JP2008502700A5 - - Google Patents
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- Publication number
- JP2008502700A5 JP2008502700A5 JP2007516703A JP2007516703A JP2008502700A5 JP 2008502700 A5 JP2008502700 A5 JP 2008502700A5 JP 2007516703 A JP2007516703 A JP 2007516703A JP 2007516703 A JP2007516703 A JP 2007516703A JP 2008502700 A5 JP2008502700 A5 JP 2008502700A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- imidazol
- substituted
- benzyl
- ethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- -1 carbocycle Chemical group 0.000 claims 144
- 125000000217 alkyl group Chemical group 0.000 claims 110
- 125000000623 heterocyclic group Chemical group 0.000 claims 101
- 125000005842 heteroatom Chemical group 0.000 claims 50
- 229910052760 oxygen Inorganic materials 0.000 claims 49
- 229910052739 hydrogen Inorganic materials 0.000 claims 45
- 229910052799 carbon Inorganic materials 0.000 claims 40
- 229910052717 sulfur Inorganic materials 0.000 claims 40
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 33
- 125000004432 carbon atom Chemical group C* 0.000 claims 32
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 28
- RSILLSRLAWUTAY-UHFFFAOYSA-N 4-(aminomethyl)cyclohexane-1-carboxamide Chemical compound NCC1CCC(C(N)=O)CC1 RSILLSRLAWUTAY-UHFFFAOYSA-N 0.000 claims 23
- 125000003118 aryl group Chemical group 0.000 claims 22
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 18
- RSILLSRLAWUTAY-LJGSYFOKSA-N NC[C@H]1CC[C@H](C(N)=O)CC1 Chemical compound NC[C@H]1CC[C@H](C(N)=O)CC1 RSILLSRLAWUTAY-LJGSYFOKSA-N 0.000 claims 18
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 17
- 150000001875 compounds Chemical class 0.000 claims 17
- 150000001721 carbon Chemical group 0.000 claims 16
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 14
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 claims 13
- 125000001072 heteroaryl group Chemical group 0.000 claims 13
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 12
- KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 11
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 10
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 9
- 125000004429 atom Chemical group 0.000 claims 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 9
- 229910052757 nitrogen Inorganic materials 0.000 claims 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 9
- 150000003839 salts Chemical class 0.000 claims 9
- 239000012453 solvate Substances 0.000 claims 9
- 125000001624 naphthyl group Chemical group 0.000 claims 8
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 7
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 7
- 125000004076 pyridyl group Chemical group 0.000 claims 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 6
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims 6
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 6
- 201000010099 disease Diseases 0.000 claims 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 6
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 5
- 125000004605 1,2,3,4-tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 claims 5
- 125000004606 5,6,7,8-tetrahydroisoquinolinyl group Chemical group C1(=NC=CC=2CCCCC12)* 0.000 claims 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 5
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims 5
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 5
- 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 claims 5
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims 5
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims 5
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 5
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims 5
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 125000002883 imidazolyl group Chemical group 0.000 claims 4
- 125000004537 indazol-5-yl group Chemical group N1N=CC2=CC(=CC=C12)* 0.000 claims 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 4
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
- 125000006413 ring segment Chemical group 0.000 claims 4
- 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 3
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims 3
- KSWRJISIQSPBCJ-UHFFFAOYSA-N 2h-isoquinoline Chemical compound C1=CC=C2[CH]NC=CC2=C1 KSWRJISIQSPBCJ-UHFFFAOYSA-N 0.000 claims 3
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000002837 carbocyclic group Chemical group 0.000 claims 3
- 125000004531 indol-5-yl group Chemical group [H]N1C([H])=C([H])C2=C([H])C(*)=C([H])C([H])=C12 0.000 claims 3
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 claims 3
- 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims 2
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 2
- 208000007536 Thrombosis Diseases 0.000 claims 2
- 206010047249 Venous thrombosis Diseases 0.000 claims 2
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- RHJVIGLEIFVHIJ-UHFFFAOYSA-N cyclohexanecarboxamide Chemical compound NC(=O)C1[CH]CCCC1 RHJVIGLEIFVHIJ-UHFFFAOYSA-N 0.000 claims 2
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 2
- 230000002526 effect on cardiovascular system Effects 0.000 claims 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 2
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 claims 2
- 125000001041 indolyl group Chemical group 0.000 claims 2
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 claims 2
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 2
- 208000010125 myocardial infarction Diseases 0.000 claims 2
- YDLAQBRNNOLMIH-UHFFFAOYSA-N n-[(4-chlorophenyl)methyl]formamide Chemical group ClC1=CC=C(CNC=O)C=C1 YDLAQBRNNOLMIH-UHFFFAOYSA-N 0.000 claims 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 2
- 125000003831 tetrazolyl group Chemical group 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000001425 triazolyl group Chemical group 0.000 claims 2
- YQMJBZVQZHKATR-GGAORHGYSA-N (6R)-1-amino-N-[(1S)-1-[5-chloro-4-(4-cyanophenyl)-1H-imidazol-2-yl]-2-phenylethyl]-5,6,7,8-tetrahydroisoquinoline-6-carboxamide Chemical compound C([C@H](NC(=O)[C@H]1CC=2C=CN=C(C=2CC1)N)C=1NC(Cl)=C(N=1)C=1C=CC(=CC=1)C#N)C1=CC=CC=C1 YQMJBZVQZHKATR-GGAORHGYSA-N 0.000 claims 1
- ICSJXVUUSDNFIJ-GCJKJVERSA-N (6r)-1-amino-n-[(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-5,6,7,8-tetrahydroisoquinoline-6-carboxamide Chemical compound C([C@@H](C1=NC(=C(N1)Cl)C=1C=C2NN=C(C2=CC=1)N)NC(=O)[C@H]1CC2=CC=NC(N)=C2CC1)C1=CC=CC=C1 ICSJXVUUSDNFIJ-GCJKJVERSA-N 0.000 claims 1
- ICSJXVUUSDNFIJ-AVRDEDQJSA-N (6s)-1-amino-n-[(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-5,6,7,8-tetrahydroisoquinoline-6-carboxamide Chemical compound C([C@@H](C1=NC(=C(N1)Cl)C=1C=C2NN=C(C2=CC=1)N)NC(=O)[C@@H]1CC2=CC=NC(N)=C2CC1)C1=CC=CC=C1 ICSJXVUUSDNFIJ-AVRDEDQJSA-N 0.000 claims 1
- YQMJBZVQZHKATR-GMAHTHKFSA-N (6s)-1-amino-n-[(1s)-1-[5-chloro-4-(4-cyanophenyl)-1h-imidazol-2-yl]-2-phenylethyl]-5,6,7,8-tetrahydroisoquinoline-6-carboxamide Chemical compound C([C@H](NC(=O)[C@@H]1CC=2C=CN=C(C=2CC1)N)C=1NC(Cl)=C(N=1)C=1C=CC(=CC=1)C#N)C1=CC=CC=C1 YQMJBZVQZHKATR-GMAHTHKFSA-N 0.000 claims 1
- ICSJXVUUSDNFIJ-HXBUSHRASA-N (6s)-1-amino-n-[1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-5,6,7,8-tetrahydroisoquinoline-6-carboxamide Chemical compound C=1C=C2C(N)=NNC2=CC=1C(=C(N1)Cl)N=C1C(NC(=O)[C@@H]1CC2=CC=NC(N)=C2CC1)CC1=CC=CC=C1 ICSJXVUUSDNFIJ-HXBUSHRASA-N 0.000 claims 1
- KNVDGWXWPWHPCC-HSTJUUNISA-N (6s)-1-amino-n-[1-[4-(4-aminoquinazolin-7-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-5,6,7,8-tetrahydroisoquinoline-6-carboxamide Chemical compound O=C([C@@H]1CC=2C=CN=C(C=2CC1)N)NC(C=1NC(Cl)=C(N=1)C=1C=C2N=CN=C(N)C2=CC=1)CC1=CC=CC=C1 KNVDGWXWPWHPCC-HSTJUUNISA-N 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 claims 1
- KCOPAESEGCGTKM-UHFFFAOYSA-N 1,3-oxazol-4-one Chemical class O=C1COC=N1 KCOPAESEGCGTKM-UHFFFAOYSA-N 0.000 claims 1
- XKNHFWHZDIOLSR-QHCPKHFHSA-N 1-amino-n-[(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-3-methylisoquinoline-6-carboxamide Chemical compound C([C@H](NC(=O)C=1C=C2C=C(N=C(N)C2=CC=1)C)C=1NC(Cl)=C(N=1)C=1C=C2NN=C(N)C2=CC=1)C1=CC=CC=C1 XKNHFWHZDIOLSR-QHCPKHFHSA-N 0.000 claims 1
- KWHJKKRXFUNBAJ-QFIPXVFZSA-N 1-amino-n-[(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]isoquinoline-6-carboxamide Chemical compound C([C@@H](C1=NC(=C(N1)Cl)C=1C=C2NN=C(C2=CC=1)N)NC(=O)C=1C=C2C=CN=C(N)C2=CC=1)C1=CC=CC=C1 KWHJKKRXFUNBAJ-QFIPXVFZSA-N 0.000 claims 1
- ZMUSBULBJACGQA-UHFFFAOYSA-N 1-n-[1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-2-chlorobenzene-1,4-dicarboxamide Chemical compound ClC1=CC(C(=O)N)=CC=C1C(=O)NC(C=1NC(Cl)=C(N=1)C=1C=C2NN=C(N)C2=CC=1)CC1=CC=CC=C1 ZMUSBULBJACGQA-UHFFFAOYSA-N 0.000 claims 1
- ZBNZAJFNDPPMDT-UHFFFAOYSA-N 1h-imidazole-5-carboxamide Chemical compound NC(=O)C1=CNC=N1 ZBNZAJFNDPPMDT-UHFFFAOYSA-N 0.000 claims 1
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 1
- WWUIZLHTDBGHFH-UHFFFAOYSA-N 2-[5-(4-carbamimidoylphenyl)-1h-imidazol-2-yl]-n,3-diphenylpropanamide Chemical compound C1=CC(C(=N)N)=CC=C1C1=CNC(C(CC=2C=CC=CC=2)C(=O)NC=2C=CC=CC=2)=N1 WWUIZLHTDBGHFH-UHFFFAOYSA-N 0.000 claims 1
- 125000004174 2-benzimidazolyl group Chemical group [H]N1C(*)=NC2=C([H])C([H])=C([H])C([H])=C12 0.000 claims 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims 1
- 125000004352 2-phenylcyclohexyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])* 0.000 claims 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- PKSAIJQAOZGOKV-IBGZPJMESA-N 3-amino-n-[(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-1,2-benzoxazole-6-carboxamide Chemical compound C([C@@H](C1=NC(=C(N1)Cl)C=1C=C2NN=C(C2=CC=1)N)NC(=O)C=1C=C2ON=C(N)C2=CC=1)C1=CC=CC=C1 PKSAIJQAOZGOKV-IBGZPJMESA-N 0.000 claims 1
- IAJDAQJCIKJYEG-FQEVSTJZSA-N 3-amino-n-[(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-1h-indazole-5-carboxamide Chemical compound C([C@@H](C1=NC(=C(N1)Cl)C=1C=C2NN=C(C2=CC=1)N)NC(=O)C=1C=C2C(N)=NNC2=CC=1)C1=CC=CC=C1 IAJDAQJCIKJYEG-FQEVSTJZSA-N 0.000 claims 1
- QEDSKDDUNJZZHC-FQEVSTJZSA-N 3-amino-n-[(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]-1h-indazole-6-carboxamide Chemical compound C([C@H](NC(=O)C=1C=C2NN=C(C2=CC=1)N)C=1NC(Cl)=C(N=1)C=1C=C2NN=C(N)C2=CC=1)C1=CC=CC=C1 QEDSKDDUNJZZHC-FQEVSTJZSA-N 0.000 claims 1
- YVUNSWOVNWOOSB-NRFANRHFSA-N 3-amino-n-[(1s)-1-[5-(4-carbamimidoylphenyl)-1h-imidazol-2-yl]-2-phenylethyl]-1h-indazole-5-carboxamide Chemical compound C1=CC(C(=N)N)=CC=C1C1=CNC([C@H](CC=2C=CC=CC=2)NC(=O)C=2C=C3C(N)=NNC3=CC=2)=N1 YVUNSWOVNWOOSB-NRFANRHFSA-N 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- OXMAFNHUBUZZQD-GRERDSQWSA-N 4-(aminomethyl)-n-[(1s)-1-[5-(1,3-benzodioxol-5-yl)-1h-imidazol-2-yl]-2-phenylethyl]cyclohexane-1-carboxamide Chemical compound C1CC(CN)CCC1C(=O)N[C@H](C=1NC=C(N=1)C=1C=C2OCOC2=CC=1)CC1=CC=CC=C1 OXMAFNHUBUZZQD-GRERDSQWSA-N 0.000 claims 1
- XFUJSTYMHFWPGW-AJTFCVKESA-N 4-(aminomethyl)-n-[(1s)-1-[5-(3-aminophenyl)-1h-imidazol-2-yl]-2-phenylethyl]cyclohexane-1-carboxamide Chemical compound C1CC(CN)CCC1C(=O)N[C@H](C=1NC=C(N=1)C=1C=C(N)C=CC=1)CC1=CC=CC=C1 XFUJSTYMHFWPGW-AJTFCVKESA-N 0.000 claims 1
- HROQHIMMOVNTMW-QFIPXVFZSA-N 4-(aminomethyl)-n-[(1s)-1-[5-(4-carbamoylphenyl)-1h-imidazol-2-yl]-2-phenylethyl]-2-fluorobenzamide Chemical compound FC1=CC(CN)=CC=C1C(=O)N[C@H](C=1NC=C(N=1)C=1C=CC(=CC=1)C(N)=O)CC1=CC=CC=C1 HROQHIMMOVNTMW-QFIPXVFZSA-N 0.000 claims 1
- MASSIHFRZVOSGL-QFIPXVFZSA-N 4-(aminomethyl)-n-[(1s)-1-[5-(4-carbamoylphenyl)-1h-imidazol-2-yl]-2-phenylethyl]benzamide Chemical compound C1=CC(CN)=CC=C1C(=O)N[C@H](C=1NC=C(N=1)C=1C=CC(=CC=1)C(N)=O)CC1=CC=CC=C1 MASSIHFRZVOSGL-QFIPXVFZSA-N 0.000 claims 1
- ZEJLTWLVGBBHBH-FYPSYCSSSA-N 4-[(1S)-1-[4-(4-aminoquinazolin-7-yl)-5-chloro-1H-imidazol-2-yl]-2-phenylethyl]-3-fluorocyclohexa-1,5-diene-1,4-dicarboxamide Chemical compound NC1=NC=NC2=CC(=CC=C12)C=1N=C(NC1Cl)[C@@H](CC1=CC=CC=C1)C1(C(=O)N)C(C=C(C(=O)N)C=C1)F ZEJLTWLVGBBHBH-FYPSYCSSSA-N 0.000 claims 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 1
- YOBXSQWDCHADCX-FQEVSTJZSA-N 4-n-[(1s)-1-[4-(3-amino-1h-indazol-6-yl)-5-chloro-1h-imidazol-2-yl]-2-phenylethyl]benzene-1,4-dicarboxamide Chemical compound C1=CC(C(=O)N)=CC=C1C(=O)N[C@H](C=1NC(Cl)=C(N=1)C=1C=C2NN=C(N)C2=CC=1)CC1=CC=CC=C1 YOBXSQWDCHADCX-FQEVSTJZSA-N 0.000 claims 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- 125000001960 7 membered carbocyclic group Chemical group 0.000 claims 1
- 208000004476 Acute Coronary Syndrome Diseases 0.000 claims 1
- 206010002388 Angina unstable Diseases 0.000 claims 1
- 200000000007 Arterial disease Diseases 0.000 claims 1
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 206010003658 Atrial Fibrillation Diseases 0.000 claims 1
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- BYMZQFRYGNATEK-HQOBLLPJSA-N n-[(1s)-1-[5-(3-amino-1h-indazol-6-yl)-1h-imidazol-2-yl]-4-[benzyl(methyl)amino]-4-oxobutyl]-4-(aminomethyl)cyclohexane-1-carboxamide Chemical compound C([C@H](NC(=O)C1CCC(CN)CC1)C=1NC(=CN=1)C=1C=C2NN=C(N)C2=CC=1)CC(=O)N(C)CC1=CC=CC=C1 BYMZQFRYGNATEK-HQOBLLPJSA-N 0.000 claims 1
- HDPAWKKAGADBEQ-QFIPXVFZSA-N n-[(1s)-1-[5-(4-carbamimidoylphenyl)-1h-imidazol-2-yl]-2-phenylethyl]-1h-indazole-6-carboxamide Chemical compound C1=CC(C(=N)N)=CC=C1C1=CNC([C@H](CC=2C=CC=CC=2)NC(=O)C=2C=C3NN=CC3=CC=2)=N1 HDPAWKKAGADBEQ-QFIPXVFZSA-N 0.000 claims 1
- AZKBLOTXRUYVCR-QHCPKHFHSA-N n-[(1s)-1-[5-(4-carbamimidoylphenyl)-1h-imidazol-2-yl]-2-phenylethyl]-1h-indole-6-carboxamide Chemical compound C1=CC(C(=N)N)=CC=C1C1=CNC([C@H](CC=2C=CC=CC=2)NC(=O)C=2C=C3NC=CC3=CC=2)=N1 AZKBLOTXRUYVCR-QHCPKHFHSA-N 0.000 claims 1
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- 239000008194 pharmaceutical composition Substances 0.000 claims 1
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-
2005
- 2005-06-13 US US11/151,667 patent/US7453002B2/en active Active
- 2005-06-14 EP EP05773261.2A patent/EP1773786B1/en not_active Expired - Lifetime
- 2005-06-14 MX MXPA06014642A patent/MXPA06014642A/es active IP Right Grant
- 2005-06-14 CA CA002570472A patent/CA2570472A1/en not_active Abandoned
- 2005-06-14 BR BRPI0512084-5A patent/BRPI0512084A/pt not_active IP Right Cessation
- 2005-06-14 WO PCT/US2005/021212 patent/WO2005123050A2/en not_active Ceased
- 2005-06-14 RU RU2007101073/04A patent/RU2007101073A/ru not_active Application Discontinuation
- 2005-06-14 ES ES05773261.2T patent/ES2628279T3/es not_active Expired - Lifetime
- 2005-06-14 JP JP2007516703A patent/JP4791460B2/ja not_active Expired - Fee Related
- 2005-06-14 AU AU2005254102A patent/AU2005254102A1/en not_active Abandoned
- 2005-06-14 KR KR1020067026365A patent/KR20070024601A/ko not_active Ceased
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2006
- 2006-12-05 IL IL179844A patent/IL179844A0/en unknown
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2008
- 2008-09-12 US US12/209,235 patent/US8101778B2/en active Active
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2011
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2014
- 2014-03-19 US US14/219,311 patent/US9079860B2/en not_active Expired - Lifetime
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2015
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2017
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