JP2007536241A - 糖尿病性腎症の処置のためのａ２ａアデノシンレセプターアゴニスト - Google Patents
糖尿病性腎症の処置のためのａ２ａアデノシンレセプターアゴニスト Download PDFInfo
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- JP2007536241A JP2007536241A JP2007511486A JP2007511486A JP2007536241A JP 2007536241 A JP2007536241 A JP 2007536241A JP 2007511486 A JP2007511486 A JP 2007511486A JP 2007511486 A JP2007511486 A JP 2007511486A JP 2007536241 A JP2007536241 A JP 2007536241A
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- Prior art keywords
- carboxylic acid
- piperidine
- alkyl
- aryl
- alkylene
- Prior art date
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- 208000007342 Diabetic Nephropathies Diseases 0.000 title claims abstract description 51
- 208000033679 diabetic kidney disease Diseases 0.000 title claims abstract description 51
- 239000003379 purinergic P1 receptor agonist Substances 0.000 title claims abstract description 30
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- 238000002560 therapeutic procedure Methods 0.000 claims abstract description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 84
- 239000001257 hydrogen Substances 0.000 claims description 82
- -1 pyrrolidino, piperidino, morpholino Chemical group 0.000 claims description 78
- 125000003118 aryl group Chemical group 0.000 claims description 70
- 150000001875 compounds Chemical class 0.000 claims description 68
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 53
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 52
- 125000002947 alkylene group Chemical group 0.000 claims description 48
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 41
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 37
- 125000001072 heteroaryl group Chemical group 0.000 claims description 37
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 36
- FLEVIENZILQUKB-DMJMAAGCSA-N methyl 4-[3-[6-amino-9-[(2r,3r,4s,5s)-5-(ethylcarbamoyl)-3,4-dihydroxyoxolan-2-yl]purin-2-yl]prop-2-ynyl]cyclohexane-1-carboxylate Chemical compound O[C@@H]1[C@H](O)[C@@H](C(=O)NCC)O[C@H]1N1C2=NC(C#CCC3CCC(CC3)C(=O)OC)=NC(N)=C2N=C1 FLEVIENZILQUKB-DMJMAAGCSA-N 0.000 claims description 35
- 125000000623 heterocyclic group Chemical group 0.000 claims description 33
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- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 19
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- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethyl cyclohexane Natural products CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 claims description 16
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- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 14
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- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 12
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- 125000003545 alkoxy group Chemical group 0.000 claims description 9
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- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 9
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- 150000001602 bicycloalkyls Chemical group 0.000 claims description 7
- XTVMZZBLCLWBPM-UHFFFAOYSA-N tert-butylcyclohexane Chemical compound CC(C)(C)C1CCCCC1 XTVMZZBLCLWBPM-UHFFFAOYSA-N 0.000 claims description 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
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- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 6
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
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- HJORMJIFDVBMOB-UHFFFAOYSA-N rolipram Chemical group COC1=CC=C(C2CC(=O)NC2)C=C1OC1CCCC1 HJORMJIFDVBMOB-UHFFFAOYSA-N 0.000 claims description 5
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- 125000001424 substituent group Chemical group 0.000 claims description 5
- XAZKFISIRYLAEE-UHFFFAOYSA-N 1,3-dimethylcyclopentane Chemical compound CC1CCC(C)C1 XAZKFISIRYLAEE-UHFFFAOYSA-N 0.000 claims description 4
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 claims description 4
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- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 4
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- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- General Health & Medical Sciences (AREA)
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| PCT/US2005/015241 WO2005107463A1 (en) | 2004-05-03 | 2005-05-03 | Agonists of a2a adenosine receptors for treatment of diabetic nephropathy |
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| JP2007536241A5 JP2007536241A5 (https=) | 2008-06-19 |
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| EP (1) | EP1746885A4 (https=) |
| JP (1) | JP2007536241A (https=) |
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Cited By (2)
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|---|---|---|---|---|
| JP2011526894A (ja) * | 2008-07-03 | 2011-10-20 | ユニバーシティ オブ バージニア パテント ファウンデーション | アパデノソンの単位投薬量 |
| WO2011158933A1 (ja) | 2010-06-17 | 2011-12-22 | 日東電工株式会社 | 腎線維症処置剤 |
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| US6232297B1 (en) * | 1999-02-01 | 2001-05-15 | University Of Virginia Patent Foundation | Methods and compositions for treating inflammatory response |
| CA2414623A1 (en) * | 2000-08-01 | 2002-02-07 | University Of Virginia Patent Foundation | Use of selective adenosine a1 receptor agonists, antagonists and allosteric enhancers to manipulate angiogenesis |
| NZ556354A (en) | 2001-10-01 | 2008-10-31 | Univ Virginia | 2-Propynyl adenosine analogs having A2A agonist activity and compositions thereof |
| EP1496911B1 (en) * | 2002-04-10 | 2007-12-19 | University Of Virginia Patent Foundation | Use of a combination comprising a2a adenosine receptor agonists and anti-pathogenic agents for the treatment of inflammatory diseases |
| US7396825B2 (en) | 2004-05-03 | 2008-07-08 | University Of Virginia Patent Foundation | Agonists of A2A adenosine receptors for treatment of diabetic nephropathy |
| US7576069B2 (en) | 2004-08-02 | 2009-08-18 | University Of Virginia Patent Foundation | 2-polycyclic propynyl adenosine analogs having A2A agonist activity |
| AU2005267706B2 (en) * | 2004-08-02 | 2011-12-08 | University Of Virginia Patent Foundation | 2-propynyl adenosine analogs with modified 5'-ribose groups having A2A agonist activity |
| GT200500281A (es) | 2004-10-22 | 2006-04-24 | Novartis Ag | Compuestos organicos. |
| GB0500785D0 (en) | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| JP2009514969A (ja) | 2005-11-09 | 2009-04-09 | コンビナトアールエックス インコーポレーティッド | 医学的状態を治療するための方法、組成物、およびキット |
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| WO2011158933A1 (ja) | 2010-06-17 | 2011-12-22 | 日東電工株式会社 | 腎線維症処置剤 |
| KR20130121813A (ko) | 2010-06-17 | 2013-11-06 | 닛토덴코 가부시키가이샤 | 신장 섬유증 치료 물질 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1746885A4 (en) | 2010-09-08 |
| US20050261236A1 (en) | 2005-11-24 |
| WO2005107463A1 (en) | 2005-11-17 |
| EP1746885A1 (en) | 2007-01-31 |
| US7396825B2 (en) | 2008-07-08 |
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