摘要:
The present disclosure relates to 4-(2-amino-1-hydroxyethyl)phenol derivatives of formula (I) as well as pharmaceutical compositions comprising them, and their use in therapy as agonists of the β2 adrenergic receptor.
摘要:
This present disclosure relates to compounds of formula (I): The present disclosure also relates to pharmaceutical compositions comprising the compounds of formula (I) and to their methods of use in therapy.
摘要:
The present disclosure relates to 4-(2-amino-1-hydroxyethyl)phenol derivatives of formula (I) as well as pharmaceutical compositions comprising them, and their use in therapy as agonists of the BETA2 adrenergic receptor.
摘要:
A compound of formula (I) or a pharmaceutically-acceptable salt, solvate or stereoisomer thereof wherein R1 is a group chosen from —CH2OH and —NHC(O)H; R2 is a hydrogen atom or R1 together with R2 form the group —NH—C(O)—CH═CH—, wherein the nitrogen atom is bound to the carbon atom in the phenyl ring holding R1 and the carbon atom is bound to the carbon atom in the phenyl ring holding R2; R3 is chosen from a hydrogen atom, a halogen atom and groups chosen from —SO—R5, —SO2—R5, —NH—CO—NH2, —CO—NH2, hydantoino, C1-4alkyl, C1-4alkoxy and —SO2NR5R6; R4 is chosen from a hydrogen atom, a halogen atom and a C1-4 alkyl group; R5 is chosen from a C1-4 alkyl group and a C3-8 cycloalkyl group; R6 is independently chosen from a hydrogen atom and a C1-4 alkyl group; n, p and q are independently 0, 1, 2, 3 or 4; m and s are independently 0, 1, 2 or 3; and r is 0, 1 or 2 with the provisos that at least one of m and r is not 0, the sum n+m+p+q+r+s is 7, 8, 9, 10, 11, 12 or 13, and the sum q+r+s is 2, 3, 4, 5 or 6.
摘要翻译:式(I)化合物或其药学上可接受的盐,溶剂合物或立体异构体,其中R 1是选自-CH 2 OH和-NHC(O)H的基团; R2是氢原子或R1与R2一起形成-NH-C(O)-CH-CH-基团,其中氮原子与保护R1的苯基中的碳原子结合,并且碳原子与 保护R2的苯环中的碳原子; R3选自氢原子,卤素原子和选自-SO-R5,-SO2-R5,-NH-CO-NH2,-CO-NH2,乙酰氧基,C1-4烷基,C1-4烷氧基和-SO2NR5R6的基团; R 4选自氢原子,卤素原子和C 1-4烷基; R5选自C 1-4烷基和C 3-8环烷基; R6独立地选自氢原子和C1-4烷基; n,p和q独立地为0,1,2,3或4; m和s独立地为0,1,2或3; 并且r为0,1或2,条件是m和r中的至少一个不为0,则和n + m + p + q + r + s为7,8,9,10,11,12或13 ,并且和q + r + s为2,3,4,5或6。
摘要:
The present disclosure relates to 4-(2-amino-1-hydroxyethyl)phenol derivatives of formula (I) as well as pharmaceutical compositions comprising them, and their use in therapy as agonists of the BETA2 adrenergic receptor.
摘要:
A compound of formula (I) or a pharmaceutically-acceptable salt, solvate or stereoisomer thereof wherein R1 is a group chosen from —CH2OH and —NHC(O)H; R2 is a hydrogen atom or R1 together with R2 form the group —NH—C(O)—CH═CH—, wherein the nitrogen atom is bound to the carbon atom in the phenyl ring holding R1 and the carbon atom is bound to the carbon atom in the phenyl ring holding R2; R3 is chosen from a hydrogen atom, a halogen atom and groups chosen from —SO—R5, —SO2—R5, —NH—CO—NH2, —CO—NH2, hydantoino, C1-4alkyl, C1-4alkoxy and —SO2NR5R6; R4 is chosen from a hydrogen atom, a halogen atom and a C1-4 alkyl group; R5 is chosen from a C1-4 alkyl group and a C3-8 cycloalkyl group; R6 is independently chosen from a hydrogen atom and a C1-4 alkyl group; n, p and q are independently 0, 1, 2, 3 or 4; m and s are independently 0, 1, 2 or 3; and r is 0, 1 or 2 with the provisos that at least one of m and r is not 0, the sum n+m+p+q+r+s is 7, 8, 9, 10, 11, 12 or 13, and the sum q+r+s is 2, 3, 4, 5 or 6.
摘要翻译:式(I)化合物或其药学上可接受的盐,溶剂合物或立体异构体,其中R 1是选自-CH 2 OH和-NHC(O)H的基团; R2是氢原子或R1与R2一起形成-NH-C(O)-CH = CH-基团,其中氮原子与保护R1的苯基中的碳原子结合,并且碳原子与 保护R2的苯环中的碳原子; R3选自氢原子,卤素原子和选自-SO-R5,-SO2-R5,-NH-CO-NH2,-CO-NH2,乙酰氧基,C1-4烷基,C1-4烷氧基和-SO2NR5R6的基团; R4选自氢原子,卤素原子和C1-4烷基; R5选自C 1-4烷基和C 3-8环烷基; R6独立地选自氢原子和C1-4烷基; n,p和q独立地为0,1,2,3或4; m和s独立地为0,1,2或3; 并且r为0,1或2,条件是m和r中的至少一个不为0,则和n + m + p + q + r + s为7,8,9,10,11,12或13 ,并且和q + r + s为2,3,4,5或6。
摘要:
The present disclosure relates to novel compounds having β2 adrenergic agonist and M3 muscarinic antagonist dual activity, to pharmaceutical compositions containing them, to the process for their preparation and to their use in respiratory therapies.
摘要:
The present disclosure relates to novel compounds having β2 adrenergic agonist and M3 muscarinic antagonist dual activity, to pharmaceutical compositions containing them, to the process for their preparation and to their use in respiratory therapies.
摘要:
The present disclosure relates to novel compounds having β2 adrenergic agonist and M3 muscarinic antagonist dual activity, to pharmaceutical compositions containing them, to the process for their preparation and to their use in respiratory therapies.
摘要:
Compounds of formula (I) and their pharmaceutically acceptable salts are provided as well as processes for the manufacture of such compounds. The compounds are useful in the treatment or prevention of inflammatory and allergic diseases.