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MAP kinase p38 inhibitors
专利权人:
Chroma Therapeutics Limited
发明人:
MOFFAT, David,PINTAT, Stéphane,DAVIES, Stephen
申请号:
ES07732629
公开号:
ES2605727T3
申请日:
2007.05.01
申请国别(地区):
ES
年份:
2017
代理人:
摘要:
A compound of formula (I): ** Formula ** 5 in which: G is -CH>; = D is an optionally substituted phenyl ring; R6 is hydrogen; P represents hydrogen and U represents a radical of formula (IA); or U represents hydrogen and P represents a radical of formula (IA); -A- (CH2) 2-X1-L1-Y-NH-CHR1R2 (IA) in which A represents an optionally substituted phenyl or cyclohexyl ring; z is or 1; Y is a link, -C (>; = O) -, -S (>; = O) 2-, -C (>; = O) NR3-, -C (>; = S) -NR3, -C (>; = NH ) NR3 or -S (>; = O) 2NR3- where R3 is hydrogen or optionally substituted C1-C6 alkyl; L1 is a divalent radical of the formula - (Alq1) m (Q) n (Alq2) p- in which m, n and p are independently 0 or 1, Q is (i) a divalent, carbocyclic or heterocyclic, mono or bicyclic radical, optionally substituted having 5-13 ring members, or (ii), in the case where myp is both 0, a divalent radical of the formula -X2-Q1- or -Q1-X2- in which X2 is -O-, S- or NRA- in which RA is optionally substituted hydrogen or C1-C3 alkyl, and Q1 is a divalent, carbocyclic or heterocyclic, mono or bicyclic, optionally substituted radical having 5-13 ring members, Alq1 and Alq2 independently represent optionally substituted C3-C7 cycloalkyl radicals, or optionally substituted C1-C6 alkylene, C2-C6 alkenylene or C2-C6 alkynylene, linear or branched, which may end in, or optionally contain, an ether (-O-) bond, thioether (-S-) or amino (-NRA-) where RA is hydrogen or optionally substituted C1-C3 alkyl; and X1 represents a link; -C (>; = O); or -S (>; = O) 2-; -NR4C (>; = O) -, -C (>; = O) NR4 -, - NR4C (>; = O) NR5-, -NR4S (>; = O) 2- or -S (>; = O) 2NR4- where R4 and R5 are independently hydrogen or optionally substituted C1-C6 alkyl; R1 is an ester group that is hydrolysable by one or more intracellular carboxylesterase enzymes to give a carboxylic acid group; R2 is the side chain of a natural or non-natural alpha amino acid selected from: (i) C1-C6 alkyl, phenyl, 2-, 3- or 4-hydroxyphenyl, 2-, 3- or 4-met
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