肾炎,动脉粥样硬化,阿尔茨海默病,老年痴呆等。 h
摘要:
Fused heterocyclic compounds of the formula (I):
wherein R¹ is an optionally substituted hydrocarbon residue which may be attached through a hetero atom; R² is a group capable of forming an anion or a group convertible thereinto; R³ is an optionally substituted aromatic hydrocarbon or heterocyclic residue which contains at least one hetero atom; X is a direct bond or a spacer having an atomic length of two or less between the R³ group and the ring W group; W is an optionally substituted aromatic hydrocarbon or heterocyclic residue which contains at least one hetero atom; a,c and d are independently selected from the group consisting of one or two optionally substituted carbon atoms and one or two optionally substituted hetero atoms; b and e are independently selected from the group consisting of one optionally substituted carbon atom and one optionally substituted nitrogen atom; the dotted line is a bond to form one double bond; n is an integer of 1 or 2 and when a, which is an optionally substituted carbon atom, is taken together with R¹, the following group:
may form a ring group; provided that when
is a benzimidazole, thieno[3,4-d]imidazole, or thieno[2,3-d]imidazole ring, at least one of the group:
and R³ is an optionally substituted heterocyclic residue ; and the pharmaceutically acceptable salts thereof, have potent angiotensinII antagonistic activity and antihypertensive activity, thus being useful as therapeutic agents for treating circulatory system diseases such as hypertensive diseases, heart diseases (e.g. hypercardia, heart failure, cardiac infarction, etc.), strokes, cerebral apoplexy, nephritis, etc.
摘要翻译:式(I)的稠合杂环化合物:其中R 1是可通过杂原子连接的任选取代的烃残基; R 2是能够形成阴离子或可转化为其的基团的基团; R 3是含有至少一个杂原子的任选取代的芳烃或杂环残基; X是在R 3基团和环W基团之间原子长度等于或小于2的直接键或间隔基; W是含有至少一个杂原子的任选取代的芳族烃或杂环残基; a,c和d独立地选自一个或两个任选取代的碳原子和一个或两个任选取代的杂原子; b和e独立地选自一个任选取代的碳原子和一个任选取代的氮原子; 虚线是形成一个双键的键; n是1或2的整数,并且当任意取代的碳原子a与R 1一起时,下列基团可以形成环基团; 条件是当为苯并咪唑,噻吩并[3,4-d]咪唑或噻吩并[2,3-d]咪唑环时,至少一个基团:和R 3是任选取代的杂环残基; 及其药学上可接受的盐具有有效的血管紧张素II拮抗活性和抗高血压活性,因此可用作治疗循环系统疾病如高血压疾病,心脏疾病(例如高血压,心力衰竭,心肌梗塞等),中风, 脑卒中,肾炎等
摘要:
This invention relates to a pharmaceutical composition for angiotensin II-mediated diseases, which comprises a compound having angiotensin II antagonistic activity of the formula wherein R is H or an optionally substituted hydrocarbon residue; R is an optionally esterified carboxyl group; R is a group capable of forming an anion or a group convertible thereinto; X is a covalent bond between the 2 phenyl rings or a spacer having a chain length of 1 to 2 atoms as the linear moiety between the adjoining phenylene group and phenyl group; n is 1 or 2; the ring A is a benzene ring having 1 or 2 optional substituents in addition to R ; and Y is a bond, -O-, -S(O)m- (wherein m is 0, 1 or 2) or -N(R )- (wherein R is H or an optionally substituted alkyl group), or a pharmaceutically acceptable salt thereof in combination with a compound having diuretic activity.
摘要:
The present invention relates to a compounds represented by the following formula or salts thereof.
The above compounds have strong angiotensin II antagonistic action, antihypertensive action and action on central nervous system, which are useful for the treatment of circulatory diseases such as hypertension, heart diseases, cerebral apoplexy, nephritis, atherosclerosis or Alzheimer's disease and senile dementia, and for agents of improving cerebral function.
摘要:
This invention relates to a compound represented by the formula
wherein the ring A stands for a 5-10 membered aromatic heterocyclic group optionally having, besides R 1 and R 2 , further substituents; R 1 stands for an optionally substituted hydrocarbon residue which is optionally bonded through a hetero-atom; R 2 stands for a group capable of liberating proton in a living body or a group convertible thereinto; R 3 stands for an 5-7 membered optionally substituted heterocyclic residue having, as a group capable of constituting the ring, carbonyl group, thiocarbonyl group, an optionally oxidized sulfur atom or a group convertible into them; X shows that the ring Y and the ring W are bonded to each other directly or through a spacer having an atomic length of two or less; the ring W and the ring Y are each an optionally substituted aromatic hydrocarbon or aromatic heterocyclic residue; and n denotes an integer of 1 to 3, or a salt thereof and to an angiotensin II antagonistic agent containing the compound (I) or a salt thereof.
摘要:
57 The present invention relates to a compounds represented by the following formula or salts thereof.
The above compounds have strong angiotensin II antagonistic action, antihypertensive action and action on central nervous system, which are useful for the treatment of circulatory diseases such as hypertension, heart diseases, cerebral apoplexy, nephritis, atherosclerosis or Alzheimer's disease and senile dementia, and for agents of improving cerebral function.