ES2608053T3 - Inhibidores de ácido graso sintasa - Google Patents
Inhibidores de ácido graso sintasa Download PDFInfo
- Publication number
- ES2608053T3 ES2608053T3 ES12826459.5T ES12826459T ES2608053T3 ES 2608053 T3 ES2608053 T3 ES 2608053T3 ES 12826459 T ES12826459 T ES 12826459T ES 2608053 T3 ES2608053 T3 ES 2608053T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- phenyl
- oxo
- oxa
- diazaspiro
- 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.)
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- 239000003112 inhibitor Substances 0.000 title description 34
- 102000015303 Fatty Acid Synthases Human genes 0.000 title description 18
- 108010039731 Fatty Acid Synthases Proteins 0.000 title description 18
- -1 -C (> = O) NR5R6 Chemical group 0.000 claims abstract description 360
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 177
- 150000001875 compounds Chemical class 0.000 claims abstract description 156
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 133
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 99
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 92
- 150000003839 salts Chemical class 0.000 claims abstract description 74
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 70
- 239000001257 hydrogen Substances 0.000 claims abstract description 70
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 62
- 150000002367 halogens Chemical class 0.000 claims abstract description 61
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 57
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 50
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 49
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 48
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 47
- 125000004043 oxo group Chemical group O=* 0.000 claims abstract description 43
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 42
- 229910052805 deuterium Inorganic materials 0.000 claims abstract description 40
- 125000001424 substituent group Chemical group 0.000 claims abstract description 40
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims abstract description 39
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 37
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 34
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 28
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims abstract description 27
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 25
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 25
- 239000001301 oxygen Substances 0.000 claims abstract description 23
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 22
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 22
- 239000011593 sulfur Substances 0.000 claims abstract description 21
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 19
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims abstract description 18
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims abstract description 18
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 18
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 15
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims abstract description 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 15
- 125000001425 triazolyl group Chemical group 0.000 claims abstract description 15
- 125000005189 alkyl hydroxy group Chemical group 0.000 claims abstract description 14
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims abstract description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 11
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims abstract description 10
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 8
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000011282 treatment Methods 0.000 claims description 73
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 58
- METKIMKYRPQLGS-UHFFFAOYSA-N atenolol Chemical compound CC(C)NCC(O)COC1=CC=C(CC(N)=O)C=C1 METKIMKYRPQLGS-UHFFFAOYSA-N 0.000 claims description 57
- 206010028980 Neoplasm Diseases 0.000 claims description 56
- 201000011510 cancer Diseases 0.000 claims description 36
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 claims description 29
- 239000002246 antineoplastic agent Substances 0.000 claims description 25
- 239000008194 pharmaceutical composition Substances 0.000 claims description 21
- 229940034982 antineoplastic agent Drugs 0.000 claims description 13
- 125000001072 heteroaryl group Chemical group 0.000 claims description 12
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 9
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 9
- 125000001041 indolyl group Chemical group 0.000 claims description 9
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 9
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 8
- 125000002883 imidazolyl group Chemical group 0.000 claims description 8
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 8
- 125000005493 quinolyl group Chemical group 0.000 claims description 8
- JACUAQUJJLQAQT-UHFFFAOYSA-N 4-cyclopropyl-9-[1-(2,6-difluoro-4-quinolin-7-ylphenyl)-2-hydroxyethyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one Chemical compound FC=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(CO)N(CC1)CCC1(OCC1=O)CN1C1CC1 JACUAQUJJLQAQT-UHFFFAOYSA-N 0.000 claims description 7
- SVGCDCWKNFLJLE-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-quinolin-7-ylphenyl)acetamide Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(C(=O)N)N(CC1)CCC1(OCC1=O)CN1C1CC1 SVGCDCWKNFLJLE-UHFFFAOYSA-N 0.000 claims description 6
- 125000005871 1,3-benzodioxolyl group Chemical group 0.000 claims description 5
- SXLYKVRZNSYRQA-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-quinolin-7-ylphenyl)-n-methylacetamide Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(C(=O)NC)N(CC1)CCC1(OCC1=O)CN1C1CC1 SXLYKVRZNSYRQA-UHFFFAOYSA-N 0.000 claims description 5
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims description 5
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 5
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims description 5
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 5
- 125000005435 dihydrobenzoxazolyl group Chemical group O1C(NC2=C1C=CC=C2)* 0.000 claims description 5
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 claims description 5
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 claims description 5
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 claims description 5
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims description 5
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims description 5
- 125000001786 isothiazolyl group Chemical group 0.000 claims description 5
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims description 5
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 claims description 5
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 claims description 5
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 5
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims description 5
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 5
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 claims description 5
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 claims description 5
- 125000001544 thienyl group Chemical group 0.000 claims description 5
- HTXPQYSWZGAGBZ-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-quinolin-7-ylphenyl)-n-hydroxyacetamide Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(C(=O)NO)N(CC1)CCC1(OCC1=O)CN1C1CC1 HTXPQYSWZGAGBZ-UHFFFAOYSA-N 0.000 claims description 4
- KBXMSZHYPWVJDC-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(4-quinolin-7-ylphenyl)acetic acid Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(C(=O)O)N(CC1)CCC1(OCC1=O)CN1C1CC1 KBXMSZHYPWVJDC-UHFFFAOYSA-N 0.000 claims description 4
- QJSMKGKRGZPBPG-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(4-quinolin-7-ylphenyl)acetonitrile Chemical compound O=C1COC2(CCN(CC2)C(C#N)C=2C=CC(=CC=2)C=2C=C3N=CC=CC3=CC=2)CN1C1CC1 QJSMKGKRGZPBPG-UHFFFAOYSA-N 0.000 claims description 4
- KLMXZFVYNBASQE-UHFFFAOYSA-N 4-cyclopropyl-9-[(2-fluoro-4-quinolin-7-ylphenyl)-(1h-1,2,4-triazol-5-yl)methyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one Chemical compound FC1=CC(C=2C=C3N=CC=CC3=CC=2)=CC=C1C(C=1NC=NN=1)N(CC1)CCC1(OCC1=O)CN1C1CC1 KLMXZFVYNBASQE-UHFFFAOYSA-N 0.000 claims description 4
- PMWLYCQCNDUYNC-UHFFFAOYSA-N 4-cyclopropyl-9-[1-(2-fluoro-4-quinolin-7-ylphenyl)-2-hydroxyethyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(CO)N(CC1)CCC1(OCC1=O)CN1C1CC1 PMWLYCQCNDUYNC-UHFFFAOYSA-N 0.000 claims description 4
- NTRJVOBNGBYMKA-UHFFFAOYSA-N 4-cyclopropyl-9-[1-(2-fluoro-4-quinolin-7-ylphenyl)ethyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(C)N(CC1)CCC1(OCC1=O)CN1C1CC1 NTRJVOBNGBYMKA-UHFFFAOYSA-N 0.000 claims description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 4
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 4
- 125000004604 benzisothiazolyl group Chemical group S1N=C(C2=C1C=CC=C2)* 0.000 claims description 4
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 claims description 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- 125000002541 furyl group Chemical group 0.000 claims description 4
- 125000005956 isoquinolyl group Chemical group 0.000 claims description 4
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 4
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 4
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- 238000002560 therapeutic procedure Methods 0.000 claims description 4
- 125000001113 thiadiazolyl group Chemical group 0.000 claims description 4
- 125000000335 thiazolyl group Chemical group 0.000 claims description 4
- WQQOGHSARCAKKL-UHFFFAOYSA-N 1-fluoro-3-(4-fluorophenyl)benzene Chemical compound C1=CC(F)=CC=C1C1=CC=CC(F)=C1 WQQOGHSARCAKKL-UHFFFAOYSA-N 0.000 claims description 3
- ZYRPFGFRKKLQCD-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-quinolin-7-ylphenyl)-n-methoxyacetamide Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(C(=O)NOC)N(CC1)CCC1(OCC1=O)CN1C1CC1 ZYRPFGFRKKLQCD-UHFFFAOYSA-N 0.000 claims description 3
- AUOFURGFEWUADQ-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-quinolin-7-ylphenyl)acetic acid Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(C(=O)O)N(CC1)CCC1(OCC1=O)CN1C1CC1 AUOFURGFEWUADQ-UHFFFAOYSA-N 0.000 claims description 3
- YRQTZANTFMPXIG-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-n,n-dimethyl-2-(4-quinolin-7-ylphenyl)acetamide Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(C(=O)N(C)C)N(CC1)CCC1(OCC1=O)CN1C1CC1 YRQTZANTFMPXIG-UHFFFAOYSA-N 0.000 claims description 3
- MMDHHBXOUDEYDT-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-n-methyl-2-(4-quinolin-7-ylphenyl)acetamide Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(C(=O)NC)N(CC1)CCC1(OCC1=O)CN1C1CC1 MMDHHBXOUDEYDT-UHFFFAOYSA-N 0.000 claims description 3
- NIXSHEWEBYWJAX-UHFFFAOYSA-N 3-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-3-(4-quinolin-7-ylphenyl)propanamide Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(CC(=O)N)N(CC1)CCC1(OCC1=O)CN1C1CC1 NIXSHEWEBYWJAX-UHFFFAOYSA-N 0.000 claims description 3
- BQDYVCDTTGKUHT-UHFFFAOYSA-N 4-cyclopropyl-9-[1-(4-quinolin-7-ylphenyl)ethyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(C)N(CC1)CCC1(OCC1=O)CN1C1CC1 BQDYVCDTTGKUHT-UHFFFAOYSA-N 0.000 claims description 3
- JDELODMNZUZMER-UHFFFAOYSA-N 4-cyclopropyl-9-[1-[2-fluoro-4-(4-methoxyphenyl)phenyl]ethyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one Chemical compound C1=CC(OC)=CC=C1C(C=C1F)=CC=C1C(C)N1CCC2(OCC(=O)N(C3CC3)C2)CC1 JDELODMNZUZMER-UHFFFAOYSA-N 0.000 claims description 3
- MKCLRYWQUNHZEV-UHFFFAOYSA-N 4-cyclopropyl-9-[2-hydroxy-1-(4-quinolin-7-ylphenyl)ethyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(CO)N(CC1)CCC1(OCC1=O)CN1C1CC1 MKCLRYWQUNHZEV-UHFFFAOYSA-N 0.000 claims description 3
- BHIMESFIENCDNE-UHFFFAOYSA-N 4-cyclopropyl-9-[2-oxo-1-(4-quinolin-7-ylphenyl)propyl]-1-oxa-4,9-diazaspiro[5.5]undecan-3-one Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(C(=O)C)N(CC1)CCC1(OCC1=O)CN1C1CC1 BHIMESFIENCDNE-UHFFFAOYSA-N 0.000 claims description 3
- 125000005037 alkyl phenyl group Chemical group 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- GFPNHOLMUGOVTH-UHFFFAOYSA-N methyl 3-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-3-(4-quinolin-7-ylphenyl)propanoate Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(CC(=O)OC)N(CC1)CCC1(OCC1=O)CN1C1CC1 GFPNHOLMUGOVTH-UHFFFAOYSA-N 0.000 claims description 3
- 125000001715 oxadiazolyl group Chemical group 0.000 claims description 3
- 125000002971 oxazolyl group Chemical group 0.000 claims description 3
- BFGRGNWRXJWRGL-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-quinolin-5-ylphenyl)acetamide Chemical compound C=1C=C(C=2C3=CC=CN=C3C=CC=2)C=C(F)C=1C(C(=O)N)N(CC1)CCC1(OCC1=O)CN1C1CC1 BFGRGNWRXJWRGL-UHFFFAOYSA-N 0.000 claims description 2
- GYVAUQIFVFTHLW-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-[2-fluoro-4-(2-oxo-1h-quinolin-7-yl)phenyl]acetamide Chemical compound C=1C=C(C=2C=C3N=C(O)C=CC3=CC=2)C=C(F)C=1C(C(=O)N)N(CC1)CCC1(OCC1=O)CN1C1CC1 GYVAUQIFVFTHLW-UHFFFAOYSA-N 0.000 claims description 2
- HGPJBHXDOVHEQG-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-[2-fluoro-4-(8-fluoroquinolin-7-yl)phenyl]acetamide Chemical compound C=1C=C(C=2C(=C3N=CC=CC3=CC=2)F)C=C(F)C=1C(C(=O)N)N(CC1)CCC1(OCC1=O)CN1C1CC1 HGPJBHXDOVHEQG-UHFFFAOYSA-N 0.000 claims description 2
- ALDBUIXUQWMDLY-UHFFFAOYSA-N 2-(4-ethyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-quinolin-7-ylphenyl)acetamide Chemical compound O1CC(=O)N(CC)CC11CCN(C(C(N)=O)C=2C(=CC(=CC=2)C=2C=C3N=CC=CC3=CC=2)F)CC1 ALDBUIXUQWMDLY-UHFFFAOYSA-N 0.000 claims description 2
- MSQOUBRPWRGJQJ-UHFFFAOYSA-N 2-(4-ethyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-[2-fluoro-4-(3-methylquinolin-7-yl)phenyl]acetamide Chemical compound O1CC(=O)N(CC)CC11CCN(C(C(N)=O)C=2C(=CC(=CC=2)C=2C=C3N=CC(C)=CC3=CC=2)F)CC1 MSQOUBRPWRGJQJ-UHFFFAOYSA-N 0.000 claims description 2
- ZTAFDQZONCDMKC-UHFFFAOYSA-N 2-[4-(3-cyanoquinolin-7-yl)-2-fluorophenyl]-2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)acetamide Chemical compound C=1C=C(C=2C=C3N=CC(=CC3=CC=2)C#N)C=C(F)C=1C(C(=O)N)N(CC1)CCC1(OCC1=O)CN1C1CC1 ZTAFDQZONCDMKC-UHFFFAOYSA-N 0.000 claims description 2
- RBKXNRBHBZDNOV-UHFFFAOYSA-N 2-[4-(3-cyanoquinolin-7-yl)-2-fluorophenyl]-2-(4-ethyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)acetamide Chemical compound O1CC(=O)N(CC)CC11CCN(C(C(N)=O)C=2C(=CC(=CC=2)C=2C=C3N=CC(=CC3=CC=2)C#N)F)CC1 RBKXNRBHBZDNOV-UHFFFAOYSA-N 0.000 claims description 2
- RWTDADOILACFPR-UHFFFAOYSA-N 3-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-3-(4-quinolin-7-ylphenyl)propanoic acid Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=CC=1C(CC(=O)O)N(CC1)CCC1(OCC1=O)CN1C1CC1 RWTDADOILACFPR-UHFFFAOYSA-N 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims description 2
- 108091008648 NR7C Proteins 0.000 claims 4
- SAIWFSNORSNDKJ-UHFFFAOYSA-N 2-(4-cyclopropyl-3-oxo-1-oxa-4,9-diazaspiro[5.5]undecan-9-yl)-2-(2-fluoro-4-quinolin-7-ylphenyl)-n,n-dimethylacetamide Chemical compound C=1C=C(C=2C=C3N=CC=CC3=CC=2)C=C(F)C=1C(C(=O)N(C)C)N(CC1)CCC1(OCC1=O)CN1C1CC1 SAIWFSNORSNDKJ-UHFFFAOYSA-N 0.000 claims 2
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 331
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
Landscapes
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
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- Hematology (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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| US201261663124P | 2012-06-22 | ||
| PCT/US2012/051064 WO2013028447A1 (en) | 2011-08-19 | 2012-08-16 | Fatty acid synthase inhibitors |
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| JP6616934B2 (ja) * | 2014-05-22 | 2019-12-04 | 株式会社 資生堂 | レナリドミドの光学分割方法 |
| TW201615643A (zh) * | 2014-06-02 | 2016-05-01 | 伊史帝夫博士實驗室股份有限公司 | 具有多重模式抗疼痛活性之１－氧雜－４，９－二氮雜螺十一烷化合物之烷基與芳基衍生物 |
| PE20180572A1 (es) | 2015-06-18 | 2018-04-04 | Cephalon Inc | Derivados de piperidina 1,4-sustituidos |
| EP3310773B1 (en) | 2015-06-18 | 2020-12-02 | 89Bio Ltd. | Substituted 4-benzyl and 4-benzoyl piperidine derivatives |
| RS59956B1 (sr) | 2015-10-23 | 2020-03-31 | Esteve Pharmaceuticals Sa | Oksa-diazaspiro jedinjenja koja imaju aktivnost protiv bola |
| CR20200263A (es) | 2017-12-13 | 2020-07-26 | Lupin Ltd | Componentes heterocíclicos bicíclicos sustituidos como inhibidores de prmt5 |
| EP3636637A1 (en) * | 2018-10-10 | 2020-04-15 | Forma Therapeutics, Inc. | Inhibiting fatty acid synthase (fasn) |
| TWI767148B (zh) | 2018-10-10 | 2022-06-11 | 美商弗瑪治療公司 | 抑制脂肪酸合成酶(fasn) |
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| US4353900A (en) | 1981-10-19 | 1982-10-12 | Syntex (U.S.A.) Inc. | 9-(Arylalkyl or aroylalkyl)-1-oxa-4,9-diazaspiro(5.5)undecan-3-ones |
| WO1997011940A1 (en) * | 1995-09-29 | 1997-04-03 | Eli Lilly And Company | Spiro compounds as inhibitors of fibrinogen-dependent platelet aggregation |
| WO2001030780A2 (en) * | 1999-10-27 | 2001-05-03 | Cor Therapeutics, Inc. | Pyridyl-containing spirocyclic compounds as inhibitors of fibrinogen-dependent platelet aggregation |
| JP2006512404A (ja) * | 2002-10-22 | 2006-04-13 | グラクソ グループ リミテッド | Ｈ３受容体リガンドとしてのアリールオキシアルキルアミン誘導体 |
| AU2006230292A1 (en) * | 2005-03-31 | 2006-10-05 | Schering Corporation | Spirocyclic thrombin receptor antagonists |
| PT1961744E (pt) * | 2005-11-18 | 2013-05-15 | Ono Pharmaceutical Co | Composto que contém um grupo básico e sua utilização |
| TW200831092A (en) * | 2006-12-21 | 2008-08-01 | Astrazeneca Ab | Therapeutic agents |
| JP2013542960A (ja) * | 2010-11-08 | 2013-11-28 | グラクソスミスクライン、インテレクチュアル、プロパティー、ナンバー２、リミテッド | 脂肪酸シンターゼ阻害剤 |
-
2012
- 2012-08-16 EP EP12826459.5A patent/EP2744333B1/en active Active
- 2012-08-16 ES ES12826459.5T patent/ES2608053T3/es active Active
- 2012-08-16 JP JP2014526199A patent/JP5964426B2/ja not_active Expired - Fee Related
- 2012-08-16 US US14/238,418 patent/US9084794B2/en not_active Expired - Fee Related
- 2012-08-16 WO PCT/US2012/051064 patent/WO2013028447A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JP5964426B2 (ja) | 2016-08-03 |
| EP2744333B1 (en) | 2016-10-05 |
| WO2013028447A1 (en) | 2013-02-28 |
| EP2744333A4 (en) | 2015-04-22 |
| US9084794B2 (en) | 2015-07-21 |
| EP2744333A1 (en) | 2014-06-25 |
| JP2014521748A (ja) | 2014-08-28 |
| US20140194415A1 (en) | 2014-07-10 |
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