发明名称 Degradation fragments
摘要 A pharmaceutical composition comprising a compound of formula (I) wherein X is an electron withdrawing group, Y<SUP>1 </SUP>is hydrogen, alkyl, alkenyl, alkynyl, aryl, heterocyclyl, -SO<SUB>2</SUB>R<SUP>4</SUP>, -CO<SUB>2</SUB>R<SUP>4</SUP>, -CONHR<SUP>4 </SUP>or -COR<SUP>4</SUP>, and each of R<SUP>1</SUP>, R<SUP>2 </SUP>and R<SUP>4</SUP>, which may be the same or different, is hydrogen, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl or heterocyclyl, or a compound of formula (II) wherein each of Y<SUP>2 </SUP>and Y<SUP>3</SUP>, which may be the same or different, is hydrogen, alkyl, alkenyl, alkynyl, aryl, heterocyclyl, -SO<SUB>2</SUB>R<SUP>9</SUP>, -CO<SUB>2</SUB>R<SUP>9</SUP>, -CONHR<SUP>9 </SUP>or -COR<SUP>9</SUP>, Z is hydrogen, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclyl, -CH-C(NHR<SUP>10</SUP>)CH((CH<SUB>2</SUB>)<SUB>m</SUB>CO<SUB>2</SUB>R<SUP>11</SUP>)(C-O)CH<SUB>3 </SUB>or -CH<SUB>2</SUB>(C-O)CH((CH<SUB>2</SUB>)<SUB>m</SUB>CO<SUB>2</SUB>R<SUP>11</SUP>)(C-O)CH<SUB>3</SUB>, R<SUP>8 </SUP>is -(CH<SUB>2</SUB>)<SUB>n</SUB>CO<SUB>2</SUB>R<SUP>12</SUP>, each of R<SUP>5 </SUP>to R<SUP>7 </SUP>and R<SUP>9 </SUP>to R<SUP>12</SUP>, which may be the same or different, is hydrogen, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl or heterocyclyl, and each of m and n, which may be the same or different, is 1 to 6 or a compound of formula (III) wherein each of Y<SUP>4 </SUP>to Y<SUP>6</SUP>, which may be the same or different, is hydrogen, alkyl, alkenyl, alkynyl, aryl, heterocyclyl, -SO<SUB>2</SUB>R<SUP>19</SUP>, -CO<SUB>2</SUB>R<SUP>19</SUP>, -CONHR<SUP>19 </SUP>or -COR<SUP>19</SUP>, each of R<SUP>16 </SUP>and R<SUP>17</SUP>, which may be the same or different, is -(CH<SUB>2</SUB>)<SUB>p</SUB>CO<SUB>2</SUB>R<SUP>20</SUP>, each of R<SUP>13 </SUP>TO R<SUP>15 </SUP>and R<SUP>18 </SUP>to R<SUP>20</SUP>, which may be the same or different, is hydrogen, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl or heterocyclyl, and p is 1 to 6, or other photolabile degradation product of bilirubin or biliverdin or derivative of a photolabile degradation fragment of bilirubin or biliverdin, or a pharmaceutically acceptable salt thereof, together with a pharmaceutically acceptable carrier or diluent
申请公布号 AU3577901(A) 申请公布日期 2001.09.03
申请号 AU20010035779 申请日期 2001.02.26
申请人 ISIS INNOVATION LIMITED 发明人 JOSEPH FLOYD CLARK;THOMAS ANDREW DANIEL CADOUX-HUDSON;CHRISTOPHER JOSEPH SCHOFIELD
分类号 G01N33/53;A61K31/40;A61K31/4015;A61K31/4025;A61K41/00;A61M1/14;A61P7/00;A61P9/00;A61P9/08;A61P9/10;C07D207/44;C07D207/448;C07D413/06;G01N33/72 主分类号 G01N33/53
代理机构 代理人
主权项
地址