Ecteinascidin analogs for use as antitumour agents
    13.
    发明授权
    Ecteinascidin analogs for use as antitumour agents 有权
    用作抗肿瘤剂的抗坏血酸类抗生素

    公开(公告)号:US07763615B2

    公开(公告)日:2010-07-27

    申请号:US10485536

    申请日:2002-08-06

    CPC分类号: C07D515/22

    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.

    摘要翻译: 基团R 1,R 2,R 3,R 4和R 5各自独立地选自H,OH,OR',SH,SR',SOR',SO 2 R',C的通式(I)的抗坏血酸素736衍生物 (= O)R',C(= O)OR',NO 2,NH 2,NHR',N(R')2,NHC(O)R',CN,卤素,= O,取代或未取代的C 1 -C 25烷基 取代或未取代的C 2 -C 18烯基,取代或未取代的C 2 -C 18炔基,取代或未取代的芳基,取代或未取代的杂环基; 其中X独立地选自OR',CN,(= O)或H; 其中每个R'基团独立地选自H,OH,NO 2,NH 2,SH,CN,卤素,= O,C(= O)H,C(= O)CH 3,CO 2 H, 未取代的C 1 -C 25烷基,取代或未取代的C 2 -C 18烯基,取代或未取代的C 2 -C 18炔基,取代或未取代的芳基; 其中m为0,1或2; 并且其中n为0,1,2,3或4,并且其用作抗肿瘤剂。

    Antitumoral analogs
    18.
    发明申请
    Antitumoral analogs 有权
    抗肿瘤类似物

    公开(公告)号:US20060128711A1

    公开(公告)日:2006-06-15

    申请号:US10485536

    申请日:2002-08-06

    IPC分类号: A61K31/498 C07D498/22

    CPC分类号: C07D515/22

    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 arly, 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 C1-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.

    摘要翻译: 基团R 1,R 2,R 3,R 4,R 3,R 3,R 3,R 3,R 3,R 3, R 3和R 5各自独立地选自H,OH,OR',SH,SR',SOR',SO 2 R',C( -O)R',C(-O)OR',NO 2,NH 2,NHR',N(R')2 ,NHC(O)R',CN,卤素,-O,取代或未取代的C 1 -C 25烷基,取代或未取代的C 2 取代或未取代的C 2 -C 18炔基,取代或未取代的芳基,取代或未取代的杂环基; 其中X独立地选自OR',CN,(-O)或H; 其中每个R'基团独立地选自H,OH,NO 2,NH 2,SH,CN,卤素,-O,C( -O)H,C(-O)CH 3,CO 2 H,取代或未取代的C 1 -C 25烷基, 取代或未取代的C 1 -C 18链烯基,取代或未取代的C 2 -C 18烷基,取代或未取代的C 1 -C 18亚烷基, 炔基,取代或未取代的芳基; 其中m为0,1或2; 并且其中n为0,1,2,3或4,并且其用作抗肿瘤剂。

    Variolin derivatives and their use as antitumor agents
    19.
    发明授权
    Variolin derivatives and their use as antitumor agents 失效
    异喹啉衍生物及其作为抗肿瘤剂的用途

    公开(公告)号:US07772241B2

    公开(公告)日:2010-08-10

    申请号:US12349813

    申请日:2009-01-07

    IPC分类号: A61K31/519 C07D473/00

    摘要: Variolin derivatives of formula (5) are provided, wherein the substituent groups defined by X2, R1, R2, R3, R6, R7, and R12 are each independently selected from the group consisting of H, OH, OR′, SH, SR′, SOR′, SO2R′, NO2, NH2, NHR′, N(R′)2, NHCOR′, NHSO2R′, CN, halogen, ═O, C(═O)H, C(═O)R′, CO2H, CO2R′, carboxyalkyl, C1-C12 alkyl, C2-C12 alkenyl, C2-C12 alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted aralkyl and substituted or unsubstituted heteroaromatic; wherein each of the R′ groups is independently selected from the group consisting of H, OH, SH, NO2, NH2, CN, halogen, ═O, C(═O)H, C(═O)CH3, CO2H, CO2CH3, C1-C12 alkyl, C2-C12 alkenyl, C2-C12 alkynyl, aryl, aralkyl and heteroaromatic; wherein the pairs of groups of R1 and R2, R2 and R3, R3 and R12, R12 and R6, or R6 and R7 may be joined into a carbocyclic or heterocyclic ring system.

    摘要翻译: 提供了式(5)的衍生物,其中由X2,R1,R2,R3,R6,R7和R12定义的取代基各自独立地选自H,OH,OR',SH,SR' ,SOR',SO2R',NO2,NH2,NHR',N(R')2,NHCOR',NHSO2R',CN,卤素,= O,C(= O)H,C(= O)R' ,CO 2 R',羧基烷基,C 1 -C 12烷基,C 2 -C 12烯基,C 2 -C 12炔基,取代或未取代的芳基,取代或未取代的芳烷基和取代或未取代的杂芳族; 其中每个R'基团独立地选自H,OH,SH,NO 2,NH 2,CN,卤素,= O,C(= O)H,C(= O)CH 3,CO 2 H,CO 2 CH 3, C 1 -C 12烷基,C 2 -C 12烯基,C 2 -C 12炔基,芳基,芳烷基和杂芳族; 其中R 1和R 2,R 2和R 3,R 3和R 12,R 12和R 6,或R 6和R 7的这些基团可以连接成碳环或杂环系。