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Melanocortin 3-aminoalkyl-1,4-diazepan-2-one receptor 5 antagonists
专利权人:
MIMETICA PTY LIMITED
发明人:
BLASKOVICH, MARK,CASSIDY, PETER
申请号:
ES09716155
公开号:
ES2445456T3
申请日:
2009.02.27
申请国别(地区):
ES
年份:
2014
代理人:
摘要:
A compound of formula (I): in which: Y is a group of formula - (CR9R10) n-; X is selected from the group consisting of -C (>; = O) -, -OC (>; = O) -, -NHC (>; = O) -, - (CR11R12) and -S (>; = O) 2-; Z is a group of formula - (CR13R14) q-; R1 is selected from the group consisting of H, optionally substituted C1-C12 alkyl, optionally substituted C2-C12 alkenyl, optionally substituted C2-C12 alkynyl, optionally substituted C1-C12 heteroaryl, optionally substituted C3-C12 cycloalkyl, optionally substituted C2-C12 heterocycloalkyl , optionally substituted C6-C18 aryl and optionally substituted C1-C18 heteroaryl; R2 and R3 are each independently selected from the group consisting of H, optionally substituted C1-C12 alkyl, optionally substituted C2-C12 alkenyl, optionally substituted C2-C12 alkynyl, optionally substituted C1-C12 heteroaryl, optionally substituted C3-C12 cycloalkyl, heterocycloalkyl Optionally substituted C2-C12, optionally substituted C6-C18 aryl and optionally substituted C1-C18 heteroaryl; R4a is selected from the group consisting of H, optionally substituted C1-C12 alkyl, optionally substituted C2-C12 alkenyl, optionally substituted C2-C12 alkynyl, heteroaryl Optionally substituted C1-C12, optionally substituted C3-C12 cycloalkyl, optionally substituted C2-C12 heterocycloalkyl, optionally substituted C6-C18 aryl, optionally substituted C1-C18 heteroaryl, C (>; = O) R15, C (>; = O) NR15R16, C (>; = O) OR15, SO2R15, C (>; = O) H, -C (>; = NR15) -NR16R17 and OR15, R4b is selected from the group consisting of H, C1-C12 alkyl optionally and substituted, optionally substituted C2-C12 alkenyl, optionally substituted C2-C12 alkynyl, optionally substituted C1-C12 heteroaryl, optionally substituted C3-C12 cycloalkyl, optionally substituted C2-C12 heterocycloalkyl, optionally substituted C6-C18 aryl, optionally substituted C1-C18 heteroaryl C (>; = O) R15, C (>; = O) NR15R16, C (>; = O) OR15, oR4a and R4b, when taken together with the nitro
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