发明名称 Antitumoral analogs of lamellarins
摘要 New lamellarins are provided of the general formula III wherein X is selected from the group consisting of N, O and S; wherein R<SUB>1</SUB>, R<SUB>2</SUB>, R<SUB>3</SUB>, R<SUB>4</SUB>, R<SUB>5</SUB>, R<SUB>6</SUB>, R<SUB>7</SUB>, R<SUB>8 </SUB>and R<SUB>9 </SUB>are each independently selected from the group consisting of H, OH, OR', SH, SR', SO<SUB>2</SUB>R', NHR', N(R')<SUB>2</SUB>, N-R', NHCOR', N(COR')<SUB>2</SUB>, NHS0<SUB>2</SUB>R', N0<SUB>2</SUB>, PO(R'<SUB>2</SUB>, P0<SUB>2</SUB>R', C(=0)H, C(=0)R', C0<SUB>2</SUB>H, C0<SUB>2</SUB>R', OPO(R')<SUB>2</SUB>, OP0<SUB>2</SUB>R', OC(=0)H, OC(=0)R', N-C(R')<SUB>2</SUB>, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>12 </SUB>alkyl, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>12 </SUB>haloalkyl, substituted or unsubstituted C<SUB>2</SUB>-C<SUB>12 </SUB>alkenyl, substituted or unsubstituted C<SUB>2</SUB>-C<SUB>12 </SUB>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, N0<SUB>2</SUB>, NH<SUB>2</SUB>, SH, CN, halogen, =0, C(=0)H, C(-O)CH<SUB>3</SUB>, C0<SUB>2</SUB>H, C(=0)R', substituted or unsubstituted C<SUB>1</SUB>-C<SUB>18 </SUB>alkyl, substituted or unsubstituted C<SUB>2</SUB>-C<SUB>18 </SUB>alkenyl, substituted or unsubstituted C<SUB>2</SUB>-C<SUB>18 </SUB>alkynyl, substituted or unsubstituted aryl, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>18 </SUB>alkoxyl, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>18 </SUB>aminoalkyl, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>18 </SUB>aminoacid, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>18 </SUB>thioalkyl, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>18 </SUB>alkylsulfinyl, substituted or unsubstituted C<SUB>1</SUB>-C<SUB>18 </SUB>alkylsulfonyl; wherein the pairs of groups R<SUB>1 </SUB>and R<SUB>2</SUB>, R<SUB>2 </SUB>and R<SUB>3</SUB>, R<SUB>3 </SUB>and R<SUB>4</SUB>, R<SUB>3 </SUB>and R<SUB>9</SUB>, R<SUB>4 </SUB>and R<SUB>9</SUB>, R<SUB>9 </SUB>and R<SUB>5</SUB>, R<SUB>9 </SUB>and R<SUB>6</SUB>, or R<SUB>6 </SUB>and R<SUB>7</SUB>, R<SUB>7 </SUB>and R<SUB>8 </SUB>may be joined into a carbocyclic or heterocyclic ring system; and the dotted line represents an single or double bond; or a pharmaceutically acceptable salt, derivative, prodrug or stereoisomer thereof.
申请公布号 US2006173030(A1) 申请公布日期 2006.08.03
申请号 US20050524151 申请日期 2005.08.01
申请人 BAILLY CHRISTIAN;FRANCESCH ANDRES;MATEO URBANO MARIA C;JIMENEZ GUERRERO JOSE A;PASTOR DEL CASTILLO ALFREDO;CUEVAS MARCHANTE CARMEN 发明人 BAILLY CHRISTIAN;FRANCESCH ANDRES;MATEO URBANO MARIA C.;JIMENEZ GUERRERO JOSE A.;PASTOR DEL CASTILLO ALFREDO;CUEVAS MARCHANTE CARMEN
分类号 A61K31/4745;C07D491/147;A61K31/437;A61K31/675;A61P35/00;A61P43/00;C07D471/14;C07D491/00;C07D491/02;C07D491/14;C07D498/02 主分类号 A61K31/4745
代理机构 代理人
主权项
地址