JP2007504271A - Crf1受容体リガンドである、ヘテロアリール縮合ピリジン類、ピラジン類及びピリミジン類 - Google Patents
Crf1受容体リガンドである、ヘテロアリール縮合ピリジン類、ピラジン類及びピリミジン類 Download PDFInfo
- Publication number
- JP2007504271A JP2007504271A JP2006526210A JP2006526210A JP2007504271A JP 2007504271 A JP2007504271 A JP 2007504271A JP 2006526210 A JP2006526210 A JP 2006526210A JP 2006526210 A JP2006526210 A JP 2006526210A JP 2007504271 A JP2007504271 A JP 2007504271A
- Authority
- JP
- Japan
- Prior art keywords
- pyridin
- pyrrolo
- alkyl
- methoxy
- ethyl
- 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.)
- Pending
Links
- 108091005471 CRHR1 Proteins 0.000 title claims abstract description 12
- 150000003230 pyrimidines Chemical class 0.000 title abstract description 5
- 239000003446 ligand Substances 0.000 title 1
- 150000003216 pyrazines Chemical class 0.000 title 1
- 150000003222 pyridines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 207
- 238000000034 method Methods 0.000 claims abstract description 173
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims abstract description 59
- 108010056643 Corticotropin-Releasing Hormone Receptors Proteins 0.000 claims abstract description 54
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 42
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 37
- 230000027455 binding Effects 0.000 claims abstract description 30
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims abstract description 30
- 208000035475 disorder Diseases 0.000 claims abstract description 24
- 208000019901 Anxiety disease Diseases 0.000 claims abstract description 14
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 14
- 208000030814 Eating disease Diseases 0.000 claims abstract description 10
- 208000019454 Feeding and Eating disease Diseases 0.000 claims abstract description 10
- 235000014632 disordered eating Nutrition 0.000 claims abstract description 10
- -1 tri-substituted phenyl Chemical group 0.000 claims description 398
- 239000000203 mixture Substances 0.000 claims description 180
- 229910052736 halogen Inorganic materials 0.000 claims description 144
- 150000002367 halogens Chemical class 0.000 claims description 144
- 125000000217 alkyl group Chemical group 0.000 claims description 117
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 115
- 229910052739 hydrogen Inorganic materials 0.000 claims description 100
- 239000001257 hydrogen Substances 0.000 claims description 97
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 87
- 229930195733 hydrocarbon Natural products 0.000 claims description 85
- 239000000243 solution Substances 0.000 claims description 83
- 150000003839 salts Chemical class 0.000 claims description 82
- 125000001424 substituent group Chemical group 0.000 claims description 81
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 72
- 150000002431 hydrogen Chemical class 0.000 claims description 70
- 229910052760 oxygen Inorganic materials 0.000 claims description 67
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 63
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 60
- 229910052717 sulfur Inorganic materials 0.000 claims description 56
- 239000004215 Carbon black (E152) Substances 0.000 claims description 48
- 125000004043 oxo group Chemical group O=* 0.000 claims description 47
- 125000004432 carbon atom Chemical group C* 0.000 claims description 43
- 229920006395 saturated elastomer Polymers 0.000 claims description 43
- 150000002430 hydrocarbons Chemical class 0.000 claims description 41
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 40
- 125000005842 heteroatom Chemical group 0.000 claims description 38
- 229910052757 nitrogen Inorganic materials 0.000 claims description 38
- 150000003462 sulfoxides Chemical class 0.000 claims description 38
- 125000004076 pyridyl group Chemical group 0.000 claims description 31
- 238000012360 testing method Methods 0.000 claims description 30
- 125000003282 alkyl amino group Chemical group 0.000 claims description 29
- 125000004122 cyclic group Chemical group 0.000 claims description 29
- 210000004027 cell Anatomy 0.000 claims description 28
- 239000001301 oxygen Substances 0.000 claims description 28
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 27
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 27
- 229910052799 carbon Inorganic materials 0.000 claims description 27
- 238000006243 chemical reaction Methods 0.000 claims description 27
- 125000005843 halogen group Chemical group 0.000 claims description 26
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 26
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 25
- 125000000623 heterocyclic group Chemical group 0.000 claims description 25
- 125000003118 aryl group Chemical group 0.000 claims description 24
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 23
- 125000004429 atom Chemical group 0.000 claims description 23
- 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 22
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims description 22
- 125000003545 alkoxy group Chemical group 0.000 claims description 21
- 238000000338 in vitro Methods 0.000 claims description 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 20
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 19
- 239000011593 sulfur Substances 0.000 claims description 18
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 17
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 17
- 230000000694 effects Effects 0.000 claims description 17
- 125000001188 haloalkyl group Chemical group 0.000 claims description 17
- 125000001544 thienyl group Chemical group 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 16
- 125000002541 furyl group Chemical group 0.000 claims description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 16
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 16
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 15
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 15
- 125000002971 oxazolyl group Chemical group 0.000 claims description 15
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 15
- 125000000335 thiazolyl group Chemical group 0.000 claims description 15
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 14
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 14
- 125000001425 triazolyl group Chemical group 0.000 claims description 13
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 12
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 11
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 11
- 241001465754 Metazoa Species 0.000 claims description 11
- 201000010099 disease Diseases 0.000 claims description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 10
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 10
- 125000002757 morpholinyl group Chemical group 0.000 claims description 10
- 125000004193 piperazinyl group Chemical group 0.000 claims description 10
- 125000003386 piperidinyl group Chemical group 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 10
- 125000004938 5-pyridyl group Chemical group N1=CC=CC(=C1)* 0.000 claims description 9
- 125000004414 alkyl thio group Chemical group 0.000 claims description 9
- 125000005605 benzo group Chemical group 0.000 claims description 9
- BAVYZALUXZFZLV-UHFFFAOYSA-N mono-methylamine Natural products NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims description 9
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 9
- 150000003457 sulfones Chemical class 0.000 claims description 9
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 9
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 8
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims description 8
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 8
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 8
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 8
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 claims description 8
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 8
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 8
- 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 7
- 125000001960 7 membered carbocyclic group Chemical group 0.000 claims description 7
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims description 7
- 125000005115 alkyl carbamoyl group Chemical group 0.000 claims description 7
- 125000002393 azetidinyl group Chemical group 0.000 claims description 7
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 7
- 125000005047 dihydroimidazolyl group Chemical group N1(CNC=C1)* 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
- 125000004621 quinuclidinyl group Chemical group N12C(CC(CC1)CC2)* 0.000 claims description 7
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 7
- 125000005432 dialkylcarboxamide group Chemical group 0.000 claims description 6
- 125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 claims description 6
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 6
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 6
- 125000005942 tetrahydropyridyl group Chemical group 0.000 claims description 6
- MTLCJOOCTPJNNV-ZDUSSCGKSA-N 1-[(2s)-1-methoxypropan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=CC2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC MTLCJOOCTPJNNV-ZDUSSCGKSA-N 0.000 claims description 5
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 239000003937 drug carrier Substances 0.000 claims description 5
- 125000006413 ring segment Chemical group 0.000 claims description 5
- 238000006467 substitution reaction Methods 0.000 claims description 5
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 4
- 238000001727 in vivo Methods 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 238000001525 receptor binding assay Methods 0.000 claims description 4
- DBVNLQXWPKYAFI-MRXNPFEDSA-N (2r)-3-methoxy-2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]propan-1-ol Chemical compound CC=1C=C2N([C@H](CO)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC DBVNLQXWPKYAFI-MRXNPFEDSA-N 0.000 claims description 3
- FJSFPDRDFLAPGN-UHFFFAOYSA-N 3-(3,7-dimethyl-5-propan-2-ylpyrrolo[2,3-b]pyrazin-2-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1N(C(C)C)C=C2C FJSFPDRDFLAPGN-UHFFFAOYSA-N 0.000 claims description 3
- BIKBEZBEIWFJNS-LBPRGKRZSA-N 3-chloro-1-[(2s)-1-methoxypropan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(Cl)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC BIKBEZBEIWFJNS-LBPRGKRZSA-N 0.000 claims description 3
- BJSJUIAUEBQBJR-ZDUSSCGKSA-N 3-chloro-5-[(2s)-1-methoxypropan-2-yl]-2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-7-methylpyrrolo[2,3-b]pyrazine Chemical compound ClC=1N=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC BJSJUIAUEBQBJR-ZDUSSCGKSA-N 0.000 claims description 3
- MQMPYVXRHMKMCD-LJQANCHMSA-N 4-[(2r)-2-[2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazin-5-yl]butyl]morpholine Chemical compound C([C@@H](CC)N1C2=NC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)OC)N1CCOCC1 MQMPYVXRHMKMCD-LJQANCHMSA-N 0.000 claims description 3
- JJBBAPZLAZRJMX-HNNXBMFYSA-N 5-(2-ethyl-6-methoxypyridin-3-yl)-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(OC)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C JJBBAPZLAZRJMX-HNNXBMFYSA-N 0.000 claims description 3
- FCCGIKZKBIBAQS-MRXNPFEDSA-N 5-[(2r)-1-methoxybutan-2-yl]-2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC FCCGIKZKBIBAQS-MRXNPFEDSA-N 0.000 claims description 3
- 208000000103 Anorexia Nervosa Diseases 0.000 claims description 3
- 208000020925 Bipolar disease Diseases 0.000 claims description 3
- 206010006550 Bulimia nervosa Diseases 0.000 claims description 3
- 208000008589 Obesity Diseases 0.000 claims description 3
- 208000028683 bipolar I disease Diseases 0.000 claims description 3
- 150000001721 carbon Chemical group 0.000 claims description 3
- 235000020824 obesity Nutrition 0.000 claims description 3
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 3
- 238000005406 washing Methods 0.000 claims description 3
- QKULNRKASLWVBK-OAHLLOKOSA-N (2r)-2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methylpyrrolo[3,2-b]pyridin-1-yl]butan-1-ol Chemical compound CC=1C=C2N([C@@H](CO)CC)C=CC2=NC=1C1=CC=C(C(C)C)N=C1OC QKULNRKASLWVBK-OAHLLOKOSA-N 0.000 claims description 2
- KPEVPNSVABOGHS-HNNXBMFYSA-N 1-[(2s)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=CC2=NC=1C1=CC=C(C(C)C)N=C1OC KPEVPNSVABOGHS-HNNXBMFYSA-N 0.000 claims description 2
- AWGFEIBQECMDIC-ZDUSSCGKSA-N 1-[1-[(2s)-1-methoxypropan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-6-methylpyrrolo[3,2-b]pyridin-7-yl]pyrrolidine-2,5-dione Chemical compound C=12N([C@@H](C)COC)C=CC2=NC(C=2C(=CC(OC(F)(F)F)=CC=2)OC)=C(C)C=1N1C(=O)CCC1=O AWGFEIBQECMDIC-ZDUSSCGKSA-N 0.000 claims description 2
- UCDGDYVDDIPKMD-UHFFFAOYSA-N 2-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,7-dimethyl-5-propan-2-ylpyrrolo[2,3-b]pyrazine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1N(C(C)C)C=C2C UCDGDYVDDIPKMD-UHFFFAOYSA-N 0.000 claims description 2
- YIJSZEYGHDZUEE-UHFFFAOYSA-N 2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethyl-5-propan-2-ylpyrrolo[2,3-b]pyrazine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1N(C(C)C)C=C2C YIJSZEYGHDZUEE-UHFFFAOYSA-N 0.000 claims description 2
- RBOSKUKWORZETB-UHFFFAOYSA-N 2-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC RBOSKUKWORZETB-UHFFFAOYSA-N 0.000 claims description 2
- GPCWPKOKMFSCRB-UHFFFAOYSA-N 3-(3,6-dimethyl-1-propylpyrrolo[3,2-b]pyridin-5-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC GPCWPKOKMFSCRB-UHFFFAOYSA-N 0.000 claims description 2
- YUIDPRYRVCCYEO-LBPRGKRZSA-N 3-bromo-1-[(2s)-1-methoxypropan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(Br)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC YUIDPRYRVCCYEO-LBPRGKRZSA-N 0.000 claims description 2
- UWWULBGQOSZTNU-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethyl-1-pentan-3-ylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC UWWULBGQOSZTNU-UHFFFAOYSA-N 0.000 claims description 2
- YMKMCFLUVMEVHP-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethyl-1-propylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC YMKMCFLUVMEVHP-UHFFFAOYSA-N 0.000 claims description 2
- ODQZETYAUCYANV-INIZCTEOSA-N 5-(6-cyclopropyl-2-ethylpyridin-3-yl)-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound C=1C=C(C=2C(=CC=3N([C@@H](C)COC)C=C(C)C=3N=2)C)C(CC)=NC=1C1CC1 ODQZETYAUCYANV-INIZCTEOSA-N 0.000 claims description 2
- OXUHZDRXXROIRN-UHFFFAOYSA-N 5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethyl-1-pentan-3-ylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC OXUHZDRXXROIRN-UHFFFAOYSA-N 0.000 claims description 2
- 210000001124 body fluid Anatomy 0.000 claims description 2
- 238000001514 detection method Methods 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- MIWLNMRIXOXROW-YADHBBJMSA-N methyl (3s,4r)-3-(2-fluoroethoxy)-4-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OC)C[C@H](OCCF)[C@@H]1N1C2=CC(C)=C(C=3C(=NC(=CC=3)C(C)C)OC)N=C2C(C)=C1 MIWLNMRIXOXROW-YADHBBJMSA-N 0.000 claims description 2
- 210000002569 neuron Anatomy 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- HNGMEXFSROUIFJ-UHFFFAOYSA-N 2-[2-methoxy-4-(trifluoromethyl)phenyl]-3,7-dimethyl-5-propan-2-ylpyrrolo[2,3-b]pyrazine Chemical compound COC1=CC(C(F)(F)F)=CC=C1C(C(=N1)C)=NC2=C1N(C(C)C)C=C2C HNGMEXFSROUIFJ-UHFFFAOYSA-N 0.000 claims 2
- GGHNFQROIOWAMJ-UHFFFAOYSA-N 6-[2-methoxy-4-(trifluoromethoxy)phenyl]-1,5-dimethyl-3-pentan-3-ylpyrrolo[2,3-b]pyridine Chemical compound CC=1C=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC GGHNFQROIOWAMJ-UHFFFAOYSA-N 0.000 claims 2
- 108010052164 Sodium Channels Proteins 0.000 claims 2
- 102000018674 Sodium Channels Human genes 0.000 claims 2
- 239000012085 test solution Substances 0.000 claims 2
- LTHHZUSIRRDOAB-MRXNPFEDSA-N (2r)-2-[2-(2-chloro-4-methoxyphenyl)-3,7-dimethylpyrrolo[2,3-b]pyrazin-5-yl]-n-ethyl-n-methylbutan-1-amine Chemical class CC=1N=C2N([C@@H](CN(C)CC)CC)C=C(C)C2=NC=1C1=CC=C(OC)C=C1Cl LTHHZUSIRRDOAB-MRXNPFEDSA-N 0.000 claims 1
- QMDJFXUCTKOXNJ-MRXNPFEDSA-N (2r)-2-[2-[4-(difluoromethoxy)-2-methoxyphenyl]-3,7-dimethylpyrrolo[2,3-b]pyrazin-5-yl]-n-ethyl-n-methylbutan-1-amine Chemical class CC=1N=C2N([C@@H](CN(C)CC)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)F)C=C1OC QMDJFXUCTKOXNJ-MRXNPFEDSA-N 0.000 claims 1
- RRDIJFSPKQHODR-QGZVFWFLSA-N (2r)-2-[5-(2-ethoxy-6-ethyl-5-methylsulfonylpyridin-3-yl)-6-ethyl-3-methylpyrrolo[3,2-b]pyridin-1-yl]butan-1-ol Chemical compound CCOC1=NC(CC)=C(S(C)(=O)=O)C=C1C(C(=C1)CC)=NC2=C1N([C@H](CC)CO)C=C2C RRDIJFSPKQHODR-QGZVFWFLSA-N 0.000 claims 1
- LVMCPHWRRJGGNR-OAHLLOKOSA-N (2r)-2-[5-(2-ethoxy-6-ethyl-5-methylsulfonylpyridin-3-yl)-6-ethyl-3-methylpyrrolo[3,2-b]pyridin-1-yl]propan-1-ol Chemical compound CCOC1=NC(CC)=C(S(C)(=O)=O)C=C1C(C(=C1)CC)=NC2=C1N([C@H](C)CO)C=C2C LVMCPHWRRJGGNR-OAHLLOKOSA-N 0.000 claims 1
- NLDWRHHOOXAXCG-QGZVFWFLSA-N (2r)-2-[6-ethyl-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridin-1-yl]butan-1-ol Chemical compound CCC=1C=C2N([C@@H](CO)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC NLDWRHHOOXAXCG-QGZVFWFLSA-N 0.000 claims 1
- BSUHHUKOJZLGBX-OAHLLOKOSA-N (2r)-2-[6-ethyl-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridin-1-yl]propan-1-ol Chemical compound CCC1=CC=2N([C@H](C)CO)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1OC BSUHHUKOJZLGBX-OAHLLOKOSA-N 0.000 claims 1
- TWHTWEBOAZACAM-OAHLLOKOSA-N (2r)-3-methoxy-2-[2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazin-5-yl]propan-1-ol Chemical compound CC=1N=C2N([C@H](CO)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC TWHTWEBOAZACAM-OAHLLOKOSA-N 0.000 claims 1
- CQPXGGBNSDNIJK-ZCNNSNEGSA-N (2r,6s)-4-[(2s)-2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl]-2,6-dimethylmorpholine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1C[C@H](C)O[C@H](C)C1 CQPXGGBNSDNIJK-ZCNNSNEGSA-N 0.000 claims 1
- YNVUQGDHCZQZBL-SFHVURJKSA-N (2s)-2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]-n,n-dimethylbutan-1-amine Chemical compound CC=1C=C2N([C@H](CN(C)C)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC YNVUQGDHCZQZBL-SFHVURJKSA-N 0.000 claims 1
- ZKXORCRISXNHAF-INIZCTEOSA-N (2s)-2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]-n,n-dimethylbutan-1-amine Chemical class CC=1C=C2N([C@H](CN(C)C)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC ZKXORCRISXNHAF-INIZCTEOSA-N 0.000 claims 1
- ZRNUFTUQKYCICK-AWEZNQCLSA-N (2s)-2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butan-1-ol Chemical compound CC=1C=C2N([C@H](CO)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC ZRNUFTUQKYCICK-AWEZNQCLSA-N 0.000 claims 1
- SOQZGQJZMOXAEA-AWEZNQCLSA-N (2s)-2-[6-bromo-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridin-1-yl]butan-1-ol Chemical compound BrC=1C=C2N([C@H](CO)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC SOQZGQJZMOXAEA-AWEZNQCLSA-N 0.000 claims 1
- BSUHHUKOJZLGBX-HNNXBMFYSA-N (2s)-2-[6-ethyl-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridin-1-yl]propan-1-ol Chemical compound CCC1=CC=2N([C@@H](C)CO)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1OC BSUHHUKOJZLGBX-HNNXBMFYSA-N 0.000 claims 1
- DBVNLQXWPKYAFI-INIZCTEOSA-N (2s)-3-methoxy-2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]propan-1-ol Chemical compound CC=1C=C2N([C@@H](CO)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC DBVNLQXWPKYAFI-INIZCTEOSA-N 0.000 claims 1
- BYKPVWNNSGKMRL-KRWDZBQOSA-N (3s)-4-methoxy-3-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butanenitrile Chemical compound CC=1C=C2N([C@@H](CC#N)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC BYKPVWNNSGKMRL-KRWDZBQOSA-N 0.000 claims 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- ZWCWGAPILYEVEV-UHFFFAOYSA-N 1-(1,3-dimethoxypropan-2-yl)-5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(COC)COC)C=C2C ZWCWGAPILYEVEV-UHFFFAOYSA-N 0.000 claims 1
- QKUZAHVNLZHHPZ-UHFFFAOYSA-N 1-(1,3-dimethoxypropan-2-yl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(COC)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC QKUZAHVNLZHHPZ-UHFFFAOYSA-N 0.000 claims 1
- KMECCOHITUUDHO-UHFFFAOYSA-N 1-(1-methoxy-2-methylpropan-2-yl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(C)(C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC KMECCOHITUUDHO-UHFFFAOYSA-N 0.000 claims 1
- YTGYNUMBKMOSRN-UHFFFAOYSA-N 1-(1-methoxypentan-2-yl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(COC)CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC YTGYNUMBKMOSRN-UHFFFAOYSA-N 0.000 claims 1
- OLUWAQSFFVASJK-UHFFFAOYSA-N 1-(1-methoxypropan-2-yl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC OLUWAQSFFVASJK-UHFFFAOYSA-N 0.000 claims 1
- DGADZOHQRGXFOV-UHFFFAOYSA-N 1-(1-methoxypropan-2-yl)-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(C)COC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC DGADZOHQRGXFOV-UHFFFAOYSA-N 0.000 claims 1
- KTMHOFKROQUWFA-UHFFFAOYSA-N 1-(2-ethoxyethyl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCOCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC KTMHOFKROQUWFA-UHFFFAOYSA-N 0.000 claims 1
- NTMRPBBYPYSEBA-UHFFFAOYSA-N 1-(2-fluoroethyl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCF)C=C2C NTMRPBBYPYSEBA-UHFFFAOYSA-N 0.000 claims 1
- NTYHFENZSKYQAM-UHFFFAOYSA-N 1-(2-methoxyethyl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCOC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC NTYHFENZSKYQAM-UHFFFAOYSA-N 0.000 claims 1
- BCIGRMIDQCDBIV-UHFFFAOYSA-N 1-(3-fluoropropyl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCCF)C=C2C BCIGRMIDQCDBIV-UHFFFAOYSA-N 0.000 claims 1
- ADVAXFRMJOTJCR-UHFFFAOYSA-N 1-(cyclopropylmethyl)-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CC1CC1)C=C2C ADVAXFRMJOTJCR-UHFFFAOYSA-N 0.000 claims 1
- DNUTZBZXLPWRJG-UHFFFAOYSA-N 1-Piperidine carboxylic acid Chemical compound OC(=O)N1CCCCC1 DNUTZBZXLPWRJG-UHFFFAOYSA-N 0.000 claims 1
- GGUAQRFGNURFHO-KRWDZBQOSA-N 1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-3,6-dimethyl-5-(6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](CF)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1 GGUAQRFGNURFHO-KRWDZBQOSA-N 0.000 claims 1
- ITZDIINMLAOWGG-INIZCTEOSA-N 1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](CF)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC ITZDIINMLAOWGG-INIZCTEOSA-N 0.000 claims 1
- OMUBYGTXDDCDAN-MRXNPFEDSA-N 1-[(2r)-1-fluorobutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](CF)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC OMUBYGTXDDCDAN-MRXNPFEDSA-N 0.000 claims 1
- UPQDJTCMBXUFHT-QGZVFWFLSA-N 1-[(2r)-1-fluoropentan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](CF)CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC UPQDJTCMBXUFHT-QGZVFWFLSA-N 0.000 claims 1
- CFOKHRZCAAUIPV-OAHLLOKOSA-N 1-[(2r)-1-fluoropropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H](C)CF)C=C2C CFOKHRZCAAUIPV-OAHLLOKOSA-N 0.000 claims 1
- WFSQCCAYGBJLFQ-GOSISDBHSA-N 1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethyl-5-(6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1 WFSQCCAYGBJLFQ-GOSISDBHSA-N 0.000 claims 1
- TVOGCLWMSRMISY-QGZVFWFLSA-N 1-[(2r)-1-methoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC TVOGCLWMSRMISY-QGZVFWFLSA-N 0.000 claims 1
- BAGGKFDFSIBFFX-MRXNPFEDSA-N 1-[(2r)-1-methoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=CC2=NC=1C1=CC=C(C(C)C)N=C1OC BAGGKFDFSIBFFX-MRXNPFEDSA-N 0.000 claims 1
- YTGYNUMBKMOSRN-GOSISDBHSA-N 1-[(2r)-1-methoxypentan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC YTGYNUMBKMOSRN-GOSISDBHSA-N 0.000 claims 1
- OLUWAQSFFVASJK-MRXNPFEDSA-N 1-[(2r)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC OLUWAQSFFVASJK-MRXNPFEDSA-N 0.000 claims 1
- HJWVECYJKJHBMA-QGZVFWFLSA-N 1-[(2r)-2-methoxybutyl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C[C@@H](CC)OC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC HJWVECYJKJHBMA-QGZVFWFLSA-N 0.000 claims 1
- FISYNTJEQPADGC-FQEVSTJZSA-N 1-[(2s)-1-(3,3-dimethylpiperidin-1-yl)butan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1CCCC(C)(C)C1 FISYNTJEQPADGC-FQEVSTJZSA-N 0.000 claims 1
- VLZNQQPZYYRDRK-SFHVURJKSA-N 1-[(2s)-1-(4,4-difluoropiperidin-1-yl)butan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1CCC(F)(F)CC1 VLZNQQPZYYRDRK-SFHVURJKSA-N 0.000 claims 1
- SEDDFSZTUSQLNM-FQEVSTJZSA-N 1-[(2s)-1-(azepan-1-yl)butan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1CCCCCC1 SEDDFSZTUSQLNM-FQEVSTJZSA-N 0.000 claims 1
- PSDREHBPEVJWGI-AWEZNQCLSA-N 1-[(2s)-1-chlorobutan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](CCl)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC PSDREHBPEVJWGI-AWEZNQCLSA-N 0.000 claims 1
- ZJHDWEFHCBXFIC-SFHVURJKSA-N 1-[(2s)-1-ethoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](CC)COCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC ZJHDWEFHCBXFIC-SFHVURJKSA-N 0.000 claims 1
- ITZDIINMLAOWGG-MRXNPFEDSA-N 1-[(2s)-1-fluoro-3-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](CF)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC ITZDIINMLAOWGG-MRXNPFEDSA-N 0.000 claims 1
- WNXIUJSYKGZMHR-KRWDZBQOSA-N 1-[(2s)-1-fluorobutan-2-yl]-3,6-dimethyl-5-(6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](CF)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1 WNXIUJSYKGZMHR-KRWDZBQOSA-N 0.000 claims 1
- OMUBYGTXDDCDAN-INIZCTEOSA-N 1-[(2s)-1-fluorobutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](CF)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC OMUBYGTXDDCDAN-INIZCTEOSA-N 0.000 claims 1
- TVOGCLWMSRMISY-KRWDZBQOSA-N 1-[(2s)-1-methoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC TVOGCLWMSRMISY-KRWDZBQOSA-N 0.000 claims 1
- JGFHDUUWMAONLV-INIZCTEOSA-N 1-[(2s)-1-methoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridine Chemical compound C=1C=C2N([C@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC JGFHDUUWMAONLV-INIZCTEOSA-N 0.000 claims 1
- IMZUXKIHQMUHDC-HNNXBMFYSA-N 1-[(2s)-1-methoxybutan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC IMZUXKIHQMUHDC-HNNXBMFYSA-N 0.000 claims 1
- RCGLZSPGSCAEQI-INIZCTEOSA-N 1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethyl-5-(2-methyl-6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1C RCGLZSPGSCAEQI-INIZCTEOSA-N 0.000 claims 1
- SLRZBOISAYCZLK-SFHVURJKSA-N 1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethyl-5-(6-propan-2-yl-2-propan-2-yloxypyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC(C)C SLRZBOISAYCZLK-SFHVURJKSA-N 0.000 claims 1
- OLUWAQSFFVASJK-INIZCTEOSA-N 1-[(2s)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC OLUWAQSFFVASJK-INIZCTEOSA-N 0.000 claims 1
- SPRSJUDLZIKCAR-HNNXBMFYSA-N 1-[(2s)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methylpyrrolo[3,2-b]pyridine-3-carbonitrile Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C#N)C2=NC=1C1=CC=C(C(C)C)N=C1OC SPRSJUDLZIKCAR-HNNXBMFYSA-N 0.000 claims 1
- DGADZOHQRGXFOV-AWEZNQCLSA-N 1-[(2s)-1-methoxypropan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC DGADZOHQRGXFOV-AWEZNQCLSA-N 0.000 claims 1
- LQMIXVMYCWOSMI-HNNXBMFYSA-N 1-[(2s)-1-methoxypropan-2-yl]-6-methyl-5-[2-(methylamino)-6-propan-2-ylpyridin-3-yl]pyrrolo[3,2-b]pyridine-3-carbonitrile Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C#N LQMIXVMYCWOSMI-HNNXBMFYSA-N 0.000 claims 1
- GMLGLUVWTUJACE-YADHBBJMSA-N 1-[(3r,4s)-4-(2-fluoroethoxy)-1-methylpyrrolidin-3-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H]1[C@H](CN(C)C1)OCCF)C=C2C GMLGLUVWTUJACE-YADHBBJMSA-N 0.000 claims 1
- NJOPGINYGSEGID-YADHBBJMSA-N 1-[(3r,4s)-4-(2-fluoroethoxy)-1-methylsulfonylpyrrolidin-3-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H]1[C@H](CN(C1)S(C)(=O)=O)OCCF)C=C2C NJOPGINYGSEGID-YADHBBJMSA-N 0.000 claims 1
- DDEGIADHENMWRC-QGZVFWFLSA-N 1-[1-[(2r)-1-methoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methylpyrrolo[3,2-b]pyridin-7-yl]pyrrolidine-2,5-dione Chemical compound C=12N([C@@H](COC)CC)C=CC2=NC(C=2C(=NC(=CC=2)C(C)C)OC)=C(C)C=1N1C(=O)CCC1=O DDEGIADHENMWRC-QGZVFWFLSA-N 0.000 claims 1
- NAOAPEWNXZRUJX-UHFFFAOYSA-N 1-[2-(2-fluoroethoxy)ethyl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCOCCF)C=C2C NAOAPEWNXZRUJX-UHFFFAOYSA-N 0.000 claims 1
- DYFGPACFQSXSOB-OAQYLSRUSA-N 1-[4-[(2r)-2-[2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazin-5-yl]butyl]piperazin-1-yl]ethanone Chemical compound C([C@@H](CC)N1C2=NC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)OC)N1CCN(C(C)=O)CC1 DYFGPACFQSXSOB-OAQYLSRUSA-N 0.000 claims 1
- DGXZGZWWHPKWRW-HNNXBMFYSA-N 1-[6-ethyl-2-methoxy-5-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]pyridin-3-yl]ethanone Chemical compound CCC1=NC(OC)=C(C(C)=O)C=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C DGXZGZWWHPKWRW-HNNXBMFYSA-N 0.000 claims 1
- VGBXSKDFSKSDNJ-UHFFFAOYSA-N 1-butan-2-yl-5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(C)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC VGBXSKDFSKSDNJ-UHFFFAOYSA-N 0.000 claims 1
- PEFFOKBTSSHVJK-UHFFFAOYSA-N 1-butan-2-yl-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(C)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC PEFFOKBTSSHVJK-UHFFFAOYSA-N 0.000 claims 1
- HSERPNAIBJURQN-UHFFFAOYSA-N 1-butan-2-yl-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(C)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC HSERPNAIBJURQN-UHFFFAOYSA-N 0.000 claims 1
- LAGGGSMPRQYHHH-UHFFFAOYSA-N 1-butan-2-yl-6-ethyl-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC=1C=C2N(C(C)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC LAGGGSMPRQYHHH-UHFFFAOYSA-N 0.000 claims 1
- VQBIPUYAVBTHAK-UHFFFAOYSA-N 1-butyl-5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC VQBIPUYAVBTHAK-UHFFFAOYSA-N 0.000 claims 1
- NYACDSKCBJAMAS-UHFFFAOYSA-N 1-butyl-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC NYACDSKCBJAMAS-UHFFFAOYSA-N 0.000 claims 1
- AKRXYEMBTILPGJ-UHFFFAOYSA-N 1-ethyl-5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CC)C=C2C AKRXYEMBTILPGJ-UHFFFAOYSA-N 0.000 claims 1
- BASDOWQNVNYFOM-UHFFFAOYSA-N 1-ethyl-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC BASDOWQNVNYFOM-UHFFFAOYSA-N 0.000 claims 1
- LHENQXAPVKABON-UHFFFAOYSA-N 1-methoxypropan-1-ol Chemical compound CCC(O)OC LHENQXAPVKABON-UHFFFAOYSA-N 0.000 claims 1
- SFTUZPUXNQAOEU-LJQANCHMSA-N 2,6-diethyl-7-[1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-4-propan-2-ylpyrido[2,3-b]pyrazin-3-one Chemical compound N1=C(CC)C(=O)N(C(C)C)C(N=C2CC)=C1C=C2C1=C(C)C=C2N([C@@H](COC)CC)C=C(C)C2=N1 SFTUZPUXNQAOEU-LJQANCHMSA-N 0.000 claims 1
- HXNACWNITLCMHI-UHFFFAOYSA-N 2-(2-ethoxy-5-methylsulfonyl-6-pent-4-en-2-ylpyridin-3-yl)-3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CCOC1=NC(C(C)CC=C)=C(S(C)(=O)=O)C=C1C(C(=N1)C)=NC2=C1N(C(CC)CC)C=C2C HXNACWNITLCMHI-UHFFFAOYSA-N 0.000 claims 1
- VPKUVCPWBCGHER-UHFFFAOYSA-N 2-(2-ethoxy-6-ethyl-5-methylsulfonylpyridin-3-yl)-3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CCOC1=NC(CC)=C(S(C)(=O)=O)C=C1C(C(=N1)C)=NC2=C1N(C(CC)CC)C=C2C VPKUVCPWBCGHER-UHFFFAOYSA-N 0.000 claims 1
- GAVRLRCRNBKKNK-UHFFFAOYSA-N 2-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC GAVRLRCRNBKKNK-UHFFFAOYSA-N 0.000 claims 1
- FRXLBMQRBFUDAM-UHFFFAOYSA-N 2-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,7-dimethyl-5-propylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC FRXLBMQRBFUDAM-UHFFFAOYSA-N 0.000 claims 1
- KKGMYPLWROEPBW-QGZVFWFLSA-N 2-(2-ethyl-6-propan-2-ylpyridin-3-yl)-5-[(2r)-1-methoxybutan-2-yl]-3,7-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC KKGMYPLWROEPBW-QGZVFWFLSA-N 0.000 claims 1
- KKGMYPLWROEPBW-KRWDZBQOSA-N 2-(2-ethyl-6-propan-2-ylpyridin-3-yl)-5-[(2s)-1-methoxybutan-2-yl]-3,7-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N([C@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC KKGMYPLWROEPBW-KRWDZBQOSA-N 0.000 claims 1
- USPILDXTYXDPNB-HXUWFJFHSA-N 2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethyl-5-[(2r)-1-(4-methylpiperazin-1-yl)butan-2-yl]pyrrolo[2,3-b]pyrazine Chemical compound C([C@@H](CC)N1C2=NC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)OC)N1CCN(C)CC1 USPILDXTYXDPNB-HXUWFJFHSA-N 0.000 claims 1
- ATSRJULUTDGNDC-LJQANCHMSA-N 2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethyl-5-[(2r)-1-pyrrolidin-1-ylbutan-2-yl]pyrrolo[2,3-b]pyrazine Chemical compound C([C@@H](CC)N1C2=NC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)OC)N1CCCC1 ATSRJULUTDGNDC-LJQANCHMSA-N 0.000 claims 1
- NZEHCAKUJVQXKG-UHFFFAOYSA-N 2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC NZEHCAKUJVQXKG-UHFFFAOYSA-N 0.000 claims 1
- YBUKMYGEETWPEW-UHFFFAOYSA-N 2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethyl-5-propylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC YBUKMYGEETWPEW-UHFFFAOYSA-N 0.000 claims 1
- KKGVEWQCJFCLMC-UHFFFAOYSA-N 2-[3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-2,5-dimethylpyrrolo[2,3-b]pyrazin-7-yl]butan-1-ol Chemical compound CC=1N=C2C(C(CO)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC KKGVEWQCJFCLMC-UHFFFAOYSA-N 0.000 claims 1
- UVKFCQSCZADXQG-UHFFFAOYSA-N 2-[3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-2,5-dimethylpyrrolo[2,3-b]pyrazin-7-yl]propan-1-ol Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1C(C(C)CO)=CN2C UVKFCQSCZADXQG-UHFFFAOYSA-N 0.000 claims 1
- FSHRMEDSESKGTE-UHFFFAOYSA-N 2-[3-[2-methoxy-4-(trifluoromethoxy)phenyl]-2,5-dimethylpyrrolo[2,3-b]pyrazin-7-yl]propan-1-ol Chemical compound COC1=CC(OC(F)(F)F)=CC=C1C(C(=N1)C)=NC2=C1C(C(C)CO)=CN2C FSHRMEDSESKGTE-UHFFFAOYSA-N 0.000 claims 1
- NGPHUFKXMZDXAZ-UHFFFAOYSA-N 2-[4-(difluoromethoxy)-2-methoxyphenyl]-3,7-dimethyl-5-propan-2-ylpyrrolo[2,3-b]pyrazine Chemical compound COC1=CC(OC(F)F)=CC=C1C(C(=N1)C)=NC2=C1N(C(C)C)C=C2C NGPHUFKXMZDXAZ-UHFFFAOYSA-N 0.000 claims 1
- GGSMWJIVCUEOKV-UHFFFAOYSA-N 2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]-n-methylpropanamide Chemical compound CC=1C=C2N(C(C)C(=O)NC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC GGSMWJIVCUEOKV-UHFFFAOYSA-N 0.000 claims 1
- XPDSGHSRZPMLEA-UHFFFAOYSA-N 2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]ethanol Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCO)C=C2C XPDSGHSRZPMLEA-UHFFFAOYSA-N 0.000 claims 1
- BWFOTNIYRHBXDQ-YOFSQIOKSA-N 2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl (2r,6s)-2,6-dimethylmorpholine-4-carboxylate Chemical compound C1=C(C)C2=NC(C=3C(=CC(OC(F)(F)F)=CC=3)OC)=C(C)C=C2N1C(CC)COC(=O)N1C[C@H](C)O[C@H](C)C1 BWFOTNIYRHBXDQ-YOFSQIOKSA-N 0.000 claims 1
- BTXZUKOZCRVGOI-UHFFFAOYSA-N 2-[6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1,5-dimethylpyrrolo[2,3-b]pyridin-3-yl]butan-1-ol Chemical compound CC=1C=C2C(C(CO)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC BTXZUKOZCRVGOI-UHFFFAOYSA-N 0.000 claims 1
- YHKPZINUTBFNCL-UHFFFAOYSA-N 2-bromo-3-[2-methoxy-4-(trifluoromethoxy)phenyl]-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound BrC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC YHKPZINUTBFNCL-UHFFFAOYSA-N 0.000 claims 1
- MRKFLBGILHSEDF-UHFFFAOYSA-N 2-ethyl-3-(2-ethyl-6-propan-2-ylpyridin-3-yl)-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CCC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC MRKFLBGILHSEDF-UHFFFAOYSA-N 0.000 claims 1
- ZPZQWZLVKSMFSR-UHFFFAOYSA-N 2-ethyl-3-(2-ethyl-6-propan-2-ylpyridin-3-yl)-5-methyl-7-propan-2-ylpyrrolo[2,3-b]pyrazine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=N1)CC)=NC2=C1C(C(C)C)=CN2C ZPZQWZLVKSMFSR-UHFFFAOYSA-N 0.000 claims 1
- YVBYQBFPVQPJNM-UHFFFAOYSA-N 2-ethyl-3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CCC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC YVBYQBFPVQPJNM-UHFFFAOYSA-N 0.000 claims 1
- HFGUWFKPPCDCOR-UHFFFAOYSA-N 2-ethyl-3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-5-methyl-7-propan-2-ylpyrrolo[2,3-b]pyrazine Chemical compound CCC1=NC=2C(C(C)C)=CN(C)C=2N=C1C1=CC=C(C(C)C)N=C1OC HFGUWFKPPCDCOR-UHFFFAOYSA-N 0.000 claims 1
- LSWLMGGALRLYEL-UHFFFAOYSA-N 2-ethyl-3-[2-methoxy-4-(trifluoromethoxy)phenyl]-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CCC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC LSWLMGGALRLYEL-UHFFFAOYSA-N 0.000 claims 1
- IQMQEJPMPJOZRA-UHFFFAOYSA-N 2-ethyl-7-(2-methoxyethyl)-3-[2-methoxy-4-(trifluoromethoxy)phenyl]-5-methylpyrrolo[2,3-b]pyrazine Chemical compound CCC1=NC=2C(CCOC)=CN(C)C=2N=C1C1=CC=C(OC(F)(F)F)C=C1OC IQMQEJPMPJOZRA-UHFFFAOYSA-N 0.000 claims 1
- BYVJZMGIFHMEFG-SXOMAYOGSA-N 2-morpholin-4-ylethyl (3s,4r)-3-(2-fluoroethoxy)-4-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]pyrrolidine-1-carboxylate Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H]1[C@H](CN(C1)C(=O)OCCN1CCOCC1)OCCF)C=C2C BYVJZMGIFHMEFG-SXOMAYOGSA-N 0.000 claims 1
- YFQCAVZGCZFBIL-UHFFFAOYSA-N 3,6-dimethyl-1-propan-2-yl-5-(6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound C1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C YFQCAVZGCZFBIL-UHFFFAOYSA-N 0.000 claims 1
- NKSFFFHRLHNFDX-UHFFFAOYSA-N 3,6-dimethyl-5-(2-methyl-6-propan-2-ylpyridin-3-yl)-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound CC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C NKSFFFHRLHNFDX-UHFFFAOYSA-N 0.000 claims 1
- LMKPKXSUDSLDBL-UHFFFAOYSA-N 3,6-dimethyl-5-(2-methyl-6-propan-2-ylpyridin-3-yl)-1-propylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1C LMKPKXSUDSLDBL-UHFFFAOYSA-N 0.000 claims 1
- ZBNYKOJAOHEVQZ-UHFFFAOYSA-N 3,6-dimethyl-5-(6-propan-2-ylpyridin-3-yl)-1-propylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1 ZBNYKOJAOHEVQZ-UHFFFAOYSA-N 0.000 claims 1
- JOEGXXVCRQULFO-UHFFFAOYSA-N 3,6-dimethyl-5-[2-(4-methylpiperazin-1-yl)-6-propan-2-ylpyridin-3-yl]-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound N=1C(C(C)C)=CC=C(C=2C(=CC=3N(C(C)C)C=C(C)C=3N=2)C)C=1N1CCN(C)CC1 JOEGXXVCRQULFO-UHFFFAOYSA-N 0.000 claims 1
- ZIJQQJHWZHEEQH-UHFFFAOYSA-N 3-(1-ethoxybutan-2-yl)-6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1,5-dimethylpyrrolo[2,3-b]pyridine Chemical compound CC=1C=C2C(C(CC)COCC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC ZIJQQJHWZHEEQH-UHFFFAOYSA-N 0.000 claims 1
- WHNQANIRXJKYCR-UHFFFAOYSA-N 3-(1-ethyl-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N(CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC WHNQANIRXJKYCR-UHFFFAOYSA-N 0.000 claims 1
- ZXZHAYSBRUBHFP-UHFFFAOYSA-N 3-(1-methoxybutan-2-yl)-6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1,5-dimethylpyrrolo[2,3-b]pyridine Chemical compound CC=1C=C2C(C(COC)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC ZXZHAYSBRUBHFP-UHFFFAOYSA-N 0.000 claims 1
- CKBBHSOZNSGYPC-UHFFFAOYSA-N 3-(2-ethyl-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazin-3-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC CKBBHSOZNSGYPC-UHFFFAOYSA-N 0.000 claims 1
- JZOPVXJEIOKAJG-UHFFFAOYSA-N 3-(2-ethyl-5-methyl-7-propan-2-ylpyrrolo[2,3-b]pyrazin-3-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC1=NC=2C(C(C)C)=CN(C)C=2N=C1C1=CC=C(C(C)C)N=C1NC JZOPVXJEIOKAJG-UHFFFAOYSA-N 0.000 claims 1
- AAGAILZTWJOHKM-UHFFFAOYSA-N 3-(2-ethyl-6-propan-2-ylpyridin-3-yl)-7-(1-methoxypropan-2-yl)-2,5-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1C(C(C)COC)=CN2C AAGAILZTWJOHKM-UHFFFAOYSA-N 0.000 claims 1
- UVGRJQCNFPCFOL-UHFFFAOYSA-N 3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-2,5-dimethyl-7-propan-2-ylpyrrolo[2,3-b]pyrazine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1C(C(C)C)=CN2C UVGRJQCNFPCFOL-UHFFFAOYSA-N 0.000 claims 1
- IVIODJAGAFAHRB-UHFFFAOYSA-N 3-(3,6-dimethyl-1-pentan-3-ylpyrrolo[3,2-b]pyridin-5-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical class CC=1C=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC IVIODJAGAFAHRB-UHFFFAOYSA-N 0.000 claims 1
- XUSBBTHVAAIJMF-UHFFFAOYSA-N 3-(3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridin-5-yl)-n,n-dimethyl-6-propan-2-ylpyridin-2-amine Chemical compound CN(C)C1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C XUSBBTHVAAIJMF-UHFFFAOYSA-N 0.000 claims 1
- KJCQQJVEIMGVQF-UHFFFAOYSA-N 3-(3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridin-5-yl)-n-(2-methoxyethyl)-6-propan-2-ylpyridin-2-amine Chemical class COCCNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C KJCQQJVEIMGVQF-UHFFFAOYSA-N 0.000 claims 1
- XZCONZUVSIZFKR-UHFFFAOYSA-N 3-(3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridin-5-yl)-n-ethyl-6-propan-2-ylpyridin-2-amine Chemical compound CCNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C XZCONZUVSIZFKR-UHFFFAOYSA-N 0.000 claims 1
- KDSGDSOOIUSTDJ-UHFFFAOYSA-N 3-(3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridin-5-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C KDSGDSOOIUSTDJ-UHFFFAOYSA-N 0.000 claims 1
- PCHCUXUJJRYZQO-UHFFFAOYSA-N 3-(3,6-dimethyl-1-propylpyrrolo[3,2-b]pyridin-5-yl)-n,n-dimethyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N(C)C PCHCUXUJJRYZQO-UHFFFAOYSA-N 0.000 claims 1
- IMUUBXMXCNCLHP-UHFFFAOYSA-N 3-(3,6-dimethyl-1-propylpyrrolo[3,2-b]pyridin-5-yl)-n-(2-methoxyethyl)-6-propan-2-ylpyridin-2-amine Chemical class CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NCCOC IMUUBXMXCNCLHP-UHFFFAOYSA-N 0.000 claims 1
- FHYWMOVEPQZGFO-UHFFFAOYSA-N 3-(3,6-dimethyl-1-propylpyrrolo[3,2-b]pyridin-5-yl)-n-ethyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NCC FHYWMOVEPQZGFO-UHFFFAOYSA-N 0.000 claims 1
- CEXQVAMBZOEYKI-UHFFFAOYSA-N 3-(3,7-dimethyl-5-propylpyrrolo[2,3-b]pyrazin-2-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1N=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC CEXQVAMBZOEYKI-UHFFFAOYSA-N 0.000 claims 1
- PXODGSQZNIVRIY-UHFFFAOYSA-N 3-(3-butan-2-yl-1,5-dimethylpyrrolo[2,3-b]pyridin-6-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2C(C(C)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC PXODGSQZNIVRIY-UHFFFAOYSA-N 0.000 claims 1
- GYYLZOISBUTECI-UHFFFAOYSA-N 3-(6-ethyl-3-methyl-1-propan-2-ylpyrrolo[3,2-b]pyridin-5-yl)-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC1=CC=2N(C(C)C)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1NC GYYLZOISBUTECI-UHFFFAOYSA-N 0.000 claims 1
- WPNKBDXSGPYICU-UHFFFAOYSA-N 3-[1-(1,3-dimethoxypropan-2-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(COC)COC)C=C2C WPNKBDXSGPYICU-UHFFFAOYSA-N 0.000 claims 1
- HXEWRJANHUWQGH-UHFFFAOYSA-N 3-[1-(1-methoxy-2-methylpropan-2-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)(C)COC)C=C2C HXEWRJANHUWQGH-UHFFFAOYSA-N 0.000 claims 1
- YOJWBDIZSSOPJW-UHFFFAOYSA-N 3-[1-(1-methoxypropan-2-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)COC)C=C2C YOJWBDIZSSOPJW-UHFFFAOYSA-N 0.000 claims 1
- FQQMUTWGBDWASM-UHFFFAOYSA-N 3-[1-(2-fluoroethyl)-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical class CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCF)C=C2C FQQMUTWGBDWASM-UHFFFAOYSA-N 0.000 claims 1
- XVAJIWRIRTXFBH-UHFFFAOYSA-N 3-[1-(3-fluoropropyl)-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical class CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCCF)C=C2C XVAJIWRIRTXFBH-UHFFFAOYSA-N 0.000 claims 1
- GHFPTCVANVGFRG-INIZCTEOSA-N 3-[1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](CF)COC)C=C2C GHFPTCVANVGFRG-INIZCTEOSA-N 0.000 claims 1
- XXASFCGNYSGFAY-QGZVFWFLSA-N 3-[1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC XXASFCGNYSGFAY-QGZVFWFLSA-N 0.000 claims 1
- SBPCQDUKKLXLJJ-GOSISDBHSA-N 3-[1-[(2r)-1-methoxypentan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N([C@@H](COC)CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC SBPCQDUKKLXLJJ-GOSISDBHSA-N 0.000 claims 1
- YOJWBDIZSSOPJW-MRXNPFEDSA-N 3-[1-[(2r)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H](C)COC)C=C2C YOJWBDIZSSOPJW-MRXNPFEDSA-N 0.000 claims 1
- KBLJODRRWZCXLM-SFHVURJKSA-N 3-[1-[(2s)-1-ethoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N([C@@H](CC)COCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC KBLJODRRWZCXLM-SFHVURJKSA-N 0.000 claims 1
- GHFPTCVANVGFRG-MRXNPFEDSA-N 3-[1-[(2s)-1-fluoro-3-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H](CF)COC)C=C2C GHFPTCVANVGFRG-MRXNPFEDSA-N 0.000 claims 1
- LLWDZRFGJCISAL-INIZCTEOSA-N 3-[1-[(2s)-1-fluorobutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N([C@H](CF)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC LLWDZRFGJCISAL-INIZCTEOSA-N 0.000 claims 1
- XIDPWFCKQOJIJD-INIZCTEOSA-N 3-[1-[(2s)-1-methoxypropan-2-yl]-3,6,7-trimethylpyrrolo[3,2-b]pyridin-5-yl]-n,n-dimethyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C(C)=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N(C)C XIDPWFCKQOJIJD-INIZCTEOSA-N 0.000 claims 1
- GYIAWRTWJIRRAL-HNNXBMFYSA-N 3-[1-[(2s)-1-methoxypropan-2-yl]-3,6,7-trimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1C)C)=NC2=C1N([C@@H](C)COC)C=C2C GYIAWRTWJIRRAL-HNNXBMFYSA-N 0.000 claims 1
- JSRKDQMOFOJRNV-SFHVURJKSA-N 3-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n,6-di(propan-2-yl)pyridin-2-amine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC(C)C JSRKDQMOFOJRNV-SFHVURJKSA-N 0.000 claims 1
- XOFAFZFSOUPTKH-KRWDZBQOSA-N 3-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n,n-dimethyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N(C)C XOFAFZFSOUPTKH-KRWDZBQOSA-N 0.000 claims 1
- YOJWBDIZSSOPJW-INIZCTEOSA-N 3-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C YOJWBDIZSSOPJW-INIZCTEOSA-N 0.000 claims 1
- OBBNXYXZIFULLR-UHFFFAOYSA-N 3-[2-ethyl-3-[2-methoxy-4-(trifluoromethoxy)phenyl]-5-methylpyrrolo[2,3-b]pyrazin-7-yl]propanenitrile Chemical compound CCC1=NC=2C(CCC#N)=CN(C)C=2N=C1C1=CC=C(OC(F)(F)F)C=C1OC OBBNXYXZIFULLR-UHFFFAOYSA-N 0.000 claims 1
- YBCJXSXCHGKIJQ-UHFFFAOYSA-N 3-[2-methoxy-4-(trifluoromethoxy)phenyl]-2,5-dimethyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC YBCJXSXCHGKIJQ-UHFFFAOYSA-N 0.000 claims 1
- JRGGNXONSYPLPT-UHFFFAOYSA-N 3-[2-methoxy-4-(trifluoromethoxy)phenyl]-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazine Chemical compound C=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC JRGGNXONSYPLPT-UHFFFAOYSA-N 0.000 claims 1
- OAECMFPXHFSBGN-UHFFFAOYSA-N 3-[3,6-dimethyl-1-(2-methylpropyl)pyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CC(C)C)C=C2C OAECMFPXHFSBGN-UHFFFAOYSA-N 0.000 claims 1
- OOFICFIVHPGPMH-HXUWFJFHSA-N 3-[3,6-dimethyl-1-[(2r)-1-morpholin-4-ylbutan-2-yl]pyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound C([C@@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)NC)N1CCOCC1 OOFICFIVHPGPMH-HXUWFJFHSA-N 0.000 claims 1
- OOFICFIVHPGPMH-FQEVSTJZSA-N 3-[3,6-dimethyl-1-[(2s)-1-morpholin-4-ylbutan-2-yl]pyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)NC)N1CCOCC1 OOFICFIVHPGPMH-FQEVSTJZSA-N 0.000 claims 1
- ICICWOCXGNDSID-LJQANCHMSA-N 3-[3,7-dimethyl-5-[(2r)-1-morpholin-4-ylbutan-2-yl]pyrrolo[2,3-b]pyrazin-2-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound C([C@@H](CC)N1C2=NC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)NC)N1CCOCC1 ICICWOCXGNDSID-LJQANCHMSA-N 0.000 claims 1
- KYCPYYIUPNKMAN-OAHLLOKOSA-N 3-[3-chloro-1-[(2r)-1-methoxybutan-2-yl]-6-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(Cl)C2=NC=1C1=CC=C(C(C)C)N=C1NC KYCPYYIUPNKMAN-OAHLLOKOSA-N 0.000 claims 1
- DRDATAVZNQSFBB-AWEZNQCLSA-N 3-[3-chloro-1-[(2s)-1-methoxypropan-2-yl]-6-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2Cl DRDATAVZNQSFBB-AWEZNQCLSA-N 0.000 claims 1
- MYZRMQNOCHQFMC-ZDUSSCGKSA-N 3-[3-chloro-5-[(2s)-1-methoxypropan-2-yl]-7-methylpyrrolo[2,3-b]pyrazin-2-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=N1)Cl)=NC2=C1N([C@@H](C)COC)C=C2C MYZRMQNOCHQFMC-ZDUSSCGKSA-N 0.000 claims 1
- QIEVDRTZANSVEK-HNNXBMFYSA-N 3-[3-ethyl-5-[(2s)-1-methoxypropan-2-yl]-7-methylpyrrolo[2,3-b]pyrazin-2-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC1=NC=2N([C@@H](C)COC)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1NC QIEVDRTZANSVEK-HNNXBMFYSA-N 0.000 claims 1
- ZOLDVIDWHMZEAI-QGZVFWFLSA-N 3-[5-[(2r)-1-ethoxybutan-2-yl]-3,7-dimethylpyrrolo[2,3-b]pyrazin-2-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1N=C2N([C@H](CC)COCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC ZOLDVIDWHMZEAI-QGZVFWFLSA-N 0.000 claims 1
- HXHYWHCVQTUVRT-QGZVFWFLSA-N 3-[5-[(2r)-1-methoxybutan-2-yl]-3,7-dimethylpyrrolo[2,3-b]pyrazin-2-yl]-n,n-dimethyl-6-propan-2-ylpyridin-2-amine Chemical compound CC=1N=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N(C)C HXHYWHCVQTUVRT-QGZVFWFLSA-N 0.000 claims 1
- HNUBZKGVMGDBGZ-AWEZNQCLSA-N 3-[6-chloro-1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)Cl)=NC2=C1N([C@@H](CF)COC)C=C2C HNUBZKGVMGDBGZ-AWEZNQCLSA-N 0.000 claims 1
- NHYNMNXNYJOZMT-HNNXBMFYSA-N 3-[6-chloro-1-[(2s)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n,n-dimethyl-6-propan-2-ylpyridin-2-amine Chemical compound ClC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N(C)C NHYNMNXNYJOZMT-HNNXBMFYSA-N 0.000 claims 1
- PYBXAFRDABTGJM-HNNXBMFYSA-N 3-[6-chloro-1-[(2s)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-ethyl-6-propan-2-ylpyridin-2-amine Chemical compound CCNC1=NC(C(C)C)=CC=C1C(C(=C1)Cl)=NC2=C1N([C@@H](C)COC)C=C2C PYBXAFRDABTGJM-HNNXBMFYSA-N 0.000 claims 1
- NIXUIZSVOAFJKY-AWEZNQCLSA-N 3-[6-chloro-1-[(2s)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)Cl)=NC2=C1N([C@@H](C)COC)C=C2C NIXUIZSVOAFJKY-AWEZNQCLSA-N 0.000 claims 1
- YVYIZCXGEHJBLC-GOSISDBHSA-N 3-[6-ethyl-1-[(2r)-1-methoxybutan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC YVYIZCXGEHJBLC-GOSISDBHSA-N 0.000 claims 1
- GIGYPNKNFKBGCX-MRXNPFEDSA-N 3-[6-ethyl-1-[(2r)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC1=CC=2N([C@H](C)COC)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1NC GIGYPNKNFKBGCX-MRXNPFEDSA-N 0.000 claims 1
- GIGYPNKNFKBGCX-INIZCTEOSA-N 3-[6-ethyl-1-[(2s)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC1=CC=2N([C@@H](C)COC)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1NC GIGYPNKNFKBGCX-INIZCTEOSA-N 0.000 claims 1
- HPRZXRYKBGRWEX-INIZCTEOSA-N 3-[6-methoxy-1-[(2s)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n,n-dimethyl-6-propan-2-ylpyridin-2-amine Chemical compound COC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N(C)C HPRZXRYKBGRWEX-INIZCTEOSA-N 0.000 claims 1
- LWFGDGSQVGUYFD-HNNXBMFYSA-N 3-[6-methoxy-1-[(2s)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=C1)OC)=NC2=C1N([C@@H](C)COC)C=C2C LWFGDGSQVGUYFD-HNNXBMFYSA-N 0.000 claims 1
- DXQKTGMDMLTGDN-UHFFFAOYSA-N 3-[7-(1-methoxypropan-2-yl)-2,5-dimethylpyrrolo[2,3-b]pyrazin-3-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1C(C(C)COC)=CN2C DXQKTGMDMLTGDN-UHFFFAOYSA-N 0.000 claims 1
- UZZILCFUGXUHIG-AWEZNQCLSA-N 3-bromo-1-[(2s)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(Br)C2=NC=1C1=CC=C(C(C)C)N=C1OC UZZILCFUGXUHIG-AWEZNQCLSA-N 0.000 claims 1
- MIXOXSWKLMRXRF-UHFFFAOYSA-N 3-bromo-5-(3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-n,4-diethyl-n-methylpyridin-2-amine Chemical compound CC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(C)CC)C(Br)=C1CC MIXOXSWKLMRXRF-UHFFFAOYSA-N 0.000 claims 1
- AFECPAVMSVAGHD-UHFFFAOYSA-N 3-butan-2-yl-6-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1,5-dimethylpyrrolo[2,3-b]pyridine Chemical compound CC=1C=C2C(C(C)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC AFECPAVMSVAGHD-UHFFFAOYSA-N 0.000 claims 1
- STCOLTWHJYIWOS-UHFFFAOYSA-N 3-butan-2-yl-6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1,5-dimethylpyrrolo[2,3-b]pyridine Chemical compound CC=1C=C2C(C(C)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC STCOLTWHJYIWOS-UHFFFAOYSA-N 0.000 claims 1
- KBWMEXYKKXIFPN-OAHLLOKOSA-N 3-chloro-1-[(2r)-1-methoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(Cl)C2=NC=1C1=CC=C(C(C)C)N=C1OC KBWMEXYKKXIFPN-OAHLLOKOSA-N 0.000 claims 1
- VOCOGJSWPFMTPN-AWEZNQCLSA-N 3-chloro-1-[(2s)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(Cl)C2=NC=1C1=CC=C(C(C)C)N=C1OC VOCOGJSWPFMTPN-AWEZNQCLSA-N 0.000 claims 1
- DRAROCBRAGNJRJ-AWEZNQCLSA-N 3-chloro-1-[(2s)-1-methoxypropan-2-yl]-6-methyl-5-(6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(Cl)C2=NC=1C1=CC=C(C(C)C)N=C1 DRAROCBRAGNJRJ-AWEZNQCLSA-N 0.000 claims 1
- UWSAUVQYBOJDOI-UHFFFAOYSA-N 3-chloro-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-6-methyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2Cl UWSAUVQYBOJDOI-UHFFFAOYSA-N 0.000 claims 1
- MEWWRIMXKHBWTF-ZDUSSCGKSA-N 3-chloro-5-[(2s)-1-methoxypropan-2-yl]-7-methyl-2-(2-methyl-6-propan-2-ylpyridin-3-yl)pyrrolo[2,3-b]pyrazine Chemical compound ClC=1N=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1C MEWWRIMXKHBWTF-ZDUSSCGKSA-N 0.000 claims 1
- KHGNQABBBCRZKJ-HNNXBMFYSA-N 3-ethyl-5-[(2s)-1-methoxypropan-2-yl]-2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-7-methylpyrrolo[2,3-b]pyrazine Chemical compound CCC1=NC=2N([C@@H](C)COC)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1OC KHGNQABBBCRZKJ-HNNXBMFYSA-N 0.000 claims 1
- SXPZIGSECPJBMG-LBPRGKRZSA-N 3-fluoro-1-[(2s)-1-methoxypropan-2-yl]-5-[2-methoxy-4-(trifluoromethoxy)phenyl]-6-methylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(F)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC SXPZIGSECPJBMG-LBPRGKRZSA-N 0.000 claims 1
- GRMTYDDSGLEKBP-HXUWFJFHSA-N 4-[(2r)-2-[2-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazin-5-yl]butyl]morpholine Chemical compound C([C@@H](CC)N1C2=NC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)CC)N1CCOCC1 GRMTYDDSGLEKBP-HXUWFJFHSA-N 0.000 claims 1
- HDKOESKTQUNERL-OAQYLSRUSA-N 4-[(2r)-2-[5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl]morpholine Chemical compound C([C@@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)CC)N1CCOCC1 HDKOESKTQUNERL-OAQYLSRUSA-N 0.000 claims 1
- MVZDNXVMVUKYFE-HXUWFJFHSA-N 4-[(2r)-2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl]morpholine Chemical compound C([C@@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)OC)N1CCOCC1 MVZDNXVMVUKYFE-HXUWFJFHSA-N 0.000 claims 1
- HDKOESKTQUNERL-NRFANRHFSA-N 4-[(2s)-2-[5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl]morpholine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)CC)N1CCOCC1 HDKOESKTQUNERL-NRFANRHFSA-N 0.000 claims 1
- MVZDNXVMVUKYFE-FQEVSTJZSA-N 4-[(2s)-2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl]morpholine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=NC(=CC=1)C(C)C)OC)N1CCOCC1 MVZDNXVMVUKYFE-FQEVSTJZSA-N 0.000 claims 1
- CCIRNHGQHDBAST-SFHVURJKSA-N 4-[(2s)-2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl]morpholine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1CCOCC1 CCIRNHGQHDBAST-SFHVURJKSA-N 0.000 claims 1
- MJZMDIMPTONIJD-SFHVURJKSA-N 4-[(2s)-2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl]thiomorpholine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1CCSCC1 MJZMDIMPTONIJD-SFHVURJKSA-N 0.000 claims 1
- IRELQQYECLKMPH-UHFFFAOYSA-N 4-[2-[3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-2,5-dimethylpyrrolo[2,3-b]pyrazin-7-yl]propyl]morpholine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1C(C(C)CN1CCOCC1)=CN2C IRELQQYECLKMPH-UHFFFAOYSA-N 0.000 claims 1
- JTNWJSHBHUAFRP-UHFFFAOYSA-N 4-[2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]ethyl]morpholine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCN1CCOCC1)C=C2C JTNWJSHBHUAFRP-UHFFFAOYSA-N 0.000 claims 1
- VFOVWUIDQLMZQN-UHFFFAOYSA-N 4-ethyl-5-(2-ethyl-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazin-3-yl)-n,n-dimethylpyridin-2-amine Chemical compound CCC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CN=C(N(C)C)C=C1CC VFOVWUIDQLMZQN-UHFFFAOYSA-N 0.000 claims 1
- BUZJYJICIXGDJA-INIZCTEOSA-N 5-(2,6-diethylpyridin-3-yl)-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(CC)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C BUZJYJICIXGDJA-INIZCTEOSA-N 0.000 claims 1
- ZFXUXPCSZDOPAO-UHFFFAOYSA-N 5-(2,6-diethylpyridin-3-yl)-3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(CC)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C ZFXUXPCSZDOPAO-UHFFFAOYSA-N 0.000 claims 1
- WPZJHBZRNNJFEF-GOSISDBHSA-N 5-(2-ethoxy-6-ethyl-5-methylsulfonylpyridin-3-yl)-6-ethyl-1-[(2r)-1-methoxybutan-2-yl]-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCOC1=NC(CC)=C(S(C)(=O)=O)C=C1C(C(=C1)CC)=NC2=C1N([C@H](CC)COC)C=C2C WPZJHBZRNNJFEF-GOSISDBHSA-N 0.000 claims 1
- UFBJCWKEEOUCET-MRXNPFEDSA-N 5-(2-ethoxy-6-ethyl-5-methylsulfonylpyridin-3-yl)-6-ethyl-1-[(2r)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCOC1=NC(CC)=C(S(C)(=O)=O)C=C1C(C(=C1)CC)=NC2=C1N([C@H](C)COC)C=C2C UFBJCWKEEOUCET-MRXNPFEDSA-N 0.000 claims 1
- OJHYFPFDOPBNIW-KRWDZBQOSA-N 5-(2-ethoxy-6-propan-2-ylpyridin-3-yl)-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCOC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C OJHYFPFDOPBNIW-KRWDZBQOSA-N 0.000 claims 1
- ISXBDNYPSSJCSY-MRXNPFEDSA-N 5-(2-ethyl-6-methoxypyridin-3-yl)-1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(OC)N=C1CC ISXBDNYPSSJCSY-MRXNPFEDSA-N 0.000 claims 1
- BJYQAYITEAAPIJ-UHFFFAOYSA-N 5-(2-ethyl-6-methoxypyridin-3-yl)-3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(OC)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C BJYQAYITEAAPIJ-UHFFFAOYSA-N 0.000 claims 1
- ZVVFOVHNFIKRIO-GOSISDBHSA-N 5-(2-ethyl-6-propan-2-yloxypyridin-3-yl)-1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(OC(C)C)N=C1CC ZVVFOVHNFIKRIO-GOSISDBHSA-N 0.000 claims 1
- MGPQAZVGRKYZNV-KRWDZBQOSA-N 5-(2-ethyl-6-propan-2-yloxypyridin-3-yl)-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(OC(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C MGPQAZVGRKYZNV-KRWDZBQOSA-N 0.000 claims 1
- CFXSBGRQSBGRSH-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-yloxypyridin-3-yl)-3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(OC(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C CFXSBGRQSBGRSH-UHFFFAOYSA-N 0.000 claims 1
- YGQHICHYUOKNQZ-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-(1-methoxy-2-methylpropan-2-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)(C)COC)C=C2C YGQHICHYUOKNQZ-UHFFFAOYSA-N 0.000 claims 1
- DJMBLQFKNGLOHF-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-(1-methoxypropan-2-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)COC)C=C2C DJMBLQFKNGLOHF-UHFFFAOYSA-N 0.000 claims 1
- RELJMCALYJBEGQ-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-(2-fluoroethyl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCF)C=C2C RELJMCALYJBEGQ-UHFFFAOYSA-N 0.000 claims 1
- MODROGVJKMWPKL-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-(3-fluoropropyl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CCCF)C=C2C MODROGVJKMWPKL-UHFFFAOYSA-N 0.000 claims 1
- LVACYZHUNJTICC-KRWDZBQOSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](CF)COC)C=C2C LVACYZHUNJTICC-KRWDZBQOSA-N 0.000 claims 1
- UTLJDDJRHZVEPW-LJQANCHMSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-[(2r)-1-methoxypentan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC UTLJDDJRHZVEPW-LJQANCHMSA-N 0.000 claims 1
- DJMBLQFKNGLOHF-QGZVFWFLSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-[(2r)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H](C)COC)C=C2C DJMBLQFKNGLOHF-QGZVFWFLSA-N 0.000 claims 1
- UCWXMWMDETYNQC-KRWDZBQOSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-[(2s)-1-fluorobutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](CF)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC UCWXMWMDETYNQC-KRWDZBQOSA-N 0.000 claims 1
- DJMBLQFKNGLOHF-KRWDZBQOSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C DJMBLQFKNGLOHF-KRWDZBQOSA-N 0.000 claims 1
- QATFVCJVPUJALI-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethyl-1-(2-methylpropyl)pyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CC(C)C)C=C2C QATFVCJVPUJALI-UHFFFAOYSA-N 0.000 claims 1
- PTOHVGGCUOWQTP-UHFFFAOYSA-N 5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C PTOHVGGCUOWQTP-UHFFFAOYSA-N 0.000 claims 1
- BRRYOWQCLPLFME-UHFFFAOYSA-N 5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1,3,6-trimethylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C)C=C2C BRRYOWQCLPLFME-UHFFFAOYSA-N 0.000 claims 1
- ILLSRBNJNNRVSD-UHFFFAOYSA-N 5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1-(3-methoxyprop-1-en-2-yl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(=C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC ILLSRBNJNNRVSD-UHFFFAOYSA-N 0.000 claims 1
- NLDODZBEVHWDED-UHFFFAOYSA-N 5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1-(3-methoxypropyl)-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCCOC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC NLDODZBEVHWDED-UHFFFAOYSA-N 0.000 claims 1
- NNUPVIYNNXPDCM-UHFFFAOYSA-N 5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethyl-1-(2-methylpropyl)pyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(CC(C)C)C=C2C NNUPVIYNNXPDCM-UHFFFAOYSA-N 0.000 claims 1
- PDWMFLICFWTMQJ-UHFFFAOYSA-N 5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethyl-1-pentan-3-ylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC PDWMFLICFWTMQJ-UHFFFAOYSA-N 0.000 claims 1
- IGQDJDAFJXCHCF-UHFFFAOYSA-N 5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C IGQDJDAFJXCHCF-UHFFFAOYSA-N 0.000 claims 1
- ASWVXKDUIXVNDT-UHFFFAOYSA-N 5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethyl-1-propylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC ASWVXKDUIXVNDT-UHFFFAOYSA-N 0.000 claims 1
- XKBLDZHMNXPXLE-UHFFFAOYSA-N 5-(3,6-dimethyl-1-pentan-3-ylpyrrolo[3,2-b]pyridin-5-yl)-4-ethyl-n,n-dimethylpyridin-2-amine Chemical class CC=1C=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(C)C)C=C1CC XKBLDZHMNXPXLE-UHFFFAOYSA-N 0.000 claims 1
- GHAINVFSRSEKTM-UHFFFAOYSA-N 5-(3,6-dimethyl-1-pentan-3-ylpyrrolo[3,2-b]pyridin-5-yl)-n,4-diethyl-n-methylpyridin-2-amine Chemical compound CC=1C=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(C)CC)C=C1CC GHAINVFSRSEKTM-UHFFFAOYSA-N 0.000 claims 1
- CXIODZDEAVSXCR-UHFFFAOYSA-N 5-(3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridin-5-yl)-6-ethyl-n,n-dimethylpyridin-2-amine Chemical compound CCC1=NC(N(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C CXIODZDEAVSXCR-UHFFFAOYSA-N 0.000 claims 1
- MJYXSUXGGLUAMB-UHFFFAOYSA-N 5-(3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-4-ethyl-n,n-dimethylpyridin-2-amine Chemical class CC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(C)C)C=C1CC MJYXSUXGGLUAMB-UHFFFAOYSA-N 0.000 claims 1
- IGUJBUALTFQKST-UHFFFAOYSA-N 5-(3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-4-methoxy-n,n-dimethylpyridin-2-amine Chemical class CC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(C)C)C=C1OC IGUJBUALTFQKST-UHFFFAOYSA-N 0.000 claims 1
- OOFULEJUQPYEHB-UHFFFAOYSA-N 5-(3,7-dimethyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-n,4-diethyl-n-methylpyridin-2-amine Chemical compound CC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(C)CC)C=C1CC OOFULEJUQPYEHB-UHFFFAOYSA-N 0.000 claims 1
- JPRSGGQOZPPJDX-UHFFFAOYSA-N 5-(3-chloro-7-methyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-4-ethyl-n,n-dimethylpyridin-2-amine Chemical compound ClC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(C)C)C=C1CC JPRSGGQOZPPJDX-UHFFFAOYSA-N 0.000 claims 1
- JYQVVBFTFIMJRQ-UHFFFAOYSA-N 5-(3-chloro-7-methyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-n,4-diethyl-n-methylpyridin-2-amine Chemical compound ClC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(C)CC)C=C1CC JYQVVBFTFIMJRQ-UHFFFAOYSA-N 0.000 claims 1
- KYMXIIPWIUIJQU-UHFFFAOYSA-N 5-(3-chloro-7-methyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-n,n,4-triethylpyridin-2-amine Chemical compound ClC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C1=CN=C(N(CC)CC)C=C1CC KYMXIIPWIUIJQU-UHFFFAOYSA-N 0.000 claims 1
- YEQAPKHQMHIDKI-QGZVFWFLSA-N 5-(6-ethoxy-2-ethylpyridin-3-yl)-1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(OCC)=CC=C1C(C(=C1)C)=NC2=C1N([C@H](CC)COC)C=C2C YEQAPKHQMHIDKI-QGZVFWFLSA-N 0.000 claims 1
- FOUNAHFZXVLJSX-INIZCTEOSA-N 5-(6-ethoxy-2-ethylpyridin-3-yl)-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(OCC)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C FOUNAHFZXVLJSX-INIZCTEOSA-N 0.000 claims 1
- XXHNBMYNAPCAKC-QGZVFWFLSA-N 5-[(2r)-1-ethoxybutan-2-yl]-2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N([C@H](CC)COCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC XXHNBMYNAPCAKC-QGZVFWFLSA-N 0.000 claims 1
- FKFLERGWUKXYPV-QGZVFWFLSA-N 5-[(2r)-1-methoxybutan-2-yl]-3,7-dimethyl-2-(2-methyl-6-propan-2-ylpyridin-3-yl)pyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1C FKFLERGWUKXYPV-QGZVFWFLSA-N 0.000 claims 1
- UPQLNKCPPNVHAJ-QGZVFWFLSA-N 5-[(2r)-1-methoxybutan-2-yl]-3,7-dimethyl-2-(6-propan-2-ylpyridin-3-yl)pyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1 UPQLNKCPPNVHAJ-QGZVFWFLSA-N 0.000 claims 1
- FCCGIKZKBIBAQS-INIZCTEOSA-N 5-[(2s)-1-methoxybutan-2-yl]-2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N([C@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC FCCGIKZKBIBAQS-INIZCTEOSA-N 0.000 claims 1
- LQSRYJXSXDGLFL-KRWDZBQOSA-N 5-[2-(3,3-difluoroazetidin-1-yl)-6-propan-2-ylpyridin-3-yl]-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N1CC(F)(F)C1 LQSRYJXSXDGLFL-KRWDZBQOSA-N 0.000 claims 1
- HVELZZIJZOWEEQ-LJQANCHMSA-N 5-[2-(azetidin-1-yl)-6-propan-2-ylpyridin-3-yl]-1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N1CCC1 HVELZZIJZOWEEQ-LJQANCHMSA-N 0.000 claims 1
- CLWBVPMWTLOQJU-KRWDZBQOSA-N 5-[2-(azetidin-1-yl)-6-propan-2-ylpyridin-3-yl]-1-[(2s)-1-methoxypropan-2-yl]-3,6,7-trimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C(C)=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N1CCC1 CLWBVPMWTLOQJU-KRWDZBQOSA-N 0.000 claims 1
- DCDSCEDRPOPAKG-SFHVURJKSA-N 5-[2-(azetidin-1-yl)-6-propan-2-ylpyridin-3-yl]-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N1CCC1 DCDSCEDRPOPAKG-SFHVURJKSA-N 0.000 claims 1
- GATNJLXVZNSEMQ-UHFFFAOYSA-N 5-[2-(azetidin-1-yl)-6-propan-2-ylpyridin-3-yl]-3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound N=1C(C(C)C)=CC=C(C=2C(=CC=3N(C(C)C)C=C(C)C=3N=2)C)C=1N1CCC1 GATNJLXVZNSEMQ-UHFFFAOYSA-N 0.000 claims 1
- QOKORLHVSDGFCX-UHFFFAOYSA-N 5-[2-(azetidin-1-yl)-6-propan-2-ylpyridin-3-yl]-3,6-dimethyl-1-propylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N(CCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N1CCC1 QOKORLHVSDGFCX-UHFFFAOYSA-N 0.000 claims 1
- ILPUKNBASIZXRD-HXUWFJFHSA-N 5-[2-(azetidin-1-yl)-6-propan-2-ylpyridin-3-yl]-6-ethyl-1-[(2r)-1-methoxybutan-2-yl]-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1N1CCC1 ILPUKNBASIZXRD-HXUWFJFHSA-N 0.000 claims 1
- SVUZACDZPFPBJJ-KRWDZBQOSA-N 5-[2-ethyl-6-(2-methoxyethoxy)pyridin-3-yl]-1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(OCCOC)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C SVUZACDZPFPBJJ-KRWDZBQOSA-N 0.000 claims 1
- ZXYFIFIEVQQMMO-IBGZPJMESA-N 5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethyl-1-[(2s)-1-(4-methylpiperazin-1-yl)butan-2-yl]pyrrolo[3,2-b]pyridine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1CCN(C)CC1 ZXYFIFIEVQQMMO-IBGZPJMESA-N 0.000 claims 1
- AIGNYRPZHNPUEC-HNNXBMFYSA-N 5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethyl-1-[(2s)-1-methylsulfonylbutan-2-yl]pyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@H](CS(C)(=O)=O)CC)C=C(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC AIGNYRPZHNPUEC-HNNXBMFYSA-N 0.000 claims 1
- YRDSHJLAAKUPPS-IBGZPJMESA-N 5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethyl-1-[(2s)-1-piperidin-1-ylbutan-2-yl]pyrrolo[3,2-b]pyridine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1CCCCC1 YRDSHJLAAKUPPS-IBGZPJMESA-N 0.000 claims 1
- VOUZMOZWFCOPDS-SFHVURJKSA-N 5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethyl-1-[(2s)-1-pyrrolidin-1-ylbutan-2-yl]pyrrolo[3,2-b]pyridine Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)N1CCCC1 VOUZMOZWFCOPDS-SFHVURJKSA-N 0.000 claims 1
- VTIWKXSKWGNOQI-UHFFFAOYSA-N 5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound COC1=CC(OC(F)(F)F)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C VTIWKXSKWGNOQI-UHFFFAOYSA-N 0.000 claims 1
- ZFDJRZWPQXLEKH-UHFFFAOYSA-N 5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethyl-1h-pyrrolo[3,2-b]pyridine Chemical compound COC1=CC(OC(F)(F)F)=CC=C1C(C(=C1)C)=NC2=C1NC=C2C ZFDJRZWPQXLEKH-UHFFFAOYSA-N 0.000 claims 1
- IRHHFPSUEJWNGL-LJQANCHMSA-N 5-[6-(cyclopropylmethoxy)-2-ethylpyridin-3-yl]-1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C(C(=N1)CC)=CC=C1OCC1CC1 IRHHFPSUEJWNGL-LJQANCHMSA-N 0.000 claims 1
- PGJGDXYZPJOSMX-HNNXBMFYSA-N 5-bromo-3-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=C(Br)C=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C PGJGDXYZPJOSMX-HNNXBMFYSA-N 0.000 claims 1
- BZQIBOXGFHDAPB-OAHLLOKOSA-N 5-bromo-3-[6-ethyl-1-[(2r)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC1=CC=2N([C@H](C)COC)C=C(C)C=2N=C1C1=CC(Br)=C(C(C)C)N=C1NC BZQIBOXGFHDAPB-OAHLLOKOSA-N 0.000 claims 1
- ZLVVETTVDNSOQI-UHFFFAOYSA-N 5-bromo-6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1-methyl-3-propan-2-ylpyrrolo[2,3-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)Br)=NC2=C1C(C(C)C)=CN2C ZLVVETTVDNSOQI-UHFFFAOYSA-N 0.000 claims 1
- VUVWOBORYVROMA-UHFFFAOYSA-N 5-bromo-6-[2-methoxy-4-(trifluoromethoxy)phenyl]-1-methyl-3-pentan-3-ylpyrrolo[2,3-b]pyridine Chemical compound BrC=1C=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC VUVWOBORYVROMA-UHFFFAOYSA-N 0.000 claims 1
- MFUKVRLBOHKDJK-UHFFFAOYSA-N 5-but-1-en-2-yl-2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N(C(=C)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC MFUKVRLBOHKDJK-UHFFFAOYSA-N 0.000 claims 1
- OHSMISVBZTXXRT-UHFFFAOYSA-N 5-butan-2-yl-2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,7-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2N(C(C)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC OHSMISVBZTXXRT-UHFFFAOYSA-N 0.000 claims 1
- XOIOAGDHULRXGP-UHFFFAOYSA-N 5-chloro-3-(3,6-dimethyl-1-propan-2-ylpyrrolo[3,2-b]pyridin-5-yl)-n-ethyl-6-propan-2-ylpyridin-2-amine Chemical compound CCNC1=NC(C(C)C)=C(Cl)C=C1C(C(=C1)C)=NC2=C1N(C(C)C)C=C2C XOIOAGDHULRXGP-UHFFFAOYSA-N 0.000 claims 1
- SDEINDYKOHDZSF-HNNXBMFYSA-N 5-chloro-3-[1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CNC1=NC(C(C)C)=C(Cl)C=C1C(C(=C1)C)=NC2=C1N([C@@H](CF)COC)C=C2C SDEINDYKOHDZSF-HNNXBMFYSA-N 0.000 claims 1
- KSEWSCJGCXRALS-OAHLLOKOSA-N 5-chloro-3-[6-ethyl-1-[(2r)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC1=CC=2N([C@H](C)COC)C=C(C)C=2N=C1C1=CC(Cl)=C(C(C)C)N=C1NC KSEWSCJGCXRALS-OAHLLOKOSA-N 0.000 claims 1
- FPGZVAIIVQQNBR-UHFFFAOYSA-N 5-chloro-6-[2-methoxy-4-(trifluoromethoxy)phenyl]-1-methyl-3-pentan-3-ylpyrrolo[2,3-b]pyridine Chemical compound ClC=1C=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC FPGZVAIIVQQNBR-UHFFFAOYSA-N 0.000 claims 1
- FPVHEVAEGCYSLO-QGZVFWFLSA-N 5-cyclopropyl-3-[6-ethyl-1-[(2r)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound CCC1=CC=2N([C@H](C)COC)C=C(C)C=2N=C1C(C(=NC=1C(C)C)NC)=CC=1C1CC1 FPVHEVAEGCYSLO-QGZVFWFLSA-N 0.000 claims 1
- XXTLMISVKFCECJ-KRWDZBQOSA-N 5-ethyl-3-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound N1=C(C(C)C)C(CC)=CC(C=2C(=CC=3N([C@@H](C)COC)C=C(C)C=3N=2)C)=C1NC XXTLMISVKFCECJ-KRWDZBQOSA-N 0.000 claims 1
- MAKHVWYFAUKTHA-QGZVFWFLSA-N 5-ethyl-3-[6-ethyl-1-[(2r)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-n-methyl-6-propan-2-ylpyridin-2-amine Chemical compound N1=C(C(C)C)C(CC)=CC(C=2C(=CC=3N([C@H](C)COC)C=C(C)C=3N=2)CC)=C1NC MAKHVWYFAUKTHA-QGZVFWFLSA-N 0.000 claims 1
- SSCSHVKGXVCWTF-UHFFFAOYSA-N 5-ethyl-6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1-methyl-3-propan-2-ylpyrrolo[2,3-b]pyridine Chemical compound CCC1=CC=2C(C(C)C)=CN(C)C=2N=C1C1=CC=C(C(C)C)N=C1OC SSCSHVKGXVCWTF-UHFFFAOYSA-N 0.000 claims 1
- CUHUVVKJCWITNC-UHFFFAOYSA-N 6-(2-ethyl-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazin-3-yl)-5-methoxy-3-propan-2-yl-2,3-dihydrofuro[3,2-b]pyridine Chemical compound CCC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C(C(=N1)OC)=CC2=C1C(C(C)C)CO2 CUHUVVKJCWITNC-UHFFFAOYSA-N 0.000 claims 1
- JIJWBWVQXZWPPV-UHFFFAOYSA-N 6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-1,5-dimethyl-3-propan-2-ylpyrrolo[2,3-b]pyridine Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1C(C(C)C)=CN2C JIJWBWVQXZWPPV-UHFFFAOYSA-N 0.000 claims 1
- DCAFQRHBYKTYEE-UHFFFAOYSA-N 6-(3,6-dimethyl-1-pentan-3-ylpyrrolo[3,2-b]pyridin-5-yl)-2,5-diethyl-3-propan-2-ylimidazo[4,5-b]pyridine Chemical compound CC=1C=C2N(C(CC)CC)C=C(C)C2=NC=1C(C(=N1)CC)=CC2=C1N(C(C)C)C(CC)=N2 DCAFQRHBYKTYEE-UHFFFAOYSA-N 0.000 claims 1
- GFZCWLDGWODXFJ-UHFFFAOYSA-N 6-(3-chloro-7-methyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-5-methoxy-3-propan-2-yl-2,3-dihydrofuro[3,2-b]pyridine Chemical compound ClC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C(C(=N1)OC)=CC2=C1C(C(C)C)CO2 GFZCWLDGWODXFJ-UHFFFAOYSA-N 0.000 claims 1
- RGTFTAHVHBEEIB-UHFFFAOYSA-N 6-(3-chloro-7-methyl-5-pentan-3-ylpyrrolo[2,3-b]pyrazin-2-yl)-5-methoxy-3-propan-2-ylfuro[3,2-b]pyridine Chemical compound ClC=1N=C2N(C(CC)CC)C=C(C)C2=NC=1C(C(=N1)OC)=CC2=C1C(C(C)C)=CO2 RGTFTAHVHBEEIB-UHFFFAOYSA-N 0.000 claims 1
- DDOAQOPGSIIJHR-HNNXBMFYSA-N 6-bromo-1-[(2s)-1-methoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridine Chemical compound BrC=1C=C2N([C@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC DDOAQOPGSIIJHR-HNNXBMFYSA-N 0.000 claims 1
- YLKDIGYWXHIZNY-YNNZGITBSA-N 6-chloro-1-[(1R)-1-fluoro-2-methoxypropyl]-3-methyl-5-(2-methyl-6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound ClC=1C=C2C(=NC1C=1C(=NC(=CC1)C(C)C)C)C(=CN2[C@@H](C(OC)C)F)C YLKDIGYWXHIZNY-YNNZGITBSA-N 0.000 claims 1
- QCVAGDDOEHAQJH-AWEZNQCLSA-N 6-chloro-1-[(2s)-1-methoxypropan-2-yl]-3-methyl-5-(6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound ClC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1 QCVAGDDOEHAQJH-AWEZNQCLSA-N 0.000 claims 1
- ZHLPYNGPPHBMPD-HNNXBMFYSA-N 6-chloro-5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC1=NC(C(C)C)=CC=C1C(C(=C1)Cl)=NC2=C1N([C@@H](CF)COC)C=C2C ZHLPYNGPPHBMPD-HNNXBMFYSA-N 0.000 claims 1
- ZLYITIUZCKESAL-KRWDZBQOSA-N 6-ethyl-1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC1=CC=2N([C@@H](CF)COC)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1OC ZLYITIUZCKESAL-KRWDZBQOSA-N 0.000 claims 1
- GEXGMAHPJDMLJI-MRXNPFEDSA-N 6-ethyl-1-[(2r)-1-fluoropropan-2-yl]-5-(2-methoxy-4-propan-2-ylphenyl)-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC1=CC=2N([C@H](C)CF)C=C(C)C=2N=C1C1=CC=C(C(C)C)C=C1OC GEXGMAHPJDMLJI-MRXNPFEDSA-N 0.000 claims 1
- DVUPIDFYTZIBRD-GOSISDBHSA-N 6-ethyl-1-[(2r)-1-methoxybutan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC DVUPIDFYTZIBRD-GOSISDBHSA-N 0.000 claims 1
- AGKNKHOVXYLXGD-QGZVFWFLSA-N 6-ethyl-1-[(2r)-1-methoxypropan-2-yl]-5-(2-methoxy-4-propan-2-ylphenyl)-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC1=CC=2N([C@H](C)COC)C=C(C)C=2N=C1C1=CC=C(C(C)C)C=C1OC AGKNKHOVXYLXGD-QGZVFWFLSA-N 0.000 claims 1
- DSZGLCUJROBHCD-INIZCTEOSA-N 6-ethyl-1-[(2s)-1-methoxypropan-2-yl]-3-methyl-5-(6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound CCC1=CC=2N([C@@H](C)COC)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1 DSZGLCUJROBHCD-INIZCTEOSA-N 0.000 claims 1
- PTDQNSILPABWCA-HNNXBMFYSA-N 6-ethyl-2-methoxy-5-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n-methylpyridine-3-carboxamide Chemical compound CCC1=NC(OC)=C(C(=O)NC)C=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C PTDQNSILPABWCA-HNNXBMFYSA-N 0.000 claims 1
- CQVPITRLKKHHQI-INIZCTEOSA-N 6-ethyl-5-(2-ethyl-6-methoxypyridin-3-yl)-1-[(2r)-1-fluoro-3-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC1=CC=2N([C@@H](CF)COC)C=C(C)C=2N=C1C1=CC=C(OC)N=C1CC CQVPITRLKKHHQI-INIZCTEOSA-N 0.000 claims 1
- MBFNADMNENQLKP-LJQANCHMSA-N 6-ethyl-5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-1-[(2r)-1-methoxybutan-2-yl]-3-methylpyrrolo[3,2-b]pyridine Chemical compound CCC=1C=C2N([C@@H](COC)CC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1CC MBFNADMNENQLKP-LJQANCHMSA-N 0.000 claims 1
- RAVROSITPQJDOR-UHFFFAOYSA-N 6-ethyl-5-(2-ethyl-6-propan-2-ylpyridin-3-yl)-3-methyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound CCC1=CC=2N(C(C)C)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1CC RAVROSITPQJDOR-UHFFFAOYSA-N 0.000 claims 1
- JDIHANWLCRAFSD-UHFFFAOYSA-N 6-ethyl-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3-methyl-1-propan-2-ylpyrrolo[3,2-b]pyridine Chemical compound CCC1=CC=2N(C(C)C)C=C(C)C=2N=C1C1=CC=C(C(C)C)N=C1OC JDIHANWLCRAFSD-UHFFFAOYSA-N 0.000 claims 1
- DOONOYDSPGMBNN-INIZCTEOSA-N 6-ethyl-5-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-n,n-dimethylpyridin-2-amine Chemical compound CCC1=NC(N(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C DOONOYDSPGMBNN-INIZCTEOSA-N 0.000 claims 1
- CMVFHSXRPSQLGG-GOSISDBHSA-N 6-ethyl-7-[1-[(2r)-1-hydroxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-2-methyl-4-propan-2-ylpyrido[2,3-b]pyrazin-3-one Chemical compound N1=C(C)C(=O)N(C(C)C)C(N=C2CC)=C1C=C2C1=C(C)C=C2N([C@@H](CO)CC)C=C(C)C2=N1 CMVFHSXRPSQLGG-GOSISDBHSA-N 0.000 claims 1
- SOLHJJQRCDOQNG-HXUWFJFHSA-N 6-ethyl-7-[1-[(2r)-1-methoxybutan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-2,4-di(propan-2-yl)pyrido[2,3-b]pyrazin-3-one Chemical compound N1=C(C(C)C)C(=O)N(C(C)C)C(N=C2CC)=C1C=C2C1=C(C)C=C2N([C@@H](COC)CC)C=C(C)C2=N1 SOLHJJQRCDOQNG-HXUWFJFHSA-N 0.000 claims 1
- REYCHCAIKSTEGD-KRWDZBQOSA-N 6-ethyl-7-[6-ethyl-1-[(2s)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-2-methyl-4-propan-2-ylpyrido[2,3-b]pyrazin-3-one Chemical compound N1=C(C)C(=O)N(C(C)C)C(N=C2CC)=C1C=C2C1=NC(C(C)=CN2[C@@H](C)COC)=C2C=C1CC REYCHCAIKSTEGD-KRWDZBQOSA-N 0.000 claims 1
- HSKQEQVONJGCCS-HNNXBMFYSA-N 6-methoxy-1-[(2s)-1-methoxypropan-2-yl]-3-methyl-5-(6-propan-2-ylpyridin-3-yl)pyrrolo[3,2-b]pyridine Chemical compound COC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1 HSKQEQVONJGCCS-HNNXBMFYSA-N 0.000 claims 1
- PGUKSOHJZKJMJY-UHFFFAOYSA-N 7-(1-methoxybutan-2-yl)-3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-2,5-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2C(C(COC)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC PGUKSOHJZKJMJY-UHFFFAOYSA-N 0.000 claims 1
- SVUGPJQVHUKYGA-UHFFFAOYSA-N 7-(1-methoxypropan-2-yl)-3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-2,5-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2C(C(C)COC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC SVUGPJQVHUKYGA-UHFFFAOYSA-N 0.000 claims 1
- ZGEWRFAULOTQNL-UHFFFAOYSA-N 7-(1-methoxypropan-2-yl)-3-[2-methoxy-4-(trifluoromethoxy)phenyl]-2,5-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2C(C(C)COC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC ZGEWRFAULOTQNL-UHFFFAOYSA-N 0.000 claims 1
- JVQFFISKMLCKND-UHFFFAOYSA-N 7-butan-2-yl-3-(2-methoxy-6-propan-2-ylpyridin-3-yl)-2,5-dimethylpyrrolo[2,3-b]pyrazine Chemical compound CC=1N=C2C(C(C)CC)=CN(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC JVQFFISKMLCKND-UHFFFAOYSA-N 0.000 claims 1
- WSNJCLABWDSADF-FQEVSTJZSA-N [(2s)-2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl] 4-acetylpiperazine-1-carboxylate Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)OC(=O)N1CCN(C(C)=O)CC1 WSNJCLABWDSADF-FQEVSTJZSA-N 0.000 claims 1
- RIQQKDPUSITTFF-IBGZPJMESA-N [(2s)-2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl] 4-methylpiperazine-1-carboxylate Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)OC(=O)N1CCN(C)CC1 RIQQKDPUSITTFF-IBGZPJMESA-N 0.000 claims 1
- KKQUFGJPRBYYCN-FQEVSTJZSA-N [(2s)-2-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]butyl] azepane-1-carboxylate Chemical compound C([C@H](CC)N1C2=CC(C)=C(N=C2C(C)=C1)C=1C(=CC(OC(F)(F)F)=CC=1)OC)OC(=O)N1CCCCCC1 KKQUFGJPRBYYCN-FQEVSTJZSA-N 0.000 claims 1
- KVVOGBABZORBND-IZLXSDGUSA-N benzyl (3s,4r)-3-(2-fluoroethoxy)-4-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]pyrrolidine-1-carboxylate Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H]1[C@H](CN(C1)C(=O)OCC=1C=CC=CC=1)OCCF)C=C2C KVVOGBABZORBND-IZLXSDGUSA-N 0.000 claims 1
- VYNSMJZUJLTAEU-VPUSJEBWSA-N benzyl (3s,4r)-3-(2-fluoroethoxy)-4-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]pyrrolidine-1-carboxylate Chemical compound COC1=CC(OC(F)(F)F)=CC=C1C(C(=C1)C)=NC2=C1N([C@H]1[C@H](CN(C1)C(=O)OCC=1C=CC=CC=1)OCCF)C=C2C VYNSMJZUJLTAEU-VPUSJEBWSA-N 0.000 claims 1
- 229940043232 butyl acetate Drugs 0.000 claims 1
- VKEOLSRHORITAD-UHFFFAOYSA-N ethyl 2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]acetate Chemical compound CC=1C=C2N(CC(=O)OCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC VKEOLSRHORITAD-UHFFFAOYSA-N 0.000 claims 1
- KPOJIIQQDBDCJC-UHFFFAOYSA-N ethyl 2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]propanoate Chemical compound CC=1C=C2N(C(C)C(=O)OCC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC KPOJIIQQDBDCJC-UHFFFAOYSA-N 0.000 claims 1
- 238000011990 functional testing Methods 0.000 claims 1
- 125000005394 methallyl group Chemical group 0.000 claims 1
- XIKDEXWRZLRDKE-CTNGQTDRSA-N methyl (3s,4r)-3-(2-fluoroethoxy)-4-[5-[2-methoxy-4-(trifluoromethoxy)phenyl]-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]pyrrolidine-1-carboxylate Chemical compound C1N(C(=O)OC)C[C@H](OCCF)[C@@H]1N1C2=CC(C)=C(C=3C(=CC(OC(F)(F)F)=CC=3)OC)N=C2C(C)=C1 XIKDEXWRZLRDKE-CTNGQTDRSA-N 0.000 claims 1
- FNKYEEIFHZMGIB-UHFFFAOYSA-N methyl 2-[3-[2-methoxy-4-(trifluoromethoxy)phenyl]-2,5-dimethylpyrrolo[2,3-b]pyrazin-7-yl]propanoate Chemical compound CC=1N=C2C(C(C)C(=O)OC)=CN(C)C2=NC=1C1=CC=C(OC(F)(F)F)C=C1OC FNKYEEIFHZMGIB-UHFFFAOYSA-N 0.000 claims 1
- MOMXNWDPJYRTQC-UHFFFAOYSA-N n,4-diethyl-5-(2-ethyl-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazin-3-yl)-n-methylpyridin-2-amine Chemical compound CCC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CN=C(N(C)CC)C=C1CC MOMXNWDPJYRTQC-UHFFFAOYSA-N 0.000 claims 1
- XOUYACVJAKAKOE-UHFFFAOYSA-N n,n,4-triethyl-5-(2-ethyl-5-methyl-7-pentan-3-ylpyrrolo[2,3-b]pyrazin-3-yl)pyridin-2-amine Chemical compound CCC=1N=C2C(C(CC)CC)=CN(C)C2=NC=1C1=CN=C(N(CC)CC)C=C1CC XOUYACVJAKAKOE-UHFFFAOYSA-N 0.000 claims 1
- VRRBIKYSOLXFRE-UHFFFAOYSA-N n-(2-methoxyethyl)-3-[1-(1-methoxypropan-2-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-6-propan-2-ylpyridin-2-amine Chemical compound COCCNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)COC)C=C2C VRRBIKYSOLXFRE-UHFFFAOYSA-N 0.000 claims 1
- WMTDJOKBWYIVFH-KRWDZBQOSA-N n-cyclopropyl-3-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-6-propan-2-ylpyridin-2-amine Chemical compound CC=1C=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1NC1CC1 WMTDJOKBWYIVFH-KRWDZBQOSA-N 0.000 claims 1
- XKBQGXCZCPXXAU-KRWDZBQOSA-N n-ethyl-3-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-6-propan-2-ylpyridin-2-amine Chemical compound CCNC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@@H](C)COC)C=C2C XKBQGXCZCPXXAU-KRWDZBQOSA-N 0.000 claims 1
- VROHHNKNINEJKL-QGZVFWFLSA-N n-ethyl-3-[5-[(2r)-1-methoxybutan-2-yl]-3,7-dimethylpyrrolo[2,3-b]pyrazin-2-yl]-6-propan-2-ylpyridin-2-amine Chemical compound CCNC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1N([C@H](CC)COC)C=C2C VROHHNKNINEJKL-QGZVFWFLSA-N 0.000 claims 1
- GCSMZSULZUXJCN-INIZCTEOSA-N n-ethyl-3-[6-methoxy-1-[(2s)-1-methoxypropan-2-yl]-3-methylpyrrolo[3,2-b]pyridin-5-yl]-6-propan-2-ylpyridin-2-amine Chemical compound CCNC1=NC(C(C)C)=CC=C1C(C(=C1)OC)=NC2=C1N([C@@H](C)COC)C=C2C GCSMZSULZUXJCN-INIZCTEOSA-N 0.000 claims 1
- 125000004944 pyrazin-3-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 1
- RTEAKYUCTSARHM-UHFFFAOYSA-N tert-butyl 2-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]propanoate Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N(C(C)C(=O)OC(C)(C)C)C=C2C RTEAKYUCTSARHM-UHFFFAOYSA-N 0.000 claims 1
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 abstract description 10
- 239000000523 sample Substances 0.000 abstract description 10
- 102000005962 receptors Human genes 0.000 abstract description 9
- 108020003175 receptors Proteins 0.000 abstract description 9
- 230000036506 anxiety Effects 0.000 abstract description 7
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 abstract description 5
- 230000004807 localization Effects 0.000 abstract description 5
- 230000002093 peripheral effect Effects 0.000 abstract description 2
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 246
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 170
- 230000008569 process Effects 0.000 description 137
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 120
- 229910001868 water Inorganic materials 0.000 description 116
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 113
- 235000019439 ethyl acetate Nutrition 0.000 description 106
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 94
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 79
- 239000000741 silica gel Substances 0.000 description 76
- 229910002027 silica gel Inorganic materials 0.000 description 76
- 238000000746 purification Methods 0.000 description 74
- 239000011541 reaction mixture Substances 0.000 description 70
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 66
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 63
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 54
- 239000012267 brine Substances 0.000 description 46
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 46
- 108010022152 Corticotropin-Releasing Hormone Proteins 0.000 description 39
- 239000000055 Corticotropin-Releasing Hormone Substances 0.000 description 39
- 102000012289 Corticotropin-Releasing Hormone Human genes 0.000 description 39
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 39
- 238000003786 synthesis reaction Methods 0.000 description 38
- 230000015572 biosynthetic process Effects 0.000 description 37
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 34
- 239000011734 sodium Substances 0.000 description 34
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 33
- 235000019341 magnesium sulphate Nutrition 0.000 description 33
- 238000003756 stirring Methods 0.000 description 33
- 239000012044 organic layer Substances 0.000 description 32
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 31
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 28
- 230000002829 reductive effect Effects 0.000 description 27
- 239000002904 solvent Substances 0.000 description 26
- 239000000047 product Substances 0.000 description 25
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 24
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 22
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 21
- 238000007872 degassing Methods 0.000 description 21
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 18
- 239000000284 extract Substances 0.000 description 18
- 238000003818 flash chromatography Methods 0.000 description 18
- 229910052938 sodium sulfate Inorganic materials 0.000 description 18
- 235000011152 sodium sulphate Nutrition 0.000 description 18
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 17
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 16
- 239000003921 oil Substances 0.000 description 16
- 235000019198 oils Nutrition 0.000 description 16
- 125000004791 2-fluoroethoxy group Chemical group FCCO* 0.000 description 15
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 239000012043 crude product Substances 0.000 description 14
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 14
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 14
- 229910000029 sodium carbonate Inorganic materials 0.000 description 14
- 235000017550 sodium carbonate Nutrition 0.000 description 14
- 238000001035 drying Methods 0.000 description 13
- 239000011159 matrix material Substances 0.000 description 13
- 229910000104 sodium hydride Inorganic materials 0.000 description 13
- 239000007787 solid Substances 0.000 description 13
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 238000001704 evaporation Methods 0.000 description 12
- 230000008020 evaporation Effects 0.000 description 12
- 239000007858 starting material Substances 0.000 description 12
- 239000000725 suspension Substances 0.000 description 12
- 239000010410 layer Substances 0.000 description 11
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 11
- 238000005160 1H NMR spectroscopy Methods 0.000 description 10
- 231100000252 nontoxic Toxicity 0.000 description 10
- 230000003000 nontoxic effect Effects 0.000 description 10
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 9
- 239000004480 active ingredient Substances 0.000 description 9
- 150000001412 amines Chemical class 0.000 description 9
- 230000008878 coupling Effects 0.000 description 9
- 238000010168 coupling process Methods 0.000 description 9
- 238000005859 coupling reaction Methods 0.000 description 9
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 9
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 239000013058 crude material Substances 0.000 description 8
- 239000003814 drug Substances 0.000 description 8
- 238000000605 extraction Methods 0.000 description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- 239000000546 pharmaceutical excipient Substances 0.000 description 8
- 210000001519 tissue Anatomy 0.000 description 8
- WJKHJLXJJJATHN-UHFFFAOYSA-N triflic anhydride Chemical compound FC(F)(F)S(=O)(=O)OS(=O)(=O)C(F)(F)F WJKHJLXJJJATHN-UHFFFAOYSA-N 0.000 description 8
- BHELZAPQIKSEDF-UHFFFAOYSA-N allyl bromide Chemical compound BrCC=C BHELZAPQIKSEDF-UHFFFAOYSA-N 0.000 description 7
- 229940079593 drug Drugs 0.000 description 7
- 239000012299 nitrogen atmosphere Substances 0.000 description 7
- 229910000027 potassium carbonate Inorganic materials 0.000 description 7
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- MUALRAIOVNYAIW-UHFFFAOYSA-N binap Chemical compound C1=CC=CC=C1P(C=1C(=C2C=CC=CC2=CC=1)C=1C2=CC=CC=C2C=CC=1P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 MUALRAIOVNYAIW-UHFFFAOYSA-N 0.000 description 6
- 239000000796 flavoring agent Substances 0.000 description 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 6
- 230000004044 response Effects 0.000 description 6
- 239000003765 sweetening agent Substances 0.000 description 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 5
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 5
- AJCQJELUJDPGEY-UHFFFAOYSA-N [2-methoxy-4-(trifluoromethoxy)phenyl]boronic acid Chemical compound COC1=CC(OC(F)(F)F)=CC=C1B(O)O AJCQJELUJDPGEY-UHFFFAOYSA-N 0.000 description 5
- 229960000583 acetic acid Drugs 0.000 description 5
- 235000011054 acetic acid Nutrition 0.000 description 5
- 229940049706 benzodiazepine Drugs 0.000 description 5
- 239000007859 condensation product Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 235000003599 food sweetener Nutrition 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000004128 high performance liquid chromatography Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000001404 mediated effect Effects 0.000 description 5
- LVWZTYCIRDMTEY-UHFFFAOYSA-N metamizole Chemical compound O=C1C(N(CS(O)(=O)=O)C)=C(C)N(C)N1C1=CC=CC=C1 LVWZTYCIRDMTEY-UHFFFAOYSA-N 0.000 description 5
- 239000006199 nebulizer Substances 0.000 description 5
- 229910052763 palladium Inorganic materials 0.000 description 5
- 238000012746 preparative thin layer chromatography Methods 0.000 description 5
- 239000003755 preservative agent Substances 0.000 description 5
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 5
- 208000024891 symptom Diseases 0.000 description 5
- 239000003643 water by type Substances 0.000 description 5
- VUIJGYPRRJGNPI-UHFFFAOYSA-N (2-methoxy-6-propan-2-ylpyridin-3-yl)boronic acid Chemical compound COC1=NC(C(C)C)=CC=C1B(O)O VUIJGYPRRJGNPI-UHFFFAOYSA-N 0.000 description 4
- PPYRIPJLBOJUNH-UHFFFAOYSA-N 2-methoxy-6-propan-2-ylpyridine Chemical compound COC1=CC=CC(C(C)C)=N1 PPYRIPJLBOJUNH-UHFFFAOYSA-N 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 4
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- 206010020751 Hypersensitivity Diseases 0.000 description 4
- 208000019022 Mood disease Diseases 0.000 description 4
- 101150003085 Pdcl gene Proteins 0.000 description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
- 230000000949 anxiolytic effect Effects 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 230000003542 behavioural effect Effects 0.000 description 4
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 4
- 210000004556 brain Anatomy 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 239000012230 colorless oil Substances 0.000 description 4
- 238000004440 column chromatography Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000002769 corticotropin releasing factor antagonist Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 235000013355 food flavoring agent Nutrition 0.000 description 4
- 235000019253 formic acid Nutrition 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000005457 ice water Substances 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 4
- 125000004430 oxygen atom Chemical group O* 0.000 description 4
- 230000036961 partial effect Effects 0.000 description 4
- 230000019491 signal transduction Effects 0.000 description 4
- 239000012312 sodium hydride Substances 0.000 description 4
- 239000000375 suspending agent Substances 0.000 description 4
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 4
- 238000004809 thin layer chromatography Methods 0.000 description 4
- 239000000080 wetting agent Substances 0.000 description 4
- NXMXETCTWNXSFG-BYPYZUCNSA-N (2s)-1-methoxypropan-2-amine Chemical compound COC[C@H](C)N NXMXETCTWNXSFG-BYPYZUCNSA-N 0.000 description 3
- KZPYGQFFRCFCPP-UHFFFAOYSA-N 1,1'-bis(diphenylphosphino)ferrocene Chemical compound [Fe+2].C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=C[C-]1P(C=1C=CC=CC=1)C1=CC=CC=C1 KZPYGQFFRCFCPP-UHFFFAOYSA-N 0.000 description 3
- SVUOLADPCWQTTE-UHFFFAOYSA-N 1h-1,2-benzodiazepine Chemical compound N1N=CC=CC2=CC=CC=C12 SVUOLADPCWQTTE-UHFFFAOYSA-N 0.000 description 3
- XWIYUCRMWCHYJR-UHFFFAOYSA-N 1h-pyrrolo[3,2-b]pyridine Chemical compound C1=CC=C2NC=CC2=N1 XWIYUCRMWCHYJR-UHFFFAOYSA-N 0.000 description 3
- LIMXEVCFAUTBCK-UHFFFAOYSA-N 2,5-dibromo-3-methylpyridine Chemical compound CC1=CC(Br)=CN=C1Br LIMXEVCFAUTBCK-UHFFFAOYSA-N 0.000 description 3
- GTBBOAUCPFNIBQ-UHFFFAOYSA-N 5-bromo-6-ethyl-2-n-propan-2-ylpyridine-2,3-diamine Chemical compound CCC1=NC(NC(C)C)=C(N)C=C1Br GTBBOAUCPFNIBQ-UHFFFAOYSA-N 0.000 description 3
- 244000215068 Acacia senegal Species 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 241000283690 Bos taurus Species 0.000 description 3
- 102100038018 Corticotropin-releasing factor receptor 1 Human genes 0.000 description 3
- 206010013883 Dwarfism Diseases 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229920000084 Gum arabic Polymers 0.000 description 3
- 241000282412 Homo Species 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 206010037660 Pyrexia Diseases 0.000 description 3
- 241000700159 Rattus Species 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
- 241000282887 Suidae Species 0.000 description 3
- LJJGMQKIIMYIGL-UHFFFAOYSA-N [6-(diethylamino)-4-ethylpyridin-3-yl]boronic acid Chemical compound CCN(CC)C1=CC(CC)=C(B(O)O)C=N1 LJJGMQKIIMYIGL-UHFFFAOYSA-N 0.000 description 3
- 235000010489 acacia gum Nutrition 0.000 description 3
- 239000000205 acacia gum Substances 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 208000026935 allergic disease Diseases 0.000 description 3
- 239000005557 antagonist Substances 0.000 description 3
- 239000002249 anxiolytic agent Substances 0.000 description 3
- 229940005530 anxiolytics Drugs 0.000 description 3
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 238000000211 autoradiogram Methods 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 125000002619 bicyclic group Chemical group 0.000 description 3
- 210000003169 central nervous system Anatomy 0.000 description 3
- 208000015114 central nervous system disease Diseases 0.000 description 3
- 210000001175 cerebrospinal fluid Anatomy 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000112 colonic effect Effects 0.000 description 3
- 235000008504 concentrate Nutrition 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000013068 control sample Substances 0.000 description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 230000002526 effect on cardiovascular system Effects 0.000 description 3
- 230000009610 hypersensitivity Effects 0.000 description 3
- 125000002883 imidazolyl group Chemical group 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 229940057995 liquid paraffin Drugs 0.000 description 3
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 238000012544 monitoring process Methods 0.000 description 3
- 125000002950 monocyclic group Chemical group 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- 150000002828 nitro derivatives Chemical class 0.000 description 3
- 239000004006 olive oil Substances 0.000 description 3
- 235000008390 olive oil Nutrition 0.000 description 3
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 3
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 3
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 3
- 108090000765 processed proteins & peptides Proteins 0.000 description 3
- 239000000651 prodrug Substances 0.000 description 3
- 229940002612 prodrug Drugs 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical compound CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 description 3
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 description 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- MAOKCLBYGZDJNX-UHFFFAOYSA-N (2-ethyl-6-methoxypyridin-3-yl)boronic acid Chemical compound CCC1=NC(OC)=CC=C1B(O)O MAOKCLBYGZDJNX-UHFFFAOYSA-N 0.000 description 2
- QDJPBFLSWVIGQY-UHFFFAOYSA-N (6-methoxy-2-propan-2-ylpyridin-3-yl)boronic acid Chemical compound COC1=CC=C(B(O)O)C(C(C)C)=N1 QDJPBFLSWVIGQY-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- YPDUJFLUTSACKH-UHFFFAOYSA-N 2,5-dibromo-6-ethyl-3-nitropyridine Chemical compound CCC1=NC(Br)=C([N+]([O-])=O)C=C1Br YPDUJFLUTSACKH-UHFFFAOYSA-N 0.000 description 2
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 description 2
- QDKQXFSDXRWWPB-LBPRGKRZSA-N 2-bromo-n-[(2s)-1-methoxypropan-2-yl]-6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-4,5-dimethylpyridin-3-amine Chemical compound CC1=C(C)C(N[C@@H](C)COC)=C(Br)N=C1C1=CC=C(C(C)C)N=C1OC QDKQXFSDXRWWPB-LBPRGKRZSA-N 0.000 description 2
- OQXPRNLEKVAZDJ-NSHDSACASA-N 2-bromo-n-[(2s)-1-methoxypropan-2-yl]-6-[2-methoxy-4-(trifluoromethoxy)phenyl]-5-methylpyridin-3-amine Chemical compound N1=C(Br)C(N[C@@H](C)COC)=CC(C)=C1C1=CC=C(OC(F)(F)F)C=C1OC OQXPRNLEKVAZDJ-NSHDSACASA-N 0.000 description 2
- VAVGOGHLNAJECD-UHFFFAOYSA-N 2-chloro-6-methoxypyridine Chemical compound COC1=CC=CC(Cl)=N1 VAVGOGHLNAJECD-UHFFFAOYSA-N 0.000 description 2
- GWNRUHJEFSOGHL-UHFFFAOYSA-N 2-ethoxy-6-ethyl-5-methylsulfonyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine Chemical compound CCOC1=NC(CC)=C(S(C)(=O)=O)C=C1B1OC(C)(C)C(C)(C)O1 GWNRUHJEFSOGHL-UHFFFAOYSA-N 0.000 description 2
- IZLTZVZEBJLVDP-ZDUSSCGKSA-N 2-ethynyl-n-[(2s)-1-methoxypropan-2-yl]-6-[2-methoxy-4-(trifluoromethoxy)phenyl]-5-methylpyridin-3-amine Chemical compound N1=C(C#C)C(N[C@@H](C)COC)=CC(C)=C1C1=CC=C(OC(F)(F)F)C=C1OC IZLTZVZEBJLVDP-ZDUSSCGKSA-N 0.000 description 2
- IZHVBANLECCAGF-UHFFFAOYSA-N 2-hydroxy-3-(octadecanoyloxy)propyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)COC(=O)CCCCCCCCCCCCCCCCC IZHVBANLECCAGF-UHFFFAOYSA-N 0.000 description 2
- NGSQLXNYUUMEIO-UHFFFAOYSA-N 3,5-dibromo-6-ethylpyridin-2-amine Chemical compound CCC1=NC(N)=C(Br)C=C1Br NGSQLXNYUUMEIO-UHFFFAOYSA-N 0.000 description 2
- RZIMNBKYMABSRW-UHFFFAOYSA-N 3-(3,7-dimethyl-5-propan-2-ylpyrrolo[2,3-b]pyrazin-2-yl)-6-propan-2-yl-1h-pyridin-2-one Chemical compound OC1=NC(C(C)C)=CC=C1C(C(=N1)C)=NC2=C1N(C(C)C)C=C2C RZIMNBKYMABSRW-UHFFFAOYSA-N 0.000 description 2
- CUYKNJBYIJFRCU-UHFFFAOYSA-N 3-aminopyridine Chemical compound NC1=CC=CN=C1 CUYKNJBYIJFRCU-UHFFFAOYSA-N 0.000 description 2
- BURZJDSIJOMHQC-JTQLQIEISA-N 3-bromo-6-chloro-n-[(2s)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)pyrazin-2-amine Chemical compound N1=C(Br)C(N[C@@H](C)COC)=NC(Cl)=C1C1=CC=C(C(C)C)N=C1OC BURZJDSIJOMHQC-JTQLQIEISA-N 0.000 description 2
- ROEPGHWJSYWGMZ-UHFFFAOYSA-N 3-bromo-6-ethyl-5-methylsulfonyl-1h-pyridin-2-one Chemical compound CCC1=NC(O)=C(Br)C=C1S(C)(=O)=O ROEPGHWJSYWGMZ-UHFFFAOYSA-N 0.000 description 2
- JOPJZYVHFBMFQU-UHFFFAOYSA-N 3-bromo-6-ethyl-5-methylsulfonylpyridin-2-amine Chemical compound CCC1=NC(N)=C(Br)C=C1S(C)(=O)=O JOPJZYVHFBMFQU-UHFFFAOYSA-N 0.000 description 2
- VTOQFOCYBTVOJZ-UHFFFAOYSA-N 3-bromopentane Chemical compound CCC(Br)CC VTOQFOCYBTVOJZ-UHFFFAOYSA-N 0.000 description 2
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 2
- AGVPSBDCZREIHN-UHFFFAOYSA-N 4-methoxy-n,n-dimethylpyridin-2-amine Chemical compound COC1=CC=NC(N(C)C)=C1 AGVPSBDCZREIHN-UHFFFAOYSA-N 0.000 description 2
- AYTPPZQSGUONRB-UHFFFAOYSA-N 5-bromo-2-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,4-dimethylpyridine Chemical compound COC1=NC(C(C)C)=CC=C1C1=NC=C(Br)C(C)=C1C AYTPPZQSGUONRB-UHFFFAOYSA-N 0.000 description 2
- PUKHGPXUBABAME-UHFFFAOYSA-N 5-bromo-2-[2-methoxy-4-(trifluoromethoxy)phenyl]-3-methylpyridine Chemical compound COC1=CC(OC(F)(F)F)=CC=C1C1=NC=C(Br)C=C1C PUKHGPXUBABAME-UHFFFAOYSA-N 0.000 description 2
- PTIDDSJVNIIEGL-UHFFFAOYSA-N 5-bromo-3,4-dimethyl-1h-pyridin-2-one Chemical compound CC1=C(C)C(O)=NC=C1Br PTIDDSJVNIIEGL-UHFFFAOYSA-N 0.000 description 2
- VBSODHLOGQXSIQ-YFKPBYRVSA-N 5-bromo-6-chloro-n-[(2s)-1-methoxypropan-2-yl]pyrazin-2-amine Chemical compound COC[C@H](C)NC1=CN=C(Br)C(Cl)=N1 VBSODHLOGQXSIQ-YFKPBYRVSA-N 0.000 description 2
- FBMFJZQNQGJFQB-UHFFFAOYSA-N 5-bromo-6-ethyl-3-nitro-n-propan-2-ylpyridin-2-amine Chemical compound CCC1=NC(NC(C)C)=C([N+]([O-])=O)C=C1Br FBMFJZQNQGJFQB-UHFFFAOYSA-N 0.000 description 2
- VWPDZMUQRAGOQK-UHFFFAOYSA-N 5-bromo-6-ethyl-3-nitropyridin-2-amine Chemical compound CCC1=NC(N)=C([N+]([O-])=O)C=C1Br VWPDZMUQRAGOQK-UHFFFAOYSA-N 0.000 description 2
- SYFQQSLPNGTEMV-UHFFFAOYSA-N 5-bromo-6-ethylpyridin-2-amine Chemical compound CCC1=NC(N)=CC=C1Br SYFQQSLPNGTEMV-UHFFFAOYSA-N 0.000 description 2
- RVYFYXRSRAJYAO-UHFFFAOYSA-N 5-ethyl-3-propan-2-yl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[4,5-b]pyridine Chemical compound CCC1=NC=2N(C(C)C)C=NC=2C=C1B1OC(C)(C)C(C)(C)O1 RVYFYXRSRAJYAO-UHFFFAOYSA-N 0.000 description 2
- JRMKAUZPIFQOAY-UHFFFAOYSA-N 6-bromo-5-ethyl-3-propan-2-ylimidazo[4,5-b]pyridine Chemical compound C1=C(Br)C(CC)=NC2=C1N=CN2C(C)C JRMKAUZPIFQOAY-UHFFFAOYSA-N 0.000 description 2
- MPVOWXAENXHCAP-NSHDSACASA-N 6-chloro-n-[(2s)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)pyrazin-2-amine Chemical compound ClC1=NC(N[C@@H](C)COC)=CN=C1C1=CC=C(C(C)C)N=C1OC MPVOWXAENXHCAP-NSHDSACASA-N 0.000 description 2
- HGXXSKFMSMTAJE-LURJTMIESA-N 6-chloro-n-[(2s)-1-methoxypropan-2-yl]pyrazin-2-amine Chemical compound COC[C@H](C)NC1=CN=CC(Cl)=N1 HGXXSKFMSMTAJE-LURJTMIESA-N 0.000 description 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- 239000000275 Adrenocorticotropic Hormone Substances 0.000 description 2
- 208000017194 Affective disease Diseases 0.000 description 2
- 208000024827 Alzheimer disease Diseases 0.000 description 2
- 241000272517 Anseriformes Species 0.000 description 2
- 235000003911 Arachis Nutrition 0.000 description 2
- 244000105624 Arachis hypogaea Species 0.000 description 2
- 241000416162 Astragalus gummifer Species 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- 102000004506 Blood Proteins Human genes 0.000 description 2
- 108010017384 Blood Proteins Proteins 0.000 description 2
- 108091005470 CRHR2 Proteins 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 206010007559 Cardiac failure congestive Diseases 0.000 description 2
- 102400000739 Corticotropin Human genes 0.000 description 2
- 101800000414 Corticotropin Proteins 0.000 description 2
- 229940122010 Corticotropin releasing factor antagonist Drugs 0.000 description 2
- 206010012735 Diarrhoea Diseases 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 241000287828 Gallus gallus Species 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 206010019280 Heart failures Diseases 0.000 description 2
- 208000023105 Huntington disease Diseases 0.000 description 2
- 206010020772 Hypertension Diseases 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 102000004856 Lectins Human genes 0.000 description 2
- 108090001090 Lectins Proteins 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
- JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 208000012902 Nervous system disease Diseases 0.000 description 2
- 208000025966 Neurological disease Diseases 0.000 description 2
- 206010033799 Paralysis Diseases 0.000 description 2
- 208000018737 Parkinson disease Diseases 0.000 description 2
- 241001494479 Pecora Species 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 241000288906 Primates Species 0.000 description 2
- 108010069820 Pro-Opiomelanocortin Proteins 0.000 description 2
- 239000000683 Pro-Opiomelanocortin Substances 0.000 description 2
- 102100027467 Pro-opiomelanocortin Human genes 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 208000013200 Stress disease Diseases 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- 208000001871 Tachycardia Diseases 0.000 description 2
- 229920001615 Tragacanth Polymers 0.000 description 2
- 208000025865 Ulcer Diseases 0.000 description 2
- YYKBBFZVNQTPHA-UHFFFAOYSA-N [6-(dimethylamino)-4-ethylpyridin-3-yl]boronic acid Chemical compound CCC1=CC(N(C)C)=NC=C1B(O)O YYKBBFZVNQTPHA-UHFFFAOYSA-N 0.000 description 2
- NEKJUWAYMREFEB-UHFFFAOYSA-N [6-(dimethylamino)-4-methoxypyridin-3-yl]boronic acid Chemical compound COC1=CC(N(C)C)=NC=C1B(O)O NEKJUWAYMREFEB-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 2
- 239000012346 acetyl chloride Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 238000000376 autoradiography Methods 0.000 description 2
- 150000001557 benzodiazepines Chemical class 0.000 description 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 2
- JPLUJHOISCAQAB-CVEARBPZSA-N benzyl (3r,4s)-3-amino-4-[tert-butyl(dimethyl)silyl]oxypyrrolidine-1-carboxylate Chemical compound C1[C@@H](N)[C@@H](O[Si](C)(C)C(C)(C)C)CN1C(=O)OCC1=CC=CC=C1 JPLUJHOISCAQAB-CVEARBPZSA-N 0.000 description 2
- 230000008499 blood brain barrier function Effects 0.000 description 2
- 210000001218 blood-brain barrier Anatomy 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 150000001649 bromium compounds Chemical class 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
- 239000001506 calcium phosphate Substances 0.000 description 2
- 229910000389 calcium phosphate Inorganic materials 0.000 description 2
- 235000011010 calcium phosphates Nutrition 0.000 description 2
- 125000002837 carbocyclic group Chemical group 0.000 description 2
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000013553 cell monolayer Substances 0.000 description 2
- 235000013330 chicken meat Nutrition 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- IDLFZVILOHSSID-OVLDLUHVSA-N corticotropin Chemical compound C([C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1NC=NC=1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](C(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC(N)=O)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C=CC=CC=1)C(O)=O)NC(=O)[C@@H](N)CO)C1=CC=C(O)C=C1 IDLFZVILOHSSID-OVLDLUHVSA-N 0.000 description 2
- 229960000258 corticotropin Drugs 0.000 description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 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 description 2
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 238000004807 desolvation Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 230000004064 dysfunction Effects 0.000 description 2
- 239000012039 electrophile Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000002124 endocrine Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000004401 flow injection analysis Methods 0.000 description 2
- 239000007903 gelatin capsule Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229940093915 gynecological organic acid Drugs 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 125000001041 indolyl group Chemical group 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 208000003243 intestinal obstruction Diseases 0.000 description 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000002523 lectin Substances 0.000 description 2
- 125000005647 linker group Chemical group 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- IUYHWZFSGMZEOG-UHFFFAOYSA-M magnesium;propane;chloride Chemical compound [Mg+2].[Cl-].C[CH-]C IUYHWZFSGMZEOG-UHFFFAOYSA-M 0.000 description 2
- 208000024714 major depressive disease Diseases 0.000 description 2
- 229940098779 methanesulfonic acid Drugs 0.000 description 2
- MLSKXPOBNQFGHW-UHFFFAOYSA-N methoxy(dioxido)borane Chemical compound COB([O-])[O-] MLSKXPOBNQFGHW-UHFFFAOYSA-N 0.000 description 2
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 2
- YYFKJEIYVOWIOS-ZDUSSCGKSA-N n-[(2s)-1-methoxypropan-2-yl]-6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-4,5-dimethylpyridin-3-amine Chemical compound CC1=C(C)C(N[C@@H](C)COC)=CN=C1C1=CC=C(C(C)C)N=C1OC YYFKJEIYVOWIOS-ZDUSSCGKSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 210000005036 nerve Anatomy 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 125000000160 oxazolidinyl group Chemical group 0.000 description 2
- 230000008506 pathogenesis Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 230000000144 pharmacologic effect Effects 0.000 description 2
- 208000028173 post-traumatic stress disease Diseases 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 2
- 208000020016 psychiatric disease Diseases 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000012453 solvate Substances 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 208000011117 substance-related disease Diseases 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
- 208000011580 syndromic disease Diseases 0.000 description 2
- 239000006188 syrup Substances 0.000 description 2
- 235000020357 syrup Nutrition 0.000 description 2
- 230000006794 tachycardia Effects 0.000 description 2
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 2
- 238000002560 therapeutic procedure Methods 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 230000032258 transport Effects 0.000 description 2
- 125000004306 triazinyl group Chemical group 0.000 description 2
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 2
- 231100000397 ulcer Toxicity 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 239000003039 volatile agent Substances 0.000 description 2
- SSJXIUAHEKJCMH-PHDIDXHHSA-N (1r,2r)-cyclohexane-1,2-diamine Chemical compound N[C@@H]1CCCC[C@H]1N SSJXIUAHEKJCMH-PHDIDXHHSA-N 0.000 description 1
- NIPVWKZBILGKCT-PGMHMLKASA-N (2r)-2-amino-3-methoxypropan-1-ol;hydrochloride Chemical compound Cl.COC[C@H](N)CO NIPVWKZBILGKCT-PGMHMLKASA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- UWYVPFMHMJIBHE-OWOJBTEDSA-N (e)-2-hydroxybut-2-enedioic acid Chemical compound OC(=O)\C=C(\O)C(O)=O UWYVPFMHMJIBHE-OWOJBTEDSA-N 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- 125000004502 1,2,3-oxadiazolyl group Chemical group 0.000 description 1
- 125000004511 1,2,3-thiadiazolyl group Chemical group 0.000 description 1
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 description 1
- 125000004504 1,2,4-oxadiazolyl group Chemical group 0.000 description 1
- 125000004514 1,2,4-thiadiazolyl group Chemical group 0.000 description 1
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 description 1
- 125000004506 1,2,5-oxadiazolyl group Chemical group 0.000 description 1
- 125000004517 1,2,5-thiadiazolyl group Chemical group 0.000 description 1
- 125000001781 1,3,4-oxadiazolyl group Chemical group 0.000 description 1
- 125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 description 1
- QHUAFQIGPJSKJC-UHFFFAOYSA-N 1,6-dimethylpyrrolo[3,2-b]pyridine Chemical compound CC1=CN=C2C=CN(C)C2=C1 QHUAFQIGPJSKJC-UHFFFAOYSA-N 0.000 description 1
- QEKMJLXEUSWIMQ-HNNXBMFYSA-N 1-[(2s)-1-methoxypropan-2-yl]-5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6,7-trimethylpyrrolo[3,2-b]pyridine Chemical compound CC=1C(C)=C2N([C@@H](C)COC)C=C(C)C2=NC=1C1=CC=C(C(C)C)N=C1OC QEKMJLXEUSWIMQ-HNNXBMFYSA-N 0.000 description 1
- ZVHZPFSWZWSDEN-UHFFFAOYSA-N 1-bromo-1-fluoroethane Chemical compound CC(F)Br ZVHZPFSWZWSDEN-UHFFFAOYSA-N 0.000 description 1
- XUQRLMCZVKFXFX-UHFFFAOYSA-N 1-bromo-2-methoxy-4-(trifluoromethoxy)benzene Chemical compound COC1=CC(OC(F)(F)F)=CC=C1Br XUQRLMCZVKFXFX-UHFFFAOYSA-N 0.000 description 1
- LOYZVRIHVZEDMW-UHFFFAOYSA-N 1-bromo-3-methylbut-2-ene Chemical compound CC(C)=CCBr LOYZVRIHVZEDMW-UHFFFAOYSA-N 0.000 description 1
- OKSRAPDSZKICKZ-UHFFFAOYSA-N 1-methoxy-3-(trifluoromethoxy)benzene Chemical compound COC1=CC=CC(OC(F)(F)F)=C1 OKSRAPDSZKICKZ-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- 125000005955 1H-indazolyl group Chemical group 0.000 description 1
- LSEAAPGIZCDEEH-UHFFFAOYSA-N 2,6-dichloropyrazine Chemical compound ClC1=CN=CC(Cl)=N1 LSEAAPGIZCDEEH-UHFFFAOYSA-N 0.000 description 1
- KKFDCBRMNNSAAW-UHFFFAOYSA-N 2-(morpholin-4-yl)ethanol Chemical compound OCCN1CCOCC1 KKFDCBRMNNSAAW-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 description 1
- RHRRKORKKIVAGJ-UHFFFAOYSA-N 2-bromo-5-(trifluoromethoxy)phenol Chemical compound OC1=CC(OC(F)(F)F)=CC=C1Br RHRRKORKKIVAGJ-UHFFFAOYSA-N 0.000 description 1
- YKHQFTANTNMYPP-UHFFFAOYSA-N 2-bromopyridin-3-ol Chemical compound OC1=CC=CN=C1Br YKHQFTANTNMYPP-UHFFFAOYSA-N 0.000 description 1
- APOYTRAZFJURPB-UHFFFAOYSA-N 2-methoxy-n-(2-methoxyethyl)-n-(trifluoro-$l^{4}-sulfanyl)ethanamine Chemical compound COCCN(S(F)(F)F)CCOC APOYTRAZFJURPB-UHFFFAOYSA-N 0.000 description 1
- HLTDBMHJSBSAOM-UHFFFAOYSA-N 2-nitropyridine Chemical compound [O-][N+](=O)C1=CC=CC=N1 HLTDBMHJSBSAOM-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- JZIBVTUXIVIFGC-UHFFFAOYSA-N 2H-pyrrole Chemical compound C1C=CC=N1 JZIBVTUXIVIFGC-UHFFFAOYSA-N 0.000 description 1
- LAQJGAKLLZAETL-UHFFFAOYSA-N 2h-pyrazin-3-one Chemical compound O=C1CN=CC=N1 LAQJGAKLLZAETL-UHFFFAOYSA-N 0.000 description 1
- XVDHMQDQXNESBM-UHFFFAOYSA-N 3-(5-bromo-3-methylpyridin-2-yl)-2-methoxy-6-propan-2-ylpyridine Chemical group COC1=NC(C(C)C)=CC=C1C1=NC=C(Br)C=C1C XVDHMQDQXNESBM-UHFFFAOYSA-N 0.000 description 1
- UWLJERQTLRORJN-UHFFFAOYSA-N 3-(trifluoromethoxy)phenol Chemical compound OC1=CC=CC(OC(F)(F)F)=C1 UWLJERQTLRORJN-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- SUERSWMCYWUEDW-UHFFFAOYSA-N 3-bromo-2-ethoxy-6-ethyl-5-methylsulfonylpyridine Chemical compound CCOC1=NC(CC)=C(S(C)(=O)=O)C=C1Br SUERSWMCYWUEDW-UHFFFAOYSA-N 0.000 description 1
- 125000005925 3-methylpentyloxy group Chemical group 0.000 description 1
- GZPHSAQLYPIAIN-UHFFFAOYSA-N 3-pyridinecarbonitrile Chemical compound N#CC1=CC=CN=C1 GZPHSAQLYPIAIN-UHFFFAOYSA-N 0.000 description 1
- SJWHILBZPGQBJE-UHFFFAOYSA-N 4-ethylpyridin-2-amine Chemical compound CCC1=CC=NC(N)=C1 SJWHILBZPGQBJE-UHFFFAOYSA-N 0.000 description 1
- BZIUQZRSHNDQTH-UHFFFAOYSA-N 4-methoxy-1h-pyridin-2-one Chemical compound COC1=CC=NC(O)=C1 BZIUQZRSHNDQTH-UHFFFAOYSA-N 0.000 description 1
- YAVKJNIMFGZBSY-UHFFFAOYSA-N 5-bromo-3,4-dimethylpyridin-2-amine Chemical compound CC1=C(C)C(N)=NC=C1Br YAVKJNIMFGZBSY-UHFFFAOYSA-N 0.000 description 1
- LAGLBZHHFADKIZ-UHFFFAOYSA-N 5-bromo-4-methoxy-n,n-dimethylpyridin-2-amine Chemical compound COC1=CC(N(C)C)=NC=C1Br LAGLBZHHFADKIZ-UHFFFAOYSA-N 0.000 description 1
- AZLVTLVOHJNYBL-UHFFFAOYSA-N 5-bromo-6-methyl-n-(3-methylbutyl)pyrazin-2-amine Chemical compound CC(C)CCNC1=CN=C(Br)C(C)=N1 AZLVTLVOHJNYBL-UHFFFAOYSA-N 0.000 description 1
- AEKPNIOSGSAUNF-UHFFFAOYSA-N 5-methoxy-3-propan-2-yl-2,3-dihydrofuro[3,2-b]pyridine Chemical compound COC1=CC=C2OCC(C(C)C)C2=N1 AEKPNIOSGSAUNF-UHFFFAOYSA-N 0.000 description 1
- HFTVJMFWJUFBNO-UHFFFAOYSA-N 5h-pyrrolo[2,3-b]pyrazine Chemical compound C1=CN=C2NC=CC2=N1 HFTVJMFWJUFBNO-UHFFFAOYSA-N 0.000 description 1
- SNKCOEGBSQBQME-UHFFFAOYSA-N 6-chloro-n-(3-methylbutyl)pyrazin-2-amine Chemical compound CC(C)CCNC1=CN=CC(Cl)=N1 SNKCOEGBSQBQME-UHFFFAOYSA-N 0.000 description 1
- JDVXOHWOZRYNND-AWEZNQCLSA-N 6-ethyl-5-[1-[(2s)-1-methoxypropan-2-yl]-3,6-dimethylpyrrolo[3,2-b]pyridin-5-yl]-1h-pyridin-2-one Chemical compound N1C(=O)C=CC(C=2C(=CC=3N([C@@H](C)COC)C=C(C)C=3N=2)C)=C1CC JDVXOHWOZRYNND-AWEZNQCLSA-N 0.000 description 1
- JXKAUUVMXZIJNZ-UHFFFAOYSA-N 6-ethylpyridin-2-amine Chemical compound CCC1=CC=CC(N)=N1 JXKAUUVMXZIJNZ-UHFFFAOYSA-N 0.000 description 1
- WDUQRIVDVQTVTJ-UHFFFAOYSA-N 7-bromo-6-ethyl-2-methyl-4-propan-2-ylpyrido[2,3-b]pyrazin-3-one Chemical compound CC(C)N1C(=O)C(C)=NC2=C1N=C(CC)C(Br)=C2 WDUQRIVDVQTVTJ-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 206010065040 AIDS dementia complex Diseases 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- 208000023275 Autoimmune disease Diseases 0.000 description 1
- 108090001008 Avidin Proteins 0.000 description 1
- 229940110385 Benzodiazepine receptor antagonist Drugs 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 208000032841 Bulimia Diseases 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- 241000283707 Capra Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 102000014914 Carrier Proteins Human genes 0.000 description 1
- 102000000844 Cell Surface Receptors Human genes 0.000 description 1
- 108010001857 Cell Surface Receptors Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 206010010144 Completed suicide Diseases 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- 241000699800 Cricetinae Species 0.000 description 1
- 208000011231 Crohn disease Diseases 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 206010012289 Dementia Diseases 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- YIIMEMSDCNDGTB-UHFFFAOYSA-N Dimethylcarbamoyl chloride Chemical compound CN(C)C(Cl)=O YIIMEMSDCNDGTB-UHFFFAOYSA-N 0.000 description 1
- 206010013654 Drug abuse Diseases 0.000 description 1
- 208000027534 Emotional disease Diseases 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 241000283073 Equus caballus Species 0.000 description 1
- XXRCUYVCPSWGCC-UHFFFAOYSA-N Ethyl pyruvate Chemical compound CCOC(=O)C(C)=O XXRCUYVCPSWGCC-UHFFFAOYSA-N 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- 208000001640 Fibromyalgia Diseases 0.000 description 1
- 208000018522 Gastrointestinal disease Diseases 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 208000011688 Generalised anxiety disease Diseases 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 206010019196 Head injury Diseases 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 101000895481 Homo sapiens Corticoliberin Proteins 0.000 description 1
- 101000878678 Homo sapiens Corticotropin-releasing factor receptor 1 Proteins 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 208000013016 Hypoglycemia Diseases 0.000 description 1
- 206010062767 Hypophysitis Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229930194542 Keto Natural products 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 229910010082 LiAlH Inorganic materials 0.000 description 1
- 101000663001 Mus musculus TNFAIP3-interacting protein 1 Proteins 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- 206010029260 Neuroblastoma Diseases 0.000 description 1
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 241000283973 Oryctolagus cuniculus Species 0.000 description 1
- 208000001132 Osteoporosis Diseases 0.000 description 1
- 101000895537 Ovis aries Corticoliberin Proteins 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 241000286209 Phasianidae Species 0.000 description 1
- 206010034912 Phobia Diseases 0.000 description 1
- 102000045595 Phosphoprotein Phosphatases Human genes 0.000 description 1
- 108700019535 Phosphoprotein Phosphatases Proteins 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 208000006399 Premature Obstetric Labor Diseases 0.000 description 1
- 206010036600 Premature labour Diseases 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- 208000028017 Psychotic disease Diseases 0.000 description 1
- 108700008625 Reporter Genes Proteins 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- 101000948733 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) Probable phospholipid translocase non-catalytic subunit CRF1 Proteins 0.000 description 1
- 208000028810 Shared psychotic disease Diseases 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 208000006011 Stroke Diseases 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 241000282898 Sus scrofa Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 1
- 229940123445 Tricyclic antidepressant Drugs 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- WERKSKAQRVDLDW-ANOHMWSOSA-N [(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO WERKSKAQRVDLDW-ANOHMWSOSA-N 0.000 description 1
- BBAWTPDTGRXPDG-UHFFFAOYSA-N [1,3]thiazolo[4,5-b]pyridine Chemical compound C1=CC=C2SC=NC2=N1 BBAWTPDTGRXPDG-UHFFFAOYSA-N 0.000 description 1
- UYAQCVPBNJMZQU-UHFFFAOYSA-N [4-ethyl-6-[ethyl(methyl)amino]pyridin-3-yl]boronic acid Chemical compound CCN(C)C1=CC(CC)=C(B(O)O)C=N1 UYAQCVPBNJMZQU-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- HFEHLDPGIKPNKL-UHFFFAOYSA-N allyl iodide Chemical compound ICC=C HFEHLDPGIKPNKL-UHFFFAOYSA-N 0.000 description 1
- 125000000746 allylic group Chemical group 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 210000004198 anterior pituitary gland Anatomy 0.000 description 1
- 239000000935 antidepressant agent Substances 0.000 description 1
- 229940005513 antidepressants Drugs 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 210000001742 aqueous humor Anatomy 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 238000011914 asymmetric synthesis Methods 0.000 description 1
- 238000000065 atmospheric pressure chemical ionisation Methods 0.000 description 1
- 230000001363 autoimmune Effects 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000004604 benzisothiazolyl group Chemical group S1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 239000000749 benzodiazepine receptor blocking agent Substances 0.000 description 1
- 239000000755 benzodiazepine receptor inverse stimulating agent Substances 0.000 description 1
- 229960004365 benzoic acid Drugs 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- UQUSRBUOCMCVJA-IZLXSDGUSA-N benzyl (3r,4s)-3-[[2-bromo-6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-5-methylpyridin-3-yl]amino]-4-[tert-butyl(dimethyl)silyl]oxypyrrolidine-1-carboxylate Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC(Br)=C1N[C@H]1[C@@H](O[Si](C)(C)C(C)(C)C)CN(C(=O)OCC=2C=CC=CC=2)C1 UQUSRBUOCMCVJA-IZLXSDGUSA-N 0.000 description 1
- IXPLJRREJIUKLG-MNOVXSKESA-N benzyl (3r,4s)-3-amino-4-hydroxypyrrolidine-1-carboxylate Chemical compound C1[C@H](O)[C@H](N)CN1C(=O)OCC1=CC=CC=C1 IXPLJRREJIUKLG-MNOVXSKESA-N 0.000 description 1
- ZBXYMRJFKSUZRT-JSOSNVBQSA-N benzyl (3s,4r)-3-[tert-butyl(dimethyl)silyl]oxy-4-[5-(2-methoxy-6-propan-2-ylpyridin-3-yl)-3,6-dimethylpyrrolo[3,2-b]pyridin-1-yl]pyrrolidine-1-carboxylate Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC2=C1N([C@H]1[C@H](CN(C1)C(=O)OCC=1C=CC=CC=1)O[Si](C)(C)C(C)(C)C)C=C2C ZBXYMRJFKSUZRT-JSOSNVBQSA-N 0.000 description 1
- KGOJMYNJOQRGCL-WDYNHAJCSA-N benzyl (3s,4r)-3-[tert-butyl(dimethyl)silyl]oxy-4-[[6-(2-methoxy-6-propan-2-ylpyridin-3-yl)-5-methylpyridin-3-yl]amino]pyrrolidine-1-carboxylate Chemical compound COC1=NC(C(C)C)=CC=C1C(C(=C1)C)=NC=C1N[C@H]1[C@@H](O[Si](C)(C)C(C)(C)C)CN(C(=O)OCC=2C=CC=CC=2)C1 KGOJMYNJOQRGCL-WDYNHAJCSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
- 102000005936 beta-Galactosidase Human genes 0.000 description 1
- 108010005774 beta-Galactosidase Proteins 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 108091008324 binding proteins Proteins 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 235000020958 biotin Nutrition 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- IPWKHHSGDUIRAH-UHFFFAOYSA-N bis(pinacolato)diboron Chemical compound O1C(C)(C)C(C)(C)OB1B1OC(C)(C)C(C)(C)O1 IPWKHHSGDUIRAH-UHFFFAOYSA-N 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- FNXLCIKXHOPCKH-UHFFFAOYSA-N bromamine Chemical compound BrN FNXLCIKXHOPCKH-UHFFFAOYSA-N 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- AEILLAXRDHDKDY-UHFFFAOYSA-N bromomethylcyclopropane Chemical compound BrCC1CC1 AEILLAXRDHDKDY-UHFFFAOYSA-N 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LFLBHTZRLVHUQC-UHFFFAOYSA-N butyl methanesulfonate Chemical compound CCCCOS(C)(=O)=O LFLBHTZRLVHUQC-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 125000001589 carboacyl group Chemical group 0.000 description 1
- 125000004623 carbolinyl group Chemical group 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 206010008118 cerebral infarction Diseases 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 230000035605 chemotaxis Effects 0.000 description 1
- 238000004296 chiral HPLC Methods 0.000 description 1
- 229960004782 chlordiazepoxide Drugs 0.000 description 1
- ANTSCNMPPGJYLG-UHFFFAOYSA-N chlordiazepoxide Chemical compound O=N=1CC(NC)=NC2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 ANTSCNMPPGJYLG-UHFFFAOYSA-N 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 description 1
- 125000004230 chromenyl group Chemical group O1C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000002920 convulsive effect Effects 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 125000000000 cycloalkoxy group Chemical group 0.000 description 1
- 125000005366 cycloalkylthio group Chemical group 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- WLVKDFJTYKELLQ-UHFFFAOYSA-N cyclopropylboronic acid Chemical compound OB(O)C1CC1 WLVKDFJTYKELLQ-UHFFFAOYSA-N 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- VRLDVERQJMEPIF-UHFFFAOYSA-N dbdmh Chemical compound CC1(C)N(Br)C(=O)N(Br)C1=O VRLDVERQJMEPIF-UHFFFAOYSA-N 0.000 description 1
- 125000004856 decahydroquinolinyl group Chemical group N1(CCCC2CCCCC12)* 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- ZJULYDCRWUEPTK-UHFFFAOYSA-N dichloromethyl Chemical compound Cl[CH]Cl ZJULYDCRWUEPTK-UHFFFAOYSA-N 0.000 description 1
- 235000005911 diet Nutrition 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- IRUNKQSGDBYUDC-UHFFFAOYSA-N diethoxymethyl acetate Chemical compound CCOC(OCC)OC(C)=O IRUNKQSGDBYUDC-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 125000006001 difluoroethyl group Chemical group 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 206010013663 drug dependence Diseases 0.000 description 1
- 230000036267 drug metabolism Effects 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 206010015037 epilepsy Diseases 0.000 description 1
- AFAXGSQYZLGZPG-UHFFFAOYSA-N ethanedisulfonic acid Chemical compound OS(=O)(=O)CCS(O)(=O)=O AFAXGSQYZLGZPG-UHFFFAOYSA-N 0.000 description 1
- 229940117360 ethyl pyruvate Drugs 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 230000029142 excretion Effects 0.000 description 1
- 210000003722 extracellular fluid Anatomy 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- OFBIFZUFASYYRE-UHFFFAOYSA-N flumazenil Chemical compound C1N(C)C(=O)C2=CC(F)=CC=C2N2C=NC(C(=O)OCC)=C21 OFBIFZUFASYYRE-UHFFFAOYSA-N 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 210000005153 frontal cortex Anatomy 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 125000003838 furazanyl group Chemical group 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 208000029364 generalized anxiety disease Diseases 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 229960002989 glutamic acid Drugs 0.000 description 1
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 description 1
- 229940074045 glyceryl distearate Drugs 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- 239000007902 hard capsule Substances 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 210000003494 hepatocyte Anatomy 0.000 description 1
- FBPFZTCFMRRESA-UHFFFAOYSA-N hexane-1,2,3,4,5,6-hexol Chemical compound OCC(O)C(O)C(O)C(O)CO FBPFZTCFMRRESA-UHFFFAOYSA-N 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- 229940091173 hydantoin Drugs 0.000 description 1
- 230000002218 hypoglycaemic effect Effects 0.000 description 1
- 125000002632 imidazolidinyl group Chemical group 0.000 description 1
- 125000002636 imidazolinyl group Chemical group 0.000 description 1
- 230000001900 immune effect Effects 0.000 description 1
- 208000026278 immune system disease Diseases 0.000 description 1
- 230000000899 immune system response Effects 0.000 description 1
- 230000036039 immunity Effects 0.000 description 1
- 230000002055 immunohistochemical effect Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000004926 indolenyl group Chemical group 0.000 description 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 208000000509 infertility Diseases 0.000 description 1
- 230000036512 infertility Effects 0.000 description 1
- 231100000535 infertility Toxicity 0.000 description 1
- 208000027866 inflammatory disease Diseases 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 229940102223 injectable solution Drugs 0.000 description 1
- 229940102213 injectable suspension Drugs 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000007913 intrathecal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- LZKLAOYSENRNKR-LNTINUHCSA-N iron;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Fe].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O LZKLAOYSENRNKR-LNTINUHCSA-N 0.000 description 1
- 208000002551 irritable bowel syndrome Diseases 0.000 description 1
- 230000000302 ischemic effect Effects 0.000 description 1
- 125000003384 isochromanyl group Chemical group C1(OCCC2=CC=CC=C12)* 0.000 description 1
- 125000005438 isoindazolyl group Chemical group 0.000 description 1
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 description 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 125000001786 isothiazolyl group Chemical group 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
- 229960005015 local anesthetics Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 210000002751 lymph Anatomy 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- QJQYPZZUKLQGGT-UHFFFAOYSA-N methyl hypobromite Chemical compound COBr QJQYPZZUKLQGGT-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 230000003228 microsomal effect Effects 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229940074096 monoolein Drugs 0.000 description 1
- 230000036651 mood Effects 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- DWLVWMUCHSLGSU-UHFFFAOYSA-M n,n-dimethylcarbamate Chemical compound CN(C)C([O-])=O DWLVWMUCHSLGSU-UHFFFAOYSA-M 0.000 description 1
- DXLNRQRGXNPJKA-LBPRGKRZSA-N n-[(2s)-1-methoxypropan-2-yl]-6-[2-methoxy-4-(trifluoromethoxy)phenyl]-5-methylpyridin-3-amine Chemical compound CC1=CC(N[C@@H](C)COC)=CN=C1C1=CC=C(OC(F)(F)F)C=C1OC DXLNRQRGXNPJKA-LBPRGKRZSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- CJYQZTZSYREQBD-UHFFFAOYSA-N n-fluorobenzenesulfonamide Chemical compound FNS(=O)(=O)C1=CC=CC=C1 CJYQZTZSYREQBD-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- PVWOIHVRPOBWPI-UHFFFAOYSA-N n-propyl iodide Chemical compound CCCI PVWOIHVRPOBWPI-UHFFFAOYSA-N 0.000 description 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 description 1
- 229940042880 natural phospholipid Drugs 0.000 description 1
- 210000000653 nervous system Anatomy 0.000 description 1
- 208000015122 neurodegenerative disease Diseases 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 239000000346 nonvolatile oil Substances 0.000 description 1
- GYCKQBWUSACYIF-UHFFFAOYSA-N o-hydroxybenzoic acid ethyl ester Natural products CCOC(=O)C1=CC=CC=C1O GYCKQBWUSACYIF-UHFFFAOYSA-N 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 125000004930 octahydroisoquinolinyl group Chemical group C1(NCCC2CCCC=C12)* 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 201000008482 osteoarthritis Diseases 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 125000004095 oxindolyl group Chemical group N1(C(CC2=CC=CC=C12)=O)* 0.000 description 1
- 230000036407 pain Effects 0.000 description 1
- 230000037324 pain perception Effects 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 230000001314 paroxysmal effect Effects 0.000 description 1
- 230000007310 pathophysiology Effects 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 description 1
- 125000004625 phenanthrolinyl group Chemical group N1=C(C=CC2=CC=C3C=CC=NC3=C12)* 0.000 description 1
- 125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- 125000004932 phenoxathinyl group Chemical group 0.000 description 1
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 208000019899 phobic disease Diseases 0.000 description 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 210000003635 pituitary gland Anatomy 0.000 description 1
- 210000002381 plasma Anatomy 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 238000002600 positron emission tomography Methods 0.000 description 1
- 230000002980 postoperative effect Effects 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 235000013594 poultry meat Nutrition 0.000 description 1
- 208000026440 premature labor Diseases 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 201000002212 progressive supranuclear palsy Diseases 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 239000013014 purified material Substances 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 0.000 description 1
- 125000002755 pyrazolinyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- UMLDUMMLRZFROX-UHFFFAOYSA-N pyridin-2-ylboronic acid Chemical compound OB(O)C1=CC=CC=N1 UMLDUMMLRZFROX-UHFFFAOYSA-N 0.000 description 1
- 125000001422 pyrrolinyl group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 229940075993 receptor modulator Drugs 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 239000012925 reference material Substances 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 238000002603 single-photon emission computed tomography Methods 0.000 description 1
- 208000019116 sleep disease Diseases 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910001467 sodium calcium phosphate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 239000012321 sodium triacetoxyborohydride Substances 0.000 description 1
- KKVTYAVXTDIPAP-UHFFFAOYSA-M sodium;methanesulfonate Chemical compound [Na+].CS([O-])(=O)=O KKVTYAVXTDIPAP-UHFFFAOYSA-M 0.000 description 1
- 239000007901 soft capsule Substances 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 208000020431 spinal cord injury Diseases 0.000 description 1
- 150000003413 spiro compounds Chemical class 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 210000001179 synovial fluid Anatomy 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001302 tertiary amino group Chemical group 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- 125000006337 tetrafluoro ethyl group Chemical group 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000003039 tetrahydroisoquinolinyl group Chemical group C1(NCCC2=CC=CC=C12)* 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 239000003029 tricyclic antidepressant agent Substances 0.000 description 1
- 150000008648 triflates Chemical class 0.000 description 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- CWMFRHBXRUITQE-UHFFFAOYSA-N trimethylsilylacetylene Chemical compound C[Si](C)(C)C#C CWMFRHBXRUITQE-UHFFFAOYSA-N 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 125000001834 xanthenyl group Chemical group C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 description 1
- LJGOZJHDEQHJRI-SITYYSIOSA-N α-helical crf Chemical compound C([C@@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(O)=O)[C@@H](C)CC)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC=1N=CNC=1)NC(=O)[C@H](CC=1C=CC=CC=1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CC(O)=O)[C@@H](C)O)C(C)C)C1=CNC=N1 LJGOZJHDEQHJRI-SITYYSIOSA-N 0.000 description 1
- MMSLSKDMIZOHRX-WYDAWZGFSA-N α-helical crf(9-41) Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(N)=O MMSLSKDMIZOHRX-WYDAWZGFSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Child & Adolescent Psychology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US50041403P | 2003-09-05 | 2003-09-05 | |
| PCT/US2004/028899 WO2005023806A2 (en) | 2003-09-05 | 2004-09-03 | Heteroaryl fused pyridines, pyrazines and pyrimidines as crf1 receptor ligands |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007504271A true JP2007504271A (ja) | 2007-03-01 |
| JP2007504271A5 JP2007504271A5 (https=) | 2007-11-29 |
Family
ID=34272952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006526210A Pending JP2007504271A (ja) | 2003-09-05 | 2004-09-03 | Crf1受容体リガンドである、ヘテロアリール縮合ピリジン類、ピラジン類及びピリミジン類 |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US20050113379A1 (https=) |
| EP (1) | EP1680424A2 (https=) |
| JP (1) | JP2007504271A (https=) |
| KR (1) | KR20060088534A (https=) |
| CN (1) | CN1878773A (https=) |
| AP (1) | AP2006003559A0 (https=) |
| AR (1) | AR045582A1 (https=) |
| AU (1) | AU2004270713A1 (https=) |
| BR (1) | BRPI0414087A (https=) |
| CA (1) | CA2537829A1 (https=) |
| CR (1) | CR8274A (https=) |
| EA (1) | EA200600372A1 (https=) |
| EC (1) | ECSP066408A (https=) |
| IL (1) | IL174084A0 (https=) |
| MA (1) | MA28086A1 (https=) |
| NO (1) | NO20061180L (https=) |
| TW (1) | TW200530232A (https=) |
| WO (1) | WO2005023806A2 (https=) |
| ZA (1) | ZA200601978B (https=) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007504243A (ja) * | 2003-09-03 | 2007-03-01 | ニューロジェン・コーポレーション | 5−アリール−ピラゾロ[4,3−d]ピリミジン類、ピリジン類、ピラジン類及び関連化合物 |
| JP2012510992A (ja) * | 2008-12-06 | 2012-05-17 | イントラ−セルラー・セラピーズ・インコーポレイテッド | 有機化合物 |
| JP5147401B2 (ja) * | 2005-09-06 | 2013-02-20 | 塩野義製薬株式会社 | Pgd2受容体アンタゴニスト活性を有するインドールカルボン酸誘導体 |
| JP2015509515A (ja) * | 2012-03-06 | 2015-03-30 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 置換アザ二環およびその使用 |
Families Citing this family (72)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8273750B2 (en) | 2005-06-06 | 2012-09-25 | Takeda Pharmaceutical Company Limited | Organic compounds |
| RU2008110941A (ru) * | 2005-08-25 | 2009-09-27 | Ф.Хоффманн-Ля Рош Аг (Ch) | ИНГИБИТОРЫ КИНАЗЫ p38 МАР И СПОСОБЫ ИХ ПРИМЕНЕНИЯ |
| US7405302B2 (en) * | 2005-10-11 | 2008-07-29 | Amira Pharmaceuticals, Inc. | 5-lipoxygenase-activating protein (FLAP) inhibitors |
| US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
| GB2431927B (en) | 2005-11-04 | 2010-03-17 | Amira Pharmaceuticals Inc | 5-Lipoxygenase-activating protein (FLAP) inhibitors |
| CN102775396B (zh) | 2005-11-08 | 2014-10-08 | 沃泰克斯药物股份有限公司 | Atp-结合弹夹转运蛋白的杂环调控剂 |
| GB0525068D0 (en) | 2005-12-08 | 2006-01-18 | Novartis Ag | Organic compounds |
| EP1961754A4 (en) | 2005-12-15 | 2009-11-11 | Ono Pharmaceutical Co | BICYCLIC HETEROCYCLIC COMPOUND |
| TW200812588A (en) * | 2006-05-15 | 2008-03-16 | Neurogen Corp | CRF1 receptor ligands comprising heteroaryl fused bicycles |
| TWI398252B (zh) | 2006-05-26 | 2013-06-11 | 諾華公司 | 吡咯并嘧啶化合物及其用途 |
| US9006258B2 (en) | 2006-12-05 | 2015-04-14 | Intra-Cellular Therapies, Inc. | Method of treating female sexual dysfunction with a PDE1 inhibitor |
| WO2008076446A1 (en) * | 2006-12-18 | 2008-06-26 | Coleman Peter R | Accelerated opiate dependence detoxification process |
| JP2010513370A (ja) * | 2006-12-19 | 2010-04-30 | エフ.ホフマン−ラ ロシュ アーゲー | ピラゾロ[3,4−d]ピリミジンp38MAPキナーゼインヒビター |
| WO2008083070A1 (en) * | 2006-12-29 | 2008-07-10 | Neurogen Corporation | Crf1 receptor ligands comprising fused bicyclic heteroaryl moieties |
| CN104447716A (zh) | 2007-05-09 | 2015-03-25 | 沃泰克斯药物股份有限公司 | Cftr调节剂 |
| ES2588238T3 (es) * | 2007-12-06 | 2016-10-31 | Intra-Cellular Therapies, Inc. | Derivados de pirazolopirimidin-4,6-diona y su uso como producto farmacéutico |
| MX365732B (es) | 2007-12-07 | 2019-06-12 | Vertex Pharma | Procesos para producir acidos cicloalquilcarboxamido-piridin benzoicos. |
| EP3683218B1 (en) | 2007-12-07 | 2024-09-18 | Vertex Pharmaceuticals Incorporated | Solid forms of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl) benzoic acid |
| NZ720282A (en) | 2008-02-28 | 2017-12-22 | Vertex Pharma | Heteroaryl derivatives as cftr modulators |
| ES2522346T3 (es) | 2008-08-22 | 2014-11-14 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de CDK |
| AU2009322904A1 (en) | 2008-12-06 | 2010-06-10 | Intra-Cellular Therapies, Inc. | Organic compounds |
| JP5989993B2 (ja) | 2008-12-06 | 2016-09-07 | イントラ−セルラー・セラピーズ・インコーポレイテッドIntra−Cellular Therapies, Inc. | 有機化合物 |
| KR20110098732A (ko) | 2008-12-06 | 2011-09-01 | 인트라-셀룰라 써래피스, 인코퍼레이티드. | 유기 화합물 |
| WO2010065147A1 (en) | 2008-12-06 | 2010-06-10 | Intra-Cellular Therapies, Inc. | Organic compounds |
| CN102231953A (zh) | 2008-12-06 | 2011-11-02 | 细胞内治疗公司 | 有机化合物 |
| US8349852B2 (en) | 2009-01-13 | 2013-01-08 | Novartis Ag | Quinazolinone derivatives useful as vanilloid antagonists |
| US8551996B2 (en) * | 2009-02-20 | 2013-10-08 | Emory University | Compounds, compositions, methods of synthesis, and methods of treatment |
| US9468637B2 (en) | 2009-05-13 | 2016-10-18 | Intra-Cellular Therapies, Inc. | Organic compounds |
| WO2011092290A1 (en) | 2010-02-01 | 2011-08-04 | Novartis Ag | Pyrazolo[5,1b]oxazole derivatives as crf-1 receptor antagonists |
| AR080056A1 (es) | 2010-02-01 | 2012-03-07 | Novartis Ag | Derivados de ciclohexil-amida como antagonistas de los receptores de crf |
| EP2531490B1 (en) | 2010-02-02 | 2014-10-15 | Novartis AG | Cyclohexyl amide derivatives as crf receptor antagonists |
| UY33227A (es) | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de la cdk4/6 |
| JP2013523833A (ja) | 2010-04-07 | 2013-06-17 | バーテックス ファーマシューティカルズ インコーポレイテッド | 3−(6−(1−(2,2−ジフルオロベンゾ[d][1,3]ジオキソール−5−イル)シクロプロパンカルボキサミド)−3−メチルピリジン−2−イル)安息香酸の医薬組成物およびその投与 |
| WO2011153135A1 (en) | 2010-05-31 | 2011-12-08 | Intra-Cellular Therapies, Inc. | Organic compounds |
| US9434730B2 (en) | 2010-05-31 | 2016-09-06 | Intra-Cellular Therapies, Inc. | PDE1 inhibitor compounds |
| US9763948B2 (en) | 2010-05-31 | 2017-09-19 | Intra-Cellular Therapies, Inc. | PDE1 inhibitory compounds and methods |
| TW201206937A (en) | 2010-05-31 | 2012-02-16 | Intra Cellular Therapies Inc | Organic compounds |
| RU2013120966A (ru) | 2010-10-08 | 2014-11-20 | Эббви Инк. | ФУРО[3,2-d]ПИРИМИДИНОВЫЕ СОЕДИНЕНИЯ |
| AR086554A1 (es) | 2011-05-27 | 2014-01-08 | Novartis Ag | Derivados de la piperidina 3-espirociclica como agonistas de receptores de la ghrelina |
| EP2717877B1 (en) | 2011-06-10 | 2017-11-08 | Intra-Cellular Therapies, Inc. | Organic compounds |
| NZ727015A (en) | 2012-01-25 | 2017-12-22 | Vertex Pharma | Formulations of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid |
| JP2015525202A (ja) | 2012-05-03 | 2015-09-03 | ノバルティス アーゲー | グレリン受容体アゴニストとしての2,7−ジアザ−スピロ[4,5]デカ−7−イル誘導体のl−リンゴ酸塩およびその結晶形態 |
| US9801882B2 (en) | 2013-02-17 | 2017-10-31 | Intra-Cellular Therapies, Inc. | Phosphodiesterase-1 inhibitors and their use in treatment of cardiovascular diseases |
| US9545406B2 (en) | 2013-03-15 | 2017-01-17 | Intra-Cellular Therapies, Inc. | Method of treating a CNS injury with a PDE1 inhibitor |
| CA2906640C (en) | 2013-03-15 | 2021-07-20 | Intra-Cellular Therapies, Inc. | Substituted imidazo-[1,2-a]pyrazolo[4.3-e]pyrimidin-4[5h]-one compounds and pharmaceutical compositions and use therof as pde1 inhibitors |
| KR102529049B1 (ko) | 2013-08-14 | 2023-05-08 | 노파르티스 아게 | 암의 치료를 위한 조합 요법 |
| AU2014349010C1 (en) | 2013-11-12 | 2020-08-06 | Vertex Pharmaceuticals Incorporated | Process of preparing pharmaceutical compositions for the treatment of CFTR mediated diseases |
| EP3102576B8 (en) | 2014-02-03 | 2019-06-19 | Vitae Pharmaceuticals, LLC | Dihydropyrrolopyridine inhibitors of ror-gamma |
| EP2940022B1 (en) * | 2014-04-30 | 2020-09-02 | Masarykova Univerzita | Furopyridines as inhibitors of protein kinases |
| WO2015196186A1 (en) | 2014-06-20 | 2015-12-23 | Intra-Cellular Therapies, Inc. | Organic compounds |
| WO2016022893A1 (en) | 2014-08-07 | 2016-02-11 | Intra-Cellular Therapies, Inc. | Organic compounds |
| US10285992B2 (en) | 2014-08-07 | 2019-05-14 | Intra-Cellular Therapies, Inc. | Combinations of PDE1 inhibitors and NEP inhibitors and associated methods |
| BR112017005533B1 (pt) | 2014-09-17 | 2023-10-10 | Intra-Cellular Therapies, Inc | Compostos inibidores de fosfodiesterase 1 (pde1), composição farmacêutica que compreende os ditos compostos e usos dos mesmos no tratamento de uma doença, distúrbio, e/ou lesão do snc e no tratamento e/ou na profilaxia de uma doença, distúrbio e/ou lesão do snp |
| PT3207043T (pt) | 2014-10-14 | 2019-03-25 | Vitae Pharmaceuticals Llc | Inibidores de di-hidropirrolopiridina de ror-gama |
| US9845308B2 (en) | 2014-11-05 | 2017-12-19 | Vitae Pharmaceuticals, Inc. | Isoindoline inhibitors of ROR-gamma |
| US9663515B2 (en) | 2014-11-05 | 2017-05-30 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| RU2691136C2 (ru) | 2014-11-18 | 2019-06-11 | Вертекс Фармасьютикалз Инкорпорейтед | Способ проведения высокопроизводительной тестовой высокоэффективной жидкостной хроматографии |
| TW201625635A (zh) | 2014-11-21 | 2016-07-16 | 默沙東藥廠 | 作為可溶性鳥苷酸環化酶活化劑之三唑并吡基衍生物 |
| WO2017024018A1 (en) | 2015-08-05 | 2017-02-09 | Vitae Pharmaceuticals, Inc. | Modulators of ror-gamma |
| US11008340B2 (en) | 2015-11-20 | 2021-05-18 | Vitae Pharmaceuticals, Llc | Modulators of ROR-gamma |
| TW202220968A (zh) | 2016-01-29 | 2022-06-01 | 美商維它藥物有限責任公司 | ROR-γ調節劑 |
| EP3436083A4 (en) | 2016-03-28 | 2019-11-27 | Intra-Cellular Therapies, Inc. | NOVEL COMPOSITIONS AND METHOD |
| US9481674B1 (en) | 2016-06-10 | 2016-11-01 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| EP3510029B1 (en) * | 2016-09-07 | 2025-11-05 | The Regents of The University of California | Allosteric corticotropin-releasing factor receptor 1 (crfr1) antagonists that decrease p-tau and improve cognition |
| WO2018049417A1 (en) | 2016-09-12 | 2018-03-15 | Intra-Cellular Therapies, Inc. | Novel uses |
| JP2020528904A (ja) | 2017-07-24 | 2020-10-01 | ヴァイティー ファーマシューティカルズ,エルエルシー | RORγの阻害剤 |
| WO2019018975A1 (en) | 2017-07-24 | 2019-01-31 | Vitae Pharmaceuticals, Inc. | INHIBITORS OF ROR GAMMA |
| JP7401442B2 (ja) | 2018-01-31 | 2023-12-19 | イントラ-セルラー・セラピーズ・インコーポレイテッド | 新規使用 |
| CN110437846B (zh) * | 2019-08-30 | 2022-02-25 | 陕西师范大学 | 含炔键的氟取代苯并噁唑液晶化合物及其制备方法 |
| EP4025202A4 (en) | 2019-09-03 | 2023-08-02 | Intra-Cellular Therapies, Inc. | NOVEL CONNECTIONS |
| KR20220140515A (ko) | 2020-01-13 | 2022-10-18 | 버지 애널리틱스, 인크. | 치환된 피라졸로-피리미딘 및 그의 용도 |
| US12364695B2 (en) | 2020-06-02 | 2025-07-22 | Intra-Cellular Therapies, Inc. | Methods of treating inflammatory disease |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000502723A (ja) * | 1996-08-28 | 2000-03-07 | ファイザー・インク | 置換された6,5―ヘテロ―二環式誘導体 |
| WO2002000623A2 (en) * | 2000-06-26 | 2002-01-03 | Neurogen Corporation | Aryl fused substituted 4-oxy-pyridines |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2153494C2 (ru) * | 1993-10-12 | 2000-07-27 | Дзе Дюпон Мерк Фармасьютикал Компани | 1-n-алкил-n-арилпиримидинамины, способ лечения заболеваний, фармацевтическая композиция |
| US6020492A (en) * | 1995-05-12 | 2000-02-01 | Neurogen Corporation | Deazapurine derivatives; a new class of CRF1 specific ligands |
| JP3964478B2 (ja) * | 1995-06-30 | 2007-08-22 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | ヘテロ環含有カルボン酸誘導体及びそれを含有する医薬 |
| JP2002510687A (ja) * | 1998-04-02 | 2002-04-09 | ニューロゲン コーポレイション | アミノアルキル置換ピロロ[2,3−b]ピリジンおよびピロロ[2,3−d]ピリミジン誘導体:crf1レセプタのモジュレータ |
| DE10229777A1 (de) * | 2002-07-03 | 2004-01-29 | Bayer Ag | Indolin-Phenylsulfonamid-Derivate |
| EP1620095A4 (en) * | 2003-04-24 | 2009-04-01 | Merck & Co Inc | HEMMER OF ACT ACTIVITY |
-
2004
- 2004-09-03 US US10/933,834 patent/US20050113379A1/en not_active Abandoned
- 2004-09-03 AP AP2006003559A patent/AP2006003559A0/xx unknown
- 2004-09-03 CN CNA2004800327037A patent/CN1878773A/zh active Pending
- 2004-09-03 KR KR1020067004564A patent/KR20060088534A/ko not_active Withdrawn
- 2004-09-03 EA EA200600372A patent/EA200600372A1/ru unknown
- 2004-09-03 WO PCT/US2004/028899 patent/WO2005023806A2/en not_active Ceased
- 2004-09-03 AU AU2004270713A patent/AU2004270713A1/en not_active Abandoned
- 2004-09-03 CA CA002537829A patent/CA2537829A1/en not_active Abandoned
- 2004-09-03 ZA ZA200601978A patent/ZA200601978B/en unknown
- 2004-09-03 BR BRPI0414087-7A patent/BRPI0414087A/pt not_active IP Right Cessation
- 2004-09-03 EP EP04788585A patent/EP1680424A2/en not_active Withdrawn
- 2004-09-03 JP JP2006526210A patent/JP2007504271A/ja active Pending
- 2004-09-03 AR ARP040103174A patent/AR045582A1/es unknown
- 2004-09-06 TW TW093126841A patent/TW200530232A/zh unknown
-
2006
- 2006-03-02 IL IL174084A patent/IL174084A0/en unknown
- 2006-03-03 CR CR8274A patent/CR8274A/es unknown
- 2006-03-03 EC EC2006006408A patent/ECSP066408A/es unknown
- 2006-03-14 NO NO20061180A patent/NO20061180L/no not_active Application Discontinuation
- 2006-03-24 US US11/389,646 patent/US20060199823A1/en not_active Abandoned
- 2006-04-05 MA MA28916A patent/MA28086A1/fr unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000502723A (ja) * | 1996-08-28 | 2000-03-07 | ファイザー・インク | 置換された6,5―ヘテロ―二環式誘導体 |
| WO2002000623A2 (en) * | 2000-06-26 | 2002-01-03 | Neurogen Corporation | Aryl fused substituted 4-oxy-pyridines |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007504243A (ja) * | 2003-09-03 | 2007-03-01 | ニューロジェン・コーポレーション | 5−アリール−ピラゾロ[4,3−d]ピリミジン類、ピリジン類、ピラジン類及び関連化合物 |
| JP5147401B2 (ja) * | 2005-09-06 | 2013-02-20 | 塩野義製薬株式会社 | Pgd2受容体アンタゴニスト活性を有するインドールカルボン酸誘導体 |
| JP2012510992A (ja) * | 2008-12-06 | 2012-05-17 | イントラ−セルラー・セラピーズ・インコーポレイテッド | 有機化合物 |
| JP2015509515A (ja) * | 2012-03-06 | 2015-03-30 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 置換アザ二環およびその使用 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20060088534A (ko) | 2006-08-04 |
| AP2006003559A0 (en) | 2006-04-30 |
| AR045582A1 (es) | 2005-11-02 |
| CR8274A (es) | 2008-06-10 |
| EP1680424A2 (en) | 2006-07-19 |
| TW200530232A (en) | 2005-09-16 |
| ZA200601978B (en) | 2007-05-30 |
| MA28086A1 (fr) | 2006-08-01 |
| AU2004270713A1 (en) | 2005-03-17 |
| WO2005023806A3 (en) | 2005-06-02 |
| CA2537829A1 (en) | 2005-03-17 |
| US20060199823A1 (en) | 2006-09-07 |
| NO20061180L (no) | 2006-03-31 |
| US20050113379A1 (en) | 2005-05-26 |
| ECSP066408A (es) | 2006-09-18 |
| WO2005023806A2 (en) | 2005-03-17 |
| BRPI0414087A (pt) | 2006-10-31 |
| IL174084A0 (en) | 2008-02-09 |
| EA200600372A1 (ru) | 2006-08-25 |
| CN1878773A (zh) | 2006-12-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2007504271A (ja) | Crf1受容体リガンドである、ヘテロアリール縮合ピリジン類、ピラジン類及びピリミジン類 | |
| JP2007504243A (ja) | 5−アリール−ピラゾロ[4,3−d]ピリミジン類、ピリジン類、ピラジン類及び関連化合物 | |
| TWI853802B (zh) | 作為a2a/a2b抑制劑之咪唑并嘧啶及三唑并嘧啶 | |
| US9458155B2 (en) | Pyrido[4,3-b]indoles containing rigid moieties | |
| DE60117568T2 (de) | Kondensierte pyrazol derivate als protein kinase inhibitoren | |
| US6936617B2 (en) | Heteroaryl substituted fused bicyclic heteroaryl compound as GABAA receptor ligands | |
| JP2002507996A (ja) | 神経学的障害を治療するためのイミダゾピリミジン類およびイミダゾピリジン類 | |
| ES2551582T3 (es) | Derivados de etinilo | |
| TW201200515A (en) | Heteroaromatic phenylimidazole derivatives as PDE10A enzyme inhibitors | |
| KR20200121823A (ko) | 약학적 6,5 헤테로비시클릭 고리 유도체 | |
| US7557103B2 (en) | Imidazopyridazine compounds | |
| KR20170005860A (ko) | 포스포디에스테라아제 10a 억제제로서 융합된 트리아졸 유도체 | |
| JP3239506B2 (ja) | 複素環式誘導体 | |
| AU2004261591A1 (en) | Imidazo-pyrimidines and triazolo-pyrimidines: benzodiazepine receptor ligands | |
| MXPA06002556A (en) | Heteroaryl fused pyridines, pyrazines and pyrimidines as crf1 receptor ligands | |
| EP3597642A1 (en) | Pharmaceutical 6,5 heterobicyclic ring derivatives | |
| CN100457756C (zh) | 咪唑-嘧啶类及三唑-嘧啶类:苯并二氮平受体配体 | |
| AU2023320660A1 (en) | TGF-β INHIBITOR COMPOUND AND USE THEREOF | |
| AU2013203621A1 (en) | Pyrido(4,3-b)indoles containing rigid moieties | |
| CN116669769A (zh) | Helios的哌啶基小分子降解剂和使用方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070831 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070831 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20071010 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20100901 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20100921 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20110308 |