ES2388485T3 - Derivados de tienopiridona como activadores de proteína quinasa activada por AMP (AMPK) - Google Patents

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Publication number

ES2388485T3

ES2388485T3 ES09741799T ES09741799T ES2388485T3 ES 2388485 T3 ES2388485 T3 ES 2388485T3 ES 09741799 T ES09741799 T ES 09741799T ES 09741799 T ES09741799 T ES 09741799T ES 2388485 T3 ES2388485 T3 ES 2388485T3

Authority

ES

Spain

Prior art keywords

pyridin

hydroxy

dihydro

thieno

phenyl

Prior art date

2008-05-05

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.)

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• 239000012190 activator Substances 0.000 title claims description 16
• 108010011376 AMP-Activated Protein Kinases Proteins 0.000 title description 30
• 102000014156 AMP-Activated Protein Kinases Human genes 0.000 title description 30
• -1 COA Chemical group 0.000 claims description 216
• 150000001875 compounds Chemical class 0.000 claims description 118
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 76
• 102100036009 5'-AMP-activated protein kinase catalytic subunit alpha-2 Human genes 0.000 claims description 68
• 101000783681 Homo sapiens 5'-AMP-activated protein kinase catalytic subunit alpha-2 Proteins 0.000 claims description 68
• 239000000203 mixture Substances 0.000 claims description 65
• 150000003839 salts Chemical class 0.000 claims description 63
• WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 39
• 239000008103 glucose Substances 0.000 claims description 39
• 238000011282 treatment Methods 0.000 claims description 28
• 239000012453 solvate Substances 0.000 claims description 24
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 21
• 239000002253 acid Substances 0.000 claims description 20
• 206010012601 diabetes mellitus Diseases 0.000 claims description 20
• 238000000034 method Methods 0.000 claims description 19
• 125000004432 carbon atom Chemical group C* 0.000 claims description 14
• 239000003814 drug Substances 0.000 claims description 14
• 229910052801 chlorine Inorganic materials 0.000 claims description 12
• 206010028980 Neoplasm Diseases 0.000 claims description 11
• 208000001145 Metabolic Syndrome Diseases 0.000 claims description 9
• 241001103145 Pentas Species 0.000 claims description 9
• 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 claims description 9
• 125000000217 alkyl group Chemical group 0.000 claims description 9
• 201000011510 cancer Diseases 0.000 claims description 9
• 125000001624 naphthyl group Chemical group 0.000 claims description 9
• 238000002360 preparation method Methods 0.000 claims description 9
• 229910052740 iodine Inorganic materials 0.000 claims description 8
• 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 8
• 208000008589 Obesity Diseases 0.000 claims description 7
• 229910052794 bromium Inorganic materials 0.000 claims description 7
• 229940079593 drug Drugs 0.000 claims description 7
• 229910052731 fluorine Inorganic materials 0.000 claims description 7
• 235000020824 obesity Nutrition 0.000 claims description 7
• 230000008569 process Effects 0.000 claims description 7
• 125000004076 pyridyl group Chemical group 0.000 claims description 7
• 229910006074 SO2NH2 Inorganic materials 0.000 claims description 6
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
• 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
• 125000000565 sulfonamide group Chemical group 0.000 claims description 6
• HKWQMQBRXWPSSR-UHFFFAOYSA-N 2-chloro-4-hydroxy-3-[4-(2-hydroxyphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound OC1=CC=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2Cl)C=C1 HKWQMQBRXWPSSR-UHFFFAOYSA-N 0.000 claims description 5
• HVTRFLDXUYTKMF-UHFFFAOYSA-N 3-[4-(2-fluorophenyl)phenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C(=CC=CC=3)F)C=2C(O)=C1C1=CC=CC=C1 HVTRFLDXUYTKMF-UHFFFAOYSA-N 0.000 claims description 5
• ZVZONVVWRDQGNE-UHFFFAOYSA-N 3-[4-(2-fluorophenyl)phenyl]-4-hydroxy-5-pyridin-3-yl-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C(=CC=CC=3)F)C=2C(O)=C1C1=CC=CN=C1 ZVZONVVWRDQGNE-UHFFFAOYSA-N 0.000 claims description 5
• TUNBRRYXMOAFGR-UHFFFAOYSA-N 3-[4-(4-fluorophenyl)phenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=CC(F)=CC=3)C=2C(O)=C1C1=CC=CC=C1 TUNBRRYXMOAFGR-UHFFFAOYSA-N 0.000 claims description 5
• HRBOTPOUTZIVDY-UHFFFAOYSA-N 4-hydroxy-3-[4-(2-hydroxyphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound OC1=CC=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 HRBOTPOUTZIVDY-UHFFFAOYSA-N 0.000 claims description 5
• KQFDGZOTTHQOMD-UHFFFAOYSA-N 4-hydroxy-3-[4-(2-hydroxyphenyl)phenyl]-5-pyridin-3-yl-7h-thieno[2,3-b]pyridin-6-one Chemical compound OC1=CC=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=NC=CC=4)C(=O)NC=3SC=2)C=C1 KQFDGZOTTHQOMD-UHFFFAOYSA-N 0.000 claims description 5
• ISXUOTBGTHNDDA-UHFFFAOYSA-N 4-hydroxy-3-[4-(4-hydroxyphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound C1=CC(O)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 ISXUOTBGTHNDDA-UHFFFAOYSA-N 0.000 claims description 5
• DTPQCCSCLMZLMM-UHFFFAOYSA-N 4-hydroxy-3-[4-(4-methylphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound C1=CC(C)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 DTPQCCSCLMZLMM-UHFFFAOYSA-N 0.000 claims description 5
• GOSMRIZUTRINQV-UHFFFAOYSA-N 4-hydroxy-3-[4-[3-(hydroxymethyl)phenyl]phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound OCC1=CC=CC(C=2C=CC(=CC=2)C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)=C1 GOSMRIZUTRINQV-UHFFFAOYSA-N 0.000 claims description 5
• YHTGTTPAZVKQBC-UHFFFAOYSA-N 4-hydroxy-5-phenyl-3-(4-phenylphenyl)-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=CC=CC=3)C=2C(O)=C1C1=CC=CC=C1 YHTGTTPAZVKQBC-UHFFFAOYSA-N 0.000 claims description 5
• 125000002950 monocyclic group Chemical group 0.000 claims description 5
• WGOZPEQUBLQTLC-UHFFFAOYSA-N 4-hydroxy-3-[4-(4-methylphenyl)phenyl]-5-pyridin-3-yl-7h-thieno[2,3-b]pyridin-6-one Chemical compound C1=CC(C)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=NC=CC=4)C(=O)NC=3SC=2)C=C1 WGOZPEQUBLQTLC-UHFFFAOYSA-N 0.000 claims description 4
• FSVYOZALIBZRKZ-UHFFFAOYSA-N 4-hydroxy-3-[4-[4-(hydroxymethyl)phenyl]phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound C1=CC(CO)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 FSVYOZALIBZRKZ-UHFFFAOYSA-N 0.000 claims description 4
• YCARLBRXUQWPTN-UHFFFAOYSA-N 4-hydroxy-5-phenyl-3-(4-pyridin-4-ylphenyl)-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=CN=CC=3)C=2C(O)=C1C1=CC=CC=C1 YCARLBRXUQWPTN-UHFFFAOYSA-N 0.000 claims description 4
• DJYMHZDZGLVPAE-UHFFFAOYSA-N 4-hydroxy-5-phenyl-3-(6-phenylpyridin-3-yl)-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=NC(=CC=3)C=3C=CC=CC=3)C=2C(O)=C1C1=CC=CC=C1 DJYMHZDZGLVPAE-UHFFFAOYSA-N 0.000 claims description 4
• 206010061218 Inflammation Diseases 0.000 claims description 4
• 239000002671 adjuvant Substances 0.000 claims description 4
• 125000004429 atom Chemical group 0.000 claims description 4
• 125000002619 bicyclic group Chemical group 0.000 claims description 4
• 229910052799 carbon Inorganic materials 0.000 claims description 4
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
• 230000004054 inflammatory process Effects 0.000 claims description 4
• 210000000663 muscle cell Anatomy 0.000 claims description 4
• XBRXAVIHKNUPSS-UHFFFAOYSA-N 4-[4-(4-hydroxy-6-oxo-5-phenyl-7h-thieno[2,3-b]pyridin-3-yl)phenyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 XBRXAVIHKNUPSS-UHFFFAOYSA-N 0.000 claims description 3
• ZCZUMSNNMVMMAS-UHFFFAOYSA-N 4-hydroxy-3-[4-(2-hydroxyphenyl)phenyl]-5-pyridin-4-yl-7H-thieno[2,3-b]pyridin-6-one Chemical compound OC1=CC=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CN=CC=4)C(=O)NC=3SC=2)C=C1 ZCZUMSNNMVMMAS-UHFFFAOYSA-N 0.000 claims description 3
• MGJOTBAPEZWQAT-UHFFFAOYSA-N 4-hydroxy-3-[6-(2-methoxyphenyl)pyridin-3-yl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=N1 MGJOTBAPEZWQAT-UHFFFAOYSA-N 0.000 claims description 3
• HZYVPJJDGTUBNS-UHFFFAOYSA-N 4-hydroxy-5-phenyl-3-(4-pyridin-3-ylphenyl)-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=NC=CC=3)C=2C(O)=C1C1=CC=CC=C1 HZYVPJJDGTUBNS-UHFFFAOYSA-N 0.000 claims description 3
• 238000006069 Suzuki reaction reaction Methods 0.000 claims description 3
• 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 3
• 150000001642 boronic acid derivatives Chemical class 0.000 claims description 3
• 125000002541 furyl group Chemical group 0.000 claims description 3
• 125000005843 halogen group Chemical group 0.000 claims description 3
• 125000002883 imidazolyl group Chemical group 0.000 claims description 3
• 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 3
• 125000001041 indolyl group Chemical group 0.000 claims description 3
• 125000001786 isothiazolyl group Chemical group 0.000 claims description 3
• 125000000842 isoxazolyl group Chemical group 0.000 claims description 3
• 125000002971 oxazolyl group Chemical group 0.000 claims description 3
• 125000003226 pyrazolyl group Chemical group 0.000 claims description 3
• 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
• 125000000168 pyrrolyl group Chemical group 0.000 claims description 3
• 125000003831 tetrazolyl group Chemical group 0.000 claims description 3
• 125000000335 thiazolyl group Chemical group 0.000 claims description 3
• 125000001544 thienyl group Chemical group 0.000 claims description 3
• 125000001425 triazolyl group Chemical group 0.000 claims description 3
• HPTTXYJXYLWZMP-UHFFFAOYSA-N 2-chloro-4-hydroxy-3-[4-(2-methoxyphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2Cl)C=C1 HPTTXYJXYLWZMP-UHFFFAOYSA-N 0.000 claims description 2
• XRKVCIPNBVUNOM-UHFFFAOYSA-N 3-[4-(2,4-dihydroxyphenyl)phenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound OC1=CC(O)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 XRKVCIPNBVUNOM-UHFFFAOYSA-N 0.000 claims description 2
• PSKVUXBFAOLMEV-UHFFFAOYSA-N 3-[4-(2,4-dimethoxyphenyl)phenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC(OC)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 PSKVUXBFAOLMEV-UHFFFAOYSA-N 0.000 claims description 2
• DKTCYOOIYQCHPU-UHFFFAOYSA-N 3-[4-(3,5-dimethoxyphenyl)phenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC(OC)=CC(C=2C=CC(=CC=2)C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)=C1 DKTCYOOIYQCHPU-UHFFFAOYSA-N 0.000 claims description 2
• MNNIVGYMKHHKLK-UHFFFAOYSA-N 3-[4-(3-fluorophenyl)phenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=C(F)C=CC=3)C=2C(O)=C1C1=CC=CC=C1 MNNIVGYMKHHKLK-UHFFFAOYSA-N 0.000 claims description 2
• DPMPJJRQUVLLNX-UHFFFAOYSA-N 3-[4-(3-fluorophenyl)phenyl]-4-hydroxy-5-pyridin-3-yl-7h-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=C(F)C=CC=3)C=2C(O)=C1C1=CC=CN=C1 DPMPJJRQUVLLNX-UHFFFAOYSA-N 0.000 claims description 2
• DYXZTQMFFQSTDS-UHFFFAOYSA-N 3-[4-(4-fluoro-2-hydroxyphenyl)phenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound OC1=CC(F)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 DYXZTQMFFQSTDS-UHFFFAOYSA-N 0.000 claims description 2
• APOWVDDKGUFNPB-UHFFFAOYSA-N 3-[4-(4-fluoro-2-methoxyphenyl)phenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC(F)=CC=C1C1=CC=C(C=2C=3C(O)=C(C(=O)NC=3SC=2)C=2C=CC=CC=2)C=C1 APOWVDDKGUFNPB-UHFFFAOYSA-N 0.000 claims description 2
• YLVCSWFJCLXOGO-UHFFFAOYSA-N 3-[4-(4-fluorophenyl)-3-methoxyphenyl]-4-hydroxy-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC(C=2C=3C(O)=C(C(=O)NC=3SC=2)C=2C=CC=CC=2)=CC=C1C1=CC=C(F)C=C1 YLVCSWFJCLXOGO-UHFFFAOYSA-N 0.000 claims description 2
• CLIWKRAIDQNDQU-UHFFFAOYSA-N 3-[4-(4-fluorophenyl)phenyl]-4-hydroxy-5-pyridin-4-yl-7H-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=CC(F)=CC=3)C=2C(O)=C1C1=CC=NC=C1 CLIWKRAIDQNDQU-UHFFFAOYSA-N 0.000 claims description 2
• ZEDRAAJXGARDIS-UHFFFAOYSA-N 3-[4-(4-hydroxy-6-oxo-5-phenyl-7h-thieno[2,3-b]pyridin-3-yl)phenyl]benzonitrile Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=C(C=CC=3)C#N)C=2C(O)=C1C1=CC=CC=C1 ZEDRAAJXGARDIS-UHFFFAOYSA-N 0.000 claims description 2
• ZBVDTJFDNXUALS-UHFFFAOYSA-N 3-[4-(furan-3-yl)phenyl]-4-hydroxy-5-pyridin-4-yl-7H-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C3=COC=C3)C=2C(O)=C1C1=CC=NC=C1 ZBVDTJFDNXUALS-UHFFFAOYSA-N 0.000 claims description 2
• 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
• MTWIMYMYPYYTRG-UHFFFAOYSA-N 4-[2-hydroxy-4-(4-hydroxy-6-oxo-5-phenyl-7h-thieno[2,3-b]pyridin-3-yl)phenyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1O MTWIMYMYPYYTRG-UHFFFAOYSA-N 0.000 claims description 2
• HXNBUOOSTZVERZ-UHFFFAOYSA-N 4-[4-(4-hydroxy-6-oxo-5-phenyl-7h-thieno[2,3-b]pyridin-3-yl)-2-methoxyphenyl]benzoic acid Chemical compound COC1=CC(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)=CC=C1C1=CC=C(C(O)=O)C=C1 HXNBUOOSTZVERZ-UHFFFAOYSA-N 0.000 claims description 2
• LFKCDHBCVZVBII-UHFFFAOYSA-N 4-[4-(4-hydroxy-6-oxo-5-phenyl-7h-thieno[2,3-b]pyridin-3-yl)phenyl]benzonitrile Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=CC(=CC=3)C#N)C=2C(O)=C1C1=CC=CC=C1 LFKCDHBCVZVBII-UHFFFAOYSA-N 0.000 claims description 2
• URQQTAXFDKYCBG-UHFFFAOYSA-N 4-[4-hydroxy-6-oxo-3-(4-phenylphenyl)-7h-thieno[2,3-b]pyridin-5-yl]benzonitrile Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=CC=CC=3)C=2C(O)=C1C1=CC=C(C#N)C=C1 URQQTAXFDKYCBG-UHFFFAOYSA-N 0.000 claims description 2
• VYXPVECHTHYTBA-UHFFFAOYSA-N 4-hydroxy-3-(2-hydroxy-4-pyridin-4-ylphenyl)-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound OC1=CC(C=2C=CN=CC=2)=CC=C1C(C=1C=2O)=CSC=1NC(=O)C=2C1=CC=CC=C1 VYXPVECHTHYTBA-UHFFFAOYSA-N 0.000 claims description 2
• SQZLYUVSATVWOY-UHFFFAOYSA-N 4-hydroxy-3-(3-methoxy-4-phenylphenyl)-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)=CC=C1C1=CC=CC=C1 SQZLYUVSATVWOY-UHFFFAOYSA-N 0.000 claims description 2
• OKDLJCJWOFSGJV-UHFFFAOYSA-N 4-hydroxy-3-(3-methoxy-4-pyridin-3-ylphenyl)-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)=CC=C1C1=CC=CN=C1 OKDLJCJWOFSGJV-UHFFFAOYSA-N 0.000 claims description 2
• WWKPQYPBDLZBFP-UHFFFAOYSA-N 4-hydroxy-3-(4-phenylphenyl)-5-pyridin-4-yl-7H-thieno[2,3-b]pyridin-6-one Chemical compound O=C1NC=2SC=C(C=3C=CC(=CC=3)C=3C=CC=CC=3)C=2C(O)=C1C1=CC=NC=C1 WWKPQYPBDLZBFP-UHFFFAOYSA-N 0.000 claims description 2
• NHERQZNYRZEFLK-UHFFFAOYSA-N 4-hydroxy-3-[3-(3-hydroxyphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound OC1=CC=CC(C=2C=C(C=CC=2)C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)=C1 NHERQZNYRZEFLK-UHFFFAOYSA-N 0.000 claims description 2
• FKZKYHYIDYMOQM-UHFFFAOYSA-N 4-hydroxy-3-[3-(4-hydroxyphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound C1=CC(O)=CC=C1C1=CC=CC(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)=C1 FKZKYHYIDYMOQM-UHFFFAOYSA-N 0.000 claims description 2
• LQMSUXUHIPMIIL-UHFFFAOYSA-N 4-hydroxy-3-[3-hydroxy-4-(4-methylphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound C1=CC(C)=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1O LQMSUXUHIPMIIL-UHFFFAOYSA-N 0.000 claims description 2
• GXRDHQVJWKNVBT-UHFFFAOYSA-N 4-hydroxy-3-[3-methoxy-4-(4-methylphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)=CC=C1C1=CC=C(C)C=C1 GXRDHQVJWKNVBT-UHFFFAOYSA-N 0.000 claims description 2
• BGJUJGNPADCDMI-UHFFFAOYSA-N 4-hydroxy-3-[4-(2-methoxyphenyl)phenyl]-5-phenyl-7h-thieno[2,3-b]pyridin-6-one Chemical compound COC1=CC=CC=C1C1=CC=C(C=2C=3C(O)=C(C=4C=CC=CC=4)C(=O)NC=3SC=2)C=C1 BGJUJGNPADCDMI-UHFFFAOYSA-N 0.000 claims description 2
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