ES2624664T3 - Derivados de fenilpirazol como potentes inhibidores de ROCK1 y ROCK2 - Google Patents
Derivados de fenilpirazol como potentes inhibidores de ROCK1 y ROCK2 Download PDFInfo
- Publication number
- ES2624664T3 ES2624664T3 ES14710732.0T ES14710732T ES2624664T3 ES 2624664 T3 ES2624664 T3 ES 2624664T3 ES 14710732 T ES14710732 T ES 14710732T ES 2624664 T3 ES2624664 T3 ES 2624664T3
- Authority
- ES
- Spain
- Prior art keywords
- pyrazol
- benzamide
- substituted
- methoxy
- chrd
- 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.)
- Active
Links
- 239000003112 inhibitor Substances 0.000 title description 14
- 150000008048 phenylpyrazoles Chemical class 0.000 title description 4
- 101000669917 Homo sapiens Rho-associated protein kinase 1 Proteins 0.000 title description 3
- 101000669921 Homo sapiens Rho-associated protein kinase 2 Proteins 0.000 title description 3
- 102100039313 Rho-associated protein kinase 1 Human genes 0.000 title description 3
- 102100039314 Rho-associated protein kinase 2 Human genes 0.000 title description 3
- 230000003389 potentiating effect Effects 0.000 title description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 179
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 130
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 122
- 150000001875 compounds Chemical class 0.000 claims abstract description 113
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 113
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 108
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 94
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 84
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 69
- 101150105130 RORB gene Proteins 0.000 claims abstract description 67
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 59
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 59
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 57
- 150000003839 salts Chemical class 0.000 claims abstract description 54
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 46
- 125000003118 aryl group Chemical group 0.000 claims abstract description 42
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 40
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 39
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 39
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 34
- 229910052702 rhenium Inorganic materials 0.000 claims abstract description 34
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 30
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract description 28
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims abstract description 22
- 229910003204 NH2 Inorganic materials 0.000 claims abstract description 19
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 19
- 229910052701 rubidium Inorganic materials 0.000 claims abstract description 18
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 18
- 239000001257 hydrogen Substances 0.000 claims abstract description 15
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 15
- 125000006706 (C3-C6) carbocyclyl group Chemical group 0.000 claims abstract description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 13
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 13
- 125000002837 carbocyclic group Chemical group 0.000 claims abstract description 8
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims abstract 6
- -1 2-hydroxy-1-phenylethyl Chemical group 0.000 claims description 159
- 238000011282 treatment Methods 0.000 claims description 21
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- 125000003342 alkenyl group Chemical group 0.000 claims description 14
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 12
- 125000000304 alkynyl group Chemical group 0.000 claims description 12
- 201000010099 disease Diseases 0.000 claims description 12
- 206010020772 Hypertension Diseases 0.000 claims description 11
- 230000000694 effects Effects 0.000 claims description 11
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 10
- 108010041788 rho-Associated Kinases Proteins 0.000 claims description 9
- 102000000568 rho-Associated Kinases Human genes 0.000 claims description 9
- 208000006011 Stroke Diseases 0.000 claims description 8
- 238000011321 prophylaxis Methods 0.000 claims description 8
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 7
- 208000035475 disorder Diseases 0.000 claims description 7
- 208000010228 Erectile Dysfunction Diseases 0.000 claims description 6
- 201000001881 impotence Diseases 0.000 claims description 6
- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- 210000002460 smooth muscle Anatomy 0.000 claims description 6
- 206010019280 Heart failures Diseases 0.000 claims description 5
- 230000001594 aberrant effect Effects 0.000 claims description 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
- 206010002383 Angina Pectoris Diseases 0.000 claims description 4
- 201000001320 Atherosclerosis Diseases 0.000 claims description 4
- 208000010412 Glaucoma Diseases 0.000 claims description 4
- 208000006673 asthma Diseases 0.000 claims description 4
- 125000004452 carbocyclyl group Chemical group 0.000 claims description 4
- 230000003176 fibrotic effect Effects 0.000 claims description 4
- 208000002815 pulmonary hypertension Diseases 0.000 claims description 4
- 238000002560 therapeutic procedure Methods 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 3
- 201000006417 multiple sclerosis Diseases 0.000 claims description 3
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 206010061216 Infarction Diseases 0.000 claims description 2
- 206010047163 Vasospasm Diseases 0.000 claims description 2
- 229910001850 copernicium Inorganic materials 0.000 claims description 2
- 208000029078 coronary artery disease Diseases 0.000 claims description 2
- 230000007574 infarction Effects 0.000 claims description 2
- 208000027866 inflammatory disease Diseases 0.000 claims description 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 9
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 claims 8
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 6
- WQKAWEFODUZYFB-UHFFFAOYSA-N N-[(2-chloro-6-fluorophenyl)methyl]-3-(1-hydroxyethyl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C(=CC=C1)F)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)C(C)O)=O WQKAWEFODUZYFB-UHFFFAOYSA-N 0.000 claims 6
- UARARIOSCGMOEN-UHFFFAOYSA-N N-[1-(2-fluorophenyl)-2-hydroxy-2-methylpropyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=CC=C1)C(C(C)(C)O)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O UARARIOSCGMOEN-UHFFFAOYSA-N 0.000 claims 6
- UHTJASDMENLSNM-UHFFFAOYSA-N N-[1-(2-fluorophenyl)-2-hydroxy-2-methylpropyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=CC=C1)C(C(C)(C)O)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O UHTJASDMENLSNM-UHFFFAOYSA-N 0.000 claims 6
- YSVQULSJUHTXBG-UHFFFAOYSA-N N-[1-(2-fluorophenyl)-2-hydroxyethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=CC=C1)C(CO)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O YSVQULSJUHTXBG-UHFFFAOYSA-N 0.000 claims 6
- WHGWETKOANDIKB-UHFFFAOYSA-N N-[1-(2-fluorophenyl)ethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=CC=C1)C(C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O WHGWETKOANDIKB-UHFFFAOYSA-N 0.000 claims 6
- ZFDYBUAPZQQBIX-UHFFFAOYSA-N N-[3-(dimethylamino)-1-phenylpropyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound CN(CCC(C1=CC=CC=C1)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C ZFDYBUAPZQQBIX-UHFFFAOYSA-N 0.000 claims 6
- PWWJBQFUGNBNDJ-KWCCSABGSA-N 3-(1-hydroxyethyl)-n-[(1r)-1-phenylethyl]-4-(1h-pyrazol-4-yl)benzamide Chemical compound CC(O)C1=CC(C(=O)N[C@H](C)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 PWWJBQFUGNBNDJ-KWCCSABGSA-N 0.000 claims 4
- SAUMCUQQDUAVFI-QMRFKDRMSA-N 3-(1-hydroxypropyl)-N-[(1R)-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC(CC)C=1C=C(C(=O)N[C@H](C)C2=CC=CC=C2)C=CC=1C=1C=NNC=1 SAUMCUQQDUAVFI-QMRFKDRMSA-N 0.000 claims 4
- FKYWIAWIDUIWFG-UHFFFAOYSA-N N-(3-hydroxy-1-phenylpropyl)-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound OCCC(C1=CC=CC=C1)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O FKYWIAWIDUIWFG-UHFFFAOYSA-N 0.000 claims 4
- YVTWDJQRSGSDSG-JHJMLUEUSA-N N-[(1R)-1-(2,6-difluorophenyl)ethyl]-3-(1-hydroxyethyl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)[C@@H](C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C(C)O)=O YVTWDJQRSGSDSG-JHJMLUEUSA-N 0.000 claims 4
- VUKPYAYVXNDTIK-MRXNPFEDSA-N N-[(1S)-1-(2,6-difluorophenyl)-2-hydroxyethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)[C@@H](CO)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O VUKPYAYVXNDTIK-MRXNPFEDSA-N 0.000 claims 4
- MVTQJLVXODOUEE-UHFFFAOYSA-N N-[1-(2-fluoro-5-methoxyphenyl)ethyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=C(C=C1)OC)C(C)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O MVTQJLVXODOUEE-UHFFFAOYSA-N 0.000 claims 4
- LTFFYNBBYLBAGX-UHFFFAOYSA-N N-[1-(2-fluoro-5-methoxyphenyl)ethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=C(C=C1)OC)C(C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O LTFFYNBBYLBAGX-UHFFFAOYSA-N 0.000 claims 4
- LYLJYIZTSPUCNP-UHFFFAOYSA-N N-[1-(2-fluorophenyl)ethyl]-3-(1-hydroxyethyl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=CC=C1)C(C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C(C)O)=O LYLJYIZTSPUCNP-UHFFFAOYSA-N 0.000 claims 4
- VBKDAAYYAUWVCA-UHFFFAOYSA-N N-[1-(2-fluorophenyl)ethyl]-3-formyl-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=CC=C1)C(C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C=O)=O VBKDAAYYAUWVCA-UHFFFAOYSA-N 0.000 claims 4
- 125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 3
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 3
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 claims 2
- KXEAONMVSCDRIF-LLVKDONJSA-N 2,5-difluoro-N-[(1R)-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=O)N[C@H](C)C2=CC=CC=C2)C=C(C(=C1)C=1C=NNC=1)F KXEAONMVSCDRIF-LLVKDONJSA-N 0.000 claims 2
- KKFYJBLOJFXLCI-OAHLLOKOSA-N 2-(2-methoxyethoxy)-N-[(1R)-1-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COCCOC1=C(C(=O)N[C@H](C)C2=CC(=CC=C2)OC)C=CC(=C1)C=1C=NNC=1 KKFYJBLOJFXLCI-OAHLLOKOSA-N 0.000 claims 2
- PHVVTCGPBIFFEL-UHFFFAOYSA-N 2-(hydroxymethyl)-N-[(3-methoxyphenyl)methyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound OCC1=C(C(=O)NCC2=CC(=CC=C2)OC)C=CC(=C1)C=1C=NNC=1 PHVVTCGPBIFFEL-UHFFFAOYSA-N 0.000 claims 2
- LWMAQRGEAMQBDS-OAHLLOKOSA-N 2-[2-(dimethylamino)ethoxy]-5-fluoro-N-[(1R)-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound CN(CCOC1=C(C(=O)N[C@H](C)C2=CC=CC=C2)C=C(C(=C1)C=1C=NNC=1)F)C LWMAQRGEAMQBDS-OAHLLOKOSA-N 0.000 claims 2
- TXAKRIXEQQYHFA-MRXNPFEDSA-N 2-[2-(dimethylamino)ethoxy]-n-[(1r)-1-(3-methoxyphenyl)ethyl]-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC=CC([C@@H](C)NC(=O)C=2C(=CC(=CC=2)C2=CNN=C2)OCCN(C)C)=C1 TXAKRIXEQQYHFA-MRXNPFEDSA-N 0.000 claims 2
- NFEOVSMGURSBHD-UHFFFAOYSA-N 2-amino-N-(3-phenylpropyl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound NC1=C(C(=O)NCCCC2=CC=CC=C2)C=CC(=C1)C=1C=NNC=1 NFEOVSMGURSBHD-UHFFFAOYSA-N 0.000 claims 2
- YQZUYMIRRIDTAO-UHFFFAOYSA-N 2-amino-N-[(3-methoxyphenyl)methyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound NC1=C(C(=O)NCC2=CC(=CC=C2)OC)C=CC(=C1)C=1C=NNC=1 YQZUYMIRRIDTAO-UHFFFAOYSA-N 0.000 claims 2
- UUZSJNLZBLNEFQ-GFCCVEGCSA-N 2-chloro-N-[(1R)-1-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C(=O)N[C@H](C)C2=CC(=CC=C2)OC)C=CC(=C1)C=1C=NNC=1 UUZSJNLZBLNEFQ-GFCCVEGCSA-N 0.000 claims 2
- BAUSMWQMIOODMY-CQSZACIVSA-N 2-ethoxy-N-[(1R)-1-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(C)OC1=C(C(=O)N[C@H](C)C2=CC(=CC=C2)OC)C=CC(=C1)C=1C=NNC=1 BAUSMWQMIOODMY-CQSZACIVSA-N 0.000 claims 2
- MQHAUPTVCAFIJM-GFCCVEGCSA-N 2-fluoro-3-methoxy-N-[(1R)-1-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=O)N[C@H](C)C2=CC(=CC=C2)OC)C=CC(=C1OC)C=1C=NNC=1 MQHAUPTVCAFIJM-GFCCVEGCSA-N 0.000 claims 2
- RJXSCRRYUBZADY-UHFFFAOYSA-N 2-fluoro-5-[[[3-methoxy-4-(1H-pyrazol-4-yl)benzoyl]amino]methyl]benzoic acid Chemical compound FC1=C(C(=O)O)C=C(C=C1)CNC(=O)C1=CC(=C(C=C1)C=1C=NNC=1)OC RJXSCRRYUBZADY-UHFFFAOYSA-N 0.000 claims 2
- SMVSFIUZEOJMAF-GFCCVEGCSA-N 2-fluoro-6-methoxy-N-[(1R)-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=O)N[C@H](C)C2=CC=CC=C2)C(=CC(=C1)C=1C=NNC=1)OC SMVSFIUZEOJMAF-GFCCVEGCSA-N 0.000 claims 2
- 125000004847 2-fluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- UUJGSCUKYQKPHU-UHFFFAOYSA-N 2-methoxy-4-(1H-pyrazol-4-yl)-N-[(3-sulfamoylphenyl)methyl]benzamide Chemical compound COC1=C(C=CC(=C1)C1=CNN=C1)C(=O)NCC1=CC(=CC=C1)S(N)(=O)=O UUJGSCUKYQKPHU-UHFFFAOYSA-N 0.000 claims 2
- GPERPWCLYBHCRW-UHFFFAOYSA-N 2-methoxy-N-[[3-[(1-methylpiperidin-4-yl)carbamoyl]phenyl]methyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC1=C(C(=O)NCC2=CC(=CC=C2)C(NC2CCN(CC2)C)=O)C=CC(=C1)C=1C=NNC=1 GPERPWCLYBHCRW-UHFFFAOYSA-N 0.000 claims 2
- QXZSUWTXBMUNHX-YBMSBYLISA-N 3-(1-hydroxyethyl)-N-[(1S)-2-methoxy-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC(C)C=1C=C(C(=O)N[C@H](COC)C2=CC=CC=C2)C=CC=1C=1C=NNC=1 QXZSUWTXBMUNHX-YBMSBYLISA-N 0.000 claims 2
- AXFQDCZRKHUGCG-OAHLLOKOSA-N 3-(2-hydroxy-2-methylpropoxy)-N-[(1R)-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC(COC=1C=C(C(=O)N[C@H](C)C2=CC=CC=C2)C=CC=1C=1C=NNC=1)(C)C AXFQDCZRKHUGCG-OAHLLOKOSA-N 0.000 claims 2
- MRSCRUMYAVOXFF-LLVKDONJSA-N 3-(difluoromethoxy)-N-[(1R)-1-(4-fluorophenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC(OC=1C=C(C(=O)N[C@H](C)C2=CC=C(C=C2)F)C=CC=1C=1C=NNC=1)F MRSCRUMYAVOXFF-LLVKDONJSA-N 0.000 claims 2
- IHJPYWIDHOPLCK-GFCCVEGCSA-N 3-(difluoromethoxy)-N-[(1R)-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC(OC=1C=C(C(=O)N[C@H](C)C2=CC=CC=C2)C=CC=1C=1C=NNC=1)F IHJPYWIDHOPLCK-GFCCVEGCSA-N 0.000 claims 2
- YXAYEZQYTJGWNT-OAHLLOKOSA-N 3-(difluoromethoxy)-N-[(1S)-1-(2,6-difluorophenyl)-2-hydroxyethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC(OC=1C=C(C(=O)N[C@H](CO)C2=C(C=CC=C2F)F)C=CC=1C=1C=NNC=1)F YXAYEZQYTJGWNT-OAHLLOKOSA-N 0.000 claims 2
- JBAFISIOKGNSRP-MRXNPFEDSA-N 3-(difluoromethoxy)-N-[(1S)-2-hydroxy-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC(OC=1C=C(C(=O)N[C@H](CO)C2=CC=CC=C2)C=CC=1C=1C=NNC=1)F JBAFISIOKGNSRP-MRXNPFEDSA-N 0.000 claims 2
- ZFFGCUGXWFNDIU-CYBMUJFWSA-N 3-(hydroxymethyl)-N-[(1R)-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound OCC=1C=C(C(=O)N[C@H](C)C2=CC=CC=C2)C=CC=1C=1C=NNC=1 ZFFGCUGXWFNDIU-CYBMUJFWSA-N 0.000 claims 2
- FPNYVINXEGJSCQ-UHFFFAOYSA-N 3-[[[3-methoxy-4-(1h-pyrazol-4-yl)benzoyl]amino]methyl]benzoic acid Chemical compound COC1=CC(C(=O)NCC=2C=C(C=CC=2)C(O)=O)=CC=C1C=1C=NNC=1 FPNYVINXEGJSCQ-UHFFFAOYSA-N 0.000 claims 2
- ZAMBLNKLSSPUQI-GFCCVEGCSA-N 3-chloro-N-[(1R)-1-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC=1C=C(C(=O)N[C@H](C)C2=CC(=CC=C2)OC)C=CC=1C=1C=NNC=1 ZAMBLNKLSSPUQI-GFCCVEGCSA-N 0.000 claims 2
- LRNKGINCBWKQIS-CYBMUJFWSA-N 3-cyano-N-[(1R)-1-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(#N)C=1C=C(C(=O)N[C@H](C)C2=CC(=CC=C2)OC)C=CC=1C=1C=NNC=1 LRNKGINCBWKQIS-CYBMUJFWSA-N 0.000 claims 2
- JKORGIDZLQYQPY-GFCCVEGCSA-N 3-cyano-N-[(1R)-1-(4-fluorophenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(#N)C=1C=C(C(=O)N[C@H](C)C2=CC=C(C=C2)F)C=CC=1C=1C=NNC=1 JKORGIDZLQYQPY-GFCCVEGCSA-N 0.000 claims 2
- BBRAFGURQIKIIF-QGZVFWFLSA-N 3-cyano-N-[(1S)-1-(2,6-difluorophenyl)-2-hydroxyethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(#N)C=1C=C(C(=O)N[C@H](CO)C2=C(C=CC=C2F)F)C=CC=1C=1C=NNC=1 BBRAFGURQIKIIF-QGZVFWFLSA-N 0.000 claims 2
- ZJTWQFQDQUDRQQ-GOSISDBHSA-N 3-cyano-N-[(1S)-2-hydroxy-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(#N)C=1C=C(C(=O)N[C@H](CO)C2=CC=CC=C2)C=CC=1C=1C=NNC=1 ZJTWQFQDQUDRQQ-GOSISDBHSA-N 0.000 claims 2
- LXGGZIPRDNFPHL-CYBMUJFWSA-N 3-ethoxy-N-[(1R)-1-(4-fluorophenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(C)OC=1C=C(C(=O)N[C@H](C)C2=CC=C(C=C2)F)C=CC=1C=1C=NNC=1 LXGGZIPRDNFPHL-CYBMUJFWSA-N 0.000 claims 2
- LVAMWHFZQXITMS-GOSISDBHSA-N 3-ethoxy-N-[(1S)-2-hydroxy-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(C)OC=1C=C(C(=O)N[C@H](CO)C2=CC=CC=C2)C=CC=1C=1C=NNC=1 LVAMWHFZQXITMS-GOSISDBHSA-N 0.000 claims 2
- HPUIONZOLCECJV-UHFFFAOYSA-N 3-methoxy-4-(1H-pyrazol-4-yl)-N-[(2,3,5-trifluorophenyl)methyl]benzamide Chemical compound COC1=C(C=CC(=C1)C(=O)NCC1=C(F)C(F)=CC(F)=C1)C1=CNN=C1 HPUIONZOLCECJV-UHFFFAOYSA-N 0.000 claims 2
- NSFLMMYRDFGKMW-UHFFFAOYSA-N 3-methoxy-4-(1H-pyrazol-4-yl)-N-[(2,3,6-trifluorophenyl)methyl]benzamide Chemical compound COC1=C(C=CC(=C1)C(=O)NCC1=C(F)C(F)=CC=C1F)C1=CNN=C1 NSFLMMYRDFGKMW-UHFFFAOYSA-N 0.000 claims 2
- FXDUJKSFLDJRPN-UHFFFAOYSA-N 3-methoxy-4-(1H-pyrazol-4-yl)-N-[(2,4,6-trifluorophenyl)methyl]benzamide Chemical compound COC1=C(C=CC(=C1)C(=O)NCC1=C(F)C=C(F)C=C1F)C1=CNN=C1 FXDUJKSFLDJRPN-UHFFFAOYSA-N 0.000 claims 2
- FTUKZMZRGJAOKF-UHFFFAOYSA-N 3-methoxy-4-(1H-pyrazol-4-yl)-N-[(3-sulfamoylphenyl)methyl]benzamide Chemical compound COC1=C(C=CC(=C1)C(=O)NCC1=CC(=CC=C1)S(N)(=O)=O)C1=CNN=C1 FTUKZMZRGJAOKF-UHFFFAOYSA-N 0.000 claims 2
- GZWZWHDONMXYLT-UHFFFAOYSA-N 3-methoxy-4-(1H-pyrazol-4-yl)-N-[2-[3-(trifluoromethyl)phenyl]ethyl]benzamide Chemical compound COC1=C(C=CC(=C1)C(=O)NCCC1=CC(=CC=C1)C(F)(F)F)C1=CNN=C1 GZWZWHDONMXYLT-UHFFFAOYSA-N 0.000 claims 2
- GYZHOJQCWGSTEZ-UHFFFAOYSA-N 3-methoxy-4-(1H-pyrazol-4-yl)-N-[2-[4-(trifluoromethyl)phenyl]ethyl]benzamide Chemical compound COC1=C(C=CC(=C1)C(=O)NCCC1=CC=C(C=C1)C(F)(F)F)C1=CNN=C1 GYZHOJQCWGSTEZ-UHFFFAOYSA-N 0.000 claims 2
- QMWOUHPEAPUFNT-UHFFFAOYSA-N 3-methoxy-4-(1h-pyrazol-4-yl)-n-(pyridin-2-ylmethyl)benzamide Chemical compound COC1=CC(C(=O)NCC=2N=CC=CC=2)=CC=C1C=1C=NNC=1 QMWOUHPEAPUFNT-UHFFFAOYSA-N 0.000 claims 2
- OFDLZAYIPJWEAV-UHFFFAOYSA-N 3-methoxy-4-(1h-pyrazol-4-yl)-n-(pyridin-3-ylmethyl)benzamide Chemical compound COC1=CC(C(=O)NCC=2C=NC=CC=2)=CC=C1C=1C=NNC=1 OFDLZAYIPJWEAV-UHFFFAOYSA-N 0.000 claims 2
- PILIWAPJQLCXKO-UHFFFAOYSA-N 3-methoxy-N-(3-oxo-1-phenylbutan-2-yl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)NC(CC2=CC=CC=C2)C(C)=O)C=CC=1C=1C=NNC=1 PILIWAPJQLCXKO-UHFFFAOYSA-N 0.000 claims 2
- VBBARCMTJPDGFK-CYBMUJFWSA-N 3-methoxy-N-[(1R)-1-(2-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)N[C@H](C)C2=C(C=CC=C2)OC)C=CC=1C=1C=NNC=1 VBBARCMTJPDGFK-CYBMUJFWSA-N 0.000 claims 2
- ZSRGQQNNHDFZKU-AWEZNQCLSA-N 3-methoxy-N-[(2R)-2-phenylpropyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)NC[C@H](C)C2=CC=CC=C2)C=CC=1C=1C=NNC=1 ZSRGQQNNHDFZKU-AWEZNQCLSA-N 0.000 claims 2
- ZSRGQQNNHDFZKU-CQSZACIVSA-N 3-methoxy-N-[(2S)-2-phenylpropyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)NC[C@@H](C)C2=CC=CC=C2)C=CC=1C=1C=NNC=1 ZSRGQQNNHDFZKU-CQSZACIVSA-N 0.000 claims 2
- RJMZRJDWOXEUNY-UHFFFAOYSA-N 3-methoxy-N-[1-(3-methoxyphenyl)cyclopropyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)NC2(CC2)C2=CC(=CC=C2)OC)C=CC=1C=1C=NNC=1 RJMZRJDWOXEUNY-UHFFFAOYSA-N 0.000 claims 2
- JQPFBPKZRBMCCY-UHFFFAOYSA-N 3-methoxy-N-[1-(6-methoxypyridin-2-yl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)NC(C)C2=NC(=CC=C2)OC)C=CC=1C=1C=NNC=1 JQPFBPKZRBMCCY-UHFFFAOYSA-N 0.000 claims 2
- YVWXLWMOJFAGPJ-UHFFFAOYSA-N 3-methoxy-N-[2-(2-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)NCCC2=C(C=CC=C2)OC)C=CC=1C=1C=NNC=1 YVWXLWMOJFAGPJ-UHFFFAOYSA-N 0.000 claims 2
- DYOILCGEGQTBTJ-UHFFFAOYSA-N 3-methoxy-N-[2-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)NCCC2=CC(=CC=C2)OC)C=CC=1C=1C=NNC=1 DYOILCGEGQTBTJ-UHFFFAOYSA-N 0.000 claims 2
- WPOIOKJTVWXYEA-UHFFFAOYSA-N 3-methoxy-N-[[3-[(1-methylpiperidin-4-yl)carbamoyl]phenyl]methyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C(=O)NCC2=CC(=CC=C2)C(NC2CCN(CC2)C)=O)C=CC=1C=1C=NNC=1 WPOIOKJTVWXYEA-UHFFFAOYSA-N 0.000 claims 2
- ZKQKBOWBNMYREE-UHFFFAOYSA-N 3-methoxy-n-(1-phenylethyl)-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC(C)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 ZKQKBOWBNMYREE-UHFFFAOYSA-N 0.000 claims 2
- SWFHDLGGWNNIBV-UHFFFAOYSA-N 3-methoxy-n-(2-phenylpropan-2-yl)-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC(C)(C)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 SWFHDLGGWNNIBV-UHFFFAOYSA-N 0.000 claims 2
- XOFDPLFMXLSAOK-UHFFFAOYSA-N 3-methoxy-n-[2-(4-methylpiperazin-1-yl)-1-phenylethyl]-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC(CN2CCN(C)CC2)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 XOFDPLFMXLSAOK-UHFFFAOYSA-N 0.000 claims 2
- 125000006497 3-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 claims 2
- CRFSDZNCOBDRQG-CQSZACIVSA-N 3-methyl-n-[(1r)-1-phenylethyl]-4-(1h-pyrazol-4-yl)benzamide Chemical compound N([C@H](C)C=1C=CC=CC=1)C(=O)C(C=C1C)=CC=C1C=1C=NNC=1 CRFSDZNCOBDRQG-CQSZACIVSA-N 0.000 claims 2
- WACNRZMKBTXEMX-CYBMUJFWSA-N 4-(3,5-dimethyl-1H-pyrazol-4-yl)-2-methoxy-N-[(1R)-1-(3-methoxyphenyl)ethyl]benzamide Chemical compound COc1cccc(c1)[C@@H](C)NC(=O)c1ccc(cc1OC)-c1c(C)n[nH]c1C WACNRZMKBTXEMX-CYBMUJFWSA-N 0.000 claims 2
- YZIKEARCAOIQTA-CQSZACIVSA-N 4-(3,5-dimethyl-1H-pyrazol-4-yl)-N-[(1R)-1-(3-methoxyphenyl)ethyl]-3-methylbenzamide Chemical compound CC1=NNC(=C1C1=C(C=C(C(=O)N[C@H](C)C2=CC(=CC=C2)OC)C=C1)C)C YZIKEARCAOIQTA-CQSZACIVSA-N 0.000 claims 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 2
- NTVGZILGUNKNME-GFCCVEGCSA-N 5-fluoro-2-methoxy-N-[(1R)-1-phenylethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC=1C(=CC(=C(C(=O)N[C@H](C)C2=CC=CC=C2)C=1)OC)C=1C=NNC=1 NTVGZILGUNKNME-GFCCVEGCSA-N 0.000 claims 2
- 208000023275 Autoimmune disease Diseases 0.000 claims 2
- SBMIMRGGSPVOAG-UHFFFAOYSA-N N-(1-amino-3-phenylpropan-2-yl)-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound NCC(CC1=CC=CC=C1)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O SBMIMRGGSPVOAG-UHFFFAOYSA-N 0.000 claims 2
- PNNANOOTMGLECQ-UHFFFAOYSA-N N-(1H-indazol-4-ylmethyl)-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound N1N=CC2=C(C=CC=C12)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O PNNANOOTMGLECQ-UHFFFAOYSA-N 0.000 claims 2
- RKGXRJNCSPXVMJ-UHFFFAOYSA-N N-(2-cyano-2-phenylethyl)-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(#N)C(CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C1=CC=CC=C1 RKGXRJNCSPXVMJ-UHFFFAOYSA-N 0.000 claims 2
- QBWKZDBFMHLSHV-CYBMUJFWSA-N N-[(1R)-1-(2,3-dihydro-1-benzofuran-5-yl)ethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O1CCC2=C1C=CC(=C2)[C@@H](C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O QBWKZDBFMHLSHV-CYBMUJFWSA-N 0.000 claims 2
- VUKPYAYVXNDTIK-INIZCTEOSA-N N-[(1R)-1-(2,6-difluorophenyl)-2-hydroxyethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)[C@H](CO)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O VUKPYAYVXNDTIK-INIZCTEOSA-N 0.000 claims 2
- LYLJYIZTSPUCNP-PZORYLMUSA-N N-[(1R)-1-(2-fluorophenyl)ethyl]-3-(1-hydroxyethyl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=CC=C1)[C@@H](C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C(C)O)=O LYLJYIZTSPUCNP-PZORYLMUSA-N 0.000 claims 2
- SEPHKODFYBTYDV-CQSZACIVSA-N N-[(1R)-1-(3-methoxyphenyl)ethyl]-3-methyl-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC=1C=C(C=CC=1)[C@@H](C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C)=O SEPHKODFYBTYDV-CQSZACIVSA-N 0.000 claims 2
- DUUFTCDTPYSKCS-GFCCVEGCSA-N N-[(1R)-1-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)-3-(trifluoromethyl)benzamide Chemical compound COC1=CC=CC(=C1)[C@@H](C)NC(=O)C1=CC(=C(C=C1)C1=CNN=C1)C(F)(F)F DUUFTCDTPYSKCS-GFCCVEGCSA-N 0.000 claims 2
- ICQSNTDFCNRKLY-GFCCVEGCSA-N N-[(1R)-1-(4-fluorophenyl)ethyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC1=C(C=CC(=C1)C1=CNN=C1)C(=O)N[C@H](C)C1=CC=C(F)C=C1 ICQSNTDFCNRKLY-GFCCVEGCSA-N 0.000 claims 2
- LFJFWJSDSCDXIT-LLVKDONJSA-N N-[(1R)-1-(4-fluorophenyl)ethyl]-3-hydroxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=CC=C(C=C1)[C@@H](C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)O)=O LFJFWJSDSCDXIT-LLVKDONJSA-N 0.000 claims 2
- ACSFOKQSDKYSPD-CYBMUJFWSA-N N-[(1R)-1-(4-fluorophenyl)ethyl]-3-methyl-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=CC=C(C=C1)[C@@H](C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C)=O ACSFOKQSDKYSPD-CYBMUJFWSA-N 0.000 claims 2
- GCKIJVYMPZVOFI-GOSISDBHSA-N N-[(1R)-3-hydroxy-1-phenylpropyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound OCC[C@H](C1=CC=CC=C1)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O GCKIJVYMPZVOFI-GOSISDBHSA-N 0.000 claims 2
- BUHHYYUWCDSWAP-IEBWSBKVSA-N N-[(1R,2R)-1,3-dihydroxy-1-phenylpropan-2-yl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O[C@@H]([C@@H](CO)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O)C1=CC=CC=C1 BUHHYYUWCDSWAP-IEBWSBKVSA-N 0.000 claims 2
- INDDLVHMKCQKDP-IEBWSBKVSA-N N-[(1R,2R)-1,3-dihydroxy-1-phenylpropan-2-yl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O[C@@H]([C@@H](CO)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C1=CC=CC=C1 INDDLVHMKCQKDP-IEBWSBKVSA-N 0.000 claims 2
- ZTDZUGXYUUIFQW-LRTDYKAYSA-N N-[(1S)-1-(2,6-difluorophenyl)-2,3-dihydroxypropyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)[C@@H](C(CO)O)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O ZTDZUGXYUUIFQW-LRTDYKAYSA-N 0.000 claims 2
- CDAZONRYNUZNMV-MRXNPFEDSA-N N-[(1S)-1-(2,6-difluorophenyl)-2-hydroxyethyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)[C@@H](CO)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O CDAZONRYNUZNMV-MRXNPFEDSA-N 0.000 claims 2
- QNIZYMHQGXFAMH-QGZVFWFLSA-N N-[(1S)-1-(2,6-difluorophenyl)-2-hydroxyethyl]-3-ethoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)[C@@H](CO)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OCC)=O QNIZYMHQGXFAMH-QGZVFWFLSA-N 0.000 claims 2
- SYAFKJOXGPOOAP-QGZVFWFLSA-N N-[(1S)-1-(2,6-difluorophenyl)-2-hydroxyethyl]-3-methyl-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)[C@@H](CO)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C)=O SYAFKJOXGPOOAP-QGZVFWFLSA-N 0.000 claims 2
- CBEMNKANJPWQCN-MRXNPFEDSA-N N-[(1S)-1-(2,6-difluorophenyl)-2-hydroxyethyl]-4-(1H-pyrazol-4-yl)-3-(trifluoromethyl)benzamide Chemical compound OC[C@@H](NC(=O)C1=CC(=C(C=C1)C1=CNN=C1)C(F)(F)F)C1=C(F)C=CC=C1F CBEMNKANJPWQCN-MRXNPFEDSA-N 0.000 claims 2
- OSDWJAUTLIVEOA-LJQANCHMSA-N N-[(1S)-2-amino-1-phenylethyl]-3-(2-hydroxy-2-methylpropoxy)-4-(1H-pyrazol-4-yl)benzamide Chemical compound NC[C@H](C1=CC=CC=C1)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OCC(C)(C)O)=O OSDWJAUTLIVEOA-LJQANCHMSA-N 0.000 claims 2
- JHZUXOVQEXDSPY-GOSISDBHSA-N N-[(1S)-2-amino-1-phenylethyl]-3-(2-hydroxyethoxy)-4-(1H-pyrazol-4-yl)benzamide Chemical compound NC[C@H](C1=CC=CC=C1)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OCCO)=O JHZUXOVQEXDSPY-GOSISDBHSA-N 0.000 claims 2
- OXNMNUGGLVTVDA-ICSRJNTNSA-N N-[(1S,2S)-1-hydroxy-3-methoxy-1-phenylpropan-2-yl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O[C@H]([C@H](COC)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C1=CC=CC=C1 OXNMNUGGLVTVDA-ICSRJNTNSA-N 0.000 claims 2
- YCNNWSRSIAKLGS-MJGOQNOKSA-N N-[(1S,2S)-2,3-dihydroxy-1-phenylpropyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O[C@@H]([C@H](C1=CC=CC=C1)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O)CO YCNNWSRSIAKLGS-MJGOQNOKSA-N 0.000 claims 2
- FRWXJFJBJPGDJM-MJGOQNOKSA-N N-[(1S,2S)-2,3-dihydroxy-1-phenylpropyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O[C@@H]([C@H](C1=CC=CC=C1)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)CO FRWXJFJBJPGDJM-MJGOQNOKSA-N 0.000 claims 2
- LIUKLYUNBUVVON-UHFFFAOYSA-N N-[(2,4-dichlorophenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C=CC(=C1)Cl)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O LIUKLYUNBUVVON-UHFFFAOYSA-N 0.000 claims 2
- FQYIMRXBBCWILN-UHFFFAOYSA-N N-[(2,6-difluorophenyl)methyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)CNC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O FQYIMRXBBCWILN-UHFFFAOYSA-N 0.000 claims 2
- PLIFSXNZAOLLSV-UHFFFAOYSA-N N-[(2,6-difluorophenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O PLIFSXNZAOLLSV-UHFFFAOYSA-N 0.000 claims 2
- SEJXTFIDDFUTMH-UHFFFAOYSA-N N-[(2-chloro-3,6-difluorophenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C(=CC=C1F)F)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O SEJXTFIDDFUTMH-UHFFFAOYSA-N 0.000 claims 2
- MBFDUQROVSLSPJ-UHFFFAOYSA-N N-[(2-chloro-4-fluorophenyl)methyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C=CC(=C1)F)CNC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O MBFDUQROVSLSPJ-UHFFFAOYSA-N 0.000 claims 2
- CWKUJWGURSJFTK-UHFFFAOYSA-N N-[(2-chloro-4-fluorophenyl)methyl]-3-methyl-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C=CC(=C1)F)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)C)=O CWKUJWGURSJFTK-UHFFFAOYSA-N 0.000 claims 2
- SOEYUSIWHOBEMJ-UHFFFAOYSA-N N-[(2-chloro-6-fluorophenyl)methyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C(=CC=C1)F)CNC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O SOEYUSIWHOBEMJ-UHFFFAOYSA-N 0.000 claims 2
- FDNZNHRDINDRLM-UHFFFAOYSA-N N-[(2-chloro-6-fluorophenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C(=CC=C1)F)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O FDNZNHRDINDRLM-UHFFFAOYSA-N 0.000 claims 2
- KUKQBSNMNWQADK-UHFFFAOYSA-N N-[(2-chloro-6-fluorophenyl)methyl]-3-methyl-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C(=CC=C1)F)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)C)=O KUKQBSNMNWQADK-UHFFFAOYSA-N 0.000 claims 2
- FRPJSZRAPBBGTE-UHFFFAOYSA-N N-[(2-ethylphenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(C)C1=C(C=CC=C1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O FRPJSZRAPBBGTE-UHFFFAOYSA-N 0.000 claims 2
- DVVOYLZXWWZJSO-UHFFFAOYSA-N N-[(2-fluoro-5-methoxyphenyl)methyl]-3-methyl-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=C(C=C1)OC)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)C)=O DVVOYLZXWWZJSO-UHFFFAOYSA-N 0.000 claims 2
- WTLKHNCRMWMEPP-QGZVFWFLSA-N N-[(2R)-1-hydroxy-3-phenylpropan-2-yl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC[C@@H](CC1=CC=CC=C1)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O WTLKHNCRMWMEPP-QGZVFWFLSA-N 0.000 claims 2
- XVWAHNBWATXACB-KRWDZBQOSA-N N-[(2R)-2-hydroxy-2-phenylethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O[C@@H](CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C1=CC=CC=C1 XVWAHNBWATXACB-KRWDZBQOSA-N 0.000 claims 2
- PZAYZTYHHVPMFG-KRWDZBQOSA-N N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC[C@H](CC1=CC=CC=C1)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O PZAYZTYHHVPMFG-KRWDZBQOSA-N 0.000 claims 2
- WTLKHNCRMWMEPP-KRWDZBQOSA-N N-[(2S)-1-hydroxy-3-phenylpropan-2-yl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC[C@H](CC1=CC=CC=C1)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O WTLKHNCRMWMEPP-KRWDZBQOSA-N 0.000 claims 2
- OORBXCUUHIIWJV-QGZVFWFLSA-N N-[(2S)-2-(3-chlorophenyl)-2-hydroxyethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC=1C=C(C=CC=1)[C@@H](CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)O OORBXCUUHIIWJV-QGZVFWFLSA-N 0.000 claims 2
- XVWAHNBWATXACB-QGZVFWFLSA-N N-[(2S)-2-hydroxy-2-phenylethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O[C@H](CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C1=CC=CC=C1 XVWAHNBWATXACB-QGZVFWFLSA-N 0.000 claims 2
- WPWSPITXILOZGO-RBUKOAKNSA-N N-[(2S,3S)-3,4-dihydroxy-1-phenylbutan-2-yl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O[C@@H]([C@H](CC1=CC=CC=C1)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O)CO WPWSPITXILOZGO-RBUKOAKNSA-N 0.000 claims 2
- DVTKMLJDBJSXHF-UHFFFAOYSA-N N-[(3-carbamoylphenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(N)(=O)C=1C=C(C=CC=1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O DVTKMLJDBJSXHF-UHFFFAOYSA-N 0.000 claims 2
- XNOBXYSDKGIVFG-UHFFFAOYSA-N N-[(3-cyanophenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(#N)C=1C=C(C=CC=1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O XNOBXYSDKGIVFG-UHFFFAOYSA-N 0.000 claims 2
- HWOQGLLRJCPMIZ-UHFFFAOYSA-N N-[(4-chloro-2-fluorophenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=CC(=C(C=C1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)F HWOQGLLRJCPMIZ-UHFFFAOYSA-N 0.000 claims 2
- WYDFGQMBIFGNSV-UHFFFAOYSA-N N-[(4-cyanophenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(#N)C1=CC=C(C=C1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O WYDFGQMBIFGNSV-UHFFFAOYSA-N 0.000 claims 2
- URYCVJWDQPAEFD-UHFFFAOYSA-N N-[(4-fluoro-3-methoxyphenyl)methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=C(C=C1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)OC URYCVJWDQPAEFD-UHFFFAOYSA-N 0.000 claims 2
- GJQXDMZVTHNNHF-UHFFFAOYSA-N N-[1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound O1CCOC2=C1C=CC(=C2)C(C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O GJQXDMZVTHNNHF-UHFFFAOYSA-N 0.000 claims 2
- FCWLESDKJOPDNI-UHFFFAOYSA-N N-[1-(2,6-difluorophenyl)ethyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)C(C)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O FCWLESDKJOPDNI-UHFFFAOYSA-N 0.000 claims 2
- YVTWDJQRSGSDSG-UHFFFAOYSA-N N-[1-(2,6-difluorophenyl)ethyl]-3-(1-hydroxyethyl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C(=CC=C1)F)C(C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C(C)O)=O YVTWDJQRSGSDSG-UHFFFAOYSA-N 0.000 claims 2
- WSXKSMSBOLIXMK-UHFFFAOYSA-N N-[1-(2,6-difluorophenyl)ethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound COC1=C(C=CC(=C1)C(=O)NC(C)C1=C(F)C=CC=C1F)C1=CNN=C1 WSXKSMSBOLIXMK-UHFFFAOYSA-N 0.000 claims 2
- IJASYRWFAWXBTH-UHFFFAOYSA-N N-[1-(2-fluoro-5-methoxyphenyl)ethyl]-3-(1-hydroxyethyl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=C(C=C1)OC)C(C)NC(C1=CC(=C(C=C1)C=1C=NNC=1)C(C)O)=O IJASYRWFAWXBTH-UHFFFAOYSA-N 0.000 claims 2
- ITMSRNJKTCZBKP-UHFFFAOYSA-N N-[1-(2-fluorophenyl)-2-hydroxyethyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound FC1=C(C=CC=C1)C(CO)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O ITMSRNJKTCZBKP-UHFFFAOYSA-N 0.000 claims 2
- XZOMFGUPUHMZFT-UHFFFAOYSA-N N-[2-(2-chlorophenyl)-2-hydroxyethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound ClC1=C(C=CC=C1)C(CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)O XZOMFGUPUHMZFT-UHFFFAOYSA-N 0.000 claims 2
- KUZSZZVWEJIXDN-UHFFFAOYSA-N N-[2-(3-hydroxyphenyl)ethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC=1C=C(C=CC=1)CCNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O KUZSZZVWEJIXDN-UHFFFAOYSA-N 0.000 claims 2
- ZQJDFLYMWBBQHF-UHFFFAOYSA-N N-[2-hydroxy-2-(3-hydroxyphenyl)ethyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC(CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C1=CC(=CC=C1)O ZQJDFLYMWBBQHF-UHFFFAOYSA-N 0.000 claims 2
- IIOMFEOXTRHVDM-UHFFFAOYSA-N N-[3-(dimethylamino)-1-phenylpropyl]-2-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound CN(CCC(C1=CC=CC=C1)NC(C1=C(C=C(C=C1)C=1C=NNC=1)OC)=O)C IIOMFEOXTRHVDM-UHFFFAOYSA-N 0.000 claims 2
- MVVFOQPCDDRVRA-UHFFFAOYSA-N N-[[3-(dimethylamino)phenyl]methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound CN(C=1C=C(C=CC=1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C MVVFOQPCDDRVRA-UHFFFAOYSA-N 0.000 claims 2
- ZAKZLDCJGVOUQE-UHFFFAOYSA-N N-[[3-(dimethylcarbamoyl)phenyl]methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound CN(C(=O)C=1C=C(C=CC=1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)C ZAKZLDCJGVOUQE-UHFFFAOYSA-N 0.000 claims 2
- JWVWCAKTWBMEPU-UHFFFAOYSA-N N-[[3-(ethylcarbamoyl)phenyl]methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(C)NC(=O)C=1C=C(C=CC=1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O JWVWCAKTWBMEPU-UHFFFAOYSA-N 0.000 claims 2
- WAOPBAUYEVWLHE-UHFFFAOYSA-N N-[[3-(ethylcarbamoyl)phenyl]methyl]-3-methyl-4-(1H-pyrazol-4-yl)benzamide Chemical compound C(C)NC(=O)C=1C=C(C=CC=1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)C)=O WAOPBAUYEVWLHE-UHFFFAOYSA-N 0.000 claims 2
- WHVMMFVGEVMVIT-UHFFFAOYSA-N N-[[3-[(2-hydroxy-2-methylpropyl)carbamoyl]phenyl]methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound OC(CNC(=O)C=1C=C(C=CC=1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O)(C)C WHVMMFVGEVMVIT-UHFFFAOYSA-N 0.000 claims 2
- GRLGITMOQAPTDO-UHFFFAOYSA-N N-[[3-[(dimethylamino)methyl]phenyl]methyl]-3-methoxy-4-(1H-pyrazol-4-yl)benzamide Chemical compound CN(C)CC=1C=C(C=CC=1)CNC(C1=CC(=C(C=C1)C=1C=NNC=1)OC)=O GRLGITMOQAPTDO-UHFFFAOYSA-N 0.000 claims 2
- YYIHXHLZFADWFM-UHFFFAOYSA-N N-benzyl-2-(2-hydroxyethyl)-4-(1H-pyrazol-4-yl)benzamide Chemical compound OCCC1=C(C=CC(=C1)C1=CNN=C1)C(=O)NCC1=CC=CC=C1 YYIHXHLZFADWFM-UHFFFAOYSA-N 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- KQDDDWVLLDDHOF-UHFFFAOYSA-N n-(2-amino-1-phenylethyl)-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC(CN)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 KQDDDWVLLDDHOF-UHFFFAOYSA-N 0.000 claims 2
- XDZHGRSCNCMGSV-QGZVFWFLSA-N n-[(1r)-1-(2,6-difluorophenyl)propyl]-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound N([C@H](CC)C=1C(=CC=CC=1F)F)C(=O)C(C=C1OC)=CC=C1C=1C=NNC=1 XDZHGRSCNCMGSV-QGZVFWFLSA-N 0.000 claims 2
- GHHRAYKNHQKBOM-GFCCVEGCSA-N n-[(1r)-1-(4-fluorophenyl)ethyl]-3-(hydroxymethyl)-4-(1h-pyrazol-4-yl)benzamide Chemical compound N([C@H](C)C=1C=CC(F)=CC=1)C(=O)C(C=C1CO)=CC=C1C=1C=NNC=1 GHHRAYKNHQKBOM-GFCCVEGCSA-N 0.000 claims 2
- KIEIVVQNVJKJFB-DJJJIMSYSA-N n-[(1r,2s)-1-hydroxy-1-phenylpropan-2-yl]-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)N[C@@H](C)[C@H](O)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 KIEIVVQNVJKJFB-DJJJIMSYSA-N 0.000 claims 2
- MXUZFINOYNQLNI-GOSISDBHSA-N n-[(1s)-1-(2,6-difluorophenyl)-2-(ethylamino)ethyl]-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound N([C@H](CNCC)C=1C(=CC=CC=1F)F)C(=O)C(C=C1OC)=CC=C1C=1C=NNC=1 MXUZFINOYNQLNI-GOSISDBHSA-N 0.000 claims 2
- KTVRJTYYMLXASQ-LJQANCHMSA-N n-[(1s)-2-(cyclopropylamino)-1-(2,6-difluorophenyl)ethyl]-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)N[C@H](CNC2CC2)C=2C(=CC=CC=2F)F)=CC=C1C=1C=NNC=1 KTVRJTYYMLXASQ-LJQANCHMSA-N 0.000 claims 2
- CYJWEDGBZCTVAV-HXUWFJFHSA-N n-[(1s)-2-(dimethylamino)-1-phenylethyl]-3-methyl-4-(1h-pyrazol-4-yl)benzamide Chemical compound N([C@H](CN(C)C)C=1C=CC=CC=1)C(=O)C(C=C1C)=CC=C1C=1C=NNC=1 CYJWEDGBZCTVAV-HXUWFJFHSA-N 0.000 claims 2
- KQDDDWVLLDDHOF-QGZVFWFLSA-N n-[(1s)-2-amino-1-phenylethyl]-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)N[C@H](CN)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 KQDDDWVLLDDHOF-QGZVFWFLSA-N 0.000 claims 2
- WPXXNWXNNZASGI-GOSISDBHSA-N n-[(1s)-2-amino-1-phenylethyl]-3-methyl-4-(1h-pyrazol-4-yl)benzamide Chemical compound CC1=CC(C(=O)N[C@H](CN)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 WPXXNWXNNZASGI-GOSISDBHSA-N 0.000 claims 2
- KIEIVVQNVJKJFB-BFUOFWGJSA-N n-[(1s,2r)-1-hydroxy-1-phenylpropan-2-yl]-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)N[C@H](C)[C@@H](O)C=2C=CC=CC=2)=CC=C1C=1C=NNC=1 KIEIVVQNVJKJFB-BFUOFWGJSA-N 0.000 claims 2
- ICBYDYURLUCFTP-UHFFFAOYSA-N n-[(2-chlorophenyl)methyl]-2-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C2=CNN=C2)=CC=C1C(=O)NCC1=CC=CC=C1Cl ICBYDYURLUCFTP-UHFFFAOYSA-N 0.000 claims 2
- PPHSCZQMXMHEGU-UHFFFAOYSA-N n-[1-(2-chlorophenyl)cyclopropyl]-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2(CC2)C=2C(=CC=CC=2)Cl)=CC=C1C=1C=NNC=1 PPHSCZQMXMHEGU-UHFFFAOYSA-N 0.000 claims 2
- VBRGZHZCCDMLQY-UHFFFAOYSA-N n-benzyl-3-methoxy-4-(1h-pyrazol-4-yl)benzamide Chemical compound COC1=CC(C(=O)NCC=2C=CC=CC=2)=CC=C1C=1C=NNC=1 VBRGZHZCCDMLQY-UHFFFAOYSA-N 0.000 claims 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 1
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- HSCQYWDDHGGJSS-CQSZACIVSA-N 2-(2-hydroxyethoxy)-N-[(1R)-1-(3-methoxyphenyl)ethyl]-4-(1H-pyrazol-4-yl)benzamide Chemical compound OCCOC1=C(C(=O)N[C@H](C)C2=CC(=CC=C2)OC)C=CC(=C1)C=1C=NNC=1 HSCQYWDDHGGJSS-CQSZACIVSA-N 0.000 claims 1
- 125000006290 2-hydroxybenzyl group Chemical group [H]OC1=C(C([H])=C([H])C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000002927 2-methoxybenzyl group Chemical group [H]C1=C([H])C([H])=C(C(OC([H])([H])[H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000006179 2-methyl benzyl group Chemical group [H]C1=C([H])C(=C(C([H])=C1[H])C([H])([H])*)C([H])([H])[H] 0.000 claims 1
- 125000006509 3,4-difluorobenzyl group Chemical group [H]C1=C(F)C(F)=C([H])C(=C1[H])C([H])([H])* 0.000 claims 1
- 125000006288 3,5-difluorobenzyl group Chemical group [H]C1=C(F)C([H])=C(C([H])=C1F)C([H])([H])* 0.000 claims 1
- QJSCJJBTPAPBQB-UHFFFAOYSA-N 3-(difluoromethyl)-n-[1-(2-fluorophenyl)ethyl]-4-(1h-pyrazol-4-yl)benzamide Chemical compound C=1C=CC=C(F)C=1C(C)NC(=O)C(C=C1C(F)F)=CC=C1C=1C=NNC=1 QJSCJJBTPAPBQB-UHFFFAOYSA-N 0.000 claims 1
- 125000003852 3-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Cl)=C1[H])C([H])([H])* 0.000 claims 1
- 125000006284 3-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(F)=C1[H])C([H])([H])* 0.000 claims 1
- 125000006291 3-hydroxybenzyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(=C1[H])C([H])([H])* 0.000 claims 1
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims 1
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 claims 1
- 239000005711 Benzoic acid Substances 0.000 claims 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 claims 1
- 208000031481 Pathologic Constriction Diseases 0.000 claims 1
- 208000018262 Peripheral vascular disease Diseases 0.000 claims 1
- 201000009594 Systemic Scleroderma Diseases 0.000 claims 1
- 206010042953 Systemic sclerosis Diseases 0.000 claims 1
- 235000010233 benzoic acid Nutrition 0.000 claims 1
- 208000026106 cerebrovascular disease Diseases 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 208000002551 irritable bowel syndrome Diseases 0.000 claims 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims 1
- 210000004165 myocardium Anatomy 0.000 claims 1
- 230000002981 neuropathic effect Effects 0.000 claims 1
- 230000000771 oncological effect Effects 0.000 claims 1
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 208000037804 stenosis Diseases 0.000 claims 1
- 230000036262 stenosis Effects 0.000 claims 1
- 201000000596 systemic lupus erythematosus Diseases 0.000 claims 1
- 125000000260 trans-2-phenylcyclopropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])[C@]1([H])C([H])([H])[C@@]1([H])* 0.000 claims 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 description 77
- 125000001715 oxadiazolyl group Chemical group 0.000 description 57
- 239000011435 rock Substances 0.000 description 43
- 239000012453 solvate Substances 0.000 description 29
- 150000001721 carbon Chemical group 0.000 description 21
- 125000001424 substituent group Chemical group 0.000 description 15
- 238000000034 method Methods 0.000 description 14
- 125000004429 atom Chemical group 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 125000000842 isoxazolyl group Chemical group 0.000 description 10
- 239000000651 prodrug Substances 0.000 description 10
- 229940002612 prodrug Drugs 0.000 description 10
- 229920006395 saturated elastomer Polymers 0.000 description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 239000003814 drug Substances 0.000 description 9
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 8
- 125000002950 monocyclic group Chemical group 0.000 description 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 7
- 125000003545 alkoxy group Chemical group 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 101100356682 Caenorhabditis elegans rho-1 gene Proteins 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 6
- 101150111584 RHOA gene Proteins 0.000 description 6
- 241000700159 Rattus Species 0.000 description 6
- 125000002619 bicyclic group Chemical group 0.000 description 6
- 125000004438 haloalkoxy group Chemical group 0.000 description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 125000002618 bicyclic heterocycle group Chemical group 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 125000001188 haloalkyl group Chemical group 0.000 description 5
- 125000001041 indolyl group Chemical group 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- 230000007170 pathology Effects 0.000 description 5
- 125000001544 thienyl group Chemical group 0.000 description 5
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 4
- 108091000080 Phosphotransferase Proteins 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 125000002527 bicyclic carbocyclic group Chemical group 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 229910052805 deuterium Inorganic materials 0.000 description 4
- NGOGFTYYXHNFQH-UHFFFAOYSA-N fasudil Chemical compound C=1C=CC2=CN=CC=C2C=1S(=O)(=O)N1CCCNCC1 NGOGFTYYXHNFQH-UHFFFAOYSA-N 0.000 description 4
- 229960002435 fasudil Drugs 0.000 description 4
- 125000002541 furyl group Chemical group 0.000 description 4
- 125000002883 imidazolyl group Chemical group 0.000 description 4
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- 208000001286 intracranial vasospasm Diseases 0.000 description 4
- 208000017169 kidney disease Diseases 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- 125000002971 oxazolyl group Chemical group 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- 102000020233 phosphotransferase Human genes 0.000 description 4
- 125000003373 pyrazinyl group Chemical group 0.000 description 4
- 125000004076 pyridyl group Chemical group 0.000 description 4
- 125000000168 pyrrolyl group Chemical group 0.000 description 4
- 230000019491 signal transduction Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000004434 sulfur atom Chemical group 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 125000000335 thiazolyl group Chemical group 0.000 description 4
- 125000004306 triazinyl group Chemical group 0.000 description 4
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 3
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 3
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 206010028980 Neoplasm Diseases 0.000 description 3
- 206010063837 Reperfusion injury Diseases 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 125000005605 benzo group Chemical group 0.000 description 3
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 3
- 230000036772 blood pressure Effects 0.000 description 3
- 201000011510 cancer Diseases 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- NLUNLVTVUDIHFE-UHFFFAOYSA-N cyclooctylcyclooctane Chemical compound C1CCCCCCC1C1CCCCCCC1 NLUNLVTVUDIHFE-UHFFFAOYSA-N 0.000 description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- 230000002526 effect on cardiovascular system Effects 0.000 description 3
- 235000019439 ethyl acetate Nutrition 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 230000001631 hypertensive effect Effects 0.000 description 3
- 125000002632 imidazolidinyl group Chemical group 0.000 description 3
- 238000001727 in vivo Methods 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 208000028867 ischemia Diseases 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 3
- 238000004949 mass spectrometry Methods 0.000 description 3
- 150000007522 mineralic acids Chemical class 0.000 description 3
- 125000002757 morpholinyl group Chemical group 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 231100000252 nontoxic Toxicity 0.000 description 3
- 230000003000 nontoxic effect Effects 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- 125000004193 piperazinyl group Chemical group 0.000 description 3
- 125000003386 piperidinyl group Chemical group 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 125000003226 pyrazolyl group Chemical group 0.000 description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 description 3
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 3
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 125000003831 tetrazolyl group Chemical group 0.000 description 3
- 229940124597 therapeutic agent Drugs 0.000 description 3
- 125000001113 thiadiazolyl group Chemical group 0.000 description 3
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 2
- 125000004514 1,2,4-thiadiazolyl group Chemical group 0.000 description 2
- BDNKZNFMNDZQMI-UHFFFAOYSA-N 1,3-diisopropylcarbodiimide Chemical compound CC(C)N=C=NC(C)C BDNKZNFMNDZQMI-UHFFFAOYSA-N 0.000 description 2
- BPXKZEMBEZGUAH-UHFFFAOYSA-N 2-(chloromethoxy)ethyl-trimethylsilane Chemical compound C[Si](C)(C)CCOCCl BPXKZEMBEZGUAH-UHFFFAOYSA-N 0.000 description 2
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 2
- FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 2
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 2
- 208000024827 Alzheimer disease Diseases 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- 206010003225 Arteriospasm coronary Diseases 0.000 description 2
- 125000000041 C6-C10 aryl group Chemical group 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 201000000057 Coronary Stenosis Diseases 0.000 description 2
- 208000003890 Coronary Vasospasm Diseases 0.000 description 2
- 239000007995 HEPES buffer Substances 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- GSCCALZHGUWNJW-UHFFFAOYSA-N N-Cyclohexyl-N-methylcyclohexanamine Chemical compound C1CCCCC1N(C)C1CCCCC1 GSCCALZHGUWNJW-UHFFFAOYSA-N 0.000 description 2
- 150000001204 N-oxides Chemical class 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 208000012902 Nervous system disease Diseases 0.000 description 2
- 208000025966 Neurological disease Diseases 0.000 description 2
- 102000010780 Platelet-Derived Growth Factor Human genes 0.000 description 2
- 108010038512 Platelet-Derived Growth Factor Proteins 0.000 description 2
- 201000004681 Psoriasis Diseases 0.000 description 2
- 208000001647 Renal Insufficiency Diseases 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 101100054666 Streptomyces halstedii sch3 gene Proteins 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 2
- 125000004450 alkenylene group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 125000004419 alkynylene group Chemical group 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 2
- 125000004604 benzisothiazolyl group Chemical group S1N=C(C2=C1C=CC=C2)* 0.000 description 2
- 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 description 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 2
- 125000004935 benzoxazolinyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 2
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 2
- 125000005512 benztetrazolyl group Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- YSHOWEKUVWPFNR-UHFFFAOYSA-N burgess reagent Chemical compound CC[N+](CC)(CC)S(=O)(=O)N=C([O-])OC YSHOWEKUVWPFNR-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 201000011634 coronary artery vasospasm Diseases 0.000 description 2
- 125000001162 cycloheptenyl group Chemical group C1(=CCCCCC1)* 0.000 description 2
- 230000034994 death Effects 0.000 description 2
- 231100000517 death Toxicity 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 2
- 230000035874 hyperreactivity Effects 0.000 description 2
- 238000000338 in vitro Methods 0.000 description 2
- 125000004926 indolenyl group Chemical group 0.000 description 2
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 2
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 2
- 125000001786 isothiazolyl group Chemical group 0.000 description 2
- 125000000468 ketone group Chemical group 0.000 description 2
- 201000006370 kidney failure Diseases 0.000 description 2
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 2
- 230000001404 mediated effect Effects 0.000 description 2
- 238000002483 medication Methods 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 208000004296 neuralgia Diseases 0.000 description 2
- 208000021722 neuropathic pain Diseases 0.000 description 2
- 125000004930 octahydroisoquinolinyl group Chemical group C1(NCCC2CCCC=C12)* 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 125000004095 oxindolyl group Chemical group N1(C(CC2=CC=CC=C12)=O)* 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 230000037361 pathway Effects 0.000 description 2
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 230000009862 primary prevention Effects 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 2
- 125000002098 pyridazinyl group Chemical group 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 208000037803 restenosis Diseases 0.000 description 2
- 230000009863 secondary prevention Effects 0.000 description 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 208000020431 spinal cord injury Diseases 0.000 description 2
- 150000003413 spiro compounds Chemical class 0.000 description 2
- 238000011699 spontaneously hypertensive rat Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- DPKBAXPHAYBPRL-UHFFFAOYSA-M tetrabutylazanium;iodide Chemical compound [I-].CCCC[N+](CCCC)(CCCC)CCCC DPKBAXPHAYBPRL-UHFFFAOYSA-M 0.000 description 2
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 description 2
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 description 2
- 125000004525 thiadiazinyl group Chemical group S1NN=C(C=C1)* 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- 125000001425 triazolyl group Chemical group 0.000 description 2
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 description 2
- ONDSBJMLAHVLMI-UHFFFAOYSA-N trimethylsilyldiazomethane Chemical compound C[Si](C)(C)[CH-][N+]#N ONDSBJMLAHVLMI-UHFFFAOYSA-N 0.000 description 2
- SFLSHLFXELFNJZ-QMMMGPOBSA-N (-)-norepinephrine Chemical compound NC[C@H](O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-QMMMGPOBSA-N 0.000 description 1
- CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 1
- AAZCFOYBTCRVEJ-YUMQZZPRSA-N (2S,5S)-2,5-diethylphospholane Chemical compound CC[C@H]1CC[C@H](CC)P1 AAZCFOYBTCRVEJ-YUMQZZPRSA-N 0.000 description 1
- YUXKOWPNKJSTPQ-AXWWPMSFSA-N (2s,3r)-2-amino-3-hydroxybutanoic acid;(2s)-2-amino-3-hydroxypropanoic acid Chemical compound OC[C@H](N)C(O)=O.C[C@@H](O)[C@H](N)C(O)=O YUXKOWPNKJSTPQ-AXWWPMSFSA-N 0.000 description 1
- CUKWUWBLQQDQAC-VEQWQPCFSA-N (3s)-3-amino-4-[[(2s)-1-[[(2s)-1-[[(2s)-1-[[(2s,3s)-1-[[(2s)-1-[(2s)-2-[[(1s)-1-carboxyethyl]carbamoyl]pyrrolidin-1-yl]-3-(1h-imidazol-5-yl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-methyl-1-ox Chemical compound C([C@@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](C)C(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CC(O)=O)C(C)C)C1=CC=C(O)C=C1 CUKWUWBLQQDQAC-VEQWQPCFSA-N 0.000 description 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 description 1
- 125000004605 1,2,3,4-tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 description 1
- 125000004607 1,2,3,4-tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000004502 1,2,3-oxadiazolyl group Chemical group 0.000 description 1
- 125000004511 1,2,3-thiadiazolyl group Chemical group 0.000 description 1
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 description 1
- 125000004504 1,2,4-oxadiazolyl group Chemical group 0.000 description 1
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 description 1
- 125000004506 1,2,5-oxadiazolyl group Chemical group 0.000 description 1
- PELXCSGCKOHGJH-UHFFFAOYSA-N 1,2-diethylphospholane Chemical compound C(C)C1P(CCC1)CC PELXCSGCKOHGJH-UHFFFAOYSA-N 0.000 description 1
- 125000001781 1,3,4-oxadiazolyl group Chemical group 0.000 description 1
- 125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 description 1
- LVEYOSJUKRVCCF-UHFFFAOYSA-N 1,3-Bis(diphenylphosphino)propane Substances C=1C=CC=CC=1P(C=1C=CC=CC=1)CCCP(C=1C=CC=CC=1)C1=CC=CC=C1 LVEYOSJUKRVCCF-UHFFFAOYSA-N 0.000 description 1
- MICMHFIQSAMEJG-UHFFFAOYSA-N 1-bromopyrrolidine-2,5-dione Chemical compound BrN1C(=O)CCC1=O.BrN1C(=O)CCC1=O MICMHFIQSAMEJG-UHFFFAOYSA-N 0.000 description 1
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000006017 1-propenyl group Chemical group 0.000 description 1
- 125000005955 1H-indazolyl group Chemical group 0.000 description 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- IEQAICDLOKRSRL-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-dodecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO IEQAICDLOKRSRL-UHFFFAOYSA-N 0.000 description 1
- 125000005273 2-acetoxybenzoic acid group Chemical group 0.000 description 1
- MLONYBFKXHEPCD-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(N)(CO)CO.OCC(N)(CO)CO MLONYBFKXHEPCD-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000006040 2-hexenyl group Chemical group 0.000 description 1
- YEDUAINPPJYDJZ-UHFFFAOYSA-N 2-hydroxybenzothiazole Chemical compound C1=CC=C2SC(O)=NC2=C1 YEDUAINPPJYDJZ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- 125000006022 2-methyl-2-propenyl group Chemical group 0.000 description 1
- 125000006024 2-pentenyl group Chemical group 0.000 description 1
- VSCBATMPTLKTOV-UHFFFAOYSA-N 2-tert-butylimino-n,n-diethyl-1,3-dimethyl-1,3,2$l^{5}-diazaphosphinan-2-amine Chemical compound CCN(CC)P1(=NC(C)(C)C)N(C)CCCN1C VSCBATMPTLKTOV-UHFFFAOYSA-N 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- 125000006041 3-hexenyl group Chemical group 0.000 description 1
- 229960000549 4-dimethylaminophenol Drugs 0.000 description 1
- 125000006042 4-hexenyl group Chemical group 0.000 description 1
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000003119 4-methyl-3-pentenyl group Chemical group [H]\C(=C(/C([H])([H])[H])C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000002471 4H-quinolizinyl group Chemical group C=1(C=CCN2C=CC=CC12)* 0.000 description 1
- 125000004608 5,6,7,8-tetrahydroquinolinyl group Chemical group N1=C(C=CC=2CCCCC12)* 0.000 description 1
- 125000006043 5-hexenyl group Chemical group 0.000 description 1
- 125000006163 5-membered heteroaryl group Chemical group 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- 239000005541 ACE inhibitor Substances 0.000 description 1
- 102100023818 ADP-ribosylation factor 3 Human genes 0.000 description 1
- OZAIFHULBGXAKX-VAWYXSNFSA-N AIBN Substances N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 102000007469 Actins Human genes 0.000 description 1
- 108010085238 Actins Proteins 0.000 description 1
- 102400000345 Angiotensin-2 Human genes 0.000 description 1
- 101800000733 Angiotensin-2 Proteins 0.000 description 1
- 102000015427 Angiotensins Human genes 0.000 description 1
- 108010064733 Angiotensins Proteins 0.000 description 1
- 229910015845 BBr3 Inorganic materials 0.000 description 1
- 229910015844 BCl3 Inorganic materials 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 1
- VATRNAJLMGEGHF-UHFFFAOYSA-K C(C)(=O)[O-].[Cu+2].C([O-])([O-])=O.[Cs+] Chemical compound C(C)(=O)[O-].[Cu+2].C([O-])([O-])=O.[Cs+] VATRNAJLMGEGHF-UHFFFAOYSA-K 0.000 description 1
- 102100021943 C-C motif chemokine 2 Human genes 0.000 description 1
- 101710155857 C-C motif chemokine 2 Proteins 0.000 description 1
- 229940127291 Calcium channel antagonist Drugs 0.000 description 1
- 206010007559 Cardiac failure congestive Diseases 0.000 description 1
- 229930186147 Cephalosporin Natural products 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 108020004635 Complementary DNA Proteins 0.000 description 1
- 238000006646 Dess-Martin oxidation reaction Methods 0.000 description 1
- 102400000686 Endothelin-1 Human genes 0.000 description 1
- 101800004490 Endothelin-1 Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 206010016654 Fibrosis Diseases 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 108091006027 G proteins Proteins 0.000 description 1
- 102000030782 GTP binding Human genes 0.000 description 1
- 108091000058 GTP-Binding Proteins 0.000 description 1
- 229910004373 HOAc Inorganic materials 0.000 description 1
- 101000684275 Homo sapiens ADP-ribosylation factor 3 Proteins 0.000 description 1
- 101001000061 Homo sapiens Protein phosphatase 1 regulatory subunit 12A Proteins 0.000 description 1
- 101001130437 Homo sapiens Ras-related protein Rap-2b Proteins 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 description 1
- 102000003777 Interleukin-1 beta Human genes 0.000 description 1
- 108090000193 Interleukin-1 beta Proteins 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- AZFKQCNGMSSWDS-UHFFFAOYSA-N MCPA-thioethyl Chemical compound CCSC(=O)COC1=CC=C(Cl)C=C1C AZFKQCNGMSSWDS-UHFFFAOYSA-N 0.000 description 1
- 229920001410 Microfiber Polymers 0.000 description 1
- 108010037801 Myosin-Light-Chain Phosphatase Proteins 0.000 description 1
- 102000011131 Myosin-Light-Chain Phosphatase Human genes 0.000 description 1
- 239000007832 Na2SO4 Substances 0.000 description 1
- 229910019213 POCl3 Inorganic materials 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- 208000005764 Peripheral Arterial Disease Diseases 0.000 description 1
- 208000030831 Peripheral arterial occlusive disease Diseases 0.000 description 1
- 108090000608 Phosphoric Monoester Hydrolases Proteins 0.000 description 1
- 102000004160 Phosphoric Monoester Hydrolases Human genes 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 102000001708 Protein Isoforms Human genes 0.000 description 1
- 108010029485 Protein Isoforms Proteins 0.000 description 1
- 102100036547 Protein phosphatase 1 regulatory subunit 12A Human genes 0.000 description 1
- 241000282941 Rangifer tarandus Species 0.000 description 1
- 102100027609 Rho-related GTP-binding protein RhoD Human genes 0.000 description 1
- 229940124639 Selective inhibitor Drugs 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- 102000050488 Urotensin II Human genes 0.000 description 1
- 108010018369 Urotensin II Proteins 0.000 description 1
- 206010047295 Ventricular hypertrophy Diseases 0.000 description 1
- WGOBPPNNYVSJTE-HSZRJFAPSA-N [(2r)-1-diphenylphosphanylpropan-2-yl]-diphenylphosphane Chemical compound C([C@@H](C)P(C=1C=CC=CC=1)C=1C=CC=CC=1)P(C=1C=CC=CC=1)C1=CC=CC=C1 WGOBPPNNYVSJTE-HSZRJFAPSA-N 0.000 description 1
- CKUAXEQHGKSLHN-UHFFFAOYSA-N [C].[N] Chemical group [C].[N] CKUAXEQHGKSLHN-UHFFFAOYSA-N 0.000 description 1
- HMHFSBLPBQMMCO-UHFFFAOYSA-N [Rh].C1=CCCC=CCC1.C1=CC=CC=C1 Chemical compound [Rh].C1=CCCC=CCC1.C1=CC=CC=C1 HMHFSBLPBQMMCO-UHFFFAOYSA-N 0.000 description 1
- PCNJCTGVMQGHAC-UHFFFAOYSA-N [Ru].C(C1=CC=CC=C1)=C1C(CCCC1)P(C1CCCCC1)C1CCCCC1 Chemical compound [Ru].C(C1=CC=CC=C1)=C1C(CCCC1)P(C1CCCCC1)C1CCCCC1 PCNJCTGVMQGHAC-UHFFFAOYSA-N 0.000 description 1
- 159000000021 acetate salts Chemical class 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 125000006177 alkyl benzyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 208000026935 allergic disease Diseases 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 229950006323 angiotensin ii Drugs 0.000 description 1
- 229940044094 angiotensin-converting-enzyme inhibitor Drugs 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000002393 azetidinyl group Chemical group 0.000 description 1
- 125000004931 azocinyl group Chemical group N1=C(C=CC=CC=C1)* 0.000 description 1
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 1
- RROBIDXNTUAHFW-UHFFFAOYSA-N benzotriazol-1-yloxy-tris(dimethylamino)phosphanium Chemical compound C1=CC=C2N(O[P+](N(C)C)(N(C)C)N(C)C)N=NC2=C1 RROBIDXNTUAHFW-UHFFFAOYSA-N 0.000 description 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 description 1
- FCDPQMAOJARMTG-UHFFFAOYSA-M benzylidene-[1,3-bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene]-dichlororuthenium;tricyclohexylphosphanium Chemical compound C1CCCCC1[PH+](C1CCCCC1)C1CCCCC1.CC1=CC(C)=CC(C)=C1N(CCN1C=2C(=CC(C)=CC=2C)C)C1=[Ru](Cl)(Cl)=CC1=CC=CC=C1 FCDPQMAOJARMTG-UHFFFAOYSA-M 0.000 description 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
- 239000002876 beta blocker Substances 0.000 description 1
- 229940097320 beta blocking agent Drugs 0.000 description 1
- 239000012867 bioactive agent Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010804 cDNA synthesis Methods 0.000 description 1
- 239000000480 calcium channel blocker Substances 0.000 description 1
- 125000004623 carbolinyl group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000021164 cell adhesion Effects 0.000 description 1
- 230000003915 cell function Effects 0.000 description 1
- 230000012292 cell migration Effects 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 229940124587 cephalosporin Drugs 0.000 description 1
- 150000001780 cephalosporins Chemical class 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- 230000035605 chemotaxis Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 125000004230 chromenyl group Chemical group O1C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 239000002299 complementary DNA Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000001047 cyclobutenyl group Chemical group C1(=CCC1)* 0.000 description 1
- XSYZCZPCBXYQTE-UHFFFAOYSA-N cyclodecylcyclodecane Chemical compound C1CCCCCCCCC1C1CCCCCCCCC1 XSYZCZPCBXYQTE-UHFFFAOYSA-N 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000522 cyclooctenyl group Chemical group C1(=CCCCCCC1)* 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 230000021953 cytokinesis Effects 0.000 description 1
- 125000004856 decahydroquinolinyl group Chemical group N1(CCCC2CCCCC12)* 0.000 description 1
- NKLCNNUWBJBICK-UHFFFAOYSA-N dess–martin periodinane Chemical compound C1=CC=C2I(OC(=O)C)(OC(C)=O)(OC(C)=O)OC(=O)C2=C1 NKLCNNUWBJBICK-UHFFFAOYSA-N 0.000 description 1
- 150000001975 deuterium Chemical group 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- WMKGGPCROCCUDY-PHEQNACWSA-N dibenzylideneacetone Chemical compound C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 WMKGGPCROCCUDY-PHEQNACWSA-N 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- ASWXNYNXAOQCCD-UHFFFAOYSA-N dichloro(triphenyl)-$l^{5}-phosphane Chemical compound C=1C=CC=CC=1P(Cl)(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 ASWXNYNXAOQCCD-UHFFFAOYSA-N 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 102000038379 digestive enzymes Human genes 0.000 description 1
- 108091007734 digestive enzymes Proteins 0.000 description 1
- BGRWYRAHAFMIBJ-UHFFFAOYSA-N diisopropylcarbodiimide Natural products CC(C)NC(=O)NC(C)C BGRWYRAHAFMIBJ-UHFFFAOYSA-N 0.000 description 1
- 239000002934 diuretic Substances 0.000 description 1
- 229940030606 diuretics Drugs 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 238000009510 drug design Methods 0.000 description 1
- 238000009509 drug development Methods 0.000 description 1
- 239000012636 effector Substances 0.000 description 1
- 238000000132 electrospray ionisation Methods 0.000 description 1
- 230000002124 endocrine Effects 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 210000001105 femoral artery Anatomy 0.000 description 1
- 230000004761 fibrosis Effects 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 125000003838 furazanyl group Chemical group 0.000 description 1
- 230000030414 genetic transfer Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000004995 haloalkylthio group Chemical group 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 208000019622 heart disease Diseases 0.000 description 1
- 125000006343 heptafluoro propyl group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004896 high resolution mass spectrometry Methods 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 208000013403 hyperactivity Diseases 0.000 description 1
- 125000002636 imidazolinyl group Chemical group 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 208000030603 inherited susceptibility to asthma Diseases 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- SYJRVVFAAIUVDH-UHFFFAOYSA-N ipa isopropanol Chemical compound CC(C)O.CC(C)O SYJRVVFAAIUVDH-UHFFFAOYSA-N 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 125000001977 isobenzofuranyl group Chemical group C=1(OC=C2C=CC=CC12)* 0.000 description 1
- 125000003384 isochromanyl group Chemical group C1(OCCC2=CC=CC=C12)* 0.000 description 1
- 125000005438 isoindazolyl group Chemical group 0.000 description 1
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000005956 isoquinolyl group Chemical group 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- ZEABYRLMGDTEAI-UHFFFAOYSA-M lithium;methanol;hydroxide Chemical compound [Li+].[OH-].OC ZEABYRLMGDTEAI-UHFFFAOYSA-M 0.000 description 1
- 238000011866 long-term treatment Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 239000003658 microfiber Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 210000001616 monocyte Anatomy 0.000 description 1
- 208000031225 myocardial ischemia Diseases 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000007971 neurological deficit Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 239000012457 nonaqueous media Substances 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- 229960002748 norepinephrine Drugs 0.000 description 1
- SFLSHLFXELFNJZ-UHFFFAOYSA-N norepinephrine Natural products NCC(O)C1=CC=C(O)C(O)=C1 SFLSHLFXELFNJZ-UHFFFAOYSA-N 0.000 description 1
- 230000001818 nuclear effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 125000000160 oxazolidinyl group Chemical group 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 230000008506 pathogenesis Effects 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000006194 pentinyl group Chemical group 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 description 1
- 125000004625 phenanthrolinyl group Chemical group N1=C(C=CC2=CC=C3C=CC=NC3=C12)* 0.000 description 1
- 125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- 125000005954 phenoxathiinyl group Chemical group 0.000 description 1
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 1
- 125000004928 piperidonyl group Chemical group 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 125000004591 piperonyl group Chemical group C(C1=CC=2OCOC2C=C1)* 0.000 description 1
- LYKMMUBOEFYJQG-UHFFFAOYSA-N piperoxan Chemical compound C1OC2=CC=CC=C2OC1CN1CCCCC1 LYKMMUBOEFYJQG-UHFFFAOYSA-N 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000009117 preventive therapy Methods 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- 125000002755 pyrazolinyl group Chemical group 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000001422 pyrrolinyl group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 125000004621 quinuclidinyl group Chemical group N12C(CC(CC1)CC2)* 0.000 description 1
- 238000011552 rat model Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000016487 regulation of smooth muscle contraction Effects 0.000 description 1
- 238000007634 remodeling Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000004007 reversed phase HPLC Methods 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 229940076279 serotonin Drugs 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 125000005309 thioalkoxy group Chemical group 0.000 description 1
- 125000005403 thiohaloalkoxy group Chemical group 0.000 description 1
- AXZWODMDQAVCJE-UHFFFAOYSA-L tin(II) chloride (anhydrous) Chemical compound [Cl-].[Cl-].[Sn+2] AXZWODMDQAVCJE-UHFFFAOYSA-L 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 125000006168 tricyclic group Chemical group 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- HFNHAPQMXICKCF-USJMABIRSA-N urotensin-ii Chemical compound N([C@@H](CC(O)=O)C(=O)N[C@H]1CSSC[C@H](NC(=O)[C@H](CC=2C=CC(O)=CC=2)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC=2C3=CC=CC=C3NC=2)NC(=O)[C@H](CC=2C=CC=CC=2)NC1=O)C(=O)N[C@@H](C(C)C)C(O)=O)C(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@@H](N)CCC(O)=O)[C@@H](C)O HFNHAPQMXICKCF-USJMABIRSA-N 0.000 description 1
- 210000005166 vasculature Anatomy 0.000 description 1
- 230000002227 vasoactive effect Effects 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- 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
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- 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
- A61P21/00—Drugs for disorders of the muscular or neuromuscular 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
-
- 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
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
- A61P37/02—Immunomodulators
-
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Vascular Medicine (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Gynecology & Obstetrics (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361770508P | 2013-02-28 | 2013-02-28 | |
| US201361770508P | 2013-02-28 | ||
| PCT/US2014/019237 WO2014134388A1 (en) | 2013-02-28 | 2014-02-28 | Phenylpyrazole derivatives as potent rock1 and rock2 inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2624664T3 true ES2624664T3 (es) | 2017-07-17 |
Family
ID=50288312
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES14710732.0T Active ES2624664T3 (es) | 2013-02-28 | 2014-02-28 | Derivados de fenilpirazol como potentes inhibidores de ROCK1 y ROCK2 |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US9458110B2 (OSRAM) |
| EP (1) | EP2961745B1 (OSRAM) |
| JP (1) | JP6423371B2 (OSRAM) |
| CN (1) | CN105358547B (OSRAM) |
| AR (1) | AR094929A1 (OSRAM) |
| ES (1) | ES2624664T3 (OSRAM) |
| TW (1) | TW201444798A (OSRAM) |
| WO (1) | WO2014134388A1 (OSRAM) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105102448B (zh) | 2013-02-28 | 2018-03-06 | 百时美施贵宝公司 | 作为rock1和rock2抑制剂的苯基吡唑衍生物 |
| US9902702B2 (en) | 2014-07-15 | 2018-02-27 | Bristol-Myers Squibb Company | Spirocycloheptanes as inhibitors of rock |
| WO2016028971A1 (en) | 2014-08-21 | 2016-02-25 | Bristol-Myers Squibb Company | Tied-back benzamide derivatives as potent rock inhibitors |
| TW201630899A (zh) * | 2015-01-09 | 2016-09-01 | 必治妥美雅史谷比公司 | 作為rock抑制劑的環狀脲類 |
| TW201706265A (zh) * | 2015-03-09 | 2017-02-16 | 必治妥美雅史谷比公司 | 做為Rho激酶(ROCK)抑制劑之內醯胺 |
| TWI730032B (zh) | 2016-01-13 | 2021-06-11 | 美商必治妥美雅史谷比公司 | 作為rock抑制劑之螺庚烷水楊酸醯胺及相關化合物 |
| KR102457933B1 (ko) * | 2016-05-27 | 2022-10-24 | 브리스톨-마이어스 스큅 컴퍼니 | Rock의 억제제로서의 트리아졸론 및 테트라졸론 |
| US10787450B2 (en) | 2016-07-07 | 2020-09-29 | Bristol-Myers Squibb Company | Spiro-fused cyclic ureas as inhibitors of rock |
| KR102491994B1 (ko) * | 2016-07-07 | 2023-01-25 | 브리스톨-마이어스 스큅 컴퍼니 | Rock의 억제제로서의 스피로락탐 |
| CN109689652B (zh) * | 2016-08-23 | 2022-04-26 | 北京诺诚健华医药科技有限公司 | 稠杂环类衍生物、其制备方法及其在医学上的应用 |
| IL266150B2 (en) * | 2016-10-24 | 2023-12-01 | Translational Drug Dev Llc | 3-substituted benzamide derivatives as kinase inhibitors |
| KR102511441B1 (ko) * | 2016-11-30 | 2023-03-16 | 브리스톨-마이어스 스큅 컴퍼니 | 트리시클릭 Rho 키나제 억제제 |
| US11046683B2 (en) | 2016-12-15 | 2021-06-29 | Ono Pharmaceutical Co., Ltd. | Activator of TREK (TWIK RElated K+ channels) channels |
| CN108203433B (zh) * | 2016-12-16 | 2020-07-03 | 成都先导药物开发股份有限公司 | 一种rock抑制剂及其应用 |
| US12060341B2 (en) | 2017-07-12 | 2024-08-13 | Bristol-Myers Squibb Company | Spiroheptanyl hydantoins as ROCK inhibitors |
| US11299488B2 (en) | 2017-07-12 | 2022-04-12 | Bristol-Myers Squibb Company | Five membered-aminoheterocycle and 5,6-or 6,6-membered bicyclic aminoheterocyclic inhibitors of rock for the treatment of heart failure |
| US11306081B2 (en) | 2017-07-12 | 2022-04-19 | Bristol-Myers Squibb Company | Phenylacetamides as inhibitors of rock |
| TW201908293A (zh) | 2017-07-12 | 2019-03-01 | 美商必治妥美雅史谷比公司 | 作為rock抑制劑之5員及雙環雜環醯胺 |
| KR102644889B1 (ko) | 2017-07-12 | 2024-03-06 | 브리스톨-마이어스 스큅 컴퍼니 | Rock 억제제로서의 스피로헵타닐 히단토인 |
| US11230541B2 (en) | 2017-07-28 | 2022-01-25 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
| US11192891B2 (en) | 2017-11-03 | 2021-12-07 | Bristol-Myers Squibb Company | Diazaspiro ROCK inhibitors |
| EP3768661B1 (en) * | 2018-03-23 | 2024-05-01 | Fochon Pharmaceuticals, Ltd. | Deuterated compounds as rock inhibitors |
| JP7187575B2 (ja) | 2018-04-18 | 2022-12-12 | メッドシャイン ディスカバリー インコーポレイテッド | Rhoキナーゼ阻害剤としてのベンゾピラゾール系化合物 |
| EP3784226B1 (en) | 2018-04-24 | 2024-08-14 | Translational Drug Development Llc | Pyrazole-phenylamide derivatives as inhibitors of the rho-associated protein kinase rock1 and rock2 for the treatment of cancer |
| CN109020977B (zh) * | 2018-10-26 | 2020-11-13 | 安庆奇创药业有限公司 | 一种Acalabrutinib的制备方法 |
| JP2021050161A (ja) | 2019-09-25 | 2021-04-01 | 武田薬品工業株式会社 | 複素環化合物及びその用途 |
| WO2021073592A1 (zh) | 2019-10-18 | 2021-04-22 | 南京明德新药研发有限公司 | 作为rho激酶抑制剂的苯并吡唑类化合物的盐型、晶型及其制备方法 |
| CN116438175B (zh) * | 2020-11-11 | 2025-07-22 | 南京明德新药研发有限公司 | 苯并脲环衍生物及其制备方法和应用 |
Family Cites Families (192)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3487851B2 (ja) | 1992-02-05 | 2004-01-19 | ベーリンガー インゲルハイム コマンディトゲゼルシャフト | 新規なアミジン誘導体、その製法、及びltb4拮抗剤としての使用 |
| KR100238346B1 (ko) | 1993-04-07 | 2000-03-02 | 오쓰까 아끼히꼬 | 피페리딘 유도체를 유효성분으로 하는 말초혈관확장제 |
| CA2155662A1 (en) | 1993-12-27 | 1995-07-06 | Fumihiro Ozaki | Anthranilic acid derivative |
| GB9500580D0 (en) | 1995-01-12 | 1995-03-01 | Merck Sharp & Dohme | Therapeutic agents |
| US5763618A (en) | 1995-05-12 | 1998-06-09 | Konica Corporation | Manufacturing method of sulfides |
| DE19545878A1 (de) | 1995-12-08 | 1997-06-12 | Basf Ag | Pyridylcarbamate, Verfahren und Zwischenprodukte zu ihrer Herstellung und ihre Verwendung |
| EP0892780B1 (en) | 1996-02-22 | 2002-11-20 | Bristol-Myers Squibb Pharma Company | M-AMIDINO PHENYL ANALOGS AS FACTOR Xa INHIBITORS |
| CA2249645A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| DE69720773T2 (de) | 1996-12-23 | 2004-01-29 | Bristol Myers Squibb Pharma Co | SAUERSTOFF ODER SCHWEFEL ENTHALTENDE 5-GLIEDRIGE HETEROAROMATISHE DERIVATIVE ALS FACTOR Xa HEMMER |
| US6187797B1 (en) | 1996-12-23 | 2001-02-13 | Dupont Pharmaceuticals Company | Phenyl-isoxazoles as factor XA Inhibitors |
| US6020357A (en) | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
| EP0946508B1 (en) | 1996-12-23 | 2009-09-23 | Bristol-Myers Squibb Pharma Company | NITROGEN CONTAINING HETEROAROMATICS AS FACTOR Xa INHIBITORS |
| PT991625E (pt) | 1997-06-19 | 2005-10-31 | Bristol Myers Squibb Pharma Co | Inibidores de factor xa com um grupo de especificidade p1 neutro |
| US6339099B1 (en) | 1997-06-20 | 2002-01-15 | Dupont Pharmaceuticals Company | Guanidine mimics as factor Xa inhibitors |
| US6511974B1 (en) | 1997-07-30 | 2003-01-28 | Wyeth | Tricyclic vasopressin agonists |
| DE69826677T2 (de) | 1997-07-30 | 2005-02-10 | Wyeth | Trizyclische Vasopressin-Agonisten |
| DK1000062T3 (da) | 1997-07-30 | 2004-11-22 | Wyeth Corp | Tricykliske vasopressinagonister |
| AU3665199A (en) | 1998-04-29 | 1999-11-16 | Vertex Pharmaceuticals Incorporated | Inhibitors of impdh enzyme |
| CN1308625A (zh) | 1998-05-12 | 2001-08-15 | 美国家用产品公司 | 萘并[2,3-b]杂芳-4-基衍生物 |
| US6121271A (en) | 1998-05-12 | 2000-09-19 | American Home Products Corporation | Naphtho[2,3-B]heteroar-4-yl derivatives |
| JP2000109465A (ja) | 1998-08-05 | 2000-04-18 | Nippon Soda Co Ltd | フェニルピラゾ―ル化合物、製法及び抗高脂血症薬 |
| WO2000026197A1 (en) | 1998-10-29 | 2000-05-11 | Bristol-Myers Squibb Company | Novel inhibitors of impdh enzyme |
| WO2000029399A1 (en) | 1998-11-12 | 2000-05-25 | Boehringer Ingelheim (Canada) Ltd. | Antiherpes compounds |
| DK1149096T3 (da) | 1999-02-04 | 2003-04-07 | Wyeth Corp | Tricykliske pyridin-N-oxider som vasopressinagonister |
| JP2000256358A (ja) | 1999-03-10 | 2000-09-19 | Yamanouchi Pharmaceut Co Ltd | ピラゾール誘導体 |
| CN101070316A (zh) | 1999-04-28 | 2007-11-14 | 萨诺费-阿文蒂斯德国有限公司 | 作为ppar受体配体的二芳基酸衍生物 |
| CA2385971A1 (en) | 1999-09-27 | 2001-04-05 | American Cyanamid Company | Vasopressin agonist formulation and process |
| AU2001239725A1 (en) | 2000-01-13 | 2001-07-24 | Tularik, Inc. | Antibacterial agents |
| WO2001068605A1 (en) | 2000-03-13 | 2001-09-20 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted benzenes useful for selective inhibition of the coagulation cascade |
| MY138097A (en) | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
| AU2001273040A1 (en) | 2000-06-27 | 2002-01-08 | Du Pont Pharmaceuticals Company | Factor xa inhibitors |
| DE10063008A1 (de) | 2000-12-16 | 2002-06-20 | Merck Patent Gmbh | Carbonsäureamidderivate |
| AU2002248432A1 (en) | 2001-02-14 | 2002-08-28 | Sankyo Company, Limited | Oxazole derivatives, their preparation and their use as cytokine inhibitors |
| PL364660A1 (en) | 2001-03-05 | 2004-12-13 | E.I.Du Pont De Nemours And Company | Heterocyclic diamide invertebrate pest control agents |
| DE10110749A1 (de) | 2001-03-07 | 2002-09-12 | Bayer Ag | Substituierte Aminodicarbonsäurederivate |
| DE10111842A1 (de) | 2001-03-13 | 2002-09-19 | Boehringer Ingelheim Pharma | Antithrombotische Carbonsäureamide, deren Herstellung und deren Verwendung als Arzneimittel |
| US7241785B2 (en) | 2001-03-23 | 2007-07-10 | Takeda Pharmaceutical Company Limited | Five-membered heterocyclic alkanoic acid derivative |
| JP2004535411A (ja) | 2001-05-25 | 2004-11-25 | ブリストルーマイヤーズ スクイブ カンパニー | マトリックスメタロプロテナーゼ及び/またはTNF−α転換酵素(TACE)の阻害剤としてのヒダントイン及び関連複素環化合物 |
| DE10130374A1 (de) | 2001-06-23 | 2003-01-02 | Boehringer Ingelheim Pharma | Substituierte N-Acyl-anilinderivate, deren Herstellung und deren Verwendung als Arzneimittel |
| CZ20033437A3 (cs) | 2001-06-28 | 2004-09-15 | Smithkline Beecham P.L.C. | N-Aroylové cyklické aminové deriváty jako antagonisté orexinového receptoru |
| GB0115862D0 (en) | 2001-06-28 | 2001-08-22 | Smithkline Beecham Plc | Compounds |
| WO2003004474A1 (en) | 2001-07-06 | 2003-01-16 | Syngenta Participations Ag | Pesticidally active aminoacetonitriles |
| CA2456187A1 (en) | 2001-08-03 | 2003-02-13 | Qing Tang | Pyrazole-derived kinase inhibitors and uses thereof |
| GB0124463D0 (en) | 2001-10-11 | 2001-12-05 | Smithkline Beecham Plc | Compounds |
| SE0103644D0 (sv) | 2001-11-01 | 2001-11-01 | Astrazeneca Ab | Therapeutic isoquinoline compounds |
| US6984735B2 (en) | 2001-12-03 | 2006-01-10 | Wyeth | Process for making an aldehyde |
| AU2003220401A1 (en) | 2002-03-18 | 2003-10-08 | Bristol-Myers Squibb Company | Uracil derivatives as inhibitors of tnf-alpha converting enzyme (tace) and matrix metalloproteinases |
| WO2003082826A1 (en) | 2002-03-28 | 2003-10-09 | Neurogen Corporation | Substituted biaryl amides as c5a receptor modulators |
| US6846838B2 (en) | 2002-06-19 | 2005-01-25 | Bristol-Myers Squibb Company | Ureido-substituted aniline compounds useful as serine protease inhibitors |
| US20040044041A1 (en) | 2002-08-06 | 2004-03-04 | Kuduk Scott D. | 2-(Biarylalkyl)amino-3-(cyanoalkanoylamino)pyridine derivatives |
| WO2004016592A1 (en) | 2002-08-14 | 2004-02-26 | Ppd Discovery, Inc. | Prenylation inhibitors and methods of their synthesis and use |
| US7041693B2 (en) | 2002-10-04 | 2006-05-09 | Bristol-Myers Squibb Company | Hydantoin derivatives as inhibitors of matrix metalloproteinases and/or TNF-α converting enzyme (TACE) |
| US20040082641A1 (en) | 2002-10-28 | 2004-04-29 | Rytved Klaus Asger | Use of glycogen phosphorylase inhibitors for treatment of cardiovascular diseases |
| AU2003276201A1 (en) | 2002-11-11 | 2004-06-03 | Bayer Healthcare Ag | Phenyl or heteroaryl amino alkane derivatives as ip receptor antagonist |
| JP2004161716A (ja) | 2002-11-15 | 2004-06-10 | Takeda Chem Ind Ltd | Jnk阻害剤 |
| CA2515544A1 (en) | 2003-02-11 | 2004-08-26 | Kemia Inc. | Compounds for the treatment of viral infection |
| DE10306250A1 (de) | 2003-02-14 | 2004-09-09 | Aventis Pharma Deutschland Gmbh | Substituierte N-Arylheterozyklen, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| CA2522080A1 (en) | 2003-04-14 | 2004-10-28 | The Institutes For Pharmaceutical Discovery, Llc | N- (((((1,3-thiazol-2-yl) amino) carbonyl) phenyl) sulfonyl) phenylalanine derivatives and related compounds for the treatment of diabetes |
| WO2005000813A1 (en) | 2003-05-30 | 2005-01-06 | Imclone Systems Incorporated | Heteroarylamino-phenylketone derivatives and their use as kinase inhibitors |
| EP1650206A4 (en) | 2003-08-01 | 2006-12-20 | Nippon Soda Co | PHENYLAZOLE COMPOUNDS, PROCESS FOR THEIR PRODUCTION AND ANTIOXIDANTS |
| US7485658B2 (en) | 2003-08-21 | 2009-02-03 | Osi Pharmaceuticals, Inc. | N-substituted pyrazolyl-amidyl-benzimidazolyl c-Kit inhibitors |
| EP1664032B1 (en) | 2003-08-21 | 2008-11-05 | OSI Pharmaceuticals, Inc. | N-substituted pyrazolyl-amidyl-benzimidazolyl c-kit inhibitors |
| JP5010917B2 (ja) | 2003-08-29 | 2012-08-29 | エグゼリクシス, インコーポレイテッド | c−Kit調節因子および使用方法 |
| EP1786815B1 (en) | 2003-09-10 | 2011-08-24 | Virochem Pharma Inc. | Spiro compounds and methods for the modulation of chemokine receptor activity |
| US7211671B2 (en) | 2003-10-01 | 2007-05-01 | Bristol Myers Squibb Company | Substituted 1,3-dihydro-imidazol-2-one and 1,3-dihydro-imidazol-2-thione derivatives as inhibitors of matrix metalloproteinases and/or TNF-α converting enzyme (TACE) |
| CA2541458C (en) | 2003-10-08 | 2011-09-20 | Eli Lilly And Company | Pyrrole and pyrazole derivatives as potentiators of glutamate receptors |
| US20050187409A1 (en) | 2003-10-21 | 2005-08-25 | Powers Gordon D. | Inhibitors of RNase P proteins as antibacterial compounds |
| JP2007519754A (ja) * | 2004-01-30 | 2007-07-19 | スミスクライン ビーチャム コーポレーション | 化合物 |
| EP1574502A1 (en) | 2004-03-08 | 2005-09-14 | Novartis AG | Use of pyrimidine compounds in the preparation of parasiticides |
| CA2578789A1 (en) | 2004-09-03 | 2006-03-16 | Celgene Corporation | Substituted heterocyclic compounds and uses thereof |
| AU2005302475A1 (en) | 2004-10-28 | 2006-05-11 | The Institutes For Pharmaceutical Discovery, Llc | Substituted phenylalkanoic acids |
| EP1831176A2 (en) | 2004-12-21 | 2007-09-12 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
| US8329703B2 (en) | 2005-02-15 | 2012-12-11 | Xtl Biopharmaceuticals Ltd. | Pyrazole compounds |
| EP1863756A1 (en) | 2005-03-24 | 2007-12-12 | Janssen Pharmaceutica N.V. | Biaryl derived amide modulators of vanilloid vr1 receptor |
| MX2008000141A (es) | 2005-06-27 | 2008-04-07 | Exelixis Inc | Moduladores de lxr basados en imidazol. |
| FR2887548B1 (fr) | 2005-06-27 | 2007-09-21 | Sanofi Aventis Sa | Derives de 4,5-diarylpyrrole, leur preparation et leur application en therapeutique |
| FR2888237B1 (fr) | 2005-07-08 | 2007-08-31 | Sanofi Aventis Sa | Derives de n-[(4,5-diphenylpyrimidin-2-yl)methyl] amine, leur preparation et leur application en therapeutique |
| AR057450A1 (es) | 2005-07-12 | 2007-12-05 | Sanofi Aventis | Derivados de n-[(1,2-difenil-1h-imidazol-4- il)metil]amina su preparacion y su aplicacion en terapeutica |
| RU2008110949A (ru) | 2005-08-23 | 2009-09-27 | Айрм Ллк (Bm) | Соединения и композиции-иммуносупрессанты |
| US7906652B2 (en) | 2005-11-28 | 2011-03-15 | Merck Sharp & Dohme Corp. | Heterocycle-substituted 3-alkyl azetidine derivatives |
| FR2894579B1 (fr) | 2005-12-12 | 2008-01-18 | Sanofi Aventis Sa | Derives diaryltriazolmethylamine, leur preparation et leur application en therapeutique. |
| FR2894578B1 (fr) | 2005-12-12 | 2008-02-01 | Sanofi Aventis Sa | Derives heterocycliques, leur preparation et leur application en therapeutique. |
| JP2009520820A (ja) | 2005-12-20 | 2009-05-28 | メルク エンド カムパニー インコーポレーテッド | ナイアシン受容体アゴニスト、前記化合物を含む組成物及び治療方法 |
| SI1962830T1 (sl) | 2005-12-23 | 2013-07-31 | Glaxosmithkline Llc | Azaindolni inhibitorji kinaz Aurora |
| MX2008010668A (es) | 2006-02-21 | 2008-10-01 | Amgen Inc | Derivados de cinolina como inhibidores de fosfodiesterasa 10. |
| AU2012200157B2 (en) | 2006-05-25 | 2014-08-21 | Synta Pharmaceuticals Corp. | Method for treating proliferative disorders associated with protooncogene products |
| WO2007146230A2 (en) | 2006-06-14 | 2007-12-21 | Merck & Co., Inc. | Non-nucleoside reverse transcriptase inhibitors |
| US9108948B2 (en) | 2006-06-23 | 2015-08-18 | Abbvie Inc. | Cyclopropyl amine derivatives |
| RU2424233C2 (ru) | 2006-06-29 | 2011-07-20 | Ф.Хоффманн-Ля Рош Аг | Производные бензимидазола, методы их получения, применение их в качестве агонистов фарнезоид-х-рецептора (fxr) и содержащие их фармацевтические препараты |
| BRPI0712795A2 (pt) | 2006-07-07 | 2012-09-04 | Boehringer Ingelheim Int | derivados de heteroarila substituìdos com fenila e uso dos mesmos como agentes antitumorais |
| WO2008016643A2 (en) | 2006-08-01 | 2008-02-07 | Cytokinetics, Incorporated | Certain chemical entities, compositions, and methods |
| FR2904827B1 (fr) | 2006-08-11 | 2008-09-19 | Sanofi Aventis Sa | Derives de 5,6-bisaryl-2-pyridine-carboxamide, leur preparation et leur application en therapeutique comme antiganistes des recepteurs a l'urotensine ii |
| CN101511828A (zh) | 2006-09-06 | 2009-08-19 | 霍夫曼-拉罗奇有限公司 | 作为蛋白激酶抑制剂的杂芳基衍生物 |
| WO2008057246A2 (en) | 2006-10-26 | 2008-05-15 | Synta Pharmaceuticals Corp. | Method for treating inflammatory disorders |
| WO2008064310A2 (en) | 2006-11-22 | 2008-05-29 | University Of Medicine And Dentistry Of New Jersey | Mixed opioid receptor active compounds |
| WO2008064317A1 (en) | 2006-11-22 | 2008-05-29 | University Of Medicine And Dentistry Of New Jersey | Lipophilic opioid receptor active compounds |
| WO2008064318A2 (en) | 2006-11-22 | 2008-05-29 | University Of Medicine And Dentistry Of New Jersey | Peripheral opioid receptor active compounds |
| EP2684871B1 (en) | 2006-12-19 | 2016-05-04 | F. Hoffmann-La Roche AG | Heteroaryl pyrrolidinyl and piperidinyl ketone derivatives |
| EP2079694B1 (en) | 2006-12-28 | 2017-03-01 | Rigel Pharmaceuticals, Inc. | N-substituted-heterocycloalkyloxybenzamide compounds and methods of use |
| FR2911136B1 (fr) | 2007-01-05 | 2009-02-20 | Sanofi Aventis Sa | Derives de n-(4-cyano-1h-pyrazol-3-yl)methylamine substitues leur preparation et leur application en therapeutique. |
| WO2008088692A2 (en) | 2007-01-12 | 2008-07-24 | Merck & Co., Inc. | Spirochromanon derivatives |
| TW200838516A (en) | 2007-01-31 | 2008-10-01 | Merck & Co Inc | Substituted pyrano[2,3-B]pyridine derivatives as cannabinoid-1 receptor modulators |
| JP2008195655A (ja) | 2007-02-14 | 2008-08-28 | Kitasato Institute | 糖尿病白内障の治療剤 |
| WO2008137102A2 (en) | 2007-05-04 | 2008-11-13 | Torreypines Therapeutics, Inc. | Methods of modulating amyloid beta and compounds useful therefor |
| EP1992625A1 (en) | 2007-05-16 | 2008-11-19 | Sanofi-Aventis | Arylamide pyrimidone compounds |
| WO2008141731A2 (en) | 2007-05-18 | 2008-11-27 | Bayer Healthcare Ag | Inhibitors of hypoxia inducible factor (hif) useful for treating hyper-proliferative disorders and diseases associated with angiogenesis |
| WO2008147518A1 (en) | 2007-05-23 | 2008-12-04 | Merck & Co., Inc. | Pyridyl piperidine orexin receptor antagonists |
| AR066834A1 (es) | 2007-06-06 | 2009-09-16 | Janssen Pharmaceutica Nv | Espirobenzoazepanos como antagonistas de vasopresina, composiciones farmaceuticas que los contienen, proceso de preparacion y usos para el tratamiento de afecciones cardiacas, renales y del sistema nervioso central. |
| EP2002838A1 (de) | 2007-06-13 | 2008-12-17 | Bayer Schering Pharma AG | Verwendung von Aryl/Hetarylamid-Derivaten als Modulatoren des EP2-Rezeptors |
| CA2690460A1 (en) | 2007-06-15 | 2008-12-18 | Markus Nett | Method for producing difluoromethyl-substituted pyrazole compounds |
| US20100240657A1 (en) | 2007-07-02 | 2010-09-23 | Boehringer Ingelheim International Gmbh | Chemical compounds |
| EP2200440B1 (en) * | 2007-07-23 | 2017-07-19 | Crestone, Inc. | Antibacterial amide and sulfonamide substituted heterocyclic urea compounds |
| EP2190466A4 (en) | 2007-08-10 | 2011-12-21 | Burnham Inst Medical Research | Tissue-specific alkaline phosphatase (TNAP) activators and their use |
| EP2193119B1 (en) * | 2007-08-27 | 2014-01-01 | Abbvie Deutschland GmbH & Co. KG | 4-(4-pyridinyl)-benzamides and their use as rock activity modulators |
| TW200920357A (en) | 2007-09-10 | 2009-05-16 | Curis Inc | HSP90 inhibitors containing a zinc binding moiety |
| WO2009036051A1 (en) | 2007-09-10 | 2009-03-19 | Curis, Inc. | Bcl-2 inhibitors containing a zinc binding moiety |
| KR20090033583A (ko) | 2007-10-01 | 2009-04-06 | 주식회사 엘지생명과학 | 글라이신 아릴 아마이드를 포함하는 신규한베타-세크리타제 저해용 화합물 |
| HRP20110953T1 (hr) | 2007-10-17 | 2012-01-31 | Sanofi | Supstituirani n-fenilbipirolidinkarboksamidi i njihova upotreba u terapiji |
| TWI440638B (zh) | 2007-10-30 | 2014-06-11 | Otsuka Pharma Co Ltd | 雜環化合物及其藥學組成物 |
| WO2009061676A2 (en) | 2007-11-06 | 2009-05-14 | Amira Pharmaceuticals, Inc. | Antagonists of pgd2 receptors |
| US8426595B2 (en) | 2007-12-11 | 2013-04-23 | Xianhai Huang | Gamma secretase modulators |
| CA2709879A1 (en) * | 2007-12-19 | 2009-06-25 | The Scripps Research Institute | Anilides and analogs as rho kinase inhibitors |
| US20110150833A1 (en) | 2007-12-21 | 2011-06-23 | The Scripps Research Institute | Benzopyrans and analogs as rho kinase inhibitors |
| CN101538245B (zh) | 2008-03-18 | 2011-02-16 | 中国科学院上海药物研究所 | 一类哒嗪酮类化合物及其制备方法和制备药物的用途 |
| EP2282742A1 (en) | 2008-04-09 | 2011-02-16 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
| EP2269993B1 (en) | 2008-04-23 | 2013-02-27 | Kyowa Hakko Kirin Co., Ltd. | 2-aminoquinazoline derivative |
| EP2278878A4 (en) | 2008-05-08 | 2014-08-27 | Bristol Myers Squibb Co | 2-ARYL-GYCINAMID DERIVATIVES |
| CN101597278B (zh) | 2008-06-04 | 2013-04-17 | 中国中化股份有限公司 | 酰胺类化合物及其制备与应用 |
| EP2361248B1 (en) | 2008-06-27 | 2018-09-19 | Celgene CAR LLC | Heteroaryl compounds and uses thereof |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| US8623238B2 (en) | 2008-06-27 | 2014-01-07 | Transitions Optical, Inc. | Mesogenic stabilizers |
| WO2010036316A1 (en) | 2008-09-24 | 2010-04-01 | Yangbo Feng | Urea and carbamate compounds and analogs as kinase inhibitors |
| US20100130522A1 (en) | 2008-10-01 | 2010-05-27 | Synta Pharmaceuticals Corp. | Compounds for inflammation and immune-related uses |
| WO2010040274A1 (zh) | 2008-10-10 | 2010-04-15 | 中国人民解放军军事医学科学院毒物药物研究所 | 新型多巴胺d3受体配体,其制备方法及其医药用途 |
| EP2375904B1 (en) | 2008-12-09 | 2014-05-28 | Merck Sharp & Dohme Corp. | Biaryl carboxamides |
| EP2379524A1 (en) | 2008-12-18 | 2011-10-26 | Boehringer Ingelheim International GmbH | Serotonin 5-ht2b receptor inhibitors |
| WO2010075290A1 (en) | 2008-12-22 | 2010-07-01 | President And Fellows Of Harvard College | Unsaturated heterocyclic inhibitors of necroptosis |
| WO2010093849A2 (en) | 2009-02-13 | 2010-08-19 | Amgen Inc. | Phenylalanine amide derivatives useful for treating insulin-related diseases and conditions |
| JP5688918B2 (ja) | 2009-04-28 | 2015-03-25 | 大塚製薬株式会社 | 医薬組成物 |
| WO2010129848A2 (en) | 2009-05-08 | 2010-11-11 | Takeda Pharmaceutical Company Limited | 2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxamides |
| EP2440048B8 (en) | 2009-06-09 | 2015-12-16 | NantBioScience, Inc. | Isoquinoline, quinoline, and quinazoline derivatives as inhibitors of hedgehog signaling |
| TW201103904A (en) * | 2009-06-11 | 2011-02-01 | Hoffmann La Roche | Janus kinase inhibitor compounds and methods |
| US20120189670A1 (en) | 2009-09-14 | 2012-07-26 | Kirkpatrick D Lynn | Pharmaceutical compositions and formulations including inhibitors of the pleckstrin homology domain and methods for using same |
| WO2011041593A1 (en) | 2009-09-30 | 2011-04-07 | University Of Kansas | Novobiocin analogues and treatment of polycystic kidney disease |
| US8993612B2 (en) | 2009-10-08 | 2015-03-31 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel and methods for treatment of non-small cell lung cancer |
| US8377970B2 (en) | 2009-10-08 | 2013-02-19 | Rhizen Pharmaceuticals Sa | Modulators of calcium release-activated calcium channel |
| EP2499139B1 (en) | 2009-11-10 | 2013-12-11 | Pfizer Inc | N1-pyrazolospiroketone acetyl-coa carboxylase inhibitors |
| US20120225900A1 (en) | 2009-11-10 | 2012-09-06 | Pfizer Inc. | N2-pyrazolospiroketone acetyl-coa carboxylase inhibitors |
| US8394858B2 (en) | 2009-12-03 | 2013-03-12 | Novartis Ag | Cyclohexane derivatives and uses thereof |
| CN102812003B (zh) | 2009-12-18 | 2015-01-21 | 欧洲筛选有限公司 | 吡咯烷羧酸衍生物、药物组合物以及在代谢紊乱中作为g-蛋白偶联受体43(gpr43)激动剂使用的方法 |
| JP2013047188A (ja) | 2009-12-24 | 2013-03-07 | Nippon Chemiphar Co Ltd | Gpr119作動薬 |
| MX2012008141A (es) | 2010-01-13 | 2012-08-03 | Glaxosmithkline Llc | Compuestos y metodos. |
| WO2011088181A1 (en) | 2010-01-13 | 2011-07-21 | Tempero Pharmaceuticals, Inc. | Compounds and methods |
| WO2011088031A1 (en) | 2010-01-13 | 2011-07-21 | Glaxosmithkline Llc | Compounds and methods |
| KR20120130104A (ko) | 2010-02-01 | 2012-11-28 | 닛뽕 케미파 가부시키가이샤 | Gpr119 작동약 |
| JP5850321B2 (ja) | 2010-02-10 | 2016-02-03 | 公立大学法人横浜市立大学 | 神経選択的転写抑制因子NRSFに特異的に結合するmSin3Bに結合する化合物の利用 |
| WO2011106632A1 (en) | 2010-02-26 | 2011-09-01 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
| US8354410B2 (en) | 2010-03-11 | 2013-01-15 | Bristol-Meyers Squibb Company | Compounds for the treatment of hepatitis C |
| EP2545042A1 (en) | 2010-03-11 | 2013-01-16 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis c |
| WO2011140425A1 (en) | 2010-05-06 | 2011-11-10 | Vertex Pharmaceuticals Incorporated | Heterocyclic chromene-spirocyclic piperidine amides as modulators of ion channels |
| WO2011156557A2 (en) | 2010-06-11 | 2011-12-15 | Thomas James B | Compounds active at the neurotensin receptor |
| US8697911B2 (en) | 2010-07-07 | 2014-04-15 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| US9079880B2 (en) | 2010-07-07 | 2015-07-14 | Boehringer Ingelheim International Gmbh | Rho kinase inhibitors |
| EP2606051B1 (en) | 2010-08-20 | 2016-10-05 | Hutchison Medipharma Limited | Pyrrolopyrimidine compounds and uses thereof |
| WO2012040444A2 (en) | 2010-09-24 | 2012-03-29 | Bristol-Myers Squibb Company | Treatment of patients with incipient alzheimer's disease |
| US9085570B2 (en) | 2010-10-11 | 2015-07-21 | The Board Of Trustees Of The Leland Stanford Junior University | Substituted benzamides and their uses |
| CN102451178A (zh) | 2010-10-29 | 2012-05-16 | 中国科学院上海药物研究所 | 二氢呋喃-2-酮类化合物在制备抗糖尿病及糖脂代谢药物中的用途 |
| WO2012068210A1 (en) | 2010-11-18 | 2012-05-24 | Janssen Pharmaceutica Nv | Pyridyl-thiazolyl inhibitors of pro-matrix metalloproteinase activation |
| US8653270B2 (en) | 2010-11-22 | 2014-02-18 | Allergan, Inc. | Compounds as receptor modulators with therapeutic utility |
| EP2457900A1 (en) | 2010-11-25 | 2012-05-30 | Almirall, S.A. | New pyrazole derivatives having CRTh2 antagonistic behaviour |
| PH12013501103A1 (en) | 2010-12-01 | 2021-06-02 | Nissan Chemical Ind Ltd | Pyrazole compounds having therapeutic effect on multiple myeloma |
| EP2647697B1 (en) | 2010-12-01 | 2016-08-24 | Nissan Chemical Industries, Ltd. | Method for producing hematopoietic stem cells using pyrazole compound |
| AU2011338561A1 (en) | 2010-12-07 | 2013-07-25 | Amira Pharmaceuticals, Inc. | Lysophosphatidic acid receptor antagonists and their use in the treatment of fibrosis |
| GB201021104D0 (en) | 2010-12-13 | 2011-01-26 | Univ Leuven Kath | Novel compounds for the treatment of neurodegenerative diseases |
| TW201604196A (zh) | 2011-02-02 | 2016-02-01 | 維泰克斯製藥公司 | 作為離子通道調節劑之吡咯并吡-螺環哌啶醯胺 |
| GB201104267D0 (en) | 2011-03-14 | 2011-04-27 | Cancer Rec Tech Ltd | Pyrrolopyridineamino derivatives |
| JP6042406B2 (ja) | 2011-03-28 | 2016-12-14 | メイ プハルマ,インコーポレーテッド | (α−置換アラルキルアミノ及びヘテロアリールアルキルアミノ)ピリミジニル及び1,3,5−トリアジニルベンズイミダゾール、それらを含む医薬組成物、並びに増殖性疾患の治療で使用するためのこれらの化合物 |
| WO2012135697A2 (en) | 2011-03-30 | 2012-10-04 | H. Lee Moffitt Cancer Center & Research Institute Inc. | Novel rho kinase inhibitors and methods of use |
| GB201107223D0 (en) | 2011-04-29 | 2011-06-15 | Amakem Nv | Novel rock inhibitors |
| WO2012160464A1 (en) | 2011-05-26 | 2012-11-29 | Daiichi Sankyo Company, Limited | Heterocyclic compounds as protein kinase inhibitors |
| KR101961884B1 (ko) | 2011-05-26 | 2019-03-25 | 티에프켐 | 아릴, 헤테로아릴, 오-아릴 및 오-헤테로 아릴 족 카르바슈가 |
| US8686184B2 (en) | 2011-05-31 | 2014-04-01 | Theravance, Inc. | Neprilysin inhibitors |
| BR112014000499A2 (pt) | 2011-07-12 | 2017-01-10 | Hoffmann La Roche | compostos de quinolona de aminometila |
| JP5967092B2 (ja) | 2011-07-29 | 2016-08-10 | 日本ゼオン株式会社 | 光学異方体の波長分散調整方法及び重合性組成物 |
| WO2013067248A1 (en) | 2011-11-04 | 2013-05-10 | Vertex Pharmaceuticals Incorporated | Benzoxazines as modulators of ion channels |
| AU2013305759C1 (en) | 2012-08-23 | 2018-01-18 | Janssen Biopharma, Inc. | Compounds for the treatment of paramoxyvirus viral infections |
| WO2014079850A1 (en) * | 2012-11-23 | 2014-05-30 | F. Hoffmann-La Roche Ag | Substituted heterocyclic derivatives |
| JP6488239B2 (ja) | 2013-01-18 | 2019-03-20 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | Rock阻害剤としてのフタラジノンおよびイソキノリノン |
| CN105102448B (zh) | 2013-02-28 | 2018-03-06 | 百时美施贵宝公司 | 作为rock1和rock2抑制剂的苯基吡唑衍生物 |
| AR096788A1 (es) | 2013-07-02 | 2016-02-03 | Bristol Myers Squibb Co | Compuestos tricíclicos de carboxamida como inhibidores potentes de rock |
| WO2015002926A1 (en) | 2013-07-02 | 2015-01-08 | Bristol-Myers Squibb Company | Tricyclic pyrido-carboxamide derivatives as rock inhibitors |
| CN106061964B (zh) | 2014-01-20 | 2019-10-25 | 豪夫迈·罗氏有限公司 | 能够刺激神经发生的n-苯基-内酰胺衍生物及其在神经性病症的治疗中的用途 |
-
2014
- 2014-02-27 AR ARP140100640A patent/AR094929A1/es unknown
- 2014-02-27 TW TW103106886A patent/TW201444798A/zh unknown
- 2014-02-28 WO PCT/US2014/019237 patent/WO2014134388A1/en not_active Ceased
- 2014-02-28 EP EP14710732.0A patent/EP2961745B1/en active Active
- 2014-02-28 US US14/770,500 patent/US9458110B2/en active Active
- 2014-02-28 ES ES14710732.0T patent/ES2624664T3/es active Active
- 2014-02-28 JP JP2015560336A patent/JP6423371B2/ja not_active Expired - Fee Related
- 2014-02-28 CN CN201480023844.6A patent/CN105358547B/zh active Active
- 2014-02-28 US US14/192,955 patent/US9126944B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| WO2014134388A1 (en) | 2014-09-04 |
| AR094929A1 (es) | 2015-09-09 |
| EP2961745B1 (en) | 2017-03-29 |
| US20160016910A1 (en) | 2016-01-21 |
| EP2961745A1 (en) | 2016-01-06 |
| US9458110B2 (en) | 2016-10-04 |
| CN105358547B (zh) | 2018-04-03 |
| US20140243338A1 (en) | 2014-08-28 |
| US9126944B2 (en) | 2015-09-08 |
| JP6423371B2 (ja) | 2018-11-14 |
| CN105358547A (zh) | 2016-02-24 |
| JP2016510032A (ja) | 2016-04-04 |
| TW201444798A (zh) | 2014-12-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES2624664T3 (es) | Derivados de fenilpirazol como potentes inhibidores de ROCK1 y ROCK2 | |
| ES2634628T3 (es) | Derivados tricíclicos de pirido-carboxamida como inhibidores ROCK | |
| ES2814325T3 (es) | Derivados de lactama, urea cíclica y carbamato y de triazolona como inhibidores potentes y selectivos de ROCK | |
| ES2937039T3 (es) | Inhibidores diazaespiro de ROCK | |
| ES2829550T3 (es) | Ureas cíclicas espiro-condensadas como inhibidores de ROCK | |
| ES2838573T3 (es) | Derivados de benzamida ligados como inhibidores potentes de ROCK | |
| ES2878054T3 (es) | Espiroheptanil hidantoínas como inhibidores de ROCK | |
| ES2829400T3 (es) | Inhibidores tricíclicos de Rho cinasa | |
| ES2951212T3 (es) | Fenilacetamidas como inhibidores de ROCK | |
| ES2684776T3 (es) | Ftalazinonas e isoquinolinonas como inhibidores de ROCK | |
| ES2855135T3 (es) | Amidas heterocíclicas como inhibidores de quinasa | |
| ES2781309T3 (es) | Triazolonas y tetrazolonas como inhibidores de ROCK | |
| CN105102448B (zh) | 作为rock1和rock2抑制剂的苯基吡唑衍生物 | |
| ES2894128T3 (es) | Inhibidores aminoheterocíclicos de cinco miembros y aminoheterocíclicos bicíclicos de 5,6 o 6,6 miembros de ROCK para el tratamiento de la insuficiencia cardíaca | |
| ES2730112T3 (es) | Lactamas como inhibidores de ROCK | |
| ES2821877T3 (es) | Espirolactamas como inhibidores de ROCK | |
| ES2815681T3 (es) | Ureas cíclicas como inhibidores de ROCK | |
| ES2854733T3 (es) | Heteroarilhidroxipirimidinonas como agonistas del receptor APJ | |
| EP3652168A1 (en) | 5-membered and bicyclic heterocyclic amides as inhibitors of rock |