发明授权
US07304092B1 Compounds and methods for treating tumors, cancer and hyperproliferative diseases
有权
用于治疗肿瘤,癌症和过度增生性疾病的化合物和方法
- 专利标题: Compounds and methods for treating tumors, cancer and hyperproliferative diseases
- 专利标题(中): 用于治疗肿瘤,癌症和过度增生性疾病的化合物和方法
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申请号: US10705483申请日: 2003-11-11
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公开(公告)号: US07304092B1公开(公告)日: 2007-12-04
- 发明人: David J. Austin , Viet-Ahn A. Nguyen , Doris Pupowicz , Albert Deisseroth , Tao Wang , Enrica Lerma
- 申请人: David J. Austin , Viet-Ahn A. Nguyen , Doris Pupowicz , Albert Deisseroth , Tao Wang , Enrica Lerma
- 申请人地址: US CT New Haven
- 专利权人: Yale University
- 当前专利权人: Yale University
- 当前专利权人地址: US CT New Haven
- 代理商 Henry D. Coleman; R. Neil Sudol; William J. Sapone
- 主分类号: A61K31/215
- IPC分类号: A61K31/215
摘要:
The present invention relates to novel compounds, pharmaceutical compositions and methods for treating tumors, cancer and hyperproliferative diseases including psoriasis, genital warts and hyperproliferative cell growth diseases, including hyperproliferative keratinocyte diseases such as hyperkeratosis, ichthyosis, keratoderma or lichen planus. These compounds are described according to the chemical structure: where R1 is H, OH, F, Cl, Br, I, a C1-C6 optionally substituted alkyl or alkenyl group, an optionally substituted aryl group or a group; Ra is a H, OH, C1-C10, optionally substituted alkyl or alkenyl group, an optionally substituted O—(C1-C7 alkyl group) or O-aryl group, an amine group which is optionally substituted with at least one C1-C10 alkyl group which may be optionally substituted, or a single optionally substituted aryl group, biphenyl group, (C1-C6) alkylenearyl group, (C1-C6) alkylenebiphenyl group, heteroaryl group, heterocyclic group, (C1-C6) alkylene heteroaryl group or (C1-C6) alkylene heterocyclic group; R2 is a group; Rb is a H, OH, C1-C10, optionally substituted alkyl or alkenyl group, an optionally substituted O—(C1-C7 alkyl group) or O-aryl group, an amine group which is optionally substituted with at least one C1-C10 alkyl group which may be optionally substituted, or a single optionally substituted aryl group, biphenyl group, (C1-C6) alkylenearyl group, (C1-C6) alkylenebiphenyl group, heteroaryl group, heterocyclic group, (C1-C6) alkylene heteroaryl group or (C1-C6) alkylene heterocyclic group; R3 and R6 are each independently selected from H, OH, F, Cl, Br, I, a C1-C6 optionally substituted alkyl or alkenyl group, an optionally substituted aryl group, a carbamate, alkylene carbamate, urethane or alkylene urethane; R4 is a group, wherein Rb is as described above; and R5 is a group, wherein Rb is as described above, with the proviso that at least one of R1 and R2 or R4 and R5 contains an Ra or Rb group which is an amine group which is optionally substituted with at least one C1-C10 alkyl group which may be optionally substituted, or a single optionally substituted aryl group, biphenyl group, (C1-C6) alkylenearyl group, (C1-C6) alkylenebiphenyl group, heteroaryl group, heterocyclic group, (C1-C6) alkylene heteroaryl group or (C1-C6) alkylene heterocyclic group; or a stereoisomer, pharmaceutically acceptable salt, solvate, and polymorph thereof.
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