KR102753110B1 - Bcl-2-관련된 데스 프로모터(bad) 인산화의 소분자 억제제 - Google Patents
Bcl-2-관련된 데스 프로모터(bad) 인산화의 소분자 억제제 Download PDFInfo
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- KR102753110B1 KR102753110B1 KR1020197034039A KR20197034039A KR102753110B1 KR 102753110 B1 KR102753110 B1 KR 102753110B1 KR 1020197034039 A KR1020197034039 A KR 1020197034039A KR 20197034039 A KR20197034039 A KR 20197034039A KR 102753110 B1 KR102753110 B1 KR 102753110B1
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- compound
- methyl
- piperazin
- dichlorophenyl
- cancer
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- 230000026731 phosphorylation Effects 0.000 title claims description 45
- 238000006366 phosphorylation reaction Methods 0.000 title claims description 45
- 102100021569 Apoptosis regulator Bcl-2 Human genes 0.000 title description 11
- 101000971171 Homo sapiens Apoptosis regulator Bcl-2 Proteins 0.000 title description 11
- 230000034994 death Effects 0.000 title description 5
- 239000003112 inhibitor Substances 0.000 title description 3
- 150000003384 small molecules Chemical class 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 114
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 81
- 201000011510 cancer Diseases 0.000 claims abstract description 58
- 239000000126 substance Substances 0.000 claims abstract description 44
- 206010061535 Ovarian neoplasm Diseases 0.000 claims abstract description 12
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims abstract description 12
- 206010014759 Endometrial neoplasm Diseases 0.000 claims abstract description 11
- 206010033128 Ovarian cancer Diseases 0.000 claims abstract description 11
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims abstract description 11
- 206010060862 Prostate cancer Diseases 0.000 claims abstract description 11
- 208000029742 colonic neoplasm Diseases 0.000 claims abstract description 11
- 208000014018 liver neoplasm Diseases 0.000 claims abstract description 11
- 206010006187 Breast cancer Diseases 0.000 claims abstract description 10
- 208000026310 Breast neoplasm Diseases 0.000 claims abstract description 10
- 206010009944 Colon cancer Diseases 0.000 claims abstract description 10
- 206010014733 Endometrial cancer Diseases 0.000 claims abstract description 10
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims abstract description 10
- 201000002528 pancreatic cancer Diseases 0.000 claims abstract description 10
- 208000008443 pancreatic carcinoma Diseases 0.000 claims abstract description 10
- 201000007270 liver cancer Diseases 0.000 claims abstract description 8
- IQLVMUSOSDGQHW-UHFFFAOYSA-N N-cyclopentyl-3-[[4-(2,3-dichlorophenyl)piperazin-1-yl]-(2-hydroxyphenyl)methyl]benzamide Chemical compound C1(CCCC1)NC(C1=CC(=CC=C1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=C(C(=CC=C1)Cl)Cl)=O IQLVMUSOSDGQHW-UHFFFAOYSA-N 0.000 claims description 98
- 125000003118 aryl group Chemical group 0.000 claims description 64
- 125000000217 alkyl group Chemical group 0.000 claims description 63
- 125000001072 heteroaryl group Chemical group 0.000 claims description 50
- 125000005843 halogen group Chemical group 0.000 claims description 39
- -1 NH 2 Chemical group 0.000 claims description 35
- 125000001424 substituent group Chemical group 0.000 claims description 34
- 229910052757 nitrogen Inorganic materials 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 20
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 20
- 125000005842 heteroatom Chemical group 0.000 claims description 17
- 229910052760 oxygen Inorganic materials 0.000 claims description 17
- 229910052717 sulfur Inorganic materials 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 16
- 239000012453 solvate Substances 0.000 claims description 16
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 14
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 10
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- QYTULDSCPQDUHU-UHFFFAOYSA-N 4-chloro-2-[(3-fluoro-4-phenylmethoxyphenyl)-[4-(4-methoxyphenyl)piperazin-1-yl]methyl]phenol Chemical compound C(C1=CC=CC=C1)OC1=C(C=C(C=C1)C(C1=C(C=CC(=C1)Cl)O)N1CCN(CC1)C1=CC=C(C=C1)OC)F QYTULDSCPQDUHU-UHFFFAOYSA-N 0.000 claims description 6
- ZVYWEULOTCSMDC-UHFFFAOYSA-N [4-[(2-hydroxyphenyl)-[4-(4-methoxyphenyl)piperazin-1-yl]methyl]phenyl]-piperidin-1-ylmethanone Chemical compound OC1=C(C=CC=C1)C(C1=CC=C(C=C1)C(=O)N1CCCCC1)N1CCN(CC1)C1=CC=C(C=C1)OC ZVYWEULOTCSMDC-UHFFFAOYSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000004193 piperazinyl group Chemical group 0.000 claims description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 5
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 5
- 125000003107 substituted aryl group Chemical group 0.000 claims description 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 4
- 229940125904 compound 1 Drugs 0.000 claims description 4
- 229940125773 compound 10 Drugs 0.000 claims description 4
- 229940125782 compound 2 Drugs 0.000 claims description 4
- 229940126214 compound 3 Drugs 0.000 claims description 4
- 229940125898 compound 5 Drugs 0.000 claims description 4
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 claims description 4
- 125000003386 piperidinyl group Chemical group 0.000 claims description 4
- 125000006413 ring segment Chemical group 0.000 claims description 4
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 3
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims description 3
- 238000006069 Suzuki reaction reaction Methods 0.000 claims description 3
- 125000001188 haloalkyl group Chemical group 0.000 claims description 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 3
- ASGMFNBUXDJWJJ-JLCFBVMHSA-N (1R,3R)-3-[[3-bromo-1-[4-(5-methyl-1,3,4-thiadiazol-2-yl)phenyl]pyrazolo[3,4-d]pyrimidin-6-yl]amino]-N,1-dimethylcyclopentane-1-carboxamide Chemical compound BrC1=NN(C2=NC(=NC=C21)N[C@H]1C[C@@](CC1)(C(=O)NC)C)C1=CC=C(C=C1)C=1SC(=NN=1)C ASGMFNBUXDJWJJ-JLCFBVMHSA-N 0.000 claims description 2
- UAOUIVVJBYDFKD-XKCDOFEDSA-N (1R,9R,10S,11R,12R,15S,18S,21R)-10,11,21-trihydroxy-8,8-dimethyl-14-methylidene-4-(prop-2-enylamino)-20-oxa-5-thia-3-azahexacyclo[9.7.2.112,15.01,9.02,6.012,18]henicosa-2(6),3-dien-13-one Chemical compound C([C@@H]1[C@@H](O)[C@@]23C(C1=C)=O)C[C@H]2[C@]12C(N=C(NCC=C)S4)=C4CC(C)(C)[C@H]1[C@H](O)[C@]3(O)OC2 UAOUIVVJBYDFKD-XKCDOFEDSA-N 0.000 claims description 2
- AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 claims description 2
- ABJSOROVZZKJGI-OCYUSGCXSA-N (1r,2r,4r)-2-(4-bromophenyl)-n-[(4-chlorophenyl)-(2-fluoropyridin-4-yl)methyl]-4-morpholin-4-ylcyclohexane-1-carboxamide Chemical compound C1=NC(F)=CC(C(NC(=O)[C@H]2[C@@H](C[C@@H](CC2)N2CCOCC2)C=2C=CC(Br)=CC=2)C=2C=CC(Cl)=CC=2)=C1 ABJSOROVZZKJGI-OCYUSGCXSA-N 0.000 claims description 2
- IUSARDYWEPUTPN-OZBXUNDUSA-N (2r)-n-[(2s,3r)-4-[[(4s)-6-(2,2-dimethylpropyl)spiro[3,4-dihydropyrano[2,3-b]pyridine-2,1'-cyclobutane]-4-yl]amino]-3-hydroxy-1-[3-(1,3-thiazol-2-yl)phenyl]butan-2-yl]-2-methoxypropanamide Chemical compound C([C@H](NC(=O)[C@@H](C)OC)[C@H](O)CN[C@@H]1C2=CC(CC(C)(C)C)=CN=C2OC2(CCC2)C1)C(C=1)=CC=CC=1C1=NC=CS1 IUSARDYWEPUTPN-OZBXUNDUSA-N 0.000 claims description 2
- YJLIKUSWRSEPSM-WGQQHEPDSA-N (2r,3r,4s,5r)-2-[6-amino-8-[(4-phenylphenyl)methylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1CNC1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O YJLIKUSWRSEPSM-WGQQHEPDSA-N 0.000 claims description 2
- STBLNCCBQMHSRC-BATDWUPUSA-N (2s)-n-[(3s,4s)-5-acetyl-7-cyano-4-methyl-1-[(2-methylnaphthalen-1-yl)methyl]-2-oxo-3,4-dihydro-1,5-benzodiazepin-3-yl]-2-(methylamino)propanamide Chemical compound O=C1[C@@H](NC(=O)[C@H](C)NC)[C@H](C)N(C(C)=O)C2=CC(C#N)=CC=C2N1CC1=C(C)C=CC2=CC=CC=C12 STBLNCCBQMHSRC-BATDWUPUSA-N 0.000 claims description 2
- IWZSHWBGHQBIML-ZGGLMWTQSA-N (3S,8S,10R,13S,14S,17S)-17-isoquinolin-7-yl-N,N,10,13-tetramethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-amine Chemical compound CN(C)[C@H]1CC[C@]2(C)C3CC[C@@]4(C)[C@@H](CC[C@@H]4c4ccc5ccncc5c4)[C@@H]3CC=C2C1 IWZSHWBGHQBIML-ZGGLMWTQSA-N 0.000 claims description 2
- UDQTXCHQKHIQMH-KYGLGHNPSA-N (3ar,5s,6s,7r,7ar)-5-(difluoromethyl)-2-(ethylamino)-5,6,7,7a-tetrahydro-3ah-pyrano[3,2-d][1,3]thiazole-6,7-diol Chemical compound S1C(NCC)=N[C@H]2[C@@H]1O[C@H](C(F)F)[C@@H](O)[C@@H]2O UDQTXCHQKHIQMH-KYGLGHNPSA-N 0.000 claims description 2
- HUWSZNZAROKDRZ-RRLWZMAJSA-N (3r,4r)-3-azaniumyl-5-[[(2s,3r)-1-[(2s)-2,3-dicarboxypyrrolidin-1-yl]-3-methyl-1-oxopentan-2-yl]amino]-5-oxo-4-sulfanylpentane-1-sulfonate Chemical compound OS(=O)(=O)CC[C@@H](N)[C@@H](S)C(=O)N[C@@H]([C@H](C)CC)C(=O)N1CCC(C(O)=O)[C@H]1C(O)=O HUWSZNZAROKDRZ-RRLWZMAJSA-N 0.000 claims description 2
- MPDDTAJMJCESGV-CTUHWIOQSA-M (3r,5r)-7-[2-(4-fluorophenyl)-5-[methyl-[(1r)-1-phenylethyl]carbamoyl]-4-propan-2-ylpyrazol-3-yl]-3,5-dihydroxyheptanoate Chemical compound C1([C@@H](C)N(C)C(=O)C2=NN(C(CC[C@@H](O)C[C@@H](O)CC([O-])=O)=C2C(C)C)C=2C=CC(F)=CC=2)=CC=CC=C1 MPDDTAJMJCESGV-CTUHWIOQSA-M 0.000 claims description 2
- MHSLDASSAFCCDO-UHFFFAOYSA-N 1-(5-tert-butyl-2-methylpyrazol-3-yl)-3-(4-pyridin-4-yloxyphenyl)urea Chemical compound CN1N=C(C(C)(C)C)C=C1NC(=O)NC(C=C1)=CC=C1OC1=CC=NC=C1 MHSLDASSAFCCDO-UHFFFAOYSA-N 0.000 claims description 2
- KQZLRWGGWXJPOS-NLFPWZOASA-N 1-[(1R)-1-(2,4-dichlorophenyl)ethyl]-6-[(4S,5R)-4-[(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]-5-methylcyclohexen-1-yl]pyrazolo[3,4-b]pyrazine-3-carbonitrile Chemical compound ClC1=C(C=CC(=C1)Cl)[C@@H](C)N1N=C(C=2C1=NC(=CN=2)C1=CC[C@@H]([C@@H](C1)C)N1[C@@H](CCC1)CO)C#N KQZLRWGGWXJPOS-NLFPWZOASA-N 0.000 claims description 2
- WZZBNLYBHUDSHF-DHLKQENFSA-N 1-[(3s,4s)-4-[8-(2-chloro-4-pyrimidin-2-yloxyphenyl)-7-fluoro-2-methylimidazo[4,5-c]quinolin-1-yl]-3-fluoropiperidin-1-yl]-2-hydroxyethanone Chemical compound CC1=NC2=CN=C3C=C(F)C(C=4C(=CC(OC=5N=CC=CN=5)=CC=4)Cl)=CC3=C2N1[C@H]1CCN(C(=O)CO)C[C@@H]1F WZZBNLYBHUDSHF-DHLKQENFSA-N 0.000 claims description 2
- ONBQEOIKXPHGMB-VBSBHUPXSA-N 1-[2-[(2s,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)propan-1-one Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1OC1=CC(O)=CC(O)=C1C(=O)CCC1=CC=C(O)C=C1 ONBQEOIKXPHGMB-VBSBHUPXSA-N 0.000 claims description 2
- LWZVCNVOTYWIHG-UHFFFAOYSA-N 2-[(2-chlorophenyl)-[4-(4-methoxyphenyl)piperazin-1-yl]methyl]phenol Chemical compound ClC1=C(C=CC=C1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=CC=C(C=C1)OC LWZVCNVOTYWIHG-UHFFFAOYSA-N 0.000 claims description 2
- LGRORZANKCYASS-UHFFFAOYSA-N 2-[(3-fluoro-4-phenylmethoxyphenyl)-[4-(4-methoxyphenyl)piperazin-1-yl]methyl]phenol Chemical compound C(C1=CC=CC=C1)OC1=C(C=C(C=C1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=CC=C(C=C1)OC)F LGRORZANKCYASS-UHFFFAOYSA-N 0.000 claims description 2
- LZVWKJVWFXFQPN-UHFFFAOYSA-N 2-[(3-methoxyphenyl)-[4-(4-methylphenyl)piperazin-1-yl]methyl]phenol Chemical compound COC=1C=C(C=CC=1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=CC=C(C=C1)C LZVWKJVWFXFQPN-UHFFFAOYSA-N 0.000 claims description 2
- ZOKWERMOMPTYTK-UHFFFAOYSA-N 2-[(4-chlorophenyl)-[4-(2,3-dichlorophenyl)piperazin-1-yl]methyl]phenol Chemical compound ClC1=CC=C(C=C1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=C(C(=CC=C1)Cl)Cl ZOKWERMOMPTYTK-UHFFFAOYSA-N 0.000 claims description 2
- ZMQCEKHZIGZVJA-UHFFFAOYSA-N 2-[(4-chlorophenyl)-[4-(4-chlorophenyl)piperazin-1-yl]methyl]phenol Chemical compound ClC1=CC=C(C=C1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=CC=C(C=C1)Cl ZMQCEKHZIGZVJA-UHFFFAOYSA-N 0.000 claims description 2
- TUQDYXHGTVCCDS-UHFFFAOYSA-N 2-[(4-chlorophenyl)-[4-(4-methylphenyl)piperazin-1-yl]methyl]phenol Chemical compound ClC1=CC=C(C=C1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=CC=C(C=C1)C TUQDYXHGTVCCDS-UHFFFAOYSA-N 0.000 claims description 2
- MKWZRSZJVRWNCP-UHFFFAOYSA-N 2-[(6-chloro-5-methylpyridin-3-yl)-[4-(2,3-dichlorophenyl)piperazin-1-yl]methyl]phenol Chemical compound ClC1=C(C=C(C=N1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=C(C(=CC=C1)Cl)Cl)C MKWZRSZJVRWNCP-UHFFFAOYSA-N 0.000 claims description 2
- FMKGJQHNYMWDFJ-CVEARBPZSA-N 2-[[4-(2,2-difluoropropoxy)pyrimidin-5-yl]methylamino]-4-[[(1R,4S)-4-hydroxy-3,3-dimethylcyclohexyl]amino]pyrimidine-5-carbonitrile Chemical compound FC(COC1=NC=NC=C1CNC1=NC=C(C(=N1)N[C@H]1CC([C@H](CC1)O)(C)C)C#N)(C)F FMKGJQHNYMWDFJ-CVEARBPZSA-N 0.000 claims description 2
- YIGQDYGEOKSEQA-UHFFFAOYSA-N 2-[[4-(2,3-dichlorophenyl)piperazin-1-yl]-(3-fluoro-4-phenylmethoxyphenyl)methyl]phenol Chemical compound C(C1=CC=CC=C1)OC1=C(C=C(C=C1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=C(C(=CC=C1)Cl)Cl)F YIGQDYGEOKSEQA-UHFFFAOYSA-N 0.000 claims description 2
- KOZQNLVEHAQHAZ-UHFFFAOYSA-N 2-[[4-(2,3-dichlorophenyl)piperazin-1-yl]-[4-(trifluoromethyl)phenyl]methyl]phenol Chemical compound ClC1=C(C=CC=C1Cl)N1CCN(CC1)C(C1=C(C=CC=C1)O)C1=CC=C(C=C1)C(F)(F)F KOZQNLVEHAQHAZ-UHFFFAOYSA-N 0.000 claims description 2
- PIMDFMSCLGZEJZ-UHFFFAOYSA-N 2-[[4-(2,3-dichlorophenyl)piperazin-1-yl]-naphthalen-1-ylmethyl]phenol Chemical compound ClC1=C(C=CC=C1Cl)N1CCN(CC1)C(C1=C(C=CC=C1)O)C1=CC=CC2=CC=CC=C12 PIMDFMSCLGZEJZ-UHFFFAOYSA-N 0.000 claims description 2
- BQLDEZCQUKBXEM-UHFFFAOYSA-N 2-[[4-(2,3-dichlorophenyl)piperazin-1-yl]-pyridin-3-ylmethyl]phenol Chemical compound ClC1=C(C=CC=C1Cl)N1CCN(CC1)C(C1=C(C=CC=C1)O)C=1C=NC=CC=1 BQLDEZCQUKBXEM-UHFFFAOYSA-N 0.000 claims description 2
- PHOXQDZFSWULCY-UHFFFAOYSA-N 2-[[4-(4-chlorophenyl)piperazin-1-yl]-(6-methylpyridin-3-yl)methyl]phenol Chemical compound ClC1=CC=C(C=C1)N1CCN(CC1)C(C1=C(C=CC=C1)O)C=1C=NC(=CC=1)C PHOXQDZFSWULCY-UHFFFAOYSA-N 0.000 claims description 2
- HSSHWNLCMCLBMN-UHFFFAOYSA-N 2-[[4-(4-methylphenyl)piperazin-1-yl]-(6-methylpyridin-3-yl)methyl]phenol Chemical compound CC1=CC=C(C=N1)C(C1=C(C=CC=C1)O)N1CCN(CC1)C1=CC=C(C=C1)C HSSHWNLCMCLBMN-UHFFFAOYSA-N 0.000 claims description 2
- FZVHKTDWQUQNDI-UHFFFAOYSA-N 2-[[4-(4-methylphenyl)piperazin-1-yl]-[4-(trifluoromethyl)phenyl]methyl]phenol Chemical compound C1(=CC=C(C=C1)N1CCN(CC1)C(C1=C(C=CC=C1)O)C1=CC=C(C=C1)C(F)(F)F)C FZVHKTDWQUQNDI-UHFFFAOYSA-N 0.000 claims description 2
- RINLWBRWBSDTOH-UHFFFAOYSA-N 2-[[4-(5,6-dichlorocyclohexa-1,5-dien-1-yl)piperazin-1-yl]-(2-fluoro-3-methylpyridin-4-yl)methyl]phenol Chemical compound ClC=1CCC=C(C=1Cl)N1CCN(CC1)C(C1=C(C=CC=C1)O)C1=C(C(=NC=C1)F)C RINLWBRWBSDTOH-UHFFFAOYSA-N 0.000 claims description 2
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- 239000000375 suspending agent Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
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- 210000004881 tumor cell Anatomy 0.000 description 1
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- 235000013311 vegetables Nutrition 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/53—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/096—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/155—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/20—Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/06—Peri-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Furan Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Management, Administration, Business Operations System, And Electronic Commerce (AREA)
- Professional, Industrial, Or Sporting Protective Garments (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1706162.3 | 2017-04-19 | ||
| GBGB1706162.3A GB201706162D0 (en) | 2017-04-19 | 2017-04-19 | Compounds |
| PCT/SG2018/050194 WO2018194520A1 (en) | 2017-04-19 | 2018-04-18 | Small molecule inhibitors of bcl-2-associated death promoter (bad) phosphorylation |
Publications (2)
| Publication Number | Publication Date |
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| KR20200029384A KR20200029384A (ko) | 2020-03-18 |
| KR102753110B1 true KR102753110B1 (ko) | 2025-01-09 |
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| EP (1) | EP3612518A4 (https=) |
| JP (1) | JP7423010B2 (https=) |
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| CN (1) | CN110719906B (https=) |
| AU (1) | AU2018256285B2 (https=) |
| CA (1) | CA3060939A1 (https=) |
| GB (1) | GB201706162D0 (https=) |
| IL (1) | IL270078B (https=) |
| MX (1) | MX2024000001A (https=) |
| SG (1) | SG11201909418WA (https=) |
| WO (1) | WO2018194520A1 (https=) |
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| GB201706162D0 (en) * | 2017-04-19 | 2017-05-31 | Nat Univ Singapore | Compounds |
| CN112481298A (zh) * | 2020-11-11 | 2021-03-12 | 清华-伯克利深圳学院筹备办公室 | 重组质粒及其应用 |
| CN115340527B (zh) * | 2021-05-13 | 2023-09-15 | 成都先导药物开发股份有限公司 | 一种bcl-xl抑制剂及其制备方法和用途 |
Citations (5)
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| JP2002518493A (ja) * | 1998-06-25 | 2002-06-25 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 3−アリール−ベンゾフラノンの製造方法 |
| JP2003505420A (ja) * | 1999-07-26 | 2003-02-12 | シェーリング コーポレイション | 咳を処置するのに使用するノシセプチンレセプタorl−1 |
| JP2007508350A (ja) * | 2003-10-15 | 2007-04-05 | イーエムテーエム ゲーエムベーハー | 異なる細胞に機能的に影響を及ぼし、免疫性疾患、炎症性疾患、神経疾患、およびその他の疾患を治療するための二重のアラニルアミノペプチダーゼおよびジペプチジルペプチダーゼivの阻害剤 |
| WO2010052448A2 (en) * | 2008-11-05 | 2010-05-14 | Ucb Pharma S.A. | Fused pyrazine derivatives as kinase inhibitors |
| US20130096133A1 (en) * | 2011-10-14 | 2013-04-18 | The Board of Trustees of the University lllinois | Procaspase-activating compounds and compositions |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8252832B2 (en) * | 2007-12-14 | 2012-08-28 | Novartis Ag | Kinesin inhibitors as cancer therapeutics |
| JP2017128541A (ja) * | 2016-01-21 | 2017-07-27 | 学校法人東京女子医科大学 | アポトーシス誘導剤 |
| GB201706162D0 (en) * | 2017-04-19 | 2017-05-31 | Nat Univ Singapore | Compounds |
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2017
- 2017-04-19 GB GBGB1706162.3A patent/GB201706162D0/en not_active Ceased
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2018
- 2018-04-18 EP EP18787822.8A patent/EP3612518A4/en active Pending
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- 2018-04-18 AU AU2018256285A patent/AU2018256285B2/en active Active
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- 2018-04-18 JP JP2020507978A patent/JP7423010B2/ja active Active
- 2018-04-18 US US16/605,630 patent/US11292773B2/en active Active
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| JP2003505420A (ja) * | 1999-07-26 | 2003-02-12 | シェーリング コーポレイション | 咳を処置するのに使用するノシセプチンレセプタorl−1 |
| JP2007508350A (ja) * | 2003-10-15 | 2007-04-05 | イーエムテーエム ゲーエムベーハー | 異なる細胞に機能的に影響を及ぼし、免疫性疾患、炎症性疾患、神経疾患、およびその他の疾患を治療するための二重のアラニルアミノペプチダーゼおよびジペプチジルペプチダーゼivの阻害剤 |
| WO2010052448A2 (en) * | 2008-11-05 | 2010-05-14 | Ucb Pharma S.A. | Fused pyrazine derivatives as kinase inhibitors |
| US20130096133A1 (en) * | 2011-10-14 | 2013-04-18 | The Board of Trustees of the University lllinois | Procaspase-activating compounds and compositions |
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Also Published As
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|---|---|
| WO2018194520A9 (en) | 2019-10-17 |
| IL270078B (en) | 2022-09-01 |
| US20200131139A1 (en) | 2020-04-30 |
| WO2018194520A1 (en) | 2018-10-25 |
| JP2020517745A (ja) | 2020-06-18 |
| EP3612518A1 (en) | 2020-02-26 |
| GB201706162D0 (en) | 2017-05-31 |
| JP7423010B2 (ja) | 2024-01-29 |
| CA3060939A1 (en) | 2018-10-25 |
| US11292773B2 (en) | 2022-04-05 |
| CN110719906A (zh) | 2020-01-21 |
| MX2024000001A (es) | 2024-02-20 |
| KR20200029384A (ko) | 2020-03-18 |
| AU2018256285B2 (en) | 2022-08-04 |
| RU2019135562A (ru) | 2021-05-19 |
| SG11201909418WA (en) | 2019-11-28 |
| AU2018256285A1 (en) | 2019-11-07 |
| CN110719906B (zh) | 2023-07-28 |
| IL270078A (https=) | 2019-12-31 |
| RU2019135562A3 (https=) | 2021-07-21 |
| BR112019022015A2 (pt) | 2020-05-12 |
| EP3612518A4 (en) | 2020-11-25 |
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