HRP20230086T1 - Inhibitori lizin specifične demetilaze-1 - Google Patents
Inhibitori lizin specifične demetilaze-1 Download PDFInfo
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- HRP20230086T1 HRP20230086T1 HRP20230086TT HRP20230086T HRP20230086T1 HR P20230086 T1 HRP20230086 T1 HR P20230086T1 HR P20230086T T HRP20230086T T HR P20230086TT HR P20230086 T HRP20230086 T HR P20230086T HR P20230086 T1 HRP20230086 T1 HR P20230086T1
- Authority
- HR
- Croatia
- Prior art keywords
- pyrimidin
- benzonitrile
- aminopiperidin
- fluorobenzonitrile
- pyridin
- Prior art date
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- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 title 1
- 239000004472 Lysine Substances 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 28
- 150000003839 salts Chemical class 0.000 claims 26
- 125000000623 heterocyclic group Chemical group 0.000 claims 12
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 150000002431 hydrogen Chemical class 0.000 claims 9
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 5
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 5
- 125000001072 heteroaryl group Chemical group 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 125000004452 carbocyclyl group Chemical group 0.000 claims 3
- -1 carbocyclylalkyloxy Chemical group 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- ANPYWBRCPZBYMQ-UHFFFAOYSA-N 4-[2-(1,2,3,3a,4,6,7,7a-octahydropyrrolo[3,2-c]pyridin-5-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound CC1=CC=C(C=C1)C=1C(=NC(=NC1)N1CC2C(CC1)NCC2)C2=CC=C(C#N)C=C2 ANPYWBRCPZBYMQ-UHFFFAOYSA-N 0.000 claims 2
- UUNDFHFDDVTMFX-UHFFFAOYSA-N 4-[2-(2,8-diazaspiro[4.5]decan-8-yl)-5-[1-(2,2,2-trifluoroethyl)pyrazol-4-yl]pyrimidin-4-yl]benzonitrile Chemical compound C1NCCC11CCN(CC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C=1C=NN(C=1)CC(F)(F)F UUNDFHFDDVTMFX-UHFFFAOYSA-N 0.000 claims 2
- ZUUIGQTXBPFVOO-UHFFFAOYSA-N 4-[2-(4-amino-3-hydroxypiperidin-1-yl)-5-(1-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1C(CN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C=1C=C2C=NN(C2=CC=1)C)O ZUUIGQTXBPFVOO-UHFFFAOYSA-N 0.000 claims 2
- WAKLZNSBSDKCIA-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-6-(methylamino)-5-(3-methyltriazolo[4,5-b]pyridin-6-yl)pyrimidin-4-yl]benzonitrile Chemical compound CNC1=NC(=NC(C2=CC=C(C=C2)C#N)=C1C1=CC2=C(N=C1)N(C)N=N2)N1CCC(N)CC1 WAKLZNSBSDKCIA-UHFFFAOYSA-N 0.000 claims 2
- 125000006519 CCH3 Chemical group 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 125000005884 carbocyclylalkyl group Chemical group 0.000 claims 2
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 2
- 125000002757 morpholinyl group Chemical group 0.000 claims 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- ZOXAXAJRWKXXOT-UHFFFAOYSA-N 2-fluoro-4-[2-[4-(methylamino)piperidin-1-yl]-5-[1-(2,2,2-trifluoroethyl)pyrazol-4-yl]pyrimidin-4-yl]benzonitrile Chemical compound FC1=C(C#N)C=CC(=C1)C1=NC(=NC=C1C=1C=NN(C=1)CC(F)(F)F)N1CCC(CC1)NC ZOXAXAJRWKXXOT-UHFFFAOYSA-N 0.000 claims 1
- QPBAZTFKTODRDF-UHFFFAOYSA-N 2-fluoro-4-[5-(2-methylindazol-5-yl)-2-piperazin-1-ylpyrimidin-4-yl]benzonitrile Chemical compound FC1=C(C#N)C=CC(=C1)C1=NC(=NC=C1C1=CC2=CN(N=C2C=C1)C)N1CCNCC1 QPBAZTFKTODRDF-UHFFFAOYSA-N 0.000 claims 1
- GLPBNBGLOOKKNX-UHFFFAOYSA-N 4-[2-(1,2,3,3a,4,6,7,7a-octahydropyrrolo[3,4-c]pyridin-5-yl)-5-(1-methylindazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCC2CN(CCC21)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C=1C=C2C=NN(C2=CC=1)C GLPBNBGLOOKKNX-UHFFFAOYSA-N 0.000 claims 1
- NZBLPSMZHWZESE-UHFFFAOYSA-N 4-[2-(1,2,3,3a,4,6,7,7a-octahydropyrrolo[3,4-c]pyridin-5-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound CC1=CC=C(C=C1)C=1C(=NC(=NC1)N1CC2C(CC1)CNC2)C2=CC=C(C#N)C=C2 NZBLPSMZHWZESE-UHFFFAOYSA-N 0.000 claims 1
- RULFXLDLMOZOEN-UHFFFAOYSA-N 4-[2-(1,3,3a,4,5,6,7,7a-octahydropyrrolo[3,4-c]pyridin-2-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound CC1=CC=C(C=C1)C=1C(=NC(=NC1)N1CC2CNCCC2C1)C1=CC=C(C#N)C=C1 RULFXLDLMOZOEN-UHFFFAOYSA-N 0.000 claims 1
- OUSGZXFWFLYBBH-UHFFFAOYSA-N 4-[2-(1,4-diazepan-1-yl)-5-(2-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound N1(CCNCCC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=CN(N=C2C=C1)C OUSGZXFWFLYBBH-UHFFFAOYSA-N 0.000 claims 1
- RYOPGHUPPWONJB-UHFFFAOYSA-N 4-[2-(1,4-diazepan-1-yl)-6-(methylamino)-5-(2-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound N1(CCNCCC1)C1=NC(=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=CN(N=C2C=C1)C)NC RYOPGHUPPWONJB-UHFFFAOYSA-N 0.000 claims 1
- MXIDFUXOFKZPNO-UHFFFAOYSA-N 4-[2-(1,4-diazepan-1-yl)-6-(methylamino)-5-(2-methylindazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound N1(CCNCCC1)C1=NC(=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC2=CN(N=C2C=C1)C)NC MXIDFUXOFKZPNO-UHFFFAOYSA-N 0.000 claims 1
- ODYGNXNVQHXTJA-UHFFFAOYSA-N 4-[2-(1,4-diazepan-1-yl)-6-methoxy-5-(2-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound N1(CCNCCC1)C1=NC(=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=CN(N=C2C=C1)C)OC ODYGNXNVQHXTJA-UHFFFAOYSA-N 0.000 claims 1
- ZQSFLZDESICNIC-UHFFFAOYSA-N 4-[2-(1,8-diazaspiro[4.5]decan-8-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound N1CCCC11CCN(CC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC=C(C=C1)C ZQSFLZDESICNIC-UHFFFAOYSA-N 0.000 claims 1
- JSWLSBADVAHSOK-UHFFFAOYSA-N 4-[2-(2,3,3a,4,5,7,8,8a-octahydro-1H-pyrrolo[3,4-d]azepin-6-yl)-5-(1,3-benzothiazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCC2C1CCN(CC2)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C=1C=CC2=C(N=CS2)C=1 JSWLSBADVAHSOK-UHFFFAOYSA-N 0.000 claims 1
- XEBPGXXUZFZIQF-UHFFFAOYSA-N 4-[2-(2,3,3a,4,5,7,8,8a-octahydro-1H-pyrrolo[3,4-d]azepin-6-yl)-5-(1,3-dimethylpyrazol-4-yl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCC2C1CCN(CC2)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C=1C(=NN(C=1)C)C XEBPGXXUZFZIQF-UHFFFAOYSA-N 0.000 claims 1
- KQZVYBXANIHJKG-UHFFFAOYSA-N 4-[2-(2,3,3a,4,5,7,8,8a-octahydro-1H-pyrrolo[3,4-d]azepin-6-yl)-5-(1-methylpyrazolo[3,4-b]pyridin-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCC2C1CCN(CC2)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C=1C=C2C(=NC=1)N(N=C2)C KQZVYBXANIHJKG-UHFFFAOYSA-N 0.000 claims 1
- QOILSXDQEISYNF-UHFFFAOYSA-N 4-[2-(2,3,3a,4,5,7,8,8a-octahydro-1H-pyrrolo[3,4-d]azepin-6-yl)-5-(1H-indazol-6-yl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCC2C1CCN(CC2)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC=C2C=NNC2=C1 QOILSXDQEISYNF-UHFFFAOYSA-N 0.000 claims 1
- UOYGTTPPDIGPCJ-UHFFFAOYSA-N 4-[2-(2,3,3a,4,5,7,8,8a-octahydro-1H-pyrrolo[3,4-d]azepin-6-yl)-5-(6,7-difluoro-1-methylbenzimidazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCC2C1CCN(CC2)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC2=C(N(C=N2)C)C(=C1F)F UOYGTTPPDIGPCJ-UHFFFAOYSA-N 0.000 claims 1
- PMFXPIYWHBPDRM-UHFFFAOYSA-N 4-[2-(2,3,3a,4,5,7,8,8a-octahydro-1H-pyrrolo[3,4-d]azepin-6-yl)-5-(6-methylpyridin-3-yl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCC2C1CCN(CC2)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C=1C=NC(=CC=1)C PMFXPIYWHBPDRM-UHFFFAOYSA-N 0.000 claims 1
- FMHQWZQROYHZQO-UHFFFAOYSA-N 4-[2-(2,7-diazaspiro[3.5]nonan-7-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCC11CCN(CC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC=C(C=C1)C FMHQWZQROYHZQO-UHFFFAOYSA-N 0.000 claims 1
- DDCBSMDYYZFKNP-UHFFFAOYSA-N 4-[2-(2,7-diazaspiro[4.4]nonan-2-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound C1N(CCC11CNCC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC=C(C=C1)C DDCBSMDYYZFKNP-UHFFFAOYSA-N 0.000 claims 1
- JZCQWXOICXKJBH-UHFFFAOYSA-N 4-[2-(2,8-diazaspiro[4.5]decan-2-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound C1N(CCC12CCNCC2)C2=NC=C(C(=N2)C2=CC=C(C#N)C=C2)C2=CC=C(C=C2)C JZCQWXOICXKJBH-UHFFFAOYSA-N 0.000 claims 1
- JWJHPTPUTHKKLJ-UHFFFAOYSA-N 4-[2-(2,8-diazaspiro[4.5]decan-8-yl)-5-(3-methylimidazo[4,5-b]pyridin-6-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound C1NCCC11CCN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C=1C=C2C(=NC=1)N(C=N2)C JWJHPTPUTHKKLJ-UHFFFAOYSA-N 0.000 claims 1
- IBDLOBBXGCGKKD-UHFFFAOYSA-N 4-[2-(2,8-diazaspiro[4.5]decan-8-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound C1NCCC11CCN(CC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC=C(C=C1)C IBDLOBBXGCGKKD-UHFFFAOYSA-N 0.000 claims 1
- ZNRPEMJJAOLLIX-UHFFFAOYSA-N 4-[2-(3,7-diazabicyclo[3.3.1]nonan-3-yl)-5-(1-methylindazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound C12CN(CC(CNC1)C2)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C=1C=C2C=NN(C2=CC=1)C ZNRPEMJJAOLLIX-UHFFFAOYSA-N 0.000 claims 1
- WHHABFYJUGNZBZ-UHFFFAOYSA-N 4-[2-(3,7-diazabicyclo[3.3.1]nonan-3-yl)-5-(4-methylphenyl)pyrimidin-4-yl]benzonitrile Chemical compound C12CN(CC(CNC1)C2)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC=C(C=C1)C WHHABFYJUGNZBZ-UHFFFAOYSA-N 0.000 claims 1
- WGHVQZMPZHYDKY-UHFFFAOYSA-N 4-[2-(3-aminopiperidin-1-yl)-5-(2-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1CN(CCC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=CN(N=C2C=C1)C WGHVQZMPZHYDKY-UHFFFAOYSA-N 0.000 claims 1
- RLCZDVULBIUWMC-UHFFFAOYSA-N 4-[2-(3-aminopyrrolidin-1-yl)-5-(2-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1CN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=CN(N=C2C=C1)C RLCZDVULBIUWMC-UHFFFAOYSA-N 0.000 claims 1
- ZHSQPHUASYYLFP-UHFFFAOYSA-N 4-[2-(4-amino-3-fluoropiperidin-1-yl)-5-(1-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1C(CN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C=1C=C2C=NN(C2=CC=1)C)F ZHSQPHUASYYLFP-UHFFFAOYSA-N 0.000 claims 1
- FQCXHJOGWCZHBR-UHFFFAOYSA-N 4-[2-(4-amino-3-fluoropiperidin-1-yl)-5-(2-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1C(CN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=CN(N=C2C=C1)C)F FQCXHJOGWCZHBR-UHFFFAOYSA-N 0.000 claims 1
- JWRLEJUAUQVTQM-UHFFFAOYSA-N 4-[2-(4-amino-3-hydroxypiperidin-1-yl)-5-(2-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1C(CN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=CN(N=C2C=C1)C)O JWRLEJUAUQVTQM-UHFFFAOYSA-N 0.000 claims 1
- VYKOATPZWNZJQB-UHFFFAOYSA-N 4-[2-(4-amino-3-hydroxypiperidin-1-yl)-5-[1-(2,2,2-trifluoroethyl)pyrazol-4-yl]pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1C(CN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C=1C=NN(C=1)CC(F)(F)F)O VYKOATPZWNZJQB-UHFFFAOYSA-N 0.000 claims 1
- ZPNWJBNJLKVPLC-UHFFFAOYSA-N 4-[2-(4-aminoazepan-1-yl)-6-methoxy-5-(2-methylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1CCN(CCC1)C1=NC(=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=CN(N=C2C=C1)C)OC ZPNWJBNJLKVPLC-UHFFFAOYSA-N 0.000 claims 1
- SYYIYGBOSRSVDI-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1,2-dimethylbenzimidazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=C(N(C(=N2)C)C)C=C1 SYYIYGBOSRSVDI-UHFFFAOYSA-N 0.000 claims 1
- DDMIJGTXTGXKKR-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1,2-dimethylbenzimidazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC2=C(N(C(=N2)C)C)C=C1 DDMIJGTXTGXKKR-UHFFFAOYSA-N 0.000 claims 1
- PEIHDJAWMDRJFQ-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1,3-dimethylindazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C=1C=C2C(=NN(C2=CC=1)C)C PEIHDJAWMDRJFQ-UHFFFAOYSA-N 0.000 claims 1
- ZQJNKVWEILGNCY-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1-methyl-3a,7a-dihydroindazol-5-yl)-6-(methylamino)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound CNC1=NC(=NC(C2=CC=C(C#N)C(F)=C2)=C1C1=CC2C=NN(C)C2C=C1)N1CCC(N)CC1 ZQJNKVWEILGNCY-UHFFFAOYSA-N 0.000 claims 1
- XEGYCYPYGHEYHX-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1-methyl-3a,7a-dihydroindazol-5-yl)-6-(methylamino)pyrimidin-4-yl]benzonitrile Chemical compound CNC1=NC(=NC(C2=CC=C(C=C2)C#N)=C1C1=CC2C=NN(C)C2C=C1)N1CCC(N)CC1 XEGYCYPYGHEYHX-UHFFFAOYSA-N 0.000 claims 1
- UNDHMJNRZKVHLE-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1-methylbenzimidazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=C(N(C=N2)C)C=C1 UNDHMJNRZKVHLE-UHFFFAOYSA-N 0.000 claims 1
- MHQGVYHZWCCMAB-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1-methylbenzimidazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC2=C(N(C=N2)C)C=C1 MHQGVYHZWCCMAB-UHFFFAOYSA-N 0.000 claims 1
- RXNINBGWXPGTLV-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1-methylbenzotriazol-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C1=CC2=C(N(N=N2)C)C=C1 RXNINBGWXPGTLV-UHFFFAOYSA-N 0.000 claims 1
- ATEZJSDCKFBRGN-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1-methylbenzotriazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC2=C(N(N=N2)C)C=C1 ATEZJSDCKFBRGN-UHFFFAOYSA-N 0.000 claims 1
- RSHWPWFPYQBIED-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1-methylindazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C=1C=C2C=NN(C2=CC=1)C RSHWPWFPYQBIED-UHFFFAOYSA-N 0.000 claims 1
- TUZMNDKMYDGZLW-UHFFFAOYSA-N 4-[2-(4-aminopiperidin-1-yl)-5-(1-methylpyrazolo[3,4-b]pyridin-5-yl)pyrimidin-4-yl]-2-fluorobenzonitrile Chemical compound NC1CCN(CC1)C1=NC=C(C(=N1)C1=CC(=C(C#N)C=C1)F)C=1C=C2C(=NC=1)N(N=C2)C TUZMNDKMYDGZLW-UHFFFAOYSA-N 0.000 claims 1
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- SZBRTCVLMWLKOE-UHFFFAOYSA-N 4-[2-[4-(dimethylamino)piperidin-1-yl]-6-(methylamino)-5-(2-methylindazol-5-yl)pyrimidin-4-yl]benzonitrile Chemical compound CN(C1CCN(CC1)C1=NC(=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC2=CN(N=C2C=C1)C)NC)C SZBRTCVLMWLKOE-UHFFFAOYSA-N 0.000 claims 1
- XLFAHCWFRUDOBL-INIZCTEOSA-N 4-[2-[[(3S)-pyrrolidin-3-yl]methylamino]-5-[4-(trifluoromethyl)phenyl]pyrimidin-4-yl]benzonitrile Chemical compound N1C[C@H](CC1)CNC1=NC=C(C(=N1)C1=CC=C(C#N)C=C1)C1=CC=C(C=C1)C(F)(F)F XLFAHCWFRUDOBL-INIZCTEOSA-N 0.000 claims 1
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- YWCTWYZDVCNIEW-UHFFFAOYSA-N 4-[5-(4-methylphenyl)-2-(piperidin-3-ylmethylamino)pyrimidin-4-yl]benzonitrile Chemical compound CC1=CC=C(C=C1)C=1C(=NC(=NC=1)NCC1CNCCC1)C1=CC=C(C#N)C=C1 YWCTWYZDVCNIEW-UHFFFAOYSA-N 0.000 claims 1
- WZPIFTGJDNFAHM-UHFFFAOYSA-N 4-[5-(4-methylphenyl)-2-(piperidin-4-ylamino)pyrimidin-4-yl]benzonitrile Chemical compound CC1=CC=C(C=C1)C=1C(=NC(=NC1)NC1CCNCC1)C1=CC=C(C#N)C=C1 WZPIFTGJDNFAHM-UHFFFAOYSA-N 0.000 claims 1
- PFNSJAQJFCJCLS-UHFFFAOYSA-N 4-[5-(4-methylphenyl)-2-(piperidin-4-ylmethylamino)pyrimidin-4-yl]benzonitrile Chemical compound CC1=CC=C(C=C1)C=1C(=NC(=NC=1)NCC1CCNCC1)C1=CC=C(C#N)C=C1 PFNSJAQJFCJCLS-UHFFFAOYSA-N 0.000 claims 1
- DVPVKYQFTVERHQ-GOSISDBHSA-N 4-[5-(4-methylphenyl)-2-[[(3R)-pyrrolidin-3-yl]methoxy]pyrimidin-4-yl]benzonitrile Chemical compound CC1=CC=C(C=C1)C=1C(=NC(=NC=1)OC[C@H]1CNCC1)C1=CC=C(C#N)C=C1 DVPVKYQFTVERHQ-GOSISDBHSA-N 0.000 claims 1
- YCCRZPBTSZSNQO-SFHVURJKSA-N 4-[5-(4-methylphenyl)-2-[[(3S)-pyrrolidin-3-yl]methylamino]pyrimidin-4-yl]benzonitrile Chemical compound CC1=CC=C(C=C1)C=1C(=NC(=NC=1)NC[C@@H]1CNCC1)C1=CC=C(C#N)C=C1 YCCRZPBTSZSNQO-SFHVURJKSA-N 0.000 claims 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims 1
- 206010005003 Bladder cancer Diseases 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- 208000026310 Breast neoplasm Diseases 0.000 claims 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
- 206010060862 Prostate cancer Diseases 0.000 claims 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000005312 heteroarylalkynyl group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 201000005202 lung cancer Diseases 0.000 claims 1
- 208000020816 lung neoplasm Diseases 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 230000035897 transcription Effects 0.000 claims 1
- 238000013518 transcription Methods 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
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- 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
- C07D405/14—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 three or more hetero rings
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- 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
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- C07D413/12—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 linked by a chain containing hetero atoms as chain links
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- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C07D471/08—Bridged systems
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- C07D471/10—Spiro-condensed systems
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/08—Bridged systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
- C07D498/18—Bridged systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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| US201361914927P | 2013-12-11 | 2013-12-11 | |
| EP14868829.4A EP3080100B1 (en) | 2013-12-11 | 2014-12-10 | Inhibitors of lysine specific demethylase-1 |
| PCT/US2014/069562 WO2015089192A1 (en) | 2013-12-11 | 2014-12-10 | Inhibitors of lysine specific demethylase-1 |
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| WO2015123408A1 (en) | 2014-02-13 | 2015-08-20 | Incyte Corporation | Cyclopropylamines as lsd1 inhibitors |
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| PE20161573A1 (es) | 2014-02-13 | 2017-01-19 | Incyte Corp | Ciclopropilamina como inhibidor de la lsd1 |
| SG11201609033TA (en) * | 2014-05-01 | 2016-11-29 | Celgene Quanticel Res Inc | Inhibitors of lysine specific demethylase-1 |
| ES2812626T3 (es) | 2014-06-27 | 2021-03-17 | Celgene Quanticel Res Inc | Inhibidores de la desmetilasa 1 específica de lisina |
| SG11201610975RA (en) * | 2014-07-03 | 2017-01-27 | Celgene Quanticel Res Inc | Inhibitors of lysine specific demethylase-1 |
| US9758523B2 (en) | 2014-07-10 | 2017-09-12 | Incyte Corporation | Triazolopyridines and triazolopyrazines as LSD1 inhibitors |
| US9695180B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted imidazo[1,2-a]pyrazines as LSD1 inhibitors |
| US9695168B2 (en) | 2014-07-10 | 2017-07-04 | Incyte Corporation | Substituted imidazo[1,5-α]pyridines and imidazo[1,5-α]pyrazines as LSD1 inhibitors |
| WO2016007722A1 (en) | 2014-07-10 | 2016-01-14 | Incyte Corporation | Triazolopyridines and triazolopyrazines as lsd1 inhibitors |
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| MY191796A (en) | 2015-04-03 | 2022-07-15 | Incyte Corp | Heterocyclic compounds as lsd1 inhibitors |
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| KR102710120B1 (ko) | 2015-08-12 | 2024-09-27 | 인사이트 홀딩스 코포레이션 | Lsd1 저해제의 염 |
| US10059668B2 (en) | 2015-11-05 | 2018-08-28 | Mirati Therapeutics, Inc. | LSD1 inhibitors |
| RU2726622C2 (ru) | 2015-11-27 | 2020-07-15 | Тайхо Фармасьютикал Ко., Лтд. | Новое соединение бифенила или его соль |
| KR102720551B1 (ko) | 2015-12-29 | 2024-10-21 | 미라티 테라퓨틱스, 인크. | Lsd1 억제제 |
| AU2017233898B2 (en) | 2016-03-15 | 2022-12-15 | Oryzon Genomics, S.A. | Combinations of LSD1 inhibitors for use in the treatment of solid tumors |
| ES3042059T3 (en) | 2016-03-16 | 2025-11-18 | Oryzon Genomics Sa | Methods to determine kdm1a target engagement and chemoprobes useful therefor |
| US10150754B2 (en) | 2016-04-19 | 2018-12-11 | Celgene Quanticel Research, Inc. | Histone demethylase inhibitors |
| PE20190377A1 (es) | 2016-04-22 | 2019-03-08 | Incyte Corp | Formulaciones de un inhibidor de lsd 1 |
| CN105924397B (zh) * | 2016-04-29 | 2017-11-24 | 河南省农业科学院植物保护研究所 | 一种1,5‑二芳基‑3‑甲酸酯吡唑类化合物、制备方法及用途 |
| US20190256929A1 (en) | 2016-11-03 | 2019-08-22 | Oryzon Genomics, S.A. | Pharmacodynamic biomarkers for personalized cancer care using epigenetic modifying agents |
| EP3535420A1 (en) | 2016-11-03 | 2019-09-11 | Oryzon Genomics, S.A. | Biomarkers for determining responsiveness to lsd1 inhibitors |
| CN110914265B (zh) * | 2017-05-15 | 2022-12-23 | 密歇根大学董事会 | 作为lsd-1抑制剂的吡咯并[2,3-c]吡啶和相关类似物 |
| WO2018216800A1 (ja) | 2017-05-26 | 2018-11-29 | 大鵬薬品工業株式会社 | 新規なビフェニル化合物又はその塩 |
| TWI727173B (zh) * | 2017-05-26 | 2021-05-11 | 日商大鵬藥品工業股份有限公司 | 使用有新穎聯苯化合物之抗腫瘤效果增強劑 |
| WO2018221555A1 (ja) | 2017-05-31 | 2018-12-06 | 大鵬薬品工業株式会社 | Insm1の発現に基づくlsd1阻害剤の治療効果の予測方法 |
| MY204406A (en) | 2017-08-03 | 2024-08-27 | Oryzon Genomics Sa | Methods of treating behavior alterations |
| AR112900A1 (es) | 2017-09-13 | 2019-12-26 | Hanmi Pharm Ind Co Ltd | Compuesto derivado de pirazol y uso de este |
| US10968200B2 (en) | 2018-08-31 | 2021-04-06 | Incyte Corporation | Salts of an LSD1 inhibitor and processes for preparing the same |
| BR112021016064A2 (pt) | 2019-03-20 | 2021-10-05 | Oryzon Genomics, S.A. | Métodos de tratamento do transtorno de personalidade borderline |
| CN120837494A (zh) | 2019-03-20 | 2025-10-28 | 奥莱松基因组股份有限公司 | 使用kdm1a抑制剂如化合物伐菲德司他治疗注意缺陷多动症的方法 |
| JP2022546908A (ja) | 2019-07-05 | 2022-11-10 | オリゾン・ゲノミクス・ソシエダッド・アノニマ | Kdm1a阻害剤を使用した小細胞肺がんの個別化された処置のためのバイオマーカーおよび方法 |
| MX2022005812A (es) | 2019-11-13 | 2022-08-16 | Taiho Pharmaceutical Co Ltd | Metodos de tratamiento de enfermedades y trastornos relacionados con desmetilasa 1 especifica de lisina con inhibidores de desmetilasa 1 especifica de lisina. |
| CN114105950B (zh) * | 2020-08-31 | 2022-09-06 | 南京明德新药研发有限公司 | 吡唑类化合物及其应用 |
| CA3231846A1 (en) | 2021-04-08 | 2022-10-13 | Tamara Maes | Combinations of lsd1 inhibitors for treating myeloid cancers |
| EP4419504A4 (en) * | 2021-10-18 | 2025-09-03 | Imago Biosciences Inc | KDM1A INHIBITORS FOR THE TREATMENT OF DISEASE |
| CN116836167B (zh) * | 2022-03-25 | 2025-09-09 | 腾讯科技(深圳)有限公司 | 咪唑并[1,2-a]吡嗪或吡唑并[1,5-a]嘧啶衍生物及其用途 |
| CN119497613A (zh) | 2022-05-09 | 2025-02-21 | 奥莱松基因组股份有限公司 | 使用lsd1抑制剂治疗nf1-突变肿瘤的方法 |
| EP4522136A1 (en) | 2022-05-09 | 2025-03-19 | Oryzon Genomics, S.A. | Methods of treating malignant peripheral nerve sheath tumor (mpnst) using lsd1 inhibitors |
| AU2023385514A1 (en) | 2022-11-24 | 2025-07-10 | Oryzon Genomics, S.A. | Combinations of lsd1 inhibitors and menin inhibitors for treating cancer |
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| US5550147A (en) * | 1992-02-05 | 1996-08-27 | Fujisawa Pharmaceutical Co., Ltd. | Pyrazole derivatives, processes for preparation thereof and pharmaceutical composition comprising the same |
| CA2450934A1 (en) * | 2001-06-19 | 2002-12-27 | Marco Dodier | Pyrimidine inhibitors of phosphodiesterase (pde) 7 |
| DE60331219D1 (de) * | 2002-03-28 | 2010-03-25 | Eisai R&D Man Co Ltd | Azaindole als hemmstoffe von c-jun n-terminalen kinasen |
| EP2316831B1 (en) | 2002-11-21 | 2013-03-06 | Novartis AG | 2-(morpholin-4-yl)pyrimidines as phosphotidylinositol (PI) 3-kinase inhibitors and their use in the treatment of cancer |
| TW200526641A (en) * | 2003-12-26 | 2005-08-16 | Daiichi Seiyaku Co | Amidopyrazole derivatives |
| US7858395B2 (en) | 2005-07-13 | 2010-12-28 | Universitaetsklinikum Freiburg | Antibodies for use in identifying and/or scoring prostate cancer and androgen receptor-dependent gene expression control |
| WO2007089768A2 (en) * | 2006-01-30 | 2007-08-09 | Exelixis, Inc. | 4-aryl-2-amino-pyrimidines or 4-aryl-2-aminoalkyl-pyrimidines as jak-2 modulators and pharmaceutical compositions containing them |
| HUE029188T2 (en) * | 2007-03-12 | 2017-03-28 | Ym Biosciences Australia Pty | Phenylamino-pyrimidine compounds and their use |
| MX2011000729A (es) * | 2008-07-29 | 2011-03-15 | Boehringer Ingelheim Int | 5-alquinil-pirimidinas. |
| WO2010046780A2 (en) * | 2008-10-22 | 2010-04-29 | Institut Pasteur Korea | Anti viral compounds |
| TWI435874B (zh) * | 2008-10-31 | 2014-05-01 | Toray Industries | 環己烷衍生物及其醫藥用途 |
| EP2258865A1 (en) | 2009-06-05 | 2010-12-08 | Universitätsklinikum Freiburg | Lysine-specific demethylase 1 (LSD1) is a biomarker for breast cancer |
| EP2258858A1 (en) | 2009-06-05 | 2010-12-08 | Universitätsklinikum Freiburg | Transgenic LSD1 animal model for cancer |
| EP2467359A4 (en) | 2009-08-18 | 2013-01-09 | Univ Johns Hopkins | (BIS-) UREA- AND (BIS-) THIOMINE COMPOUNDS AS EPIGENE MODULATORS OF THE LYSINE-SPECIFIC DEMETHYLASE 1 AND METHODS OF DISEASE TREATMENT THEREWITH |
| TW201111378A (en) * | 2009-09-11 | 2011-04-01 | Bayer Schering Pharma Ag | Substituted (heteroarylmethyl) thiohydantoins |
| US9365539B2 (en) * | 2010-05-11 | 2016-06-14 | Merck Sharp & Dohme Corp. | Prolylcarboxypeptidase inhibitors |
| US9006449B2 (en) * | 2010-07-29 | 2015-04-14 | Oryzon Genomics, S.A. | Cyclopropylamine derivatives useful as LSD1 inhibitors |
| GB201106829D0 (en) * | 2011-04-21 | 2011-06-01 | Proximagen Ltd | Heterocyclic compounds |
| WO2013033688A1 (en) | 2011-09-01 | 2013-03-07 | The Brigham And Women's Hospital, Inc. | Treatment of cancer |
| AR088351A1 (es) * | 2011-10-31 | 2014-05-28 | Lilly Co Eli | Analogos de pirazol sustituidos |
| PL2770994T3 (pl) * | 2012-05-04 | 2020-03-31 | Samumed, Llc | 1H-Pirazolo[3,4-b]pirydyny i ich zastosowania terapeutyczne |
| JP6195828B2 (ja) * | 2012-05-24 | 2017-09-13 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子用材料、及びそれを用いた有機エレクトロルミネッセンス素子 |
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Also Published As
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| CA3161836A1 (en) | 2015-06-18 |
| EP3080100A1 (en) | 2016-10-19 |
| DK3080100T3 (da) | 2023-02-06 |
| LT3080100T (lt) | 2023-02-27 |
| MX2020010496A (es) | 2020-10-28 |
| PT3080100T (pt) | 2023-01-19 |
| JP2017502940A (ja) | 2017-01-26 |
| US20160304516A1 (en) | 2016-10-20 |
| US10131664B2 (en) | 2018-11-20 |
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| CA2933480C (en) | 2022-08-23 |
| CA2933480A1 (en) | 2015-06-18 |
| FI3080100T3 (fi) | 2023-03-15 |
| EP3080100B1 (en) | 2022-11-30 |
| US20180179204A1 (en) | 2018-06-28 |
| RS63939B1 (sr) | 2023-02-28 |
| WO2015089192A1 (en) | 2015-06-18 |
| EP3080100A4 (en) | 2017-09-06 |
| EP4257591A2 (en) | 2023-10-11 |
| PL3080100T3 (pl) | 2023-03-06 |
| US20190055242A1 (en) | 2019-02-21 |
| US9944636B2 (en) | 2018-04-17 |
| HUE061252T2 (hu) | 2023-05-28 |
| SI3080100T1 (sl) | 2023-04-28 |
| SMT202300014T1 (it) | 2023-05-12 |
| EP4257591A3 (en) | 2023-11-22 |
| MX2016007585A (es) | 2016-12-16 |
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