ES2660822T3 - Inhibidores de beta-hidrolasa para tratamiento del cáncer - Google Patents
Inhibidores de beta-hidrolasa para tratamiento del cáncer Download PDFInfo
- Publication number
- ES2660822T3 ES2660822T3 ES13838498.7T ES13838498T ES2660822T3 ES 2660822 T3 ES2660822 T3 ES 2660822T3 ES 13838498 T ES13838498 T ES 13838498T ES 2660822 T3 ES2660822 T3 ES 2660822T3
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- ES
- Spain
- Prior art keywords
- amino
- furanone
- oxy
- methyl
- chlorophenyl
- Prior art date
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- 238000011282 treatment Methods 0.000 title claims abstract description 31
- 206010028980 Neoplasm Diseases 0.000 title claims description 77
- 201000011510 cancer Diseases 0.000 title description 29
- 239000004093 hydrolase inhibitor Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 251
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 129
- 210000004027 cell Anatomy 0.000 claims abstract description 104
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 92
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 72
- 125000003118 aryl group Chemical group 0.000 claims abstract description 68
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 60
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 54
- 239000003112 inhibitor Substances 0.000 claims abstract description 46
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims abstract description 44
- 150000003839 salts Chemical class 0.000 claims abstract description 42
- 238000000034 method Methods 0.000 claims abstract description 39
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 38
- 239000012453 solvate Substances 0.000 claims abstract description 38
- 150000002148 esters Chemical class 0.000 claims abstract description 33
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 32
- 210000004881 tumor cell Anatomy 0.000 claims abstract description 22
- 239000001257 hydrogen Substances 0.000 claims abstract description 19
- 230000002062 proliferating effect Effects 0.000 claims abstract description 16
- 238000013508 migration Methods 0.000 claims abstract description 15
- 206010027476 Metastases Diseases 0.000 claims abstract description 14
- 230000009545 invasion Effects 0.000 claims abstract description 14
- 230000005012 migration Effects 0.000 claims abstract description 13
- 230000009401 metastasis Effects 0.000 claims abstract description 12
- 125000006736 (C6-C20) aryl group Chemical group 0.000 claims abstract description 10
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 9
- 230000035755 proliferation Effects 0.000 claims abstract description 9
- 125000000613 asparagine group Chemical group N[C@@H](CC(N)=O)C(=O)* 0.000 claims abstract description 6
- -1 2-thiazolyl Chemical group 0.000 claims description 598
- 125000001424 substituent group Chemical group 0.000 claims description 78
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 72
- 125000000217 alkyl group Chemical group 0.000 claims description 49
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 49
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 49
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 46
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 42
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 41
- 229910003827 NRaRb Inorganic materials 0.000 claims description 41
- 206010073071 hepatocellular carcinoma Diseases 0.000 claims description 37
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 34
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 25
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims description 24
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 23
- 201000002528 pancreatic cancer Diseases 0.000 claims description 23
- 208000008443 pancreatic carcinoma Diseases 0.000 claims description 23
- 125000001624 naphthyl group Chemical group 0.000 claims description 19
- 125000006708 (C5-C14) heteroaryl group Chemical group 0.000 claims description 14
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 14
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims description 13
- 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 description 12
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 12
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 12
- 239000008194 pharmaceutical composition Substances 0.000 claims description 12
- 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 description 11
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 11
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 11
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 11
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 11
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 11
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 11
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 11
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims description 11
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 11
- SZPWXAOBLNYOHY-UHFFFAOYSA-N [C]1=CC=NC2=CC=CC=C12 Chemical group [C]1=CC=NC2=CC=CC=C12 SZPWXAOBLNYOHY-UHFFFAOYSA-N 0.000 claims description 11
- 125000001617 2,3-dimethoxy phenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 10
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 10
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 10
- 125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 10
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 10
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 10
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
- ZCRZCMUDOWDGOB-UHFFFAOYSA-N ethanesulfonimidic acid Chemical compound CCS(N)(=O)=O ZCRZCMUDOWDGOB-UHFFFAOYSA-N 0.000 claims description 10
- 229960002317 succinimide Drugs 0.000 claims description 10
- 239000003937 drug carrier Substances 0.000 claims description 8
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims description 7
- 206010009944 Colon cancer Diseases 0.000 claims description 7
- 230000037396 body weight Effects 0.000 claims description 7
- 208000006990 cholangiocarcinoma Diseases 0.000 claims description 7
- 208000029742 colonic neoplasm Diseases 0.000 claims description 7
- 208000005017 glioblastoma Diseases 0.000 claims description 7
- 208000014018 liver neoplasm Diseases 0.000 claims description 7
- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 claims description 6
- 206010006187 Breast cancer Diseases 0.000 claims description 6
- 208000026310 Breast neoplasm Diseases 0.000 claims description 6
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 6
- 206010060862 Prostate cancer Diseases 0.000 claims description 6
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 6
- WRYVLBKLGDJEPA-UHFFFAOYSA-N [2-amino-5-(4-chlorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C=CC(Cl)=CC=2)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 WRYVLBKLGDJEPA-UHFFFAOYSA-N 0.000 claims description 6
- 201000005202 lung cancer Diseases 0.000 claims description 6
- 208000020816 lung neoplasm Diseases 0.000 claims description 6
- HJEJFKVSAXODHG-UHFFFAOYSA-N n-[5-(4-chlorophenyl)-3,4-dihydroxyfuran-2-yl]methanesulfonamide Chemical compound OC1=C(NS(=O)(=O)C)OC(C=2C=CC(Cl)=CC=2)=C1O HJEJFKVSAXODHG-UHFFFAOYSA-N 0.000 claims description 5
- NAXKDCHVHXHQRK-UHFFFAOYSA-N 1-[5-(4-chlorophenyl)-3,4-dihydroxyfuran-2-yl]pyrrolidin-2-one Chemical compound OC=1C(O)=C(C=2C=CC(Cl)=CC=2)OC=1N1CCCC1=O NAXKDCHVHXHQRK-UHFFFAOYSA-N 0.000 claims description 4
- UVBJSQGBODUPEH-UHFFFAOYSA-N 2-[3-(5-amino-4-benzylsulfonyloxy-3-oxofuran-2-yl)phenyl]acetic acid Chemical compound NC1=C(OS(=O)(=O)Cc2ccccc2)C(=O)C(O1)c1cccc(CC(O)=O)c1 UVBJSQGBODUPEH-UHFFFAOYSA-N 0.000 claims description 4
- LUMHNZAEHOKQLV-UHFFFAOYSA-N 5-amino-2-(4-chlorophenyl)-2-methyl-4-trimethylsilyloxyfuran-3-one Chemical compound C=1C=C(Cl)C=CC=1C1(C)OC(N)=C(O[Si](C)(C)C)C1=O LUMHNZAEHOKQLV-UHFFFAOYSA-N 0.000 claims description 4
- VRDRWMHTNNYGDU-UHFFFAOYSA-N 5-amino-2-(4-chlorophenyl)-4-hydroxy-2-methylfuran-3-one Chemical compound C=1C=C(Cl)C=CC=1C1(C)OC(N)=C(O)C1=O VRDRWMHTNNYGDU-UHFFFAOYSA-N 0.000 claims description 4
- XWHLBEUFQUKZHR-UHFFFAOYSA-N [2-(4-bromobutanoylamino)-5-(4-chlorophenyl)-4-hydroxyfuran-3-yl] acetate Chemical compound O1C(NC(=O)CCCBr)=C(OC(=O)C)C(O)=C1C1=CC=C(Cl)C=C1 XWHLBEUFQUKZHR-UHFFFAOYSA-N 0.000 claims description 4
- OWVQJWLKTXHRKW-UHFFFAOYSA-N [2-(benzenesulfonamido)-5-(4-chlorophenyl)-4-hydroxyfuran-3-yl] acetate Chemical compound CC(=O)OC=1C(O)=C(C=2C=CC(Cl)=CC=2)OC=1NS(=O)(=O)C1=CC=CC=C1 OWVQJWLKTXHRKW-UHFFFAOYSA-N 0.000 claims description 4
- YOJILVOCMQSCAB-UHFFFAOYSA-N [2-acetamido-5-(4-chlorophenyl)-4-hydroxyfuran-3-yl] acetate Chemical compound CC(=O)OC1=C(NC(=O)C)OC(C=2C=CC(Cl)=CC=2)=C1O YOJILVOCMQSCAB-UHFFFAOYSA-N 0.000 claims description 4
- JSENTRJIUXBCNY-UHFFFAOYSA-N [2-amino-4-oxo-5-[4-(trifluoromethyl)phenyl]furan-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C=CC(=CC=2)C(F)(F)F)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 JSENTRJIUXBCNY-UHFFFAOYSA-N 0.000 claims description 4
- RKSVAVTXWOUTKP-UHFFFAOYSA-N [2-amino-5-(2,3-dichlorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=C(Cl)C=CC=2)Cl)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 RKSVAVTXWOUTKP-UHFFFAOYSA-N 0.000 claims description 4
- FSAGXOYHOPYBLM-UHFFFAOYSA-N [2-amino-5-(2,4-dichlorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC(Cl)=CC=2)Cl)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 FSAGXOYHOPYBLM-UHFFFAOYSA-N 0.000 claims description 4
- NRSDXXYHJSXZIM-UHFFFAOYSA-N [2-amino-5-(2,5-dichlorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC=C(Cl)C=2)Cl)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 NRSDXXYHJSXZIM-UHFFFAOYSA-N 0.000 claims description 4
- ZINZHCFHUQQGOC-UHFFFAOYSA-N [2-amino-5-(2,5-difluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC=C(F)C=2)F)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 ZINZHCFHUQQGOC-UHFFFAOYSA-N 0.000 claims description 4
- UXLGTLOXBAKPJN-UHFFFAOYSA-N [2-amino-5-(2,6-difluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2F)F)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 UXLGTLOXBAKPJN-UHFFFAOYSA-N 0.000 claims description 4
- FOGWFWDJRVMWKA-UHFFFAOYSA-N [2-amino-5-(2-chlorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2)Cl)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 FOGWFWDJRVMWKA-UHFFFAOYSA-N 0.000 claims description 4
- RMXWGKXYBJIXBE-UHFFFAOYSA-N [2-amino-5-(2-fluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2)F)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 RMXWGKXYBJIXBE-UHFFFAOYSA-N 0.000 claims description 4
- XITRFEDNNGVURT-UHFFFAOYSA-N [2-amino-5-(3,4-dichlorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C=C(Cl)C(Cl)=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 XITRFEDNNGVURT-UHFFFAOYSA-N 0.000 claims description 4
- QRSZCGYMHKMZOG-UHFFFAOYSA-N [2-amino-5-(3,4-difluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C=C(F)C(F)=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 QRSZCGYMHKMZOG-UHFFFAOYSA-N 0.000 claims description 4
- TYLBFGJWPMBOSE-UHFFFAOYSA-N [2-amino-5-(3,5-dichlorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C=C(Cl)C=C(Cl)C=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 TYLBFGJWPMBOSE-UHFFFAOYSA-N 0.000 claims description 4
- GCYOEKPCUFCJOL-UHFFFAOYSA-N [2-amino-5-(3,5-difluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C=C(F)C=C(F)C=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 GCYOEKPCUFCJOL-UHFFFAOYSA-N 0.000 claims description 4
- SDGJJRNVCOGVAG-UHFFFAOYSA-N [2-amino-5-(3-chlorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C=C(Cl)C=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 SDGJJRNVCOGVAG-UHFFFAOYSA-N 0.000 claims description 4
- NHVBIMUJMMJGDO-UHFFFAOYSA-N [2-amino-5-(3-fluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C=C(F)C=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 NHVBIMUJMMJGDO-UHFFFAOYSA-N 0.000 claims description 4
- UKZKOHRWARZTOS-UHFFFAOYSA-N [2-amino-5-(4-chlorophenyl)-4-oxofuran-3-yl] (4-fluorophenyl)methanesulfonate Chemical compound O=C1C(C=2C=CC(Cl)=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=C(F)C=C1 UKZKOHRWARZTOS-UHFFFAOYSA-N 0.000 claims description 4
- XXJFDCICKAWHSZ-UHFFFAOYSA-N [2-amino-5-(4-chlorophenyl)-4-oxofuran-3-yl] butane-1-sulfonate Chemical compound O=C1C(OS(=O)(=O)CCCC)=C(N)OC1C1=CC=C(Cl)C=C1 XXJFDCICKAWHSZ-UHFFFAOYSA-N 0.000 claims description 4
- VCNOSHCOKRGAFH-UHFFFAOYSA-N [2-amino-5-(4-chlorophenyl)-4-oxofuran-3-yl] ethanesulfonate Chemical compound O=C1C(OS(=O)(=O)CC)=C(N)OC1C1=CC=C(Cl)C=C1 VCNOSHCOKRGAFH-UHFFFAOYSA-N 0.000 claims description 4
- AFTCLAGEFNWDOX-UHFFFAOYSA-N [2-amino-5-(4-chlorophenyl)-4-oxofuran-3-yl] methanesulfonate Chemical compound O=C1C(OS(=O)(=O)C)=C(N)OC1C1=CC=C(Cl)C=C1 AFTCLAGEFNWDOX-UHFFFAOYSA-N 0.000 claims description 4
- OWVBFOSPAPHJPY-UHFFFAOYSA-N [2-amino-5-(4-chlorophenyl)-4-oxofuran-3-yl] propane-1-sulfonate Chemical compound O=C1C(OS(=O)(=O)CCC)=C(N)OC1C1=CC=C(Cl)C=C1 OWVBFOSPAPHJPY-UHFFFAOYSA-N 0.000 claims description 4
- SYCCMZVSTUCIHF-UHFFFAOYSA-N [2-amino-5-(4-chlorophenyl)-4-oxofuran-3-yl] propane-2-sulfonate Chemical compound O=C1C(OS(=O)(=O)C(C)C)=C(N)OC1C1=CC=C(Cl)C=C1 SYCCMZVSTUCIHF-UHFFFAOYSA-N 0.000 claims description 4
- SLYSOBIJVWDZBX-UHFFFAOYSA-N [2-amino-5-(4-fluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C=CC(F)=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 SLYSOBIJVWDZBX-UHFFFAOYSA-N 0.000 claims description 4
- WFNHVZXNKPPPBO-UHFFFAOYSA-N [2-benzamido-5-(4-chlorophenyl)-4-hydroxyfuran-3-yl] acetate Chemical compound CC(=O)OC=1C(O)=C(C=2C=CC(Cl)=CC=2)OC=1NC(=O)C1=CC=CC=C1 WFNHVZXNKPPPBO-UHFFFAOYSA-N 0.000 claims description 4
- YGGYXRLVTAYOMN-UHFFFAOYSA-N [3-acetyloxy-5-(4-chlorophenyl)-4-hydroxyfuran-2-yl]carbamic acid Chemical compound C(C)(=O)OC1=C(OC(=C1O)C1=CC=C(C=C1)Cl)NC(O)=O YGGYXRLVTAYOMN-UHFFFAOYSA-N 0.000 claims description 4
- KSEDCPKLLWHSHW-UHFFFAOYSA-N [5-(4-chlorophenyl)-2-(2,5-dioxopyrrolidin-1-yl)-4-hydroxyfuran-3-yl] acetate Chemical compound CC(=O)OC=1C(O)=C(C=2C=CC(Cl)=CC=2)OC=1N1C(=O)CCC1=O KSEDCPKLLWHSHW-UHFFFAOYSA-N 0.000 claims description 4
- OGHXRSPEMPMFOE-UHFFFAOYSA-N [5-(4-chlorophenyl)-2-(ethylsulfonylamino)-4-hydroxyfuran-3-yl] acetate Chemical compound CC(=O)OC1=C(NS(=O)(=O)CC)OC(C=2C=CC(Cl)=CC=2)=C1O OGHXRSPEMPMFOE-UHFFFAOYSA-N 0.000 claims description 4
- VDQHKMUPBQTWTQ-UHFFFAOYSA-N [5-(4-chlorophenyl)-4-hydroxy-2-(2-oxopyrrolidin-1-yl)furan-3-yl] acetate Chemical compound CC(=O)OC=1C(O)=C(C=2C=CC(Cl)=CC=2)OC=1N1CCCC1=O VDQHKMUPBQTWTQ-UHFFFAOYSA-N 0.000 claims description 4
- FVIJYPJRMDJNGO-UHFFFAOYSA-N [5-(4-chlorophenyl)-4-hydroxy-2-(methanesulfonamido)furan-3-yl] acetate Chemical compound O1C(NS(C)(=O)=O)=C(OC(=O)C)C(O)=C1C1=CC=C(Cl)C=C1 FVIJYPJRMDJNGO-UHFFFAOYSA-N 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- DJGXIYUUEOOIOJ-UHFFFAOYSA-N n-[5-(4-chlorophenyl)-3,4-dihydroxyfuran-2-yl]acetamide Chemical compound OC1=C(NC(=O)C)OC(C=2C=CC(Cl)=CC=2)=C1O DJGXIYUUEOOIOJ-UHFFFAOYSA-N 0.000 claims description 4
- DPLHXRNPGUNHRQ-UHFFFAOYSA-N n-[5-(4-chlorophenyl)-3,4-dihydroxyfuran-2-yl]benzamide Chemical compound OC=1C(O)=C(C=2C=CC(Cl)=CC=2)OC=1NC(=O)C1=CC=CC=C1 DPLHXRNPGUNHRQ-UHFFFAOYSA-N 0.000 claims description 4
- XMIREYMMILAEME-UHFFFAOYSA-N n-[5-(4-chlorophenyl)-3,4-dihydroxyfuran-2-yl]benzenesulfonamide Chemical compound OC=1C(O)=C(C=2C=CC(Cl)=CC=2)OC=1NS(=O)(=O)C1=CC=CC=C1 XMIREYMMILAEME-UHFFFAOYSA-N 0.000 claims description 4
- WWHUSZQHRUNRSB-UHFFFAOYSA-N n-[5-(4-chlorophenyl)-3,4-dihydroxyfuran-2-yl]ethanesulfonamide Chemical compound OC1=C(NS(=O)(=O)CC)OC(C=2C=CC(Cl)=CC=2)=C1O WWHUSZQHRUNRSB-UHFFFAOYSA-N 0.000 claims description 4
- VRGPSZZFSFLPEF-UHFFFAOYSA-N o-[2-amino-5-(4-chlorophenyl)-4-oxofuran-3-yl] n-phenylcarbamothioate Chemical compound O=C1C(C=2C=CC(Cl)=CC=2)OC(N)=C1OC(=S)NC1=CC=CC=C1 VRGPSZZFSFLPEF-UHFFFAOYSA-N 0.000 claims description 4
- KZMXJOUETCOJAX-UHFFFAOYSA-N 1-[5-(4-chlorophenyl)-3,4-dihydroxyfuran-2-yl]pyrrolidine-2,5-dione Chemical compound OC=1C(O)=C(C=2C=CC(Cl)=CC=2)OC=1N1C(=O)CCC1=O KZMXJOUETCOJAX-UHFFFAOYSA-N 0.000 claims description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- TYAYBWQIEWVCKO-UHFFFAOYSA-N [2-(3-bromopropylsulfonylamino)-5-(4-chlorophenyl)-4-hydroxyfuran-3-yl] acetate Chemical compound O1C(NS(=O)(=O)CCCBr)=C(OC(=O)C)C(O)=C1C1=CC=C(Cl)C=C1 TYAYBWQIEWVCKO-UHFFFAOYSA-N 0.000 claims description 3
- UEIXZUNCVZXURR-UHFFFAOYSA-N [2-amino-5-(2,3-difluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=C(F)C=CC=2)F)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 UEIXZUNCVZXURR-UHFFFAOYSA-N 0.000 claims description 3
- UZMVSVRIMLYTFC-UHFFFAOYSA-N [2-amino-5-(2,3-dimethoxyphenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound COC1=CC=CC(C2C(C(OS(=O)(=O)CC=3C=CC=CC=3)=C(N)O2)=O)=C1OC UZMVSVRIMLYTFC-UHFFFAOYSA-N 0.000 claims description 3
- MRANPYZDQRPVMQ-UHFFFAOYSA-N [2-amino-5-(2,4-difluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC(F)=CC=2)F)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 MRANPYZDQRPVMQ-UHFFFAOYSA-N 0.000 claims description 3
- UTLRIETUSATVLU-UHFFFAOYSA-N [2-amino-5-(2,4-dimethoxyphenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound COC1=CC(OC)=CC=C1C1C(=O)C(OS(=O)(=O)CC=2C=CC=CC=2)=C(N)O1 UTLRIETUSATVLU-UHFFFAOYSA-N 0.000 claims description 3
- ABEXEQNVKLVRTN-UHFFFAOYSA-N [2-amino-5-(2,5-dimethoxyphenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound COC1=CC=C(OC)C(C2C(C(OS(=O)(=O)CC=3C=CC=CC=3)=C(N)O2)=O)=C1 ABEXEQNVKLVRTN-UHFFFAOYSA-N 0.000 claims description 3
- NWAYGVMPOGETRW-UHFFFAOYSA-N [2-amino-5-(2,6-dimethoxyphenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound COC1=CC=CC(OC)=C1C1C(=O)C(OS(=O)(=O)CC=2C=CC=CC=2)=C(N)O1 NWAYGVMPOGETRW-UHFFFAOYSA-N 0.000 claims description 3
- LBPGBBOUMNREPT-UHFFFAOYSA-N [2-amino-5-(2-chloro-4-fluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC(F)=CC=2)Cl)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 LBPGBBOUMNREPT-UHFFFAOYSA-N 0.000 claims description 3
- KFIICSGBLRSJPA-UHFFFAOYSA-N [2-amino-5-(2-chloro-5-fluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC=C(F)C=2)Cl)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 KFIICSGBLRSJPA-UHFFFAOYSA-N 0.000 claims description 3
- MDJJAEKJZSERFA-UHFFFAOYSA-N [2-amino-5-(2-chloro-6-fluorophenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2F)Cl)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 MDJJAEKJZSERFA-UHFFFAOYSA-N 0.000 claims description 3
- YXFYSGOXEMVSMD-UHFFFAOYSA-N [2-amino-5-(2-methoxyphenyl)-4-oxofuran-3-yl] phenylmethanesulfonate Chemical compound COC1=CC=CC=C1C1C(=O)C(OS(=O)(=O)CC=2C=CC=CC=2)=C(N)O1 YXFYSGOXEMVSMD-UHFFFAOYSA-N 0.000 claims description 3
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- VUFCEWCXUGOJHE-UHFFFAOYSA-N (2-amino-4-oxo-5-pyridin-3-ylfuran-3-yl) phenylmethanesulfonate Chemical compound O=C1C(C=2C=NC=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 VUFCEWCXUGOJHE-UHFFFAOYSA-N 0.000 claims description 2
- LPLKWAFFHXFBLQ-UHFFFAOYSA-N (2-amino-4-oxo-5-pyridin-4-ylfuran-3-yl) phenylmethanesulfonate Chemical compound O=C1C(C=2C=CN=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 LPLKWAFFHXFBLQ-UHFFFAOYSA-N 0.000 claims description 2
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- NWJKACQHXANJDX-UHFFFAOYSA-N (2-amino-5-naphthalen-2-yl-4-oxofuran-3-yl) phenylmethanesulfonate Chemical compound O=C1C(C=2C=C3C=CC=CC3=CC=2)OC(N)=C1OS(=O)(=O)CC1=CC=CC=C1 NWJKACQHXANJDX-UHFFFAOYSA-N 0.000 claims description 2
- 229910020364 ClSO2 Inorganic materials 0.000 claims description 2
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- 125000001475 halogen functional group Chemical group 0.000 claims 25
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- YUQKKNQBFGXOKN-UHFFFAOYSA-N [2-amino-4-oxo-5-(1,3-thiazol-2-yl)furan-3-yl] benzenesulfonate Chemical compound O=C1C(C=2SC=CN=2)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 YUQKKNQBFGXOKN-UHFFFAOYSA-N 0.000 description 1
- IAZUJSBYPKUENN-UHFFFAOYSA-N [2-amino-5-(2,3-dichlorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=CC(Cl)=C1Cl IAZUJSBYPKUENN-UHFFFAOYSA-N 0.000 description 1
- VRJDKZLPFQTSCX-UHFFFAOYSA-N [2-amino-5-(2,3-dichlorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=C(Cl)C=CC=2)Cl)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 VRJDKZLPFQTSCX-UHFFFAOYSA-N 0.000 description 1
- WHSNAVZHMKCVDP-UHFFFAOYSA-N [2-amino-5-(2,3-dichlorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC=CC(Cl)=C1Cl WHSNAVZHMKCVDP-UHFFFAOYSA-N 0.000 description 1
- MXIGMWGLAZDIBP-UHFFFAOYSA-N [2-amino-5-(2,3-difluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound CC(=O)OC1=C(N)OC(C1=O)c1cccc(F)c1F MXIGMWGLAZDIBP-UHFFFAOYSA-N 0.000 description 1
- SZPQTUZCIQHRCN-UHFFFAOYSA-N [2-amino-5-(2,3-difluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=C(F)C=CC=2)F)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 SZPQTUZCIQHRCN-UHFFFAOYSA-N 0.000 description 1
- PFCRHOBCDYQPJM-UHFFFAOYSA-N [2-amino-5-(2,3-dimethoxyphenyl)-4-oxofuran-3-yl] acetate Chemical compound COC1=CC=CC(C2C(C(OC(C)=O)=C(N)O2)=O)=C1OC PFCRHOBCDYQPJM-UHFFFAOYSA-N 0.000 description 1
- SFNMSLUOLHZDSK-UHFFFAOYSA-N [2-amino-5-(2,3-dimethoxyphenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound COC1=CC=CC(C2C(C(OS(=O)(=O)C=3C=CC=CC=3)=C(N)O2)=O)=C1OC SFNMSLUOLHZDSK-UHFFFAOYSA-N 0.000 description 1
- ZYCNUHAHVIJHJY-UHFFFAOYSA-N [2-amino-5-(2,3-dimethoxyphenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound COc1cccc(c1OC)C1(C)OC(N)=C(OC(C)=O)C1=O ZYCNUHAHVIJHJY-UHFFFAOYSA-N 0.000 description 1
- KXOOYLLKBAEHSY-UHFFFAOYSA-N [2-amino-5-(2,4-dichlorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=C(Cl)C=C1Cl KXOOYLLKBAEHSY-UHFFFAOYSA-N 0.000 description 1
- OHHRFXAVRNIYLS-UHFFFAOYSA-N [2-amino-5-(2,4-dichlorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC(Cl)=CC=2)Cl)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 OHHRFXAVRNIYLS-UHFFFAOYSA-N 0.000 description 1
- IJSWZKDLUPRKFT-UHFFFAOYSA-N [2-amino-5-(2,4-dichlorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC=C(Cl)C=C1Cl IJSWZKDLUPRKFT-UHFFFAOYSA-N 0.000 description 1
- GFZBICPYEYJDEF-UHFFFAOYSA-N [2-amino-5-(2,4-difluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=C(F)C=C1F GFZBICPYEYJDEF-UHFFFAOYSA-N 0.000 description 1
- SNAUJVRREQYERY-UHFFFAOYSA-N [2-amino-5-(2,4-difluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC(F)=CC=2)F)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 SNAUJVRREQYERY-UHFFFAOYSA-N 0.000 description 1
- ISFGFJGJOFKYSG-UHFFFAOYSA-N [2-amino-5-(2,4-difluorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC=C(F)C=C1F ISFGFJGJOFKYSG-UHFFFAOYSA-N 0.000 description 1
- VIMXSEYLOLBBKO-UHFFFAOYSA-N [2-amino-5-(2,4-dimethoxyphenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound COC1=CC(OC)=CC=C1C1C(=O)C(OS(=O)(=O)C=2C=CC=CC=2)=C(N)O1 VIMXSEYLOLBBKO-UHFFFAOYSA-N 0.000 description 1
- DLUHDFMIUBOWTD-UHFFFAOYSA-N [2-amino-5-(2,4-dimethoxyphenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound COc1ccc(c(OC)c1)C1(C)OC(N)=C(OC(C)=O)C1=O DLUHDFMIUBOWTD-UHFFFAOYSA-N 0.000 description 1
- ILEDDHIDOILLGM-UHFFFAOYSA-N [2-amino-5-(2,5-dichlorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC(Cl)=CC=C1Cl ILEDDHIDOILLGM-UHFFFAOYSA-N 0.000 description 1
- XEOWHUIHICYMTA-UHFFFAOYSA-N [2-amino-5-(2,5-dichlorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC=C(Cl)C=2)Cl)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 XEOWHUIHICYMTA-UHFFFAOYSA-N 0.000 description 1
- RNOLXSXGBMEJCT-UHFFFAOYSA-N [2-amino-5-(2,5-dichlorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC(Cl)=CC=C1Cl RNOLXSXGBMEJCT-UHFFFAOYSA-N 0.000 description 1
- MYKYSAFTRITHJG-UHFFFAOYSA-N [2-amino-5-(2,5-difluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC(F)=CC=C1F MYKYSAFTRITHJG-UHFFFAOYSA-N 0.000 description 1
- RNRJGZXQGGOSKH-UHFFFAOYSA-N [2-amino-5-(2,5-difluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound NC1=C(OS(=O)(=O)c2ccccc2)C(=O)C(O1)c1cc(F)ccc1F RNRJGZXQGGOSKH-UHFFFAOYSA-N 0.000 description 1
- DZXJSUDKVNVBAM-UHFFFAOYSA-N [2-amino-5-(2,5-difluorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC(F)=CC=C1F DZXJSUDKVNVBAM-UHFFFAOYSA-N 0.000 description 1
- GZEOSTIBUAQHSZ-UHFFFAOYSA-N [2-amino-5-(2,5-dimethoxyphenyl)-4-oxofuran-3-yl] acetate Chemical compound COC1=CC=C(OC)C(C2C(C(OC(C)=O)=C(N)O2)=O)=C1 GZEOSTIBUAQHSZ-UHFFFAOYSA-N 0.000 description 1
- GWLBRJJMJBABLD-UHFFFAOYSA-N [2-amino-5-(2,5-dimethoxyphenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound COC1=CC=C(OC)C(C2C(C(OS(=O)(=O)C=3C=CC=CC=3)=C(N)O2)=O)=C1 GWLBRJJMJBABLD-UHFFFAOYSA-N 0.000 description 1
- DGJAJVNMEWSBDK-UHFFFAOYSA-N [2-amino-5-(2,5-dimethoxyphenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound COc1ccc(OC)c(c1)C1(C)OC(N)=C(OC(C)=O)C1=O DGJAJVNMEWSBDK-UHFFFAOYSA-N 0.000 description 1
- IODUIQVANHEXKN-UHFFFAOYSA-N [2-amino-5-(2,6-dichlorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=C(Cl)C=CC=C1Cl IODUIQVANHEXKN-UHFFFAOYSA-N 0.000 description 1
- IEKWYOUMOLCHKW-UHFFFAOYSA-N [2-amino-5-(2,6-dichlorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2Cl)Cl)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 IEKWYOUMOLCHKW-UHFFFAOYSA-N 0.000 description 1
- FUAZXQIGWXKSTA-UHFFFAOYSA-N [2-amino-5-(2,6-dichlorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=C(Cl)C=CC=C1Cl FUAZXQIGWXKSTA-UHFFFAOYSA-N 0.000 description 1
- BQHVRSFIKAIJEL-UHFFFAOYSA-N [2-amino-5-(2,6-difluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=C(F)C=CC=C1F BQHVRSFIKAIJEL-UHFFFAOYSA-N 0.000 description 1
- BXUALRSNSBTXQB-UHFFFAOYSA-N [2-amino-5-(2,6-difluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2F)F)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 BXUALRSNSBTXQB-UHFFFAOYSA-N 0.000 description 1
- IPAJEBBSTXYVCR-UHFFFAOYSA-N [2-amino-5-(2,6-difluorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=C(F)C=CC=C1F IPAJEBBSTXYVCR-UHFFFAOYSA-N 0.000 description 1
- NRDXIJFRXBQGEH-UHFFFAOYSA-N [2-amino-5-(2,6-dimethoxyphenyl)-4-oxofuran-3-yl] acetate Chemical compound COC1=CC=CC(OC)=C1C1C(=O)C(OC(C)=O)=C(N)O1 NRDXIJFRXBQGEH-UHFFFAOYSA-N 0.000 description 1
- WYHTXEHHZIYMMP-UHFFFAOYSA-N [2-amino-5-(2,6-dimethoxyphenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound COC1=CC=CC(OC)=C1C1C(=O)C(OS(=O)(=O)C=2C=CC=CC=2)=C(N)O1 WYHTXEHHZIYMMP-UHFFFAOYSA-N 0.000 description 1
- CKBDABZTHILGTH-UHFFFAOYSA-N [2-amino-5-(2,6-dimethoxyphenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound COc1cccc(OC)c1C1(C)OC(N)=C(OC(C)=O)C1=O CKBDABZTHILGTH-UHFFFAOYSA-N 0.000 description 1
- YOWYZJWQVOLGOH-UHFFFAOYSA-N [2-amino-5-(2-chloro-4-fluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=C(F)C=C1Cl YOWYZJWQVOLGOH-UHFFFAOYSA-N 0.000 description 1
- GXLRGKKDYSCJPR-UHFFFAOYSA-N [2-amino-5-(2-chloro-4-fluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC(F)=CC=2)Cl)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 GXLRGKKDYSCJPR-UHFFFAOYSA-N 0.000 description 1
- ZPJWRKRCXMROJV-UHFFFAOYSA-N [2-amino-5-(2-chloro-4-fluorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC=C(F)C=C1Cl ZPJWRKRCXMROJV-UHFFFAOYSA-N 0.000 description 1
- BRQIHLGKUQAROQ-UHFFFAOYSA-N [2-amino-5-(2-chloro-5-fluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC(F)=CC=C1Cl BRQIHLGKUQAROQ-UHFFFAOYSA-N 0.000 description 1
- PKMDHALYVILUCA-UHFFFAOYSA-N [2-amino-5-(2-chloro-5-fluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC=C(F)C=2)Cl)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 PKMDHALYVILUCA-UHFFFAOYSA-N 0.000 description 1
- DKHJMFILTVWGBB-UHFFFAOYSA-N [2-amino-5-(2-chloro-5-fluorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC(F)=CC=C1Cl DKHJMFILTVWGBB-UHFFFAOYSA-N 0.000 description 1
- DLXSDJVYRAGRJE-UHFFFAOYSA-N [2-amino-5-(2-chloro-6-fluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=C(F)C=CC=C1Cl DLXSDJVYRAGRJE-UHFFFAOYSA-N 0.000 description 1
- KPKFBCUEFMLDGC-UHFFFAOYSA-N [2-amino-5-(2-chloro-6-fluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2F)Cl)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 KPKFBCUEFMLDGC-UHFFFAOYSA-N 0.000 description 1
- USCVGGPTWJKLCN-UHFFFAOYSA-N [2-amino-5-(2-chloro-6-fluorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=C(F)C=CC=C1Cl USCVGGPTWJKLCN-UHFFFAOYSA-N 0.000 description 1
- GRZPSWNJXULSOA-UHFFFAOYSA-N [2-amino-5-(2-chlorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=CC=C1Cl GRZPSWNJXULSOA-UHFFFAOYSA-N 0.000 description 1
- LANZQBDLGIUMFO-UHFFFAOYSA-N [2-amino-5-(2-chlorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2)Cl)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 LANZQBDLGIUMFO-UHFFFAOYSA-N 0.000 description 1
- GDMNOGWOYRQEOW-UHFFFAOYSA-N [2-amino-5-(2-chlorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC=CC=C1Cl GDMNOGWOYRQEOW-UHFFFAOYSA-N 0.000 description 1
- CXVQTAKFWFDBRJ-UHFFFAOYSA-N [2-amino-5-(2-fluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=CC=C1F CXVQTAKFWFDBRJ-UHFFFAOYSA-N 0.000 description 1
- UXUIDNZBMAWGOL-UHFFFAOYSA-N [2-amino-5-(2-fluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=CC=CC=2)F)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 UXUIDNZBMAWGOL-UHFFFAOYSA-N 0.000 description 1
- YMQVMZZYYRZUEF-UHFFFAOYSA-N [2-amino-5-(2-methoxyphenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound COc1ccccc1C1OC(N)=C(OS(=O)(=O)c2ccccc2)C1=O YMQVMZZYYRZUEF-UHFFFAOYSA-N 0.000 description 1
- GGROGJPCDXAHNK-UHFFFAOYSA-N [2-amino-5-(2-methoxyphenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound COC1=CC=CC=C1C1(C)C(=O)C(OC(C)=O)=C(N)O1 GGROGJPCDXAHNK-UHFFFAOYSA-N 0.000 description 1
- UAXZJDXJNUQGQI-UHFFFAOYSA-N [2-amino-5-(3,4-dichlorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=C(Cl)C(Cl)=C1 UAXZJDXJNUQGQI-UHFFFAOYSA-N 0.000 description 1
- AVKMPECSIBQYRX-UHFFFAOYSA-N [2-amino-5-(3,4-dichlorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C=C(Cl)C(Cl)=CC=2)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 AVKMPECSIBQYRX-UHFFFAOYSA-N 0.000 description 1
- KBLBNCUEDDUEEI-UHFFFAOYSA-N [2-amino-5-(3,4-dichlorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC=C(Cl)C(Cl)=C1 KBLBNCUEDDUEEI-UHFFFAOYSA-N 0.000 description 1
- UTHXJPXONYGHOD-UHFFFAOYSA-N [2-amino-5-(3,4-difluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=C(F)C(F)=C1 UTHXJPXONYGHOD-UHFFFAOYSA-N 0.000 description 1
- BXVAYUGHSCEXDY-UHFFFAOYSA-N [2-amino-5-(3,4-difluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound NC1=C(OS(=O)(=O)c2ccccc2)C(=O)C(O1)c1ccc(F)c(F)c1 BXVAYUGHSCEXDY-UHFFFAOYSA-N 0.000 description 1
- CXXVCCDYVAVBLL-UHFFFAOYSA-N [2-amino-5-(3,4-difluorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC=C(F)C(F)=C1 CXXVCCDYVAVBLL-UHFFFAOYSA-N 0.000 description 1
- FIZAOYJRNDGYRX-UHFFFAOYSA-N [2-amino-5-(3,4-dimethoxyphenyl)-4-oxofuran-3-yl] acetate Chemical compound C1=C(OC)C(OC)=CC=C1C1C(=O)C(OC(C)=O)=C(N)O1 FIZAOYJRNDGYRX-UHFFFAOYSA-N 0.000 description 1
- USJCDHLBHAYGSR-UHFFFAOYSA-N [2-amino-5-(3,4-dimethoxyphenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound C1=C(OC)C(OC)=CC=C1C1C(=O)C(OS(=O)(=O)C=2C=CC=CC=2)=C(N)O1 USJCDHLBHAYGSR-UHFFFAOYSA-N 0.000 description 1
- SJAKAHOSCAZZPW-UHFFFAOYSA-N [2-amino-5-(3,4-dimethoxyphenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound COc1ccc(cc1OC)C1(C)OC(N)=C(OC(C)=O)C1=O SJAKAHOSCAZZPW-UHFFFAOYSA-N 0.000 description 1
- ZQSUGUORWWFBKC-UHFFFAOYSA-N [2-amino-5-(3,5-dichlorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC(Cl)=CC(Cl)=C1 ZQSUGUORWWFBKC-UHFFFAOYSA-N 0.000 description 1
- INDXVQDMMXFVLI-UHFFFAOYSA-N [2-amino-5-(3,5-dichlorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C=C(Cl)C=C(Cl)C=2)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 INDXVQDMMXFVLI-UHFFFAOYSA-N 0.000 description 1
- JYBATYLRAVUYBP-UHFFFAOYSA-N [2-amino-5-(3,5-dichlorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC(Cl)=CC(Cl)=C1 JYBATYLRAVUYBP-UHFFFAOYSA-N 0.000 description 1
- ZEHANCIPCFXJGP-UHFFFAOYSA-N [2-amino-5-(3,5-difluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC(F)=CC(F)=C1 ZEHANCIPCFXJGP-UHFFFAOYSA-N 0.000 description 1
- PMAUEXFYSIEQRE-UHFFFAOYSA-N [2-amino-5-(3,5-difluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C=C(F)C=C(F)C=2)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 PMAUEXFYSIEQRE-UHFFFAOYSA-N 0.000 description 1
- FGSLDKGEKUFQAM-UHFFFAOYSA-N [2-amino-5-(3,5-difluorophenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1(C)C1=CC(F)=CC(F)=C1 FGSLDKGEKUFQAM-UHFFFAOYSA-N 0.000 description 1
- LMFIEEHVCBAMGC-UHFFFAOYSA-N [2-amino-5-(3,5-dimethoxyphenyl)-4-oxofuran-3-yl] acetate Chemical compound COC1=CC(OC)=CC(C2C(C(OC(C)=O)=C(N)O2)=O)=C1 LMFIEEHVCBAMGC-UHFFFAOYSA-N 0.000 description 1
- WPQXMLHJJFCBSI-UHFFFAOYSA-N [2-amino-5-(3,5-dimethoxyphenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound COC1=CC(OC)=CC(C2C(C(OS(=O)(=O)C=3C=CC=CC=3)=C(N)O2)=O)=C1 WPQXMLHJJFCBSI-UHFFFAOYSA-N 0.000 description 1
- VYQQDWDKWRZYGA-UHFFFAOYSA-N [2-amino-5-(3,5-dimethoxyphenyl)-5-methyl-4-oxofuran-3-yl] acetate Chemical compound COc1cc(OC)cc(c1)C1(C)OC(N)=C(OC(C)=O)C1=O VYQQDWDKWRZYGA-UHFFFAOYSA-N 0.000 description 1
- GQIDGFDRMXDMBO-UHFFFAOYSA-N [2-amino-5-(3-chloro-2-fluorophenyl)-4-oxofuran-3-yl] acetate Chemical compound O=C1C(OC(=O)C)=C(N)OC1C1=CC=CC(Cl)=C1F GQIDGFDRMXDMBO-UHFFFAOYSA-N 0.000 description 1
- WXALLPITIJSDEZ-UHFFFAOYSA-N [2-amino-5-(3-chloro-2-fluorophenyl)-4-oxofuran-3-yl] benzenesulfonate Chemical compound O=C1C(C=2C(=C(Cl)C=CC=2)F)OC(N)=C1OS(=O)(=O)C1=CC=CC=C1 WXALLPITIJSDEZ-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/32—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/66—Nitrogen atoms
-
- 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
- C07D405/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/26—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261704014P | 2012-09-21 | 2012-09-21 | |
| US201261704014P | 2012-09-21 | ||
| PCT/US2013/061050 WO2014047519A2 (en) | 2012-09-21 | 2013-09-20 | Inhibitors of beta-hydrolase for treatment of cancer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2660822T3 true ES2660822T3 (es) | 2018-03-26 |
Family
ID=50342080
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES13838498.7T Active ES2660822T3 (es) | 2012-09-21 | 2013-09-20 | Inhibidores de beta-hidrolasa para tratamiento del cáncer |
| ES17202827T Active ES2865412T3 (es) | 2012-09-21 | 2013-09-20 | Inhibidores de beta-hidrolasa para tratamiento del cáncer |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES17202827T Active ES2865412T3 (es) | 2012-09-21 | 2013-09-20 | Inhibidores de beta-hidrolasa para tratamiento del cáncer |
Country Status (10)
| Country | Link |
|---|---|
| US (8) | US9771356B2 (https=) |
| EP (2) | EP3345596B1 (https=) |
| JP (1) | JP6469009B2 (https=) |
| KR (1) | KR102137180B1 (https=) |
| CN (2) | CN104902889A (https=) |
| AU (1) | AU2013317791B2 (https=) |
| CA (1) | CA2885762C (https=) |
| ES (2) | ES2660822T3 (https=) |
| HK (1) | HK1208805A1 (https=) |
| WO (2) | WO2014047519A2 (https=) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2660822T3 (es) | 2012-09-21 | 2018-03-26 | Rhode Island Hospital | Inhibidores de beta-hidrolasa para tratamiento del cáncer |
| EP3652542A1 (en) * | 2017-07-14 | 2020-05-20 | Protea Biopharma N.V. | Methods and means for diagnosing and/or treating a fatiguing illness |
| WO2019246093A1 (en) * | 2018-06-18 | 2019-12-26 | Midwestern University | Monoclonal antibodies targeting epitopes of asph |
| CN109364251A (zh) * | 2018-12-06 | 2019-02-22 | 苏州大学 | Tet蛋白在治疗抑郁症中的应用 |
| CA3130396A1 (en) | 2019-02-15 | 2020-08-20 | Midwestern University | Isotopically-stabilized tetronimide compounds |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD39717A (https=) | ||||
| DE39717C (de) | H. LEHMANN in München, Enhuberstr. 5 part | Bleistifthalter | ||
| EP0232258B1 (en) | 1985-08-02 | 1990-05-02 | Chevron Research And Technology Company | Herbicidal 2-(oxa or thia heterocycle)5-amino-3-oxo-4-(substituted-phenyl)-2,3-dihydrofurans |
| US5314913A (en) * | 1992-12-08 | 1994-05-24 | American Home Products Corporation | 4- or 5-(substituted sulfonyl)methyl-3(2H)-furanones |
| JPH09110853A (ja) * | 1995-10-12 | 1997-04-28 | Kikkoman Corp | 4‐アシルオキシフラノン誘導体又はその塩及びその製造方法 |
| US5698585A (en) | 1995-04-13 | 1997-12-16 | Kikkoman Corporation | Pharmaceutical preparation for prevention and/or treatment for cataract |
| UA57002C2 (uk) | 1995-10-13 | 2003-06-16 | Мерк Фросст Кенада Енд Ко./Мерк Фросст Кенада Енд Сі. | Похідне (метилсульфоніл)феніл-2-(5н)-фуранону, фармацевтична композиція та спосіб лікування |
| US5877193A (en) * | 1996-07-19 | 1999-03-02 | Hoffmann-La Roche Inc. | Use of N-(4-aryl-thiazol-2-yl)-sulfonamides |
| TW528755B (en) * | 1996-12-24 | 2003-04-21 | Glaxo Group Ltd | 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives |
| CA2283100A1 (en) | 1997-03-14 | 1998-09-24 | Merck Frosst Canada & Co. | (methylsulfonyl)phenyl-2-(5h)-furanones with oxygen link as cox-2 inhibitors |
| US20030031670A1 (en) | 1999-11-08 | 2003-02-13 | Jack R. Wands | Diagnosis and treatment of malignant neoplasms |
| US6835370B2 (en) | 1999-11-08 | 2004-12-28 | Rhode Island Hospital | Diagnosis and treatment of malignant neoplasms |
| US20050123545A1 (en) | 1999-11-08 | 2005-06-09 | Wands Jack R. | Diagnosis and treatment of malignant neoplasms |
| WO2003018575A1 (en) * | 2001-08-24 | 2003-03-06 | Wyeth Holdings Corporation | 5-substituted-3(2h)-furanones useful for inhibition of farnesyl-protein transferase |
| US6667330B2 (en) * | 2002-01-31 | 2003-12-23 | Galileo Pharmaceuticals, Inc. | Furanone derivatives |
| AU2002950862A0 (en) | 2002-08-19 | 2002-09-12 | Biosignal Pty Ltd | Furanone derivatives and methods of making same |
| WO2004035812A2 (en) | 2002-10-16 | 2004-04-29 | Isis Innovation Limited | Asparaginyl hydroxylases and modulators thereof |
| US7642361B2 (en) * | 2004-01-09 | 2010-01-05 | Eli Lilly And Company | Thiophene and furan compounds |
| JP5583592B2 (ja) | 2007-11-30 | 2014-09-03 | ニューリンク ジェネティクス コーポレイション | Ido阻害剤 |
| MX2012014273A (es) * | 2010-06-07 | 2013-03-22 | Novomedix Llc | Compuestos furanilo y su uso. |
| ES2660822T3 (es) | 2012-09-21 | 2018-03-26 | Rhode Island Hospital | Inhibidores de beta-hidrolasa para tratamiento del cáncer |
-
2013
- 2013-09-20 ES ES13838498.7T patent/ES2660822T3/es active Active
- 2013-09-20 KR KR1020157010188A patent/KR102137180B1/ko not_active Expired - Fee Related
- 2013-09-20 WO PCT/US2013/061050 patent/WO2014047519A2/en not_active Ceased
- 2013-09-20 CN CN201380061004.4A patent/CN104902889A/zh active Pending
- 2013-09-20 US US14/430,101 patent/US9771356B2/en active Active
- 2013-09-20 HK HK15109523.0A patent/HK1208805A1/xx unknown
- 2013-09-20 AU AU2013317791A patent/AU2013317791B2/en not_active Ceased
- 2013-09-20 ES ES17202827T patent/ES2865412T3/es active Active
- 2013-09-20 EP EP17202827.6A patent/EP3345596B1/en not_active Not-in-force
- 2013-09-20 CA CA2885762A patent/CA2885762C/en active Active
- 2013-09-20 JP JP2015533237A patent/JP6469009B2/ja not_active Expired - Fee Related
- 2013-09-20 WO PCT/US2013/060934 patent/WO2014047447A2/en not_active Ceased
- 2013-09-20 EP EP13838498.7A patent/EP2897607B1/en not_active Not-in-force
- 2013-09-20 CN CN201910949656.0A patent/CN110818660B/zh not_active Expired - Fee Related
-
2017
- 2017-07-17 US US15/651,842 patent/US10106532B2/en active Active
- 2017-09-26 US US15/715,989 patent/US10710995B2/en active Active
-
2018
- 2018-09-14 US US16/131,275 patent/US10351555B2/en active Active
-
2019
- 2019-06-12 US US16/439,253 patent/US10787445B2/en active Active
-
2020
- 2020-06-02 US US16/890,680 patent/US20200361925A1/en not_active Abandoned
- 2020-09-23 US US17/029,127 patent/US20210032233A1/en not_active Abandoned
-
2022
- 2022-04-14 US US17/720,472 patent/US20220251076A1/en not_active Abandoned
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