JP2013518892A5 - - Google Patents
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- JP2013518892A5 JP2013518892A5 JP2012552070A JP2012552070A JP2013518892A5 JP 2013518892 A5 JP2013518892 A5 JP 2013518892A5 JP 2012552070 A JP2012552070 A JP 2012552070A JP 2012552070 A JP2012552070 A JP 2012552070A JP 2013518892 A5 JP2013518892 A5 JP 2013518892A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- pyrido
- dihydro
- methyl
- phthalazin
- 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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- 239000008194 pharmaceutical composition Substances 0.000 claims 48
- -1 C 1 -C 6 alkyl Chemical group 0.000 claims 21
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 18
- 229910052739 hydrogen Inorganic materials 0.000 claims 16
- 239000001257 hydrogen Substances 0.000 claims 16
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 16
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 13
- 125000003545 alkoxy group Chemical group 0.000 claims 13
- 125000003118 aryl group Chemical group 0.000 claims 13
- 229910052794 bromium Inorganic materials 0.000 claims 13
- 229910052801 chlorine Inorganic materials 0.000 claims 13
- 229910052731 fluorine Inorganic materials 0.000 claims 13
- 229910052740 iodine Inorganic materials 0.000 claims 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 11
- 150000003839 salts Chemical class 0.000 claims 11
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 10
- 125000001072 heteroaryl group Chemical group 0.000 claims 10
- 102000014160 PTEN Phosphohydrolase Human genes 0.000 claims 9
- 108010011536 PTEN Phosphohydrolase Proteins 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims 9
- 125000001188 haloalkyl group Chemical group 0.000 claims 9
- 206010028980 Neoplasm Diseases 0.000 claims 8
- 102000012338 Poly(ADP-ribose) Polymerases Human genes 0.000 claims 8
- 108010061844 Poly(ADP-ribose) Polymerases Proteins 0.000 claims 8
- 229920000776 Poly(Adenosine diphosphate-ribose) polymerase Polymers 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 201000011510 cancer Diseases 0.000 claims 8
- 230000007812 deficiency Effects 0.000 claims 8
- 201000010099 disease Diseases 0.000 claims 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 8
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 8
- 125000001424 substituent group Chemical group 0.000 claims 8
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 7
- 125000006354 carbonyl alkylene group Chemical group 0.000 claims 7
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 6
- 125000002947 alkylene group Chemical group 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 239000000651 prodrug Substances 0.000 claims 6
- 229940002612 prodrug Drugs 0.000 claims 6
- 239000012453 solvate Substances 0.000 claims 6
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 5
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims 5
- 125000004438 haloalkoxy group Chemical group 0.000 claims 5
- 125000005842 heteroatom Chemical group 0.000 claims 5
- 125000004043 oxo group Chemical group O=* 0.000 claims 5
- 150000003852 triazoles Chemical class 0.000 claims 5
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 4
- 206010041067 Small cell lung cancer Diseases 0.000 claims 4
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 125000000304 alkynyl group Chemical group 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 230000002401 inhibitory effect Effects 0.000 claims 4
- 208000000587 small cell lung carcinoma Diseases 0.000 claims 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 3
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 230000005782 double-strand break Effects 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 125000005114 heteroarylalkoxy group Chemical group 0.000 claims 3
- 125000005367 heteroarylalkylthio group Chemical group 0.000 claims 3
- 125000005553 heteroaryloxy group Chemical group 0.000 claims 3
- 125000005368 heteroarylthio group Chemical group 0.000 claims 3
- 125000004470 heterocyclooxy group Chemical group 0.000 claims 3
- 230000006801 homologous recombination Effects 0.000 claims 3
- 238000002744 homologous recombination Methods 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000002883 imidazolyl group Chemical group 0.000 claims 3
- 206010027191 meningioma Diseases 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 2
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical compound C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 claims 2
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims 2
- WGZMUTVUDVLUJL-UHFFFAOYSA-N 12-phenyl-11-pyridin-2-yl-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound N1C(C2=3)=CC=CC=3C(=O)NN=C2C(C=2C=CC=CC=2)C1C1=CC=CC=N1 WGZMUTVUDVLUJL-UHFFFAOYSA-N 0.000 claims 2
- VZYOBZPMHSMQGJ-UHFFFAOYSA-N 12-phenyl-11-pyridin-4-yl-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound N1C(C2=3)=CC=CC=3C(=O)NN=C2C(C=2C=CC=CC=2)C1C1=CC=NC=C1 VZYOBZPMHSMQGJ-UHFFFAOYSA-N 0.000 claims 2
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 2
- HWGQMRYQVZSGDQ-UHFFFAOYSA-N 7-fluoro-11-(4-fluorophenyl)-12-(2-methyl-1,2,4-triazol-3-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1N=CN=C1C(C(N1)C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 HWGQMRYQVZSGDQ-UHFFFAOYSA-N 0.000 claims 2
- 206010005003 Bladder cancer Diseases 0.000 claims 2
- 206010006187 Breast cancer Diseases 0.000 claims 2
- 208000026310 Breast neoplasm Diseases 0.000 claims 2
- 206010009944 Colon cancer Diseases 0.000 claims 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims 2
- 206010014733 Endometrial cancer Diseases 0.000 claims 2
- 206010014759 Endometrial neoplasm Diseases 0.000 claims 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 2
- 208000008839 Kidney Neoplasms Diseases 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 206010060862 Prostate cancer Diseases 0.000 claims 2
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 2
- 206010038389 Renal cancer Diseases 0.000 claims 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 2
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 2
- 201000008395 adenosquamous carcinoma Diseases 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 125000005129 aryl carbonyl group Chemical group 0.000 claims 2
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 2
- 230000002950 deficient Effects 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 208000005017 glioblastoma Diseases 0.000 claims 2
- 201000010536 head and neck cancer Diseases 0.000 claims 2
- 208000014829 head and neck neoplasm Diseases 0.000 claims 2
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 claims 2
- 125000005885 heterocycloalkylalkyl group Chemical group 0.000 claims 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims 2
- 201000010982 kidney cancer Diseases 0.000 claims 2
- 201000010893 malignant breast melanoma Diseases 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 108090000623 proteins and genes Proteins 0.000 claims 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 2
- 201000005112 urinary bladder cancer Diseases 0.000 claims 2
- SOMLCVOFFCJGNU-IRXDYDNUSA-N (11R,12S)-11-(4-fluorophenyl)-12-(1-methylimidazol-2-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1C=CN=C1[C@@H]([C@@H](N1)C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC=C3 SOMLCVOFFCJGNU-IRXDYDNUSA-N 0.000 claims 1
- VGCYLQAHCSEGLE-HOTGVXAUSA-N (11R,12S)-11-(4-fluorophenyl)-12-(2-methyl-1,2,4-triazol-3-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1N=CN=C1[C@@H]([C@@H](N1)C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC=C3 VGCYLQAHCSEGLE-HOTGVXAUSA-N 0.000 claims 1
- UMTZOWPWZLHANK-UPVQGACJSA-N (11R,12S)-11-[4-(azetidin-1-ylmethyl)phenyl]-12-(4-fluorophenyl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C1=CC(F)=CC=C1[C@@H]([C@@H](N1)C=2C=CC(CN3CCC3)=CC=2)C2=NNC(=O)C3=C2C1=CC=C3 UMTZOWPWZLHANK-UPVQGACJSA-N 0.000 claims 1
- OWJGUHRNNJVRHR-OALUTQOASA-N (11R,12S)-11-[4-[(dimethylamino)methyl]phenyl]-7-fluoro-12-(2-methyl-1,2,4-triazol-3-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C1=CC(CN(C)C)=CC=C1[C@H](N1)[C@H](C=2N(N=CN=2)C)C2=NNC(=O)C3=C2C1=CC(F)=C3 OWJGUHRNNJVRHR-OALUTQOASA-N 0.000 claims 1
- LJXPYHXSPQXFKB-IRXDYDNUSA-N (11R,12S)-7-fluoro-11-(4-fluorophenyl)-12-(1-methylimidazol-2-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1C=CN=C1[C@@H]([C@@H](N1)C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 LJXPYHXSPQXFKB-IRXDYDNUSA-N 0.000 claims 1
- HWGQMRYQVZSGDQ-HOTGVXAUSA-N (11R,12S)-7-fluoro-11-(4-fluorophenyl)-12-(2-methyl-1,2,4-triazol-3-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1N=CN=C1[C@@H]([C@@H](N1)C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 HWGQMRYQVZSGDQ-HOTGVXAUSA-N 0.000 claims 1
- JMRVJHACGJMVJK-IRXDYDNUSA-N (11R,12S)-7-fluoro-12-(1-methylimidazol-2-yl)-11-phenyl-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1C=CN=C1[C@@H]([C@@H](N1)C=2C=CC=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 JMRVJHACGJMVJK-IRXDYDNUSA-N 0.000 claims 1
- RJXIQUMBMLJTTJ-HOTGVXAUSA-N (11R,12S)-7-fluoro-12-(2-methyl-1,2,4-triazol-3-yl)-11-phenyl-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1N=CN=C1[C@@H]([C@@H](N1)C=2C=CC=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 RJXIQUMBMLJTTJ-HOTGVXAUSA-N 0.000 claims 1
- SOMLCVOFFCJGNU-IAGOWNOFSA-N (11S,12R)-11-(4-fluorophenyl)-12-(1-methylimidazol-2-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1C=CN=C1[C@H]([C@H](N1)C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC=C3 SOMLCVOFFCJGNU-IAGOWNOFSA-N 0.000 claims 1
- VGCYLQAHCSEGLE-HZPDHXFCSA-N (11S,12R)-11-(4-fluorophenyl)-12-(2-methyl-1,2,4-triazol-3-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1N=CN=C1[C@H]([C@H](N1)C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC=C3 VGCYLQAHCSEGLE-HZPDHXFCSA-N 0.000 claims 1
- UMTZOWPWZLHANK-ISKFKSNPSA-N (11S,12R)-11-[4-(azetidin-1-ylmethyl)phenyl]-12-(4-fluorophenyl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C1=CC(F)=CC=C1[C@H]([C@H](N1)C=2C=CC(CN3CCC3)=CC=2)C2=NNC(=O)C3=C2C1=CC=C3 UMTZOWPWZLHANK-ISKFKSNPSA-N 0.000 claims 1
- OWJGUHRNNJVRHR-RTBURBONSA-N (11S,12R)-11-[4-[(dimethylamino)methyl]phenyl]-7-fluoro-12-(2-methyl-1,2,4-triazol-3-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C1=CC(CN(C)C)=CC=C1[C@@H](N1)[C@@H](C=2N(N=CN=2)C)C2=NNC(=O)C3=C2C1=CC(F)=C3 OWJGUHRNNJVRHR-RTBURBONSA-N 0.000 claims 1
- LJXPYHXSPQXFKB-IAGOWNOFSA-N (11S,12R)-7-fluoro-11-(4-fluorophenyl)-12-(1-methylimidazol-2-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1C=CN=C1[C@H]([C@H](N1)C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 LJXPYHXSPQXFKB-IAGOWNOFSA-N 0.000 claims 1
- JMRVJHACGJMVJK-IAGOWNOFSA-N (11S,12R)-7-fluoro-12-(1-methylimidazol-2-yl)-11-phenyl-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1C=CN=C1[C@H]([C@H](N1)C=2C=CC=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 JMRVJHACGJMVJK-IAGOWNOFSA-N 0.000 claims 1
- RJXIQUMBMLJTTJ-HZPDHXFCSA-N (11S,12R)-7-fluoro-12-(2-methyl-1,2,4-triazol-3-yl)-11-phenyl-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1N=CN=C1[C@H]([C@H](N1)C=2C=CC=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 RJXIQUMBMLJTTJ-HZPDHXFCSA-N 0.000 claims 1
- BBVIDBNAYOIXOE-UHFFFAOYSA-N 1,2,4-oxadiazole Chemical compound C=1N=CON=1 BBVIDBNAYOIXOE-UHFFFAOYSA-N 0.000 claims 1
- FYADHXFMURLYQI-UHFFFAOYSA-N 1,2,4-triazine Chemical compound C1=CN=NC=N1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 claims 1
- 125000001414 1,2,4-triazol-5-yl group Chemical group [H]N1N=C([H])N=C1[*] 0.000 claims 1
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims 1
- HLMLLKFCRNXDCU-UHFFFAOYSA-N 10-ethyl-11,12-diphenyl-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C=12C3=NNC(=O)C2=CC=CC=1N(CC)C(C=1C=CC=CC=1)C3C1=CC=CC=C1 HLMLLKFCRNXDCU-UHFFFAOYSA-N 0.000 claims 1
- OVSNPTZKZPHLSC-UHFFFAOYSA-N 11,12-bis(1-methylimidazol-2-yl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN1C=CN=C1C(N1)C(C=2N(C=CN=2)C)C2=NNC(=O)C3=C2C1=CC=C3 OVSNPTZKZPHLSC-UHFFFAOYSA-N 0.000 claims 1
- XCTHABQHPYGJGY-UHFFFAOYSA-N 11,12-bis(4-fluorophenyl)-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C1=CC(F)=CC=C1C(N1)C(C=2C=CC(F)=CC=2)C2=NNC(=O)C3=C2C1=CC=C3 XCTHABQHPYGJGY-UHFFFAOYSA-N 0.000 claims 1
- ALFPJVGIQSAMIR-UHFFFAOYSA-N 11,12-bis[3-(methylaminomethyl)phenyl]-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CNCC1=CC=CC(C2C(C=3C4=C(C(NN=3)=O)C=CC=C4N2)C=2C=C(CNC)C=CC=2)=C1 ALFPJVGIQSAMIR-UHFFFAOYSA-N 0.000 claims 1
- HGZOJDBSTWKIKE-UHFFFAOYSA-N 11,12-bis[3-[(dimethylamino)methyl]phenyl]-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound CN(C)CC1=CC=CC(C2C(C=3C4=C(C(NN=3)=O)C=CC=C4N2)C=2C=C(CN(C)C)C=CC=2)=C1 HGZOJDBSTWKIKE-UHFFFAOYSA-N 0.000 claims 1
- UWMAULNVNHANQX-UHFFFAOYSA-N 11,12-bis[3-[4-(2-methylpropanoyl)piperazine-1-carbonyl]phenyl]-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C1CN(C(=O)C(C)C)CCN1C(=O)C1=CC=CC(C2C(C=3C4=C(C(NN=3)=O)C=CC=C4N2)C=2C=C(C=CC=2)C(=O)N2CCN(CC2)C(=O)C(C)C)=C1 UWMAULNVNHANQX-UHFFFAOYSA-N 0.000 claims 1
- UMCZUCYEMNNRPS-UHFFFAOYSA-N 11,12-bis[4-[(dimethylamino)methyl]phenyl]-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C1=CC(CN(C)C)=CC=C1C(N1)C(C=2C=CC(CN(C)C)=CC=2)C2=NNC(=O)C3=C2C1=CC=C3 UMCZUCYEMNNRPS-UHFFFAOYSA-N 0.000 claims 1
- PVKRHCUUSZTERO-UHFFFAOYSA-N 11,12-bis[4-[(dimethylamino)methyl]phenyl]-7-fluoro-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound C1=CC(CN(C)C)=CC=C1C(N1)C(C=2C=CC(CN(C)C)=CC=2)C2=NNC(=O)C3=C2C1=CC(F)=C3 PVKRHCUUSZTERO-UHFFFAOYSA-N 0.000 claims 1
- ULPMFQRNYGWKAD-UHFFFAOYSA-N 11,12-dipyridin-2-yl-2,3,10-triazatricyclo[7.3.1.05,13]trideca-1,5(13),6,8-tetraen-4-one Chemical compound N1C(C2=3)=CC=CC=3C(=O)NN=C2C(C=2N=CC=CC=2)C1C1=CC=CC=N1 ULPMFQRNYGWKAD-UHFFFAOYSA-N 0.000 claims 1
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-
2011
- 2011-02-03 CA CA2787844A patent/CA2787844C/en not_active Expired - Fee Related
- 2011-02-03 US US13/020,619 patent/US8541403B2/en not_active Expired - Fee Related
- 2011-02-03 AU AU2011212928A patent/AU2011212928B2/en not_active Ceased
- 2011-02-03 CN CN201180017703XA patent/CN102869258A/zh active Pending
- 2011-02-03 EP EP11740322.0A patent/EP2531033A4/en not_active Withdrawn
- 2011-02-03 CN CN201710081268.6A patent/CN106943406A/zh active Pending
- 2011-02-03 JP JP2012552070A patent/JP5883397B2/ja not_active Expired - Fee Related
- 2011-02-03 WO PCT/US2011/023532 patent/WO2011097334A1/en not_active Ceased
-
2013
- 2013-08-21 US US13/972,166 patent/US9018201B2/en not_active Expired - Fee Related
-
2015
- 2015-03-27 US US14/671,944 patent/US20150209363A1/en not_active Abandoned
-
2016
- 2016-02-05 JP JP2016020358A patent/JP2016128492A/ja not_active Withdrawn
- 2016-09-22 AU AU2016231573A patent/AU2016231573A1/en not_active Abandoned
-
2017
- 2017-06-20 JP JP2017120148A patent/JP2017197565A/ja active Pending
-
2018
- 2018-07-20 AU AU2018206826A patent/AU2018206826A1/en not_active Abandoned
- 2018-08-03 US US16/054,899 patent/US10493078B2/en not_active Expired - Fee Related
- 2018-09-27 JP JP2018182009A patent/JP2019011356A/ja not_active Withdrawn
-
2020
- 2020-07-09 JP JP2020118694A patent/JP2020176136A/ja active Pending
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