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NOVEL PYRROLE COMPOUNDS, SYNTHESIS METHOD THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME
专利权人:
LE LABORATUAR SERVE
发明人:
LE-TIRAN Arno (FR),ЛЕ-ТИРАН Арно (FR),LE-DIGORE Terri (FR),ЛЕ-ДИГОРЕ Тьерри (FR),STARK Zherom-Benua (FR),СТАРК Жером-Бенуа (FR),ANLEN Zhan-Mishel (FR),АНЛЕН Жан-Мишель (FR),GIJUZIK Ann-Fransuaz (FR),Г,LE-TIRAN Arno,ЛЕ-ТИРАН Арно,LE-DIGORE Terri,ЛЕ-ДИГОРЕ Тьерри,STARK Zherom-Benua,СТАРК Жером-Бенуа,ANLEN Zhan-Mishel,АНЛЕН Жан-Мишель,GIJUZIK Ann-Fransuaz,ГИЙУЗИК Анн-Франсуаз,DE-NANTEJ Gijom,ДЕ-НАНТЁЙ
申请号:
RU2014130125
公开号:
RU0002607788C2
申请日:
2014.07.22
申请国别(地区):
RU
年份:
2017
代理人:
摘要:
FIELD: chemistry.SUBSTANCE: invention relates to a compound of formula (I) possessing inhibitory activity on Bcl-2 family proteins. In formula (I) (I) A1 is hydrogen, (C1-C6)polyhaloalkyl group or (C1-C6)alkyl group, A2 is hydrogen, (C1-C6)polyhaloalkyl group, (C1-C6)alkyl group or cycloalkyl group, T denotes a hydrogen atom, (C1-C6)alkyl group, optionally substituted with one-three halogen atoms, group (C1-C4)alkyl-NR1R2 or group (C1-C4)alkyl-OR6, R1 and R2 each independently from each other is a hydrogen atom or (C1-C6)alkyl group, or R1 and R2 form with a nitrogen atom bearing them, heterocycloalkyl, R3 is (C1-C6)alkyl group, cycloalkyl group, heterocycloalkyl group, aryl group or heteroaryl group, wherein one or more carbon atoms of previous groups or their possible substitutes can be deuterated, R4 is an aryl group or heteroaryl group, wherein one or more carbon atoms of previous groups or their possible substitutes can be deuterated, R5 is hydrogen or halogen atom, R6 is a hydrogen atom or a linear or branched (C1-C6)alkyl group, Ra, Rb, Rc and Rd each independently from other represents hydrogen, linear or branched (C1-C6)alkyl, halogen atom, a linear or branched (C1-C6)alkoxy group, hydroxy group, R7-CO-NH-(C0-C6)alkyl-, R7-SO2-NH-(C0-C6)alkyl-, R7-NH-CO-NH-(C0-C6)alkyl-, R7-O-CO-NH-(C0-C6)alkyl-, or substitutes of pair (Rb, Rc) form together with carbon atoms carrying them, a ring consisting of 5–6 ring members, which may contain 1–2 oxygen atoms, R7 is hydrogen, linear or branched (C1-C6)alkyl, aryl or heteroaryl. Invention also relates to methods of producing compounds of formula (I), to a pharmaceutical composition, use of a pharmaceutical composition for preparing a drug, use of compound of formula (I) for preparing a drug.EFFECT: obtaining novel compounds of formula (I) possessing inhibitory activity on Bcl-2 family proteins.37 cl, 2 tbl, 473 exИзобретение относится к соединению формулы (I), обладающего ингибирующей активностью в отношении белков семе
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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