AR066386A1 - Compuestos heterociclicos condensados, metodos e intermediarios para su preparacion, una composicion farmaceutica que los comprende y su uso en el tratamiento de enfermedades mediadas por la inhibicion de la pde-4 - Google Patents
Compuestos heterociclicos condensados, metodos e intermediarios para su preparacion, una composicion farmaceutica que los comprende y su uso en el tratamiento de enfermedades mediadas por la inhibicion de la pde-4Info
- Publication number
- AR066386A1 AR066386A1 ARP050105281A ARP050105281A AR066386A1 AR 066386 A1 AR066386 A1 AR 066386A1 AR P050105281 A ARP050105281 A AR P050105281A AR P050105281 A ARP050105281 A AR P050105281A AR 066386 A1 AR066386 A1 AR 066386A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- unsubstituted
- carboxylate
- methoxy
- furan
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 101100296719 Caenorhabditis elegans pde-4 gene Proteins 0.000 title 1
- 201000010099 disease Diseases 0.000 title 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 1
- 230000005764 inhibitory process Effects 0.000 title 1
- 230000001404 mediated effect Effects 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- -1 -OH Chemical group 0.000 abstract 10
- 229910003827 NRaRb Inorganic materials 0.000 abstract 8
- 125000001072 heteroaryl group Chemical group 0.000 abstract 7
- 229910003813 NRa Inorganic materials 0.000 abstract 6
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 5
- 229910052760 oxygen Inorganic materials 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 3
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 3
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 125000006239 protecting group Chemical group 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- IHCCAYCGZOLTEU-UHFFFAOYSA-N 3-furoic acid Chemical compound OC(=O)C=1C=COC=1 IHCCAYCGZOLTEU-UHFFFAOYSA-N 0.000 abstract 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 abstract 2
- 206010010744 Conjunctivitis allergic Diseases 0.000 abstract 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 abstract 2
- 206010040070 Septic Shock Diseases 0.000 abstract 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 208000002205 allergic conjunctivitis Diseases 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 2
- 230000010410 reperfusion Effects 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- OTVIRSQEMRZCJH-UHFFFAOYSA-N (4-nitrophenyl) 6-(difluoromethoxy)-[1]benzofuro[2,3-d]pyridazine-9-carboxylate Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC(=O)C1=CC=C(OC(F)F)C2=C1C1=CN=NC=C1O2 OTVIRSQEMRZCJH-UHFFFAOYSA-N 0.000 abstract 1
- FXQZROFFMQIOEA-UHFFFAOYSA-N (4-nitrophenyl) 6-methoxy-[1]benzofuro[2,3-d]pyridazine-9-carboxylate Chemical compound O1C2=CN=NC=C2C2=C1C(OC)=CC=C2C(=O)OC1=CC=C([N+]([O-])=O)C=C1 FXQZROFFMQIOEA-UHFFFAOYSA-N 0.000 abstract 1
- XRQKPLIBQNKZFX-UHFFFAOYSA-N (4-nitrophenyl) 6-methoxy-[1]benzofuro[3,2-d]pyrimidine-9-carboxylate Chemical compound O1C2=CN=CN=C2C2=C1C(OC)=CC=C2C(=O)OC1=CC=C([N+]([O-])=O)C=C1 XRQKPLIBQNKZFX-UHFFFAOYSA-N 0.000 abstract 1
- UONRIEVHDZSAIW-TWGQIWQCSA-N (z)-3-(7-cyclopentyloxy-4-methoxycarbonyl-1-benzofuran-2-yl)prop-2-enoic acid Chemical compound C1=2OC(\C=C/C(O)=O)=CC=2C(C(=O)OC)=CC=C1OC1CCCC1 UONRIEVHDZSAIW-TWGQIWQCSA-N 0.000 abstract 1
- DHWRZDFGCCSMOD-UTCJRWHESA-N (z)-3-(7-methoxy-4-methoxycarbonyl-1-benzofuran-2-yl)prop-2-enoic acid Chemical compound COC(=O)C1=CC=C(OC)C2=C1C=C(\C=C/C(O)=O)O2 DHWRZDFGCCSMOD-UTCJRWHESA-N 0.000 abstract 1
- TVCVZPPTRJJNOP-UHFFFAOYSA-N 1,2-dihydropyridine-2-carboxylic acid Chemical compound OC(=O)C1NC=CC=C1 TVCVZPPTRJJNOP-UHFFFAOYSA-N 0.000 abstract 1
- DLSRMWYAGDCOKK-UHFFFAOYSA-N 1H-[1]benzofuro[2,3-c]pyridine-2-carboxylic acid Chemical compound C1N(C=CC2=C1OC1=C2C=CC=C1)C(=O)O DLSRMWYAGDCOKK-UHFFFAOYSA-N 0.000 abstract 1
- CMGPABVOJJVRSY-UHFFFAOYSA-N 2,4-diethyl-7-hydroxy-3-methyl-1-benzofuran-2,4-dicarboxylic acid Chemical compound C1=CC(CC)(C(O)=O)C2=C(C)C(CC)(C(O)=O)OC2=C1O CMGPABVOJJVRSY-UHFFFAOYSA-N 0.000 abstract 1
- ZDYFSZAOYGZRQN-UHFFFAOYSA-N 2-(7-methoxy-1-benzofuran-2-yl)ethanamine Chemical compound COC1=CC=CC2=C1OC(CCN)=C2 ZDYFSZAOYGZRQN-UHFFFAOYSA-N 0.000 abstract 1
- YSJIQYFAFSUMAR-UHFFFAOYSA-N 2-ethoxycarbonyl-7-hydroxy-3-methyl-1-benzofuran-4-carboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C)=C(C(=O)OCC)OC2=C1O YSJIQYFAFSUMAR-UHFFFAOYSA-N 0.000 abstract 1
- PZLSGUCLHNPDKP-UHFFFAOYSA-N 2-ethoxycarbonyl-7-methoxy-3-methyl-1-benzofuran-4-carboxylic acid Chemical compound C1=CC(C(O)=O)=C2C(C)=C(C(=O)OCC)OC2=C1OC PZLSGUCLHNPDKP-UHFFFAOYSA-N 0.000 abstract 1
- XAEHFKPEJSYWGQ-UHFFFAOYSA-N 2-ethyl-7-methoxy-3,4-dimethyl-1-benzofuran-2,4-dicarboxylic acid Chemical compound C1=CC(C)(C(O)=O)C2=C(C)C(CC)(C(O)=O)OC2=C1OC XAEHFKPEJSYWGQ-UHFFFAOYSA-N 0.000 abstract 1
- KZLAYEFPKQCHEP-UHFFFAOYSA-N 3-(bromomethyl)-2-ethyl-7-methoxy-4-methyl-1-benzofuran-2,4-dicarboxylic acid Chemical compound C1=CC(C)(C(O)=O)C2=C(CBr)C(CC)(C(O)=O)OC2=C1OC KZLAYEFPKQCHEP-UHFFFAOYSA-N 0.000 abstract 1
- JFFUQYKOVKSKLJ-UHFFFAOYSA-N 6-(difluoromethoxy)-[1]benzofuro[2,3-d]pyridazine-9-carboxylic acid Chemical compound O1C2=CN=NC=C2C2=C1C(OC(F)F)=CC=C2C(=O)O JFFUQYKOVKSKLJ-UHFFFAOYSA-N 0.000 abstract 1
- KPRMKWDXGLPXIR-UHFFFAOYSA-N 6-methoxy-1h-[1]benzofuro[3,2-d]pyrimidin-4-one Chemical compound N1=CNC(=O)C2=C1C(C=CC=C1OC)=C1O2 KPRMKWDXGLPXIR-UHFFFAOYSA-N 0.000 abstract 1
- QWOQUANZBGCZSR-UHFFFAOYSA-N 6-methoxy-[1]benzofuro[2,3-d]pyridazine-9-carboxylic acid Chemical compound C12=CN=NC=C2OC2=C1C(C(O)=O)=CC=C2OC QWOQUANZBGCZSR-UHFFFAOYSA-N 0.000 abstract 1
- ARDQEHWVAJIYGN-UHFFFAOYSA-N 6-methoxy-[1]benzofuro[3,2-c]pyridine-9-carboxylic acid Chemical compound C12=CN=CC=C2OC2=C1C(C(O)=O)=CC=C2OC ARDQEHWVAJIYGN-UHFFFAOYSA-N 0.000 abstract 1
- IWYBHOOJCQFRCR-UHFFFAOYSA-N 6-methoxy-[1]benzofuro[3,2-d]pyrimidine Chemical compound O1C2=CN=CN=C2C2=C1C(OC)=CC=C2 IWYBHOOJCQFRCR-UHFFFAOYSA-N 0.000 abstract 1
- VDHDWEMGDGLVQG-UHFFFAOYSA-N 6-methoxy-[1]benzofuro[3,2-d]pyrimidine-9-carbonitrile Chemical compound O1C2=CN=CN=C2C2=C1C(OC)=CC=C2C#N VDHDWEMGDGLVQG-UHFFFAOYSA-N 0.000 abstract 1
- IMTAMGSIJJNXET-UHFFFAOYSA-N 6-methoxy-[1]benzofuro[3,2-d]pyrimidine-9-carboxylic acid Chemical compound O1C2=CN=CN=C2C2=C1C(OC)=CC=C2C(O)=O IMTAMGSIJJNXET-UHFFFAOYSA-N 0.000 abstract 1
- ZGBFQCSZMNHVSB-UHFFFAOYSA-N 7-(difluoromethoxy)-2,4-diethyl-3-methyl-1-benzofuran-2,4-dicarboxylic acid Chemical compound C1=CC(CC)(C(O)=O)C2=C(C)C(CC)(C(O)=O)OC2=C1OC(F)F ZGBFQCSZMNHVSB-UHFFFAOYSA-N 0.000 abstract 1
- HGHMCNGBTJOMCM-UHFFFAOYSA-N 7-cyclopentyloxy-2-methyl-1-benzofuran-4-carbaldehyde Chemical compound C=12OC(C)=CC2=C(C=O)C=CC=1OC1CCCC1 HGHMCNGBTJOMCM-UHFFFAOYSA-N 0.000 abstract 1
- DPAYSHNIQOADKU-UHFFFAOYSA-N 7-cyclopentyloxy-2-methyl-1-benzofuran-4-carboxylic acid Chemical compound C=12OC(C)=CC2=C(C(O)=O)C=CC=1OC1CCCC1 DPAYSHNIQOADKU-UHFFFAOYSA-N 0.000 abstract 1
- XXXPYUMNOJLCQC-UHFFFAOYSA-N 7-hydroxy-2-methyl-1-benzofuran-4-carbaldehyde Chemical compound C1=CC(O)=C2OC(C)=CC2=C1C=O XXXPYUMNOJLCQC-UHFFFAOYSA-N 0.000 abstract 1
- PSGKIVSGXXTASY-UHFFFAOYSA-N 8-methoxy-2-[(2-methylpropan-2-yl)oxycarbonyl]-3,4-dihydro-1h-[1]benzothiolo[2,3-c]pyridine-5-carboxylic acid Chemical compound C1CN(C(=O)OC(C)(C)C)CC2=C1C(C(C(O)=O)=CC=C1OC)=C1S2 PSGKIVSGXXTASY-UHFFFAOYSA-N 0.000 abstract 1
- PEIZMWALXHMTFZ-UHFFFAOYSA-N 9-bromo-6-methoxy-[1]benzofuro[3,2-d]pyrimidine Chemical compound O1C2=CN=CN=C2C2=C1C(OC)=CC=C2Br PEIZMWALXHMTFZ-UHFFFAOYSA-N 0.000 abstract 1
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 abstract 1
- 206010006458 Bronchitis chronic Diseases 0.000 abstract 1
- NYUTUOKOZYMJIF-UHFFFAOYSA-N CC1=C2C(=C(N=N1)Cl)OC1=C2C=CC=C1OC Chemical compound CC1=C2C(=C(N=N1)Cl)OC1=C2C=CC=C1OC NYUTUOKOZYMJIF-UHFFFAOYSA-N 0.000 abstract 1
- XLVRNPOJNREXJT-UHFFFAOYSA-N CC1=C2C(=CN=N1)OC1=C2C=CC=C1OC Chemical compound CC1=C2C(=CN=N1)OC1=C2C=CC=C1OC XLVRNPOJNREXJT-UHFFFAOYSA-N 0.000 abstract 1
- 206010009900 Colitis ulcerative Diseases 0.000 abstract 1
- 208000011231 Crohn disease Diseases 0.000 abstract 1
- 206010012438 Dermatitis atopic Diseases 0.000 abstract 1
- 206010014824 Endotoxic shock Diseases 0.000 abstract 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract 1
- 206010018367 Glomerulonephritis chronic Diseases 0.000 abstract 1
- 206010069698 Langerhans' cell histiocytosis Diseases 0.000 abstract 1
- 201000004681 Psoriasis Diseases 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 1
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 abstract 1
- 206010039085 Rhinitis allergic Diseases 0.000 abstract 1
- 201000006704 Ulcerative Colitis Diseases 0.000 abstract 1
- 208000024780 Urticaria Diseases 0.000 abstract 1
- 208000026935 allergic disease Diseases 0.000 abstract 1
- 230000000172 allergic effect Effects 0.000 abstract 1
- 201000010105 allergic rhinitis Diseases 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 208000024998 atopic conjunctivitis Diseases 0.000 abstract 1
- 201000008937 atopic dermatitis Diseases 0.000 abstract 1
- 230000006931 brain damage Effects 0.000 abstract 1
- 231100000874 brain damage Toxicity 0.000 abstract 1
- 208000029028 brain injury Diseases 0.000 abstract 1
- 206010006451 bronchitis Diseases 0.000 abstract 1
- 208000007451 chronic bronchitis Diseases 0.000 abstract 1
- IMNLSIUSAYXPQK-UHFFFAOYSA-N diethyl 3-(bromomethyl)-7-(difluoromethoxy)-1-benzofuran-2,4-dicarboxylate Chemical compound C1=CC(C(=O)OCC)=C2C(CBr)=C(C(=O)OCC)OC2=C1OC(F)F IMNLSIUSAYXPQK-UHFFFAOYSA-N 0.000 abstract 1
- XHVRJECSWOEJBL-UHFFFAOYSA-N diethyl 7-(difluoromethoxy)-3-formyl-1-benzofuran-2,4-dicarboxylate Chemical compound C1=CC(C(=O)OCC)=C2C(C=O)=C(C(=O)OCC)OC2=C1OC(F)F XHVRJECSWOEJBL-UHFFFAOYSA-N 0.000 abstract 1
- 208000003401 eosinophilic granuloma Diseases 0.000 abstract 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 abstract 1
- WSINVGWTMNYZCJ-UHFFFAOYSA-N ethyl 4-chloro-6-(difluoromethoxy)-[1]benzofuro[2,3-d]pyridazine-9-carboxylate Chemical compound O1C2=C(Cl)N=NC=C2C2=C1C(OC(F)F)=CC=C2C(=O)OCC WSINVGWTMNYZCJ-UHFFFAOYSA-N 0.000 abstract 1
- PEXYJIOXSZOZBT-UHFFFAOYSA-N ethyl 4-formyl-7-methoxy-3-methyl-1-benzofuran-2-carboxylate Chemical compound C1=CC(C=O)=C2C(C)=C(C(=O)OCC)OC2=C1OC PEXYJIOXSZOZBT-UHFFFAOYSA-N 0.000 abstract 1
- KHNOEKPAJYAEGM-UHFFFAOYSA-N ethyl 5-formyl-8-methoxy-3,4-dihydro-1h-[1]benzothiolo[2,3-c]pyridine-2-carboxylate Chemical compound S1C2=C(OC)C=CC(C=O)=C2C2=C1CN(C(=O)OCC)CC2 KHNOEKPAJYAEGM-UHFFFAOYSA-N 0.000 abstract 1
- FKYKSGFJUMTFKT-UHFFFAOYSA-N ethyl 6-(difluoromethoxy)-4-oxo-3h-[1]benzofuro[2,3-d]pyridazine-9-carboxylate Chemical compound C1=2C(C(=O)OCC)=CC=C(OC(F)F)C=2OC2=C1C=NNC2=O FKYKSGFJUMTFKT-UHFFFAOYSA-N 0.000 abstract 1
- SHSWCAHUMSOMDM-UHFFFAOYSA-N ethyl 6-(difluoromethoxy)-[1]benzofuro[2,3-d]pyridazine-9-carboxylate Chemical compound O1C2=CN=NC=C2C2=C1C(OC(F)F)=CC=C2C(=O)OCC SHSWCAHUMSOMDM-UHFFFAOYSA-N 0.000 abstract 1
- PMJRJLBAPXIOKR-UHFFFAOYSA-N ethyl 6-methoxy-3,4-dihydro-1h-[1]benzofuro[3,2-c]pyridine-2-carboxylate Chemical compound O1C2=C(OC)C=CC=C2C2=C1CCN(C(=O)OCC)C2 PMJRJLBAPXIOKR-UHFFFAOYSA-N 0.000 abstract 1
- IDEWKXNUUFCNKC-UHFFFAOYSA-N ethyl 8-methoxy-3,4-dihydro-1h-[1]benzothiolo[2,3-c]pyridine-2-carboxylate Chemical compound S1C2=C(OC)C=CC=C2C2=C1CN(C(=O)OCC)CC2 IDEWKXNUUFCNKC-UHFFFAOYSA-N 0.000 abstract 1
- UJVLZLXFQPGKTP-UHFFFAOYSA-N ethyl n-[2-(7-methoxy-1-benzofuran-2-yl)ethyl]carbamate Chemical compound C1=CC(OC)=C2OC(CCNC(=O)OCC)=CC2=C1 UJVLZLXFQPGKTP-UHFFFAOYSA-N 0.000 abstract 1
- UYPJHELHHLFJSX-UHFFFAOYSA-N ethyl n-[2-(7-methoxy-1-benzofuran-3-yl)ethyl]carbamate Chemical compound C1=CC=C2C(CCNC(=O)OCC)=COC2=C1OC UYPJHELHHLFJSX-UHFFFAOYSA-N 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- JOTDFEIYNHTJHZ-UHFFFAOYSA-N furan-2,4-dicarboxylic acid Chemical compound OC(=O)C1=COC(C(O)=O)=C1 JOTDFEIYNHTJHZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- BDBWMKJQRNCCNU-UHFFFAOYSA-N methyl 1-chloro-6-methoxy-[1]benzofuro[3,2-c]pyridine-9-carboxylate Chemical compound O1C2=CC=NC(Cl)=C2C2=C1C(OC)=CC=C2C(=O)OC BDBWMKJQRNCCNU-UHFFFAOYSA-N 0.000 abstract 1
- BHBABKPTSDRVLE-UHFFFAOYSA-N methyl 2-(bromomethyl)-7-cyclopentyloxy-1-benzofuran-4-carboxylate Chemical compound C1=2OC(CBr)=CC=2C(C(=O)OC)=CC=C1OC1CCCC1 BHBABKPTSDRVLE-UHFFFAOYSA-N 0.000 abstract 1
- JYEKGXMBMUVVSR-UHFFFAOYSA-N methyl 2-(bromomethyl)-7-methoxy-1-benzofuran-4-carboxylate Chemical compound COC(=O)C1=CC=C(OC)C2=C1C=C(CBr)O2 JYEKGXMBMUVVSR-UHFFFAOYSA-N 0.000 abstract 1
- AMMYCWWFXKQDTE-UHFFFAOYSA-N methyl 2-formyl-7-methoxy-1-benzofuran-4-carboxylate Chemical compound COC(=O)C1=CC=C(OC)C2=C1C=C(C=O)O2 AMMYCWWFXKQDTE-UHFFFAOYSA-N 0.000 abstract 1
- QQRXTKRNACQOAE-UHFFFAOYSA-N methyl 4-methoxy-3-[2-(1-methyl-2-oxopiperidin-3-ylidene)hydrazinyl]benzoate Chemical compound COC(=O)C1=CC=C(OC)C(NN=C2C(N(C)CCC2)=O)=C1 QQRXTKRNACQOAE-UHFFFAOYSA-N 0.000 abstract 1
- ZOUTZVLMUQGAKH-UHFFFAOYSA-N methyl 6-methoxy-1-oxo-2h-[1]benzofuro[3,2-c]pyridine-9-carboxylate Chemical compound O1C2=CC=NC(O)=C2C2=C1C(OC)=CC=C2C(=O)OC ZOUTZVLMUQGAKH-UHFFFAOYSA-N 0.000 abstract 1
- WXXKJCOMRDZOIC-UHFFFAOYSA-N methyl 7-cyclopentyloxy-2-formyl-1-benzofuran-4-carboxylate Chemical compound C1=2OC(C=O)=CC=2C(C(=O)OC)=CC=C1OC1CCCC1 WXXKJCOMRDZOIC-UHFFFAOYSA-N 0.000 abstract 1
- CGUZLIXUEQPZPB-UHFFFAOYSA-N methyl 7-cyclopentyloxy-2-methyl-1-benzofuran-4-carboxylate Chemical compound C1=2OC(C)=CC=2C(C(=O)OC)=CC=C1OC1CCCC1 CGUZLIXUEQPZPB-UHFFFAOYSA-N 0.000 abstract 1
- DZVQCNHEYYKZFC-UHFFFAOYSA-N methyl 7-methoxy-2-methyl-1-benzofuran-4-carboxylate Chemical compound COC(=O)C1=CC=C(OC)C2=C1C=C(C)O2 DZVQCNHEYYKZFC-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000003680 myocardial damage Effects 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-M picolinate Chemical compound [O-]C(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-M 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000036303 septic shock Effects 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 201000005539 vernal conjunctivitis Diseases 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4355—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/16—Central respiratory analeptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/14—Decongestants or antiallergics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/08—Plasma substitutes; Perfusion solutions; Dialytics or haemodialytics; Drugs for electrolytic or acid-base disorders, e.g. hypovolemic shock
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pulmonology (AREA)
- Neurology (AREA)
- Epidemiology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Ophthalmology & Optometry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Otolaryngology (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Composiciones farmacéuticas que los contengan, que son utiles en el tratamiento de enfermedades alérgicas e inflamatorias incluyendo asma, bronquitis cronica, dermatitis atopica, urticaria, rinitis alérgica, conjuntivitis alérgica, conjuntivitis vernal, granuloma eosinofílico, psoriasis, artritis reumatoide, shock séptico, colitis ulcerante, enfermedad de Crohn, dano del miocardio por reperfusion, dano del cerebro por reperfusion, glomerulonefritis cronica, shock endotoxico y síndrome de dificultad respiratoria en adultos. Reivindicacion 1: Un compuesto de formula (1) en la cual; en cada caso R1, R2 y R3 pueden ser idénticos o diferentes, y son, independientemente, hidrogeno, alquilo substituido o no substituido, alquenilo substituido o no substituido, alquinilo substituido o no substituido, cicloalquilo substituido o no substituido, cicloalquilalquilo substituido o no substituido, cicloalquenilo substituido o no substituido, cicloalquenilalquilo substituido o no substituido, arilo substituido o no substituido, arilalquilo substituido o no substituido, heteroarilo substituido á no substituido, heteroarilalquilo substituido o no substituido, un grupo heterocíclico substituido o no substituido, heterociclilalquilo substituido o no substituido, -NR5R6, -C(=L)-R5, -C(O)-R5, -C(O)O-R5, -C(O)NR5R6, -S(O)m-R5, -S(O)m-NR5R6, nitro, -OH, ciano, oxo, formilo, acetilo, halogeno, -OR5, -SR5, o un grupo protector, o cuando dos substituyentes R2 o dos substituyentes R3 se encuentran en posicion orto entre sí, los dos substituyentes pueden estar unidos para formar un anillo cíclico de 3-7 miembros opcionalmente substituido, saturado o no saturado, que de manera opcional puede incluir hasta dos heteroátomos seleccionados de entre O, NR5 o S; en cada caso, R5 y R6 pueden ser idénticos o diferentes y son, de manera independiente, hidrogeno, alquilo substituido o no substituido, alquenilo substituido o no substituido, alquinilo substituido o no substituido, cicloalquilo substituido o no substituido, cicloalquilalquilo substituido o no substituido, cicloalquenilo substituido o no substituido, cicloalquenilalquilo substituido o no substituido, arilo substituido o no substituido, arilalquilo substituido o no substituido, heteroarilo substituido o no substituido, heteroarilalquilo substituido o no substituido, un grupo heterocíclico substituido o no substituido, heterociclilalquilo substituido o no substituido, nitro, halo, -OH, ciano, -C(O)-Ra, -C(O)O-Ra, -C(O)NRaRb, -S(O)m-Ra, -S(O)m-NRaRb, -C(=NRa)-Rb, -C(=NRa)-NRaRb, -C(=S)-NRaRb, -C(=S)-Ra, -N=C(RaRb), -NRaRb, -ORa, -SRa, o un grupo protector, o R5 y R6 pueden estar unidos entre sí junto con el átomo al cual están enlazados para formar un anillo cíclico de 3-7 miembros opcionalmente substituido, saturado o no saturado, que de manera opcional puede incluir hasta dos heteroátomos seleccionados de entre O, NRa o S; en cada caso, Ra y Rb pueden ser idénticos o diferentes, y son, de manera independiente, hidrogeno, alquilo substituido o no substituido, alquenilo substituido o no substituido, alquinilo substituido o no substituido, cicloalquilo substituido o no substituido, cicloalquilalquilo substituido o no substituido, cicloalquenilo substituido o no substituido, cicloalquenilalquilo substituido o no substituido, arilo substituido o no substituido, arilalquilo substituido o no substituido, heteroarilo substituido o no substituido, heteroarilalquilo substituido o no substituido, un grupo heterocíclico substituido o no substituido, heterociclilalquilo substituido o no substituido, nitro, -OH, ciano, formilo, acetilo, halogeno, un grupo protector, -C(O)-Ra, -C(O)O-Ra, -C(O)NRaRb, -S(O)m-Ra, -S(O)m-NRaRb, NRaRb, -ORa, o -SRa; Ar es arilo substituido o no substituido, arilalquilo substituido o no substituido, anillo heterocíclico substituido o no substituido, heterocicloalquilo substituido o no substituido, un anillo heteroarilo substituido o no substituido, o heteroarilalquilo substituido o no substituido; L es O, S o NRa, en donde Ra es tal como se define anteriormente; n es un entero desde 0 a 2; p es un entero desde 0 a 8; T, U, V y W son cada uno, de manera independiente, C, C=O, N, NRa, O o S, siempre que al menos uno de T, U, V y W sea N, NRa, O o S, y en donde Ra es tal como se define anteriormente; cada línea entrecortada [-----] en el anillo representa un enlace opcionalmente doble; X es O, S(O)m o NRb, en donde Rb es tal como se define anteriormente; en cada caso, m es independientemente 0, 1 o 2; Y es -C(O)NR4-, -NR4SO2-, -SO2NR4- o -NR4C(O)-; R4 es hidrogeno, alquilo substituido o no substituido, hidroxilo, -ORa (en donde Ra es tal como se define anteriormente) , cicloalquilo substituido o no substituido, cicloalquilalquilo substituido o no substituido, arilo substituido o no substituido, arilalquilo substituido o no substituido, un anillo heterocíclico substituido o no substituido, heterocicloalquilo substituido o no substituido, un anillo heteroarilo substituido o no substituido o heteroarilalquilo substituido o no substituido, o un análogo, tautomero, regioisomero, estereoisomero, enantiomero, diasteromero, polimorfo, sal farmacéuticamente aceptable, N-oxido, o un solvato farmacéuticamente aceptable de los mismos. Reivindicacion 56: Un compuesto que es: etil 4-formil-7-metoxi-3-metilbenzo[b] furan-2-carboxilato; ácido 2-etoxicarbonil-7-metoxi-3-metilbenzo[b] furan-4-carboxílico; 2-etil-4-metil-7-metoxi-3-metilbenzo [b] furan-2,4-dicarboxilato; 2-etil-4-metil-3-bromometil-7-metoxibenzo [b] furan-2,4-dicarboxilato; 2-etil-4-metil 3-formil-7-metilbenzo[b)furan-2,4-dicarboxilato; metil-7-metoxi-2-metilbenzo [b] furan-4-carboxilato; metil-2-bromometil-7-metoxibenzo [b] furan-4-carboxilato; metil-2-formil-7-metoxibenzo [b] furan-4-carboxilato; ácido (Z)-3-(7-metoxi-4-metiloxicarbonilbenzo [b] furan-2-il)-2-propenoico; metil-2-[(Z)-2-azidocarbonil)-1-etenil]-7-metoxibenzo [b] furan-4-carboxilato; ácido 2-etoxicarbonil-7-hidroxi-3-metilbenzo [b] furan-4-carboxílico; 2,4-dietil-7-hidroxi-3-metilbenzo[b]furan-2,4-dicarboxilato, 2,4-dietil-7-difluorometoxi-3-metilbenzo [b] furan-2,4-dicarboxilato; dietil 3-bromometil-7-difluorometoxibenzo [b] furan-2,4-dicarboxilato; dietil 7-difluorometoxi-3-formilbenzo [b] furan-2,4-dicarboxilato; 2-(7-metoxi-1-benzofuran-2-il) etanamina; etil 2-(7-metoxi-1-benzofuran-2-il) etilcarbamato; 7-hidroxi-2-metilbenzo [b] furan-4-carbaldehido; 7-ciclopentiloxi-2-metilbenzo [b) furan-4-carboxaldehído; ácido 7-ciclopentiloxi-2-metilbenzo [b] furan-4-carboxílico; metil-7-ciclopentiloxi-2-metilbenzo [b] furan-4-carboxilato; metil-7-ciclopentiloxi-2-bromometilbenzo [b] furan-4-carboxilato; metil-2-formil-7-ciclopentiloxibenzo [b] furan-4-carboxilato; ácido (Z)-3-(7-ciclopentiloxi-4-metiloxicarbonilbenzo [b] furan-2-il)-2-propenoico; metil-2-[(Z)-2-azidocarbonil)-1-etenil]-7-metoxibenzo [b] furan-4-carboxilato; 2-(7-metoxibenceno [b] tiofen-3-il) acetamida; 2-(7-metoxibenceno [b] tiofen-3-il) etilamina; etil 2-(7-metoxibenceno [b] tiofen-3-il) etilcarbamato; etil-2-(7-metoxi-1-benzofuran-3-il)etilcarbamato; o 1-metil-3-(2-metoxi-5-carbmetoxi-fenil-hidrazono)-piperidin-2-ona. Reivindicacion 57 Un compuesto que es metil(6-metoxi-4-oxo-3,4-dihidrobenzo[4,5] furo[2,3-d]piridazin-9-carboxilato; metil(4-cloro-6-metoxibenzo [4,5] furo[2,3-d] piridazin)-9-carboxilato; metil (6-metoxibenzo [4,5]furo[2,3-d]piridazin)-9-carboxilato; 6-metoxibenzo [4,5] furo [2,3-d] piridazin-9-carboxílico ácido; 4-nitrofenil 6-metoxibenzo [4,5] furo [2,3-d] piridazin-9-carboxilato, 6-metoxi-3,4-dihidrobenzo [4,5] furo [3,2-d] pirimidin-4-ona; 6-metoxibenzo [4,5] furo [3,2-d] pirimidina; 9-bromo-6-metoxibenzo [4,5] furo [3,2-d] pirimidina; 6-metoxibenzo [4,5] furo [3,2-d] pirimidin-9-il cianida; ácido 6-metoxibenzo [4,5] furo [3,2-d]pirimidin-9-carboxílico; 4-nitrofenil 6-metoxibenzo [4,5] furo [3,2-d]pirimidin-9-carboxilato; etil-8-metoxi-1,2,3,4-tetrahidrobenzo [4,5] tieno [2,3-c]piridin-2-carboxilato; etil-5-formil-8-metoxi-1,2,3,4-tetrahidrobenzo [4,5] tieno[2,3-c]piridin-2-carboxilato; ácido 2-etoxicarbonil-8-metoxi-1,2,3,4-tetrahidrobenzo [4,5] tieno [2,3-] piridin-5-carboxílico; 2-etil-5-(4-nitrofenil)-8-metoxi-1,2,3,4-tetrahidrobenzo[4, 5] tieno [2,3-c] piridin-2,5-dicarboxilato; 2-etil-5-(4-nitrofenil)-8-metoxi-1,2,3,4-tetrahidrobenzo [4,5] tieno [2,3-c] piridin-2,5-dicarboxilato; etil-6-difluorometoxi-4-oxo-3,4-dihidrobenzo [4,5] furo [2,3-d]piridazin-9-carboxilato; etil-4-cloro-6-difluorometoxibenzo [4,5] furo [2,3-d] piridazin-9-carboxilato; etil-6-difluorometoxibenzo [4,5] furo [2,3-d]piridazin-9-carboxilato; ácido 6-Difluorometoxibenzo [4,5] furo [2,3-d] piridazin-9-carboxílico; 4-nitrofenil 6-difluorometoxibenzo [4,5] furo [2,3-d]piridazin-9-carboxilato; ácido 2-tert-butiloxicarbonil-8-metoxi-1,2,3,4-tetrahidrobenzo[4,5]tieno[2,3-c] piridin-5-carboxílico; 2(tert-butil)-5-(4-nitrofenil)-8-metoxi-1,2,3,4-tetrahidrobenzo [4,5]tieno [2,3-c] piridin-2,5-dicarboxilato; tert-butil-5-(3,5-dicloro-4-piridilcarbamoil)-8-metoxi-1,2,3,4-tetrahidrobenzo [4,5] tieno[2,3-c)piridin-2-carboxilato; 2-etoxicarbonil-6-metoxi-1,2,3,4-tetrahidro[1]benzofuro[3,2-c]piridina; 2-etoxicarbonil-6-metoxi-1,2,3,4-tetrahidro [1]benzofuro(3,2-c]piridin-9-carbaldehído; ácido 2-etoxicarbonil-6-metoxi-1,2,3,4-tetrahidro[12]benzofuro(3,2-c]piridin-9-carboxílico; 4-nitrofenil-(2-etoxicarbonil]-6-metoxi-1,2,3,4-tetrahidro[1]benzofuro[3,2-c]piridin)-9-carboxilato; metil-1-hidroxi-6-metoxibenzo[4,5]furo[3,2-c] piridin-9-carboxilato; metil-1-cloro-6-metoxibenzo[4,5]furo[3,2-c]piridin-9-carboxilato; meti6-metoxibenzo[4,5]furo[3,2-c)piridin-9-carboxilato; 6-metoxibenzo[4,5]furo[3,2-c]piridin-9-carboxílico ácido; 4-nitrofenil-6-metoxibenzo[4.5] furo[3,2-c]piridin-9-carboxilato; etil 8-metoxi-3,4-dihidro[1]benzofuro[2,3-c]piridin-2(1H)-carboxilato; etil 5-formil-8-metoxi-3,4-dihidro[1]-benzofuro[2,3-c]piridin-2(1H)-carboxilato; ácido 2-(etoxicarbonil)-8-metoxi-1,2,3,4-tetrahidro[1]benzofuro [2,3-c] piridin-5-carbox
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63723204P | 2004-12-17 | 2004-12-17 | |
| IN1352MU2004 | 2004-12-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR066386A1 true AR066386A1 (es) | 2009-08-19 |
Family
ID=36384379
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050105281A AR066386A1 (es) | 2004-12-17 | 2005-12-15 | Compuestos heterociclicos condensados, metodos e intermediarios para su preparacion, una composicion farmaceutica que los comprende y su uso en el tratamiento de enfermedades mediadas por la inhibicion de la pde-4 |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US8129401B2 (es) |
| EP (1) | EP1831227B1 (es) |
| JP (1) | JP5122974B2 (es) |
| KR (1) | KR101317119B1 (es) |
| AP (1) | AP2334A (es) |
| AR (1) | AR066386A1 (es) |
| AU (1) | AU2005315319B2 (es) |
| BR (1) | BRPI0517211B8 (es) |
| CA (1) | CA2591438C (es) |
| EA (1) | EA014956B1 (es) |
| IL (1) | IL183827A (es) |
| MA (1) | MA29231B1 (es) |
| MX (1) | MX2007007345A (es) |
| MY (1) | MY143483A (es) |
| NZ (1) | NZ555809A (es) |
| PL (1) | PL1831227T3 (es) |
| TW (1) | TWI359814B (es) |
| WO (1) | WO2006064355A2 (es) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008032171A1 (en) * | 2006-09-11 | 2008-03-20 | Matrix Laboratories Ltd. | Dibenzofuran derivatives as inhibitors of pde-4 and pde-10 |
| RU2334514C1 (ru) * | 2006-12-01 | 2008-09-27 | Институт физиологически активных веществ Российской Академии наук | СРЕДСТВО ДЛЯ УЛУЧШЕНИЯ КОГНИТИВНЫХ ФУНКЦИЙ И ПАМЯТИ НА ОСНОВЕ ГИДРИРОВАННЫХ ПИРИДО (4,3-b) ИНДОЛОВ (ВАРИАНТЫ), ФАРМАКОЛОГИЧЕСКОЕ СРЕДСТВО НА ЕГО ОСНОВЕ И СПОСОБ ЕГО ПРИМЕНЕНИЯ |
| WO2008081282A2 (en) * | 2006-12-20 | 2008-07-10 | Glenmark Pharmaceuticals S.A. | Process for the synthesis of n9-(3,5-dichloro-4-pyridyl)-6- difluoromethoxybenzo(4,5)furo(3,2-c)pyridine-9-carboxamide and salts thereof |
| WO2008093221A2 (en) * | 2007-02-01 | 2008-08-07 | Glenmark Pharmaceuticals, S.A. | Pharmaceutical compositions containing pde4 inhibitor for the treatment of inflammatory and allergic disorders |
| US8524905B2 (en) | 2007-05-22 | 2013-09-03 | Glenmark Pharmaceuticals S.A. | Processes for preparing 6-(difluoromethoxy)[1]benzofuro[3,2-c]pyridine-9-carbaldehyde, a novel intermediate for the synthesis of PDE IV inhibitors |
| RU2007139634A (ru) | 2007-10-25 | 2009-04-27 | Сергей Олегович Бачурин (RU) | Новые тиазол-, триазол- или оксадиазол-содержащие тетрациклические соединения |
| MX382569B (es) | 2007-11-16 | 2025-03-13 | Rigel Pharmaceuticals Inc | Compuesto de carboxamida, sulfonamida y amina para trastornos metabolicos. |
| WO2009076631A1 (en) | 2007-12-12 | 2009-06-18 | Rigel Pharmaceuticals, Inc. | Carboxamide, sulfonamide and amine compounds for metabolic disorders |
| EP2070913A1 (en) | 2007-12-14 | 2009-06-17 | CHIESI FARMACEUTICI S.p.A. | Ester derivatives as phosphodiesterase inhibitors |
| ES2523580T3 (es) | 2008-01-11 | 2014-11-27 | Albany Molecular Research, Inc. | Piridoindoles substituidos con (1-Azinona) |
| CN102099357B (zh) | 2008-04-23 | 2014-07-02 | 里格尔药品股份有限公司 | 用于治疗代谢障碍的甲酰胺化合物 |
| JP5643290B2 (ja) | 2009-04-09 | 2014-12-17 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Hiv複製の阻害薬 |
| CN102480955B (zh) | 2009-04-29 | 2015-08-05 | 梅迪维新技术公司 | 吡啶并[4,3-b]吲哚类和使用方法 |
| BRPI1006608A2 (pt) | 2009-04-29 | 2015-08-25 | Medivation Technologies Inc | Composto, método para modular um receptor de histamina em um indivíduo, composição farmacêutica, kit e método para tratar um distúrbio cognitivo ou um distúrbio induzido por pelo menos um sintoma associado com a alteração da cognição |
| EP2448585B1 (en) | 2009-07-01 | 2014-01-01 | Albany Molecular Research, Inc. | Azinone-substituted azepino[b]indole and pyrido-pyrrolo-azepine mch-1 antagonists, methods of making, and use thereof |
| WO2011003012A1 (en) | 2009-07-01 | 2011-01-06 | Albany Molecular Research, Inc. | Azinone-substituted azapolycycle mch-1 antagonists, methods of making, and use thereof |
| US9073925B2 (en) | 2009-07-01 | 2015-07-07 | Albany Molecular Research, Inc. | Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof |
| US8629158B2 (en) | 2009-07-01 | 2014-01-14 | Albany Molecular Research, Inc. | Azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof |
| WO2011044134A1 (en) | 2009-10-05 | 2011-04-14 | Albany Molecular Research, Inc. | Epiminocycloalkyl(b)indole derivatives as serotonin sub-type 6 (5-ht6) modulators and uses thereof |
| WO2011132051A2 (en) * | 2010-04-19 | 2011-10-27 | Glenmark Pharmaceuticals S.A. | Tricycle compounds as phosphodiesterase-10 inhibitors |
| RU2417081C1 (ru) * | 2010-05-07 | 2011-04-27 | Ольга Филипповна Сибирева | Способ лечения больных хроническим гломерулонефритом в сочетании с хроническим описторхозом |
| SI2585469T1 (sl) * | 2010-06-24 | 2016-11-30 | Leo Pharma A/S | Heterociklične spojine benzodioksola ali benzodioksepina kot zaviralci fostodiesteraze |
| US8697700B2 (en) | 2010-12-21 | 2014-04-15 | Albany Molecular Research, Inc. | Piperazinone-substituted tetrahydro-carboline MCH-1 antagonists, methods of making, and uses thereof |
| WO2012088124A2 (en) | 2010-12-21 | 2012-06-28 | Albany Molecular Research, Inc. | Tetrahydro-azacarboline mch-1 antagonists, methods of making, and uses thereof |
| CA2823955A1 (en) | 2011-01-19 | 2012-07-26 | Albany Molecular Research, Inc. | Benzofuro[3,2-c] pyridines and related analogs as serotonin sub-type 6 (5-ht6) modulators for the treatment of obesity, metabolic syndrome, cognition and schizophrenia |
| WO2012098495A1 (en) | 2011-01-19 | 2012-07-26 | Glenmark Pharmaceuticals Sa | Pharmaceutical composition that includes revamilast and a beta-2 agonist |
| WO2012110946A1 (en) | 2011-02-17 | 2012-08-23 | Glenmark Pharmaceuticals Sa | Pharmaceutical composition comprising the pde4 enzyme inhibitor revamilast and a disease modifying agent, preferably methotrexate |
| JP2014505738A (ja) | 2011-02-18 | 2014-03-06 | メディベイション テクノロジーズ, インコーポレイテッド | 高血圧を処置するための化合物および方法 |
| WO2012168907A1 (en) | 2011-06-10 | 2012-12-13 | Glenmark Pharmaceuticals Sa | Pharmaceutical composition comprising revamilast and montelukast or zafirlukast |
| WO2013084182A1 (en) | 2011-12-08 | 2013-06-13 | Glenmark Pharmaceuticals S.A. | Pharmaceutical composition that includes a pde4 enzyme inhibitor and an analgesic agent |
| JP6545148B2 (ja) | 2013-03-13 | 2019-07-17 | フラットリー ディスカバリー ラブ,エルエルシー | ピリダジノン化合物及び嚢胞性線維症の治療のための方法 |
| US9714234B2 (en) | 2013-06-25 | 2017-07-25 | Bristol-Myers Squibb Company | Carbazole carboxamide compounds |
| AR096721A1 (es) | 2013-06-25 | 2016-01-27 | Bristol Myers Squibb Co | Compuestos de tetrahidrocarbazol y carbazol carboxamida sustituidos |
| CA2965517C (en) | 2014-10-24 | 2023-05-02 | Bristol-Myers Squibb Company | Indole carboxamides compounds useful as kinase inhibitors |
| WO2016065222A1 (en) | 2014-10-24 | 2016-04-28 | Bristol-Myers Squibb Company | Tricyclic atropisomer compounds |
| PH12017500724B1 (en) | 2014-10-24 | 2023-07-05 | Bristol Myers Squibb Co | Carbazole derivatives |
| CN106496322A (zh) * | 2015-09-07 | 2017-03-15 | 江苏恒瑞医药股份有限公司 | 人胰岛素或其类似物的酰化衍生物的制备方法 |
| JP6472428B2 (ja) * | 2015-12-09 | 2019-02-20 | 財團法人食品工業發展研究所 | キサンチンオキシダーゼ活性の阻害におけるβ−カルボリンアルカロイドの使用 |
| CN112898376B (zh) * | 2019-12-02 | 2022-06-24 | 首都医科大学 | 二氧六环修饰的四氢咔啉-3-甲酰-The-HGK,其制备,抗肿瘤活性和应用 |
| CN112979667B (zh) * | 2019-12-02 | 2022-04-22 | 首都医科大学 | 二氧六环修饰的四氢咔啉-3-甲酰-The,其合成,活性和应用 |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1041861A (en) | 1962-03-14 | 1966-09-07 | Organon Labor Ltd | Pyrrolidone derivatives and pharmaceutical preparations containing them |
| US3759948A (en) | 1969-06-25 | 1973-09-18 | Merck & Co Inc | Non-steroid anti-inflammatory compounds |
| NL7008628A (es) | 1969-06-25 | 1970-12-29 | ||
| US3846553A (en) | 1969-12-03 | 1974-11-05 | Merck & Co Inc | 3-substituted-2-pyridones in the treatment of pain, fever or inflammation |
| NL7016899A (es) | 1969-12-03 | 1971-06-07 | ||
| US4222944A (en) | 1978-07-31 | 1980-09-16 | Hoffmann-La Roche Inc. | Halo-3-dibenzofuran alkanonitriles |
| JPS62158253A (ja) | 1985-12-28 | 1987-07-14 | Kirin Brewery Co Ltd | 4−アミノピリジンアミド誘導体 |
| JPH0812430B2 (ja) | 1986-07-07 | 1996-02-07 | キヤノン株式会社 | 電子写真感光体 |
| DE3779221D1 (de) | 1986-08-19 | 1992-06-25 | Genentech Inc | Einrichtung und dispersion zum intrapulmonalen eingeben von polypeptidwuchsstoffen und -zytokinen. |
| JPS63250378A (ja) * | 1987-04-07 | 1988-10-18 | Mitsubishi Kasei Corp | インド−ル誘導体 |
| US5202344A (en) | 1990-12-11 | 1993-04-13 | G. D. Searle & Co. | N-substituted lactams useful as cholecystokinin antagonists |
| IE71647B1 (en) | 1991-01-28 | 1997-02-26 | Rhone Poulenc Rorer Ltd | Benzamide derivatives |
| MX9301903A (es) | 1992-04-02 | 1994-08-31 | Smithkline Beecham Corp | Compuestos. |
| PL307265A1 (en) | 1992-07-28 | 1995-05-15 | Rhone Poulenc Rorer Ltd | Compounds containing a phenyl group bonded with aryl or heteroaryl group through their bonding aliphatic group or that containing heteroatom |
| MX9306311A (es) | 1992-10-13 | 1994-04-29 | Smithkline Beecham Plc | Compuestos antagonistas del receptor de 5-ht4, procedimiento para su preparacion y composiciones farmaceuticas que los contienen |
| US5814651A (en) | 1992-12-02 | 1998-09-29 | Pfizer Inc. | Catechol diethers as selective PDEIV inhibitors |
| GB9304920D0 (en) | 1993-03-10 | 1993-04-28 | Celltech Ltd | Chemical compounds |
| PL178314B1 (pl) | 1993-07-02 | 2000-04-28 | Byk Gulden Lomberg Chem Fab | Benzamidy podstawione grupą fluoroalkoksylową, hamujące fosfodiesterazę cyklicznych nukleotydów, sposób ich otrzymywania i lek zawierający podstawione benzamidy |
| GB9315595D0 (en) | 1993-07-28 | 1993-09-08 | Res Inst Medicine Chem | New compounds |
| WO1995009837A1 (en) | 1993-10-01 | 1995-04-13 | Smithkline Beecham Corporation | Cyano compounds |
| GB9401460D0 (en) | 1994-01-26 | 1994-03-23 | Rhone Poulenc Rorer Ltd | Compositions of matter |
| GB9404706D0 (en) | 1994-03-11 | 1994-04-27 | Smithkline Beecham Corp | Compounds |
| CN1166169A (zh) | 1994-07-27 | 1997-11-26 | 三共株式会社 | 用作毒蕈碱性受体别构效应物的杂环化合物 |
| CA2217950C (en) | 1995-04-14 | 2001-12-25 | Glaxo Wellcome Inc. | Metered dose inhaler for albuterol |
| US6514996B2 (en) * | 1995-05-19 | 2003-02-04 | Kyowa Hakko Kogyo Co., Ltd. | Derivatives of benzofuran or benzodioxole |
| DE19616573C2 (de) | 1996-04-25 | 1999-03-04 | Pari Gmbh | Verwendung unterkritischer Treibmittelmischungen und Aerosole für die Mikronisierung von Arzneimitteln mit Hilfe dichter Gase |
| CA2256716A1 (en) | 1996-09-04 | 1998-03-12 | Warner-Lambert Company | Matrix metalloproteinase inhibitors and their therapeutic uses |
| US6177440B1 (en) * | 1996-10-30 | 2001-01-23 | Eli Lilly And Company | Substituted tricyclics |
| JP3530004B2 (ja) | 1998-02-06 | 2004-05-24 | 株式会社日立ユニシアオートモティブ | 吸入式投薬器 |
| EP2261235A3 (en) | 1998-03-19 | 2011-04-20 | Vertex Pharmaceuticals Incorporated | Inhibitors of caspases |
| CN1308627A (zh) | 1998-05-12 | 2001-08-15 | 美国家用产品公司 | 可用于治疗胰岛素抗性和高血糖的11-芳基-苯并[b]萘并[2,3-d]呋喃和11-芳基-苯并[b]萘并[2,3-d]噻吩 |
| US6110962A (en) | 1998-05-12 | 2000-08-29 | American Home Products Corporation | 11-aryl-benzo[B]naphtho[2,3-D]furans and 11-aryl-benzo[B]naphtho[2,3-D]thiophenes useful in the treatment of insulin resistance and hyperglycemia |
| US6887870B1 (en) | 1999-10-12 | 2005-05-03 | Bristol-Myers Squibb Company | Heterocyclic sodium/proton exchange inhibitors and method |
| CZ20023033A3 (cs) | 2000-03-17 | 2003-01-15 | Bristol-Myers Squibb Pharma Company | Deriváty cyklických beta-aminokyselin jako inhibitory matrixových metaloproteáz a TNF-alfa |
| US6924292B2 (en) | 2000-03-23 | 2005-08-02 | Takeda Chemical Industries, Ltd. | Furoisoquinoline derivatives, process for producing the same and use thereof |
| WO2002060867A2 (en) | 2001-01-29 | 2002-08-08 | Insight Strategy And Marketing Ltd | Carbazole derivatives and their uses as heparanase inhibitors |
| US20020128920A1 (en) | 2001-03-06 | 2002-09-12 | Dilip Chopra | System and method for providing lowest costs purchasing |
| AU2002306687A1 (en) | 2001-03-13 | 2002-09-24 | Glenmark Pharmaceuticals Limited | Heterocyclic compounds, process for their preparation and pharmaceutical compositions containing them |
| WO2004016596A1 (en) | 2002-08-19 | 2004-02-26 | Glenmark Pharmaceuticals Limited | Condensed heterocyclic compounds as pde-iv inhibitors for the treatment of inflammatory and allergic disorders |
| WO2004022536A1 (en) | 2002-09-04 | 2004-03-18 | Glenmark Pharmaceuticals Limited | New heterocyclic amide compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them |
| AU2003269317B2 (en) * | 2002-10-23 | 2009-10-29 | Glenmark Pharmaceuticals Ltd. | Novel tricyclic compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them |
| WO2004069831A1 (en) * | 2003-02-10 | 2004-08-19 | Glenmark Pharmaceuticals Ltd. | Tricyclic compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation |
| WO2004089940A1 (en) | 2003-04-11 | 2004-10-21 | Glenmark Pharmaceuticals S.A. | Novel heterocyclic compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them |
-
2005
- 2005-12-15 AR ARP050105281A patent/AR066386A1/es unknown
- 2005-12-15 WO PCT/IB2005/003798 patent/WO2006064355A2/en not_active Ceased
- 2005-12-15 JP JP2007546221A patent/JP5122974B2/ja not_active Expired - Fee Related
- 2005-12-15 NZ NZ555809A patent/NZ555809A/en not_active IP Right Cessation
- 2005-12-15 AU AU2005315319A patent/AU2005315319B2/en not_active Ceased
- 2005-12-15 EA EA200701268A patent/EA014956B1/ru not_active IP Right Cessation
- 2005-12-15 CA CA2591438A patent/CA2591438C/en not_active Expired - Lifetime
- 2005-12-15 AP AP2007004031A patent/AP2334A/xx active
- 2005-12-15 MX MX2007007345A patent/MX2007007345A/es active IP Right Grant
- 2005-12-15 KR KR1020077014219A patent/KR101317119B1/ko not_active Expired - Fee Related
- 2005-12-15 PL PL05826587T patent/PL1831227T3/pl unknown
- 2005-12-15 EP EP05826587.7A patent/EP1831227B1/en not_active Expired - Lifetime
- 2005-12-15 BR BRPI0517211A patent/BRPI0517211B8/pt not_active IP Right Cessation
- 2005-12-16 MY MYPI20055953A patent/MY143483A/en unknown
- 2005-12-16 TW TW094144699A patent/TWI359814B/zh not_active IP Right Cessation
-
2007
- 2007-06-10 IL IL183827A patent/IL183827A/en not_active IP Right Cessation
- 2007-07-12 MA MA30075A patent/MA29231B1/fr unknown
-
2011
- 2011-04-15 US US13/087,826 patent/US8129401B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| NZ555809A (en) | 2010-07-30 |
| HK1111147A1 (en) | 2008-08-01 |
| IL183827A (en) | 2013-02-28 |
| CA2591438C (en) | 2014-04-29 |
| KR20070100254A (ko) | 2007-10-10 |
| CA2591438A1 (en) | 2006-06-22 |
| EA014956B1 (ru) | 2011-04-29 |
| MA29231B1 (fr) | 2008-02-01 |
| WO2006064355A3 (en) | 2006-08-03 |
| AP2007004031A0 (en) | 2007-06-30 |
| AU2005315319A1 (en) | 2006-06-22 |
| EP1831227B1 (en) | 2013-06-19 |
| MX2007007345A (es) | 2007-09-07 |
| AU2005315319B2 (en) | 2011-07-07 |
| TWI359814B (en) | 2012-03-11 |
| JP2008524201A (ja) | 2008-07-10 |
| WO2006064355A2 (en) | 2006-06-22 |
| EA200701268A1 (ru) | 2007-12-28 |
| US20110190303A1 (en) | 2011-08-04 |
| BRPI0517211A (pt) | 2008-09-30 |
| PL1831227T3 (pl) | 2013-10-31 |
| IL183827A0 (en) | 2007-09-20 |
| MY143483A (en) | 2011-05-31 |
| TW200634015A (en) | 2006-10-01 |
| JP5122974B2 (ja) | 2013-01-16 |
| BRPI0517211B8 (pt) | 2021-05-25 |
| US8129401B2 (en) | 2012-03-06 |
| EP1831227A2 (en) | 2007-09-12 |
| BRPI0517211B1 (pt) | 2020-08-11 |
| KR101317119B1 (ko) | 2013-10-11 |
| AP2334A (en) | 2011-12-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR066386A1 (es) | Compuestos heterociclicos condensados, metodos e intermediarios para su preparacion, una composicion farmaceutica que los comprende y su uso en el tratamiento de enfermedades mediadas por la inhibicion de la pde-4 | |
| AU2007268749B2 (en) | Novel heterocyclic compound or salt thereof and intermediate thereof | |
| AU2011330850B2 (en) | Inhibitors of HIV replication | |
| AU2016262969B2 (en) | Substituted tetrahydroquinolinone compounds as ROR gamma modulators | |
| ES2759253T3 (es) | Derivados de imidazol tricíclicos condensados como moduladores de la actividad de TNF | |
| JP5872027B2 (ja) | ニコチンアミドホスホリボシルトランスフェラーゼ(nampt)を阻害するためのピペリジン誘導体および組成物 | |
| US20040087577A1 (en) | Anti-infective agents | |
| BR112020012644A2 (pt) | derivados de cromenopiridina como inibidores da fosfatidilinositol fosfato quinase | |
| AU2013225533A1 (en) | Amido spirocyclic amide and sulfonamide derivatives | |
| CA3085460A1 (en) | Aryl-bipyridine amine derivatives as phosphatidylinositol phosphate kinase inhibitors | |
| CZ294027B6 (cs) | Derivát thienopyrimidinu, jeho použití a farmaceutický prostředek, který ho obsahuje | |
| AU2018316254B2 (en) | Carboxamides as ubiquitin-specific protease inhibitors | |
| BR112020012635A2 (pt) | derivados de aminopiridina como inibidores de fosfatidilinositol fosfato quinase | |
| WO2017139778A1 (en) | Thienopyridine carboxamides as ubiquitin-specific protease inhibitors | |
| EP0885894A1 (en) | Pyrido [2,3-d] pyrimidine derivatives and medicinal compositions thereof | |
| WO2006044826A2 (en) | Thiophens and their use as anti-tumor agents | |
| TWI856471B (zh) | 一種DNA聚合酶theta抑制劑及其應用 | |
| JP2013519681A (ja) | 7−アミノフロピリジン誘導体 | |
| CA3189706A1 (en) | Casein kinase 1 delta modulators | |
| JP2018510203A5 (es) | ||
| PT76868A (fr) | Nouveaux derives du thioformamide leur preparation et des medicaments qui les contiennent | |
| JPS5959665A (ja) | 三環式ラクタム類の製造法およびそれらの医薬組成物 | |
| TW202426460A (zh) | 並環含氮化合物、其中間體、製備方法和應用 | |
| EP4182299A2 (en) | Cyclic cyanoenone derivatives as modulators of keap1 | |
| CZ2002818A3 (cs) | Pouľití thienopyrimidinů |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |