JP2012526798A5 - - Google Patents
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- Publication number
- JP2012526798A5 JP2012526798A5 JP2012510440A JP2012510440A JP2012526798A5 JP 2012526798 A5 JP2012526798 A5 JP 2012526798A5 JP 2012510440 A JP2012510440 A JP 2012510440A JP 2012510440 A JP2012510440 A JP 2012510440A JP 2012526798 A5 JP2012526798 A5 JP 2012526798A5
- Authority
- JP
- Japan
- Prior art keywords
- composition according
- agonist
- iop
- meca
- subject
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000556 agonist Substances 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- 239000000969 carrier Substances 0.000 claims 3
- 125000006482 3-iodobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(I)=C1[H])C([H])([H])* 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- XTPOZVLRZZIEBW-SCFUHWHPSA-N (2R,3R,4S,5R)-2-[6-[2-(4-aminophenyl)ethylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical group C1=CC(N)=CC=C1CCNC1=NC=NC2=C1N=CN2[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 XTPOZVLRZZIEBW-SCFUHWHPSA-N 0.000 claims 1
- IPSYPUKKXMNCNQ-PFHKOEEOSA-N (2S,3S,4R,5R)-5-[2-chloro-6-[(3-iodophenyl)methylamino]purin-9-yl]-3,4-dihydroxy-N-methyloxolane-2-carboxamide Chemical compound O[C@@H]1[C@H](O)[C@@H](C(=O)NC)O[C@H]1N1C2=NC(Cl)=NC(NCC=3C=C(I)C=CC=3)=C2N=C1 IPSYPUKKXMNCNQ-PFHKOEEOSA-N 0.000 claims 1
- 125000003853 4-amino-3-iodobenzyl group Chemical group [H]N([H])C1=C(I)C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 208000008784 Apnea Diseases 0.000 claims 1
- 206010002974 Apnoea Diseases 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 239000002552 dosage form Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 230000000699 topical Effects 0.000 claims 1
Claims (9)
- A3AR作動薬がIOPの被検者のIOPの低下に有効であり有効成分として前記A3AR作動薬および生理学的に許容される担体を含有する、前記被検者のIOPを低下させる医薬組成物。
- 前記被検者がヒト被検者である、請求項1に記載に医薬組成物。
- 亢進したIOPを有する被験者のIOPを低下させるための、請求項1または2に記載の医薬組成物。
- 前記担体がA3 AR作動薬の経口投与に好適である、請求項1から3のいずれか1項に記載の組成物。
- 1日2回の投与に好適な剤形で製剤された、請求項4記載の組成物。
- 前記担体が前記A3 AR作動薬の局所投与に好適である、請求項1から5のいずれか1項に記載の組成物。
- 目に前記A3 AR作動薬を投与するために製剤した、請求項6記載の組成物。
- 前記A 3 AR作動薬がN6−2‐(4−アミノフェニル)エチルアデノシン(APNEA)、N6‐(4‐アミノ‐3‐ヨードベンジル)‐アデノシン‐5’‐N‐メチルウロンアミド(AB−MECA)、N6‐(3‐ヨードベンジル)‐アデノシン‐5’‐N‐メチルウロンアミド(IB‐MECA)および2−クロロ−N6−(3−ヨードベンジル)−アデノシン‐5’‐N‐メチルウロンアミド(CI‐IB−MECA)からなる群から選択される、請求項1から7のいずれか1項に記載の組成物。
- 前記A 3 AR作動薬がIB−MECAである、請求項8記載の組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IL198787 | 2009-05-17 | ||
IL19878709 | 2009-05-17 | ||
PCT/IL2010/000393 WO2010134067A1 (en) | 2009-05-17 | 2010-05-16 | A3 adenosine receptor agonists for the reduction of intraocular pressure |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2012526798A JP2012526798A (ja) | 2012-11-01 |
JP2012526798A5 true JP2012526798A5 (ja) | 2013-07-04 |
JP5849044B2 JP5849044B2 (ja) | 2016-01-27 |
Family
ID=42352183
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012510440A Expired - Fee Related JP5849044B2 (ja) | 2009-05-17 | 2010-05-16 | 眼圧低下のためのa3アデノシン受容体作動薬 |
Country Status (10)
Country | Link |
---|---|
US (1) | US8557790B2 (ja) |
EP (1) | EP2432475A1 (ja) |
JP (1) | JP5849044B2 (ja) |
KR (1) | KR20120022919A (ja) |
CN (1) | CN102427819A (ja) |
AU (1) | AU2010250759B2 (ja) |
CA (1) | CA2761499A1 (ja) |
IL (1) | IL216114A (ja) |
MX (1) | MX2011012229A (ja) |
WO (1) | WO2010134067A1 (ja) |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5443836A (en) | 1993-03-15 | 1995-08-22 | Gensia, Inc. | Methods for protecting tissues and organs from ischemic damage |
AU7331094A (en) | 1993-07-13 | 1995-02-13 | United States Of America, As Represented By The Secretary, Department Of Health And Human Services, The | A3 adenosine receptor agonists |
US5688774A (en) | 1993-07-13 | 1997-11-18 | The United States Of America As Represented By The Department Of Health And Human Services | A3 adenosine receptor agonists |
AU1399297A (en) | 1996-01-24 | 1997-08-20 | Sumitomo Chemical Company, Limited | Dihalopropene compounds, their use as insecticides/acaricides and intermediates for their production |
US6048865A (en) | 1997-07-29 | 2000-04-11 | Medco Research, Inc. | N6 -substituted-adenosine-5'-uronamides as adenosine receptor modulator |
WO1999006053A1 (en) | 1997-07-29 | 1999-02-11 | Medco Research, Inc. | N6-substituted-adenosine-5'-uronamides as adenosine receptor modulators |
US6329349B1 (en) | 1997-10-23 | 2001-12-11 | Trustees Of The University Of Pennsylvania | Methods for reducing ischemic injury of the heart via the sequential administration of monophosphoryl lipid A and adenosine receptor agents |
US6217896B1 (en) | 1999-04-01 | 2001-04-17 | Uab Research Foundation | Conjunctival inserts for topical delivery of medication or lubrication |
IL133680A0 (en) | 1999-09-10 | 2001-04-30 | Can Fite Technologies Ltd | Pharmaceutical compositions comprising an adenosine receptor agonist or antagonist |
AU2003282359A1 (en) * | 2002-11-19 | 2004-06-15 | Can-Fite Biopharma Ltd. | A3ar agonists for the treatment of inflammatory arthritis |
BRPI0517639A (pt) * | 2004-11-08 | 2008-10-14 | Can Fite Biopharma Ltd | método para o tratamento de ressorção óssea acelerada, composição farmacêutica, e, uso de um agonista de a3ar |
CN101083998A (zh) * | 2004-11-22 | 2007-12-05 | 王者制药研究发展有限公司 | 用腺苷a3受体激动剂强化治疗hif-1介导的病症 |
WO2007002139A2 (en) * | 2005-06-22 | 2007-01-04 | The Trustees Of The University Of Pennsylvania | Neuroprotection of retinal ganglion cells |
DK1983990T3 (da) * | 2006-01-26 | 2011-07-11 | Us Gov Health & Human Serv | Allosteriske A3-adenosin-receptormodulatorer |
BRPI0621052A2 (pt) * | 2006-01-27 | 2012-07-17 | Can Fite Biopharma Ltd | uso de um agonista de receptor de adenosina a3 (a3ar) |
US8153781B2 (en) * | 2007-06-29 | 2012-04-10 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Dendrimer conjugates of agonists and antagonists of the GPCR superfamily |
EP3039030B1 (en) * | 2013-08-29 | 2018-09-19 | Yeda Research and Development Co. Ltd. | Selective inhibitors of alpha2 isoform of na,k-atpase and use for reduction of intra-ocular pressure |
-
2010
- 2010-05-16 JP JP2012510440A patent/JP5849044B2/ja not_active Expired - Fee Related
- 2010-05-16 EP EP10726312A patent/EP2432475A1/en not_active Withdrawn
- 2010-05-16 MX MX2011012229A patent/MX2011012229A/es not_active Application Discontinuation
- 2010-05-16 AU AU2010250759A patent/AU2010250759B2/en not_active Ceased
- 2010-05-16 KR KR1020117026858A patent/KR20120022919A/ko not_active Application Discontinuation
- 2010-05-16 US US13/320,715 patent/US8557790B2/en not_active Expired - Fee Related
- 2010-05-16 CA CA2761499A patent/CA2761499A1/en not_active Abandoned
- 2010-05-16 CN CN2010800212202A patent/CN102427819A/zh active Pending
- 2010-05-16 WO PCT/IL2010/000393 patent/WO2010134067A1/en active Application Filing
-
2011
- 2011-11-03 IL IL216114A patent/IL216114A/en not_active IP Right Cessation
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