JP2017501983A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2017501983A5 JP2017501983A5 JP2016535650A JP2016535650A JP2017501983A5 JP 2017501983 A5 JP2017501983 A5 JP 2017501983A5 JP 2016535650 A JP2016535650 A JP 2016535650A JP 2016535650 A JP2016535650 A JP 2016535650A JP 2017501983 A5 JP2017501983 A5 JP 2017501983A5
- Authority
- JP
- Japan
- Prior art keywords
- methoxy
- dihydroimidazo
- quinazolin
- morpholin
- ylpropoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 nitro, hydroxy Chemical group 0.000 claims 30
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 10
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 9
- 239000012453 solvate Substances 0.000 claims 9
- 150000001875 compounds Chemical class 0.000 claims 8
- 206010060862 Prostate cancer Diseases 0.000 claims 5
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 5
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 5
- 125000000623 heterocyclic group Chemical group 0.000 claims 5
- 229960003966 nicotinamide Drugs 0.000 claims 5
- 235000005152 nicotinamide Nutrition 0.000 claims 5
- 239000011570 nicotinamide Substances 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 4
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 4
- 206010027476 Metastases Diseases 0.000 claims 4
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 4
- 125000004429 atom Chemical group 0.000 claims 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 4
- 150000003857 carboxamides Chemical class 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 201000005202 lung cancer Diseases 0.000 claims 4
- 208000020816 lung neoplasm Diseases 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 4
- QDXGKRWDQCEABB-UHFFFAOYSA-N pyrimidine-5-carboxamide Chemical compound NC(=O)C1=CN=CN=C1 QDXGKRWDQCEABB-UHFFFAOYSA-N 0.000 claims 4
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 3
- MWYDSXOGIBMAET-UHFFFAOYSA-N 2-amino-N-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydro-1H-imidazo[1,2-c]quinazolin-5-ylidene]pyrimidine-5-carboxamide Chemical compound NC1=NC=C(C=N1)C(=O)N=C1N=C2C(=C(C=CC2=C2N1CCN2)OCCCN1CCOCC1)OC MWYDSXOGIBMAET-UHFFFAOYSA-N 0.000 claims 3
- 206010006187 Breast cancer Diseases 0.000 claims 3
- 208000026310 Breast neoplasm Diseases 0.000 claims 3
- NIQHXSFKSLJILV-UHFFFAOYSA-N NC1N(C=CC=N1)C1=NC=2C(=C(C=CC2C=2N1CCN2)OCCCN2CCOCC2)OC Chemical compound NC1N(C=CC=N1)C1=NC=2C(=C(C=CC2C=2N1CCN2)OCCCN2CCOCC2)OC NIQHXSFKSLJILV-UHFFFAOYSA-N 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 150000001408 amides Chemical class 0.000 claims 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 3
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- PFAXMTRQGWBENF-UHFFFAOYSA-N n-[8-[3-[2-(hydroxymethyl)morpholin-4-yl]propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCCN1CCOC(CO)C1 PFAXMTRQGWBENF-UHFFFAOYSA-N 0.000 claims 3
- 229910052705 radium Inorganic materials 0.000 claims 3
- HCWPIIXVSYCSAN-UHFFFAOYSA-N radium atom Chemical compound [Ra] HCWPIIXVSYCSAN-UHFFFAOYSA-N 0.000 claims 3
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 2
- 206010009944 Colon cancer Diseases 0.000 claims 2
- 208000034578 Multiple myelomas Diseases 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 2
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims 2
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 201000011510 cancer Diseases 0.000 claims 2
- 208000029742 colonic neoplasm Diseases 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 206010073071 hepatocellular carcinoma Diseases 0.000 claims 2
- 231100000844 hepatocellular carcinoma Toxicity 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims 2
- 201000001441 melanoma Diseases 0.000 claims 2
- 230000009401 metastasis Effects 0.000 claims 2
- VOJJBKFDVYAHHS-UHFFFAOYSA-N n-[7-methoxy-8-(2-morpholin-4-ylethoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCN1CCOCC1 VOJJBKFDVYAHHS-UHFFFAOYSA-N 0.000 claims 2
- VLPUKEZMPQNOHW-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-2,4-dimethyl-1,3-thiazole-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C3=C(N=C(C)S3)C)=NC=2C(OC)=C1OCCCN1CCOCC1 VLPUKEZMPQNOHW-UHFFFAOYSA-N 0.000 claims 2
- WCRDAUWROGEPIU-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-6-methylpyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC(C)=CC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 WCRDAUWROGEPIU-UHFFFAOYSA-N 0.000 claims 2
- PTBHOHFIBIMRLB-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 PTBHOHFIBIMRLB-UHFFFAOYSA-N 0.000 claims 2
- MYZQRTALORWOFJ-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=NC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 MYZQRTALORWOFJ-UHFFFAOYSA-N 0.000 claims 2
- IGDWQPUGKSBEED-UHFFFAOYSA-N n-[8-[2-(dimethylamino)ethoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-2,4-dimethyl-1,3-thiazole-5-carboxamide Chemical compound N=1C=2C(OC)=C(OCCN(C)C)C=CC=2C2=NCCN2C=1NC(=O)C=1SC(C)=NC=1C IGDWQPUGKSBEED-UHFFFAOYSA-N 0.000 claims 2
- WNUPSDDMPRHUPR-UHFFFAOYSA-N n-[8-[2-(dimethylamino)ethoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound N=1C=2C(OC)=C(OCCN(C)C)C=CC=2C2=NCCN2C=1NC(=O)C1=CC=CN=C1 WNUPSDDMPRHUPR-UHFFFAOYSA-N 0.000 claims 2
- XYVNDTVSILQGKM-UHFFFAOYSA-N n-[8-[2-(dimethylamino)ethoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamide Chemical compound N=1C=2C(OC)=C(OCCN(C)C)C=CC=2C2=NCCN2C=1NC(=O)C1=CN=CN=C1 XYVNDTVSILQGKM-UHFFFAOYSA-N 0.000 claims 2
- SBJDLHJPWPQZLP-UHFFFAOYSA-N n-[8-[3-(dimethylamino)propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound N=1C=2C(OC)=C(OCCCN(C)C)C=CC=2C2=NCCN2C=1NC(=O)C1=CC=CN=C1 SBJDLHJPWPQZLP-UHFFFAOYSA-N 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 201000002528 pancreatic cancer Diseases 0.000 claims 2
- 208000008443 pancreatic carcinoma Diseases 0.000 claims 2
- 230000002265 prevention Effects 0.000 claims 2
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 2
- HCWPIIXVSYCSAN-OIOBTWANSA-N radium-223 Chemical compound [223Ra] HCWPIIXVSYCSAN-OIOBTWANSA-N 0.000 claims 2
- 229960005562 radium-223 Drugs 0.000 claims 2
- 229910052717 sulfur Chemical group 0.000 claims 2
- 239000011593 sulfur Chemical group 0.000 claims 2
- 229930192474 thiophene Natural products 0.000 claims 2
- 102000010400 1-phosphatidylinositol-3-kinase activity proteins Human genes 0.000 claims 1
- LNMCRSJMLGCLCZ-UHFFFAOYSA-N 2-amino-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-1,3-oxazole-4-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3N=C(N)OC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 LNMCRSJMLGCLCZ-UHFFFAOYSA-N 0.000 claims 1
- AQMSKYKATADCTL-UHFFFAOYSA-N 2-amino-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-1,3-oxazole-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3OC(N)=NC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 AQMSKYKATADCTL-UHFFFAOYSA-N 0.000 claims 1
- RWCMUSCEPMWINC-UHFFFAOYSA-N 2-amino-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-1,3-thiazole-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3SC(N)=NC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 RWCMUSCEPMWINC-UHFFFAOYSA-N 0.000 claims 1
- NFNLEBOQOSHXAE-UHFFFAOYSA-N 2-amino-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-4-methyl-1,3-thiazole-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C3=C(N=C(N)S3)C)=NC=2C(OC)=C1OCCCN1CCOCC1 NFNLEBOQOSHXAE-UHFFFAOYSA-N 0.000 claims 1
- JVNVQISIPQMGQT-UHFFFAOYSA-N 2-amino-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-4-methylpyrimidine-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C(=NC(N)=NC=3)C)=NC=2C(OC)=C1OCCCN1CCOCC1 JVNVQISIPQMGQT-UHFFFAOYSA-N 0.000 claims 1
- BEMUPKPURPXIOV-UHFFFAOYSA-N 2-amino-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-4-propylpyrimidine-5-carboxamide Chemical compound CCCC1=NC(N)=NC=C1C(=O)NC1=NC2=C(OC)C(OCCCN3CCOCC3)=CC=C2C2=NCCN12 BEMUPKPURPXIOV-UHFFFAOYSA-N 0.000 claims 1
- HTXHYBJJPFAYJF-UHFFFAOYSA-N 2-amino-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrimidine-4-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3N=C(N)N=CC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 HTXHYBJJPFAYJF-UHFFFAOYSA-N 0.000 claims 1
- LTMJJJRJLOZDKC-UHFFFAOYSA-N 2-amino-n-[8-[3-(dimethylamino)propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamide Chemical compound N=1C=2C(OC)=C(OCCCN(C)C)C=CC=2C2=NCCN2C=1NC(=O)C1=CN=C(N)N=C1 LTMJJJRJLOZDKC-UHFFFAOYSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- BMALKTLCGJCSFT-UHFFFAOYSA-N 2-methoxy-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamide Chemical compound C1=NC(OC)=NC=C1C(=O)NC1=NC2=C(OC)C(OCCCN3CCOCC3)=CC=C2C2=NCCN12 BMALKTLCGJCSFT-UHFFFAOYSA-N 0.000 claims 1
- 125000004176 4-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1F)C([H])([H])* 0.000 claims 1
- PRGHVANXJBUMMP-UHFFFAOYSA-N 6-amino-n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-2-methylpyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C(=NC(N)=CC=3)C)=NC=2C(OC)=C1OCCCN1CCOCC1 PRGHVANXJBUMMP-UHFFFAOYSA-N 0.000 claims 1
- YREMFJUNYZTERX-UHFFFAOYSA-N C(C(C)C)(=O)NN1C(N2C(C=3C=CC(=C(C13)OC)OCCCN1CCOCC1)=NCC2)N2CC=CC(=C2)C2N(C)CCC2 Chemical compound C(C(C)C)(=O)NN1C(N2C(C=3C=CC(=C(C13)OC)OCCCN1CCOCC1)=NCC2)N2CC=CC(=C2)C2N(C)CCC2 YREMFJUNYZTERX-UHFFFAOYSA-N 0.000 claims 1
- UTSTWSBQVYVZAL-UHFFFAOYSA-N C1(CCC1)CN1CC(OCC1)CCOC=1C=CC=2C=3N(C(=NC2C1OC)N1CC=CC(=C1)C1N(C)CCC1)CCN3 Chemical compound C1(CCC1)CN1CC(OCC1)CCOC=1C=CC=2C=3N(C(=NC2C1OC)N1CC=CC(=C1)C1N(C)CCC1)CCN3 UTSTWSBQVYVZAL-UHFFFAOYSA-N 0.000 claims 1
- KQVLFZDOTHDTAM-HDICACEKSA-N C[C@@H]1CN(C[C@@H](O1)C)CCCOC=1C=CC=2C=3N(C(=NC=2C=1OC)C1=C(C(=O)N)C=CC(=N1)C)CCN=3 Chemical compound C[C@@H]1CN(C[C@@H](O1)C)CCCOC=1C=CC=2C=3N(C(=NC=2C=1OC)C1=C(C(=O)N)C=CC(=N1)C)CCN=3 KQVLFZDOTHDTAM-HDICACEKSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 206010027454 Metastases to breast Diseases 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 108091007960 PI3Ks Proteins 0.000 claims 1
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 1
- 210000000988 bone and bone Anatomy 0.000 claims 1
- 210000000481 breast Anatomy 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 125000006312 cyclopentyl amino group Chemical group [H]N(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000006255 cyclopropyl carbonyl group Chemical group [H]C1([H])C([H])([H])C1([H])C(*)=O 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 210000004072 lung Anatomy 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- LOTBYPQQWICYBB-UHFFFAOYSA-N methyl n-hexyl-n-[2-(hexylamino)ethyl]carbamate Chemical compound CCCCCCNCCN(C(=O)OC)CCCCCC LOTBYPQQWICYBB-UHFFFAOYSA-N 0.000 claims 1
- FTPSRPZIUIMGJG-UHFFFAOYSA-N n-[7-methoxy-8-(2-piperidin-1-ylethoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCN1CCCCC1 FTPSRPZIUIMGJG-UHFFFAOYSA-N 0.000 claims 1
- HTWHGWBGGRQZIH-UHFFFAOYSA-N n-[7-methoxy-8-(2-pyrrolidin-1-ylethoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCN1CCCC1 HTWHGWBGGRQZIH-UHFFFAOYSA-N 0.000 claims 1
- KWJLJTBSGLETMV-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-2-(methylamino)-1,3-thiazole-4-carboxamide Chemical compound S1C(NC)=NC(C(=O)NC=2N3CCN=C3C3=CC=C(OCCCN4CCOCC4)C(OC)=C3N=2)=C1 KWJLJTBSGLETMV-UHFFFAOYSA-N 0.000 claims 1
- SGKLUDAKPNLYEE-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-2-methyl-1,3-thiazole-4-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3N=C(C)SC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 SGKLUDAKPNLYEE-UHFFFAOYSA-N 0.000 claims 1
- ZIDFUBHWWUXLRT-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-2-morpholin-4-ylpyrimidine-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC(=NC=3)N3CCOCC3)=NC=2C(OC)=C1OCCCN1CCOCC1 ZIDFUBHWWUXLRT-UHFFFAOYSA-N 0.000 claims 1
- JLKWVDHZVRQTKD-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-2-pyrrolidin-1-ylpyrimidine-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC(=NC=3)N3CCCC3)=NC=2C(OC)=C1OCCCN1CCOCC1 JLKWVDHZVRQTKD-UHFFFAOYSA-N 0.000 claims 1
- WKMOTJBONANCJS-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-6-piperazin-1-ylpyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC(=CC=3)N3CCNCC3)=NC=2C(OC)=C1OCCCN1CCOCC1 WKMOTJBONANCJS-UHFFFAOYSA-N 0.000 claims 1
- ZWIHOWYOWLAPOW-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-6-pyrrolidin-1-ylpyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC(=CC=3)N3CCCC3)=NC=2C(OC)=C1OCCCN1CCOCC1 ZWIHOWYOWLAPOW-UHFFFAOYSA-N 0.000 claims 1
- HERHMVXJRQROEC-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]furan-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C3=COC=C3)=NC=2C(OC)=C1OCCCN1CCOCC1 HERHMVXJRQROEC-UHFFFAOYSA-N 0.000 claims 1
- VSBKXPZKOULKMN-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrazine-2-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3N=CC=NC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 VSBKXPZKOULKMN-UHFFFAOYSA-N 0.000 claims 1
- CUZHQMVTVIFZLN-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-4-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=CN=CC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 CUZHQMVTVIFZLN-UHFFFAOYSA-N 0.000 claims 1
- CCLXFYQHHORRCJ-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyrimidine-4-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3N=CN=CC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 CCLXFYQHHORRCJ-UHFFFAOYSA-N 0.000 claims 1
- LCPXEFLYSZVIKX-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]thiophene-2-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3SC=CC=3)=NC=2C(OC)=C1OCCCN1CCOCC1 LCPXEFLYSZVIKX-UHFFFAOYSA-N 0.000 claims 1
- HAMKTMLNCPASGR-UHFFFAOYSA-N n-[7-methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]thiophene-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C3=CSC=C3)=NC=2C(OC)=C1OCCCN1CCOCC1 HAMKTMLNCPASGR-UHFFFAOYSA-N 0.000 claims 1
- ZHUXRHRQKUDHHC-UHFFFAOYSA-N n-[7-methoxy-8-(3-piperidin-1-ylpropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCCN1CCCCC1 ZHUXRHRQKUDHHC-UHFFFAOYSA-N 0.000 claims 1
- IWNNQCNMNDPRNM-UHFFFAOYSA-N n-[7-methoxy-8-(morpholin-2-ylmethoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCC1CNCCO1 IWNNQCNMNDPRNM-UHFFFAOYSA-N 0.000 claims 1
- CLTOGHIOSYMIGR-UHFFFAOYSA-N n-[7-methoxy-8-[(4-methylmorpholin-2-yl)methoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCC1CN(C)CCO1 CLTOGHIOSYMIGR-UHFFFAOYSA-N 0.000 claims 1
- HGFPIMYEUVQSNS-UHFFFAOYSA-N n-[7-methoxy-8-[2-[4-(2-methoxyethyl)morpholin-2-yl]ethoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1N(CCOC)CCOC1CCOC1=CC=C(C=2N(CCN=2)C(NC(=O)C=2C=NC=CC=2)=N2)C2=C1OC HGFPIMYEUVQSNS-UHFFFAOYSA-N 0.000 claims 1
- MBTCIYIPCNTFMO-UHFFFAOYSA-N n-[7-methoxy-8-[3-(3-methylmorpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCCN1CCOCC1C MBTCIYIPCNTFMO-UHFFFAOYSA-N 0.000 claims 1
- FJLAKZHXRUSKFW-UHFFFAOYSA-N n-[7-methoxy-8-[3-(4-methylpiperazin-1-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCCN1CCN(C)CC1 FJLAKZHXRUSKFW-UHFFFAOYSA-N 0.000 claims 1
- PUKCESPXCWGTSN-UHFFFAOYSA-N n-[7-methoxy-8-[3-(methylamino)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound N=1C2=C(OC)C(OCCCNC)=CC=C2C2=NCCN2C=1NC(=O)C1=CC=CN=C1 PUKCESPXCWGTSN-UHFFFAOYSA-N 0.000 claims 1
- GZVXBDSYVFNCFF-UHFFFAOYSA-N n-[7-methoxy-8-[[4-(2-methoxyethyl)morpholin-2-yl]methoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1N(CCOC)CCOC1COC1=CC=C(C=2N(CCN=2)C(NC(=O)C=2C=NC=CC=2)=N2)C2=C1OC GZVXBDSYVFNCFF-UHFFFAOYSA-N 0.000 claims 1
- KUJFQKOTPRLKLL-UHFFFAOYSA-N n-[8-(2-aminoethoxy)-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound N=1C=2C(OC)=C(OCCN)C=CC=2C2=NCCN2C=1NC(=O)C1=CC=CN=C1 KUJFQKOTPRLKLL-UHFFFAOYSA-N 0.000 claims 1
- YTWYXKYMMKOBOM-UHFFFAOYSA-N n-[8-(2-hydroxy-3-morpholin-4-ylpropoxy)-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCC(O)CN1CCOCC1 YTWYXKYMMKOBOM-UHFFFAOYSA-N 0.000 claims 1
- YYVUROKADZATNZ-UHFFFAOYSA-N n-[8-(3-aminopropoxy)-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.N=1C=2C(OC)=C(OCCCN)C=CC=2C2=NCCN2C=1NC(=O)C1=CC=CN=C1 YYVUROKADZATNZ-UHFFFAOYSA-N 0.000 claims 1
- XKVDGFQUQVVMRN-UHFFFAOYSA-N n-[8-[(4-ethylmorpholin-2-yl)methoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1N(CC)CCOC1COC1=CC=C(C=2N(CCN=2)C(NC(=O)C=2C=NC=CC=2)=N2)C2=C1OC XKVDGFQUQVVMRN-UHFFFAOYSA-N 0.000 claims 1
- WJTQKNQTKYYWRW-UHFFFAOYSA-N n-[8-[2-(4-ethylmorpholin-2-yl)ethoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1N(CC)CCOC1CCOC1=CC=C(C=2N(CCN=2)C(NC(=O)C=2C=NC=CC=2)=N2)C2=C1OC WJTQKNQTKYYWRW-UHFFFAOYSA-N 0.000 claims 1
- UUMDZEMRXJMVLW-UHFFFAOYSA-N n-[8-[2-(diethylamino)ethoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound N=1C2=C(OC)C(OCCN(CC)CC)=CC=C2C2=NCCN2C=1NC(=O)C1=CC=CN=C1 UUMDZEMRXJMVLW-UHFFFAOYSA-N 0.000 claims 1
- ABYVJGMYXVHJSH-UHFFFAOYSA-N n-[8-[2-(dimethylamino)ethoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-6-methylpyridine-3-carboxamide Chemical compound N=1C=2C(OC)=C(OCCN(C)C)C=CC=2C2=NCCN2C=1NC(=O)C1=CC=C(C)N=C1 ABYVJGMYXVHJSH-UHFFFAOYSA-N 0.000 claims 1
- AXWMUMUBHLBJJW-UHFFFAOYSA-N n-[8-[2-[di(propan-2-yl)amino]ethoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound N=1C=2C(OC)=C(OCCN(C(C)C)C(C)C)C=CC=2C2=NCCN2C=1NC(=O)C1=CC=CN=C1 AXWMUMUBHLBJJW-UHFFFAOYSA-N 0.000 claims 1
- AITFHDROVDHPHJ-UHFFFAOYSA-N n-[8-[3-(diethylamino)propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound N=1C2=C(OC)C(OCCCN(CC)CC)=CC=C2C2=NCCN2C=1NC(=O)C1=CC=CN=C1 AITFHDROVDHPHJ-UHFFFAOYSA-N 0.000 claims 1
- FYGKNFXODIEWJB-UHFFFAOYSA-N n-[8-[3-(dimethylamino)propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-1-oxidopyridin-1-ium-3-carboxamide Chemical compound N=1C=2C(OC)=C(OCCCN(C)C)C=CC=2C2=NCCN2C=1NC(=O)C1=CC=C[N+]([O-])=C1 FYGKNFXODIEWJB-UHFFFAOYSA-N 0.000 claims 1
- BQDLTRWPXDTWFK-HDICACEKSA-N n-[8-[3-[(2r,6s)-2,6-dimethylmorpholin-4-yl]propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]pyridine-3-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C=3C=NC=CC=3)=NC=2C(OC)=C1OCCCN1C[C@H](C)O[C@H](C)C1 BQDLTRWPXDTWFK-HDICACEKSA-N 0.000 claims 1
- LTQFHGCERMMMMZ-IYBDPMFKSA-N n-[8-[3-[(2s,6r)-2,6-dimethylmorpholin-4-yl]propoxy]-7-methoxy-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl]-2,4-dimethyl-1,3-thiazole-5-carboxamide Chemical compound C1=CC=2C3=NCCN3C(NC(=O)C3=C(N=C(C)S3)C)=NC=2C(OC)=C1OCCCN1C[C@H](C)O[C@H](C)C1 LTQFHGCERMMMMZ-IYBDPMFKSA-N 0.000 claims 1
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims 1
- OBLVPWTUALCMGD-UHFFFAOYSA-N pyridin-1-ium-3-carboxamide;chloride Chemical compound Cl.NC(=O)C1=CC=CN=C1 OBLVPWTUALCMGD-UHFFFAOYSA-N 0.000 claims 1
- WLCIHZQHQBOALC-UHFFFAOYSA-N pyridine-3-carboxamide hydrate hydrochloride Chemical compound O.Cl.C(C1=CN=CC=C1)(=O)N WLCIHZQHQBOALC-UHFFFAOYSA-N 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims 1
- 0 *C(NC(N1C(c2ccc3OI)=NCC1)=Nc2c3O*)=O Chemical compound *C(NC(N1C(c2ccc3OI)=NCC1)=Nc2c3O*)=O 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13195485.1 | 2013-12-03 | ||
| EP13195485 | 2013-12-03 | ||
| PCT/EP2014/075886 WO2015082322A1 (en) | 2013-12-03 | 2014-11-28 | COMBINATION of PI3K-INHIBITORS |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017501983A JP2017501983A (ja) | 2017-01-19 |
| JP2017501983A5 true JP2017501983A5 (enExample) | 2017-12-28 |
| JP6499657B2 JP6499657B2 (ja) | 2019-04-10 |
Family
ID=49683606
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016535650A Expired - Fee Related JP6499657B2 (ja) | 2013-12-03 | 2014-11-28 | Ｐｉ３ｋ阻害剤の組み合わせ |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US10117874B2 (enExample) |
| EP (1) | EP3077002B1 (enExample) |
| JP (1) | JP6499657B2 (enExample) |
| CN (1) | CN105934256B (enExample) |
| CA (1) | CA2932221C (enExample) |
| WO (1) | WO2015082322A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2168583A1 (en) | 2008-09-24 | 2010-03-31 | Bayer Schering Pharma Aktiengesellschaft | Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines for the treatment of myeloma |
| EP2508525A1 (en) | 2011-04-05 | 2012-10-10 | Bayer Pharma Aktiengesellschaft | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline salts |
| UA119537C2 (uk) | 2013-04-08 | 2019-07-10 | Байєр Фарма Акцієнгезелльшафт | ЗАСТОСУВАННЯ ЗАМІЩЕНИХ 2,3-ДИГІДРОІМІДАЗО[1,2-c]ХІНАЗОЛІНІВ ДЛЯ ЛІКУВАННЯ ЛІМФОМ |
| US10124007B2 (en) | 2013-12-03 | 2018-11-13 | Bayer Pharma Aktiengesellschaft | Combination of PI3K-inhibitors |
| EP3018127A1 (en) | 2014-11-07 | 2016-05-11 | Bayer Pharma Aktiengesellschaft | Synthesis of copanlisib and its dihydrochloride salt |
| CA2978830A1 (en) | 2015-03-09 | 2016-09-15 | Bayer Pharma Aktiengesellschaft | Substituted 2,3-dihydroimidazo[1,2-c]quinazoline-containing combinations |
| CA3016584A1 (en) | 2016-03-08 | 2017-09-14 | Bayer Pharma Aktiengesellschaft | 2-amino-n-[7-methoxy-2,3-dihydroimidazo-[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamides |
| CA3037626A1 (en) * | 2016-09-23 | 2018-03-29 | Bayer Pharma Aktiengesellschaft | Combination of pi3k-inhibitors |
| CN110366417A (zh) | 2017-01-05 | 2019-10-22 | Mbc制药公司 | 使用骨靶向治疗剂的针对骨和骨相关疾病的药物组合治疗 |
| EP3645005A1 (en) * | 2017-06-28 | 2020-05-06 | Bayer Consumer Care AG | Combination of a pi3k-inhibitor with an androgen receptor antagonist |
| AU2022262350B2 (en) | 2021-04-20 | 2026-05-07 | Terrapower Isotopes, Llc | Titania based generators for ac-225 generation |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO310544B1 (no) | 1999-01-04 | 2001-07-23 | Algeta As | Opparbeidelse og anvendelse av radium-223 til fremstilling av preparat samt kit til behandling av kalsifisert vev for palliasjon, benkreft-terapi og/eller overflatebehandling av ben |
| WO2005079867A2 (en) | 2004-02-20 | 2005-09-01 | Algeta As | Alpha-emitting hydroxyapatite particles |
| CA2633593A1 (en) * | 2005-12-16 | 2007-10-04 | Genentech, Inc. | Method for diagnosing, prognosing and treating glioma |
| AR064106A1 (es) * | 2006-12-05 | 2009-03-11 | Bayer Schering Pharma Ag | Derivados de 2,3-dihidroimidazo [1,2-c] quinazolina sustituida utiles para el tratamiento de enfermedades y trastornos hiper-proliferativos asociados con la angiogenesis |
| GB201007353D0 (en) | 2010-04-30 | 2010-06-16 | Algeta Asa | Method |
| GB201007354D0 (en) | 2010-04-30 | 2010-06-16 | Algeta Asa | Method |
| UA113280C2 (xx) | 2010-11-11 | 2017-01-10 | АМІНОСПИРТЗАМІЩЕНІ ПОХІДНІ 2,3-ДИГІДРОІМІДАЗО$1,2-c]ХІНАЗОЛІНУ, ПРИДАТНІ ДЛЯ ЛІКУВАННЯ ГІПЕРПРОЛІФЕРАТИВНИХ ПОРУШЕНЬ І ЗАХВОРЮВАНЬ, ПОВ'ЯЗАНИХ З АНГІОГЕНЕЗОМ | |
| US9730943B2 (en) | 2010-11-11 | 2017-08-15 | Bayer Intellectual Property Gmbh | Alkoxy-substituted 2,3-dihydroimidazo[1,2-C]quinazolines |
| CN103370320B (zh) | 2010-11-11 | 2016-04-27 | 拜耳知识产权有限责任公司 | 芳基氨基醇取代的2,3-二氢咪唑并[1,2-c]喹啉 |
| DE102011079031A1 (de) | 2011-07-12 | 2013-01-17 | Algeta Asa | Flüssigkeitsbehälter |
-
2014
- 2014-11-28 JP JP2016535650A patent/JP6499657B2/ja not_active Expired - Fee Related
- 2014-11-28 CA CA2932221A patent/CA2932221C/en active Active
- 2014-11-28 WO PCT/EP2014/075886 patent/WO2015082322A1/en not_active Ceased
- 2014-11-28 EP EP14805266.5A patent/EP3077002B1/en active Active
- 2014-11-28 US US15/101,638 patent/US10117874B2/en active Active
- 2014-11-28 CN CN201480074721.5A patent/CN105934256B/zh not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2018226470B2 (en) | Compounds for treatment of cancer | |
| KR102534028B1 (ko) | 트리아졸로피리미딘 화합물 및 그의 용도 | |
| CA2737999A1 (en) | Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines for the treatment of myeloma | |
| ES2430614T3 (es) | Métodos de tratamiento del cáncer usando inhibidores de piridopirimidinona de PI3K alfa | |
| JP2018512403A5 (enExample) | ||
| RU2017145026A (ru) | Соединение, ингибирующее brk | |
| HRP20191821T1 (hr) | Antiproliferativni spojevi i načini njihove uporabe | |
| JP2018531983A (ja) | タンパク質分解誘導キメラ化合物ならびにその調製方法および使用方法 | |
| RU2014152790A (ru) | Пирролопиразоновые ингибиторы танкиразы | |
| JP6695353B2 (ja) | Ｆｇｆｒ４阻害剤としてのホルミル化ｎ−複素環式誘導体 | |
| RU2016102137A (ru) | Первичные карбоксамиды в качестве ингибиторов bik | |
| RU2016141645A (ru) | ИНГИБИТОРЫ TrkA КИНАЗЫ, ОСНОВАННЫЕ НА НИХ КОМПОЗИЦИИ И СПОСОБЫ | |
| EA019064B1 (ru) | Способы лечения рака с применением хинаксолинового ингибитора pi3k-альфа | |
| RU2018106453A (ru) | Соединения | |
| RU2015148189A (ru) | ПРОИЗВОДНЫЕ 2-АМИДОПИРИДО[4, 3-d]ПИРИМИДИН-5-ОНА И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ИНГИБИТОРОВ WEE-1 | |
| JP2017528487A5 (enExample) | ||
| JP2017532360A5 (enExample) | ||
| JP2014518544A5 (enExample) | ||
| RU2015121424A (ru) | Комбинированная терапия | |
| JP2015536986A5 (enExample) | ||
| RU2014135436A (ru) | Комбинация ингибитора rtk с антиэстрогеном и ее применение для лечения рака | |
| JP2017513887A5 (enExample) | ||
| RU2015103151A (ru) | Усилитель противоопухолевого эффекта, содержащий имидазооксазиновое соединение | |
| RU2018103174A (ru) | Ингибиторы рекомбинантного белка человека enhancer of zeste homolog 2 | |
| CN1511036B (zh) | 包含信号转导抑制剂和埃坡霉素衍生物的联合形式 |