JP2008526866A5 - - Google Patents
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- JP2008526866A5 JP2008526866A5 JP2007550457A JP2007550457A JP2008526866A5 JP 2008526866 A5 JP2008526866 A5 JP 2008526866A5 JP 2007550457 A JP2007550457 A JP 2007550457A JP 2007550457 A JP2007550457 A JP 2007550457A JP 2008526866 A5 JP2008526866 A5 JP 2008526866A5
- Authority
- JP
- Japan
- Prior art keywords
- optionally substituted
- methyl
- biphenyl
- difluoro
- isonicotinamide
- 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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- 150000001875 compounds Chemical class 0.000 claims 57
- 125000000217 alkyl group Chemical group 0.000 claims 27
- 125000005843 halogen group Chemical group 0.000 claims 26
- 239000000651 prodrug Substances 0.000 claims 16
- 229940002612 prodrug Drugs 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 16
- 239000012453 solvate Substances 0.000 claims 16
- 125000003545 alkoxy group Chemical group 0.000 claims 14
- 125000001188 haloalkyl group Chemical group 0.000 claims 13
- 125000000623 heterocyclic group Chemical group 0.000 claims 12
- 125000004414 alkyl thio group Chemical group 0.000 claims 11
- 125000001072 heteroaryl group Chemical group 0.000 claims 11
- 125000004438 haloalkoxy group Chemical group 0.000 claims 10
- 238000000034 method Methods 0.000 claims 10
- 125000004093 cyano group Chemical group *C#N 0.000 claims 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 8
- -1 1H-tetrazolyl Chemical group 0.000 claims 7
- 125000000547 substituted alkyl group Chemical group 0.000 claims 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims 6
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 6
- 125000004475 heteroaralkyl group Chemical group 0.000 claims 6
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 6
- 125000002971 oxazolyl group Chemical group 0.000 claims 6
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 6
- 125000004426 substituted alkynyl group Chemical group 0.000 claims 6
- 125000003107 substituted aryl group Chemical group 0.000 claims 6
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 6
- 125000000335 thiazolyl group Chemical group 0.000 claims 6
- 125000003282 alkyl amino group Chemical group 0.000 claims 5
- 125000004663 dialkyl amino group Chemical group 0.000 claims 5
- 125000006582 (C5-C6) heterocycloalkyl group Chemical group 0.000 claims 3
- PUTFMOAOKZNUSN-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(2h-tetrazol-5-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2NN=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F PUTFMOAOKZNUSN-UHFFFAOYSA-N 0.000 claims 3
- 102000004310 Ion Channels Human genes 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 125000002883 imidazolyl group Chemical group 0.000 claims 3
- 230000005931 immune cell recruitment Effects 0.000 claims 3
- 230000002401 inhibitory effect Effects 0.000 claims 3
- 125000000842 isoxazolyl group Chemical group 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims 3
- 125000000168 pyrrolyl group Chemical group 0.000 claims 3
- 125000003831 tetrazolyl group Chemical group 0.000 claims 3
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 3
- 125000001544 thienyl group Chemical group 0.000 claims 3
- 125000001425 triazolyl group Chemical group 0.000 claims 3
- NHEMHKBZHHLNLI-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(1,2-oxazol-5-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2ON=CC=2)C)C=C1 NHEMHKBZHHLNLI-UHFFFAOYSA-N 0.000 claims 2
- XKTZWZSXRKNGGM-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(1,3,4-oxadiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2OC=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1C XKTZWZSXRKNGGM-UHFFFAOYSA-N 0.000 claims 2
- WIMBOLXNLFZPHG-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(1,3-oxazol-5-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2OC=NC=2)C)C=C1 WIMBOLXNLFZPHG-UHFFFAOYSA-N 0.000 claims 2
- CMXASVOPXKZDOI-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(1,3-thiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2SC=CN=2)C)C=C1 CMXASVOPXKZDOI-UHFFFAOYSA-N 0.000 claims 2
- WQTHUZBGFPUICL-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(2h-tetrazol-5-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2NN=NN=2)C)C=C1 WQTHUZBGFPUICL-UHFFFAOYSA-N 0.000 claims 2
- 210000001744 T-lymphocyte Anatomy 0.000 claims 2
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 2
- 210000003719 b-lymphocyte Anatomy 0.000 claims 2
- 210000004027 cell Anatomy 0.000 claims 2
- 230000016396 cytokine production Effects 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 125000002757 morpholinyl group Chemical group 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 1
- ACZGJZKDSJLKPZ-UHFFFAOYSA-N 2,6-difluoro-n-[4-(2-methyl-5-pyridin-2-ylphenyl)phenyl]benzamide Chemical compound CC1=CC=C(C=2N=CC=CC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F ACZGJZKDSJLKPZ-UHFFFAOYSA-N 0.000 claims 1
- RJOOCBTVZKGDSW-UHFFFAOYSA-N 2,6-difluoro-n-[4-(2-methyl-5-pyridin-3-ylphenyl)phenyl]benzamide Chemical compound CC1=CC=C(C=2C=NC=CC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F RJOOCBTVZKGDSW-UHFFFAOYSA-N 0.000 claims 1
- DYJBJACFGHRXMH-UHFFFAOYSA-N 2,6-difluoro-n-[4-(2-methyl-5-pyridin-4-ylphenyl)phenyl]benzamide Chemical compound CC1=CC=C(C=2C=CN=CC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F DYJBJACFGHRXMH-UHFFFAOYSA-N 0.000 claims 1
- YCQQPBDGYUQILO-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methoxy-5-(1,3-oxazol-2-yl)phenyl]phenyl]benzamide Chemical compound COC1=CC=C(C=2OC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F YCQQPBDGYUQILO-UHFFFAOYSA-N 0.000 claims 1
- FRIGRPXYZRZZKE-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(1,3,4-oxadiazol-2-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2OC=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F FRIGRPXYZRZZKE-UHFFFAOYSA-N 0.000 claims 1
- PRCNEOSMANURNW-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(1,3,4-thiadiazol-2-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2SC=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F PRCNEOSMANURNW-UHFFFAOYSA-N 0.000 claims 1
- ZOHBMCUPFMAUSR-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(1,3-oxazol-2-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2OC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F ZOHBMCUPFMAUSR-UHFFFAOYSA-N 0.000 claims 1
- VNYPBEICPYEHMU-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(1,3-oxazol-4-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2N=COC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F VNYPBEICPYEHMU-UHFFFAOYSA-N 0.000 claims 1
- JJJUQDROKHOMAQ-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(1,3-oxazol-5-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2OC=NC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F JJJUQDROKHOMAQ-UHFFFAOYSA-N 0.000 claims 1
- HDILCULZLSYGHY-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(1-methyltetrazol-5-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2N(N=NN=2)C)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F HDILCULZLSYGHY-UHFFFAOYSA-N 0.000 claims 1
- VMGWUJGHNODFSG-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(1h-pyrrol-2-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2NC=CC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F VMGWUJGHNODFSG-UHFFFAOYSA-N 0.000 claims 1
- FOBDRCIFVMXTIZ-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(2-methyl-1,2,4-triazol-3-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2N(N=CN=2)C)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F FOBDRCIFVMXTIZ-UHFFFAOYSA-N 0.000 claims 1
- LIODNSHJTIDZIW-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(2-methyltetrazol-5-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C2=NN(C)N=N2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F LIODNSHJTIDZIW-UHFFFAOYSA-N 0.000 claims 1
- HEYNONRWYRATQB-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(3-methyl-1,2-oxazol-5-yl)phenyl]phenyl]benzamide Chemical compound O1N=C(C)C=C1C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=C1 HEYNONRWYRATQB-UHFFFAOYSA-N 0.000 claims 1
- GYWJWMIPARWTPX-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]phenyl]benzamide Chemical compound CC1=CSC(C=2C=C(C(C)=CC=2)C=2C=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=N1 GYWJWMIPARWTPX-UHFFFAOYSA-N 0.000 claims 1
- DZXZUWXTRUTBAZ-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(4-methyl-5-methylsulfanyl-1,2,4-triazol-3-yl)phenyl]phenyl]benzamide Chemical compound CN1C(SC)=NN=C1C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=C1 DZXZUWXTRUTBAZ-UHFFFAOYSA-N 0.000 claims 1
- XGHSASJTYJAMBM-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(5-methyl-1h-pyrazol-3-yl)phenyl]phenyl]benzamide Chemical compound N1N=C(C)C=C1C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=C1 XGHSASJTYJAMBM-UHFFFAOYSA-N 0.000 claims 1
- RBKOFVZSWPUDHN-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-(5-oxo-2h-1,2,4-oxadiazol-3-yl)phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2NC(=O)ON=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F RBKOFVZSWPUDHN-UHFFFAOYSA-N 0.000 claims 1
- ADNXESORVNANSH-UHFFFAOYSA-N 2,6-difluoro-n-[4-[2-methyl-5-[4-(trifluoromethyl)-1,3-thiazol-2-yl]phenyl]phenyl]benzamide Chemical compound CC1=CC=C(C=2SC=C(N=2)C(F)(F)F)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F ADNXESORVNANSH-UHFFFAOYSA-N 0.000 claims 1
- HXUWFCJSAZOUHC-UHFFFAOYSA-N 3,5-difluoro-n-[4-[2-methoxy-5-(1,3-oxazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound COC1=CC=C(C=2OC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=NC=C1F HXUWFCJSAZOUHC-UHFFFAOYSA-N 0.000 claims 1
- IBXFTAMPNIFRLP-UHFFFAOYSA-N 3,5-difluoro-n-[4-[2-methyl-5-(1,3,4-oxadiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2OC=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=NC=C1F IBXFTAMPNIFRLP-UHFFFAOYSA-N 0.000 claims 1
- GGFLWLCIACQRTN-UHFFFAOYSA-N 3,5-difluoro-n-[4-[2-methyl-5-(1,3,4-thiadiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2SC=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=NC=C1F GGFLWLCIACQRTN-UHFFFAOYSA-N 0.000 claims 1
- ABHZATVUDHEZLF-UHFFFAOYSA-N 3,5-difluoro-n-[4-[2-methyl-5-(1,3-oxazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2OC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=NC=C1F ABHZATVUDHEZLF-UHFFFAOYSA-N 0.000 claims 1
- YGSAGYAPEBUCNA-UHFFFAOYSA-N 3,5-difluoro-n-[4-[2-methyl-5-(1,3-thiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2SC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=NC=C1F YGSAGYAPEBUCNA-UHFFFAOYSA-N 0.000 claims 1
- GUETUBNIKSOXBL-UHFFFAOYSA-N 3,5-difluoro-n-[4-[2-methyl-5-(4-methyl-5-methylsulfanyl-1,2,4-triazol-3-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CN1C(SC)=NN=C1C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CN=CC=3F)F)=CC=2)=C1 GUETUBNIKSOXBL-UHFFFAOYSA-N 0.000 claims 1
- NMPQFYMAMREFNS-UHFFFAOYSA-N 3-fluoro-n-[4-[2-methyl-5-(1,3,4-oxadiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2OC=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1F NMPQFYMAMREFNS-UHFFFAOYSA-N 0.000 claims 1
- FEUMTZNEZOBMOK-UHFFFAOYSA-N 3-fluoro-n-[4-[2-methyl-5-(1,3,4-thiadiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2SC=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1F FEUMTZNEZOBMOK-UHFFFAOYSA-N 0.000 claims 1
- WPCGQXNFVBKJKW-UHFFFAOYSA-N 3-fluoro-n-[4-[2-methyl-5-(1,3-oxazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2OC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1F WPCGQXNFVBKJKW-UHFFFAOYSA-N 0.000 claims 1
- QCEDPLCXHVYYHI-UHFFFAOYSA-N 3-fluoro-n-[4-[2-methyl-5-(1,3-oxazol-4-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2N=COC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1F QCEDPLCXHVYYHI-UHFFFAOYSA-N 0.000 claims 1
- PJPOZVMUALBLIM-UHFFFAOYSA-N 3-fluoro-n-[4-[2-methyl-5-(1,3-thiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2SC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1F PJPOZVMUALBLIM-UHFFFAOYSA-N 0.000 claims 1
- MLZFLMBXBPPYEA-UHFFFAOYSA-N 3-fluoro-n-[4-[2-methyl-5-(2-methyl-1,2,4-triazol-3-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2N(N=CN=2)C)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1F MLZFLMBXBPPYEA-UHFFFAOYSA-N 0.000 claims 1
- CEIRNGJBZOTXOK-UHFFFAOYSA-N 3-methyl-n-[4-(2-methyl-5-pyridin-3-ylphenyl)phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2C=NC=CC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1C CEIRNGJBZOTXOK-UHFFFAOYSA-N 0.000 claims 1
- GONHYCZCLJNREV-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(1,3,4-thiadiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2SC=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1C GONHYCZCLJNREV-UHFFFAOYSA-N 0.000 claims 1
- ZNMMURJWVGDXBJ-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(1,3-oxazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2OC=CN=2)C)C=C1 ZNMMURJWVGDXBJ-UHFFFAOYSA-N 0.000 claims 1
- RWWRLUIPEDCHLY-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(1,3-oxazol-4-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2N=COC=2)C)C=C1 RWWRLUIPEDCHLY-UHFFFAOYSA-N 0.000 claims 1
- AOUOIIJWWFSLCP-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(1-methyltetrazol-5-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CC=C(C=2N(N=NN=2)C)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1C AOUOIIJWWFSLCP-UHFFFAOYSA-N 0.000 claims 1
- AXNLDNHUWVCRPF-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(3-methyl-1,2-oxazol-5-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound O1N=C(C)C=C1C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CN=CC=3)C)=CC=2)=C1 AXNLDNHUWVCRPF-UHFFFAOYSA-N 0.000 claims 1
- FOHRUTIEUZNDIQ-UHFFFAOYSA-N 3-methyl-n-[4-[2-methyl-5-(4-methyl-1,3-thiazol-2-yl)phenyl]phenyl]pyridine-4-carboxamide Chemical compound CC1=CSC(C=2C=C(C(C)=CC=2)C=2C=CC(NC(=O)C=3C(=CN=CC=3)C)=CC=2)=N1 FOHRUTIEUZNDIQ-UHFFFAOYSA-N 0.000 claims 1
- WOUMRZCHSWVQTK-UHFFFAOYSA-N 4-methyl-n-[4-(2-methyl-5-pyridin-2-ylphenyl)phenyl]thiadiazole-5-carboxamide Chemical compound N1=NSC(C(=O)NC=2C=CC(=CC=2)C=2C(=CC=C(C=2)C=2N=CC=CC=2)C)=C1C WOUMRZCHSWVQTK-UHFFFAOYSA-N 0.000 claims 1
- CLGKUTCVDXQFFI-UHFFFAOYSA-N 4-methyl-n-[4-(2-methyl-5-pyridin-3-ylphenyl)phenyl]thiadiazole-5-carboxamide Chemical compound N1=NSC(C(=O)NC=2C=CC(=CC=2)C=2C(=CC=C(C=2)C=2C=NC=CC=2)C)=C1C CLGKUTCVDXQFFI-UHFFFAOYSA-N 0.000 claims 1
- CLQLZLCGPUHVLW-UHFFFAOYSA-N 4-methyl-n-[4-[2-methyl-5-(1,2-oxazol-5-yl)phenyl]phenyl]thiadiazole-5-carboxamide Chemical compound N1=NSC(C(=O)NC=2C=CC(=CC=2)C=2C(=CC=C(C=2)C=2ON=CC=2)C)=C1C CLQLZLCGPUHVLW-UHFFFAOYSA-N 0.000 claims 1
- PTTPWZUIZKXKGY-UHFFFAOYSA-N 4-methyl-n-[4-[2-methyl-5-(1,3-thiazol-2-yl)phenyl]phenyl]thiadiazole-5-carboxamide Chemical compound N1=NSC(C(=O)NC=2C=CC(=CC=2)C=2C(=CC=C(C=2)C=2SC=CN=2)C)=C1C PTTPWZUIZKXKGY-UHFFFAOYSA-N 0.000 claims 1
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims 1
- 208000026935 allergic disease Diseases 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 239000000427 antigen Substances 0.000 claims 1
- 102000036639 antigens Human genes 0.000 claims 1
- 108091007433 antigens Proteins 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 230000004663 cell proliferation Effects 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- 210000000987 immune system Anatomy 0.000 claims 1
- 208000026278 immune system disease Diseases 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- 230000003834 intracellular effect Effects 0.000 claims 1
- JKAOBMCPBFAEQR-UHFFFAOYSA-N methyl 3-[4-[(2,6-difluorobenzoyl)amino]phenyl]-4-methylbenzoate Chemical compound COC(=O)C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=C1 JKAOBMCPBFAEQR-UHFFFAOYSA-N 0.000 claims 1
- UUROVLXVZCQYKJ-UHFFFAOYSA-N methyl 3-[4-[(3,5-difluoropyridine-4-carbonyl)amino]phenyl]-4-methylbenzoate Chemical compound COC(=O)C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CN=CC=3F)F)=CC=2)=C1 UUROVLXVZCQYKJ-UHFFFAOYSA-N 0.000 claims 1
- NOBHVWOAQXWKFL-UHFFFAOYSA-N methyl 3-[4-[(3-fluoropyridine-4-carbonyl)amino]phenyl]-4-methylbenzoate Chemical compound COC(=O)C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CN=CC=3)F)=CC=2)=C1 NOBHVWOAQXWKFL-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
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- REPOWMBMZCESPG-UHFFFAOYSA-N n-[4-(5-chloro-2-methoxypyridin-3-yl)phenyl]-2,6-difluorobenzamide Chemical compound COC1=NC=C(Cl)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F REPOWMBMZCESPG-UHFFFAOYSA-N 0.000 claims 1
- FFQDNYZYQQTJCY-UHFFFAOYSA-N n-[4-(5-chloro-2-methoxypyridin-3-yl)phenyl]-3-methylpyridine-4-carboxamide Chemical compound COC1=NC=C(Cl)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1C FFQDNYZYQQTJCY-UHFFFAOYSA-N 0.000 claims 1
- BVDBPRBGCAMVIK-UHFFFAOYSA-N n-[4-[2-(dimethylamino)-5-(1,3-oxazol-2-yl)phenyl]phenyl]-3-methylpyridine-4-carboxamide Chemical compound CN(C)C1=CC=C(C=2OC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1C BVDBPRBGCAMVIK-UHFFFAOYSA-N 0.000 claims 1
- BIIGGBDTMAWGEQ-UHFFFAOYSA-N n-[4-[2-chloro-5-(1,3-oxazol-2-yl)phenyl]phenyl]-2,6-difluorobenzamide Chemical compound FC1=CC=CC(F)=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2OC=CN=2)Cl)C=C1 BIIGGBDTMAWGEQ-UHFFFAOYSA-N 0.000 claims 1
- VJEMLWSCIVANKS-UHFFFAOYSA-N n-[4-[2-chloro-5-(1,3-oxazol-2-yl)phenyl]phenyl]-3,5-difluoropyridine-4-carboxamide Chemical compound FC1=CN=CC(F)=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2OC=CN=2)Cl)C=C1 VJEMLWSCIVANKS-UHFFFAOYSA-N 0.000 claims 1
- DOIRCJTXASVGPW-UHFFFAOYSA-N n-[4-[2-chloro-5-(1,3-oxazol-2-yl)phenyl]phenyl]-3-methylpyridine-4-carboxamide Chemical compound CC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2OC=CN=2)Cl)C=C1 DOIRCJTXASVGPW-UHFFFAOYSA-N 0.000 claims 1
- FBPZZKCLQCACGD-UHFFFAOYSA-N n-[4-[2-chloro-5-(1,3-thiazol-2-yl)phenyl]phenyl]-2,6-difluorobenzamide Chemical compound FC1=CC=CC(F)=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2SC=CN=2)Cl)C=C1 FBPZZKCLQCACGD-UHFFFAOYSA-N 0.000 claims 1
- RRPPHAPIBOIGBN-UHFFFAOYSA-N n-[4-[2-chloro-5-(1,3-thiazol-2-yl)phenyl]phenyl]-3,5-difluoropyridine-4-carboxamide Chemical compound FC1=CN=CC(F)=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2SC=CN=2)Cl)C=C1 RRPPHAPIBOIGBN-UHFFFAOYSA-N 0.000 claims 1
- CDXPRTPWAIUPGS-UHFFFAOYSA-N n-[4-[2-chloro-5-(1,3-thiazol-2-yl)phenyl]phenyl]-3-fluoropyridine-4-carboxamide Chemical compound FC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2SC=CN=2)Cl)C=C1 CDXPRTPWAIUPGS-UHFFFAOYSA-N 0.000 claims 1
- JOMGPQQJXLLZEM-UHFFFAOYSA-N n-[4-[2-chloro-5-(1,3-thiazol-2-yl)phenyl]phenyl]-3-methylpyridine-4-carboxamide Chemical compound CC1=CN=CC=C1C(=O)NC1=CC=C(C=2C(=CC=C(C=2)C=2SC=CN=2)Cl)C=C1 JOMGPQQJXLLZEM-UHFFFAOYSA-N 0.000 claims 1
- KOKVANSMRRJMMS-UHFFFAOYSA-N n-[4-[2-methoxy-5-(1,3-oxazol-2-yl)phenyl]phenyl]-3-methylpyridine-4-carboxamide Chemical compound COC1=CC=C(C=2OC=CN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1C KOKVANSMRRJMMS-UHFFFAOYSA-N 0.000 claims 1
- SOOVPSRHNUYTBZ-UHFFFAOYSA-N n-[4-[2-methoxy-5-(1,3-oxazol-5-yl)phenyl]phenyl]-4-methylthiadiazole-5-carboxamide Chemical compound COC1=CC=C(C=2OC=NC=2)C=C1C(C=C1)=CC=C1NC(=O)C=1SN=NC=1C SOOVPSRHNUYTBZ-UHFFFAOYSA-N 0.000 claims 1
- OSZIQZHRROTGTD-UHFFFAOYSA-N n-[4-[5-(5-amino-1,3,4-thiadiazol-2-yl)-2-methylphenyl]phenyl]-2,6-difluorobenzamide Chemical compound CC1=CC=C(C=2SC(N)=NN=2)C=C1C(C=C1)=CC=C1NC(=O)C1=C(F)C=CC=C1F OSZIQZHRROTGTD-UHFFFAOYSA-N 0.000 claims 1
- GEXVQFXUKFJYCI-UHFFFAOYSA-N n-[4-[5-(furan-2-yl)-2-methoxyphenyl]phenyl]-3-methylpyridine-4-carboxamide Chemical compound COC1=CC=C(C=2OC=CC=2)C=C1C(C=C1)=CC=C1NC(=O)C1=CC=NC=C1C GEXVQFXUKFJYCI-UHFFFAOYSA-N 0.000 claims 1
- PKVFLLHAPLTWRZ-UHFFFAOYSA-N n-[4-[5-[5-(dimethylamino)-1,3,4-thiadiazol-2-yl]-2-methylphenyl]phenyl]-2,6-difluoro-n-methylbenzamide Chemical compound S1C(N(C)C)=NN=C1C1=CC=C(C)C(C=2C=CC(=CC=2)N(C)C(=O)C=2C(=CC=CC=2F)F)=C1 PKVFLLHAPLTWRZ-UHFFFAOYSA-N 0.000 claims 1
- BZUOMZUMVYMSMW-UHFFFAOYSA-N n-[4-[5-[5-(dimethylamino)-1,3,4-thiadiazol-2-yl]-2-methylphenyl]phenyl]-2,6-difluorobenzamide Chemical compound S1C(N(C)C)=NN=C1C1=CC=C(C)C(C=2C=CC(NC(=O)C=3C(=CC=CC=3F)F)=CC=2)=C1 BZUOMZUMVYMSMW-UHFFFAOYSA-N 0.000 claims 1
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- 230000001105 regulatory effect Effects 0.000 claims 1
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 1
- 0 *C1C=CC(*)=CC1c(cc1)ccc1I* Chemical compound *C1C=CC(*)=CC1c(cc1)ccc1I* 0.000 description 1
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2006
- 2006-01-06 NZ NZ556546A patent/NZ556546A/en not_active IP Right Cessation
- 2006-01-06 US US11/326,872 patent/US8202999B2/en not_active Expired - Fee Related
- 2006-01-06 KR KR1020137034625A patent/KR20140018997A/ko not_active Ceased
- 2006-01-06 EP EP06733619.8A patent/EP1846372B1/en active Active
- 2006-01-06 MX MX2007008290A patent/MX2007008290A/es active IP Right Grant
- 2006-01-06 BR BRPI0606476-0A patent/BRPI0606476A2/pt not_active IP Right Cessation
- 2006-01-06 TW TW095100558A patent/TWI441819B/zh not_active IP Right Cessation
- 2006-01-06 AU AU2006211646A patent/AU2006211646B2/en not_active Ceased
- 2006-01-06 CA CA002593550A patent/CA2593550A1/en not_active Abandoned
- 2006-01-06 WO PCT/US2006/000296 patent/WO2006083477A2/en not_active Ceased
- 2006-01-06 JP JP2007550457A patent/JP5184891B2/ja not_active Expired - Fee Related
- 2006-01-06 KR KR1020077017923A patent/KR20070107022A/ko not_active Ceased
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2007
- 2007-07-05 IL IL184445A patent/IL184445A0/en unknown
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2012
- 2012-04-25 JP JP2012100291A patent/JP2012176959A/ja active Pending
- 2012-05-14 US US13/470,772 patent/US8592486B2/en not_active Expired - Fee Related
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2013
- 2013-10-15 US US14/053,896 patent/US20140039009A1/en not_active Abandoned