发明名称 |
DERIVATIVES OF IMIDAZOLE ELICITING INHIBITORY ACTIVITY WITH RESPECT TO FARNESYLTRANSFERASE, METHOD OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS, PHARMACEUTICAL COMPOSITION |
摘要 |
organic chemistry, biochemistry, pharmacy. SUBSTANCE: invention relates to novel derivatives of imidazole of the general formula (I) where n1 means a whole number from 1 to 3; A means hydrogen atom, linear or branched C1-C10-alkyl that can be optionally substituted with C3-C7- cycloalkyl or lower alkoxy-group, or radical taken among the group indicated in the invention claim; Y means radical taken among the group described in the invention claim, or to its novel pharmaceutically acceptable salts. Compounds show inhibitory activity with respect to activity of farnesyltransferase. Also, invention relates to method of synthesis of these compounds, intermediate compounds and pharmaceutical composition based on new derivatives of imidazole. Invention can be used in medicine for prophylaxis and treatment of cancer. EFFECT: new compounds indicated above, improved method of synthesis, valuable antitumor properties. 12 cl, 7 tbl
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申请公布号 |
RU2179975(C1) |
申请公布日期 |
2002.02.27 |
申请号 |
RU20000116633 |
申请日期 |
1998.11.25 |
申请人 |
EHL DZHI KEMIKAL LTD. |
发明人 |
LI KHIUN IL;KOKH DZONG SUNG;LI DZIN KHO;DZUNG VON KHI;SHIN JU SEUNG;CHUNG KHIUN KHO;KIM DZONG KHIUN;RO SEONG GU;CHOJ TAE SAENG;DZEONG SHIN VU;KVAK TAE KHVAN;AKHN IN AE;KIM KHIUN SUNG;LI SUN KHVA;KIM KVI KHVA;JOO DZUNG KVON |
分类号 |
A61K31/415;A61K31/4178;A61K31/42;A61K31/422;A61K31/425;A61K31/427;A61K31/4427;A61K31/443;A61K31/4433;A61K31/454;A61K31/496;A61K31/5377;A61K31/541;A61P9/00;A61P9/10;A61P13/12;A61P35/00;A61P43/00;C07D207/416;C07D401/14;C07D403/06;C07D403/14;C07D405/14;C07D409/12;C07D409/14;C07D413/06;C07D413/14;C07D417/06;C07D417/14;(IPC1-7):C07D403/06 |
主分类号 |
A61K31/415 |
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