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MULTITARGET INHIBITORS OF TUMOUR GROWTH BASED ON LINEAR HETEROARENE ANTHRACENEDIONES
MULTITARGET INHIBITORS OF TUMOUR GROWTH BASED ON LINEAR HETEROARENE ANTHRACENEDIONES
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机译:基于线性杂芳烃蒽二酮的肿瘤生长多靶标抑制剂
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FIELD: chemistry.;SUBSTANCE: invention relates to derivatives of linear tetracyclic heteroarene anthracehediones, which contain in side chains residues of halogen acetamidines and correspond to formula: as well as to their pharmacologically acceptable salts, where X, Y, Z independently stand for CH- or Nh-groups or heteroatoms, selected from O, N and S, forming five-member heteroarene, optionally substituted with alkyl; Hal independently stands for fluorine, chlorine, bromine or iodine atom; m and n independently stand for number from 2 to 4 and equal quantity of spacer CH2-groups, connecting aminogroups in peri-positions of heteroarene anthracenedione with nitrogen atoms of residues of halogenacylamidines, located in side chain; W stands for substituents, independently selected from the group: amino, hydroxy, alkoxy, fluorine; k stands for number of substituents W in anthracenedione fragment, independently equal from 0.;EFFECT: novel compounds, which can be applied in medicine for therapy of oncological diseases, have been obtained.;3 tbl, 4 dwg, 12 ex
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机译:技术领域本发明涉及线性四环杂芳基蒽二酮的衍生物,其在侧链中含有卤素乙am的残基,并且对应于下式:<图像文件=“ 00000027.GIF” he =“ 33” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 67” />及其药理学上可接受的盐,其中X,Y,Z独立代表CH-或Nh-基团或选自O,N和S的杂原子,形成五个杂芳基成员,任选地被烷基取代; Hal独立地代表氟,氯,溴或碘原子; m和n独立地表示2-4个数,并且是等量的间隔CH 2 Sub>-基团,其连接杂芳基蒽二酮周围位置的氨基与位于侧链的卤代酰基lam的残基的氮原子。 W代表取代基,其独立地选自:氨基,羟基,烷氧基,氟; k代表蒽二酮片段中取代基W的数目,独立地等于0 .;作用:获得了可用于治疗肿瘤疾病的新化合物。; 3 tbl,4 dwg,12 ex
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