发明授权
- 专利标题: Ecteinascidin analogs for use as antitumour agents
- 专利标题(中): 用作抗肿瘤剂的抗坏血酸类抗生素
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申请号: US10485536申请日: 2002-08-06
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公开(公告)号: US07763615B2公开(公告)日: 2010-07-27
- 发明人: Pilar Gallego , Carmen Cuevas , Simon Munt , Ignacio Manzanares , Valentin Martinez
- 申请人: Pilar Gallego , Carmen Cuevas , Simon Munt , Ignacio Manzanares , Valentin Martinez
- 申请人地址: ES Madrid
- 专利权人: Pharma Mar, S.A.
- 当前专利权人: Pharma Mar, S.A.
- 当前专利权人地址: ES Madrid
- 代理机构: King & Spalding LLP
- 代理商 Kenneth H. Sonnenfeld
- 优先权: GB0119243.4 20010807
- 国际申请: PCT/GB02/03592 WO 20020806
- 国际公布: WO03/014127 WO 20030220
- 主分类号: A01N43/58
- IPC分类号: A01N43/58 ; A01N43/60 ; A61K31/50 ; A61K31/495 ; C07D487/00 ; C07D491/00 ; C07D513/00
摘要:
Derivatives of ecteinascidin 736 of general formula (I) wherein the groups R1, R2, R3, R4 and R5 are each independently selected from the group consisting of H, OH, OR′, SH, SR′, SOR′, SO2R′, C(═O)R′, C(═O)OR′, NO2, NH2, NHR′, N(R′)2, NHC(O)R′, CN, halogen, ═O, substituted or unsubstituted C1-C25 alkyl, substituted or unsubstituted C2-C18 alkenyl, substituted or unsubstituted C2-C18 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted heterocyclic; wherein X is independently selected of OR′, CN, (═O), or H; wherein each of the R′ groups is independently selected from the group consisting of H, OH, NO2, NH2, SH, CN, halogen, ═O, C(═O)H, C(═O)CH3, CO2H, substituted or unsubstituted C1-C25 alkyl, substituted or unsubstituted C2-C18 alkenyl, substituted or unsubstituted C2-C18 alkynyl, substituted or unsubstituted aryl; wherein m is 0, 1 or 2; and wherein n is 0, 1, 2, 3, or 4, and their use as antitumoral agent.
公开/授权文献
- US20060128711A1 Antitumoral analogs 公开/授权日:2006-06-15
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