ES2618352T3 - Antagonistas del receptor de prostaglandina D2 para el tratamiento de la alopecia androgenética - Google Patents
Antagonistas del receptor de prostaglandina D2 para el tratamiento de la alopecia androgenética Download PDFInfo
- Publication number
- ES2618352T3 ES2618352T3 ES07809581.7T ES07809581T ES2618352T3 ES 2618352 T3 ES2618352 T3 ES 2618352T3 ES 07809581 T ES07809581 T ES 07809581T ES 2618352 T3 ES2618352 T3 ES 2618352T3
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- ES
- Spain
- Prior art keywords
- methyl
- benzoyl
- ylmethoxy
- indole
- dihydro
- 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.)
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- 201000004384 Alopecia Diseases 0.000 title abstract 2
- 206010068168 androgenetic alopecia Diseases 0.000 title abstract 2
- 201000002996 androgenic alopecia Diseases 0.000 title abstract 2
- 239000002464 receptor antagonist Substances 0.000 title description 6
- 229940044551 receptor antagonist Drugs 0.000 title description 6
- 102000009389 Prostaglandin D receptors Human genes 0.000 title 1
- 108050000258 Prostaglandin D receptors Proteins 0.000 title 1
- 229940122913 Prostaglandin D2 receptor antagonist Drugs 0.000 abstract 1
- 102000005962 receptors Human genes 0.000 abstract 1
- 108020003175 receptors Proteins 0.000 abstract 1
- 210000004761 scalp Anatomy 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 22
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 22
- -1 benzyl ester Chemical class 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 8
- 125000004430 oxygen atom Chemical group O* 0.000 description 7
- 125000004434 sulfur atom Chemical group 0.000 description 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 5
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 125000004953 trihalomethyl group Chemical group 0.000 description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 description 2
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 description 2
- FWFRRGYZSXNHEN-NRFANRHFSA-N 2-[1-[2-methyl-4-[[(2s)-4-methyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]indol-4-yl]acetic acid Chemical compound O1C2=CC=CC=C2N(C)C[C@H]1COC(C=C1C)=CC=C1C(=O)N1C2=CC=CC(CC(O)=O)=C2C=C1 FWFRRGYZSXNHEN-NRFANRHFSA-N 0.000 description 2
- LYXITARYJFNGKJ-FQEVSTJZSA-N 2-[1-[4-[[(3s)-2,3-dihydro-1-benzofuran-3-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound C1OC2=CC=CC=C2[C@H]1COC(C=C1)=CC=C1C(=O)N1C2=CC=CC(CC(O)=O)=C2C=C1C LYXITARYJFNGKJ-FQEVSTJZSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 125000002837 carbocyclic group Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 125000004043 oxo group Chemical group O=* 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 description 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 1
- LRYXCWKTCRUSKY-QHCPKHFHSA-N 2-[1-[4-[[(2s)-1-ethyl-2,3-dihydroindol-2-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound C1C2=CC=CC=C2N(CC)[C@@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CC(O)=O)=C3C=C2C)C=C1 LRYXCWKTCRUSKY-QHCPKHFHSA-N 0.000 description 1
- PDLHJVXUGHZZQP-QHCPKHFHSA-N 2-[1-[4-[[(2s)-4,6-dimethyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound O1C2=CC=C(C)C=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CC(O)=O)=C3C=C2C)C=C1 PDLHJVXUGHZZQP-QHCPKHFHSA-N 0.000 description 1
- IYHQJRACZJPXQR-QHCPKHFHSA-N 2-[1-[4-[[(2s)-4,7-dimethyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound O1C2=CC(C)=CC=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CC(O)=O)=C3C=C2C)C=C1 IYHQJRACZJPXQR-QHCPKHFHSA-N 0.000 description 1
- PKELGWLBIVXMAL-QHCPKHFHSA-N 2-[1-[4-[[(2s)-4,8-dimethyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound O1C2=C(C)C=CC=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CC(O)=O)=C3C=C2C)C=C1 PKELGWLBIVXMAL-QHCPKHFHSA-N 0.000 description 1
- BTHUBRJFQVQARS-NRFANRHFSA-N 2-[1-[4-[[(2s)-4-methyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]indol-4-yl]acetic acid Chemical compound O1C2=CC=CC=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CC(O)=O)=C3C=C2)C=C1 BTHUBRJFQVQARS-NRFANRHFSA-N 0.000 description 1
- RGWJLTVSSDJWIX-QFIPXVFZSA-N 2-[1-[4-[[(2s)-5-methoxy-4-methyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound CC1=CC2=C(CC(O)=O)C=CC=C2N1C(=O)C(C=C1)=CC=C1OC[C@H]1OC(C=CC=C2OC)=C2N(C)C1 RGWJLTVSSDJWIX-QFIPXVFZSA-N 0.000 description 1
- OOSKJUCSXNQQLG-QFIPXVFZSA-N 2-[1-[4-[[(2s)-7-fluoro-4-methyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound O1C2=CC(F)=CC=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CC(O)=O)=C3C=C2C)C=C1 OOSKJUCSXNQQLG-QFIPXVFZSA-N 0.000 description 1
- OCCPUDPMKJXBQC-OAQYLSRUSA-N 2-[1-[4-[[(3r)-2,3-dihydro-1,4-benzodioxin-3-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound C1OC2=CC=CC=C2O[C@@H]1COC(C=C1)=CC=C1C(=O)N1C2=CC=CC(CC(O)=O)=C2C=C1C OCCPUDPMKJXBQC-OAQYLSRUSA-N 0.000 description 1
- LYXITARYJFNGKJ-HXUWFJFHSA-N 2-[1-[4-[[(3r)-2,3-dihydro-1-benzofuran-3-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound C1OC2=CC=CC=C2[C@@H]1COC(C=C1)=CC=C1C(=O)N1C2=CC=CC(CC(O)=O)=C2C=C1C LYXITARYJFNGKJ-HXUWFJFHSA-N 0.000 description 1
- UBJVBXKPUVQJGZ-LJQANCHMSA-N 2-[1-[4-[[(3r)-5-fluoro-2,3-dihydro-1-benzofuran-3-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound C1OC2=CC=C(F)C=C2[C@@H]1COC(C=C1)=CC=C1C(=O)N1C2=CC=CC(CC(O)=O)=C2C=C1C UBJVBXKPUVQJGZ-LJQANCHMSA-N 0.000 description 1
- JPRFNTRHBYRBKQ-LJQANCHMSA-N 2-[1-[4-[[(3r)-7-fluoro-2,3-dihydro-1-benzofuran-3-yl]methoxy]benzoyl]-2-methylindol-4-yl]acetic acid Chemical compound C1OC(C(=CC=C2)F)=C2[C@@H]1COC(C=C1)=CC=C1C(=O)N1C2=CC=CC(CC(O)=O)=C2C=C1C JPRFNTRHBYRBKQ-LJQANCHMSA-N 0.000 description 1
- XECAIYOLUPUKEJ-QFIPXVFZSA-N 2-[2-methyl-1-[4-[[(2s)-4-methyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]indol-4-yl]acetic acid Chemical compound O1C2=CC=CC=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CC(O)=O)=C3C=C2C)C=C1 XECAIYOLUPUKEJ-QFIPXVFZSA-N 0.000 description 1
- MBWGGQJQWWBUQO-NRFANRHFSA-N 2-[2-methyl-1-[4-[[(2s)-4-methyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]benzoyl]indol-4-yl]oxyacetic acid Chemical compound O1C2=CC=CC=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(OCC(O)=O)=C3C=C2C)C=C1 MBWGGQJQWWBUQO-NRFANRHFSA-N 0.000 description 1
- OGLLEKOVLBGGFR-OAQYLSRUSA-N 2-[2-methyl-1-[4-[[(3r)-5-methyl-2,3-dihydro-1-benzofuran-3-yl]methoxy]benzoyl]indol-4-yl]acetic acid Chemical compound C1OC2=CC=C(C)C=C2[C@@H]1COC(C=C1)=CC=C1C(=O)N1C2=CC=CC(CC(O)=O)=C2C=C1C OGLLEKOVLBGGFR-OAQYLSRUSA-N 0.000 description 1
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJWJUGPRGZKPRH-QHCPKHFHSA-N [4-(2-hydroxyethyl)-2-methylindol-1-yl]-[4-[[(2s)-4-methyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]phenyl]methanone Chemical compound O1C2=CC=CC=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CCO)=C3C=C2C)C=C1 ZJWJUGPRGZKPRH-QHCPKHFHSA-N 0.000 description 1
- YJFPPZQJDJTIKZ-QHCPKHFHSA-N [4-[[(2s)-2,3-dihydro-1-benzofuran-2-yl]methoxy]phenyl]-[4-(2-hydroxyethyl)-2-methylindol-1-yl]methanone Chemical compound C1C2=CC=CC=C2O[C@@H]1COC(C=C1)=CC=C1C(=O)N1C2=CC=CC(CCO)=C2C=C1C YJFPPZQJDJTIKZ-QHCPKHFHSA-N 0.000 description 1
- INTXHZGEKJSHIF-DEOSSOPVSA-N [4-[[(2s)-4,6-dimethyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]phenyl]-[4-(2-hydroxyethyl)-2-methylindol-1-yl]methanone Chemical compound O1C2=CC=C(C)C=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CCO)=C3C=C2C)C=C1 INTXHZGEKJSHIF-DEOSSOPVSA-N 0.000 description 1
- ISSBBMRIFOTHGB-QHCPKHFHSA-N [4-[[(2s)-6-fluoro-4-methyl-2,3-dihydro-1,4-benzoxazin-2-yl]methoxy]phenyl]-[4-(2-hydroxyethyl)-2-methylindol-1-yl]methanone Chemical compound O1C2=CC=C(F)C=C2N(C)C[C@H]1COC1=CC=C(C(=O)N2C3=CC=CC(CCO)=C3C=C2C)C=C1 ISSBBMRIFOTHGB-QHCPKHFHSA-N 0.000 description 1
- RMDDXYZPBZKIMO-OAQYLSRUSA-N [4-[[(3r)-2,3-dihydro-1-benzofuran-3-yl]methoxy]phenyl]-[4-(2-hydroxyethyl)-2-methylindol-1-yl]methanone Chemical compound C1OC2=CC=CC=C2[C@@H]1COC(C=C1)=CC=C1C(=O)N1C2=CC=CC(CCO)=C2C=C1C RMDDXYZPBZKIMO-OAQYLSRUSA-N 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
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- A01K67/00—Rearing or breeding animals, not otherwise provided for; New or modified breeds of animals
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Abstract
Un antagonista del receptor de prostaglandina D2 (receptor DP) para su uso en el tratamiento de la alopecia androgenética (AAG) en el cuero cabelludo de un sujeto.
Description
En otra realización, el antagonista del receptor DP es una variante de la estructura anterior, en la que el grupo ciclopentilo de la derecha arriba está sustituido por un grupo ciclohexilo. Cada uno de los sustituyentes enumerados 5 para la estructura anterior puede usarse para esta estructura que contiene ciclohexilo.
En otra realización, el antagonista del receptor DP tiene una de las siguientes estructuras:
7
En otras realizaciones, el antagonista del receptor DP es una sal no tóxica de uno de los compuestos anteriores.
En otras realizaciones, el antagonista del receptor DP se selecciona entre los siguientes compuestos: (1) éster bencílico del ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético,
- (2)
- ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (3) ácido 1-(4-((2R)-1,4-benzodioxan-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (4) ácido 1-(4-((2S)-1,4-benzodioxan-2ilmetoxi)benzoil)-2-metil-1H-indolo-4-il-acético, (5) ácido 1-(4-((2S)-1-metilindolin-2-ilmetoxi)benzoil)-2-metil-1H-indol4-il-acético, (6) ácido 1-(4-((2R)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-ilacético, (7) ácido 1-(4-((2S)-4,6-dimetil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-ilacético, (8) ácido 1-(4-((2S)-6-fluoro-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-ilacético, (9) ácido 1-(4-((2S)-6-metoxi-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-ilacético, (10) ácido 1-(4-((2S)-7-metoxi-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-ilacético, (11) ácido 1-(4-((2S)-4,7-dimetil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4ilacético, (12) ácido 1-(4-((2 S)-7-fluoro-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4il-acético, (13) ácido 1-(4-((2S)-1-etilindolin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (14) ácido 1-(4-((2S)-4,8dimetil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (15) ácido 1-(4-((2S)-5-metoxi4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (16) ácido 1-(4-((2S)-5-fluoro4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (17) ácido 1-(4-((2S)-2,3dihidrobenzofuran-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (18) ácido 1-(4-((2R)-2,3-dihidrobenzofuran-2ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (19) ácido 1-(4-((2S)-8-fluoro-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2ilmetoxi)benzoil)-2-metil-1H-indol-4-ilacético, (20) ácido 1-(4-((2R)-1,4-benzoxatian-2-ilmetoxi)benzoil)-2-metil-1Hindol-4-il-acético, (21) ácido 1-(4-((3S)-2,3-dihidrobenzofuran-3-ilmetoxi)benzoil)-2-metil-1H-indol-4-ilacético, (22) ácido 1-(4-((3R)-2,3-dihidrobenzofuran-3-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (23) ácido 1-(4-((3R)-5-fluoro2,3-dihidrobenzofuran-3-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (24) ácido 1-(4-((3R)-5-metil-2,3dihidrobenzofuran-3-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (25) ácido 1-(4-((3R)-6-fluoro-2,3dihidrobenzofuran-3-ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (26) ácido 1-(4-((3R)-7-metil-2,3dihidrobenzofuran-3-ilmetoxi)benzoil)-2-metil-1H-indol-4-ilacético, (27) ácido 1-(4-((2R)-5-fluoro-1,4-benzodioxan-2ilmetoxi)benzoil)-2-metil-1H-indol-4-il-acético, (28) ácido 1-(4-((2S)-8-fluoro-1,4-benzodioxan-2-ilmetoxi)benzoil)-2metil-1H-indol-4-il-acético, (29) ácido 1-(4-((3R)-7-fluoro-2,3-dihidrobenzofuran-3-ilmetoxi)benzoil)-2-metil-1H-indol-4il-acético, (30) éster alílico del ácido 3-(1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil1H-indol-4-il)acrílico, (31) ácido 3-(1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1Hindol-4-il)acrílico, (32) ácido 3-(1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol4-il)propanoico, (33) éster bencílico del ácido (1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2metil-1H-indol-4-il)oxiacético, (34) ácido (1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil1H-indol-4-il)oxiacético, (35) éster bencílico del ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2ilmetoxi)benzoil)-2-metil-1H-indol-4-carboxílico, (36) ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2ilmetoxi)benzoil)-2-metil-1H-indol-4-carboxílico, (37) éster bencílico del ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4benzoxazin-2-ilmetoxi)benzoil)-1H-indol-4-il-acético, (38) ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2ilmetoxi)benzoil)-1H-indol-4-il-acético, (39) ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)2,3-dihidro-1H-indol-4-il-acético, (40) ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2metil-2,3-dihidro-1H-indol-4-il-acético, (41) 2-(1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2metil-1H-indol-4-il)etanol, (42) 2-(1-(4-((2S)-4,6-dimetil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1Hindol-4-il)etanol, (43) 2-(1-(4-((2S)-6-fluoro-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1Hindol-4-il)etanol, (44) 2-(1-(4-((2S)-7-fluoro-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1Hindol-4-il)etanol, (45) 2-(1-(4-((2S)-2,3-dihidrobenzofuran-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il)etanol, (46) 2-(1-(4((3R)-2,3-dihidrobenzofuran-3-ilmetoxi)benzoil)-2-metil-1H-indol-4-il)etanol, (47) N-metilsulfonil-( 1-(4-((2S)-4-metil3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il)acetamida, (48) N-fenilsulfonil-(1-(4-((2S)-4metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il)acetamida, (49) acetato de 2-(1-(4-((2S)4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)benzoil)-2-metil-1H-indol-4-il)etilo, (50) éster bencílico del ácido 1(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)-2-metilbenzoil)-2-metil-1H-indol-4-il-acético, (51) éster bencílico del ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)-2-metilbenzoil)-1H-indol-4-il-acético,
- (52)
- ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)-2-metilbenzoil)-2-metil-1H-indol-4-il-acético, y
- (53)
- ácido 1-(4-((2S)-4-metil-3,4-dihidro-2H-1,4-benzoxazin-2-ilmetoxi)-2-metilbenzoil)-1H-indol-4-il-acético o una sal no tóxica de los mismos.
En otras realizaciones, el antagonista del receptor DP tiene la estructura:
21
en la que
R.sup.1 representa hidroxi, alcoxi C1-6, o NR.sup.8R.sup.9, en la que cada uno de R.sup.8 y R.sup.9 representa independientemente un átomo de hidrógeno, alquilo C1-6, o SO.sub.2R.sup.13, en la que R.sup.13 representa alquilo C1-6, un anillo carbocíclico saturado o insaturado C3-15 o un anillo heterocíclico de 4 a 15 miembros que contiene de 1 a 5 átomos de nitrógeno, átomos de azufre y/o átomos de oxígeno; R.sup.2 representa un átomo de hidrógeno, alquilo C1-6, alcoxi C1-6, alcoxialquilo C2-6, un átomo de halógeno, amino, trihalometilo, ciano, hidroxi, bencilo, o 4-metoxibencilo; R.sup.3 representa un átomo de hidrógeno, alquilo C1-6, alcoxi C1-6, un átomo de halógeno, trihalometilo, ciano, o hidroxi; cada uno de R.sup.4 y R.sup.5 representa independientemente un átomo de hidrógeno, alquilo C1-6, alcoxi C1-6, alcoxialquilo C2-6, un átomo de halógeno, nitro, amino, trihalometilo, ciano, o hidroxi; D representa un enlace sencillo, alquileno C1-6, alquenileno C2-6, u oxialquileno C1-6; en --G--R.sup.6,
1) G representa un enlace sencillo, alquileno C1-6 que puede estar sustituido con 1 a 2 átomos de oxígeno y/o átomos de azufre, alquenileno C2-6 que puede estar sustituido con 1 a 2 átomos de oxígeno y/o átomos de azufre, en la que el alquileno y el alquenileno pueden estar sustituidos con hidroxi o alcoxi C1-4, --C(O)NH--, --NHC(O)--, -SO.sub.2NH--,-NHSO.sub.2--, o diazo; R.sup.6 representa un anillo carbocíclico saturado o insaturado C3-15, o un anillo heterocíclico de 4 a 15 miembros que contiene de 1 a 5 átomos de nitrógeno, átomos de azufre y/o átomos de oxígeno, en la que el anillo puede estar sustituido con 1 a 5 sustituyentes seleccionados entre alquilo C1-6, alcoxi C1-10, alcoxialquilo C2-6, un átomo de halógeno, hidroxi, trihalometilo, nitro, amino, fenilo, fenoxi, oxo, acilo C2-6, alcanosulfonilo C1-6 y ciano,
2) G y R.sup.6 se toman juntos para representar
- (i)
- alquilo C1-15 que puede estar sustituido con 1 a 5 átomos de oxígeno y/o átomos de azufre;
- (ii)
- alquenilo C2-15 que puede estar sustituido con 1 a 5 átomos de oxígeno y/o átomos de azufre; o
(iii) alquinilo C2-15 que puede estar sustituido con 1 a 5 átomos de oxígeno y/o átomos de azufre, en la que el alquilo, el alquenilo y el alquinilo pueden estar sustituidos con 1 a 12 sustituyentes seleccionados entre alcoxi C1-6, un átomo de halógeno, hidroxi, ciano, oxo y NR.sup.11R.sup.12, en la que cada uno de R.sup.11 y R.sup.12 representa independientemente un átomo de hidrógeno, alquilo C1-6, alquenilo C2-6, fenilo, benzoílo, naftilo, fenilo sustituido con alquilo C1-6, o alquilo C1-6 sustituido con fenilo o ciano; n representa de 1 a 3; m representa de 1 a 3; i representa de 1 a 4; y
22
Claims (1)
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-
2007
- 2007-06-15 SI SI200731896A patent/SI2037967T1/sl unknown
- 2007-06-15 US US12/303,998 patent/US9254293B2/en active Active
- 2007-06-15 PL PL07809581T patent/PL2037967T3/pl unknown
- 2007-06-15 PT PT78095817T patent/PT2037967T/pt unknown
- 2007-06-15 ES ES07809581.7T patent/ES2618352T3/es active Active
- 2007-06-15 EP EP16196670.0A patent/EP3175856A1/en active Pending
- 2007-06-15 EP EP07809581.7A patent/EP2037967B1/en active Active
- 2007-06-15 WO PCT/US2007/014031 patent/WO2007149312A2/en active Application Filing
- 2007-06-15 HU HUE07809581A patent/HUE030850T2/en unknown
- 2007-06-15 DK DK07809581.7T patent/DK2037967T3/en active
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2015
- 2015-08-24 US US14/833,470 patent/US9889082B2/en active Active
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Also Published As
Publication number | Publication date |
---|---|
EP2037967A4 (en) | 2010-07-07 |
US20160346186A1 (en) | 2016-12-01 |
EP3175856A1 (en) | 2017-06-07 |
WO2007149312A3 (en) | 2009-04-02 |
US20110021599A1 (en) | 2011-01-27 |
DK2037967T3 (en) | 2017-03-13 |
SI2037967T1 (sl) | 2017-04-26 |
US10849841B2 (en) | 2020-12-01 |
PT2037967T (pt) | 2017-03-14 |
EP2037967A2 (en) | 2009-03-25 |
CY1118737T1 (el) | 2018-03-07 |
US9254293B2 (en) | 2016-02-09 |
EP2037967B1 (en) | 2016-12-07 |
WO2007149312A2 (en) | 2007-12-27 |
US9889082B2 (en) | 2018-02-13 |
US20190380942A1 (en) | 2019-12-19 |
HUE030850T2 (en) | 2017-06-28 |
PL2037967T3 (pl) | 2017-07-31 |
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