MX2014005714A - Inhibidores de fosfodiesterasa del tipo 10a. - Google Patents

Info

Publication number

MX2014005714A

MX2014005714A MX2014005714A MX2014005714A MX2014005714A MX 2014005714 A MX2014005714 A MX 2014005714A MX 2014005714 A MX2014005714 A MX 2014005714A MX 2014005714 A MX2014005714 A MX 2014005714A MX 2014005714 A MX2014005714 A MX 2014005714A

Authority

MX

Mexico

Prior art keywords

ethyl

quinolin

pyridin

thieno

cyclopropyl

Prior art date

2011-11-09

Links

• Espacenet
• Global Dossier
• Discuss

• 108090001050 Phosphoric Diester Hydrolases Proteins 0.000 title claims abstract description 13
• 102000004861 Phosphoric Diester Hydrolases Human genes 0.000 title claims abstract description 13
• 239000003112 inhibitor Substances 0.000 title abstract description 5
• 150000001875 compounds Chemical class 0.000 claims abstract description 383
• 229910052799 carbon Inorganic materials 0.000 claims abstract description 246
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 187
• 239000001257 hydrogen Substances 0.000 claims abstract description 181
• 229910052717 sulfur Inorganic materials 0.000 claims abstract description 106
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 99
• 229910052760 oxygen Inorganic materials 0.000 claims abstract description 97
• 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 94
• 150000002431 hydrogen Chemical class 0.000 claims abstract description 80
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 58
• 229910052736 halogen Inorganic materials 0.000 claims abstract description 49
• 150000002367 halogens Chemical class 0.000 claims abstract description 49
• 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 41
• 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims abstract description 21
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 20
• 208000020016 psychiatric disease Diseases 0.000 claims abstract description 15
• 208000012902 Nervous system disease Diseases 0.000 claims abstract description 11
• 208000025966 Neurological disease Diseases 0.000 claims abstract description 11
• -1 heterobicyclic radicals Chemical class 0.000 claims description 1127
• 150000003254 radicals Chemical class 0.000 claims description 167
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 157
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 124
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 121
• 125000004429 atom Chemical group 0.000 claims description 100
• 229910052731 fluorine Inorganic materials 0.000 claims description 92
• 239000011737 fluorine Substances 0.000 claims description 92
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 90
• 150000003839 salts Chemical class 0.000 claims description 89
• 229940002612 prodrug Drugs 0.000 claims description 84
• 239000000651 prodrug Substances 0.000 claims description 84
• 229920006395 saturated elastomer Polymers 0.000 claims description 84
• 150000004677 hydrates Chemical class 0.000 claims description 76
• 150000001204 N-oxides Chemical class 0.000 claims description 74
• 125000004159 quinolin-2-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C([H])C(*)=NC2=C1[H] 0.000 claims description 67
• 239000000126 substance Substances 0.000 claims description 64
• IJAPPYDYQCXOEF-UHFFFAOYSA-N phthalazin-1(2H)-one Chemical compound C1=CC=C2C(=O)NN=CC2=C1 IJAPPYDYQCXOEF-UHFFFAOYSA-N 0.000 claims description 63
• 125000001072 heteroaryl group Chemical group 0.000 claims description 57
• 125000004432 carbon atom Chemical group C* 0.000 claims description 53
• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 49
• IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 48
• 125000001424 substituent group Chemical group 0.000 claims description 44
• 238000000034 method Methods 0.000 claims description 43
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 36
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 35
• 239000000460 chlorine Substances 0.000 claims description 35
• 229910052801 chlorine Inorganic materials 0.000 claims description 35
• 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 35
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 28
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 26
• 241000124008 Mammalia Species 0.000 claims description 26
• 125000004076 pyridyl group Chemical group 0.000 claims description 25
• 125000000335 thiazolyl group Chemical group 0.000 claims description 25
• 125000002971 oxazolyl group Chemical group 0.000 claims description 24
• 125000000714 pyrimidinyl group Chemical group 0.000 claims description 24
• 125000000168 pyrrolyl group Chemical group 0.000 claims description 24
• 125000001544 thienyl group Chemical group 0.000 claims description 24
• 125000002541 furyl group Chemical group 0.000 claims description 23
• 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 22
• 125000002883 imidazolyl group Chemical group 0.000 claims description 22
• 125000003226 pyrazolyl group Chemical group 0.000 claims description 22
• VOIKXRQSXFJVMT-UHFFFAOYSA-N 5h-thieno[2,3-d]pyridazin-4-one Chemical compound O=C1NN=CC2=C1C=CS2 VOIKXRQSXFJVMT-UHFFFAOYSA-N 0.000 claims description 21
• DUPNPBCUJHMSFZ-UHFFFAOYSA-N 5h-thieno[3,2-c]pyridin-4-one Chemical compound O=C1NC=CC2=C1C=CS2 DUPNPBCUJHMSFZ-UHFFFAOYSA-N 0.000 claims description 21
• 125000004430 oxygen atom Chemical group O* 0.000 claims description 21
• 125000000623 heterocyclic group Chemical group 0.000 claims description 20
• 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 20
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 18
• 201000000980 schizophrenia Diseases 0.000 claims description 18
• MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 17
• 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims description 17
• 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 15
• 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 14
• 208000019901 Anxiety disease Diseases 0.000 claims description 12
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
• 239000001301 oxygen Substances 0.000 claims description 12
• 239000008194 pharmaceutical composition Substances 0.000 claims description 12
• 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 11
• UTCSSFWDNNEEBH-UHFFFAOYSA-N imidazo[1,2-a]pyridine Chemical compound C1=CC=CC2=NC=CN21 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 claims description 11
• DWHIRSWNWDXFMQ-UHFFFAOYSA-N 4h-pyridazin-5-one Chemical compound O=C1CC=NN=C1 DWHIRSWNWDXFMQ-UHFFFAOYSA-N 0.000 claims description 10
• 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 10
• VDBNYAPERZTOOF-UHFFFAOYSA-N isoquinolin-1(2H)-one Chemical compound C1=CC=C2C(=O)NC=CC2=C1 VDBNYAPERZTOOF-UHFFFAOYSA-N 0.000 claims description 10
• 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 10
• 230000036506 anxiety Effects 0.000 claims description 9
• 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims description 9
• 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 claims description 8
• 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 claims description 8
• 125000004571 thiomorpholin-4-yl group Chemical group N1(CCSCC1)* 0.000 claims description 8
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 7
• CYQLXLAJVANNIE-UHFFFAOYSA-N 8-pyridin-4-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=CC=NC=C1 CYQLXLAJVANNIE-UHFFFAOYSA-N 0.000 claims description 7
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 7
• 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 7
• 208000010877 cognitive disease Diseases 0.000 claims description 7
• 239000000546 pharmaceutical excipient Substances 0.000 claims description 7
• ASNUDELVENWRMB-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CC=NC=C1 ASNUDELVENWRMB-UHFFFAOYSA-N 0.000 claims description 6
• MQKXIURELWPBHC-UHFFFAOYSA-N 8-pyridin-4-yl-2-(2-quinolin-2-ylcyclopropyl)phthalazin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CC=NC=C1 MQKXIURELWPBHC-UHFFFAOYSA-N 0.000 claims description 6
• LCSGWIUZBNBGDL-UHFFFAOYSA-N 8-(2-fluoropyridin-4-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=NC(F)=CC(C=2C=3C(=O)N(C4C(C4)C=4N=C5C=CC=CC5=CC=4)C=CC=3C=CC=2)=C1 LCSGWIUZBNBGDL-UHFFFAOYSA-N 0.000 claims description 5
• 208000020925 Bipolar disease Diseases 0.000 claims description 5
• 208000023105 Huntington disease Diseases 0.000 claims description 5
• 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 5
• NALBLJLOBICXRH-UHFFFAOYSA-N dinitrogen monohydride Chemical compound N=[N] NALBLJLOBICXRH-UHFFFAOYSA-N 0.000 claims description 5
• 125000004428 fluoroalkoxy group Chemical group 0.000 claims description 5
• 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims description 5
• 125000001041 indolyl group Chemical group 0.000 claims description 5
• 230000002401 inhibitory effect Effects 0.000 claims description 5
• 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims description 5
• 125000002911 monocyclic heterocycle group Chemical group 0.000 claims description 5
• 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 5
• OEZPXSYTAGOBNS-UHFFFAOYSA-N 2-[2-(6-fluoroquinolin-2-yl)cyclopropyl]-8-pyridin-4-ylisoquinolin-1-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1C1CC1N(C(C1=2)=O)C=CC1=CC=CC=2C1=CC=NC=C1 OEZPXSYTAGOBNS-UHFFFAOYSA-N 0.000 claims description 4
• NZGNEUSBEOWIEE-UHFFFAOYSA-N 2-[2-(6-fluoroquinolin-2-yl)cyclopropyl]-8-pyridin-4-ylphthalazin-1-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1C1CC1N(C(C1=2)=O)N=CC1=CC=CC=2C1=CC=NC=C1 NZGNEUSBEOWIEE-UHFFFAOYSA-N 0.000 claims description 4
• 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
• RROZJMWKQNSJOL-UHFFFAOYSA-N 3-pyrimidin-5-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CN=CN=C1 RROZJMWKQNSJOL-UHFFFAOYSA-N 0.000 claims description 4
• RQDUVXXBTYJKIN-UHFFFAOYSA-N 5-[2-(6-fluoroquinolin-2-yl)cyclopropyl]-3-pyridin-4-ylthieno[3,2-c]pyridin-4-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1C1CC1N(C(C=12)=O)C=CC=1SC=C2C1=CC=NC=C1 RQDUVXXBTYJKIN-UHFFFAOYSA-N 0.000 claims description 4
• XDCLDCDNXHQJEI-UHFFFAOYSA-N 5-pyridin-3-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=CC=C2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=C1C1=CC=CN=C1 XDCLDCDNXHQJEI-UHFFFAOYSA-N 0.000 claims description 4
• XHCLSIRVDUTRAS-UHFFFAOYSA-N 5-pyridin-4-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=CC=C2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=C1C1=CC=NC=C1 XHCLSIRVDUTRAS-UHFFFAOYSA-N 0.000 claims description 4
• QEUNFNUYYKEICD-UHFFFAOYSA-N 5-pyrimidin-5-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=CC=C2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=C1C1=CN=CN=C1 QEUNFNUYYKEICD-UHFFFAOYSA-N 0.000 claims description 4
• JJRDWBQFQAZETF-UHFFFAOYSA-N 7-fluoro-3-pyridin-4-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C=1SC=2C(F)=CN(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C(=O)C=2C=1C1=CC=NC=C1 JJRDWBQFQAZETF-UHFFFAOYSA-N 0.000 claims description 4
• PJBHVFBLRDATND-UHFFFAOYSA-N 8-(1-methylpyrazol-4-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=NN(C)C=C1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 PJBHVFBLRDATND-UHFFFAOYSA-N 0.000 claims description 4
• HMEUYKQNWQWISF-UHFFFAOYSA-N 8-(2-oxa-7-azaspiro[3.4]octan-7-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1N(C1)CCC21COC2 HMEUYKQNWQWISF-UHFFFAOYSA-N 0.000 claims description 4
• DAVWDBKMWVHGSV-UHFFFAOYSA-N 8-(4-fluorophenyl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=CC(F)=CC=C1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 DAVWDBKMWVHGSV-UHFFFAOYSA-N 0.000 claims description 4
• HATHYQZLFTULDK-UHFFFAOYSA-N 8-(4-methoxyphenyl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=CC(OC)=CC=C1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 HATHYQZLFTULDK-UHFFFAOYSA-N 0.000 claims description 4
• VNLWXEZYYWYETD-UHFFFAOYSA-N 8-(4-methoxypiperidin-1-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1CC(OC)CCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 VNLWXEZYYWYETD-UHFFFAOYSA-N 0.000 claims description 4
• UCSFMOYQPXDGJS-UHFFFAOYSA-N 8-(furan-3-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C=1C=COC=1 UCSFMOYQPXDGJS-UHFFFAOYSA-N 0.000 claims description 4
• ITVWXGUTBHQGBK-UHFFFAOYSA-N 8-(oxetan-3-ylamino)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1NC1COC1 ITVWXGUTBHQGBK-UHFFFAOYSA-N 0.000 claims description 4
• BLBLGVHZYVRYPY-BLWHJXEHSA-N 8-[(3r,4r)-4-fluoro-3-hydroxypiperidin-1-yl]-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1C[C@@H](F)[C@H](O)CN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 BLBLGVHZYVRYPY-BLWHJXEHSA-N 0.000 claims description 4
• ZUCWYTLCOZARHE-HGCBZUSOSA-N 8-[(3s)-3-hydroxypyrrolidin-1-yl]-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1[C@@H](O)CCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 ZUCWYTLCOZARHE-HGCBZUSOSA-N 0.000 claims description 4
• PGYRAFRFQRTAEP-UHFFFAOYSA-N 8-pyridazin-4-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=CC=NN=C1 PGYRAFRFQRTAEP-UHFFFAOYSA-N 0.000 claims description 4
• WQZGDHBUYPHNFQ-UHFFFAOYSA-N 8-pyridin-3-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=CC=CN=C1 WQZGDHBUYPHNFQ-UHFFFAOYSA-N 0.000 claims description 4
• GNICBZPWMYAWHI-UHFFFAOYSA-N 8-pyrimidin-5-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=CN=CN=C1 GNICBZPWMYAWHI-UHFFFAOYSA-N 0.000 claims description 4
• 208000024827 Alzheimer disease Diseases 0.000 claims description 4
• 208000008589 Obesity Diseases 0.000 claims description 4
• 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims description 4
• 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
• 125000002837 carbocyclic group Chemical group 0.000 claims description 4
• 235000005911 diet Nutrition 0.000 claims description 4
• 230000037213 diet Effects 0.000 claims description 4
• 125000002950 monocyclic group Chemical group 0.000 claims description 4
• 125000001624 naphthyl group Chemical group 0.000 claims description 4
• 235000020824 obesity Nutrition 0.000 claims description 4
• 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims description 4
• 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims description 4
• 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 4
• 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims description 4
• 229910052702 rhenium Inorganic materials 0.000 claims description 4
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
• 238000002560 therapeutic procedure Methods 0.000 claims description 4
• 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 3
• DBEXXZREBNIVIE-UHFFFAOYSA-N 1-[1-oxo-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-8-yl]piperidine-4-carbonitrile Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1N1CCC(C#N)CC1 DBEXXZREBNIVIE-UHFFFAOYSA-N 0.000 claims description 3
• 125000005983 2,5-diazabicyclo[2.2.1]heptan-2-yl group Chemical group 0.000 claims description 3
• YYKZVHXBOVKANS-UHFFFAOYSA-N 2-[2-(6-fluoroquinolin-2-yl)cyclopropyl]-8-pyrimidin-5-ylisoquinolin-1-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1C1CC1N(C(C1=2)=O)C=CC1=CC=CC=2C1=CN=CN=C1 YYKZVHXBOVKANS-UHFFFAOYSA-N 0.000 claims description 3
• 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 3
• 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
• MYOKVRYNQIVFJX-UHFFFAOYSA-N 4-chloro-8-pyrimidin-5-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=CC=C2C(Cl)=CN(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C(=O)C2=C1C1=CN=CN=C1 MYOKVRYNQIVFJX-UHFFFAOYSA-N 0.000 claims description 3
• PPQAGFQZBYYBPQ-UHFFFAOYSA-N 4-fluoro-8-pyridin-4-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=CC=C2C(F)=CN(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C(=O)C2=C1C1=CC=NC=C1 PPQAGFQZBYYBPQ-UHFFFAOYSA-N 0.000 claims description 3
• 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 3
• OKKDTIKQKNZBFH-UHFFFAOYSA-N 8-(4,4-difluoropiperidin-1-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1CC(F)(F)CCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 OKKDTIKQKNZBFH-UHFFFAOYSA-N 0.000 claims description 3
• BEQNPWNIWYZXKT-UHFFFAOYSA-N 8-(4-hydroxypiperidin-1-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1CC(O)CCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 BEQNPWNIWYZXKT-UHFFFAOYSA-N 0.000 claims description 3
• PXUKFUXBASUFNE-UHFFFAOYSA-N 8-[3-(fluoromethyl)pyrrolidin-1-yl]-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1C(CF)CCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 PXUKFUXBASUFNE-UHFFFAOYSA-N 0.000 claims description 3
• KNYZQKSPNAILGJ-UHFFFAOYSA-N 8-[methyl(oxetan-3-yl)amino]-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=1C=CC=2C=CN(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C(=O)C=2C=1N(C)C1COC1 KNYZQKSPNAILGJ-UHFFFAOYSA-N 0.000 claims description 3
• XPPXUDVPZXZMHC-UHFFFAOYSA-N 8-morpholin-4-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1N1CCOCC1 XPPXUDVPZXZMHC-UHFFFAOYSA-N 0.000 claims description 3
• KPOZQDBDLQTIGV-GHRIWEEISA-N 8-pyridin-4-yl-2-[(e)-2-quinolin-2-ylethenyl]isoquinolin-1-one Chemical compound C=12C(=O)N(\C=C\C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=CC=NC=C1 KPOZQDBDLQTIGV-GHRIWEEISA-N 0.000 claims description 3
• JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Substances N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 3
• 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 3
• BGHVTPXKDAVZDD-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-5-pyridin-3-ylphthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=C1C1=CC=CN=C1 BGHVTPXKDAVZDD-UHFFFAOYSA-N 0.000 claims description 2
• FJJZNBZJFQVYRT-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1,2,3,6-tetrahydropyridin-4-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1=CCNCC1 FJJZNBZJFQVYRT-UHFFFAOYSA-N 0.000 claims description 2
• LEDAISWHEVRGMO-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1,2-oxazolidin-2-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N1CCCO1 LEDAISWHEVRGMO-UHFFFAOYSA-N 0.000 claims description 2
• SNEHAQOYYRJELH-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1,4-oxazepan-4-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N1CCCOCC1 SNEHAQOYYRJELH-UHFFFAOYSA-N 0.000 claims description 2
• NZAAMDAAXLPMLH-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1h-pyrazol-5-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C=1C=CNN=1 NZAAMDAAXLPMLH-UHFFFAOYSA-N 0.000 claims description 2
• DZDFVQFBSZHODZ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(4-methylpiperazin-1-yl)phthalazin-1-one Chemical compound C1CN(C)CCN1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 DZDFVQFBSZHODZ-UHFFFAOYSA-N 0.000 claims description 2
• GHKGNRPMXWTDJJ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(morpholin-4-ylmethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1CN1CCOCC1 GHKGNRPMXWTDJJ-UHFFFAOYSA-N 0.000 claims description 2
• DXCMCCZFNKZAMD-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxetan-3-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1COC1 DXCMCCZFNKZAMD-UHFFFAOYSA-N 0.000 claims description 2
• BYBQUXPEWFXGOZ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxetan-3-yloxy)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1OC1COC1 BYBQUXPEWFXGOZ-UHFFFAOYSA-N 0.000 claims description 2
• AZFURDPSTMAEGN-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(pyridin-4-ylmethoxy)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1OCC1=CC=NC=C1 AZFURDPSTMAEGN-UHFFFAOYSA-N 0.000 claims description 2
• MUIRKGPMSUPADS-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-[4-(trifluoromethyl)piperidin-1-yl]phthalazin-1-one Chemical compound C1CC(C(F)(F)F)CCN1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 MUIRKGPMSUPADS-UHFFFAOYSA-N 0.000 claims description 2
• YGMWDYMNXOAZCG-QGZVFWFLSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-[[(3r)-oxolan-3-yl]amino]phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N[C@@H]1CCOC1 YGMWDYMNXOAZCG-QGZVFWFLSA-N 0.000 claims description 2
• QYMINYZRMQLHLP-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-piperazin-1-ylphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N1CCNCC1 QYMINYZRMQLHLP-UHFFFAOYSA-N 0.000 claims description 2
• YTKDXEZBJIZKAR-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-pyridin-4-ylphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1=CC=NC=C1 YTKDXEZBJIZKAR-UHFFFAOYSA-N 0.000 claims description 2
• AVBWILVLIMXUQN-UHFFFAOYSA-N 2-(2-quinolin-2-ylethyl)-8-[4-(trifluoromethyl)phenyl]phthalazin-1-one Chemical compound C1=CC(C(F)(F)F)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 AVBWILVLIMXUQN-UHFFFAOYSA-N 0.000 claims description 2
• PCVUPNNIMVDXTJ-UHFFFAOYSA-N 2-[2-(1,3-benzothiazol-2-yl)ethyl]-8-pyridin-4-ylisoquinolin-1-one Chemical compound C=12C(=O)N(CCC=3SC4=CC=CC=C4N=3)C=CC2=CC=CC=1C1=CC=NC=C1 PCVUPNNIMVDXTJ-UHFFFAOYSA-N 0.000 claims description 2
• CSEIXJZKDKGRQL-UHFFFAOYSA-N 2-[2-(1,6-naphthyridin-2-yl)ethyl]-8-pyridin-4-ylisoquinolin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CN=CC4=CC=3)C=CC2=CC=CC=1C1=CC=NC=C1 CSEIXJZKDKGRQL-UHFFFAOYSA-N 0.000 claims description 2
• VCCQOLDSXGLKJY-UHFFFAOYSA-N 2-[2-(1h-benzimidazol-2-yl)ethyl]-5-pyridin-4-ylphthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3NC4=CC=CC=C4N=3)N=CC2=C1C1=CC=NC=C1 VCCQOLDSXGLKJY-UHFFFAOYSA-N 0.000 claims description 2
• RNZOPJWJVAXPFR-UHFFFAOYSA-N 2-[2-(3-methylquinolin-2-yl)ethyl]-8-pyridin-4-ylisoquinolin-1-one Chemical compound CC1=CC2=CC=CC=C2N=C1CCN(C(C1=2)=O)C=CC1=CC=CC=2C1=CC=NC=C1 RNZOPJWJVAXPFR-UHFFFAOYSA-N 0.000 claims description 2
• GUSZZCFDFJEHQY-UHFFFAOYSA-N 2-[2-(5-methylpyridin-2-yl)ethyl]-8-pyridin-4-ylisoquinolin-1-one Chemical compound N1=CC(C)=CC=C1CCN1C(=O)C2=C(C=3C=CN=CC=3)C=CC=C2C=C1 GUSZZCFDFJEHQY-UHFFFAOYSA-N 0.000 claims description 2
• SIXKYHRABSUILN-UHFFFAOYSA-N 2-[2-(6-fluoroquinolin-2-yl)cyclopropyl]-8-morpholin-4-ylisoquinolin-1-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1C1CC1N(C(C1=2)=O)C=CC1=CC=CC=2N1CCOCC1 SIXKYHRABSUILN-UHFFFAOYSA-N 0.000 claims description 2
• GBLUIIINCIVDDD-UHFFFAOYSA-N 2-[2-(8-fluoroquinolin-2-yl)ethyl]-8-pyridin-4-ylisoquinolin-1-one Chemical compound N1=C2C(F)=CC=CC2=CC=C1CCN(C(C1=2)=O)C=CC1=CC=CC=2C1=CC=NC=C1 GBLUIIINCIVDDD-UHFFFAOYSA-N 0.000 claims description 2
• 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
• ZFOQJELBBAXKQI-UHFFFAOYSA-N 3,7-dipyridin-4-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2SC=C(C=3C=CN=CC=3)C=2C(=O)N(CCC=2N=C3C=CC=CC3=CC=2)N=C1C1=CC=NC=C1 ZFOQJELBBAXKQI-UHFFFAOYSA-N 0.000 claims description 2
• KAFNLLKMKIWPCP-UHFFFAOYSA-N 3-(1,3-benzodioxol-5-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C2OCOC2=CC(C2=CSC=3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C2=3)=O)=C1 KAFNLLKMKIWPCP-UHFFFAOYSA-N 0.000 claims description 2
• ULMDVRBWINKKKT-UHFFFAOYSA-N 3-(1-benzofuran-2-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC=C2OC(C3=CSC=4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C3=4)=O)=CC2=C1 ULMDVRBWINKKKT-UHFFFAOYSA-N 0.000 claims description 2
• IZLNFMAGGHABDR-UHFFFAOYSA-N 3-(1-methylpyrazol-4-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=NN(C)C=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 IZLNFMAGGHABDR-UHFFFAOYSA-N 0.000 claims description 2
• JNSCTURGBBDPJR-UHFFFAOYSA-N 3-(1h-indazol-5-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C2NN=CC2=CC(C2=CSC=3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C2=3)=O)=C1 JNSCTURGBBDPJR-UHFFFAOYSA-N 0.000 claims description 2
• DCJOQZGUMMATNR-UHFFFAOYSA-N 3-(1h-indol-4-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CC=CC2=C1C=CN2 DCJOQZGUMMATNR-UHFFFAOYSA-N 0.000 claims description 2
• UPPVMIBSCMUMFC-UHFFFAOYSA-N 3-(1h-indol-6-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C2C=CNC2=CC(C2=CSC=3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C2=3)=O)=C1 UPPVMIBSCMUMFC-UHFFFAOYSA-N 0.000 claims description 2
• BUEPDTHRTIHMEC-UHFFFAOYSA-N 3-(2,3-difluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound FC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1F BUEPDTHRTIHMEC-UHFFFAOYSA-N 0.000 claims description 2
• FVDXMNXFJQEXSP-UHFFFAOYSA-N 3-(2,3-dihydro-1-benzofuran-5-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C2OCCC2=CC(C2=CSC=3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C2=3)=O)=C1 FVDXMNXFJQEXSP-UHFFFAOYSA-N 0.000 claims description 2
• XINPVAVWVVDEAK-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1OC XINPVAVWVVDEAK-UHFFFAOYSA-N 0.000 claims description 2
• UPJKOCYDAPUPBN-UHFFFAOYSA-N 3-(2,4-dimethoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC(OC)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 UPJKOCYDAPUPBN-UHFFFAOYSA-N 0.000 claims description 2
• PUCCFQQFKJXEIK-UHFFFAOYSA-N 3-(2,5-dichlorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound ClC1=CC=C(Cl)C(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 PUCCFQQFKJXEIK-UHFFFAOYSA-N 0.000 claims description 2
• QLKPJNKSMMRWIC-UHFFFAOYSA-N 3-(2,5-difluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound FC1=CC=C(F)C(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 QLKPJNKSMMRWIC-UHFFFAOYSA-N 0.000 claims description 2
• JYRDMQKOYPEEMB-UHFFFAOYSA-N 3-(2,5-dimethoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=C(OC)C(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 JYRDMQKOYPEEMB-UHFFFAOYSA-N 0.000 claims description 2
• DNGAPPWFPQYXHZ-UHFFFAOYSA-N 3-(2-chloro-4-fluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound ClC1=CC(F)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 DNGAPPWFPQYXHZ-UHFFFAOYSA-N 0.000 claims description 2
• CAAYDVZTNZIUSM-UHFFFAOYSA-N 3-(2-ethoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CCOC1=CC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 CAAYDVZTNZIUSM-UHFFFAOYSA-N 0.000 claims description 2
• RYORFSMHEDEJPU-UHFFFAOYSA-N 3-(2-fluoro-4-methylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound FC1=CC(C)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 RYORFSMHEDEJPU-UHFFFAOYSA-N 0.000 claims description 2
• HJGIQUYRMXQHCG-UHFFFAOYSA-N 3-(2-fluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound FC1=CC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 HJGIQUYRMXQHCG-UHFFFAOYSA-N 0.000 claims description 2
• IWSYGBCUTRXSMZ-UHFFFAOYSA-N 3-(2-hydroxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound OC1=CC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 IWSYGBCUTRXSMZ-UHFFFAOYSA-N 0.000 claims description 2
• ABRIEEOFOWGNFG-UHFFFAOYSA-N 3-(2-methoxy-5-methylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=C(C)C=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 ABRIEEOFOWGNFG-UHFFFAOYSA-N 0.000 claims description 2
• FVIYJDJDXDTQKE-UHFFFAOYSA-N 3-(2-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 FVIYJDJDXDTQKE-UHFFFAOYSA-N 0.000 claims description 2
• SPMRLIHQISMBCB-UHFFFAOYSA-N 3-(2-methoxypyridin-3-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=NC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 SPMRLIHQISMBCB-UHFFFAOYSA-N 0.000 claims description 2
• ZYXIVTZVKLFZKM-UHFFFAOYSA-N 3-(2-methylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CC1=CC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 ZYXIVTZVKLFZKM-UHFFFAOYSA-N 0.000 claims description 2
• JMRQRIZTIIZPEI-UHFFFAOYSA-N 3-(2-methylpyridin-4-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=NC(C)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 JMRQRIZTIIZPEI-UHFFFAOYSA-N 0.000 claims description 2
• ZGDQKGYAOYVOIH-UHFFFAOYSA-N 3-(2-methylpyrimidin-5-yl)-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=NC(C)=NC=C1C1=CSC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 ZGDQKGYAOYVOIH-UHFFFAOYSA-N 0.000 claims description 2
• YGBCPOLEDWOMSR-UHFFFAOYSA-N 3-(2-pyridin-3-ylethynyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C#CC1=CC=CN=C1 YGBCPOLEDWOMSR-UHFFFAOYSA-N 0.000 claims description 2
• IPEHQBRQXCJXMI-UHFFFAOYSA-N 3-(3,4-dimethoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C(OC)C(OC)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 IPEHQBRQXCJXMI-UHFFFAOYSA-N 0.000 claims description 2
• KFSIBWDMINRVGU-UHFFFAOYSA-N 3-(3,4-dimethylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C(C)C(C)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 KFSIBWDMINRVGU-UHFFFAOYSA-N 0.000 claims description 2
• VBPCKGWTMWNDBQ-UHFFFAOYSA-N 3-(3,5-difluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound FC1=CC(F)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 VBPCKGWTMWNDBQ-UHFFFAOYSA-N 0.000 claims description 2
• YDMWKMJIKYUHRE-UHFFFAOYSA-N 3-(3-chloro-4-fluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C(Cl)C(F)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 YDMWKMJIKYUHRE-UHFFFAOYSA-N 0.000 claims description 2
• VRDKPRWGIPWKAY-UHFFFAOYSA-N 3-(3-fluoro-4-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C(F)C(OC)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 VRDKPRWGIPWKAY-UHFFFAOYSA-N 0.000 claims description 2
• NBVQYERGRIFTBT-UHFFFAOYSA-N 3-(3-fluoro-5-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC(F)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 NBVQYERGRIFTBT-UHFFFAOYSA-N 0.000 claims description 2
• HISVDBNUIFMAEV-UHFFFAOYSA-N 3-(3-methylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 HISVDBNUIFMAEV-UHFFFAOYSA-N 0.000 claims description 2
• ZRXFASXFGKYWSL-UHFFFAOYSA-N 3-(4,5-difluoro-2-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC(F)=C(F)C=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 ZRXFASXFGKYWSL-UHFFFAOYSA-N 0.000 claims description 2
• QVWRXKGQVFZOOL-UHFFFAOYSA-N 3-(4-ethoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(OCC)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 QVWRXKGQVFZOOL-UHFFFAOYSA-N 0.000 claims description 2
• LEKKMNVDZORIHF-UHFFFAOYSA-N 3-(4-fluoro-2-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC(F)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 LEKKMNVDZORIHF-UHFFFAOYSA-N 0.000 claims description 2
• WFRMHEYXUIDBSD-UHFFFAOYSA-N 3-(4-fluoro-2-methylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CC1=CC(F)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 WFRMHEYXUIDBSD-UHFFFAOYSA-N 0.000 claims description 2
• BAUWWUYLSMLXDE-UHFFFAOYSA-N 3-(4-fluoro-3-methylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=C(F)C(C)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 BAUWWUYLSMLXDE-UHFFFAOYSA-N 0.000 claims description 2
• SGJXOCUUXPGHKQ-UHFFFAOYSA-N 3-(4-methoxypyridin-3-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=NC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 SGJXOCUUXPGHKQ-UHFFFAOYSA-N 0.000 claims description 2
• YFMBLVALFCERPI-UHFFFAOYSA-N 3-(4-methylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(C)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 YFMBLVALFCERPI-UHFFFAOYSA-N 0.000 claims description 2
• RDYGHZZGCVCTFA-UHFFFAOYSA-N 3-(4-propan-2-ylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(C(C)C)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 RDYGHZZGCVCTFA-UHFFFAOYSA-N 0.000 claims description 2
• RAQYNIRCJNRTMJ-UHFFFAOYSA-N 3-(5-fluoro-2-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=C(F)C=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 RAQYNIRCJNRTMJ-UHFFFAOYSA-N 0.000 claims description 2
• YHEMNUWGXLMLDC-UHFFFAOYSA-N 3-(6-methoxypyridin-3-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=NC(OC)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 YHEMNUWGXLMLDC-UHFFFAOYSA-N 0.000 claims description 2
• HDWZWZSDSQKEFK-UHFFFAOYSA-N 3-[3-(dimethylamino)phenyl]-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CN(C)C1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 HDWZWZSDSQKEFK-UHFFFAOYSA-N 0.000 claims description 2
• TZPCJCUERYPQHQ-UHFFFAOYSA-N 3-[3-(methoxymethyl)phenyl]-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COCC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 TZPCJCUERYPQHQ-UHFFFAOYSA-N 0.000 claims description 2
• 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 2
• ITIJUGYBZDLPAG-UHFFFAOYSA-N 3-isoquinolin-5-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound N1=CC=C2C(C3=CSC=4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C3=4)=O)=CC=CC2=C1 ITIJUGYBZDLPAG-UHFFFAOYSA-N 0.000 claims description 2
• XGUYQFMFVOSCNY-UHFFFAOYSA-N 3-methyl-7-pyridin-4-yl-5-(2-quinolin-2-ylethyl)thieno[3,2-c]pyridin-4-one Chemical compound C=1N(CCC=2N=C3C=CC=CC3=CC=2)C(=O)C=2C(C)=CSC=2C=1C1=CC=NC=C1 XGUYQFMFVOSCNY-UHFFFAOYSA-N 0.000 claims description 2
• YAXLKDIIBKDITJ-UHFFFAOYSA-N 3-naphthalen-2-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC=CC2=CC(C3=CSC=4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C3=4)=O)=CC=C21 YAXLKDIIBKDITJ-UHFFFAOYSA-N 0.000 claims description 2
• VLBVRYOYJYGBAE-UHFFFAOYSA-N 3-phenyl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CC=CC=C1 VLBVRYOYJYGBAE-UHFFFAOYSA-N 0.000 claims description 2
• VPGCNSZZYKECJJ-UHFFFAOYSA-N 3-piperidin-4-yl-5-(2-quinolin-2-ylethyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1CCNCC1 VPGCNSZZYKECJJ-UHFFFAOYSA-N 0.000 claims description 2
• FKKFWPZJMQQYAB-UHFFFAOYSA-N 3-pyridazin-4-yl-5-(2-quinolin-2-ylcyclopropyl)furo[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2OC=C1C1=CC=NN=C1 FKKFWPZJMQQYAB-UHFFFAOYSA-N 0.000 claims description 2
• PZSUHIDQNAZRJU-UHFFFAOYSA-N 3-pyridazin-4-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CC=NN=C1 PZSUHIDQNAZRJU-UHFFFAOYSA-N 0.000 claims description 2
• AOKVZGMQMSKCEQ-UHFFFAOYSA-N 3-pyridin-3-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CC=CN=C1 AOKVZGMQMSKCEQ-UHFFFAOYSA-N 0.000 claims description 2
• BPFGZUCGZGHFRD-UHFFFAOYSA-N 3-pyridin-3-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CC=CN=C1 BPFGZUCGZGHFRD-UHFFFAOYSA-N 0.000 claims description 2
• QELJOMYMWSPTSR-UHFFFAOYSA-N 3-pyridin-3-yl-5-(2-thieno[3,2-b]pyridin-5-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CSC4=CC=3)C=CC=2SC=C1C1=CC=CN=C1 QELJOMYMWSPTSR-UHFFFAOYSA-N 0.000 claims description 2
• SKSQYABGUVJJEB-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-pyridin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound N1=CC=2SC=C(C=3C=CN=CC=3)C=2C(=O)N1CCC1=CC=CC=N1 SKSQYABGUVJJEB-UHFFFAOYSA-N 0.000 claims description 2
• MGRMNBJBPWQARR-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CC=NC=C1 MGRMNBJBPWQARR-UHFFFAOYSA-N 0.000 claims description 2
• QJXQBZZLXDICMT-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CC=NC=C1 QJXQBZZLXDICMT-UHFFFAOYSA-N 0.000 claims description 2
• ZLFDZSFURHBDLR-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-thieno[3,2-b]pyridin-5-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CSC4=CC=3)C=CC=2SC=C1C1=CC=NC=C1 ZLFDZSFURHBDLR-UHFFFAOYSA-N 0.000 claims description 2
• FWOVGPICLCXZHT-UKTHLTGXSA-N 3-pyridin-4-yl-5-[(e)-2-quinolin-2-ylethenyl]thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(\C=C\C=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CC=NC=C1 FWOVGPICLCXZHT-UKTHLTGXSA-N 0.000 claims description 2
• OIYGMNYTGALGEQ-UHFFFAOYSA-N 3-pyridin-4-yl-5-[2-(5,6,7,8-tetrahydroquinolin-2-yl)ethyl]thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4CCCCC4=CC=3)N=CC=2SC=C1C1=CC=NC=C1 OIYGMNYTGALGEQ-UHFFFAOYSA-N 0.000 claims description 2
• HSJUJKCRPYXEPU-UHFFFAOYSA-N 3-pyrimidin-5-yl-5-(2-quinolin-2-ylethyl)furo[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)C=CC=2OC=C1C1=CN=CN=C1 HSJUJKCRPYXEPU-UHFFFAOYSA-N 0.000 claims description 2
• JIRYNXNYQFOFAU-UHFFFAOYSA-N 3-pyrimidin-5-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CN=CN=C1 JIRYNXNYQFOFAU-UHFFFAOYSA-N 0.000 claims description 2
• HMECCLFCJDDNEH-UHFFFAOYSA-N 3-quinolin-3-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC=CC2=CC(C3=CSC=4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C3=4)=O)=CN=C21 HMECCLFCJDDNEH-UHFFFAOYSA-N 0.000 claims description 2
• IXXONYPEYIBQBU-UHFFFAOYSA-N 3-quinolin-5-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC=C2C(C3=CSC=4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C3=4)=O)=CC=CC2=N1 IXXONYPEYIBQBU-UHFFFAOYSA-N 0.000 claims description 2
• NVOZAEATMWXGLJ-UHFFFAOYSA-N 3-quinolin-6-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound N1=CC=CC2=CC(C3=CSC=4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C3=4)=O)=CC=C21 NVOZAEATMWXGLJ-UHFFFAOYSA-N 0.000 claims description 2
• ZBZBBGGENJZXQQ-UHFFFAOYSA-N 4-(oxetan-3-ylamino)-6-(2-quinolin-2-ylethyl)pyrido[2,3-d]pyridazin-5-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=NC=CC=1NC1COC1 ZBZBBGGENJZXQQ-UHFFFAOYSA-N 0.000 claims description 2
• 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
• 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 2
• SNDDOEOHYUBNTL-UHFFFAOYSA-N 4-morpholin-4-yl-6-(2-quinolin-2-ylethyl)pyrido[2,3-d]pyridazin-5-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=NC=CC=1N1CCOCC1 SNDDOEOHYUBNTL-UHFFFAOYSA-N 0.000 claims description 2
• JMHFKEWHJJGYTP-UHFFFAOYSA-N 4-pyridin-4-yl-6-(2-quinolin-2-ylcyclopropyl)pyrido[2,3-d]pyridazin-5-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)N=CC2=NC=CC=1C1=CC=NC=C1 JMHFKEWHJJGYTP-UHFFFAOYSA-N 0.000 claims description 2
• AZGBNIZGMABJEK-UHFFFAOYSA-N 4-pyridin-4-yl-6-(2-quinolin-2-ylethyl)pyrido[2,3-d]pyridazin-5-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=NC=CC=1C1=CC=NC=C1 AZGBNIZGMABJEK-UHFFFAOYSA-N 0.000 claims description 2
• WZSXORXZGIVIER-UHFFFAOYSA-N 5-(1,1-dioxo-1,4-thiazinan-4-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=C1N1CCS(=O)(=O)CC1 WZSXORXZGIVIER-UHFFFAOYSA-N 0.000 claims description 2
• MZZKQGOPXKBFIO-UHFFFAOYSA-N 5-(2-imidazo[1,2-a]pyridin-2-ylethyl)-3-pyridin-4-ylfuro[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CN4C=3)C=CC=2OC=C1C1=CC=NC=C1 MZZKQGOPXKBFIO-UHFFFAOYSA-N 0.000 claims description 2
• AGRKZDAWQAWXDN-UHFFFAOYSA-N 5-(2-indazol-1-ylethyl)-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCN3C4=CC=CC=C4C=N3)N=CC=2SC=C1C1=CC=NC=C1 AGRKZDAWQAWXDN-UHFFFAOYSA-N 0.000 claims description 2
• YKPOIRPJGYUVSM-UHFFFAOYSA-N 5-(2-pyrazin-2-ylethyl)-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound N1=CC=2SC=C(C=3C=CN=CC=3)C=2C(=O)N1CCC1=CN=CC=N1 YKPOIRPJGYUVSM-UHFFFAOYSA-N 0.000 claims description 2
• ATISANFQFYTXEY-UHFFFAOYSA-N 5-(2-quinolin-2-ylethyl)-3-(2,3,4-trifluorophenyl)thieno[2,3-d]pyridazin-4-one Chemical compound FC1=C(F)C(F)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 ATISANFQFYTXEY-UHFFFAOYSA-N 0.000 claims description 2
• WWMKQPOEEVFZBP-UHFFFAOYSA-N 5-(2-quinolin-2-ylethyl)-3-[2-(trifluoromethyl)phenyl]thieno[2,3-d]pyridazin-4-one Chemical compound FC(F)(F)C1=CC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 WWMKQPOEEVFZBP-UHFFFAOYSA-N 0.000 claims description 2
• JKSFRKPCZZEAHH-UHFFFAOYSA-N 5-(2-quinolin-2-ylethyl)-3-[4-(trifluoromethyl)phenyl]thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(C(F)(F)F)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 JKSFRKPCZZEAHH-UHFFFAOYSA-N 0.000 claims description 2
• OZUSTWWQMHVVOX-UHFFFAOYSA-N 5-(2-quinolin-2-ylethyl)-3-thiophen-2-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CC=CS1 OZUSTWWQMHVVOX-UHFFFAOYSA-N 0.000 claims description 2
• RWRGYTCBRXICLF-UHFFFAOYSA-N 5-(3-hydroxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound OC1=CC=CC(C=2C3=C(C(N(CCC=4N=C5C=CC=CC5=CC=4)N=C3)=O)C=CC=2)=C1 RWRGYTCBRXICLF-UHFFFAOYSA-N 0.000 claims description 2
• PLTVGJQELISXRT-XYOKQWHBSA-N 5-[(e)-2-(1,3-benzothiazol-2-yl)ethenyl]-3-pyridin-4-ylthieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(\C=C\C=3SC4=CC=CC=C4N=3)C=CC=2SC=C1C1=CC=NC=C1 PLTVGJQELISXRT-XYOKQWHBSA-N 0.000 claims description 2
• WUSHTKKHBFTHNQ-XYOKQWHBSA-N 5-[(e)-2-(3-methylquinolin-2-yl)ethenyl]-3-pyridin-4-ylthieno[3,2-c]pyridin-4-one Chemical compound CC1=CC2=CC=CC=C2N=C1\C=C\N(C(C=12)=O)C=CC=1SC=C2C1=CC=NC=C1 WUSHTKKHBFTHNQ-XYOKQWHBSA-N 0.000 claims description 2
• XOEVLTCSMYOOSC-XYOKQWHBSA-N 5-[(e)-2-(6-methoxyquinolin-2-yl)ethenyl]-3-pyridin-4-ylthieno[3,2-c]pyridin-4-one Chemical compound C1=CC2=CC(OC)=CC=C2N=C1\C=C\N(C(C=12)=O)C=CC=1SC=C2C1=CC=NC=C1 XOEVLTCSMYOOSC-XYOKQWHBSA-N 0.000 claims description 2
• LFVZXKCRLFXGPA-UHFFFAOYSA-N 5-[2-(1,5-naphthyridin-2-yl)ethyl]-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=NC4=CC=3)N=CC=2SC=C1C1=CC=NC=C1 LFVZXKCRLFXGPA-UHFFFAOYSA-N 0.000 claims description 2
• OPPVYQFCPBWYOL-UHFFFAOYSA-N 5-[2-(1h-benzimidazol-2-yl)ethyl]-3-pyridin-4-ylfuro[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3NC4=CC=CC=C4N=3)C=CC=2OC=C1C1=CC=NC=C1 OPPVYQFCPBWYOL-UHFFFAOYSA-N 0.000 claims description 2
• RYIZXDMCAXBLGG-UHFFFAOYSA-N 5-[2-(5-ethylpyridin-2-yl)ethyl]-3-pyridin-4-ylthieno[3,2-c]pyridin-4-one Chemical compound N1=CC(CC)=CC=C1CCN1C(=O)C(C(C=2C=CN=CC=2)=CS2)=C2C=C1 RYIZXDMCAXBLGG-UHFFFAOYSA-N 0.000 claims description 2
• RSAKLROOLZQYNB-UHFFFAOYSA-N 5-[2-(6-chloroquinolin-2-yl)ethyl]-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=CC2=CC(Cl)=CC=C2N=C1CCN(C(C=12)=O)N=CC=1SC=C2C1=CC=NC=C1 RSAKLROOLZQYNB-UHFFFAOYSA-N 0.000 claims description 2
• UMWVILFMSHQJHT-UHFFFAOYSA-N 5-[2-(6-chloroquinolin-2-yl)ethyl]-3-pyridin-4-ylthieno[3,2-c]pyridin-4-one Chemical compound C1=CC2=CC(Cl)=CC=C2N=C1CCN(C(C=12)=O)C=CC=1SC=C2C1=CC=NC=C1 UMWVILFMSHQJHT-UHFFFAOYSA-N 0.000 claims description 2
• XGUCJGKGBVWPPR-UHFFFAOYSA-N 5-[2-(6-fluoroquinolin-2-yl)ethyl]-3-pyridin-3-ylthieno[3,2-c]pyridin-4-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1CCN(C(C=12)=O)C=CC=1SC=C2C1=CC=CN=C1 XGUCJGKGBVWPPR-UHFFFAOYSA-N 0.000 claims description 2
• ZKZYHJUFYIHZIS-UHFFFAOYSA-N 5-morpholin-4-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=C1N1CCOCC1 ZKZYHJUFYIHZIS-UHFFFAOYSA-N 0.000 claims description 2
• MFGXCNXNPGFFGW-UHFFFAOYSA-N 5-pyridin-3-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=C1C1=CC=CN=C1 MFGXCNXNPGFFGW-UHFFFAOYSA-N 0.000 claims description 2
• XHIMEOLPDDADGU-UHFFFAOYSA-N 5-pyridin-4-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=C1C1=CC=NC=C1 XHIMEOLPDDADGU-UHFFFAOYSA-N 0.000 claims description 2
• BILLTUXMZNLKOD-UHFFFAOYSA-N 5-pyrimidin-5-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=C1C1=CN=CN=C1 BILLTUXMZNLKOD-UHFFFAOYSA-N 0.000 claims description 2
• DHLCTHXZKHGREA-UHFFFAOYSA-N 6h-pyrido[2,3-d]pyridazin-5-one Chemical compound C1=CC=C2C(=O)NN=CC2=N1 DHLCTHXZKHGREA-UHFFFAOYSA-N 0.000 claims description 2
• IKPPQKUZZDMBIY-UHFFFAOYSA-N 7-pyridin-4-yl-5-(2-quinolin-2-ylethyl)furo[3,2-c]pyridin-4-one Chemical compound C1=2OC=CC=2C(=O)N(CCC=2N=C3C=CC=CC3=CC=2)C=C1C1=CC=NC=C1 IKPPQKUZZDMBIY-UHFFFAOYSA-N 0.000 claims description 2
• YVBSOAHXHUBZBG-UHFFFAOYSA-N 7-pyridin-4-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2SC=CC=2C(=O)N(CCC=2N=C3C=CC=CC3=CC=2)N=C1C1=CC=NC=C1 YVBSOAHXHUBZBG-UHFFFAOYSA-N 0.000 claims description 2
• ANWMTJXMGCVPSL-UHFFFAOYSA-N 8-(1,1-dioxo-1,4-thiazinan-4-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1N1CCS(=O)(=O)CC1 ANWMTJXMGCVPSL-UHFFFAOYSA-N 0.000 claims description 2
• GYNDNUHIODKUEL-UHFFFAOYSA-N 8-(1,3-benzodioxol-5-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C2OCOC2=CC(C=2C=CC=C3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C=23)=O)=C1 GYNDNUHIODKUEL-UHFFFAOYSA-N 0.000 claims description 2
• CQKNFSSBFDPAIT-UHFFFAOYSA-N 8-(1-benzofuran-5-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C2OC=CC2=CC(C=2C=CC=C3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C=23)=O)=C1 CQKNFSSBFDPAIT-UHFFFAOYSA-N 0.000 claims description 2
• VVOQHEUMTCCHMM-UHFFFAOYSA-N 8-(1-methylpyrazol-4-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=NN(C)C=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 VVOQHEUMTCCHMM-UHFFFAOYSA-N 0.000 claims description 2
• QGFFXJRVGBXMJF-UHFFFAOYSA-N 8-(1h-indol-5-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C2NC=CC2=CC(C=2C=CC=C3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C=23)=O)=C1 QGFFXJRVGBXMJF-UHFFFAOYSA-N 0.000 claims description 2
• SKLJKIRYYKHHGJ-UHFFFAOYSA-N 8-(2,3,3a,4,6,6a-hexahydrofuro[2,3-c]pyrrol-5-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound N1=CC2=CC=CC(N3CC4OCCC4C3)=C2C(=O)N1CCC1=CN(C=CC=C2)C2=N1 SKLJKIRYYKHHGJ-UHFFFAOYSA-N 0.000 claims description 2
• HMVCKYIKOYKEAZ-UHFFFAOYSA-N 8-(2,3-difluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound FC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1F HMVCKYIKOYKEAZ-UHFFFAOYSA-N 0.000 claims description 2
• SZIBUDQVFZLYQL-UHFFFAOYSA-N 8-(2,4-dimethoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC(OC)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 SZIBUDQVFZLYQL-UHFFFAOYSA-N 0.000 claims description 2
• BNGIOLANESYJGX-UHFFFAOYSA-N 8-(2,5-difluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound FC1=CC=C(F)C(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 BNGIOLANESYJGX-UHFFFAOYSA-N 0.000 claims description 2
• GHCSQONACBFQCS-UHFFFAOYSA-N 8-(2,5-dimethoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC=C(OC)C(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 GHCSQONACBFQCS-UHFFFAOYSA-N 0.000 claims description 2
• PIJPDFOZENNOON-UHFFFAOYSA-N 8-(2-chlorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound ClC1=CC=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 PIJPDFOZENNOON-UHFFFAOYSA-N 0.000 claims description 2
• HDIMXYLZNNQPNS-UHFFFAOYSA-N 8-(2-ethylphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound CCC1=CC=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 HDIMXYLZNNQPNS-UHFFFAOYSA-N 0.000 claims description 2
• GWZUSCSPXHLREQ-UHFFFAOYSA-N 8-(2-fluoro-3-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1F GWZUSCSPXHLREQ-UHFFFAOYSA-N 0.000 claims description 2
• CRPXYLHFHXOXIA-UHFFFAOYSA-N 8-(2-fluoro-4-methylphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound FC1=CC(C)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 CRPXYLHFHXOXIA-UHFFFAOYSA-N 0.000 claims description 2
• HGDWZYBPOHRWEG-UHFFFAOYSA-N 8-(2-fluoro-5-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC=C(F)C(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 HGDWZYBPOHRWEG-UHFFFAOYSA-N 0.000 claims description 2
• YTLAMKCZSDOOMC-UHFFFAOYSA-N 8-(2-methylphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound CC1=CC=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 YTLAMKCZSDOOMC-UHFFFAOYSA-N 0.000 claims description 2
• JOJRFNRLHIGGAQ-UHFFFAOYSA-N 8-(2-methylpyridin-4-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=NC(C)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 JOJRFNRLHIGGAQ-UHFFFAOYSA-N 0.000 claims description 2
• QNISTLHNQGTRFO-UHFFFAOYSA-N 8-(3,4-difluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C(F)C(F)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 QNISTLHNQGTRFO-UHFFFAOYSA-N 0.000 claims description 2
• USEFFUABFNRNFQ-UHFFFAOYSA-N 8-(3,4-dihydro-2h-1,5-benzodioxepin-7-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound O1CCCOC2=CC(C=3C=CC=C4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C=34)=O)=CC=C21 USEFFUABFNRNFQ-UHFFFAOYSA-N 0.000 claims description 2
• BWEJHNZISLZJHX-UHFFFAOYSA-N 8-(3,4-dimethoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 BWEJHNZISLZJHX-UHFFFAOYSA-N 0.000 claims description 2
• DQVGRVRVQIFJIN-UHFFFAOYSA-N 8-(3,4-dimethylphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C(C)C(C)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 DQVGRVRVQIFJIN-UHFFFAOYSA-N 0.000 claims description 2
• YJUMMXDZZOGXIJ-UHFFFAOYSA-N 8-(3,5-dimethoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC(OC)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 YJUMMXDZZOGXIJ-UHFFFAOYSA-N 0.000 claims description 2
• USPNZGLIPIPHMG-UHFFFAOYSA-N 8-(3,5-dimethyl-1h-pyrazol-4-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound CC1=NNC(C)=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 USPNZGLIPIPHMG-UHFFFAOYSA-N 0.000 claims description 2
• GAWJYLBMHMKZTQ-UHFFFAOYSA-N 8-(3-chloro-4-fluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C(Cl)C(F)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 GAWJYLBMHMKZTQ-UHFFFAOYSA-N 0.000 claims description 2
• BFRDNLJBXSBZFE-UHFFFAOYSA-N 8-(3-fluoro-4-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C(F)C(OC)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 BFRDNLJBXSBZFE-UHFFFAOYSA-N 0.000 claims description 2
• ZWUJMPYIBCPCPW-UHFFFAOYSA-N 8-(3-fluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound FC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 ZWUJMPYIBCPCPW-UHFFFAOYSA-N 0.000 claims description 2
• ADWMCIGCCIDWOV-UHFFFAOYSA-N 8-(3-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 ADWMCIGCCIDWOV-UHFFFAOYSA-N 0.000 claims description 2
• PWCXNISNHONFFV-UHFFFAOYSA-N 8-(3-methoxypiperidin-1-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1C(OC)CCCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 PWCXNISNHONFFV-UHFFFAOYSA-N 0.000 claims description 2
• YEAMKDJHJDLGSV-UHFFFAOYSA-N 8-(3-methylphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound CC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 YEAMKDJHJDLGSV-UHFFFAOYSA-N 0.000 claims description 2
• SSBGUENBVWTZDN-UHFFFAOYSA-N 8-(4,5-difluoro-2-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC(F)=C(F)C=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 SSBGUENBVWTZDN-UHFFFAOYSA-N 0.000 claims description 2
• AMRSVPSVBBXEHP-UHFFFAOYSA-N 8-(4-fluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC(F)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 AMRSVPSVBBXEHP-UHFFFAOYSA-N 0.000 claims description 2
• NHVDGQWAVIRLAB-UHFFFAOYSA-N 8-(4-hydroxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC(O)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 NHVDGQWAVIRLAB-UHFFFAOYSA-N 0.000 claims description 2
• OBLGCZAAFNWEEK-UHFFFAOYSA-N 8-(4-propan-2-ylphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC(C(C)C)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 OBLGCZAAFNWEEK-UHFFFAOYSA-N 0.000 claims description 2
• KGGSKYQXRPEXPF-UHFFFAOYSA-N 8-(5-fluoro-2-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC=C(F)C=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 KGGSKYQXRPEXPF-UHFFFAOYSA-N 0.000 claims description 2
• LXGJGIKPAZRBBH-UHFFFAOYSA-N 8-(5-fluoropyridin-3-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound FC1=CN=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 LXGJGIKPAZRBBH-UHFFFAOYSA-N 0.000 claims description 2
• RPAPNQNOVOQGHN-UHFFFAOYSA-N 8-(6-fluoropyridin-3-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=NC(F)=CC=C1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 RPAPNQNOVOQGHN-UHFFFAOYSA-N 0.000 claims description 2
• OCQOVHUDZAGSKS-UHFFFAOYSA-N 8-(6-methoxypyridin-3-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=NC(OC)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 OCQOVHUDZAGSKS-UHFFFAOYSA-N 0.000 claims description 2
• CRMLDRMUJSVAKJ-UHFFFAOYSA-N 8-(furan-3-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C=1C=COC=1 CRMLDRMUJSVAKJ-UHFFFAOYSA-N 0.000 claims description 2
• NBXHUSUIIANDCL-UHFFFAOYSA-N 8-(oxan-4-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1CCOCC1 NBXHUSUIIANDCL-UHFFFAOYSA-N 0.000 claims description 2
• HUWZHIQDPOGDRQ-UHFFFAOYSA-N 8-(piperidin-4-ylamino)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1NC1CCNCC1 HUWZHIQDPOGDRQ-UHFFFAOYSA-N 0.000 claims description 2
• VIQRKAXKNCTFIL-GOSISDBHSA-N 8-[(3r)-3-hydroxypiperidin-1-yl]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1[C@H](O)CCCN1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 VIQRKAXKNCTFIL-GOSISDBHSA-N 0.000 claims description 2
• MBZYXTRDGUBSIB-UHFFFAOYSA-N 8-[1-(2-methylpropyl)pyrazol-4-yl]-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=NN(CC(C)C)C=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 MBZYXTRDGUBSIB-UHFFFAOYSA-N 0.000 claims description 2
• GOKKCGWUSHZOSO-UHFFFAOYSA-N 8-[2-(3,4-difluorophenyl)morpholin-4-yl]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1=C(F)C(F)=CC=C1C1OCCN(C=2C=3C(=O)N(CCC=4N=C5C=CC=CN5C=4)N=CC=3C=CC=2)C1 GOKKCGWUSHZOSO-UHFFFAOYSA-N 0.000 claims description 2
• VBLCGBMNUHGMPA-UHFFFAOYSA-N 8-[3-(difluoromethyl)pyrrolidin-1-yl]-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1C(C(F)F)CCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 VBLCGBMNUHGMPA-UHFFFAOYSA-N 0.000 claims description 2
• VWJIBWOVEOCMLC-UHFFFAOYSA-N 8-naphthalen-2-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=CC2=CC(C=3C=CC=C4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C=34)=O)=CC=C21 VWJIBWOVEOCMLC-UHFFFAOYSA-N 0.000 claims description 2
• FFRMASCYWRZWMG-UHFFFAOYSA-N 8-pyridin-4-yl-2-(1-quinolin-2-ylpropan-2-yl)isoquinolin-1-one Chemical compound C=1C=C2C=CC=CC2=NC=1CC(C)N(C(C1=2)=O)C=CC1=CC=CC=2C1=CC=NC=C1 FFRMASCYWRZWMG-UHFFFAOYSA-N 0.000 claims description 2
• KEBSXAABDDVRNS-UHFFFAOYSA-N 8-pyridin-4-yl-2-(2-quinolin-2-ylethyl)isoquinolin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=CC=NC=C1 KEBSXAABDDVRNS-UHFFFAOYSA-N 0.000 claims description 2
• FXSVKGDGQZAEMN-UHFFFAOYSA-N 8-pyridin-4-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CC=NC=C1 FXSVKGDGQZAEMN-UHFFFAOYSA-N 0.000 claims description 2
• DSBQLIPPWLAUAO-RVDMUPIBSA-N 8-pyridin-4-yl-2-[(e)-2-quinazolin-2-ylethenyl]isoquinolin-1-one Chemical compound C=12C(=O)N(\C=C\C=3N=C4C=CC=CC4=CN=3)C=CC2=CC=CC=1C1=CC=NC=C1 DSBQLIPPWLAUAO-RVDMUPIBSA-N 0.000 claims description 2
• QTAYILSEAREWPM-NTCAYCPXSA-N 8-pyridin-4-yl-2-[(e)-2-quinolin-2-ylethenyl]phthalazin-1-one Chemical compound C=12C(=O)N(\C=C\C=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CC=NC=C1 QTAYILSEAREWPM-NTCAYCPXSA-N 0.000 claims description 2
• YKMDALRGEMWMID-UHFFFAOYSA-N 8-quinolin-3-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=CC2=CC(C=3C=CC=C4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C=34)=O)=CN=C21 YKMDALRGEMWMID-UHFFFAOYSA-N 0.000 claims description 2
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
• 101000609942 Dictyostelium discoideum cGMP-dependent 3',5'-cGMP phosphodiesterase A Proteins 0.000 claims description 2
• 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 2
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
• 125000003003 spiro group Chemical group 0.000 claims description 2
• YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 22
• 125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 claims 3
• HXFHTFGZTNXCET-UHFFFAOYSA-N 8-(3-fluoropyridin-4-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound FC1=CN=CC=C1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 HXFHTFGZTNXCET-UHFFFAOYSA-N 0.000 claims 2
• LGJTXRMGYFXHRE-HDJSMCDHSA-N 8-[(3s)-3-hydroxypiperidin-1-yl]-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1[C@@H](O)CCCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 LGJTXRMGYFXHRE-HDJSMCDHSA-N 0.000 claims 2
• KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical group [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 claims 2
• KGMRCSFKZMMGRS-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1,3-oxazol-2-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1=NC=CO1 KGMRCSFKZMMGRS-UHFFFAOYSA-N 0.000 claims 1
• IXMPEMSGOMZKGC-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1-methylpyrazol-3-yl)phthalazin-1-one Chemical compound CN1C=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CN5C=4)N=CC=3C=CC=2)=N1 IXMPEMSGOMZKGC-UHFFFAOYSA-N 0.000 claims 1
• QYDOEPJNJJZBJP-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxan-3-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1CCCOC1 QYDOEPJNJJZBJP-UHFFFAOYSA-N 0.000 claims 1
• CAJOMULDHTXCCJ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxan-4-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1CCOCC1 CAJOMULDHTXCCJ-UHFFFAOYSA-N 0.000 claims 1
• MFNGOWHRKORXFO-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxetan-3-ylmethylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NCC1COC1 MFNGOWHRKORXFO-UHFFFAOYSA-N 0.000 claims 1
• YGMWDYMNXOAZCG-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxolan-3-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1CCOC1 YGMWDYMNXOAZCG-UHFFFAOYSA-N 0.000 claims 1
• UJIVFCYJTRNPQW-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(piperidin-3-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1CCCNC1 UJIVFCYJTRNPQW-UHFFFAOYSA-N 0.000 claims 1
• ZTVMSECUCXZQCH-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(piperidin-4-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1CCNCC1 ZTVMSECUCXZQCH-UHFFFAOYSA-N 0.000 claims 1
• VQUXWBJKOCSWQH-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-[2-(trifluoromethyl)pyridin-4-yl]phthalazin-1-one Chemical compound C1=NC(C(F)(F)F)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CN5C=4)N=CC=3C=CC=2)=C1 VQUXWBJKOCSWQH-UHFFFAOYSA-N 0.000 claims 1
• WMKPAWNMKJMZSQ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-[methyl(oxetan-3-yl)amino]phthalazin-1-one Chemical compound C=1C=CC=2C=NN(CCC=3N=C4C=CC=CN4C=3)C(=O)C=2C=1N(C)C1COC1 WMKPAWNMKJMZSQ-UHFFFAOYSA-N 0.000 claims 1
• SDWQWDWHSDNWLU-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-piperidin-1-ylphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N1CCCCC1 SDWQWDWHSDNWLU-UHFFFAOYSA-N 0.000 claims 1
• ILBALRRYSDZQQD-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-piperidin-4-ylphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1CCNCC1 ILBALRRYSDZQQD-UHFFFAOYSA-N 0.000 claims 1
• CNYARIHSCWKDBT-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-pyrimidin-5-ylphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1=CN=CN=C1 CNYARIHSCWKDBT-UHFFFAOYSA-N 0.000 claims 1
• IDRPQGPZVKLIFY-UHFFFAOYSA-N 2-[2-(6-methoxypyridin-2-yl)ethyl]-8-pyridin-4-ylisoquinolin-1-one Chemical compound COC1=CC=CC(CCN2C(C3=C(C=4C=CN=CC=4)C=CC=C3C=C2)=O)=N1 IDRPQGPZVKLIFY-UHFFFAOYSA-N 0.000 claims 1
• 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
• SDOXLUOIIPDGMK-UHFFFAOYSA-N 3-(2,4-difluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound FC1=CC(F)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 SDOXLUOIIPDGMK-UHFFFAOYSA-N 0.000 claims 1
• HVDLBYARLPPWIF-UHFFFAOYSA-N 3-(2,4-dimethylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CC1=CC(C)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 HVDLBYARLPPWIF-UHFFFAOYSA-N 0.000 claims 1
• TWQSIYVSIGASMZ-UHFFFAOYSA-N 3-(2-chlorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound ClC1=CC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 TWQSIYVSIGASMZ-UHFFFAOYSA-N 0.000 claims 1
• XUPANYHEJOSCDA-UHFFFAOYSA-N 3-(2-ethylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CCC1=CC=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 XUPANYHEJOSCDA-UHFFFAOYSA-N 0.000 claims 1
• NMLZCHNXGCJDPI-UHFFFAOYSA-N 3-(2-fluoro-3-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1F NMLZCHNXGCJDPI-UHFFFAOYSA-N 0.000 claims 1
• FVHHUOKOJFNQHF-UHFFFAOYSA-N 3-(2-fluoro-5-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=C(F)C(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 FVHHUOKOJFNQHF-UHFFFAOYSA-N 0.000 claims 1
• IJVFXZRAODURBL-UHFFFAOYSA-N 3-(2-fluoropyridin-4-yl)-5-[2-(6-fluoroquinolin-2-yl)cyclopropyl]thieno[3,2-c]pyridin-4-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1C1CC1N(C(C=12)=O)C=CC=1SC=C2C1=CC=NC(F)=C1 IJVFXZRAODURBL-UHFFFAOYSA-N 0.000 claims 1
• MHRGRGWBBXZGIR-UHFFFAOYSA-N 3-(2-methylpyrazol-3-yl)-5-(2-quinolin-2-ylethyl)thieno[3,2-c]pyridin-4-one Chemical compound CN1N=CC=C1C1=CSC2=C1C(=O)N(CCC1=NC3=CC=CC=C3C=C1)C=C2 MHRGRGWBBXZGIR-UHFFFAOYSA-N 0.000 claims 1
• RFVNCAFZOXTBAU-UHFFFAOYSA-N 3-(3,5-dimethoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC(OC)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 RFVNCAFZOXTBAU-UHFFFAOYSA-N 0.000 claims 1
• HPXIBHJLBJHPKR-UHFFFAOYSA-N 3-(3,5-dimethyl-1,2-oxazol-4-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CC1=NOC(C)=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 HPXIBHJLBJHPKR-UHFFFAOYSA-N 0.000 claims 1
• MBGVVLXDXVCQGN-UHFFFAOYSA-N 3-(3-ethoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CCOC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 MBGVVLXDXVCQGN-UHFFFAOYSA-N 0.000 claims 1
• SSCOIHCJCLALID-UHFFFAOYSA-N 3-(3-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 SSCOIHCJCLALID-UHFFFAOYSA-N 0.000 claims 1
• JDGUULVDBSWWLL-UHFFFAOYSA-N 3-(5-methoxypyridin-3-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound COC1=CN=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 JDGUULVDBSWWLL-UHFFFAOYSA-N 0.000 claims 1
• XQUMGKVAAPDXJQ-UHFFFAOYSA-N 3-(6-fluoropyridin-3-yl)-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=NC(F)=CC=C1C1=CSC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 XQUMGKVAAPDXJQ-UHFFFAOYSA-N 0.000 claims 1
• CMDPRGIKUUDGPI-UHFFFAOYSA-N 3-(6-morpholin-4-ylpyridin-3-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C(C=N1)=CC=C1N1CCOCC1 CMDPRGIKUUDGPI-UHFFFAOYSA-N 0.000 claims 1
• ZDNPTHXSPSJNMQ-UHFFFAOYSA-N 3-(furan-3-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C=1C=COC=1 ZDNPTHXSPSJNMQ-UHFFFAOYSA-N 0.000 claims 1
• NHDWNERLXZJDOX-UHFFFAOYSA-N 3-isoquinolin-4-yl-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC=C2C(C3=CSC=4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C3=4)=O)=CN=CC2=C1 NHDWNERLXZJDOX-UHFFFAOYSA-N 0.000 claims 1
• JRECDFQWSARPCO-UHFFFAOYSA-N 3-morpholin-4-yl-5-(2-quinolin-2-ylethyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1N1CCOCC1 JRECDFQWSARPCO-UHFFFAOYSA-N 0.000 claims 1
• DESVUEMSTZOZEE-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-quinolin-2-ylethyl)furo[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)C=CC=2OC=C1C1=CC=NC=C1 DESVUEMSTZOZEE-UHFFFAOYSA-N 0.000 claims 1
• OTQVJTJWFXTDLK-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-thieno[3,2-b]pyridin-5-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CSC4=CC=3)N=CC=2SC=C1C1=CC=NC=C1 OTQVJTJWFXTDLK-UHFFFAOYSA-N 0.000 claims 1
• JHJQPTRQWWQDQJ-UHFFFAOYSA-N 4-bromo-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-pyridin-4-ylphthalazin-1-one Chemical compound C1=CC=C2C(Br)=NN(CCC=3N=C4C=CC=CN4C=3)C(=O)C2=C1C1=CC=NC=C1 JHJQPTRQWWQDQJ-UHFFFAOYSA-N 0.000 claims 1
• 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
• 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
• MRJYSRAHMFKHSB-UHFFFAOYSA-N 4-pyridin-3-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C12=CC=CC=C2C(=O)N(CCC=2N=C3C=CC=CC3=CC=2)N=C1C1=CC=CN=C1 MRJYSRAHMFKHSB-UHFFFAOYSA-N 0.000 claims 1
• MKPWXXGSRXDBMR-UHFFFAOYSA-N 5-(1,3,3a,4,6,6a-hexahydrofuro[3,4-c]pyrrol-5-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound N1=CC2=C(N3CC4COCC4C3)C=CC=C2C(=O)N1CCC1=CN(C=CC=C2)C2=N1 MKPWXXGSRXDBMR-UHFFFAOYSA-N 0.000 claims 1
• RIUPBWLBPKIHNC-UHFFFAOYSA-N 5-(2,2-difluoro-2-quinolin-2-ylethyl)-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C=1C=C2C=CC=CC2=NC=1C(F)(F)CN(C(C=12)=O)N=CC=1SC=C2C1=CC=NC=C1 RIUPBWLBPKIHNC-UHFFFAOYSA-N 0.000 claims 1
• AAPUOJXPNUDEGU-UHFFFAOYSA-N 5-(2-imidazo[1,2-a]pyridin-2-ylethyl)-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC=2SC=C1C1=CC=NC=C1 AAPUOJXPNUDEGU-UHFFFAOYSA-N 0.000 claims 1
• BHTXGQUUUWAGLV-UHFFFAOYSA-N 5-(2-imidazo[1,2-a]pyridin-2-ylethyl)-7-pyridin-3-yl-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=2SC=C(C=3C=CN=CC=3)C=2C(=O)N(CCC=2N=C3C=CC=CN3C=2)N=C1C1=CC=CN=C1 BHTXGQUUUWAGLV-UHFFFAOYSA-N 0.000 claims 1
• IRLXRKYHRIWIAT-UHFFFAOYSA-N 5-(2-quinolin-2-ylethyl)-3-(1,2,3,6-tetrahydropyridin-4-yl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CCNCC1 IRLXRKYHRIWIAT-UHFFFAOYSA-N 0.000 claims 1
• KQDJRRHPJRLMHO-YRNVUSSQSA-N 5-[(e)-2-(6-chloroquinolin-2-yl)ethenyl]-3-pyridin-4-ylthieno[3,2-c]pyridin-4-one Chemical compound C1=CC2=CC(Cl)=CC=C2N=C1\C=C\N(C(C=12)=O)C=CC=1SC=C2C1=CC=NC=C1 KQDJRRHPJRLMHO-YRNVUSSQSA-N 0.000 claims 1
• MJDDRKFLLPXAQN-UHFFFAOYSA-N 5-[2-(1h-benzimidazol-2-yl)ethyl]-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3NC4=CC=CC=C4N=3)N=CC=2SC=C1C1=CC=NC=C1 MJDDRKFLLPXAQN-UHFFFAOYSA-N 0.000 claims 1
• FQNWDYVYKPTBLY-UHFFFAOYSA-N 5-[2-(3,5-dimethylpyridin-2-yl)ethyl]-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound CC1=CC(C)=CN=C1CCN1C(=O)C(C(C=2C=CN=CC=2)=CS2)=C2C=N1 FQNWDYVYKPTBLY-UHFFFAOYSA-N 0.000 claims 1
• JHHLCWVSRJESDJ-UHFFFAOYSA-N 5-[2-(3-methylquinolin-2-yl)ethyl]-3-pyridin-4-ylthieno[3,2-c]pyridin-4-one Chemical compound CC1=CC2=CC=CC=C2N=C1CCN(C(C=12)=O)C=CC=1SC=C2C1=CC=NC=C1 JHHLCWVSRJESDJ-UHFFFAOYSA-N 0.000 claims 1
• FAFSADVWNGOAQV-UHFFFAOYSA-N 5-[2-(6-fluoroquinolin-2-yl)ethyl]-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1CCN(C(C=12)=O)N=CC=1SC=C2C1=CC=NC=C1 FAFSADVWNGOAQV-UHFFFAOYSA-N 0.000 claims 1
• SHDSPNVSPWZXQK-UHFFFAOYSA-N 5-[2-(benzimidazol-1-yl)ethyl]-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCN3C4=CC=CC=C4N=C3)N=CC=2SC=C1C1=CC=NC=C1 SHDSPNVSPWZXQK-UHFFFAOYSA-N 0.000 claims 1
• FYNCIYHECMWXPK-UHFFFAOYSA-N 5h-furo[3,2-c]pyridin-4-one Chemical compound O=C1NC=CC2=C1C=CO2 FYNCIYHECMWXPK-UHFFFAOYSA-N 0.000 claims 1
• DEBVRECAXOMUKB-UHFFFAOYSA-N 8-(1,3,3a,4,6,6a-hexahydrofuro[3,4-c]pyrrol-5-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=CC=CC2=NC(C3CC3N3C(C4=C(N5CC6COCC6C5)C=CC=C4C=C3)=O)=CC=C21 DEBVRECAXOMUKB-UHFFFAOYSA-N 0.000 claims 1
• LXVJRNOUEDUIIE-UHFFFAOYSA-N 8-(1-benzofuran-2-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=C2OC(C=3C=CC=C4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C=34)=O)=CC2=C1 LXVJRNOUEDUIIE-UHFFFAOYSA-N 0.000 claims 1
• WGBJQZVYZDTKIY-UHFFFAOYSA-N 8-(2,2-dimethylmorpholin-4-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1COC(C)(C)CN1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 WGBJQZVYZDTKIY-UHFFFAOYSA-N 0.000 claims 1
• SCXXDISADHSQQW-UHFFFAOYSA-N 8-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound O1CCOC2=CC(C=3C=CC=C4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C=34)=O)=CC=C21 SCXXDISADHSQQW-UHFFFAOYSA-N 0.000 claims 1
• UTYZFWQHDODEQT-UHFFFAOYSA-N 8-(2,3-dihydro-1-benzofuran-5-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C2OCCC2=CC(C=2C=CC=C3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C=23)=O)=C1 UTYZFWQHDODEQT-UHFFFAOYSA-N 0.000 claims 1
• FUJSQVCEXWRUTI-UHFFFAOYSA-N 8-(2,6-dimethylmorpholin-4-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1C(C)OC(C)CN1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 FUJSQVCEXWRUTI-UHFFFAOYSA-N 0.000 claims 1
• AGCFZDDKWQPNRV-UHFFFAOYSA-N 8-(2,7-diazaspiro[4.4]nonan-2-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N(C1)CCC21CCNC2 AGCFZDDKWQPNRV-UHFFFAOYSA-N 0.000 claims 1
• UWYXBOUXFFBGDZ-UHFFFAOYSA-N 8-(2-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 UWYXBOUXFFBGDZ-UHFFFAOYSA-N 0.000 claims 1
• NJEOVZBHBJGJBT-UHFFFAOYSA-N 8-(2-methoxypyridin-3-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=NC=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 NJEOVZBHBJGJBT-UHFFFAOYSA-N 0.000 claims 1
• BHRLRJMCBKPDIT-UHFFFAOYSA-N 8-(2-methylpyrazol-3-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound CN1N=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 BHRLRJMCBKPDIT-UHFFFAOYSA-N 0.000 claims 1
• JIRCMBTUPSBKDM-UHFFFAOYSA-N 8-(3,5-difluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound FC1=CC(F)=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 JIRCMBTUPSBKDM-UHFFFAOYSA-N 0.000 claims 1
• DSQRBAZCKPKNNG-UHFFFAOYSA-N 8-(4-ethylphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC(CC)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 DSQRBAZCKPKNNG-UHFFFAOYSA-N 0.000 claims 1
• PASMGXRZNQPTIQ-UHFFFAOYSA-N 8-(4-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC(OC)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 PASMGXRZNQPTIQ-UHFFFAOYSA-N 0.000 claims 1
• YZNVYUPCDBYVDK-UHFFFAOYSA-N 8-(4-methylphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC(C)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 YZNVYUPCDBYVDK-UHFFFAOYSA-N 0.000 claims 1
• YFCSELPIEXZQJO-UHFFFAOYSA-N 8-(5-fluoropyridin-3-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound FC1=CN=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CN5C=4)N=CC=3C=CC=2)=C1 YFCSELPIEXZQJO-UHFFFAOYSA-N 0.000 claims 1
• TYLSRGVVYMTMQL-UHFFFAOYSA-N 8-[(1-acetylpiperidin-3-yl)amino]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1N(C(=O)C)CCCC1NC1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 TYLSRGVVYMTMQL-UHFFFAOYSA-N 0.000 claims 1
• WYHULGFAYFYQOK-UHFFFAOYSA-N 8-[(1-acetylpiperidin-4-yl)amino]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1CN(C(=O)C)CCC1NC1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 WYHULGFAYFYQOK-UHFFFAOYSA-N 0.000 claims 1
• OJWMESYCDJWTOA-FXELSEDVSA-N 8-[(1S,2R,6S,7R)-4,10-diazatricyclo[5.2.1.02,6]decan-10-yl]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound N1=CC2=CC=CC(N3[C@@H]4CC[C@H]3[C@H]3CNC[C@H]34)=C2C(=O)N1CCC1=CN(C=CC=C2)C2=N1 OJWMESYCDJWTOA-FXELSEDVSA-N 0.000 claims 1
• IJPREFCEFQXMFI-ROUUACIJSA-N 8-[(1s,4s)-2,5-diazabicyclo[2.2.1]heptan-2-yl]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC=CC2=NC(CCN3N=CC=4C=CC=C(C=4C3=O)N3C[C@]4(NC[C@]3([H])C4)[H])=CN21 IJPREFCEFQXMFI-ROUUACIJSA-N 0.000 claims 1
• SPDWRQMREDRMBU-FUHWJXTLSA-N 8-[(1s,5s)-3,6-diazabicyclo[3.2.0]heptan-3-yl]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound N1=CC2=CC=CC(N3C[C@H]4NC[C@H]4C3)=C2C(=O)N1CCC1=CN(C=CC=C2)C2=N1 SPDWRQMREDRMBU-FUHWJXTLSA-N 0.000 claims 1
• YNUMIMIPUOEQKI-UHFFFAOYSA-N 8-[2-(4-chlorophenyl)morpholin-4-yl]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1=CC(Cl)=CC=C1C1OCCN(C=2C=3C(=O)N(CCC=4N=C5C=CC=CN5C=4)N=CC=3C=CC=2)C1 YNUMIMIPUOEQKI-UHFFFAOYSA-N 0.000 claims 1
• GADWXTSPBAPGEO-UHFFFAOYSA-N 8-[4-(chloromethyl)-4-(hydroxymethyl)piperidin-1-yl]-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1CC(CO)(CCl)CCN1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 GADWXTSPBAPGEO-UHFFFAOYSA-N 0.000 claims 1
• GCFILDDIVOZJJL-UHFFFAOYSA-N 8-morpholin-4-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1N1CCOCC1 GCFILDDIVOZJJL-UHFFFAOYSA-N 0.000 claims 1
• SPOXUQKAORHVPZ-UHFFFAOYSA-N 8-phenyl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CC=CC=C1 SPOXUQKAORHVPZ-UHFFFAOYSA-N 0.000 claims 1
• QEGSAUPKYWNROX-UHFFFAOYSA-N 8-piperidin-4-yl-2-[2-(5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-2-yl)ethyl]phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4CCCCN4C=3)N=CC2=CC=CC=1C1CCNCC1 QEGSAUPKYWNROX-UHFFFAOYSA-N 0.000 claims 1
• LNUGJMVVSXZAIJ-UHFFFAOYSA-N 8-pyridin-4-yl-2-(2-quinolin-2-ylethyl)pyrido[3,4-d]pyridazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CN=CC=1C1=CC=NC=C1 LNUGJMVVSXZAIJ-UHFFFAOYSA-N 0.000 claims 1
• ARDQUSAPLNXNNB-UHFFFAOYSA-N 8-pyrimidin-5-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CN=CN=C1 ARDQUSAPLNXNNB-UHFFFAOYSA-N 0.000 claims 1
• 101100043731 Caenorhabditis elegans syx-3 gene Proteins 0.000 claims 1
• 101100535673 Drosophila melanogaster Syn gene Proteins 0.000 claims 1
• 101100368134 Mus musculus Syn1 gene Proteins 0.000 claims 1
• ZHYNEISCZBAWGN-UHFFFAOYSA-N N1=C(C=CC2=CC=CC=C12)C1C(C1)C1=CC=2C(NC=CC=2S1)=O Chemical compound N1=C(C=CC2=CC=CC=C12)C1C(C1)C1=CC=2C(NC=CC=2S1)=O ZHYNEISCZBAWGN-UHFFFAOYSA-N 0.000 claims 1
• 150000007942 carboxylates Chemical class 0.000 claims 1
• 208000015114 central nervous system disease Diseases 0.000 claims 1
• 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
• UFBBWLWUIISIPW-UHFFFAOYSA-N imidazo[2,1-b][1,3]thiazole Chemical compound C1=CSC2=NC=CN21 UFBBWLWUIISIPW-UHFFFAOYSA-N 0.000 claims 1
• LPQZERIRKRYGGM-UHFFFAOYSA-N tert-butyl pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCC1 LPQZERIRKRYGGM-UHFFFAOYSA-N 0.000 claims 1
• 239000003814 drug Substances 0.000 abstract description 40
• 150000001721 carbon Chemical group 0.000 abstract description 14
• 208000024891 symptom Diseases 0.000 abstract description 14
• 238000004519 manufacturing process Methods 0.000 abstract description 4
• 125000002619 bicyclic group Chemical group 0.000 abstract description 2
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
• 101150052500 cic-1 gene Proteins 0.000 abstract 1
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 70
• 208000035475 disorder Diseases 0.000 description 41
• 239000000203 mixture Substances 0.000 description 38
• 238000006243 chemical reaction Methods 0.000 description 33
• 101001072037 Homo sapiens cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A Proteins 0.000 description 28
• 102100036377 cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A Human genes 0.000 description 28
• 229940079593 drug Drugs 0.000 description 26
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical group CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 25
• 229910052805 deuterium Inorganic materials 0.000 description 22
• YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 21
• 230000005764 inhibitory process Effects 0.000 description 18
• 239000004480 active ingredient Substances 0.000 description 17
• 125000000753 cycloalkyl group Chemical group 0.000 description 16
• 238000011282 treatment Methods 0.000 description 15
• 229910001868 water Inorganic materials 0.000 description 15
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 14
• 239000000243 solution Substances 0.000 description 14
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 13
• 230000000694 effects Effects 0.000 description 13
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
• 239000002585 base Substances 0.000 description 12
• 201000010099 disease Diseases 0.000 description 12
• 229910052740 iodine Inorganic materials 0.000 description 12
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
• 238000003745 diagnosis Methods 0.000 description 11
• 235000019439 ethyl acetate Nutrition 0.000 description 11
• 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 10
• XQYZDYMELSJDRZ-UHFFFAOYSA-N papaverine Chemical compound C1=C(OC)C(OC)=CC=C1CC1=NC=CC2=CC(OC)=C(OC)C=C12 XQYZDYMELSJDRZ-UHFFFAOYSA-N 0.000 description 10
• 108010015742 Cytochrome P-450 Enzyme System Proteins 0.000 description 9
• 102000002004 Cytochrome P-450 Enzyme System Human genes 0.000 description 9
• 241000282414 Homo sapiens Species 0.000 description 9
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
• 125000000217 alkyl group Chemical group 0.000 description 9
• 208000011117 substance-related disease Diseases 0.000 description 9
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
• 229910000288 alkali metal carbonate Inorganic materials 0.000 description 8
• 150000008041 alkali metal carbonates Chemical class 0.000 description 8
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 8
• 229910052794 bromium Inorganic materials 0.000 description 8
• 125000003709 fluoroalkyl group Chemical group 0.000 description 8
• 239000004615 ingredient Substances 0.000 description 8
• 230000002503 metabolic effect Effects 0.000 description 8
• 239000000047 product Substances 0.000 description 8
• 108091006146 Channels Proteins 0.000 description 7
• 208000020401 Depressive disease Diseases 0.000 description 7
• KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 7
• 125000003545 alkoxy group Chemical group 0.000 description 7
• 125000002947 alkylene group Chemical group 0.000 description 7
• 230000006399 behavior Effects 0.000 description 7
• 239000003795 chemical substances by application Substances 0.000 description 7
• 230000000155 isotopic effect Effects 0.000 description 7
• 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 7
• 239000012074 organic phase Substances 0.000 description 7
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 7
• 230000002829 reductive effect Effects 0.000 description 7
• 125000006413 ring segment Chemical group 0.000 description 7
• 125000004174 2-benzimidazolyl group Chemical group [H]N1C(*)=NC2=C([H])C([H])=C([H])C([H])=C12 0.000 description 6
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 6
• 102000004190 Enzymes Human genes 0.000 description 6
• 108090000790 Enzymes Proteins 0.000 description 6
• 229940123773 Phosphodiesterase 10A inhibitor Drugs 0.000 description 6
• 239000004698 Polyethylene Substances 0.000 description 6
• 241000700159 Rattus Species 0.000 description 6
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
• 239000002253 acid Substances 0.000 description 6
• 210000004556 brain Anatomy 0.000 description 6
• 239000012267 brine Substances 0.000 description 6
• 230000006872 improvement Effects 0.000 description 6
• 239000000543 intermediate Substances 0.000 description 6
• 230000004060 metabolic process Effects 0.000 description 6
• JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 6
• 238000000746 purification Methods 0.000 description 6
• 239000011734 sodium Substances 0.000 description 6
• HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 6
• 239000007787 solid Substances 0.000 description 6
• 239000003981 vehicle Substances 0.000 description 6
• ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 5
• 229930008281 A03AD01 - Papaverine Natural products 0.000 description 5
• 241001465754 Metazoa Species 0.000 description 5
• 208000028017 Psychotic disease Diseases 0.000 description 5
• 229910052784 alkaline earth metal Inorganic materials 0.000 description 5
• 230000004075 alteration Effects 0.000 description 5
• 150000004649 carbonic acid derivatives Chemical class 0.000 description 5
• 125000004431 deuterium atom Chemical group 0.000 description 5
• 239000011630 iodine Substances 0.000 description 5
• 231100000252 nontoxic Toxicity 0.000 description 5
• 230000003000 nontoxic effect Effects 0.000 description 5
• 229960001789 papaverine Drugs 0.000 description 5
• 238000002360 preparation method Methods 0.000 description 5
• 230000008569 process Effects 0.000 description 5
• 230000004044 response Effects 0.000 description 5
• 239000003826 tablet Substances 0.000 description 5
• 230000001225 therapeutic effect Effects 0.000 description 5
• CYPYTURSJDMMMP-WVCUSYJESA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 CYPYTURSJDMMMP-WVCUSYJESA-N 0.000 description 4
• 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 4
• MPOYBFYHRQBZPM-UHFFFAOYSA-N 3h-pyridin-4-one Chemical compound O=C1CC=NC=C1 MPOYBFYHRQBZPM-UHFFFAOYSA-N 0.000 description 4
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
• MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
• 230000009471 action Effects 0.000 description 4
• 125000003342 alkenyl group Chemical group 0.000 description 4
• 125000003302 alkenyloxy group Chemical group 0.000 description 4
• 125000004183 alkoxy alkyl group Chemical group 0.000 description 4
• 125000004686 alkyl sulfanyl alkyl group Chemical group 0.000 description 4
• 125000004390 alkyl sulfonyl group Chemical group 0.000 description 4
• 150000001412 amines Chemical class 0.000 description 4
• 230000015572 biosynthetic process Effects 0.000 description 4
• RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 4
• 239000003054 catalyst Substances 0.000 description 4
• 238000004587 chromatography analysis Methods 0.000 description 4
• 238000009109 curative therapy Methods 0.000 description 4
• VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 description 4
• 239000003937 drug carrier Substances 0.000 description 4
• 125000001153 fluoro group Chemical group F* 0.000 description 4
• 238000009472 formulation Methods 0.000 description 4
• 238000001990 intravenous administration Methods 0.000 description 4
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
• ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 4
• 210000002569 neuron Anatomy 0.000 description 4
• 239000003921 oil Substances 0.000 description 4
• 235000019198 oils Nutrition 0.000 description 4
• 230000000144 pharmacologic effect Effects 0.000 description 4
• 238000011321 prophylaxis Methods 0.000 description 4
• 239000000377 silicon dioxide Substances 0.000 description 4
• 238000003786 synthesis reaction Methods 0.000 description 4
• FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
• LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 3
• ZOOGRGPOEVQQDX-UUOKFMHZSA-N 3',5'-cyclic GMP Chemical compound C([C@H]1O2)OP(O)(=O)O[C@H]1[C@@H](O)[C@@H]2N1C(N=C(NC2=O)N)=C2N=C1 ZOOGRGPOEVQQDX-UUOKFMHZSA-N 0.000 description 3
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
• YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
• 241000282412 Homo Species 0.000 description 3
• DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
• PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
• 229910052783 alkali metal Inorganic materials 0.000 description 3
• 125000005083 alkoxyalkoxy group Chemical group 0.000 description 3
• 125000004448 alkyl carbonyl group Chemical group 0.000 description 3
• 235000001014 amino acid Nutrition 0.000 description 3
• 150000001413 amino acids Chemical class 0.000 description 3
• 230000037396 body weight Effects 0.000 description 3
• FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 3
• 229910000024 caesium carbonate Inorganic materials 0.000 description 3
• 150000004657 carbamic acid derivatives Chemical class 0.000 description 3
• 235000013877 carbamide Nutrition 0.000 description 3
• 230000015556 catabolic process Effects 0.000 description 3
• 239000003153 chemical reaction reagent Substances 0.000 description 3
• 230000001149 cognitive effect Effects 0.000 description 3
• 230000000875 corresponding effect Effects 0.000 description 3
• 238000009826 distribution Methods 0.000 description 3
• 208000024732 dysthymic disease Diseases 0.000 description 3
• 238000001914 filtration Methods 0.000 description 3
• 239000007903 gelatin capsule Substances 0.000 description 3
• 125000001183 hydrocarbyl group Chemical group 0.000 description 3
• 208000013403 hyperactivity Diseases 0.000 description 3
• RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
• 239000007943 implant Substances 0.000 description 3
• 150000007529 inorganic bases Chemical class 0.000 description 3
• 238000007918 intramuscular administration Methods 0.000 description 3
• 239000002207 metabolite Substances 0.000 description 3
• 210000001589 microsome Anatomy 0.000 description 3
• 208000015238 neurotic disease Diseases 0.000 description 3
• 230000003647 oxidation Effects 0.000 description 3
• 238000007254 oxidation reaction Methods 0.000 description 3
• 229910052763 palladium Inorganic materials 0.000 description 3
• PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 3
• 239000000843 powder Substances 0.000 description 3
• 230000002265 prevention Effects 0.000 description 3
• 230000002285 radioactive effect Effects 0.000 description 3
• 239000011541 reaction mixture Substances 0.000 description 3
• 108020003175 receptors Proteins 0.000 description 3
• 102000005962 receptors Human genes 0.000 description 3
• 238000011160 research Methods 0.000 description 3
• 229910052938 sodium sulfate Inorganic materials 0.000 description 3
• 235000011152 sodium sulphate Nutrition 0.000 description 3
• 239000002904 solvent Substances 0.000 description 3
• 238000007920 subcutaneous administration Methods 0.000 description 3
• 239000011593 sulfur Substances 0.000 description 3
• 239000000725 suspension Substances 0.000 description 3
• LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 3
• 239000000080 wetting agent Substances 0.000 description 3
• 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 description 2
• AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 2
• 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 2
• YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-UHFFFAOYSA-N 0.000 description 2
• HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
• AVTACHRNMUXQIN-UHFFFAOYSA-N 2-[2-(6-fluoroquinolin-2-yl)cyclopropyl]-8-pyridin-3-ylisoquinolin-1-one Chemical compound C1=CC2=CC(F)=CC=C2N=C1C1CC1N(C(C1=2)=O)C=CC1=CC=CC=2C1=CC=CN=C1 AVTACHRNMUXQIN-UHFFFAOYSA-N 0.000 description 2
• VPDAGUVEZGEHJJ-UHFFFAOYSA-N 2-quinolin-2-ylethanol Chemical compound C1=CC=CC2=NC(CCO)=CC=C21 VPDAGUVEZGEHJJ-UHFFFAOYSA-N 0.000 description 2
• NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 2
• YFDQPCLLOLSBMJ-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-quinolin-2-ylcyclopropyl)furo[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2OC=C1C1=CC=NC=C1 YFDQPCLLOLSBMJ-UHFFFAOYSA-N 0.000 description 2
• ZUCWYTLCOZARHE-MVBMGLOESA-N 8-[(3r)-3-hydroxypyrrolidin-1-yl]-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1[C@H](O)CCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 ZUCWYTLCOZARHE-MVBMGLOESA-N 0.000 description 2
• 208000008811 Agoraphobia Diseases 0.000 description 2
• QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
• 239000004215 Carbon black (E152) Substances 0.000 description 2
• 206010012218 Delirium Diseases 0.000 description 2
• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
• 101100406515 Drosophila melanogaster orb2 gene Proteins 0.000 description 2
• ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 description 2
• DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
• 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 2
• LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 2
• FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
• KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 2
• FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
• SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
• 239000007832 Na2SO4 Substances 0.000 description 2
• 229910002666 PdCl2 Inorganic materials 0.000 description 2
• GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
• NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
• ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
• KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
• LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
• 241000283984 Rodentia Species 0.000 description 2
• 101100258025 Schizosaccharomyces pombe (strain 972 / ATCC 24843) shk1 gene Proteins 0.000 description 2
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
• YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
• 239000007983 Tris buffer Substances 0.000 description 2
• 238000010521 absorption reaction Methods 0.000 description 2
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
• 150000007513 acids Chemical class 0.000 description 2
• 230000004913 activation Effects 0.000 description 2
• 150000001342 alkaline earth metals Chemical class 0.000 description 2
• 150000004703 alkoxides Chemical class 0.000 description 2
• 125000004414 alkyl thio group Chemical group 0.000 description 2
• 150000001408 amides Chemical class 0.000 description 2
• 238000004458 analytical method Methods 0.000 description 2
• 239000000164 antipsychotic agent Substances 0.000 description 2
• 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 2
• 239000011230 binding agent Substances 0.000 description 2
• 230000033228 biological regulation Effects 0.000 description 2
• 208000028683 bipolar I disease Diseases 0.000 description 2
• 125000001246 bromo group Chemical group Br* 0.000 description 2
• 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
• 229960001948 caffeine Drugs 0.000 description 2
• VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 2
• 239000004202 carbamide Substances 0.000 description 2
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
• 229940082638 cardiac stimulant phosphodiesterase inhibitors Drugs 0.000 description 2
• 206010007776 catatonia Diseases 0.000 description 2
• 210000004027 cell Anatomy 0.000 description 2
• 238000000576 coating method Methods 0.000 description 2
• ZPUCINDJVBIVPJ-LJISPDSOSA-N cocaine Chemical compound O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1=CC=CC=C1 ZPUCINDJVBIVPJ-LJISPDSOSA-N 0.000 description 2
• 230000001143 conditioned effect Effects 0.000 description 2
• 230000001276 controlling effect Effects 0.000 description 2
• 238000005859 coupling reaction Methods 0.000 description 2
• 239000006071 cream Substances 0.000 description 2
• 125000004966 cyanoalkyl group Chemical group 0.000 description 2
• 125000000000 cycloalkoxy group Chemical group 0.000 description 2
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
• 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 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
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
• 238000005888 cyclopropanation reaction Methods 0.000 description 2
• 230000003247 decreasing effect Effects 0.000 description 2
• 230000006735 deficit Effects 0.000 description 2
• 238000006731 degradation reaction Methods 0.000 description 2
• 230000003111 delayed effect Effects 0.000 description 2
• 150000001975 deuterium Chemical group 0.000 description 2
• 238000011161 development Methods 0.000 description 2
• BABWHSBPEIVBBZ-UHFFFAOYSA-N diazete Chemical compound C1=CN=N1 BABWHSBPEIVBBZ-UHFFFAOYSA-N 0.000 description 2
• FAMRKDQNMBBFBR-BQYQJAHWSA-N diethyl azodicarboxylate Substances CCOC(=O)\N=N\C(=O)OCC FAMRKDQNMBBFBR-BQYQJAHWSA-N 0.000 description 2
• 239000002270 dispersing agent Substances 0.000 description 2
• IXTMWRCNAAVVAI-UHFFFAOYSA-N dofetilide Chemical compound C=1C=C(NS(C)(=O)=O)C=CC=1CCN(C)CCOC1=CC=C(NS(C)(=O)=O)C=C1 IXTMWRCNAAVVAI-UHFFFAOYSA-N 0.000 description 2
• 229960002994 dofetilide Drugs 0.000 description 2
• 229960003638 dopamine Drugs 0.000 description 2
• 230000008030 elimination Effects 0.000 description 2
• 238000003379 elimination reaction Methods 0.000 description 2
• 150000002148 esters Chemical class 0.000 description 2
• 230000029142 excretion Effects 0.000 description 2
• 235000019197 fats Nutrition 0.000 description 2
• 239000000945 filler Substances 0.000 description 2
• 239000000706 filtrate Substances 0.000 description 2
• 239000000796 flavoring agent Substances 0.000 description 2
• 235000019634 flavors Nutrition 0.000 description 2
• 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 description 2
• 235000003599 food sweetener Nutrition 0.000 description 2
• KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
• 239000008187 granular material Substances 0.000 description 2
• 150000008282 halocarbons Chemical class 0.000 description 2
• LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
• 230000036541 health Effects 0.000 description 2
• GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 2
• 229930195733 hydrocarbon Natural products 0.000 description 2
• 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
• NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 2
• 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 2
• 238000001727 in vivo Methods 0.000 description 2
• 238000010348 incorporation Methods 0.000 description 2
• 238000001802 infusion Methods 0.000 description 2
• 238000002347 injection Methods 0.000 description 2
• 239000007924 injection Substances 0.000 description 2
• 230000003993 interaction Effects 0.000 description 2
• 238000007912 intraperitoneal administration Methods 0.000 description 2
• PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
• 150000002500 ions Chemical class 0.000 description 2
• 230000000670 limiting effect Effects 0.000 description 2
• 229910052744 lithium Inorganic materials 0.000 description 2
• 239000011777 magnesium Substances 0.000 description 2
• 229910052749 magnesium Inorganic materials 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
• 208000024714 major depressive disease Diseases 0.000 description 2
• NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
• 230000001404 mediated effect Effects 0.000 description 2
• 230000037353 metabolic pathway Effects 0.000 description 2
• HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 description 2
• LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
• 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
• 150000007522 mineralic acids Chemical class 0.000 description 2
• 238000002156 mixing Methods 0.000 description 2
• 239000002674 ointment Substances 0.000 description 2
• 150000007524 organic acids Chemical class 0.000 description 2
• 150000007530 organic bases Chemical class 0.000 description 2
• 239000003960 organic solvent Substances 0.000 description 2
• 229950010883 phencyclidine Drugs 0.000 description 2
• 239000002571 phosphodiesterase inhibitor Substances 0.000 description 2
• 229920001223 polyethylene glycol Polymers 0.000 description 2
• 239000011591 potassium Substances 0.000 description 2
• 229910052700 potassium Inorganic materials 0.000 description 2
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
• 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 2
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 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
• 235000018102 proteins Nutrition 0.000 description 2
• 108090000623 proteins and genes Proteins 0.000 description 2
• 102000004169 proteins and genes Human genes 0.000 description 2
• NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical compound OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 description 2
• 239000002994 raw material Substances 0.000 description 2
• 230000009467 reduction Effects 0.000 description 2
• 239000011347 resin Substances 0.000 description 2
• 229920005989 resin Polymers 0.000 description 2
• 229930195734 saturated hydrocarbon Natural products 0.000 description 2
• 239000000741 silica gel Substances 0.000 description 2
• 229910002027 silica gel Inorganic materials 0.000 description 2
• 229910052708 sodium Inorganic materials 0.000 description 2
• 239000012453 solvate Substances 0.000 description 2
• 241000894007 species Species 0.000 description 2
• 239000003381 stabilizer Substances 0.000 description 2
• 239000007858 starting material Substances 0.000 description 2
• 201000009032 substance abuse Diseases 0.000 description 2
• 231100000736 substance abuse Toxicity 0.000 description 2
• 125000004434 sulfur atom Chemical group 0.000 description 2
• 239000000829 suppository Substances 0.000 description 2
• 239000000375 suspending agent Substances 0.000 description 2
• 239000003765 sweetening agent Substances 0.000 description 2
• 210000001519 tissue Anatomy 0.000 description 2
• 230000000699 topical effect Effects 0.000 description 2
• 231100000331 toxic Toxicity 0.000 description 2
• 230000002588 toxic effect Effects 0.000 description 2
• 230000002110 toxicologic effect Effects 0.000 description 2
• 231100000027 toxicology Toxicity 0.000 description 2
• 230000009466 transformation Effects 0.000 description 2
• 238000000844 transformation Methods 0.000 description 2
• GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
• RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
• 150000003672 ureas Chemical class 0.000 description 2
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
• UGOMMVLRQDMAQQ-UHFFFAOYSA-N xphos Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 UGOMMVLRQDMAQQ-UHFFFAOYSA-N 0.000 description 2
• 229910052727 yttrium Inorganic materials 0.000 description 2
• 239000011701 zinc Substances 0.000 description 2
• DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
• SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 description 1
• MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
• 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 1
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 1
• KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 description 1
• 125000001724 1,2,3-oxadiazol-4-yl group Chemical group [H]C1=C(*)N=NO1 0.000 description 1
• 125000004503 1,2,3-oxadiazol-5-yl group Chemical group O1N=NC=C1* 0.000 description 1
• 125000004512 1,2,3-thiadiazol-4-yl group Chemical group S1N=NC(=C1)* 0.000 description 1
• 125000001607 1,2,3-triazol-1-yl group Chemical group [*]N1N=NC([H])=C1[H] 0.000 description 1
• 125000001359 1,2,3-triazol-4-yl group Chemical group [H]N1N=NC([*])=C1[H] 0.000 description 1
• 125000001766 1,2,4-oxadiazol-3-yl group Chemical group [H]C1=NC(*)=NO1 0.000 description 1
• 125000004516 1,2,4-thiadiazol-5-yl group Chemical group S1N=CN=C1* 0.000 description 1
• 125000004509 1,3,4-oxadiazol-2-yl group Chemical group O1C(=NN=C1)* 0.000 description 1
• 125000004317 1,3,5-triazin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=N1 0.000 description 1
• YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
• OMIVCRYZSXDGAB-UHFFFAOYSA-N 1,4-butanediyl Chemical group [CH2]CC[CH2] OMIVCRYZSXDGAB-UHFFFAOYSA-N 0.000 description 1
• IBXMKLPFLZYRQZ-UHFFFAOYSA-N 1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].[Pd].C=1C=CC=CC=1C=CC(=O)C=CC1=CC=CC=C1 IBXMKLPFLZYRQZ-UHFFFAOYSA-N 0.000 description 1
• 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
• 125000006420 1-fluorocyclopropyl group Chemical group [H]C1([H])C([H])([H])C1(F)* 0.000 description 1
• HNEGJTWNOOWEMH-UHFFFAOYSA-N 1-fluoropropane Chemical group [CH2]CCF HNEGJTWNOOWEMH-UHFFFAOYSA-N 0.000 description 1
• 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 description 1
• 125000006019 1-methyl-1-propenyl group Chemical group 0.000 description 1
• 125000006021 1-methyl-2-propenyl group Chemical group 0.000 description 1
• 125000006017 1-propenyl group Chemical group 0.000 description 1
• 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 description 1
• 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 description 1
• MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 1
• VEUACMGMFIDCST-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-5-pyrimidin-5-ylphthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=C1C1=CN=CN=C1 VEUACMGMFIDCST-UHFFFAOYSA-N 0.000 description 1
• GOPOXQNQVLGYPW-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2-methylpyrimidin-5-yl)phthalazin-1-one Chemical compound C1=NC(C)=NC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 GOPOXQNQVLGYPW-UHFFFAOYSA-N 0.000 description 1
• GUGMALZEBFWGRM-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2-oxa-7-azaspiro[3.5]nonan-7-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N(CC1)CCC21COC2 GUGMALZEBFWGRM-UHFFFAOYSA-N 0.000 description 1
• NVDGEXVYORQXAV-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(3-methoxypyridin-4-yl)phthalazin-1-one Chemical compound COC1=CN=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 NVDGEXVYORQXAV-UHFFFAOYSA-N 0.000 description 1
• HZTFBULEZQUNSO-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(3-oxa-8-azabicyclo[3.2.1]octan-8-yl)phthalazin-1-one Chemical compound C1OCC2CCC1N2C(C=CC=C1C=N2)=C1C(=O)N2CCC1=CN(C=CC=C2)C2=N1 HZTFBULEZQUNSO-UHFFFAOYSA-N 0.000 description 1
• PWXUZKKXTLUZSF-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxolan-3-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1CCOC1 PWXUZKKXTLUZSF-UHFFFAOYSA-N 0.000 description 1
• YIXZIGNYQFLREH-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-[(1-methylazetidin-3-yl)amino]phthalazin-1-one Chemical compound C1N(C)CC1NC1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 YIXZIGNYQFLREH-UHFFFAOYSA-N 0.000 description 1
• YGMWDYMNXOAZCG-KRWDZBQOSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-[[(3s)-oxolan-3-yl]amino]phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N[C@H]1CCOC1 YGMWDYMNXOAZCG-KRWDZBQOSA-N 0.000 description 1
• XPJZDWHNPGTAOG-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-morpholin-4-ylphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N1CCOCC1 XPJZDWHNPGTAOG-UHFFFAOYSA-N 0.000 description 1
• CRHZLJYSERGJMO-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-pyridazin-4-ylphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1=CC=NN=C1 CRHZLJYSERGJMO-UHFFFAOYSA-N 0.000 description 1
• GRVGYMSXORAJPI-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-pyridin-3-yloxyphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1OC1=CC=CN=C1 GRVGYMSXORAJPI-UHFFFAOYSA-N 0.000 description 1
• YAKOTIWFALPZOJ-UHFFFAOYSA-N 2-(2-quinolin-2-ylethyl)-8-thiophen-2-ylphthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CC=CS1 YAKOTIWFALPZOJ-UHFFFAOYSA-N 0.000 description 1
• 125000000134 2-(methylsulfanyl)ethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])[*] 0.000 description 1
• MCDDLRLLWOQIHT-UHFFFAOYSA-N 2-[4-[4-oxo-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-3-yl]phenyl]acetonitrile Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CC=C(CC#N)C=C1 MCDDLRLLWOQIHT-UHFFFAOYSA-N 0.000 description 1
• MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 description 1
• GRWKNBPOGBTZMN-UHFFFAOYSA-N 2-benzyl-3-phenylpropane-1,2-diamine Chemical compound C=1C=CC=CC=1CC(N)(CN)CC1=CC=CC=C1 GRWKNBPOGBTZMN-UHFFFAOYSA-N 0.000 description 1
• QKJAZPHKNWSXDF-UHFFFAOYSA-N 2-bromoquinoline Chemical compound C1=CC=CC2=NC(Br)=CC=C21 QKJAZPHKNWSXDF-UHFFFAOYSA-N 0.000 description 1
• 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
• 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
• 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 1
• BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
• 229940013085 2-diethylaminoethanol Drugs 0.000 description 1
• GIMXWZYFIFOCBJ-UHFFFAOYSA-N 2-fluorobenzene-1,4-diol Chemical compound OC1=CC=C(O)C(F)=C1 GIMXWZYFIFOCBJ-UHFFFAOYSA-N 0.000 description 1
• 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
• YEDUAINPPJYDJZ-UHFFFAOYSA-N 2-hydroxybenzothiazole Chemical compound C1=CC=C2SC(O)=NC2=C1 YEDUAINPPJYDJZ-UHFFFAOYSA-N 0.000 description 1
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
• 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 1
• 125000006020 2-methyl-1-propenyl group Chemical group 0.000 description 1
• 125000006022 2-methyl-2-propenyl group Chemical group 0.000 description 1
• NNOSLZKFMRDJTM-UHFFFAOYSA-N 2-pyridin-4-ylphthalazin-1-one Chemical compound N1=CC2=CC=CC=C2C(=O)N1C1=CC=NC=C1 NNOSLZKFMRDJTM-UHFFFAOYSA-N 0.000 description 1
• 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 description 1
• ONTRQBLGZCFMEX-UHFFFAOYSA-N 2-thieno[3,2-b]pyridin-5-ylethanol Chemical compound OCCC1=CC=C2SC=CC2=N1 ONTRQBLGZCFMEX-UHFFFAOYSA-N 0.000 description 1
• JMTMSDXUXJISAY-UHFFFAOYSA-N 2H-benzotriazol-4-ol Chemical group OC1=CC=CC2=C1N=NN2 JMTMSDXUXJISAY-UHFFFAOYSA-N 0.000 description 1
• 125000004326 2H-pyran-2-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])(*)O1 0.000 description 1
• 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 description 1
• UMBMLDDVTGHFSQ-UHFFFAOYSA-N 3,7-dipyridin-4-yl-5-(2-pyridin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound N1=C(C=2C=CN=CC=2)C=2SC=C(C=3C=CN=CC=3)C=2C(=O)N1CCC1=CC=CC=N1 UMBMLDDVTGHFSQ-UHFFFAOYSA-N 0.000 description 1
• IHOIKIWAGBXMTK-UHFFFAOYSA-N 3-(1-methylindol-5-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC=CC2=NC(CCN3N=CC=4SC=C(C=4C3=O)C=3C=C4C=CN(C4=CC=3)C)=CC=C21 IHOIKIWAGBXMTK-UHFFFAOYSA-N 0.000 description 1
• HRAMAKGPDRKFFD-UHFFFAOYSA-N 3-(1h-pyrazol-5-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C=1C=CNN=1 HRAMAKGPDRKFFD-UHFFFAOYSA-N 0.000 description 1
• GWWYZNKLDFJASM-UHFFFAOYSA-N 3-(2,3-dihydro-1,4-benzodioxin-6-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound O1CCOC2=CC(C3=CSC=4C=NN(CCC=5N=C6C=CC=CC6=CC=5)C(C3=4)=O)=CC=C21 GWWYZNKLDFJASM-UHFFFAOYSA-N 0.000 description 1
• YCTIMOAODOWOEI-UHFFFAOYSA-N 3-(2-methoxypyrimidin-5-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=NC(OC)=NC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 YCTIMOAODOWOEI-UHFFFAOYSA-N 0.000 description 1
• LJSRZOPHTPAEEZ-UHFFFAOYSA-N 3-(2-methylpyrazol-3-yl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound CN1N=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 LJSRZOPHTPAEEZ-UHFFFAOYSA-N 0.000 description 1
• CIIOAWIXDWJHJF-UHFFFAOYSA-N 3-(2-oxo-1,3-dihydroindol-6-yl)-5-(2-quinolin-2-ylethyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=CC=CC2=NC(CCN3C=CC=4SC=C(C=4C3=O)C3=CC=C4CC(NC4=C3)=O)=CC=C21 CIIOAWIXDWJHJF-UHFFFAOYSA-N 0.000 description 1
• XIZJMWMNGPCFFF-UHFFFAOYSA-N 3-(3-fluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound FC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 XIZJMWMNGPCFFF-UHFFFAOYSA-N 0.000 description 1
• WVFAYBUSNQRFQL-UHFFFAOYSA-N 3-(3-hydroxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound OC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3SC=2)=C1 WVFAYBUSNQRFQL-UHFFFAOYSA-N 0.000 description 1
• YLUAVPASONNKNY-UHFFFAOYSA-N 3-(3-hydroxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[3,2-c]pyridin-4-one Chemical compound OC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)C=CC=3SC=2)=C1 YLUAVPASONNKNY-UHFFFAOYSA-N 0.000 description 1
• JCZJEAVBOXBNIM-UHFFFAOYSA-N 3-(3-methoxypyridin-4-yl)-5-(2-quinolin-2-ylethyl)thieno[3,2-c]pyridin-4-one Chemical compound COC1=CN=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)C=C2 JCZJEAVBOXBNIM-UHFFFAOYSA-N 0.000 description 1
• QLLGSNSIQMHGCH-UHFFFAOYSA-N 3-(4-ethylphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(CC)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 QLLGSNSIQMHGCH-UHFFFAOYSA-N 0.000 description 1
• HYVRQNWOIHSVIE-UHFFFAOYSA-N 3-(4-fluorophenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(F)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 HYVRQNWOIHSVIE-UHFFFAOYSA-N 0.000 description 1
• FWTSFAIGMJGHNF-UHFFFAOYSA-N 3-(4-hydroxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(O)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 FWTSFAIGMJGHNF-UHFFFAOYSA-N 0.000 description 1
• ZYKSSUUTHFODIP-UHFFFAOYSA-N 3-(4-methoxyphenyl)-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(OC)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 ZYKSSUUTHFODIP-UHFFFAOYSA-N 0.000 description 1
• FPQQSJJWHUJYPU-UHFFFAOYSA-N 3-(dimethylamino)propyliminomethylidene-ethylazanium;chloride Chemical compound Cl.CCN=C=NCCCN(C)C FPQQSJJWHUJYPU-UHFFFAOYSA-N 0.000 description 1
• NWYBBEUETPVNJY-UHFFFAOYSA-N 3-[4-(dimethylamino)phenyl]-5-(2-quinolin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=CC(N(C)C)=CC=C1C1=CSC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 NWYBBEUETPVNJY-UHFFFAOYSA-N 0.000 description 1
• 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
• QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
• 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 description 1
• XBGKDDYOBIDYGP-UHFFFAOYSA-N 3-morpholin-4-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1N1CCOCC1 XBGKDDYOBIDYGP-UHFFFAOYSA-N 0.000 description 1
• ZMDYNOAKXSXGDB-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-quinolin-2-ylethyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CC=NC=C1 ZMDYNOAKXSXGDB-UHFFFAOYSA-N 0.000 description 1
• LAZKBVHPUMNCNL-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-quinoxalin-2-ylethyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CC4=NC=3)N=CC=2SC=C1C1=CC=NC=C1 LAZKBVHPUMNCNL-UHFFFAOYSA-N 0.000 description 1
• BIZBRYQFLGWKRS-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-thieno[3,2-b]pyridin-5-ylcyclopropyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CSC4=CC=3)N=CC=2SC=C1C1=CC=NC=C1 BIZBRYQFLGWKRS-UHFFFAOYSA-N 0.000 description 1
• FVKSBWFXOSEBOR-UHFFFAOYSA-N 3-pyrimidin-5-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[2,3-d]pyridazin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)N=CC=2SC=C1C1=CN=CN=C1 FVKSBWFXOSEBOR-UHFFFAOYSA-N 0.000 description 1
• 125000001397 3-pyrrolyl group Chemical group [H]N1C([H])=C([*])C([H])=C1[H] 0.000 description 1
• 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 description 1
• CICPLKAJEGYYGM-UHFFFAOYSA-N 3h-pyridazin-4-one Chemical compound O=C1CN=NC=C1 CICPLKAJEGYYGM-UHFFFAOYSA-N 0.000 description 1
• RDIZZNVGOLUAFG-UHFFFAOYSA-N 4-(oxetan-3-yl)-1,1-dioxo-1,4-thiazinan-3-amine Chemical compound O1CC(C1)N1C(CS(CC1)(=O)=O)N RDIZZNVGOLUAFG-UHFFFAOYSA-N 0.000 description 1
• HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-UHFFFAOYSA-N 0.000 description 1
• 125000004860 4-ethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])C([H])([H])[H] 0.000 description 1
• SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
• 125000004315 4H-pyran-2-yl group Chemical group [H]C1=C([H])C([H])([H])C([H])=C(*)O1 0.000 description 1
• 125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
• ZYIHAXAZLQIEFK-UHFFFAOYSA-N 5-(2-imidazo[1,2-a]pyridin-2-ylethyl)-3-pyridin-3-ylthieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(CCC=3N=C4C=CC=CN4C=3)C=CC=2SC=C1C1=CC=CN=C1 ZYIHAXAZLQIEFK-UHFFFAOYSA-N 0.000 description 1
• ZYAHQJHDXMVUFO-UHFFFAOYSA-N 5-[2-(7-fluoroquinolin-2-yl)ethyl]-3-pyridin-4-ylthieno[2,3-d]pyridazin-4-one Chemical compound N=1C2=CC(F)=CC=C2C=CC=1CCN(C(C=12)=O)N=CC=1SC=C2C1=CC=NC=C1 ZYAHQJHDXMVUFO-UHFFFAOYSA-N 0.000 description 1
• 125000004938 5-pyridyl group Chemical group N1=CC=CC(=C1)* 0.000 description 1
• IVPQULUXGFANGE-UHFFFAOYSA-N 8-(1,1-dioxo-1,4-thiazinan-4-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N1CCS(=O)(=O)CC1 IVPQULUXGFANGE-UHFFFAOYSA-N 0.000 description 1
• VZVMSIYCOVYMAD-UHFFFAOYSA-N 8-(1,3,3a,4,6,6a-hexahydrofuro[3,4-c]pyrrol-5-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound N1=CC2=CC=CC(N3CC4COCC4C3)=C2C(=O)N1CCC1=CN(C=CC=C2)C2=N1 VZVMSIYCOVYMAD-UHFFFAOYSA-N 0.000 description 1
• MMRXOAWVKWYOFF-UHFFFAOYSA-N 8-(1h-indol-4-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CC=CC2=C1C=CN2 MMRXOAWVKWYOFF-UHFFFAOYSA-N 0.000 description 1
• NIANGUGNOKCGIX-UHFFFAOYSA-N 8-(1h-indol-6-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C1=C2C=CNC2=CC(C=2C=CC=C3C=NN(CCC=4N=C5C=CC=CC5=CC=4)C(C=23)=O)=C1 NIANGUGNOKCGIX-UHFFFAOYSA-N 0.000 description 1
• BMGJUJKGLPWRFY-UHFFFAOYSA-N 8-(2,3-dihydro-1,4-benzoxazin-4-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C1COC2=CC=CC=C2N1C(C=CC=C1C=N2)=C1C(=O)N2CCC1=CN(C=CC=C2)C2=N1 BMGJUJKGLPWRFY-UHFFFAOYSA-N 0.000 description 1
• INBIIFXPBZMYKQ-UHFFFAOYSA-N 8-(2,3-dihydrofuran-4-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=COCC1 INBIIFXPBZMYKQ-UHFFFAOYSA-N 0.000 description 1
• YNMBGCQXVBXWRV-UHFFFAOYSA-N 8-(2,7-diazaspiro[3.5]nonan-7-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N(CC1)CCC21CNC2 YNMBGCQXVBXWRV-UHFFFAOYSA-N 0.000 description 1
• LHTPZOZMDHLOLP-UHFFFAOYSA-N 8-(2-chloro-4-fluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound ClC1=CC(F)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 LHTPZOZMDHLOLP-UHFFFAOYSA-N 0.000 description 1
• GLTGKZUTXNYACM-UHFFFAOYSA-N 8-(2-fluorophenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound FC1=CC=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 GLTGKZUTXNYACM-UHFFFAOYSA-N 0.000 description 1
• FNOVBOOFIYVYLI-UHFFFAOYSA-N 8-(3-hydroxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound OC1=CC=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 FNOVBOOFIYVYLI-UHFFFAOYSA-N 0.000 description 1
• ZUDOREUYXPCAOS-UHFFFAOYSA-N 8-(4-fluoro-2-methoxyphenyl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CC(F)=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CC3=CC=1)N=C2 ZUDOREUYXPCAOS-UHFFFAOYSA-N 0.000 description 1
• WYIOMEWWIORQAU-UHFFFAOYSA-N 8-(4-methylpiperazin-1-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1CN(C)CCN1C1=CC=CC2=C1C(=O)N(C1C(C1)C=1N=C3C=CC=CC3=CC=1)C=C2 WYIOMEWWIORQAU-UHFFFAOYSA-N 0.000 description 1
• XBYIOBJIDZZOLI-UHFFFAOYSA-N 8-(5-methoxypyridin-3-yl)-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound COC1=CN=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CC5=CC=4)N=CC=3C=CC=2)=C1 XBYIOBJIDZZOLI-UHFFFAOYSA-N 0.000 description 1
• DIUVFUVAQLFMKK-UHFFFAOYSA-N 8-(furan-2-yl)-2-(2-imidazo[1,2-a]pyridin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1=CC=CO1 DIUVFUVAQLFMKK-UHFFFAOYSA-N 0.000 description 1
• UGZYEVNNJNSNHU-UHFFFAOYSA-N 8-pyridin-3-yl-2-(2-quinolin-2-ylethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CC=CN=C1 UGZYEVNNJNSNHU-UHFFFAOYSA-N 0.000 description 1
• 206010001497 Agitation Diseases 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
• 206010002859 Anxiety disorder due to a general medical condition Diseases 0.000 description 1
• 239000004475 Arginine Substances 0.000 description 1
• 208000021465 Brief psychotic disease Diseases 0.000 description 1
• 238000006443 Buchwald-Hartwig cross coupling reaction Methods 0.000 description 1
• COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 1
• DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 1
• OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
• BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
• 241000282472 Canis lupus familiaris Species 0.000 description 1
• 244000025254 Cannabis sativa Species 0.000 description 1
• 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
• 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
• 208000009132 Catalepsy Diseases 0.000 description 1
• RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
• 108010074922 Cytochrome P-450 CYP1A2 Proteins 0.000 description 1
• 102000008144 Cytochrome P-450 CYP1A2 Human genes 0.000 description 1
• 108010001237 Cytochrome P-450 CYP2D6 Proteins 0.000 description 1
• 208000009011 Cytochrome P-450 CYP3A Inhibitors Diseases 0.000 description 1
• 101150049660 DRD2 gene Proteins 0.000 description 1
• 101100296720 Dictyostelium discoideum Pde4 gene Proteins 0.000 description 1
• 101100135868 Dictyostelium discoideum pde3 gene Proteins 0.000 description 1
• 208000007590 Disorders of Excessive Somnolence Diseases 0.000 description 1
• 102000004980 Dopamine D2 Receptors Human genes 0.000 description 1
• 108090001111 Dopamine D2 Receptors Proteins 0.000 description 1
• 206010013654 Drug abuse Diseases 0.000 description 1
• PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
• CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
• WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
• 108010010803 Gelatin Proteins 0.000 description 1
• 208000011688 Generalised anxiety disease Diseases 0.000 description 1
• 239000004471 Glycine Substances 0.000 description 1
• 208000004547 Hallucinations Diseases 0.000 description 1
• XLYOFNOQVPJJNP-ZSJDYOACSA-N Heavy water Chemical compound [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
• 101001047090 Homo sapiens Potassium voltage-gated channel subfamily H member 2 Proteins 0.000 description 1
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
• 206010022998 Irritability Diseases 0.000 description 1
• QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
• ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
• HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
• KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
• COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-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
• WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
• 239000004472 Lysine Substances 0.000 description 1
• KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
• 238000006751 Mitsunobu reaction Methods 0.000 description 1
• 102000008109 Mixed Function Oxygenases Human genes 0.000 description 1
• 108010074633 Mixed Function Oxygenases Proteins 0.000 description 1
• 102000004868 N-Methyl-D-Aspartate Receptors Human genes 0.000 description 1
• 108090001041 N-Methyl-D-Aspartate Receptors Proteins 0.000 description 1
• UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
• HTLZVHNRZJPSMI-UHFFFAOYSA-N N-ethylpiperidine Chemical compound CCN1CCCCC1 HTLZVHNRZJPSMI-UHFFFAOYSA-N 0.000 description 1
• MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 description 1
• 208000021384 Obsessive-Compulsive disease Diseases 0.000 description 1
• 235000019502 Orange oil Nutrition 0.000 description 1
• 102000004316 Oxidoreductases Human genes 0.000 description 1
• 108090000854 Oxidoreductases Proteins 0.000 description 1
• 229910019142 PO4 Inorganic materials 0.000 description 1
• 206010034912 Phobia Diseases 0.000 description 1
• XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 1
• 101100082610 Plasmodium falciparum (isolate 3D7) PDEdelta gene Proteins 0.000 description 1
• 239000002202 Polyethylene glycol Substances 0.000 description 1
• 102100022807 Potassium voltage-gated channel subfamily H member 2 Human genes 0.000 description 1
• 208000001431 Psychomotor Agitation Diseases 0.000 description 1
• 206010037211 Psychomotor hyperactivity Diseases 0.000 description 1
• 206010061921 Psychotic disorder due to a general medical condition Diseases 0.000 description 1
• WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
• CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
• 208000020114 Schizophrenia and other psychotic disease Diseases 0.000 description 1
• 208000036750 Schizophrenia, residual type Diseases 0.000 description 1
• 229940124639 Selective inhibitor Drugs 0.000 description 1
• MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
• 208000019568 Shared Paranoid disease Diseases 0.000 description 1
• 208000028810 Shared psychotic disease Diseases 0.000 description 1
• 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
• 206010041250 Social phobia Diseases 0.000 description 1
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
• FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
• 229920002472 Starch Polymers 0.000 description 1
• 238000006619 Stille reaction Methods 0.000 description 1
• 229930006000 Sucrose Natural products 0.000 description 1
• 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 1
• 239000000150 Sympathomimetic Substances 0.000 description 1
• FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric Acid Chemical class [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
• 208000018452 Torsade de pointes Diseases 0.000 description 1
• 208000002363 Torsades de Pointes Diseases 0.000 description 1
• 208000031674 Traumatic Acute Stress disease Diseases 0.000 description 1
• 241000927721 Tritia Species 0.000 description 1
• 229910052770 Uranium Inorganic materials 0.000 description 1
• 206010047853 Waxy flexibility Diseases 0.000 description 1
• 238000007239 Wittig reaction Methods 0.000 description 1
• HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
• GRTJBNJOHNTQBO-UHFFFAOYSA-N [2-(2-diphenylphosphanylphenyl)phenyl]-diphenylphosphane Chemical group C1=CC=CC=C1P(C=1C(=CC=CC=1)C=1C(=CC=CC=1)P(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 GRTJBNJOHNTQBO-UHFFFAOYSA-N 0.000 description 1
• 239000013543 active substance Substances 0.000 description 1
• 230000001154 acute effect Effects 0.000 description 1
• 208000026345 acute stress disease Diseases 0.000 description 1
• 125000002252 acyl group Chemical group 0.000 description 1
• 239000000654 additive Substances 0.000 description 1
• 208000012826 adjustment disease Diseases 0.000 description 1
• 230000002411 adverse Effects 0.000 description 1
• 239000000443 aerosol Substances 0.000 description 1
• 230000002776 aggregation Effects 0.000 description 1
• 238000004220 aggregation Methods 0.000 description 1
• 238000013019 agitation Methods 0.000 description 1
• 235000004279 alanine Nutrition 0.000 description 1
• 125000001931 aliphatic group Chemical group 0.000 description 1
• 150000001340 alkali metals Chemical class 0.000 description 1
• 229910052782 aluminium Inorganic materials 0.000 description 1
• XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
• 229940025084 amphetamine Drugs 0.000 description 1
• 125000000129 anionic group Chemical group 0.000 description 1
• 208000022531 anorexia Diseases 0.000 description 1
• 230000008485 antagonism Effects 0.000 description 1
• 230000000561 anti-psychotic effect Effects 0.000 description 1
• 230000002421 anti-septic effect Effects 0.000 description 1
• 239000003963 antioxidant agent Substances 0.000 description 1
• 229940005529 antipsychotics Drugs 0.000 description 1
• 229940064004 antiseptic throat preparations Drugs 0.000 description 1
• 239000002249 anxiolytic agent Substances 0.000 description 1
• 230000000949 anxiolytic effect Effects 0.000 description 1
• 229940005530 anxiolytics Drugs 0.000 description 1
• VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 description 1
• 229960004046 apomorphine Drugs 0.000 description 1
• 238000013459 approach Methods 0.000 description 1
• 239000000010 aprotic solvent Substances 0.000 description 1
• 239000008346 aqueous phase Substances 0.000 description 1
• 239000007864 aqueous solution Substances 0.000 description 1
• 239000007900 aqueous suspension Substances 0.000 description 1
• ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
• 229960003121 arginine Drugs 0.000 description 1
• 125000003118 aryl group Chemical group 0.000 description 1
• 238000000889 atomisation Methods 0.000 description 1
• 208000025748 atypical depressive disease Diseases 0.000 description 1
• KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 1
• 125000005605 benzo group Chemical group 0.000 description 1
• 229940049706 benzodiazepine Drugs 0.000 description 1
• 125000003310 benzodiazepinyl group Chemical class N1N=C(C=CC2=C1C=CC=C2)* 0.000 description 1
• WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
• 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
• 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
• MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 description 1
• 229960003237 betaine Drugs 0.000 description 1
• 230000004071 biological effect Effects 0.000 description 1
• 208000022257 bipolar II disease Diseases 0.000 description 1
• 210000005013 brain tissue Anatomy 0.000 description 1
• OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 description 1
• 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 229910052792 caesium Inorganic materials 0.000 description 1
• TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
• 239000011575 calcium Substances 0.000 description 1
• 229910052791 calcium Inorganic materials 0.000 description 1
• 229910001424 calcium ion Inorganic materials 0.000 description 1
• 230000000711 cancerogenic effect Effects 0.000 description 1
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
• 231100000315 carcinogenic Toxicity 0.000 description 1
• 230000002903 catalepsic effect Effects 0.000 description 1
• 125000002091 cationic group Chemical group 0.000 description 1
• 210000001159 caudate nucleus Anatomy 0.000 description 1
• 239000001913 cellulose Substances 0.000 description 1
• 229920002678 cellulose Polymers 0.000 description 1
• 210000003169 central nervous system Anatomy 0.000 description 1
• 210000003793 centrosome Anatomy 0.000 description 1
• 230000008859 change Effects 0.000 description 1
• 239000002738 chelating agent Substances 0.000 description 1
• 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
• IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 1
• OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
• 229960001231 choline Drugs 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
• CCGSUNCLSOWKJO-UHFFFAOYSA-N cimetidine Chemical compound N#CNC(=N/C)\NCCSCC1=NC=N[C]1C CCGSUNCLSOWKJO-UHFFFAOYSA-N 0.000 description 1
• 229960001380 cimetidine Drugs 0.000 description 1
• 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 description 1
• 230000009194 climbing Effects 0.000 description 1
• 239000011248 coating agent Substances 0.000 description 1
• 229960003920 cocaine Drugs 0.000 description 1
• 229940110456 cocoa butter Drugs 0.000 description 1
• 235000019868 cocoa butter Nutrition 0.000 description 1
• 239000003086 colorant Substances 0.000 description 1
• 238000002648 combination therapy Methods 0.000 description 1
• 229940125782 compound 2 Drugs 0.000 description 1
• 229940126214 compound 3 Drugs 0.000 description 1
• 229940125898 compound 5 Drugs 0.000 description 1
• 230000001010 compromised effect Effects 0.000 description 1
• 230000003750 conditioning effect Effects 0.000 description 1
• 238000010276 construction Methods 0.000 description 1
• 238000007796 conventional method Methods 0.000 description 1
• 229910052802 copper Inorganic materials 0.000 description 1
• 239000010949 copper Substances 0.000 description 1
• 230000001054 cortical effect Effects 0.000 description 1
• 230000008878 coupling Effects 0.000 description 1
• 238000010168 coupling process Methods 0.000 description 1
• 239000013058 crude material Substances 0.000 description 1
• 239000012043 crude product Substances 0.000 description 1
• 239000013078 crystal Substances 0.000 description 1
• 125000004093 cyano group Chemical group *C#N 0.000 description 1
• WZHCOOQXZCIUNC-UHFFFAOYSA-N cyclandelate Chemical compound C1C(C)(C)CC(C)CC1OC(=O)C(O)C1=CC=CC=C1 WZHCOOQXZCIUNC-UHFFFAOYSA-N 0.000 description 1
• 150000004292 cyclic ethers Chemical class 0.000 description 1
• 125000000392 cycloalkenyl group Chemical group 0.000 description 1
• 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 1
• 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 description 1
• 125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 description 1
• ZBCKWHYWPLHBOK-UHFFFAOYSA-N cyclohexylphosphane Chemical compound PC1CCCCC1 ZBCKWHYWPLHBOK-UHFFFAOYSA-N 0.000 description 1
• NXQGGXCHGDYOHB-UHFFFAOYSA-L cyclopenta-1,4-dien-1-yl(diphenyl)phosphane;dichloropalladium;iron(2+) Chemical compound [Fe+2].Cl[Pd]Cl.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1.[CH-]1C=CC(P(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 NXQGGXCHGDYOHB-UHFFFAOYSA-L 0.000 description 1
• 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 description 1
• 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
• 208000026725 cyclothymic disease Diseases 0.000 description 1
• 210000000172 cytosol Anatomy 0.000 description 1
• 230000006378 damage Effects 0.000 description 1
• 206010061428 decreased appetite Diseases 0.000 description 1
• 239000002274 desiccant Substances 0.000 description 1
• 238000013461 design Methods 0.000 description 1
• 206010012601 diabetes mellitus Diseases 0.000 description 1
• 238000010586 diagram Methods 0.000 description 1
• HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
• 238000009792 diffusion process Methods 0.000 description 1
• 230000029087 digestion Effects 0.000 description 1
• 125000001070 dihydroindolyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
• 125000004611 dihydroisoindolyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 description 1
• 125000005045 dihydroisoquinolinyl group Chemical group C1(NC=CC2=CC=CC=C12)* 0.000 description 1
• 125000005044 dihydroquinolinyl group Chemical group N1(CC=CC2=CC=CC=C12)* 0.000 description 1
• 239000003085 diluting agent Substances 0.000 description 1
• 239000007884 disintegrant Substances 0.000 description 1
• 239000006185 dispersion Substances 0.000 description 1
• 238000006073 displacement reaction Methods 0.000 description 1
• 238000010494 dissociation reaction Methods 0.000 description 1
• 230000005593 dissociations Effects 0.000 description 1
• 239000002552 dosage form Substances 0.000 description 1
• 238000004980 dosimetry Methods 0.000 description 1
• 238000007876 drug discovery Methods 0.000 description 1
• 239000003480 eluent Substances 0.000 description 1
• 239000003995 emulsifying agent Substances 0.000 description 1
• 230000001804 emulsifying effect Effects 0.000 description 1
• 239000000839 emulsion Substances 0.000 description 1
• 230000002255 enzymatic effect Effects 0.000 description 1
• 238000006735 epoxidation reaction Methods 0.000 description 1
• 229960003276 erythromycin Drugs 0.000 description 1
• NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
• OQQYMAOGIWMABG-UHFFFAOYSA-N ethyl 2-quinolin-2-ylacetate Chemical compound C1=CC=CC2=NC(CC(=O)OCC)=CC=C21 OQQYMAOGIWMABG-UHFFFAOYSA-N 0.000 description 1
• PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 1
• FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 1
• 125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
• 238000002474 experimental method Methods 0.000 description 1
• RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 description 1
• 238000003818 flash chromatography Methods 0.000 description 1
• 239000012530 fluid Substances 0.000 description 1
• 125000001207 fluorophenyl group Chemical group 0.000 description 1
• 235000011087 fumaric acid Nutrition 0.000 description 1
• 210000001222 gaba-ergic neuron Anatomy 0.000 description 1
• 229960003692 gamma aminobutyric acid Drugs 0.000 description 1
• BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 1
• 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
• 239000000499 gel Substances 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
• 102000054767 gene variant Human genes 0.000 description 1
• 229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 1
• 208000029364 generalized anxiety disease Diseases 0.000 description 1
• 229960002442 glucosamine Drugs 0.000 description 1
• 235000015201 grapefruit juice Nutrition 0.000 description 1
• 150000003278 haem Chemical class 0.000 description 1
• 239000000380 hallucinogen Substances 0.000 description 1
• 150000002366 halogen compounds Chemical class 0.000 description 1
• 230000002140 halogenating effect Effects 0.000 description 1
• 229960003878 haloperidol Drugs 0.000 description 1
• 210000003494 hepatocyte Anatomy 0.000 description 1
• 125000006343 heptafluoro propyl group Chemical group 0.000 description 1
• 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 125000005842 heteroatom Chemical group 0.000 description 1
• 238000004128 high performance liquid chromatography Methods 0.000 description 1
• HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
• XGIHQYAWBCFNPY-AZOCGYLKSA-N hydrabamine Chemical compound C([C@@H]12)CC3=CC(C(C)C)=CC=C3[C@@]2(C)CCC[C@@]1(C)CNCCNC[C@@]1(C)[C@@H]2CCC3=CC(C(C)C)=CC=C3[C@@]2(C)CCC1 XGIHQYAWBCFNPY-AZOCGYLKSA-N 0.000 description 1
• 239000000416 hydrocolloid Substances 0.000 description 1
• 238000005984 hydrogenation reaction Methods 0.000 description 1
• 206010020765 hypersomnia Diseases 0.000 description 1
• 239000003326 hypnotic agent Substances 0.000 description 1
• 230000000147 hypnotic effect Effects 0.000 description 1
• UVNXNSUKKOLFBM-UHFFFAOYSA-N imidazo[2,1-b][1,3,4]thiadiazole Chemical compound N1=CSC2=NC=CN21 UVNXNSUKKOLFBM-UHFFFAOYSA-N 0.000 description 1
• 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 description 1
• 125000003037 imidazol-2-yl group Chemical group [H]N1C([*])=NC([H])=C1[H] 0.000 description 1
• 125000002140 imidazol-4-yl group Chemical group [H]N1C([H])=NC([*])=C1[H] 0.000 description 1
• 230000001771 impaired effect Effects 0.000 description 1
• 238000000338 in vitro Methods 0.000 description 1
• 206010021654 increased appetite Diseases 0.000 description 1
• 125000003114 inden-1-yl group Chemical group [H]C1=C([H])C([H])(*)C2=C([H])C([H])=C([H])C([H])=C12 0.000 description 1
• 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 description 1
• 229940060367 inert ingredients Drugs 0.000 description 1
• 206010022437 insomnia Diseases 0.000 description 1
• 239000003456 ion exchange resin Substances 0.000 description 1
• 229920003303 ion-exchange polymer Polymers 0.000 description 1
• 239000002085 irritant Substances 0.000 description 1
• 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
• JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
• 150000002537 isoquinolines Chemical class 0.000 description 1
• 125000001793 isothiazol-3-yl group Chemical group [H]C1=C([H])C(*)=NS1 0.000 description 1
• 125000004500 isothiazol-4-yl group Chemical group S1N=CC(=C1)* 0.000 description 1
• 125000004501 isothiazol-5-yl group Chemical group S1N=CC=C1* 0.000 description 1
• 125000004284 isoxazol-3-yl group Chemical group [H]C1=C([H])C(*)=NO1 0.000 description 1
• 125000004499 isoxazol-5-yl group Chemical group O1N=CC=C1* 0.000 description 1
• 238000002372 labelling Methods 0.000 description 1
• 150000003951 lactams Chemical class 0.000 description 1
• 239000008101 lactose Substances 0.000 description 1
• 239000003446 ligand Substances 0.000 description 1
• 150000002632 lipids Chemical class 0.000 description 1
• 239000002502 liposome Substances 0.000 description 1
• 239000011344 liquid material Substances 0.000 description 1
• XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
• 229910052808 lithium carbonate Inorganic materials 0.000 description 1
• 210000004185 liver Anatomy 0.000 description 1
• 230000033001 locomotion Effects 0.000 description 1
• 239000006210 lotion Substances 0.000 description 1
• 235000019359 magnesium stearate Nutrition 0.000 description 1
• 239000002075 main ingredient Substances 0.000 description 1
• 230000014759 maintenance of location Effects 0.000 description 1
• 239000003550 marker Substances 0.000 description 1
• 230000000873 masking effect Effects 0.000 description 1
• 238000005259 measurement Methods 0.000 description 1
• 230000010534 mechanism of action Effects 0.000 description 1
• 239000012907 medicinal substance Substances 0.000 description 1
• 201000003995 melancholia Diseases 0.000 description 1
• 108020004999 messenger RNA Proteins 0.000 description 1
• LULAYUGMBFYYEX-UHFFFAOYSA-N metachloroperbenzoic acid Natural products OC(=O)C1=CC=CC(Cl)=C1 LULAYUGMBFYYEX-UHFFFAOYSA-N 0.000 description 1
• 229910052751 metal Inorganic materials 0.000 description 1
• 239000002184 metal Substances 0.000 description 1
• TWEQNZZOOFKOER-UHFFFAOYSA-N methyl 3-aminothiophene-2-carboxylate Chemical compound COC(=O)C=1SC=CC=1N TWEQNZZOOFKOER-UHFFFAOYSA-N 0.000 description 1
• 239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
• 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
• 229960002216 methylparaben Drugs 0.000 description 1
• 239000003094 microcapsule Substances 0.000 description 1
• 239000002480 mineral oil Substances 0.000 description 1
• 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
• 125000006124 n-propyl sulfonyl group Chemical group 0.000 description 1
• 125000006252 n-propylcarbonyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C(*)=O 0.000 description 1
• 230000000926 neurological effect Effects 0.000 description 1
• 208000025319 neurotic depression Diseases 0.000 description 1
• 230000003472 neutralizing effect Effects 0.000 description 1
• 229960002715 nicotine Drugs 0.000 description 1
• SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
• 239000012299 nitrogen atmosphere Substances 0.000 description 1
• 125000005246 nonafluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
• 210000001009 nucleus accumben Anatomy 0.000 description 1
• 210000001010 olfactory tubercle Anatomy 0.000 description 1
• 229940127240 opiate Drugs 0.000 description 1
• 239000010502 orange oil Substances 0.000 description 1
• 150000002894 organic compounds Chemical class 0.000 description 1
• 150000004967 organic peroxy acids Chemical class 0.000 description 1
• AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
• 125000004287 oxazol-2-yl group Chemical group [H]C1=C([H])N=C(*)O1 0.000 description 1
• 125000003145 oxazol-4-yl group Chemical group O1C=NC(=C1)* 0.000 description 1
• 125000004304 oxazol-5-yl group Chemical group O1C=NC=C1* 0.000 description 1
• 239000007800 oxidant agent Substances 0.000 description 1
• YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
• 208000019906 panic disease Diseases 0.000 description 1
• 238000007911 parenteral administration Methods 0.000 description 1
• 230000037361 pathway Effects 0.000 description 1
• 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
• 239000003208 petroleum Substances 0.000 description 1
• 230000003285 pharmacodynamic effect Effects 0.000 description 1
• 239000012071 phase Substances 0.000 description 1
• DHHVAGZRUROJKS-UHFFFAOYSA-N phentermine Chemical compound CC(C)(N)CC1=CC=CC=C1 DHHVAGZRUROJKS-UHFFFAOYSA-N 0.000 description 1
• COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
• 208000019899 phobic disease Diseases 0.000 description 1
• 235000021317 phosphate Nutrition 0.000 description 1
• 150000003003 phosphines Chemical class 0.000 description 1
• 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
• 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
• LFSXCDWNBUNEEM-UHFFFAOYSA-N phthalazine Chemical class C1=NN=CC2=CC=CC=C21 LFSXCDWNBUNEEM-UHFFFAOYSA-N 0.000 description 1
• 230000000704 physical effect Effects 0.000 description 1
• 230000004962 physiological condition Effects 0.000 description 1
• 230000035790 physiological processes and functions Effects 0.000 description 1
• 239000000049 pigment Substances 0.000 description 1
• 125000004574 piperidin-2-yl group Chemical group N1C(CCCC1)* 0.000 description 1
• 125000004483 piperidin-3-yl group Chemical group N1CC(CCC1)* 0.000 description 1
• FSDNTQSJGHSJBG-UHFFFAOYSA-N piperidine-4-carbonitrile Chemical compound N#CC1CCNCC1 FSDNTQSJGHSJBG-UHFFFAOYSA-N 0.000 description 1
• IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
• 229920000768 polyamine Polymers 0.000 description 1
• 229920001296 polysiloxane Polymers 0.000 description 1
• 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
• 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
• 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
• 208000028173 post-traumatic stress disease Diseases 0.000 description 1
• 229910000027 potassium carbonate Inorganic materials 0.000 description 1
• 235000011181 potassium carbonates Nutrition 0.000 description 1
• 230000003389 potentiating effect Effects 0.000 description 1
• 238000002953 preparative HPLC Methods 0.000 description 1
• 238000009117 preventive therapy Methods 0.000 description 1
• 150000003141 primary amines Chemical class 0.000 description 1
• MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
• 229960004919 procaine Drugs 0.000 description 1
• 102000004196 processed proteins & peptides Human genes 0.000 description 1
• 108090000765 processed proteins & peptides Proteins 0.000 description 1
• 230000002035 prolonged effect Effects 0.000 description 1
• VVWRJUBEIPHGQF-MDZDMXLPSA-N propan-2-yl (ne)-n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)\N=N\C(=O)OC(C)C VVWRJUBEIPHGQF-MDZDMXLPSA-N 0.000 description 1
• VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 1
• SUVIGLJNEAMWEG-UHFFFAOYSA-N propane-1-thiol Chemical compound CCCS SUVIGLJNEAMWEG-UHFFFAOYSA-N 0.000 description 1
• KJRCEJOSASVSRA-UHFFFAOYSA-N propane-2-thiol Chemical compound CC(C)S KJRCEJOSASVSRA-UHFFFAOYSA-N 0.000 description 1
• 239000003380 propellant Substances 0.000 description 1
• 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
• 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
• 229960003415 propylparaben Drugs 0.000 description 1
• 150000003212 purines Chemical class 0.000 description 1
• 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 description 1
• 125000004289 pyrazol-3-yl group Chemical group [H]N1N=C(*)C([H])=C1[H] 0.000 description 1
• 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 description 1
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
• BEJXOECDIXUTLN-UHFFFAOYSA-N pyrido[2,3-c]pyridazine Chemical class N1=NC=CC2=CC=CN=C21 BEJXOECDIXUTLN-UHFFFAOYSA-N 0.000 description 1
• 229940107700 pyruvic acid Drugs 0.000 description 1
• 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
• 150000003246 quinazolines Chemical group 0.000 description 1
• 238000009790 rate-determining step (RDS) Methods 0.000 description 1
• 230000009257 reactivity Effects 0.000 description 1
• 229940044551 receptor antagonist Drugs 0.000 description 1
• 239000002464 receptor antagonist Substances 0.000 description 1
• 238000001953 recrystallisation Methods 0.000 description 1
• 230000000306 recurrent effect Effects 0.000 description 1
• 238000010992 reflux Methods 0.000 description 1
• 230000001105 regulatory effect Effects 0.000 description 1
• 230000033764 rhythmic process Effects 0.000 description 1
• 208000012672 seasonal affective disease Diseases 0.000 description 1
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
• 239000000932 sedative agent Substances 0.000 description 1
• 229940125723 sedative agent Drugs 0.000 description 1
• 239000012056 semi-solid material Substances 0.000 description 1
• 230000019491 signal transduction Effects 0.000 description 1
• 230000011664 signaling Effects 0.000 description 1
• 235000012239 silicon dioxide Nutrition 0.000 description 1
• 229910000029 sodium carbonate Inorganic materials 0.000 description 1
• 235000017550 sodium carbonate Nutrition 0.000 description 1
• 239000011343 solid material Substances 0.000 description 1
• 239000008247 solid mixture Substances 0.000 description 1
• 201000001716 specific phobia Diseases 0.000 description 1
• 239000008107 starch Substances 0.000 description 1
• 235000019698 starch Nutrition 0.000 description 1
• 238000003756 stirring Methods 0.000 description 1
• 201000006152 substance dependence Diseases 0.000 description 1
• 210000003523 substantia nigra Anatomy 0.000 description 1
• 238000006467 substitution reaction Methods 0.000 description 1
• 239000000758 substrate Substances 0.000 description 1
• 239000005720 sucrose Substances 0.000 description 1
• 238000005987 sulfurization reaction Methods 0.000 description 1
• 230000001629 suppression Effects 0.000 description 1
• 239000012730 sustained-release form Substances 0.000 description 1
• 230000001975 sympathomimetic effect Effects 0.000 description 1
• 229940064707 sympathomimetics Drugs 0.000 description 1
• 239000006188 syrup Substances 0.000 description 1
• 235000020357 syrup Nutrition 0.000 description 1
• 238000007910 systemic administration Methods 0.000 description 1
• 239000000454 talc Substances 0.000 description 1
• 229910052623 talc Inorganic materials 0.000 description 1
• 235000012222 talc Nutrition 0.000 description 1
• 235000002906 tartaric acid Nutrition 0.000 description 1
• UXAWXZDXVOYLII-UHFFFAOYSA-N tert-butyl 2,5-diazabicyclo[2.2.1]heptane-2-carboxylate Chemical compound C1C2N(C(=O)OC(C)(C)C)CC1NC2 UXAWXZDXVOYLII-UHFFFAOYSA-N 0.000 description 1
• 125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
• 125000004187 tetrahydropyran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
• 125000004297 tetrahydropyrrol-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])C1([H])* 0.000 description 1
• 125000004523 tetrazol-1-yl group Chemical group N1(N=NN=C1)* 0.000 description 1
• 125000004299 tetrazol-5-yl group Chemical group [H]N1N=NC(*)=N1 0.000 description 1
• 230000000542 thalamic effect Effects 0.000 description 1
• 229940126585 therapeutic drug Drugs 0.000 description 1
• 230000004797 therapeutic response Effects 0.000 description 1
• 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 description 1
• 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
• 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 description 1
• 239000002562 thickening agent Substances 0.000 description 1
• 229930192474 thiophene Natural products 0.000 description 1
• 238000011200 topical administration Methods 0.000 description 1
• 231100000419 toxicity Toxicity 0.000 description 1
• 230000001988 toxicity Effects 0.000 description 1
• 239000003053 toxin Substances 0.000 description 1
• 231100000765 toxin Toxicity 0.000 description 1
• 229910052723 transition metal Inorganic materials 0.000 description 1
• 150000003624 transition metals Chemical class 0.000 description 1
• TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
• 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
• 239000013638 trimer Substances 0.000 description 1
• YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
• LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
• COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
• BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 1
• 229960000281 trometamol Drugs 0.000 description 1
• 208000001072 type 2 diabetes mellitus Diseases 0.000 description 1
• DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 1
• 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
• 239000003039 volatile agent Substances 0.000 description 1
• 239000001993 wax Substances 0.000 description 1
• 208000016261 weight loss Diseases 0.000 description 1
• 230000004580 weight loss Effects 0.000 description 1
• 239000002676 xenobiotic agent Substances 0.000 description 1
• 229910052725 zinc Inorganic materials 0.000 description 1