ES2287739T3 - Inhibidores de metaloproteinasa de matriz. - Google Patents
Inhibidores de metaloproteinasa de matriz. Download PDFInfo
- Publication number
- ES2287739T3 ES2287739T3 ES04739544T ES04739544T ES2287739T3 ES 2287739 T3 ES2287739 T3 ES 2287739T3 ES 04739544 T ES04739544 T ES 04739544T ES 04739544 T ES04739544 T ES 04739544T ES 2287739 T3 ES2287739 T3 ES 2287739T3
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- Spain
- Prior art keywords
- sup
- sub
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- alkyl
- biphenyl
- 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.)
- Expired - Lifetime
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- 239000003112 inhibitor Substances 0.000 title abstract description 8
- 239000011159 matrix material Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 62
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 6
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 5
- 125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 4
- 125000001475 halogen functional group Chemical group 0.000 claims abstract 2
- 239000003814 drug Substances 0.000 claims description 8
- 238000011282 treatment Methods 0.000 claims description 6
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
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- 229940124597 therapeutic agent Drugs 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 15
- 102000002274 Matrix Metalloproteinases Human genes 0.000 abstract description 10
- 108010000684 Matrix Metalloproteinases Proteins 0.000 abstract description 10
- 125000003118 aryl group Chemical group 0.000 abstract description 6
- 238000002360 preparation method Methods 0.000 abstract description 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract description 3
- 125000006168 tricyclic group Chemical group 0.000 abstract 1
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
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- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
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- YPPNVJXWEXSSHZ-UHFFFAOYSA-N tert-butyl 3-hydroxy-5-(4-phenylphenyl)pentanoate Chemical compound C1=CC(CCC(O)CC(=O)OC(C)(C)C)=CC=C1C1=CC=CC=C1 YPPNVJXWEXSSHZ-UHFFFAOYSA-N 0.000 description 3
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- DJIIKVXNEHYGKS-UHFFFAOYSA-N 3-hydroxy-2-(4-phenylphenyl)pentanoic acid Chemical compound C1=CC(C(C(O)=O)C(O)CC)=CC=C1C1=CC=CC=C1 DJIIKVXNEHYGKS-UHFFFAOYSA-N 0.000 description 2
- IVJJRBPCKGCPJK-UHFFFAOYSA-N 3-hydroxy-2-methyl-5-(4-phenylphenyl)pentanoic acid Chemical compound C1=CC(CCC(O)C(C)C(O)=O)=CC=C1C1=CC=CC=C1 IVJJRBPCKGCPJK-UHFFFAOYSA-N 0.000 description 2
- SJCUUBUCSXBNFV-UHFFFAOYSA-N 3-hydroxy-5-(4-iodophenyl)pentanoic acid Chemical compound OC(=O)CC(O)CCC1=CC=C(I)C=C1 SJCUUBUCSXBNFV-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
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- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 2
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- 201000004624 Dermatitis Diseases 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 102000005741 Metalloproteases Human genes 0.000 description 2
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- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical compound [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
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- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
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- C07C233/54—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of a saturated carbon skeleton
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- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
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- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/04—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
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GB0321538D0 (en) * | 2003-09-13 | 2003-10-15 | Glaxo Group Ltd | Therapeutically useful compounds |
EA013539B1 (ru) * | 2005-02-22 | 2010-06-30 | Рэнбакси Лабораториз Лимитед | Производные 5-фенилпентановой кислоты в качестве ингибиторов матричной металлопротеиназы для лечения астмы и других заболеваний |
SI2074093T1 (sl) | 2006-08-22 | 2012-12-31 | Ranbaxy Laboratories Limited | Postopek za pridobitev inhibitorjev matrične metalproteinaze in kiralni pomožnik zanj |
ES2569660T3 (es) | 2007-06-08 | 2016-05-12 | Mannkind Corporation | Inhibidores de la IRE-1alfa |
JP2013537533A (ja) | 2010-07-30 | 2013-10-03 | ランバクシー ラボラトリーズ リミテッド | マトリックスメタロプロテイナーゼ阻害剤 |
AU2011306396A1 (en) | 2010-09-24 | 2013-05-02 | Ranbaxy Laboratories Limited | Matrix metalloproteinase inhibitors |
AU2011323617B2 (en) | 2010-11-03 | 2015-02-05 | Corteva Agriscience Llc | Pesticidal compositions and processes related thereto |
US9750789B2 (en) * | 2011-02-18 | 2017-09-05 | The Trustees Of Columbia University In The City Of New York | Use of matrix metalloproteinase inhibitors to treat tuberculosis |
US8937083B2 (en) | 2011-10-26 | 2015-01-20 | DowAgroSciences, LLC | Pesticidal compositions and processes related thereto |
EP2601941A1 (en) * | 2011-12-06 | 2013-06-12 | Ludwig-Maximilians-Universität München | Beta-O/S/N fatty acid based compounds as antibacterial and antiprotozoal agents |
US9282739B2 (en) | 2012-04-27 | 2016-03-15 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
US9708288B2 (en) | 2012-04-27 | 2017-07-18 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
US20130291227A1 (en) | 2012-04-27 | 2013-10-31 | Dow Agrosciences Llc | Pesticidal compositions and processes related thereto |
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US6350885B1 (en) * | 1998-07-30 | 2002-02-26 | Warner-Lambert Company | Tricyclic heteroaromatics and their derivatives as inhibitors of matrix metalloproteinases |
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US20060160875A1 (en) | 2006-07-20 |
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WO2004110974A1 (en) | 2004-12-23 |
ATE362910T1 (de) | 2007-06-15 |
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