Invention Application
US20120322815A1 PHARMACEUTICAL COMPOSITION CONTAINING A3 ADENOSINE RECEPTOR AGONIST
审中-公开
含有腺苷受体激动剂的药物组合物
- Patent Title: PHARMACEUTICAL COMPOSITION CONTAINING A3 ADENOSINE RECEPTOR AGONIST
- Patent Title (中): 含有腺苷受体激动剂的药物组合物
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Application No.: US13516634Application Date: 2010-12-16
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Publication No.: US20120322815A1Publication Date: 2012-12-20
- Inventor: Lak Shin Jeong , Sang Kook Lee , Hwa Jin Chung , Hyuk Woo Lee
- Applicant: Lak Shin Jeong , Sang Kook Lee , Hwa Jin Chung , Hyuk Woo Lee
- Applicant Address: KR Seoul
- Assignee: EWHA UNIVERSITY-INDUSTRY COLLABORATION FOUNDATION
- Current Assignee: EWHA UNIVERSITY-INDUSTRY COLLABORATION FOUNDATION
- Current Assignee Address: KR Seoul
- Priority: KR10-2009-0126190 20091217; KR10-2009-0126195 20091217; KR10-2010-0009630 20100202
- International Application: PCT/KR2010/009036 WO 20101216
- Main IPC: A61K31/52
- IPC: A61K31/52 ; C07D473/40 ; A61P35/00 ; A61P29/00 ; A61P37/00 ; A61P1/00 ; A61P31/14 ; A61P11/08 ; A61P17/00 ; A61P1/04 ; A61P25/00 ; C07D473/34 ; A61P19/02

Abstract:
The present invention relates to a pharmaceutical composition for preventing or treating inflammatory disease, colorectal cancer and prostate cancer, which contains an A3 adenosine receptor agonist, 2-chloro-N6-(3-iodobenzyl)-4′-thioadenosine-5′-N-methyluronamide (thio-Cl-IB-MECA), N6-(3-iodobenzyl)-4′-thioadenosine-5′-N-methyluronamide (thio-IB-MECA), or a pharmaceutically acceptable salt thereof. The pharmaceutical composition of the invention is significantly less toxic than conventional A3 adenosine agonists, and thus is useful for prevention or treatment of inflammatory disease. In addition, it more selectively inhibits the growth of androgen receptor-dependent or independent prostate cancer cells than other A3 adenosine receptor agonists and thus is useful for prevention or treatment of colorectal cancer or prostate cancer.
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