摘要:
A catechol derivative represented by the formula wherein R' represents a hydrogen atom or a C, to C 5 alkyl group; R 2 represents a hydrogen atom or a halogen atom; X represents a straight chain or branched alkylene group having 1 to 15 carbon atoms or a vinylene group; Y represents a carbonyl group or a group represented by represents a hydrogen atom or a C, to C. alkyl group) and Z represents a hydrogen atom, a straight chain or branched alkyl group having 1 to 15 carbon atoms ora cycloalkyl group; the sum of the carbon atoms of said X and Z being at least 3. The compounds of this invention are useful for the prophylaxis and treatment for various allergic diseases, ischemic heart diseases an inflammations caused by slow reacting substance of anaphylaxis (SRS-A), since the compounds inhibit very potently the formation and release of SRS-A.
摘要:
Novel 2-phenylimidazo[2,1-b]benzothiazole compounds shown by general formula I TAKE IN and the salts thereof, a process of producing the compounds, and pharmaceutical compositions containing the compounds. The compounds of this invention act on immune response, in particular, suppress delayed type hypersensitivity reaction, and are useful as antiallergic agents, antirheumatics, therapeutic agents for autoimmune diseases, and suppressants of rejection after tissue transplantation and skin graft.
摘要:
2-hydroxyoxanilic acid derivatives shown by the following formula and salts thereof possess an immunoregulatory action and can be useful as antiallergic agents, antiasthmatics, antirheumatics, carcinostatic agents, therapeutic agents for autoimmune disease, and suppressants of rejection in tissue transplants and skin grafts. They can be made from the corresponding aminophenols and oxalylic acids.
摘要:
Novel 2-phenylimidazo[2,1-b]benzothiazole compounds shown by general formula I TAKE IN and the salts thereof, a process of producing the compounds, and pharmaceutical compositions containing the compounds. The compounds of this invention act on immune response, in particular, suppress delayed type hypersensitivity reaction, and are useful as antiallergic agents, antirheumatics, therapeutic agents for autoimmune diseases, and suppressants of rejection after tissue transplantation and skin graft.
摘要:
A heterocyclic compound of the formula (I): and a pharmacologically acceptable salt thereof which have platelet activating factor (PAF) antagonizing activity are disclosed.
摘要:
A saturated heterocyclic carboxamide derivative of the following general formula (I) and salts thereof which have platelet activating factor (PAF) antagonizing activity.
摘要翻译:具有下列通式(I)的饱和杂环羧酰胺衍生物及其盐,其具有血小板活化因子(PAF)拮抗活性。 v
摘要:
Heterocyclic compound of formula (I) and salts thereof are SRS-A antagonists: wherein R' is a C 1 to C 8 acyl group; R 2 is a C 1 to C a alkyl group; Het- is a 5- or 6-membered heterocyclic ring which contains 1 to 3 nitrogen atoms and may additionally contain a sulfur atom or an oxygen atom; R 3 is a carboxy group, an amino group, a C 1 to C 8 alkylamino group which may be carboxy-substituted, a C, to C 8 alkanoylamino group which may be carboxy-substituted, a di-(C 1 -C 8 alkyl) amino group, a hydroxy group, a C 1 to C 8 alkoxy group which may be carboxy-substituted, a mercapto group, a C 1 -C 8 alkylthio group which may be carboxy-substituted, a group of formula: or formula: (wherein p is integer of 1 to 5, q is 0, 1 or 2, r is an integer of 1 to 5; R 4 is a carboxy group, a C 1 -C 8 alkoxy group which may be carboxy-substituted or a C 1 -C 8 alkyl group which may be carboxy-substituted and optionally additionally contain a sulfur atom or an oxygen atom in the carbon chain thereof); and n is 0 or an integer of to 3; provided that when the compound is substituted by a carboxy group, said carboxy group may be in the form of an ester, and when n is 2 or 3 different R 3 's is may be present.
摘要:
A catechol derivative represented by the formula wherein R' represents a hydrogen atom or a C, to C 5 alkyl group; R 2 represents a hydrogen atom or a halogen atom; X represents a straight chain or branched alkylene group having 1 to 15 carbon atoms or a vinylene group; Y represents a carbonyl group or a group represented by represents a hydrogen atom or a C, to C. alkyl group) and Z represents a hydrogen atom, a straight chain or branched alkyl group having 1 to 15 carbon atoms ora cycloalkyl group; the sum of the carbon atoms of said X and Z being at least 3. The compounds of this invention are useful for the prophylaxis and treatment for various allergic diseases, ischemic heart diseases an inflammations caused by slow reacting substance of anaphylaxis (SRS-A), since the compounds inhibit very potently the formation and release of SRS-A.