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用來治療癌症之雙(硫醯肼醯胺)鹽
专利权人:
SYNTA PHARMACEUTICALS CORP.
发明人:
KOSTIK, ELENA,艾雷娜 高斯提克,VAGHEFI, FARID,法利德 梵奇菲,LIANG, GUIQING,梁桂青,KOYA, KEIZO,古屋圭三,SUN, LIJUN,孙利军,孫利軍,TATSUTA, NORIAKI,辰田宪昭,辰田憲昭,CHEN, SHOUJUN,陈寿军,陳壽軍,INOUE, TAKAYO,井上孝也,艾雷娜 高斯提克,法利德 梵奇菲
申请号:
TW094120599
公开号:
TWI389684B
申请日:
2005.06.21
申请国别(地区):
TW
年份:
2013
代理人:
摘要:
Disclosed are bis (thio-hydrazide amide) disalts, which are represented by Structural Formula (I):Y is a covalent bond or a substituted or unsubstituted straight chained hydrocarbyl group. R1-R4are independently-H, an aliphatic group, a substituted aliphatic group, an aryl group or a substituted aryl group, or R1and R3taken together with the carbon and nitrogen atoms to which they are bonded, and/or R2and R4taken together with the carbon and nitrogen atoms to which they are bonded, form a non-aromatic heterocyclic ring optionally fused to an aromatic ring. Z is-O or-S. M+is a pharmaceutically acceptable monovalent cation and M2+is a pharmaceutically acceptable divalent cation.Also, disclosed are pharmaceutical compositions comprising a bis (thio-hydrazide amide) disalt described above. Further disclosed are methods of treating a subject with cancer. The methods comprise the step of administering an effective amount of a bis (thio-hydrazide amide) disalt described above.本發明係揭示雙(硫醯肼醯胺)二鹽,其由結構式(I)所代表:Y是共價鍵或經取代或未經取代之直鏈氫碳基。R1-R4獨立為-H、脂肪基、經取代的脂肪基、芳基或經取代的芳基,或R1和R3與其所鍵結的碳及氮原子結合在一起,和/或R2和R4與其所鍵結的碳及氮原子結合在一起形成非芳香族雜環,其視需要與芳環融合。Z是-O或-S。M+是醫藥上可接受的單價陽離子並且M2+是醫藥上可接受的二價陽離子。同時,本發明亦揭示包含以上所說明的雙(硫醯肼醯胺)二鹽之醫藥組成物。本發明還揭示治療罹患癌症的患者之方法。該方法包括施用有效量之以上所說明的雙(硫醯肼醯胺)二鹽之步驟。
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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