JP2016523911A5 - - Google Patents
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- Publication number
- JP2016523911A5 JP2016523911A5 JP2016524175A JP2016524175A JP2016523911A5 JP 2016523911 A5 JP2016523911 A5 JP 2016523911A5 JP 2016524175 A JP2016524175 A JP 2016524175A JP 2016524175 A JP2016524175 A JP 2016524175A JP 2016523911 A5 JP2016523911 A5 JP 2016523911A5
- Authority
- JP
- Japan
- Prior art keywords
- carboxamide
- indole
- methyl
- methylphenyl
- optionally substituted
- 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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- -1 substituted Chemical class 0.000 claims 47
- 150000001875 compounds Chemical class 0.000 claims 37
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 32
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 19
- 125000001072 heteroaryl group Chemical group 0.000 claims 12
- 125000000623 heterocyclic group Chemical group 0.000 claims 12
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims 10
- 102100000129 CHURC1 Human genes 0.000 claims 10
- 101710014631 CHURC1 Proteins 0.000 claims 10
- 229910052736 halogen Inorganic materials 0.000 claims 10
- 150000002367 halogens Chemical class 0.000 claims 10
- 125000003386 piperidinyl group Chemical group 0.000 claims 10
- 150000003857 carboxamides Chemical class 0.000 claims 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 8
- 125000002757 morpholinyl group Chemical group 0.000 claims 8
- 125000003226 pyrazolyl group Chemical group 0.000 claims 8
- 229910052757 nitrogen Inorganic materials 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 7
- 239000011780 sodium chloride Substances 0.000 claims 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 6
- 125000004076 pyridyl group Chemical group 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 5
- 208000000429 Leukemia, Lymphocytic, Chronic, B-Cell Diseases 0.000 claims 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 5
- 210000003719 B-Lymphocytes Anatomy 0.000 claims 4
- 206010012818 Diffuse large B-cell lymphoma Diseases 0.000 claims 4
- 206010029592 Non-Hodgkin's lymphomas Diseases 0.000 claims 4
- 125000002393 azetidinyl group Chemical group 0.000 claims 4
- YZCKVEUIGOORGS-OUBTZVSYSA-N deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 4
- 229910052805 deuterium Inorganic materials 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 4
- 125000003107 substituted aryl group Chemical group 0.000 claims 4
- 125000000335 thiazolyl group Chemical group 0.000 claims 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 3
- QWEWLLNSJDTOKH-UHFFFAOYSA-N 1,3-thiazole-2-carboxamide Chemical compound NC(=O)C1=NC=CS1 QWEWLLNSJDTOKH-UHFFFAOYSA-N 0.000 claims 3
- HJNRNIXTGYJMOH-UHFFFAOYSA-N 2-(1-methylpyrazol-4-yl)-4-(1-prop-2-enoylpiperidin-3-yl)-1H-indole-7-carboxamide Chemical compound C1=NN(C)C=C1C1=CC2=C(C3CN(CCC3)C(=O)C=C)C=CC(C(N)=O)=C2N1 HJNRNIXTGYJMOH-UHFFFAOYSA-N 0.000 claims 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- ZVLPFZCGSSCGDH-QWRGUYRKSA-N NC(=O)c1ccc([C@H]2CC[C@@H](C2)NC(=O)C=C)c2cc[nH]c12 Chemical compound NC(=O)c1ccc([C@H]2CC[C@@H](C2)NC(=O)C=C)c2cc[nH]c12 ZVLPFZCGSSCGDH-QWRGUYRKSA-N 0.000 claims 3
- 230000001684 chronic Effects 0.000 claims 3
- 125000005842 heteroatoms Chemical group 0.000 claims 3
- 125000003566 oxetanyl group Chemical group 0.000 claims 3
- 125000004193 piperazinyl group Chemical group 0.000 claims 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 3
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 3
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 3
- 125000004605 1,2,3,4-tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 claims 2
- 125000005940 1,4-dioxanyl group Chemical group 0.000 claims 2
- OXCXIABGNNQZOF-UHFFFAOYSA-N 1H-indole-7-carboxamide Chemical compound NC(=O)C1=CC=CC2=C1NC=C2 OXCXIABGNNQZOF-UHFFFAOYSA-N 0.000 claims 2
- NXYHVXAWMQRIQZ-UHFFFAOYSA-N 2-(4-methylphenyl)-4-(1H-pyrazol-5-yl)-1H-indole-7-carboxamide Chemical compound C1=CC(C)=CC=C1C1=CC2=C(C=3NN=CC=3)C=CC(C(N)=O)=C2N1 NXYHVXAWMQRIQZ-UHFFFAOYSA-N 0.000 claims 2
- 125000004485 2-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])C1([H])* 0.000 claims 2
- AUDNGNGLLRZLDR-UHFFFAOYSA-N 4-(2-aminoethylamino)-2-(4-methylphenyl)-1H-indole-7-carboxamide Chemical compound C1=CC(C)=CC=C1C1=CC2=C(NCCN)C=CC(C(N)=O)=C2N1 AUDNGNGLLRZLDR-UHFFFAOYSA-N 0.000 claims 2
- NTKHIMDXLAINBM-UHFFFAOYSA-N 4-(2-aminophenyl)-2-(1-methylsulfonyl-3,6-dihydro-2H-pyridin-4-yl)-1H-indole-7-carboxamide Chemical compound C1N(S(=O)(=O)C)CCC(C=2NC3=C(C(N)=O)C=CC(=C3C=2)C=2C(=CC=CC=2)N)=C1 NTKHIMDXLAINBM-UHFFFAOYSA-N 0.000 claims 2
- SEZNBUSTSPNUEM-UHFFFAOYSA-N 4-(3-amino-2-methylphenyl)-2-(1-methylsulfonyl-3,6-dihydro-2H-pyridin-4-yl)-1H-indole-7-carboxamide Chemical compound CC1=C(N)C=CC=C1C1=CC=C(C(N)=O)C2=C1C=C(C=1CCN(CC=1)S(C)(=O)=O)N2 SEZNBUSTSPNUEM-UHFFFAOYSA-N 0.000 claims 2
- YLUGQOCWOPDIMD-UHFFFAOYSA-N 4-(dimethylamino)but-2-enamide Chemical compound CN(C)CC=CC(N)=O YLUGQOCWOPDIMD-UHFFFAOYSA-N 0.000 claims 2
- LPBGWJZEPAVKJF-UHFFFAOYSA-N 4-[2-methyl-3-(1-oxo-3,4-dihydroisoquinolin-2-yl)phenyl]-2-(1-methylsulfonyl-3,6-dihydro-2H-pyridin-4-yl)-1H-indole-7-carboxamide Chemical compound CC1=C(N2C(C3=CC=CC=C3CC2)=O)C=CC=C1C(C=1C=2)=CC=C(C(N)=O)C=1NC=2C1=CCN(S(C)(=O)=O)CC1 LPBGWJZEPAVKJF-UHFFFAOYSA-N 0.000 claims 2
- OUTWFGLFYFYILF-UHFFFAOYSA-N 4-[3-(6-fluoro-4-oxoquinazolin-3-yl)-2-methylphenyl]-2-pyridin-3-yl-1H-indole-7-carboxamide Chemical compound C1=CC=C(N2C(C3=CC(F)=CC=C3N=C2)=O)C(C)=C1C(C=1C=2)=CC=C(C(N)=O)C=1NC=2C1=CC=CN=C1 OUTWFGLFYFYILF-UHFFFAOYSA-N 0.000 claims 2
- MMGQHMNFRYJGPY-UHFFFAOYSA-N 4-[methyl-(1-prop-2-enoylazetidin-3-yl)amino]-1H-indole-7-carboxamide Chemical compound C=1C=C(C(N)=O)C=2NC=CC=2C=1N(C)C1CN(C(=O)C=C)C1 MMGQHMNFRYJGPY-UHFFFAOYSA-N 0.000 claims 2
- 206010002556 Ankylosing spondylitis Diseases 0.000 claims 2
- 208000006673 Asthma Diseases 0.000 claims 2
- VOJDSPGXWOOAFB-NWDGAFQWSA-N C(C=C)(=O)N[C@H]1C[C@H](CCC1)C1=C2C=CNC2=C(C=C1)C(=O)N Chemical compound C(C=C)(=O)N[C@H]1C[C@H](CCC1)C1=C2C=CNC2=C(C=C1)C(=O)N VOJDSPGXWOOAFB-NWDGAFQWSA-N 0.000 claims 2
- MZSBJBIISWWHIV-UHFFFAOYSA-N CC(C)n1cc(cn1)-c1cc2c(ccc(C(N)=O)c2[nH]1)-c1cccc(NC(=O)C=C)c1C Chemical compound CC(C)n1cc(cn1)-c1cc2c(ccc(C(N)=O)c2[nH]1)-c1cccc(NC(=O)C=C)c1C MZSBJBIISWWHIV-UHFFFAOYSA-N 0.000 claims 2
- UZSXYSMMCLOEHN-UHFFFAOYSA-N CCc1cc2c(ccc(C(N)=O)c2[nH]1)-c1cccc(NC(=O)C=C)c1 Chemical compound CCc1cc2c(ccc(C(N)=O)c2[nH]1)-c1cccc(NC(=O)C=C)c1 UZSXYSMMCLOEHN-UHFFFAOYSA-N 0.000 claims 2
- WYNJLPVFWIJNOU-UHFFFAOYSA-N CCn1cc(cn1)-c1cc2c(ccc(C(N)=O)c2[nH]1)-c1cccc(NC(=O)C=C)c1C Chemical compound CCn1cc(cn1)-c1cc2c(ccc(C(N)=O)c2[nH]1)-c1cccc(NC(=O)C=C)c1C WYNJLPVFWIJNOU-UHFFFAOYSA-N 0.000 claims 2
- BBIXMNJGTVMMCL-UHFFFAOYSA-N CN1CCC(CC1)C(=O)Nc1cccc(c1C)-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound CN1CCC(CC1)C(=O)Nc1cccc(c1C)-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O BBIXMNJGTVMMCL-UHFFFAOYSA-N 0.000 claims 2
- YROFMPHUAZCMHI-UHFFFAOYSA-N CS(=O)(=O)N1CCC(=CC1)c1cc2c(ccc(C(N)=O)c2[nH]1)-c1cccc(CNC(=O)C=C)c1 Chemical compound CS(=O)(=O)N1CCC(=CC1)c1cc2c(ccc(C(N)=O)c2[nH]1)-c1cccc(CNC(=O)C=C)c1 YROFMPHUAZCMHI-UHFFFAOYSA-N 0.000 claims 2
- 206010009900 Colitis ulcerative Diseases 0.000 claims 2
- 206010011401 Crohn's disease Diseases 0.000 claims 2
- 206010021972 Inflammatory bowel disease Diseases 0.000 claims 2
- 208000005615 Interstitial Cystitis Diseases 0.000 claims 2
- 208000003456 Juvenile Arthritis Diseases 0.000 claims 2
- 206010059176 Juvenile idiopathic arthritis Diseases 0.000 claims 2
- 208000005777 Lupus Nephritis Diseases 0.000 claims 2
- 206010052178 Lymphocytic lymphoma Diseases 0.000 claims 2
- 206010026798 Mantle cell lymphomas Diseases 0.000 claims 2
- NATHNSVCDVBPTA-UHFFFAOYSA-N N-[3-[7-carbamoyl-2-(1-methylsulfonyl-3,6-dihydro-2H-pyridin-4-yl)-1H-indol-4-yl]-2-methylphenyl]-1,3-thiazole-2-carboxamide Chemical compound C1=CC=C(C=2C=3C=C(NC=3C(C(N)=O)=CC=2)C=2CCN(CC=2)S(C)(=O)=O)C(C)=C1NC(=O)C1=NC=CS1 NATHNSVCDVBPTA-UHFFFAOYSA-N 0.000 claims 2
- YPHQUSNPXDGUHL-UHFFFAOYSA-N N-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 claims 2
- FRIIAQXQWLDHKH-UHFFFAOYSA-N NC(=O)c1ccc(-c2cccc(NC(=O)C=C)c2)c2cc(CCO)[nH]c12 Chemical compound NC(=O)c1ccc(-c2cccc(NC(=O)C=C)c2)c2cc(CCO)[nH]c12 FRIIAQXQWLDHKH-UHFFFAOYSA-N 0.000 claims 2
- UNHZLHSLZZWMNP-NSHDSACASA-N NC(=O)c1ccc([C@H]2CCCN(C2)C(=O)C=C)c2cc[nH]c12 Chemical compound NC(=O)c1ccc([C@H]2CCCN(C2)C(=O)C=C)c2cc[nH]c12 UNHZLHSLZZWMNP-NSHDSACASA-N 0.000 claims 2
- VOJDSPGXWOOAFB-RYUDHWBXSA-N NC(=O)c1ccc([C@H]2CCC[C@@H](C2)NC(=O)C=C)c2cc[nH]c12 Chemical compound NC(=O)c1ccc([C@H]2CCC[C@@H](C2)NC(=O)C=C)c2cc[nH]c12 VOJDSPGXWOOAFB-RYUDHWBXSA-N 0.000 claims 2
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 2
- 208000006664 Precursor Cell Lymphoblastic Leukemia-Lymphoma Diseases 0.000 claims 2
- 206010037162 Psoriatic arthropathy Diseases 0.000 claims 2
- 206010039073 Rheumatoid arthritis Diseases 0.000 claims 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 201000003444 follicular lymphoma Diseases 0.000 claims 2
- 201000009277 hairy cell leukemia Diseases 0.000 claims 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims 2
- 201000002215 juvenile rheumatoid arthritis Diseases 0.000 claims 2
- 201000011649 lymphoblastic lymphoma Diseases 0.000 claims 2
- 125000004312 morpholin-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])OC([H])(*)C1([H])[H] 0.000 claims 2
- 201000006417 multiple sclerosis Diseases 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 201000008482 osteoarthritis Diseases 0.000 claims 2
- 125000003551 oxepanyl group Chemical group 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 201000004681 psoriasis Diseases 0.000 claims 2
- 201000001263 psoriatic arthritis Diseases 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 201000000596 systemic lupus erythematosus Diseases 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 201000006704 ulcerative colitis Diseases 0.000 claims 2
- HFBYLYCMISIEMM-FFHNEAJVSA-N (4R,4aR,7S,7aR,12bS)-9-methoxy-3-methyl-2,4,4a,5,6,7,7a,13-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-7-ol;phosphoric acid Chemical class OP(O)(O)=O.C([C@H]1[C@H](N(CC[C@@]112)C)C3)C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC HFBYLYCMISIEMM-FFHNEAJVSA-N 0.000 claims 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 1
- BSSNZUFKXJJCBG-OWOJBTEDSA-N (E)-but-2-enediamide Chemical compound NC(=O)\C=C\C(N)=O BSSNZUFKXJJCBG-OWOJBTEDSA-N 0.000 claims 1
- ICJNPIYNARHAEK-UHFFFAOYSA-N 1-methyl-3,6-dihydro-2H-pyridine-5-carboxamide Chemical compound CN1CCC=C(C(N)=O)C1 ICJNPIYNARHAEK-UHFFFAOYSA-N 0.000 claims 1
- IICSRUINYZLIGZ-UHFFFAOYSA-N 2-(1-acetyl-2,5-dihydropyrrol-3-yl)-4-[2-methyl-3-(4-oxoquinazolin-3-yl)phenyl]-1H-indole-7-carboxamide Chemical compound C1N(C(=O)C)CC=C1C1=CC2=C(C=3C(=C(C=CC=3)N3C(C4=CC=CC=C4N=C3)=O)C)C=CC(C(N)=O)=C2N1 IICSRUINYZLIGZ-UHFFFAOYSA-N 0.000 claims 1
- SKCMEXAMJWCEBX-UHFFFAOYSA-N 2-(1-acetyl-3,6-dihydro-2H-pyridin-4-yl)-4-[2-methyl-3-(4-oxoquinazolin-3-yl)phenyl]-1H-indole-7-carboxamide Chemical compound C1N(C(=O)C)CCC(C=2NC3=C(C(N)=O)C=CC(=C3C=2)C=2C(=C(C=CC=2)N2C(C3=CC=CC=C3N=C2)=O)C)=C1 SKCMEXAMJWCEBX-UHFFFAOYSA-N 0.000 claims 1
- RJPBBDLEQSWCJW-UHFFFAOYSA-N 2-(1-acetyl-3,6-dihydro-2H-pyridin-4-yl)-4-[3-(6-fluoro-4-oxoquinazolin-3-yl)-2-methylphenyl]-1H-indole-7-carboxamide Chemical compound C1N(C(=O)C)CCC(C=2NC3=C(C(N)=O)C=CC(=C3C=2)C=2C(=C(C=CC=2)N2C(C3=CC(F)=CC=C3N=C2)=O)C)=C1 RJPBBDLEQSWCJW-UHFFFAOYSA-N 0.000 claims 1
- POUHUOHPRFEYLG-UHFFFAOYSA-N 2-(1-acetyl-3,6-dihydro-2H-pyridin-4-yl)-4-[3-[(4-cyclopropylbenzoyl)amino]-2-methylphenyl]-1H-indole-7-carboxamide Chemical compound C1N(C(=O)C)CCC(C=2NC3=C(C(N)=O)C=CC(=C3C=2)C=2C(=C(NC(=O)C=3C=CC(=CC=3)C3CC3)C=CC=2)C)=C1 POUHUOHPRFEYLG-UHFFFAOYSA-N 0.000 claims 1
- APLKJSDZPXJSHT-UHFFFAOYSA-N 2-(1-acetyl-3,6-dihydro-2H-pyridin-4-yl)-4-[3-[(4-tert-butylbenzoyl)amino]-2-methylphenyl]-1H-indole-7-carboxamide Chemical compound C1N(C(=O)C)CCC(C=2NC3=C(C(N)=O)C=CC(=C3C=2)C=2C(=C(NC(=O)C=3C=CC(=CC=3)C(C)(C)C)C=CC=2)C)=C1 APLKJSDZPXJSHT-UHFFFAOYSA-N 0.000 claims 1
- JRPNURORIBAHHP-UHFFFAOYSA-N 2-(1-acetyl-3,6-dihydro-2H-pyridin-4-yl)-4-[3-[[4-(2-cyanopropan-2-yl)benzoyl]amino]-2-methylphenyl]-1H-indole-7-carboxamide Chemical compound C1N(C(=O)C)CCC(C=2NC3=C(C(N)=O)C=CC(=C3C=2)C=2C(=C(NC(=O)C=3C=CC(=CC=3)C(C)(C)C#N)C=CC=2)C)=C1 JRPNURORIBAHHP-UHFFFAOYSA-N 0.000 claims 1
- YWZCROIWSUOWHD-UHFFFAOYSA-N 2-(1-acetylpiperidin-4-yl)-4-(3-amino-2-methylphenyl)-1H-indole-7-carboxamide Chemical compound C1CN(C(=O)C)CCC1C1=CC2=C(C=3C(=C(N)C=CC=3)C)C=CC(C(N)=O)=C2N1 YWZCROIWSUOWHD-UHFFFAOYSA-N 0.000 claims 1
- NFRZDNDHJBQTBD-UHFFFAOYSA-N 2-(1-methyl-2,5-dihydropyrrol-3-yl)-4-[2-methyl-3-(4-oxoquinazolin-3-yl)phenyl]-1H-indole-7-carboxamide Chemical compound C1N(C)CC=C1C1=CC2=C(C=3C(=C(C=CC=3)N3C(C4=CC=CC=C4N=C3)=O)C)C=CC(C(N)=O)=C2N1 NFRZDNDHJBQTBD-UHFFFAOYSA-N 0.000 claims 1
- TZQAYSKKISJPLV-UHFFFAOYSA-N 2-(1-methyl-3,6-dihydro-2H-pyridin-4-yl)-4-[2-methyl-3-(4-oxoquinazolin-3-yl)phenyl]-1H-indole-7-carboxamide Chemical compound C1N(C)CCC(C=2NC3=C(C(N)=O)C=CC(=C3C=2)C=2C(=C(C=CC=2)N2C(C3=CC=CC=C3N=C2)=O)C)=C1 TZQAYSKKISJPLV-UHFFFAOYSA-N 0.000 claims 1
- YUEIHKMWPVHCRD-QGZVFWFLSA-N 2-(1-methylpyrazol-4-yl)-4-[(3R)-3-(4-oxoquinazolin-3-yl)piperidin-1-yl]-1H-indole-7-carboxamide Chemical compound C1=NN(C)C=C1C1=CC2=C(N3C[C@@H](CCC3)N3C(C4=CC=CC=C4N=C3)=O)C=CC(C(N)=O)=C2N1 YUEIHKMWPVHCRD-QGZVFWFLSA-N 0.000 claims 1
- CNKOAUCEOSHPNA-QGZVFWFLSA-N 2-(1-methylpyrazol-4-yl)-4-[(3R)-3-[[4-(trifluoromethoxy)benzoyl]amino]piperidin-1-yl]-1H-indole-7-carboxamide Chemical compound C1=NN(C)C=C1C1=CC2=C(N3C[C@@H](CCC3)NC(=O)C=3C=CC(OC(F)(F)F)=CC=3)C=CC(C(N)=O)=C2N1 CNKOAUCEOSHPNA-QGZVFWFLSA-N 0.000 claims 1
- LLJRVOOYABPRCT-GOSISDBHSA-N 2-(1-methylpyrazol-4-yl)-4-[(3R)-3-[[4-(trifluoromethyl)benzoyl]amino]piperidin-1-yl]-1H-indole-7-carboxamide Chemical compound C1=NN(C)C=C1C1=CC2=C(N3C[C@@H](CCC3)NC(=O)C=3C=CC(=CC=3)C(F)(F)F)C=CC(C(N)=O)=C2N1 LLJRVOOYABPRCT-GOSISDBHSA-N 0.000 claims 1
- SEXZUTLAWKTNBR-UHFFFAOYSA-N 2-(1-methylpyrazol-4-yl)-4-[2-methyl-3-(4,5,6,7-tetrahydro-1-benzothiophene-2-carbonylamino)phenyl]-1H-indole-7-carboxamide Chemical compound CC1=C(NC(=O)C=2SC=3CCCCC=3C=2)C=CC=C1C(C=1C=2)=CC=C(C(N)=O)C=1NC=2C=1C=NN(C)C=1 SEXZUTLAWKTNBR-UHFFFAOYSA-N 0.000 claims 1
- COUFPWFCNDXODQ-UHFFFAOYSA-N 2-(1-methylsulfonyl-3,6-dihydro-2H-pyridin-4-yl)-4-phenyl-1H-indole-7-carboxamide Chemical compound C1N(S(=O)(=O)C)CCC(C=2NC3=C(C(N)=O)C=CC(=C3C=2)C=2C=CC=CC=2)=C1 COUFPWFCNDXODQ-UHFFFAOYSA-N 0.000 claims 1
- RVXZOOCMGWQPPY-UHFFFAOYSA-N 2-(2,5-dihydro-1H-pyrrol-3-yl)-4-[2-methyl-3-(4-oxoquinazolin-3-yl)phenyl]-1H-indole-7-carboxamide Chemical compound C1=CC=C(N2C(C3=CC=CC=C3N=C2)=O)C(C)=C1C(C=1C=2)=CC=C(C(N)=O)C=1NC=2C1=CCNC1 RVXZOOCMGWQPPY-UHFFFAOYSA-N 0.000 claims 1
- BEZFSGBAWXYAAH-UHFFFAOYSA-N 2-(3,6-dihydro-2H-pyran-4-yl)-4-[2-methyl-3-(4-oxoquinazolin-3-yl)phenyl]-1H-indole-7-carboxamide Chemical compound C1=CC=C(N2C(C3=CC=CC=C3N=C2)=O)C(C)=C1C(C=1C=2)=CC=C(C(N)=O)C=1NC=2C1=CCOCC1 BEZFSGBAWXYAAH-UHFFFAOYSA-N 0.000 claims 1
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- IXEINPQFWGGODG-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(cc1)C(=O)N1CCOCC1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(cc1)C(=O)N1CCOCC1 IXEINPQFWGGODG-UHFFFAOYSA-N 0.000 claims 1
- OEVFVKCGDGRVEB-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(cc1)C(N)=O Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(cc1)C(N)=O OEVFVKCGDGRVEB-UHFFFAOYSA-N 0.000 claims 1
- FMYJZEZIFCKMTC-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(cc1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(cc1)S(C)(=O)=O FMYJZEZIFCKMTC-UHFFFAOYSA-N 0.000 claims 1
- WXZZGTWRPAYESB-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(nc1)N1CCOCC1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(nc1)N1CCOCC1 WXZZGTWRPAYESB-UHFFFAOYSA-N 0.000 claims 1
- YVPLIJIFPOCTRM-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc2OCCc2c1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc2OCCc2c1 YVPLIJIFPOCTRM-UHFFFAOYSA-N 0.000 claims 1
- VYWBAOZNJXBKJR-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccc(F)c1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccc(F)c1 VYWBAOZNJXBKJR-UHFFFAOYSA-N 0.000 claims 1
- GYJNMTQJNFJMLH-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccc(c1)C#N Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccc(c1)C#N GYJNMTQJNFJMLH-UHFFFAOYSA-N 0.000 claims 1
- VHDUKPLNPHRVSN-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccc(c1)C(N)=O Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccc(c1)C(N)=O VHDUKPLNPHRVSN-UHFFFAOYSA-N 0.000 claims 1
- NNNYJFPVGYYKJO-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1 NNNYJFPVGYYKJO-UHFFFAOYSA-N 0.000 claims 1
- GMIFXZYGXOORIR-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1F Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1F GMIFXZYGXOORIR-UHFFFAOYSA-N 0.000 claims 1
- VPYZMMAUEHCYKO-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1S(C)(=O)=O Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1S(C)(=O)=O VPYZMMAUEHCYKO-UHFFFAOYSA-N 0.000 claims 1
- NCNWONLJFVNBTJ-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccnc1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccnc1 NCNWONLJFVNBTJ-UHFFFAOYSA-N 0.000 claims 1
- KKTDMBARBZCGTO-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccnc1F Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cccnc1F KKTDMBARBZCGTO-UHFFFAOYSA-N 0.000 claims 1
- HZKIOPURNJHCMO-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccncc1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccncc1 HZKIOPURNJHCMO-UHFFFAOYSA-N 0.000 claims 1
- DNLNHLRBNUVBAK-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccnn1C Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccnn1C DNLNHLRBNUVBAK-UHFFFAOYSA-N 0.000 claims 1
- ZXZGHIWUVGGGQY-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccnn1C1CCCCO1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccnn1C1CCCCO1 ZXZGHIWUVGGGQY-UHFFFAOYSA-N 0.000 claims 1
- SDOUSUDTGZHQIF-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cncnc1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cncnc1 SDOUSUDTGZHQIF-UHFFFAOYSA-N 0.000 claims 1
- ABISGEILENTRHF-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cnn(CCN2CCOCC2)c1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cnn(CCN2CCOCC2)c1 ABISGEILENTRHF-UHFFFAOYSA-N 0.000 claims 1
- XNYPZZORGISRKE-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCC(F)(F)CC1 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCC(F)(F)CC1 XNYPZZORGISRKE-UHFFFAOYSA-N 0.000 claims 1
- IDSMWPFVTYNYBE-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O IDSMWPFVTYNYBE-UHFFFAOYSA-N 0.000 claims 1
- VCUVORGMNPBWLP-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 VCUVORGMNPBWLP-UHFFFAOYSA-N 0.000 claims 1
- KNTQACBDFZPUAI-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1cnc(C(N)=O)c2[nH]ccc12 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1cnc(C(N)=O)c2[nH]ccc12 KNTQACBDFZPUAI-UHFFFAOYSA-N 0.000 claims 1
- WPFNZFRAJWFDBQ-UHFFFAOYSA-N Cc1c(NC(=O)C=C)cccc1-c1ncc(C(N)=O)c2[nH]ccc12 Chemical compound Cc1c(NC(=O)C=C)cccc1-c1ncc(C(N)=O)c2[nH]ccc12 WPFNZFRAJWFDBQ-UHFFFAOYSA-N 0.000 claims 1
- KRTFWIGPHTZTGK-UHFFFAOYSA-N Cc1c(NC(=O)CC#N)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)CC#N)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O KRTFWIGPHTZTGK-UHFFFAOYSA-N 0.000 claims 1
- JXORORQAIWDLFE-UHFFFAOYSA-N Cc1c(NC(=O)CCN2CCCC2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)CCN2CCCC2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O JXORORQAIWDLFE-UHFFFAOYSA-N 0.000 claims 1
- DIRNHKSZAKHEQA-UHFFFAOYSA-N Cc1c(NC(=O)CCN2CCCC2)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 Chemical compound Cc1c(NC(=O)CCN2CCCC2)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 DIRNHKSZAKHEQA-UHFFFAOYSA-N 0.000 claims 1
- DYANIUIJLWLJBU-UHFFFAOYSA-N Cc1c(NC(=O)CCN2CCCCC2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)CCN2CCCCC2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O DYANIUIJLWLJBU-UHFFFAOYSA-N 0.000 claims 1
- OCHVPBKNFYRGKT-UHFFFAOYSA-N Cc1c(NC(=O)CCN2CCOCC2)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 Chemical compound Cc1c(NC(=O)CCN2CCOCC2)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 OCHVPBKNFYRGKT-UHFFFAOYSA-N 0.000 claims 1
- NZDAGGSEHOPPBG-UHFFFAOYSA-N Cc1c(NC(=O)CF)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)CF)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O NZDAGGSEHOPPBG-UHFFFAOYSA-N 0.000 claims 1
- XXNMXUFOUXMWOW-UHFFFAOYSA-N Cc1c(NC(=O)COc2ccc(F)cc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)COc2ccc(F)cc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O XXNMXUFOUXMWOW-UHFFFAOYSA-N 0.000 claims 1
- QFTJOBWGFASQPI-UHFFFAOYSA-N Cc1c(NC(=O)COc2ccc(cc2)C#N)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)COc2ccc(cc2)C#N)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O QFTJOBWGFASQPI-UHFFFAOYSA-N 0.000 claims 1
- WEZDWRNDISJZEE-UHFFFAOYSA-N Cc1c(NC(=O)COc2ccccc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)COc2ccccc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O WEZDWRNDISJZEE-UHFFFAOYSA-N 0.000 claims 1
- WXNZZODLMFNGAW-UHFFFAOYSA-N Cc1c(NC(=O)COc2ccccn2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)COc2ccccn2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O WXNZZODLMFNGAW-UHFFFAOYSA-N 0.000 claims 1
- NVOMWEQSOKZEGG-UHFFFAOYSA-N Cc1c(NC(=O)COc2cccnc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)COc2cccnc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O NVOMWEQSOKZEGG-UHFFFAOYSA-N 0.000 claims 1
- RWZLIADCPQKFDV-UHFFFAOYSA-N Cc1c(NC(=O)COc2cccnn2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)COc2cccnn2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O RWZLIADCPQKFDV-UHFFFAOYSA-N 0.000 claims 1
- KDNPGULZWGMNFO-KTKRTIGZSA-N Cc1c(NC(=O)\C=C/C(=O)NCC)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 Chemical compound Cc1c(NC(=O)\C=C/C(=O)NCC)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 KDNPGULZWGMNFO-KTKRTIGZSA-N 0.000 claims 1
- IZMWRRVTBHSCIP-UHFFFAOYSA-N Cc1c(NC(=O)c2ccc(cc2)C(F)F)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cncnc1 Chemical compound Cc1c(NC(=O)c2ccc(cc2)C(F)F)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cncnc1 IZMWRRVTBHSCIP-UHFFFAOYSA-N 0.000 claims 1
- UOLJFIHJIRWYNQ-UHFFFAOYSA-N Cc1c(NC(=O)c2ccc(cc2)C(F)F)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)c2ccc(cc2)C(F)F)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O UOLJFIHJIRWYNQ-UHFFFAOYSA-N 0.000 claims 1
- XWFZDPTZWPUQHG-UHFFFAOYSA-N Cc1c(NC(=O)c2ccc(cc2)C(F)F)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 Chemical compound Cc1c(NC(=O)c2ccc(cc2)C(F)F)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 XWFZDPTZWPUQHG-UHFFFAOYSA-N 0.000 claims 1
- DMNKXNXZJKNAJD-UHFFFAOYSA-N Cc1c(NC(=O)c2ccc(cc2)C2CC2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cncnc1 Chemical compound Cc1c(NC(=O)c2ccc(cc2)C2CC2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1cncnc1 DMNKXNXZJKNAJD-UHFFFAOYSA-N 0.000 claims 1
- REPAKHRVIRKAAQ-UHFFFAOYSA-N Cc1c(NC(=O)c2cccnc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)c2cccnc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O REPAKHRVIRKAAQ-UHFFFAOYSA-N 0.000 claims 1
- QLZMSPIHINMENP-UHFFFAOYSA-N Cc1c(NC(=O)c2cnsc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O Chemical compound Cc1c(NC(=O)c2cnsc2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)C1=CCN(CC1)S(C)(=O)=O QLZMSPIHINMENP-UHFFFAOYSA-N 0.000 claims 1
- GYHOMRUVKPOPQG-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(=O)n(C)c1 Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccc(=O)n(C)c1 GYHOMRUVKPOPQG-UHFFFAOYSA-N 0.000 claims 1
- IILZYARQHIQTSF-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)C#C Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)C#C IILZYARQHIQTSF-UHFFFAOYSA-N 0.000 claims 1
- WPCKMHXUQFOUKH-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)CC#N Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)CC#N WPCKMHXUQFOUKH-UHFFFAOYSA-N 0.000 claims 1
- HWSHQIRKGWPDRF-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)CCN1CCCCC1 Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)CCN1CCCCC1 HWSHQIRKGWPDRF-UHFFFAOYSA-N 0.000 claims 1
- DJSLPTIFRSGIHG-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)CCl Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)CCl DJSLPTIFRSGIHG-UHFFFAOYSA-N 0.000 claims 1
- ITPDNVDAJJQZKL-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)COc1ccc(F)cc1 Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)COc1ccc(F)cc1 ITPDNVDAJJQZKL-UHFFFAOYSA-N 0.000 claims 1
- ZVJZHAYDXXCUQZ-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)COc1ccccc1 Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]c(cc12)-c1ccccc1CNC(=O)COc1ccccc1 ZVJZHAYDXXCUQZ-UHFFFAOYSA-N 0.000 claims 1
- RVEPFVVEAZFKDW-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]cc(NC(=O)C=C)c12 Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]cc(NC(=O)C=C)c12 RVEPFVVEAZFKDW-UHFFFAOYSA-N 0.000 claims 1
- LHFKQYKLXFGFJW-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]cc(NC(=O)CC#N)c12 Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]cc(NC(=O)CC#N)c12 LHFKQYKLXFGFJW-UHFFFAOYSA-N 0.000 claims 1
- BAUJUCGDWMMZGI-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]cc(NC(=O)CCl)c12 Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]cc(NC(=O)CCl)c12 BAUJUCGDWMMZGI-UHFFFAOYSA-N 0.000 claims 1
- RCYDYQAACYUQKF-UHFFFAOYSA-N Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]cc(NC(=O)COc3ccc(F)cc3)c12 Chemical compound Cc1c(NC(=O)c2nccs2)cccc1-c1ccc(C(N)=O)c2[nH]cc(NC(=O)COc3ccc(F)cc3)c12 RCYDYQAACYUQKF-UHFFFAOYSA-N 0.000 claims 1
- VDZGMBDHKREWFJ-UHFFFAOYSA-N Cc1c(NC2COC2)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 Chemical compound Cc1c(NC2COC2)cccc1-c1ccc(C(N)=O)c2[nH]ccc12 VDZGMBDHKREWFJ-UHFFFAOYSA-N 0.000 claims 1
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NZ754039A (en) * | 2013-06-26 | 2021-06-25 | Abbvie Inc | Primary carboxamides as btk inhibitors |
KR102272792B1 (ko) | 2013-09-30 | 2021-07-05 | 광저우 이노케어 파마 테크 씨오., 엘티디. | Btk의 치환된 니코틴이미드 저해제 및 그의 제조 방법 및 암, 염증 및 자가면역 질환에의 용도 |
KR102001745B1 (ko) | 2014-10-24 | 2019-07-18 | 브리스톨-마이어스 스큅 컴퍼니 | 키나제 억제제로서 유용한 인돌 카르복스아미드 화합물 |
AR104259A1 (es) * | 2015-04-15 | 2017-07-05 | Celgene Quanticel Res Inc | Inhibidores de bromodominio |
WO2017019429A1 (en) * | 2015-07-27 | 2017-02-02 | Eli Lilly And Company | 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds and theit use as mutant idh1 inhibitors |
TW201718581A (zh) | 2015-10-19 | 2017-06-01 | 英塞特公司 | 作為免疫調節劑之雜環化合物 |
JP6891173B2 (ja) * | 2015-11-17 | 2021-06-18 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Btk阻害活性を有するピリミジン及びピリジン化合物を用いたmsの治療方法 |
LT3377488T (lt) | 2015-11-19 | 2023-01-10 | Incyte Corporation | Heterocikliniai junginiai, kaip imunomoduliatoriai |
DK3889145T3 (da) | 2015-12-17 | 2024-03-18 | Merck Patent Gmbh | 8-cyano-5-piperidino-quinoliner som TLR7/8-antagonister og anvendelser deraf til behandling af immunsygdomme |
SI3394033T1 (sl) | 2015-12-22 | 2021-03-31 | Incyte Corporation | Heterociklične spojine kot imunomodulatorji |
MA44860A (fr) | 2016-05-06 | 2019-03-13 | Incyte Holdings Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
US20170335530A1 (en) * | 2016-05-23 | 2017-11-23 | Fatu K. Kofa | Pet waste vacuum and disposal device and method |
WO2017205464A1 (en) | 2016-05-26 | 2017-11-30 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
CN106083707B (zh) * | 2016-06-01 | 2018-10-26 | 温州大学 | 一种非对称杂芳基硫醚的合成方法 |
CN105837993A (zh) * | 2016-06-01 | 2016-08-10 | 扬州兰都塑料科技有限公司 | 一种阻燃电力电缆用阻燃剂 |
CN105924840A (zh) * | 2016-06-01 | 2016-09-07 | 扬州兰都塑料科技有限公司 | 一种阻燃电力电缆 |
CN105884673B (zh) * | 2016-06-03 | 2018-05-11 | 温州大学 | 一种吲哚衍生物的合成方法 |
EP4137489A1 (en) | 2016-06-20 | 2023-02-22 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
WO2018013789A1 (en) | 2016-07-14 | 2018-01-18 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
BR112019000696A2 (pt) | 2016-08-08 | 2019-04-24 | Merck Patent Gmbh | antagonistas de tlr7/8 e uso dos mesmos |
EP3504198B1 (en) | 2016-08-29 | 2023-01-25 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
PT3507282T (pt) * | 2016-09-02 | 2020-12-23 | Bristol Myers Squibb Co | Processo para a preparação de compostos de indol carboxamida |
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