JP2015504061A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015504061A5 JP2015504061A5 JP2014550525A JP2014550525A JP2015504061A5 JP 2015504061 A5 JP2015504061 A5 JP 2015504061A5 JP 2014550525 A JP2014550525 A JP 2014550525A JP 2014550525 A JP2014550525 A JP 2014550525A JP 2015504061 A5 JP2015504061 A5 JP 2015504061A5
- Authority
- JP
- Japan
- Prior art keywords
- pyridin
- halo
- group
- imidazo
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000005843 halogen group Chemical group 0.000 claims 35
- 125000000217 alkyl group Chemical group 0.000 claims 33
- 150000003839 salts Chemical class 0.000 claims 21
- -1 cyano, carboxy Chemical group 0.000 claims 20
- 150000001875 compounds Chemical class 0.000 claims 18
- 125000003342 alkenyl group Chemical group 0.000 claims 14
- 125000000304 alkynyl group Chemical group 0.000 claims 14
- 229910052739 hydrogen Inorganic materials 0.000 claims 14
- 125000001072 heteroaryl group Chemical group 0.000 claims 11
- 239000001257 hydrogen Substances 0.000 claims 10
- FWCVZAQENIZVMY-UHFFFAOYSA-N 2-hydroxy-6-[[2-(2-propan-2-ylpyrazol-3-yl)pyridin-3-yl]methoxy]benzaldehyde Chemical compound CC(C)N1N=CC=C1C1=NC=CC=C1COC1=CC=CC(O)=C1C=O FWCVZAQENIZVMY-UHFFFAOYSA-N 0.000 claims 8
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 8
- 150000002431 hydrogen Chemical class 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- LAFDCOJCHVMHEK-UHFFFAOYSA-N 3-formyl-4-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzonitrile Chemical compound O=CC1=CC(C#N)=CC=C1OCC1=CC=CN2C1=NC=C2 LAFDCOJCHVMHEK-UHFFFAOYSA-N 0.000 claims 2
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims 2
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 2
- KRGGDHHVSYRSIR-UHFFFAOYSA-N 5-methoxy-2-(1h-pyrrolo[2,3-b]pyridin-4-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=NC2=C1C=CN2 KRGGDHHVSYRSIR-UHFFFAOYSA-N 0.000 claims 2
- XNLXMKUOZPVVAY-UHFFFAOYSA-N 5-methoxy-2-(pyrrolo[1,2-a]pyrazin-6-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=C2N1C=CN=C2 XNLXMKUOZPVVAY-UHFFFAOYSA-N 0.000 claims 2
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims 2
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims 2
- 150000001299 aldehydes Chemical group 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 208000007056 sickle cell anemia Diseases 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- OYRNMRHRANZAEA-UHFFFAOYSA-N 2-(1h-indazol-4-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=C1C=NN2 OYRNMRHRANZAEA-UHFFFAOYSA-N 0.000 claims 1
- SXHIWHCDGVVVIB-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-3-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN=C2N1C=CC=C2 SXHIWHCDGVVVIB-UHFFFAOYSA-N 0.000 claims 1
- HITDPUASURIIIM-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-5-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=NC=CN12 HITDPUASURIIIM-UHFFFAOYSA-N 0.000 claims 1
- QHLPHLHHFIJUTA-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-6-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN2C=CN=C2C=C1 QHLPHLHHFIJUTA-UHFFFAOYSA-N 0.000 claims 1
- BOVHKSDADHYZQJ-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-7-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC2=NC=CN2C=C1 BOVHKSDADHYZQJ-UHFFFAOYSA-N 0.000 claims 1
- XJOOEFTYEAKFPQ-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-3-methoxybenzaldehyde Chemical compound COC1=CC=CC(C=O)=C1OCC1=CC=CN2C1=NC=C2 XJOOEFTYEAKFPQ-UHFFFAOYSA-N 0.000 claims 1
- IGCYNZLPHDJAFF-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-4-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C(OCC=2C3=NC=CN3C=CC=2)=C1 IGCYNZLPHDJAFF-UHFFFAOYSA-N 0.000 claims 1
- AJERFTOKIJSSNV-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CN2C1=NC=C2 AJERFTOKIJSSNV-UHFFFAOYSA-N 0.000 claims 1
- JIPTXLQISRYEFG-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methylbenzaldehyde Chemical compound O=CC1=CC(C)=CC=C1OCC1=CC=CN2C1=NC=C2 JIPTXLQISRYEFG-UHFFFAOYSA-N 0.000 claims 1
- DQAWRCYLXLPFGX-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC=CC=C1OCC1=CC=CN2C1=NC=C2 DQAWRCYLXLPFGX-UHFFFAOYSA-N 0.000 claims 1
- CXANJHAMRLLDTK-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-5-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=CN=CN12 CXANJHAMRLLDTK-UHFFFAOYSA-N 0.000 claims 1
- FKALBRNKMNOVHC-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-6-ylmethoxy)-4-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C(OCC2=CN3C=NC=C3C=C2)=C1 FKALBRNKMNOVHC-UHFFFAOYSA-N 0.000 claims 1
- QDLUTGMUCKWBAN-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-6-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN2C=NC=C2C=C1 QDLUTGMUCKWBAN-UHFFFAOYSA-N 0.000 claims 1
- OBVSYIPVNMKXQV-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-8-ylmethoxy)-4-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C(OCC=2C3=CN=CN3C=CC=2)=C1 OBVSYIPVNMKXQV-UHFFFAOYSA-N 0.000 claims 1
- VKOMJTJRYAGKIV-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CN2C1=CN=C2 VKOMJTJRYAGKIV-UHFFFAOYSA-N 0.000 claims 1
- RVRQTALZXUANFL-UHFFFAOYSA-N 2-[(1-methylimidazol-2-yl)methoxy]benzaldehyde Chemical compound CN1C=CN=C1COC1=CC=CC=C1C=O RVRQTALZXUANFL-UHFFFAOYSA-N 0.000 claims 1
- QNMDAKAPCVVQQP-UHFFFAOYSA-N 2-[(2-nitropyridin-3-yl)oxymethyl]benzene-1,3-dicarbaldehyde Chemical compound [O-][N+](=O)C1=NC=CC=C1OCC1=C(C=O)C=CC=C1C=O QNMDAKAPCVVQQP-UHFFFAOYSA-N 0.000 claims 1
- INLKHRAYLFROSM-UHFFFAOYSA-N 2-[(7-chloroquinolin-2-yl)methoxy]-5-nitrobenzaldehyde Chemical compound O=CC1=CC([N+](=O)[O-])=CC=C1OCC1=CC=C(C=CC(Cl)=C2)C2=N1 INLKHRAYLFROSM-UHFFFAOYSA-N 0.000 claims 1
- WEWBVBKSBQBVFI-UHFFFAOYSA-N 2-[(7-chloroquinolin-2-yl)methoxy]benzene-1,3-dicarbaldehyde Chemical compound N=1C2=CC(Cl)=CC=C2C=CC=1COC1=C(C=O)C=CC=C1C=O WEWBVBKSBQBVFI-UHFFFAOYSA-N 0.000 claims 1
- LJUWDMROBYYYNX-UHFFFAOYSA-N 2-[[1-[2-(2-methyl-5-nitroimidazol-1-yl)ethyl]triazol-4-yl]methoxy]benzaldehyde Chemical compound CC1=NC=C([N+]([O-])=O)N1CCN1N=NC(COC=2C(=CC=CC=2)C=O)=C1 LJUWDMROBYYYNX-UHFFFAOYSA-N 0.000 claims 1
- HYEMCPMRYDUHSN-UHFFFAOYSA-N 2-[[2-(4-tert-butyl-1,3-thiazol-2-yl)-1-benzofuran-5-yl]oxymethyl]benzaldehyde Chemical compound CC(C)(C)C1=CSC(C=2OC3=CC=C(OCC=4C(=CC=CC=4)C=O)C=C3C=2)=N1 HYEMCPMRYDUHSN-UHFFFAOYSA-N 0.000 claims 1
- GTAYSDREQLXNMN-UHFFFAOYSA-N 2-fluoro-6-[[2-(2-propan-2-ylpyrazol-3-yl)pyridin-3-yl]methoxy]benzaldehyde Chemical compound CC(C)N1N=CC=C1C1=NC=CC=C1COC1=CC=CC(F)=C1C=O GTAYSDREQLXNMN-UHFFFAOYSA-N 0.000 claims 1
- QZQXJMNHOPSYBC-UHFFFAOYSA-N 2-fluoro-6-[[2-[2-(2,2,2-trifluoroethyl)pyrazol-3-yl]pyridin-3-yl]methoxy]benzaldehyde Chemical compound FC1=CC=CC(OCC=2C(=NC=CC=2)C=2N(N=CC=2)CC(F)(F)F)=C1C=O QZQXJMNHOPSYBC-UHFFFAOYSA-N 0.000 claims 1
- LLNUXVXQOAESCE-UHFFFAOYSA-N 2-fluoro-6-[[2-[2-(3,3,3-trifluoropropyl)pyrazol-3-yl]pyridin-3-yl]methoxy]benzaldehyde Chemical compound FC1=CC=CC(OCC=2C(=NC=CC=2)C=2N(N=CC=2)CCC(F)(F)F)=C1C=O LLNUXVXQOAESCE-UHFFFAOYSA-N 0.000 claims 1
- BUSDPAIYNWOKOG-UHFFFAOYSA-N 2-hydroxy-6-[[2-[2-(2,2,2-trifluoroethyl)pyrazol-3-yl]pyridin-3-yl]methoxy]benzaldehyde Chemical compound OC1=CC=CC(OCC=2C(=NC=CC=2)C=2N(N=CC=2)CC(F)(F)F)=C1C=O BUSDPAIYNWOKOG-UHFFFAOYSA-N 0.000 claims 1
- VPPVYRNEOIHMAM-UHFFFAOYSA-N 2-hydroxy-6-[[2-[2-(3,3,3-trifluoropropyl)pyrazol-3-yl]pyridin-3-yl]methoxy]benzaldehyde Chemical compound OC1=CC=CC(OCC=2C(=NC=CC=2)C=2N(N=CC=2)CCC(F)(F)F)=C1C=O VPPVYRNEOIHMAM-UHFFFAOYSA-N 0.000 claims 1
- RCLXRECDHREUJS-UHFFFAOYSA-N 3-(imidazo[1,2-a]pyridin-8-ylmethyl)-1,3-dihydro-2-benzofuran-1-ol Chemical compound C12=CC=CC=C2C(O)OC1CC1=CC=CN2C1=NC=C2 RCLXRECDHREUJS-UHFFFAOYSA-N 0.000 claims 1
- VWXGYOFEFGXHLR-UHFFFAOYSA-N 3-formyl-4-(imidazo[1,5-a]pyridin-5-ylmethoxy)benzonitrile Chemical compound O=CC1=CC(C#N)=CC=C1OCC1=CC=CC2=CN=CN12 VWXGYOFEFGXHLR-UHFFFAOYSA-N 0.000 claims 1
- PRYOWPXXQMPLLX-UHFFFAOYSA-N 3-methyl-2-[(2-nitropyridin-3-yl)oxymethyl]benzaldehyde Chemical compound CC1=CC=CC(C=O)=C1COC1=CC=CN=C1[N+]([O-])=O PRYOWPXXQMPLLX-UHFFFAOYSA-N 0.000 claims 1
- CIVJRNZQBJFPEY-UHFFFAOYSA-N 4-[(7-chloroquinolin-2-yl)methoxy]benzene-1,3-dicarbaldehyde Chemical compound N=1C2=CC(Cl)=CC=C2C=CC=1COC1=CC=C(C=O)C=C1C=O CIVJRNZQBJFPEY-UHFFFAOYSA-N 0.000 claims 1
- BERKGZQCMWOMFH-UHFFFAOYSA-N 4-chloro-2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound ClC1=CC=C(C=O)C(OCC=2C3=NC=CN3C=CC=2)=C1 BERKGZQCMWOMFH-UHFFFAOYSA-N 0.000 claims 1
- BJRVCVXCUZTNOT-UHFFFAOYSA-N 4-fluoro-2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound FC1=CC=C(C=O)C(OCC=2C3=NC=CN3C=CC=2)=C1 BJRVCVXCUZTNOT-UHFFFAOYSA-N 0.000 claims 1
- IOLJMWNHXRPCSE-UHFFFAOYSA-N 4-formyl-3-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzonitrile Chemical compound O=CC1=CC=C(C#N)C=C1OCC1=CC=CN2C1=NC=C2 IOLJMWNHXRPCSE-UHFFFAOYSA-N 0.000 claims 1
- QSPXWFLFNPDJTF-UHFFFAOYSA-N 5-bromo-2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(Br)=CC=C1OCC1=CC=CN2C1=NC=C2 QSPXWFLFNPDJTF-UHFFFAOYSA-N 0.000 claims 1
- WCVNZCJUHMJOEH-UHFFFAOYSA-N 5-bromo-2-[(6-methylpyridin-3-yl)methoxy]benzaldehyde Chemical compound C1=NC(C)=CC=C1COC1=CC=C(Br)C=C1C=O WCVNZCJUHMJOEH-UHFFFAOYSA-N 0.000 claims 1
- MOHKJHQLXKCGPV-UHFFFAOYSA-N 5-ethyl-2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(CC)=CC=C1OCC1=CC=CN2C1=NC=C2 MOHKJHQLXKCGPV-UHFFFAOYSA-N 0.000 claims 1
- OAKLOYATUAFQQI-UHFFFAOYSA-N 5-methoxy-2-(1h-pyrazolo[3,4-b]pyridin-4-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=NC2=C1C=NN2 OAKLOYATUAFQQI-UHFFFAOYSA-N 0.000 claims 1
- ZGAQYTGICSHQIN-UHFFFAOYSA-N 5-methoxy-2-(pyrazolo[1,5-a]pyrazin-3-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=C2C=NC=CN2N=C1 ZGAQYTGICSHQIN-UHFFFAOYSA-N 0.000 claims 1
- NRGBAMJCLLKMCZ-UHFFFAOYSA-N 5-methoxy-2-(pyrrolo[1,2-a]pyrazin-4-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN=CC2=CC=CN12 NRGBAMJCLLKMCZ-UHFFFAOYSA-N 0.000 claims 1
- QHYINIBXOSBMIT-UHFFFAOYSA-N 5-methoxy-2-(quinolin-5-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=NC=CC=C12 QHYINIBXOSBMIT-UHFFFAOYSA-N 0.000 claims 1
- PHGADRUHZNQNFN-UHFFFAOYSA-N 5-methoxy-2-[(1-methylindazol-4-yl)methoxy]benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=C1C=NN2C PHGADRUHZNQNFN-UHFFFAOYSA-N 0.000 claims 1
- QSJNCVCFMKNDKW-UHFFFAOYSA-N 5-methoxy-2-[(8-methylimidazo[1,2-a]pyridin-2-yl)methoxy]benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN(C=CC=C2C)C2=N1 QSJNCVCFMKNDKW-UHFFFAOYSA-N 0.000 claims 1
- OFTYDSFWKUUDNZ-UHFFFAOYSA-N 5-methoxy-2-[[2-(2-propan-2-ylpyrazol-3-yl)pyridin-3-yl]methoxy]benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CN=C1C1=CC=NN1C(C)C OFTYDSFWKUUDNZ-UHFFFAOYSA-N 0.000 claims 1
- GLQWIOMIMKQPFA-UHFFFAOYSA-N 6-[(2-formyl-4-methoxyphenoxy)methyl]pyrrolo[1,2-a]pyrazine-7-carbonitrile Chemical compound O=CC1=CC(OC)=CC=C1OCC1=C(C#N)C=C2N1C=CN=C2 GLQWIOMIMKQPFA-UHFFFAOYSA-N 0.000 claims 1
- CWDLNRKREBPISR-UHFFFAOYSA-N 6-[(2-formyl-4-methoxyphenoxy)methyl]pyrrolo[1,2-a]pyrazine-7-carboxamide Chemical compound O=CC1=CC(OC)=CC=C1OCC1=C(C(N)=O)C=C2N1C=CN=C2 CWDLNRKREBPISR-UHFFFAOYSA-N 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 206010011985 Decubitus ulcer Diseases 0.000 claims 1
- 206010021143 Hypoxia Diseases 0.000 claims 1
- 208000004852 Lung Injury Diseases 0.000 claims 1
- 208000019693 Lung disease Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000004210 Pressure Ulcer Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 206010069363 Traumatic lung injury Diseases 0.000 claims 1
- 208000025865 Ulcer Diseases 0.000 claims 1
- 206010052428 Wound Diseases 0.000 claims 1
- 208000027418 Wounds and injury Diseases 0.000 claims 1
- 208000008445 altitude sickness Diseases 0.000 claims 1
- 125000005214 aminoheteroaryl group Chemical group 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 150000004292 cyclic ethers Chemical class 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 230000007954 hypoxia Effects 0.000 claims 1
- 231100000515 lung injury Toxicity 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- MEADIYLUVHACCV-UHFFFAOYSA-N n,n-diethyl-2-formyl-4-methoxy-3-(pyridin-4-ylmethoxy)benzamide Chemical compound CCN(CC)C(=O)C1=CC=C(OC)C(OCC=2C=CN=CC=2)=C1C=O MEADIYLUVHACCV-UHFFFAOYSA-N 0.000 claims 1
- KHPCVTBRFJFTGV-UHFFFAOYSA-N n-(2-formyl-4-methoxyphenyl)imidazo[1,2-a]pyridine-8-carboxamide Chemical compound O=CC1=CC(OC)=CC=C1NC(=O)C1=CC=CN2C1=NC=C2 KHPCVTBRFJFTGV-UHFFFAOYSA-N 0.000 claims 1
- RXFXGKDBNOKILL-UHFFFAOYSA-N n-(2-formylphenyl)imidazo[1,2-a]pyridine-8-carboxamide Chemical compound O=CC1=CC=CC=C1NC(=O)C1=CC=CN2C1=NC=C2 RXFXGKDBNOKILL-UHFFFAOYSA-N 0.000 claims 1
- BXNFZMDIMWCBHR-UHFFFAOYSA-N n-[6-[(2-formylphenoxy)methyl]pyridin-2-yl]acetamide Chemical compound CC(=O)NC1=CC=CC(COC=2C(=CC=CC=2)C=O)=N1 BXNFZMDIMWCBHR-UHFFFAOYSA-N 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000004944 pyrazin-3-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000003831 tetrazolyl group Chemical group 0.000 claims 1
- DENPQNAWGQXKCU-UHFFFAOYSA-N thiophene-2-carboxamide Chemical compound NC(=O)C1=CC=CS1 DENPQNAWGQXKCU-UHFFFAOYSA-N 0.000 claims 1
- 230000000287 tissue oxygenation Effects 0.000 claims 1
- 231100000397 ulcer Toxicity 0.000 claims 1
- ATEDQANYWGMZND-UHFFFAOYSA-N CC(C)[n]1nccc1-c1c(CCl)cccn1 Chemical compound CC(C)[n]1nccc1-c1c(CCl)cccn1 ATEDQANYWGMZND-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161581053P | 2011-12-28 | 2011-12-28 | |
| US61/581,053 | 2011-12-28 | ||
| US201261661320P | 2012-06-18 | 2012-06-18 | |
| US61/661,320 | 2012-06-18 | ||
| PCT/US2012/072177 WO2013102142A1 (en) | 2011-12-28 | 2012-12-28 | Substituted benzaldehyde compounds and methods for their use in increasing tissue oxygenation |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017077318A Division JP6424399B2 (ja) | 2011-12-28 | 2017-04-10 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015504061A JP2015504061A (ja) | 2015-02-05 |
| JP2015504061A5 true JP2015504061A5 (enExample) | 2016-07-28 |
| JP6242810B2 JP6242810B2 (ja) | 2017-12-06 |
Family
ID=48698669
Family Applications (7)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014550525A Active JP6242810B2 (ja) | 2011-12-28 | 2012-12-28 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2017077318A Active JP6424399B2 (ja) | 2011-12-28 | 2017-04-10 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2018189280A Active JP6585261B2 (ja) | 2011-12-28 | 2018-10-04 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2019161066A Active JP6848026B2 (ja) | 2011-12-28 | 2019-09-04 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2021033123A Pending JP2021104996A (ja) | 2011-12-28 | 2021-03-03 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2022154128A Pending JP2022191281A (ja) | 2011-12-28 | 2022-09-27 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2024008428A Pending JP2024050663A (ja) | 2011-12-28 | 2024-01-24 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
Family Applications After (6)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017077318A Active JP6424399B2 (ja) | 2011-12-28 | 2017-04-10 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2018189280A Active JP6585261B2 (ja) | 2011-12-28 | 2018-10-04 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2019161066A Active JP6848026B2 (ja) | 2011-12-28 | 2019-09-04 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2021033123A Pending JP2021104996A (ja) | 2011-12-28 | 2021-03-03 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2022154128A Pending JP2022191281A (ja) | 2011-12-28 | 2022-09-27 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2024008428A Pending JP2024050663A (ja) | 2011-12-28 | 2024-01-24 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
Country Status (33)
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3142817A1 (en) | 2011-12-28 | 2013-07-04 | Global Blood Therapeutics, Inc. | Substituted benzaldehyde compounds and methods for their use in increasing tissue oxygenation |
| ES2790358T3 (es) | 2011-12-28 | 2020-10-27 | Global Blood Therapeutics Inc | Compuestos de heteroaril aldehído sustituido y métodos para su uso en el aumento de la oxigenación tisular |
| US9802900B2 (en) | 2013-03-15 | 2017-10-31 | Global Blood Therapeutics, Inc. | Bicyclic heteroaryl compounds and uses thereof for the modulation of hemoglobin |
| EP3919056B1 (en) * | 2013-03-15 | 2024-08-28 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| CN112500338A (zh) | 2013-03-15 | 2021-03-16 | 全球血液疗法股份有限公司 | 化合物及其用于调节血红蛋白的用途 |
| US9422279B2 (en) | 2013-03-15 | 2016-08-23 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| EA201591427A1 (ru) * | 2013-03-15 | 2016-01-29 | Глобал Блад Терапьютикс, Инк. | Соединения и их применения для модуляции гемоглобина |
| US9604999B2 (en) | 2013-03-15 | 2017-03-28 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US20140274961A1 (en) * | 2013-03-15 | 2014-09-18 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US10100043B2 (en) | 2013-03-15 | 2018-10-16 | Global Blood Therapeutics, Inc. | Substituted aldehyde compounds and methods for their use in increasing tissue oxygenation |
| US9458139B2 (en) | 2013-03-15 | 2016-10-04 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US8952171B2 (en) | 2013-03-15 | 2015-02-10 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US10266551B2 (en) | 2013-03-15 | 2019-04-23 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| CA2902709A1 (en) * | 2013-03-15 | 2014-09-25 | Global Blood Therapeutics, Inc. | Compositions and methods for the modulation of hemoglobin (s) |
| ES2710380T3 (es) * | 2013-03-15 | 2019-04-24 | Global Blood Therapeutics Inc | Compuestos y usos de los mismos para la modulación de hemoglobina |
| EP2968299B1 (en) | 2013-03-15 | 2021-01-20 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| EP3036222A2 (en) * | 2013-08-23 | 2016-06-29 | Virginia Commonwealth University | Ester nitrates derivatives of aromatic aldehydes with multiple pharmalogic properties to treat sickle cell disease |
| US20160206604A1 (en) * | 2013-08-26 | 2016-07-21 | Global Blood Therapeutics, Inc. | Formulations comprising wetting agents and compounds for the modulation of hemoglobin (s) |
| WO2015031285A1 (en) * | 2013-08-27 | 2015-03-05 | Global Blood Therapeutics, Inc. | Crystalline 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde ansolvate salts |
| US20160207904A1 (en) * | 2013-08-27 | 2016-07-21 | Global Blood Therapeutics, Inc. | Crystalline 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde ansolvate salts |
| EA202092627A1 (ru) | 2013-11-18 | 2021-09-30 | Глобал Блад Терапьютикс, Инк. | Соединения и их применения для модуляции гемоглобина |
| WO2015116061A1 (en) * | 2014-01-29 | 2015-08-06 | Global Blood Therapeutics, Inc. | 1:1 adducts of sickle hemoglobin |
| US9248199B2 (en) | 2014-01-29 | 2016-02-02 | Global Blood Therapeutics, Inc. | 1:1 adducts of sickle hemoglobin |
| SG10201911662YA (en) | 2014-02-07 | 2020-02-27 | Global Blood Therapeutics Inc | Crystalline polymorphs of the free base of 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde |
| WO2016043849A2 (en) * | 2014-07-24 | 2016-03-24 | Global Blood Therapeutics, Inc. | Compounds for treating acute respiratory distress syndrome or a negative effect thereof |
| MA41841A (fr) | 2015-03-30 | 2018-02-06 | Global Blood Therapeutics Inc | Composés aldéhyde pour le traitement de la fibrose pulmonaire, de l'hypoxie, et de maladies auto-immunes et des tissus conjonctifs |
| WO2016161572A1 (en) * | 2015-04-08 | 2016-10-13 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
| EP3288933B1 (en) | 2015-04-30 | 2021-10-06 | Musc Foundation for Research Development | Oxindole compounds and pharmaceutical compositions thereof |
| HUE072191T2 (hu) | 2015-12-04 | 2025-10-28 | Global Blood Therapeutics Inc | A 2-hidoxi-6-((2-(1-izopropil-1H-pirazol-5-il)piridin-3-il)metoxi)benzaldehid adagolási rendje |
| TWI825524B (zh) * | 2016-05-12 | 2023-12-11 | 美商全球血液治療公司 | 用於合成2-羥基-6-((2-(1-異丙基-1h-吡唑-5-基)-吡啶-3-基)甲氧基)苯甲醛之方法 |
| US10787430B2 (en) | 2016-06-17 | 2020-09-29 | Fronthera U.S. Pharmaceuticals Llc | Hemoglobin modifier compounds and uses thereof |
| TWI778983B (zh) | 2016-10-12 | 2022-10-01 | 美商全球血液治療公司 | 包含2-羥基-6-((2-(1-異丙基-1h-吡唑-5-基)吡啶-3-基)甲氧基)-苯甲醛之片劑 |
| PT3448859T (pt) | 2017-03-20 | 2019-10-25 | Forma Therapeutics Inc | Composições de pirrolopirrole como ativadores de piruvato quinase (pkr). |
| EP3624885B1 (en) | 2017-05-19 | 2026-02-18 | Trudell Medical International Inc. | Positive expiratory pressure device |
| CN108276405A (zh) * | 2018-03-12 | 2018-07-13 | 南安市创培电子科技有限公司 | 一种医药中间体咪唑并[1,2-a]吡啶-2-羧酸乙酯的合成工艺 |
| WO2019182938A1 (en) * | 2018-03-22 | 2019-09-26 | Virginia Commonwealth University | Aromatic aldehydes with sustained and enhanced in vitro and in vivo pharmacologic activity to treat sickle cell disease |
| USD874064S1 (en) | 2018-05-18 | 2020-01-28 | Trudell Medical International | Mask |
| USD903097S1 (en) | 2018-05-18 | 2020-11-24 | Trudell Medical International | Mask |
| US12053458B2 (en) | 2018-09-19 | 2024-08-06 | Novo Nordisk Health Care Ag | Treating sickle cell disease with a pyruvate kinase R activating compound |
| ES2989438T3 (es) | 2018-09-19 | 2024-11-26 | Novo Nordisk Healthcare Ag | Activación de la piruvato cinasa R |
| US11014884B2 (en) | 2018-10-01 | 2021-05-25 | Global Blood Therapeutics, Inc. | Modulators of hemoglobin |
| USD893806S1 (en) | 2018-11-09 | 2020-08-18 | Trudell Medical Internationl | Mask and shroud |
| CR20210335A (es) | 2018-11-19 | 2021-09-14 | Global Blood Therapeutics Inc | Compuestos de 2-formil-3-hidroxifeniloximetilo capaces de modular la hemoglobina |
| MX2021006095A (es) | 2018-11-29 | 2021-07-06 | Pfizer | Pirazoles como moduladores de hemoglobina. |
| WO2020127945A1 (en) | 2018-12-21 | 2020-06-25 | Bionice, S.L.U. | Process and intermediates for the synthesis of voxelotor |
| US12492180B2 (en) | 2018-12-21 | 2025-12-09 | Curia Spain, S.A.U. | Process and intermediates for the preparation of Voxelotor |
| US12479816B2 (en) | 2019-02-08 | 2025-11-25 | University of Pittsburgh—of the Commonwealth System of Higher Education | 20-HETE formation inhibitors |
| EP3693364A1 (en) | 2019-02-11 | 2020-08-12 | Sandoz Ag | Crystalline salts of a hemoglobin s allosteric modulator |
| CN114615977B (zh) | 2019-09-19 | 2025-01-14 | 诺沃挪第克健康护理股份公司 | 丙酮酸激酶r(pkr)活化组合物 |
| US20230015823A1 (en) | 2019-11-19 | 2023-01-19 | Global Blood Therapeutics, Inc. | Methods of administering voxelotor |
| GB202002560D0 (en) | 2020-02-24 | 2020-04-08 | Johnson Matthey Plc | Crystalline forms of voxelotor, and processes for the preparation thereof |
| EP3888750A1 (en) | 2020-04-02 | 2021-10-06 | Sandoz AG | Crystalline form of voxelotor |
| WO2021224280A1 (en) * | 2020-05-05 | 2021-11-11 | Dipharma Francis S.R.L. | Synthesis of a sickle cell disease agent and intermediates thereof |
| IT202000009970A1 (it) * | 2020-05-05 | 2021-11-05 | Dipharma Francis Srl | Procedimento per la preparazione di un farmaco per il trattamento dell’anemia falciforme |
| IT202000025135A1 (it) | 2020-10-23 | 2022-04-23 | Dipharma Francis Srl | Procedimento per la preparazione di un farmaco per il trattamento dell’anemia falciforme |
| WO2022013052A1 (en) | 2020-07-15 | 2022-01-20 | Sandoz Ag | Compounds comprising voxelotor and 2,5-dihydroxybenzoic acid and crystal forms |
| CN112047924B (zh) * | 2020-10-10 | 2023-04-18 | 山东汇海医药化工有限公司 | 一种沃克洛多的制备方法 |
| CN116710441A (zh) * | 2020-11-06 | 2023-09-05 | 全球血液疗法公司 | 制备2-羟基-6-((2-(1-异丙基-1h-吡唑-5-基)吡啶-3-基)甲氧基)苯甲醛的方法 |
| TW202233589A (zh) | 2020-11-06 | 2022-09-01 | 美商全球血液治療公司 | 2-羥基-6-((2-(1-異丙基-1h-吡唑-5-基)吡啶-3-基)甲氧基)苯甲醛之製備方法 |
| US12128035B2 (en) | 2021-03-19 | 2024-10-29 | Novo Nordisk Health Care Ag | Activating pyruvate kinase R |
| AU2022381755A1 (en) | 2021-11-05 | 2024-05-16 | Global Blood Therapeutics, Inc. | Methods of treating sickle cell disease with voxelotor |
| AU2023376662B2 (en) * | 2022-11-07 | 2025-06-05 | Children's Hospital Of Philadelphia (Chop) | Benzaldehyde compounds with direct polymer destabilizing effects to treat sickle cell disease |
| WO2025106877A1 (en) * | 2023-11-16 | 2025-05-22 | The J. David Gladstone Institutes, A Testamentary Trust Established Under The Will Of J. David Gladstone | Inhaled hypoxia and small molecule forms of hypoxia as novel anticancer agents |
Family Cites Families (257)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL218146A (enExample) | 1956-02-13 | 1900-01-01 | ||
| BE787580A (fr) | 1971-08-13 | 1973-02-14 | Hoechst Ag | Procede de preparation de derives du furanne |
| BE787576A (fr) | 1971-08-13 | 1973-02-14 | Hoechst Ag | Derives de benzofuranne et leur utilisation comme azureurs optiques |
| GB1409865A (en) | 1973-02-13 | 1975-10-15 | Science Union & Cie | Dihydropyridines derivatives their preparation and pharmaceu tical compositions containing them |
| US4062858A (en) | 1976-12-22 | 1977-12-13 | E. R. Squibb & Sons, Inc. | Derivatives of 5,6-dihydrobenzo[5,6]cyclohepta[1,2-b]pyrazolo[4,3-e]pyridin-11(1H)-ones and 11(1H)-imines |
| GB1593417A (en) | 1976-12-22 | 1981-07-15 | Squibb & Sons Inc | Carbocyclic-fused pyrazolopyridine derivatives |
| DE2964427D1 (en) | 1978-10-04 | 1983-02-03 | Ciba Geigy Ag | Process for the preparation of furanyl-benzazoles |
| DE2853765A1 (de) | 1978-12-13 | 1980-06-26 | Bayer Ag | Verfahren zur herstellung von benzimidazolylbenzofuranen |
| DE2904829A1 (de) | 1979-02-08 | 1980-08-14 | Bayer Ag | Verfahren zur herstellung von benzimidazolylbenzofuran |
| HU190774B (en) * | 1979-06-29 | 1986-11-28 | The Wellcome Foundation Ltd,Gb | Process for preparing ether derivatives with pharmacological activity |
| GB2090830B (en) | 1980-12-18 | 1984-09-26 | Wellcome Found | Formyl ether derivatives |
| JPS5929667A (ja) | 1982-08-13 | 1984-02-16 | Otsuka Pharmaceut Co Ltd | カルボスチリル誘導体および強心剤 |
| US4478834A (en) | 1983-02-11 | 1984-10-23 | Usv Pharmaceutical Corporation | Dihydropyridines and their use in the treatment of asthma |
| GB8402740D0 (en) | 1984-02-02 | 1984-03-07 | Scras | Furo-(3 4-c)-pyridine derivatives |
| JPS6140236A (ja) | 1984-08-02 | 1986-02-26 | Yamanouchi Pharmaceut Co Ltd | ハイドロキノン誘導体 |
| DE3431004A1 (de) | 1984-08-23 | 1986-03-06 | Hoechst Ag, 6230 Frankfurt | Neue 3-pyridylverbindungen und verfahren zu ihrer herstellung |
| DD226590A1 (de) | 1984-09-07 | 1985-08-28 | Univ Leipzig | Mittel zur phagenhemmung in mikrobiellen produktionsprozessen |
| GB8603475D0 (en) | 1986-02-12 | 1986-03-19 | Glaxo Group Ltd | Chemical compounds |
| DK111387A (da) | 1986-03-05 | 1987-09-06 | Otsuka Pharma Co Ltd | Carbostyrilderivater og salte deraf, laegemiddel indeholdende saadanne derivater samt fremgangsmaade til fremstilling af derivaterne |
| US4831041A (en) * | 1986-11-26 | 1989-05-16 | Fujisawa Pharmaceutical Co., Ltd. | Imidazopyridine compounds and processes for preparation thereof |
| GB8628262D0 (en) * | 1986-11-26 | 1986-12-31 | Fujisawa Pharmaceutical Co | Imidazopyridine compounds |
| EP0278686A1 (en) | 1987-02-07 | 1988-08-17 | The Wellcome Foundation Limited | Pyridopyrimidines methods for their preparation and pharmaceutical formulations thereof |
| DD258226A1 (de) | 1987-03-05 | 1988-07-13 | Fahlberg List Veb | Verfahren zur herstellung von aroxymethylchinoxalinen |
| JPH07121937B2 (ja) | 1987-03-18 | 1995-12-25 | 大塚製薬株式会社 | カルボスチリル誘導体 |
| JPS63258463A (ja) | 1987-04-14 | 1988-10-25 | Kumiai Chem Ind Co Ltd | 2−フエノキシピリミジン誘導体及び除草剤 |
| GB8711802D0 (en) | 1987-05-19 | 1987-06-24 | Fujisawa Pharmaceutical Co | Dithioacetal compounds |
| GB8718940D0 (en) | 1987-08-11 | 1987-09-16 | Glaxo Group Ltd | Chemical compounds |
| US4920131A (en) | 1987-11-03 | 1990-04-24 | Rorer Pharmaceutical Corp. | Quinoline derivatives and use thereof as antagonists of leukotriene D4 |
| JP2650038B2 (ja) | 1988-01-27 | 1997-09-03 | サントリー株式会社 | ピロリチジン化合物およびその用途 |
| EP0336369A1 (en) | 1988-04-04 | 1989-10-11 | E.R. Squibb & Sons, Inc. | 3-Acylamino-1-[[[(substituted sulfonyl)amino]carbonyl]amino]2-azetidinones |
| US4952574A (en) | 1988-09-26 | 1990-08-28 | Riker Laboratories, Inc. | Antiarrhythmic substituted N-(2-piperidylmethyl)benzamides |
| IE81170B1 (en) * | 1988-10-21 | 2000-05-31 | Zeneca Ltd | Pyridine derivatives |
| DD276480A1 (de) | 1988-10-26 | 1990-02-28 | Fahlberg List Veb | Verfahren zur herstellung von naphtho/2,1-b/fur-2-ylchinoxalinen |
| DD276479A1 (de) | 1988-10-26 | 1990-02-28 | Fahlberg List Veb | Verfahren zur herstellung von benzo/b/fur-2-ylchinoxalinen |
| US5236917A (en) | 1989-05-04 | 1993-08-17 | Sterling Winthrop Inc. | Saccharin derivatives useful as proteolytic enzyme inhibitors and compositions and method of use thereof |
| IT1230859B (it) | 1989-06-05 | 1991-11-08 | Corvi Camillo Spa | 2 alchinilfenoli sostituiti ad azione anti infiammatoria, procedimento per la loro preparazione e composizioni farmaceutiche che li contengono. |
| EP0453210A3 (en) | 1990-04-19 | 1993-01-13 | Imperial Chemical Industries Plc | Pyridine derivatives |
| AU641769B2 (en) | 1990-06-18 | 1993-09-30 | Merck & Co., Inc. | Inhibitors of HIV reverse transcriptase |
| CN1034934C (zh) | 1990-06-19 | 1997-05-21 | 明治制果株式会社 | 血管紧张素ii拮抗性吡啶衍生物的制备方法 |
| NL9001752A (nl) | 1990-08-02 | 1992-03-02 | Cedona Pharm Bv | Nieuwe 1,4-dihydropyridinederivaten. |
| IL99731A0 (en) | 1990-10-18 | 1992-08-18 | Merck & Co Inc | Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them |
| JPH05301872A (ja) | 1992-04-23 | 1993-11-16 | Kumiai Chem Ind Co Ltd | ピコリン酸誘導体及び除草剤 |
| US5403816A (en) | 1990-10-25 | 1995-04-04 | Kumiai Chemical Industry Co., Ltd. | Picolinic acid derivative and herbicidal composition |
| AU1183992A (en) | 1991-02-08 | 1992-09-07 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Complexing agents |
| JPH0641118A (ja) | 1991-05-31 | 1994-02-15 | Kumiai Chem Ind Co Ltd | ピコリン酸誘導体及び除草剤 |
| US5185251A (en) | 1991-06-07 | 1993-02-09 | Merck & Co., Inc. | Microbial transformation of a substituted pyridinone using actinoplanacete sp. MA 6559 |
| JP2600644B2 (ja) | 1991-08-16 | 1997-04-16 | 藤沢薬品工業株式会社 | チアゾリルベンゾフラン誘導体 |
| FR2680512B1 (fr) | 1991-08-20 | 1995-01-20 | Adir | Nouveaux derives de 2,4-thiazolidinedione, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
| US5202243A (en) | 1991-10-04 | 1993-04-13 | Merck & Co., Inc. | Method of hydroxylating 3-[2-(benzoxazol-2-yl)ethyl]-5-ethyl-6-methyl-2-(1H)-pyridinone by incubation with liver slices |
| GB9203798D0 (en) | 1992-02-21 | 1992-04-08 | Fujisawa Pharmaceutical Co | Quinolylbenzofuran derivatives,processes for preparation thereof and pharmaceutical composition comprising the same |
| WO1994001406A1 (de) | 1992-07-01 | 1994-01-20 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Kontrastmittel für die mr diagnostik |
| US5290941A (en) | 1992-10-14 | 1994-03-01 | Merck & Co., Inc. | Facile condensation of methylbenzoxazoles with aromatic aldehydes |
| HU224548B1 (hu) | 1993-04-07 | 2005-10-28 | Taiho Pharmaceutical Co. Ltd. | Tiazolidinszármazékok és ezeket tartalmazó gyógyszerkészítmények, valamint eljárás előállításukra |
| DE4318550A1 (de) | 1993-06-04 | 1994-12-08 | Boehringer Mannheim Gmbh | Aryliden-4-oxo-2-thioxo-3- thiazolidincarbonsäuren, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel |
| AU672699B2 (en) | 1993-06-30 | 1996-10-10 | Sankyo Company Limited | Amide and urea derivatives having anti-hypercholesteremic activity, their preparation and their therapeutic uses |
| JPH0725882A (ja) | 1993-07-07 | 1995-01-27 | Res Dev Corp Of Japan | アクロメリン酸bおよびeを製造するための中間体と、その製造方法 |
| DE69418789T2 (de) * | 1993-08-05 | 1999-12-02 | Hoechst Marion Roussel, Inc. | 2-(Piperidin-4-yl, Pyridin-4-yl und Tetrahydropyridin-4-yl)-benzofuran-7-carbamat Derivate, ihre Herstellung und Verwendung als Acetylcholinesterase Inhibitoren |
| EP0640609A1 (en) | 1993-08-24 | 1995-03-01 | Ono Pharmaceutical Co., Ltd. | Fused phenol derivatives having inhibitory activity on TXA2 synthetase, and 5-lipoxygenase and scavenging activity on oxygen species |
| US5840900A (en) | 1993-10-20 | 1998-11-24 | Enzon, Inc. | High molecular weight polymer-based prodrugs |
| US5965566A (en) | 1993-10-20 | 1999-10-12 | Enzon, Inc. | High molecular weight polymer-based prodrugs |
| US5880131A (en) | 1993-10-20 | 1999-03-09 | Enzon, Inc. | High molecular weight polymer-based prodrugs |
| US5605976A (en) | 1995-05-15 | 1997-02-25 | Enzon, Inc. | Method of preparing polyalkylene oxide carboxylic acids |
| WO1995014015A1 (en) | 1993-11-19 | 1995-05-26 | Ciba-Geigy Ag | Benzothiophene derivatives possessing a methoxyimino substituent as microbicides |
| EP0658559A1 (de) * | 1993-12-14 | 1995-06-21 | Chemisch Pharmazeutische Forschungsgesellschaft m.b.H. | Thienothiazinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als 5-dipoxygenase und Cyclooxygenaseinhibitoren |
| HUT74385A (en) | 1994-02-14 | 1996-12-30 | Merrell Pharma Inc | Novel mercaptoacetylamido 1,3,4,5-tetrahydro-benzo[c]azepin-3-one disulfide derivatives useful as inhibitors of enkephalinase and ace |
| GB9420557D0 (en) | 1994-10-12 | 1994-11-30 | Zeneca Ltd | Aromatic compounds |
| DE4442050A1 (de) | 1994-11-25 | 1996-05-30 | Hoechst Ag | Heterospiroverbindungen und ihre Verwendung als Elektrolumineszenzmaterialien |
| US5650408A (en) | 1995-06-07 | 1997-07-22 | Karanewsky; Donald S. | Thiazolo benzazepine containing dual action inhibitors |
| TW434240B (en) | 1995-06-20 | 2001-05-16 | Zeneca Ltd | Aromatic compounds, preparation thereof and pharmaceutical composition comprising same |
| JP3895404B2 (ja) | 1996-05-17 | 2007-03-22 | 興和株式会社 | カルコン誘導体及びこれを含有する医薬 |
| WO1997041120A1 (en) | 1996-07-26 | 1997-11-06 | Dr. Reddy's Research Foundation | Thiazolidinedione compounds having antidiabetic, hypolipidaemic, antihypertensive properties, process for their preparation and pharmaceutical compositions thereof |
| US6630496B1 (en) | 1996-08-26 | 2003-10-07 | Genetics Institute Llc | Inhibitors of phospholipase enzymes |
| CA2264020A1 (en) | 1996-08-26 | 1998-03-05 | Jean Bemis | Inhibitors of phospholipase enzymes |
| WO1998009967A1 (fr) | 1996-09-09 | 1998-03-12 | Kyowa Hakko Kogyo Co., Ltd. | Derives de pyrrolocarbazole |
| BR9713027A (pt) | 1996-11-12 | 2000-01-25 | Novartis Ag | Derivados de pirazol úteis como herbicidas |
| US6043389A (en) | 1997-03-11 | 2000-03-28 | Mor Research Applications, Ltd. | Hydroxy and ether-containing oxyalkylene esters and uses thereof |
| US5760232A (en) | 1997-06-16 | 1998-06-02 | Schering Corporation | Synthesis of intermediates useful in preparing bromo-substituted tricyclic compounds |
| US6214817B1 (en) | 1997-06-20 | 2001-04-10 | Monsanto Company | Substituted pyridino pentaazamacrocyle complexes having superoxide dismutase activity |
| US6011042A (en) | 1997-10-10 | 2000-01-04 | Enzon, Inc. | Acyl polymeric derivatives of aromatic hydroxyl-containing compounds |
| US6111107A (en) | 1997-11-20 | 2000-08-29 | Enzon, Inc. | High yield method for stereoselective acylation of tertiary alcohols |
| HUP0301166A2 (en) * | 1997-12-12 | 2003-08-28 | Euro Celtique Sa | 3-substituted adenines via2-thioxanthines |
| KR20010041346A (ko) | 1998-02-25 | 2001-05-15 | 브루스 엠. 에이센, 토마스 제이 데스로저 | 포스포리파제 a2 억제제 |
| JP2002506873A (ja) | 1998-03-18 | 2002-03-05 | アリアド・ファーマシューティカルズ・インコーポレイテッド | 複素環式シグナル伝達阻害剤、それを含む組成物 |
| US6214879B1 (en) * | 1998-03-24 | 2001-04-10 | Virginia Commonwealth University | Allosteric inhibitors of pyruvate kinase |
| US6153655A (en) | 1998-04-17 | 2000-11-28 | Enzon, Inc. | Terminally-branched polymeric linkers and polymeric conjugates containing the same |
| GB9810860D0 (en) | 1998-05-20 | 1998-07-22 | Hoechst Schering Agrevo Gmbh | Substituted pyridine and pyrimidines, processes for their preparation and their use as pesticides |
| IL139811A0 (en) | 1998-06-04 | 2002-02-10 | Abbott Lab | Cell adhesion-inhibiting antinflammatory compounds |
| US6232320B1 (en) | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| GB9818627D0 (en) * | 1998-08-26 | 1998-10-21 | Glaxo Group Ltd | Improvements in dva vaccination |
| GB9823871D0 (en) * | 1998-10-30 | 1998-12-23 | Pharmacia & Upjohn Spa | 2-Amino-thiazole derivatives, process for their preparation, and their use as antitumour agents |
| US20030060425A1 (en) | 1998-11-24 | 2003-03-27 | Ahlem Clarence N. | Immune modulation method using steroid compounds |
| HRP20010427A2 (en) | 1998-12-14 | 2002-06-30 | Hoffmann La Roche | Phenylglycine derivatives |
| US6544980B2 (en) | 1998-12-31 | 2003-04-08 | Aventis Pharmaceuticals Inc. | N-carboxymethyl substituted benzolactams as inhibitors of matrix metalloproteinase |
| EP1150957A1 (en) | 1998-12-31 | 2001-11-07 | Aventis Pharmaceuticals Inc. | N-carboxymethyl substituted benzolactams as inhibitors of matrix metalloproteinase |
| JP2002541134A (ja) | 1999-03-31 | 2002-12-03 | ビーエーエスエフ アクチェンゲゼルシャフト | 置換アニリン化合物 |
| US6251927B1 (en) | 1999-04-20 | 2001-06-26 | Medinox, Inc. | Methods for treatment of sickle cell anemia |
| WO2000069472A2 (en) | 1999-05-14 | 2000-11-23 | Boehringer Ingelheim Pharmaceuticals, Inc. | Enzyme-activated anti-tumor prodrug compounds |
| US6184228B1 (en) | 1999-05-25 | 2001-02-06 | Anadys Pharmaceuticals, Inc. | Anti-sickling agents: selection methods and effective compounds |
| HK1045306A1 (zh) | 1999-06-03 | 2002-11-22 | Abbott Laboratories | 抑制细胞黏附的抗炎化合物 |
| AUPQ105499A0 (en) | 1999-06-18 | 1999-07-08 | Biota Scientific Management Pty Ltd | Antiviral agents |
| EA005027B1 (ru) | 1999-06-28 | 2004-10-28 | Янссен Фармацевтика Н.В. | Ингибиторы репликации респираторно-синцитиального вируса |
| US6599917B1 (en) | 1999-09-28 | 2003-07-29 | Eisai Co., Ltd. | Quinuclidine compounds and drugs containing the same as the active ingredient |
| AU2622301A (en) | 1999-11-05 | 2001-05-14 | Emisphere Technologies, Inc. | Phenyl amine carboxylic acid compounds and compositions for delivering active agents |
| AUPQ407699A0 (en) | 1999-11-16 | 1999-12-09 | Fujisawa Pharmaceutical Co., Ltd. | Aminoalcohol derivatives |
| AU2001230537A1 (en) | 2000-02-01 | 2001-08-14 | Daiichi Pharmaceutical Co., Ltd. | Pyridoxazine derivatives |
| US6506755B2 (en) | 2000-02-03 | 2003-01-14 | Hoffmann-La Roche Inc. | Thiazolidinecarboxyl acids |
| AUPQ585000A0 (en) | 2000-02-28 | 2000-03-16 | Fujisawa Pharmaceutical Co., Ltd. | Aminoalcohol derivatives |
| CN1311198A (zh) | 2000-03-02 | 2001-09-05 | 上海博德基因开发有限公司 | 一种新的多肽——网格蛋白轻链37和编码这种多肽的多核苷酸 |
| WO2001070663A2 (en) | 2000-03-17 | 2001-09-27 | Corixa Corporation | Novel amphipathic aldehydes and their use as adjuvants and immunoeffectors |
| AUPQ841300A0 (en) | 2000-06-27 | 2000-07-20 | Fujisawa Pharmaceutical Co., Ltd. | New aminoalcohol derivatives |
| CA2415890C (en) | 2000-07-14 | 2009-04-07 | F. Hoffmann-La Roche Ag | N-oxides as nk1 receptor antagonist prodrugs of 4-phenyl-pyridine derivatives |
| AU2001281071A1 (en) * | 2000-08-01 | 2002-02-13 | Gmp Companies, Inc. | Ammonium salts of hemoglobin allosteric effectors, and uses thereof |
| US6653313B2 (en) | 2000-08-10 | 2003-11-25 | Warner-Lambert Company Llc | 1,4-dihydropyridine compounds as bradykinin antagonists |
| JP4272338B2 (ja) | 2000-09-22 | 2009-06-03 | バイエル アクチェンゲゼルシャフト | ピリジン誘導体 |
| AUPR034000A0 (en) | 2000-09-25 | 2000-10-19 | Fujisawa Pharmaceutical Co., Ltd. | Aminoalcohol derivatives |
| IL155702A0 (en) * | 2000-11-20 | 2003-11-23 | Biovitrum Ab | Piperazinylpyrazine compounds as agonist or antagonist of serotonin 5-ht2 receptor |
| WO2002051849A1 (en) | 2000-12-26 | 2002-07-04 | Daiichi Pharmaceutical Co., Ltd. | Cdk4 inhibitors |
| ATE433964T1 (de) | 2000-12-28 | 2009-07-15 | Takeda Pharmaceutical | Alkansäurederivate, verfahren zu deren herstellung und deren verwendung |
| US20030022923A1 (en) | 2001-03-01 | 2003-01-30 | Medinox, Inc. | Methods for treatment of sickle cell anemia |
| US6627646B2 (en) | 2001-07-17 | 2003-09-30 | Sepracor Inc. | Norastemizole polymorphs |
| EP1435894A4 (en) * | 2001-07-23 | 2005-07-06 | Galileo Pharmaceuticals Inc | CYTOPROTECTIVE COMPOUNDS, PHARMACEUTICAL AND COSMETIC FORMULATIONS AND METHOD |
| JP2003075970A (ja) | 2001-08-31 | 2003-03-12 | Konica Corp | ハロゲン化銀カラー写真感光材料、カラー写真感光材料、その画像形成方法及びデジタル画像情報作製方法 |
| KR100467313B1 (ko) | 2001-11-22 | 2005-01-24 | 한국전자통신연구원 | 적색 유기 전기발광 화합물 및 그 제조 방법과 전기발광소자 |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
| MXPA04005864A (es) | 2001-12-19 | 2004-10-29 | Atherogenics Inc | Derivados de charcona y su uso para tratar enfermedades. |
| US20030190333A1 (en) | 2002-02-04 | 2003-10-09 | Corixa Corporation | Immunostimulant compositions comprising aminoalkyl glucosaminide phosphates and saponins |
| EP1542704A1 (en) | 2002-04-18 | 2005-06-22 | Stephen H. Embury | Method and composition for preventing pain in sickle cell patients |
| US6608076B1 (en) | 2002-05-16 | 2003-08-19 | Enzon, Inc. | Camptothecin derivatives and polymeric conjugates thereof |
| GB0212785D0 (en) | 2002-05-31 | 2002-07-10 | Glaxo Group Ltd | Compounds |
| BR0313160A (pt) * | 2002-08-08 | 2005-07-12 | Smithkline Beecham Corp | Composto, composição farmacêutica, métodos para tratar uma condição e um neoplasmo suscetìvel em um animal em um animal, processo para preparar um composto e uso de um composto |
| AU2003257666A1 (en) | 2002-08-23 | 2004-03-11 | Kirin Beer Kabushiki Kaisha | COMPOUND HAVING TGFss INHIBITORY ACTIVITY AND MEDICINAL COMPOSITION CONTAINING THE SAME |
| WO2004024705A1 (ja) | 2002-09-10 | 2004-03-25 | Takeda Pharmaceutical Company Limited | 5員複素環化合物 |
| AU2003296022B2 (en) | 2002-12-04 | 2007-01-25 | Virginia Commonwealth University | Anti-sickling agents |
| AU2003303239A1 (en) | 2002-12-19 | 2004-07-14 | Atherogenics, Inc. | Process of making chalcone derivatives |
| WO2004058790A1 (ja) | 2002-12-25 | 2004-07-15 | Kissei Pharmaceutical Co., Ltd. | 含窒素複素環誘導体、それを含有する医薬組成物およびその医薬用途 |
| WO2004073675A1 (de) | 2003-02-24 | 2004-09-02 | Randolph Riemschneider | Kosmetische zusammensetzung mit whitening-effekt, verfahren zu ihrer herstellung und ihre verwendung |
| US20040186077A1 (en) | 2003-03-17 | 2004-09-23 | Medicure International Inc. | Novel heteroaryl phosphonates as cardioprotective agents |
| ZA200507752B (en) | 2003-03-28 | 2007-01-31 | Threshold Pharmaceuticals Inc | Compositions and methods for treating cancer |
| EP1613613B1 (en) | 2003-04-11 | 2021-06-02 | Genzyme Corporation | Cxcr4 chemokine receptor binding compounds |
| RU2337908C2 (ru) | 2003-06-12 | 2008-11-10 | Ново Нордиск А/С | Пиридинилкарбаматы в качестве ингибиторов гормон-чувствительной липазы |
| WO2005019220A2 (en) * | 2003-08-11 | 2005-03-03 | Cellular Genomics Inc. | Substituted imidazo[1,2-a]pyrazines as modulators of kinase activity |
| US7411083B2 (en) | 2003-09-25 | 2008-08-12 | Wyeth | Substituted acetic acid derivatives |
| BRPI0416283A (pt) | 2003-11-05 | 2007-01-23 | Hoffmann La Roche | compostos, processo para a fabricação de compostos, composição farmacêutica, método para o tratamento e/ou prevenção de doenças que são moduladas por agonistas de ppar(delta) e/ou ppar(alfa) e uso destes compostos |
| AU2004289690A1 (en) * | 2003-11-10 | 2005-05-26 | Schering Aktiengesellschaft | Benzylether amine compounds useful as CCR-5 antagonists |
| EP1694328A4 (en) | 2003-12-02 | 2010-02-17 | Celgene Corp | METHOD AND COMPOSITIONS FOR THE TREATMENT AND SUPPLY OF HEMOGLOBINOPATHY AND ANEMIA |
| US7378439B2 (en) | 2004-01-20 | 2008-05-27 | Usv, Ltd. | Process for the preparation of 4-(2-dipropylaminoethyl)-1,3-dihydro-2H-indol-2-one hydrochloride |
| AU2005211349A1 (en) | 2004-01-30 | 2005-08-18 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | N-benzyl-3,4-dihyroxypyridine-2-carboxamide and N-benzyl-2,3-dihydroxypyridine-4-carboxamide compounds useful as HIV integrase inhibitors |
| GB0403038D0 (en) | 2004-02-11 | 2004-03-17 | Novartis Ag | Organic compounds |
| WO2005087766A1 (en) | 2004-03-09 | 2005-09-22 | Istituto Di Ricerche Di Biologia Molecolare P Angeletti Spa | Hiv integrase inhibitors |
| WO2005086951A2 (en) | 2004-03-10 | 2005-09-22 | Threshold Pharmaceuticals, Inc. | Hypoxia-activated anti-cancer agents |
| DE102004015226B3 (de) | 2004-03-24 | 2005-08-25 | Siemens Ag | Verfahren zum Plasmareinigen eines Werkstücks und zu dessen Durchführung geeignete Vorrichtung |
| JP2007534691A (ja) | 2004-04-22 | 2007-11-29 | アロス・セラピューティクス・インコーポレーテッド | アロステリックヘモグロビン修飾体の組成物および前記組成物の製造法 |
| TW200606133A (en) * | 2004-06-30 | 2006-02-16 | Sankyo Co | Substituted benzene compounds |
| TW200606129A (en) | 2004-07-26 | 2006-02-16 | Chugai Pharmaceutical Co Ltd | Novel cyclohexane derivative, its prodrug, its salt and diabetic therapeutic agent containing the same |
| GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| CA2585165A1 (en) | 2004-10-28 | 2006-05-18 | Medicure International Inc. | Dual antiplatelet/anticoagulant pyridoxine analogs |
| EP1831170A4 (en) | 2004-12-14 | 2009-10-14 | Astrazeneca Ab | SUBSTITUTED AMINOPYRIDINES AND THEIR USE |
| ATE516026T1 (de) | 2005-02-21 | 2011-07-15 | Shionogi & Co | Bicyclisches carbamoylpyridonderivat mit hiv- integrase-hemmender wirkung |
| EP1861357B1 (en) | 2005-03-19 | 2013-04-24 | Amorepacific Corporation | Novel compounds or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and pharmaceutical compositions containing the same |
| WO2006106711A1 (ja) | 2005-03-30 | 2006-10-12 | Eisai R & D Management Co., Ltd. | ピリジン誘導体を含有する抗真菌剤 |
| GB0506677D0 (en) | 2005-04-01 | 2005-05-11 | Btg Int Ltd | Iron modulators |
| DK1874117T3 (da) | 2005-04-28 | 2013-09-23 | Viiv Healthcare Co | Polycyklisk carbamoylpyridonderivat med hiv-integrasehæmmende aktivitet |
| DE102005025989A1 (de) | 2005-06-07 | 2007-01-11 | Bayer Cropscience Ag | Carboxamide |
| JP2006342115A (ja) | 2005-06-10 | 2006-12-21 | Shionogi & Co Ltd | Hivインテグラーゼ阻害活性を有する多環性化合物 |
| EP2308840A1 (en) | 2005-06-30 | 2011-04-13 | Prosidion Limited | GPCR agonists |
| CN100562514C (zh) | 2005-07-22 | 2009-11-25 | 中国科学院上海药物研究所 | 一类取代丙酰胺衍生物、其制备方法和用途 |
| GB0516270D0 (en) | 2005-08-08 | 2005-09-14 | Glaxo Group Ltd | Novel compounds |
| SI1945622T1 (sl) | 2005-10-11 | 2012-05-31 | Univ Pittsburgh | Izotopično markirane spojine benzfurana kot označevalne snovi za amiloidogenske proteine |
| JP5131689B2 (ja) | 2005-10-27 | 2013-01-30 | 塩野義製薬株式会社 | Hivインテグラーゼ阻害活性を有する多環性カルバモイルピリドン誘導体 |
| WO2007061923A2 (en) * | 2005-11-18 | 2007-05-31 | Takeda San Diego, Inc. | Glucokinase activators |
| WO2007084914A2 (en) | 2006-01-17 | 2007-07-26 | Neurocrine Biosciences, Inc. | Phenoxy-substituted pyrimidines as adenosine receptor antagonists |
| WO2007095495A2 (en) * | 2006-02-13 | 2007-08-23 | Pharmacopeia, Inc. | Benzodiazepine gcnf modulators for stem cell modulation |
| RU2318818C1 (ru) | 2006-04-12 | 2008-03-10 | Общество С Ограниченной Ответственностью "Исследовательский Институт Химического Разнообразия" | Азагетероциклы, комбинаторная библиотека, фокусированная библиотека, фармацевтическая композиция и способ получения (варианты) |
| GB0614586D0 (en) | 2006-07-22 | 2006-08-30 | Pliva Istrazivacki Inst D O O | Pharmaceutical Formulation |
| CN101113148A (zh) | 2006-07-26 | 2008-01-30 | 中国海洋大学 | 二氧哌嗪类化合物及其制备方法和用途 |
| CA2658925C (en) | 2006-07-27 | 2015-07-14 | Amorepacific Corporation | Novel sulfonylamino acrylamide derivatives, isomer thereof,or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist; and pharmaceutical compositions containing the same |
| TW200817424A (en) | 2006-08-04 | 2008-04-16 | Daiichi Sankyo Co Ltd | Benzylphenyl glucopyranoside derivatives |
| TWI389895B (zh) | 2006-08-21 | 2013-03-21 | Infinity Discovery Inc | 抑制bcl蛋白質與結合夥伴間之交互作用的化合物及方法 |
| CA2661649C (en) | 2006-09-03 | 2014-12-30 | Techfields Biochem Co. Ltd | Positively charged water-soluble prodrugs of acetaminophen and related compounds with very fast skin penetration rate |
| JP2010505811A (ja) | 2006-10-04 | 2010-02-25 | ファイザー・プロダクツ・インク | カルシウム受容体アンタゴニストとしてのピリド[4,3−d]ピリミジン−4(3H)−オン誘導体 |
| MX2009004385A (es) | 2006-10-23 | 2009-05-22 | Merck & Co Inc | Derivados de 2-[1-fenil-5-hidroxi-4alfa-metil-hexahidrociclopenta [f]indazol-5-il]etil fenilo como ligandos del receptor glucocorticoide. |
| EP2123637A4 (en) * | 2006-11-30 | 2011-12-21 | Tokyo Inst Tech | NEW CURCUMIN DERIVATIVES |
| TW200835687A (en) | 2006-11-30 | 2008-09-01 | R Tech Ueno Ltd | Thiazole derivatives and their use as VAP-1 inhibitor |
| FR2909379B1 (fr) | 2006-11-30 | 2009-01-16 | Servier Lab | Nouveaux derives heterocycliques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
| WO2008101682A2 (en) | 2007-02-22 | 2008-08-28 | Syngenta Participations Ag | Iminipyridine derivatives and their uses as microbiocides |
| TWI407960B (zh) | 2007-03-23 | 2013-09-11 | Jerini Ag | 小分子緩激肽b2受體調節劑 |
| CN101679172B (zh) | 2007-05-22 | 2013-05-29 | 住友化学株式会社 | 苯甲醛化合物的制造方法 |
| WO2009001214A2 (en) | 2007-06-28 | 2008-12-31 | Pfizer Products Inc. | Thieno[2,3-d]pyrimidin-4(3h)-one, isoxazolo[5,4-d]pyrimidin-4(5h)-one and isothiazolo[5,4-d]pyrimidin-4(5h)-one derivatives as calcium receptor antagonists |
| WO2009011850A2 (en) | 2007-07-16 | 2009-01-22 | Abbott Laboratories | Novel therapeutic compounds |
| KR101158191B1 (ko) | 2007-07-17 | 2012-06-19 | 에프. 호프만-라 로슈 아게 | 11b-하이드록시스테로이드 탈수소효소의 억제제 |
| ATE522249T1 (de) | 2007-07-26 | 2011-09-15 | Novartis Ag | Organische verbindungen |
| TW200918521A (en) | 2007-08-31 | 2009-05-01 | Astrazeneca Ab | Heterocyclic amides and methods of use thereof |
| JP5456681B2 (ja) | 2007-10-17 | 2014-04-02 | ノバルティス アーゲー | ALK阻害剤として有用なイミダゾ[1,2−a]ピリジン誘導体 |
| JP5301557B2 (ja) | 2007-12-04 | 2013-09-25 | エフ.ホフマン−ラ ロシュ アーゲー | イソオキサゾロ−ピリジン誘導体 |
| US7776875B2 (en) | 2007-12-19 | 2010-08-17 | Hoffman-La Roche Inc. | Spiroindolinone derivatives |
| JP2009203230A (ja) | 2008-01-31 | 2009-09-10 | Daiichi Sankyo Co Ltd | ベンジルフェニルグルコピラノシド誘導体を含有する医薬組成物 |
| BRPI0906348A2 (pt) | 2008-04-11 | 2019-07-16 | Inst Of Medicinal Molecular Designer Inc | composto representado pela fórmula (1), composição farmacêutica; inibidor pai-1 e medicamento para prevenção para prevenção e/ou tratamento terapêutico de doença causada pela manifestação de pai-1 ou pelo aumento da ação de pai-1 |
| US8633245B2 (en) | 2008-04-11 | 2014-01-21 | Institute Of Medicinal Molecular Design, Inc. | PAI-1 inhibitor |
| JP2011136906A (ja) | 2008-04-18 | 2011-07-14 | Otsuka Pharmaceut Co Ltd | 複素環化合物 |
| US8119647B2 (en) | 2008-04-23 | 2012-02-21 | Glenmark Pharmaceuticals S.A. | Fused pyrimidineone compounds as TRPV3 modulators |
| CA2723233C (en) | 2008-05-08 | 2017-06-13 | Nova Southeastern University | Specific inhibitors for vascular endothelial growth factor receptors |
| WO2009146555A1 (en) | 2008-06-04 | 2009-12-10 | Ambrilia Biopharma Inc. | Hiv integrase inhibitors from pyridoxine |
| DE102008027574A1 (de) | 2008-06-10 | 2009-12-17 | Merck Patent Gmbh | Neue Pyrrolidinderivate als MetAP-2 Inhibitoren |
| JP5314330B2 (ja) | 2008-06-16 | 2013-10-16 | 住友化学株式会社 | 2−(アリールオキシメチル)ベンズアルデヒドの製造方法およびその中間体 |
| GB0811451D0 (en) | 2008-06-20 | 2008-07-30 | Syngenta Participations Ag | Novel microbiocides |
| JP5494482B2 (ja) * | 2008-07-03 | 2014-05-14 | アステラス製薬株式会社 | トリアゾール誘導体またはその塩 |
| AR073304A1 (es) | 2008-09-22 | 2010-10-28 | Jerini Ag | Moduladores del receptor de bradiquinina b2 de molecula pequena |
| JP2012508692A (ja) | 2008-11-12 | 2012-04-12 | シェーリング コーポレイション | 脂肪酸結合タンパク質(fabp)の阻害薬 |
| TW201033201A (en) | 2009-02-19 | 2010-09-16 | Hoffmann La Roche | Isoxazole-isoxazole and isoxazole-isothiazole derivatives |
| HUE049450T2 (hu) | 2009-03-31 | 2020-09-28 | Ligand Pharm Inc | Endotelin és angiotenzin II receptor antagonista bifenilszulfonamid glomeruloszklerózis és IgA által kiváltott nefropátia kezelésére |
| ES2440000T3 (es) | 2009-05-08 | 2014-01-27 | Tetraphase Pharmaceuticals, Inc. | Compuestos de 8-aza-tetraciclina |
| EP2471789B9 (en) | 2009-08-26 | 2015-03-25 | Takeda Pharmaceutical Company Limited | Fused heterocyclic ring derivative and use thereof |
| EP2474540A4 (en) | 2009-08-31 | 2013-03-13 | Nippon Chemiphar Co | GPR119 AGONIST |
| BR112012005616A2 (pt) | 2009-09-21 | 2016-06-21 | Hoffmann La Roche | compostos antivirais heterocíclicos |
| NZ599763A (en) | 2009-11-09 | 2014-06-27 | Wyeth Llc | Tablet formulations of neratinib maleate |
| TW201139406A (en) | 2010-01-14 | 2011-11-16 | Glaxo Group Ltd | Voltage-gated sodium channel blockers |
| KR101698153B1 (ko) | 2010-04-26 | 2017-01-23 | 광주과학기술원 | P2x1 및 p2x3 수용체 길항제로 사용되는 신규한 피리딘 카르복실산계 화합물, 이의 제조방법 및 이를 포함하는 조성물 |
| CN102232949A (zh) | 2010-04-27 | 2011-11-09 | 孙远 | 提高药物溶出度的组合物及其制备方法 |
| TWI535442B (zh) | 2010-05-10 | 2016-06-01 | Kyowa Hakko Kirin Co Ltd | A nitrogen-containing heterocyclic compound having an action of inhibiting the production of canine erythritine |
| US20120122928A1 (en) | 2010-08-11 | 2012-05-17 | Bayer Cropscience Ag | Heteroarylpiperidine and -Piperazine Derivatives as Fungicides |
| CN102116772B (zh) | 2010-09-28 | 2013-08-28 | 上海大学 | 二氢查尔酮化合物的筛选方法 |
| JP2014501224A (ja) | 2010-12-27 | 2014-01-20 | 武田薬品工業株式会社 | 口腔内崩壊錠 |
| BR112013025680A2 (pt) | 2011-04-06 | 2017-01-03 | Teva Pharma | Novos intermediários e processos para preparar ticagrelor |
| CN103717588B (zh) | 2011-04-11 | 2016-08-03 | 绿色科技株式会社 | 吡唑衍生物 |
| CN102952062B (zh) | 2011-08-12 | 2016-06-08 | 中国医学科学院医药生物技术研究所 | 取代苯并杂环类化合物及其制备方法和应用 |
| PE20142353A1 (es) | 2011-09-15 | 2015-01-10 | Demerx Inc | Ansolvatos de sal de noribogaina |
| US20140308260A1 (en) | 2011-10-07 | 2014-10-16 | Radiorx, Inc. | Methods and compositions comprising a nitrite-reductase promoter for treatment of medical disorders and preservation of blood products |
| CA3142817A1 (en) * | 2011-12-28 | 2013-07-04 | Global Blood Therapeutics, Inc. | Substituted benzaldehyde compounds and methods for their use in increasing tissue oxygenation |
| ES2790358T3 (es) | 2011-12-28 | 2020-10-27 | Global Blood Therapeutics Inc | Compuestos de heteroaril aldehído sustituido y métodos para su uso en el aumento de la oxigenación tisular |
| BR112015015216B1 (pt) | 2012-12-27 | 2020-01-07 | Sumitomo Chemical Company, Limited | Composto de tetrazolinona, agente e método de controle de peste |
| US20150057251A1 (en) | 2013-08-26 | 2015-02-26 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US9458139B2 (en) | 2013-03-15 | 2016-10-04 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US20140271591A1 (en) | 2013-03-15 | 2014-09-18 | Global Blood Therapeutics, Inc. | Compositions and methods for the modulation of hemoglobin (s) |
| US20140274961A1 (en) | 2013-03-15 | 2014-09-18 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| CA2902709A1 (en) | 2013-03-15 | 2014-09-25 | Global Blood Therapeutics, Inc. | Compositions and methods for the modulation of hemoglobin (s) |
| US9802900B2 (en) | 2013-03-15 | 2017-10-31 | Global Blood Therapeutics, Inc. | Bicyclic heteroaryl compounds and uses thereof for the modulation of hemoglobin |
| ES2710380T3 (es) | 2013-03-15 | 2019-04-24 | Global Blood Therapeutics Inc | Compuestos y usos de los mismos para la modulación de hemoglobina |
| EP3919056B1 (en) | 2013-03-15 | 2024-08-28 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| EP2968299B1 (en) | 2013-03-15 | 2021-01-20 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US10100043B2 (en) | 2013-03-15 | 2018-10-16 | Global Blood Therapeutics, Inc. | Substituted aldehyde compounds and methods for their use in increasing tissue oxygenation |
| CN112500338A (zh) | 2013-03-15 | 2021-03-16 | 全球血液疗法股份有限公司 | 化合物及其用于调节血红蛋白的用途 |
| US8952171B2 (en) | 2013-03-15 | 2015-02-10 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US10266551B2 (en) | 2013-03-15 | 2019-04-23 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| EA201591427A1 (ru) | 2013-03-15 | 2016-01-29 | Глобал Блад Терапьютикс, Инк. | Соединения и их применения для модуляции гемоглобина |
| US9604999B2 (en) | 2013-03-15 | 2017-03-28 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US9422279B2 (en) | 2013-03-15 | 2016-08-23 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US20160206604A1 (en) | 2013-08-26 | 2016-07-21 | Global Blood Therapeutics, Inc. | Formulations comprising wetting agents and compounds for the modulation of hemoglobin (s) |
| WO2015031285A1 (en) | 2013-08-27 | 2015-03-05 | Global Blood Therapeutics, Inc. | Crystalline 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde ansolvate salts |
| US20160207904A1 (en) | 2013-08-27 | 2016-07-21 | Global Blood Therapeutics, Inc. | Crystalline 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde ansolvate salts |
| EA202092627A1 (ru) | 2013-11-18 | 2021-09-30 | Глобал Блад Терапьютикс, Инк. | Соединения и их применения для модуляции гемоглобина |
| US20150141465A1 (en) | 2013-11-18 | 2015-05-21 | Global Blood Therapeutics, Inc. | Compounds and uses thereof for the modulation of hemoglobin |
| US9248199B2 (en) | 2014-01-29 | 2016-02-02 | Global Blood Therapeutics, Inc. | 1:1 adducts of sickle hemoglobin |
| SG10201911662YA (en) | 2014-02-07 | 2020-02-27 | Global Blood Therapeutics Inc | Crystalline polymorphs of the free base of 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde |
| MA41841A (fr) | 2015-03-30 | 2018-02-06 | Global Blood Therapeutics Inc | Composés aldéhyde pour le traitement de la fibrose pulmonaire, de l'hypoxie, et de maladies auto-immunes et des tissus conjonctifs |
| HUE072191T2 (hu) | 2015-12-04 | 2025-10-28 | Global Blood Therapeutics Inc | A 2-hidoxi-6-((2-(1-izopropil-1H-pirazol-5-il)piridin-3-il)metoxi)benzaldehid adagolási rendje |
| TWI825524B (zh) | 2016-05-12 | 2023-12-11 | 美商全球血液治療公司 | 用於合成2-羥基-6-((2-(1-異丙基-1h-吡唑-5-基)-吡啶-3-基)甲氧基)苯甲醛之方法 |
| TWI778983B (zh) | 2016-10-12 | 2022-10-01 | 美商全球血液治療公司 | 包含2-羥基-6-((2-(1-異丙基-1h-吡唑-5-基)吡啶-3-基)甲氧基)-苯甲醛之片劑 |
-
2012
- 2012-12-28 CA CA3142817A patent/CA3142817A1/en active Pending
- 2012-12-28 MX MX2018009537A patent/MX372804B/es unknown
- 2012-12-28 IL IL292366A patent/IL292366A/en unknown
- 2012-12-28 WO PCT/US2012/072177 patent/WO2013102142A1/en not_active Ceased
- 2012-12-28 LT LTEP12862525.8T patent/LT2797416T/lt unknown
- 2012-12-28 LT LTEP16194019.2T patent/LT3141542T/lt unknown
- 2012-12-28 SG SG11201403645VA patent/SG11201403645VA/en unknown
- 2012-12-28 SI SI201231797T patent/SI3141542T1/sl unknown
- 2012-12-28 RS RS20170968A patent/RS56388B1/sr unknown
- 2012-12-28 JP JP2014550525A patent/JP6242810B2/ja active Active
- 2012-12-28 PL PL12862525T patent/PL2797416T3/pl unknown
- 2012-12-28 EP EP20167746.5A patent/EP3738434B1/en active Active
- 2012-12-28 SI SI201232045T patent/SI3738434T1/sl unknown
- 2012-12-28 ES ES16194019T patent/ES2811129T3/es active Active
- 2012-12-28 RS RS20201021A patent/RS60740B1/sr unknown
- 2012-12-28 EP EP16194019.2A patent/EP3141542B1/en active Active
- 2012-12-28 MX MX2014007971A patent/MX358992B/es active IP Right Grant
- 2012-12-28 DK DK20167746.5T patent/DK3738434T3/da active
- 2012-12-28 EP EP12862525.8A patent/EP2797416B1/en active Active
- 2012-12-28 CN CN201710403045.7A patent/CN107176953B/zh active Active
- 2012-12-28 DK DK16194019.2T patent/DK3141542T3/da active
- 2012-12-28 BR BR112014016165-8A patent/BR112014016165B1/pt active IP Right Grant
- 2012-12-28 EP EP23190105.9A patent/EP4289813A3/en not_active Withdrawn
- 2012-12-28 SM SM20170483T patent/SMT201700483T1/it unknown
- 2012-12-28 AP AP2014007805A patent/AP2014007805A0/xx unknown
- 2012-12-28 PT PT161940192T patent/PT3141542T/pt unknown
- 2012-12-28 AU AU2012362236A patent/AU2012362236B2/en active Active
- 2012-12-28 PE PE2022001477A patent/PE20221914A1/es unknown
- 2012-12-28 HU HUE20167746A patent/HUE064226T2/hu unknown
- 2012-12-28 HU HUE12862525A patent/HUE035069T2/en unknown
- 2012-12-28 HU HUE16194019A patent/HUE050189T2/hu unknown
- 2012-12-28 ES ES12862525.8T patent/ES2643403T3/es active Active
- 2012-12-28 SG SG10201912411RA patent/SG10201912411RA/en unknown
- 2012-12-28 FI FIEP20167746.5T patent/FI3738434T3/fi active
- 2012-12-28 PE PE2018001322A patent/PE20181519A1/es unknown
- 2012-12-28 PT PT128625258T patent/PT2797416T/pt unknown
- 2012-12-28 SG SG10201702513SA patent/SG10201702513SA/en unknown
- 2012-12-28 CA CA2860323A patent/CA2860323C/en active Active
- 2012-12-28 SM SM20200370T patent/SMT202000370T1/it unknown
- 2012-12-28 HR HRP20171665TT patent/HRP20171665T1/hr unknown
- 2012-12-28 SI SI201231103T patent/SI2797416T1/sl unknown
- 2012-12-28 US US13/730,674 patent/US9018210B2/en active Active
- 2012-12-28 SG SG10201912409XA patent/SG10201912409XA/en unknown
- 2012-12-28 PL PL20167746.5T patent/PL3738434T3/pl unknown
- 2012-12-28 ES ES20167746T patent/ES2963218T3/es active Active
- 2012-12-28 DK DK12862525.8T patent/DK2797416T3/en active
- 2012-12-28 CN CN201280070743.5A patent/CN104135859B/zh active Active
- 2012-12-28 PL PL16194019T patent/PL3141542T3/pl unknown
- 2012-12-28 PT PT201677465T patent/PT3738434T/pt unknown
- 2012-12-28 PE PE2014001050A patent/PE20142454A1/es active IP Right Grant
-
2014
- 2014-06-23 IL IL233329A patent/IL233329A0/en active IP Right Grant
- 2014-06-27 GT GT201400136A patent/GT201400136A/es unknown
- 2014-06-27 MX MX2020005645A patent/MX2020005645A/es unknown
- 2014-06-27 NI NI201400070A patent/NI201400070A/es unknown
- 2014-06-27 MX MX2022008867A patent/MX2022008867A/es unknown
- 2014-06-30 CL CL2014001762A patent/CL2014001762A1/es unknown
- 2014-07-28 CO CO14163228A patent/CO7101245A2/es unknown
-
2015
- 2015-03-18 US US14/662,156 patent/US20150344472A1/en not_active Abandoned
-
2016
- 2016-03-16 IL IL24462616A patent/IL244626B/en active IP Right Grant
- 2016-03-25 US US15/081,704 patent/US20160206614A1/en not_active Abandoned
- 2016-06-06 AU AU2016203755A patent/AU2016203755B2/en active Active
-
2017
- 2017-04-10 JP JP2017077318A patent/JP6424399B2/ja active Active
- 2017-09-22 AU AU2017232206A patent/AU2017232206C1/en active Active
- 2017-10-18 CY CY20171101090T patent/CY1119575T1/el unknown
- 2017-12-22 US US15/852,406 patent/US10034879B2/en active Active
-
2018
- 2018-06-25 US US16/017,248 patent/US10806733B2/en active Active
- 2018-10-04 JP JP2018189280A patent/JP6585261B2/ja active Active
-
2019
- 2019-09-04 JP JP2019161066A patent/JP6848026B2/ja active Active
- 2019-10-15 IL IL269977A patent/IL269977B/en unknown
- 2019-12-04 AU AU2019275607A patent/AU2019275607B2/en active Active
-
2020
- 2020-07-01 HR HRP20201045TT patent/HRP20201045T1/hr unknown
- 2020-08-18 CY CY20201100773T patent/CY1123270T1/el unknown
-
2021
- 2021-03-03 JP JP2021033123A patent/JP2021104996A/ja active Pending
- 2021-05-28 US US17/334,213 patent/US20210290619A1/en not_active Abandoned
- 2021-09-17 AU AU2021232806A patent/AU2021232806B2/en active Active
-
2022
- 2022-01-07 US US17/571,183 patent/US20220125786A1/en not_active Abandoned
- 2022-07-20 NO NO2022031C patent/NO2022031I1/no unknown
- 2022-08-01 LU LU00276C patent/LUC00276I2/en unknown
- 2022-08-02 HU HUS2200037C patent/HUS2200037I1/hu unknown
- 2022-08-03 NL NL301191C patent/NL301191I2/nl unknown
- 2022-08-03 FR FR22C1042C patent/FR22C1042I2/fr active Active
- 2022-08-10 CY CY2022025C patent/CY2022025I2/el unknown
- 2022-08-11 LT LTPA2022517C patent/LTPA2022517I1/lt unknown
- 2022-09-27 JP JP2022154128A patent/JP2022191281A/ja active Pending
-
2023
- 2023-04-20 US US18/137,210 patent/US20230255963A1/en not_active Abandoned
-
2024
- 2024-01-24 JP JP2024008428A patent/JP2024050663A/ja active Pending
- 2024-01-29 AU AU2024200515A patent/AU2024200515A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2015504061A5 (enExample) | ||
| AU2012362236B2 (en) | Substituted benzaldehyde compounds and methods for their use in increasing tissue oxygenation | |
| ES2451659T3 (es) | Derivados de 2-[(2-sustituido)-indolizin-3-il]-2-oxo-acetamida como agentes antifúngicos | |
| JP2018507214A5 (enExample) | ||
| JP2006523193A5 (enExample) | ||
| JP2013529196A5 (enExample) | ||
| JP2013510124A5 (enExample) | ||
| JP2013531684A5 (enExample) | ||
| ES2838004T3 (es) | Inhibidores de cinasa relacionada con tropomiosina (TRK) | |
| TWI455939B (zh) | cMET抑制劑 | |
| JP2016525075A5 (enExample) | ||
| JP2019503337A5 (enExample) | ||
| JP2016520116A5 (enExample) | ||
| JP2013540119A5 (enExample) | ||
| JP2009529047A5 (enExample) | ||
| HRP20161178T1 (hr) | N1-PIRAZOLOSPIROKETONSKI INHIBITORI ACETIL-CoA-KARBOKSILAZE | |
| JP2013507425A5 (enExample) | ||
| JP2019536768A5 (enExample) | ||
| JP2014521725A5 (enExample) | ||
| CA2725445A1 (en) | Antifungal combination therapy | |
| JP2016520618A5 (enExample) | ||
| JP2013512953A5 (enExample) | ||
| JP2007523151A5 (enExample) | ||
| JP2017510576A5 (enExample) | ||
| JP2011527684A5 (enExample) |