EA028057B1 - Производные аминопиримидина для применения в качестве модуляторов киназной активности - Google Patents
Производные аминопиримидина для применения в качестве модуляторов киназной активности Download PDFInfo
- Publication number
- EA028057B1 EA028057B1 EA201400338A EA201400338A EA028057B1 EA 028057 B1 EA028057 B1 EA 028057B1 EA 201400338 A EA201400338 A EA 201400338A EA 201400338 A EA201400338 A EA 201400338A EA 028057 B1 EA028057 B1 EA 028057B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- amino
- pyrimidin
- piperazin
- ethyl
- fluorophenyl
- Prior art date
Links
- 230000000694 effects Effects 0.000 title claims description 12
- 108091000080 Phosphotransferase Proteins 0.000 title claims description 10
- 102000020233 phosphotransferase Human genes 0.000 title claims description 10
- 150000005005 aminopyrimidines Chemical class 0.000 title 1
- -1 heterocyclic amine compounds Chemical class 0.000 claims abstract description 101
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 19
- 201000011510 cancer Diseases 0.000 claims abstract description 16
- 238000004519 manufacturing process Methods 0.000 claims abstract description 5
- 150000001875 compounds Chemical class 0.000 claims description 355
- 238000000034 method Methods 0.000 claims description 226
- 150000003839 salts Chemical class 0.000 claims description 46
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 32
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 30
- 239000012453 solvate Substances 0.000 claims description 29
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 24
- 150000001408 amides Chemical class 0.000 claims description 23
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 15
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims description 12
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 12
- 239000008194 pharmaceutical composition Substances 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 10
- 125000004076 pyridyl group Chemical group 0.000 claims description 10
- 239000004480 active ingredient Substances 0.000 claims description 9
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 8
- HYXXLNCSACYDRW-UHFFFAOYSA-N 6-[4-[2-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN(C)C)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 HYXXLNCSACYDRW-UHFFFAOYSA-N 0.000 claims description 7
- 125000003277 amino group Chemical group 0.000 claims description 7
- 239000003814 drug Substances 0.000 claims description 7
- 239000003937 drug carrier Substances 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- LFZNGMFPCMRNTM-UHFFFAOYSA-N 4-amino-1-[6-amino-5-(1h-pyrazol-4-yl)pyrimidin-4-yl]piperidine-4-carboxylic acid Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N1CCC(N)(C(O)=O)CC1 LFZNGMFPCMRNTM-UHFFFAOYSA-N 0.000 claims description 5
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- QWLMSTZXMUMIFV-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-[6-(trifluoromethyl)pyridin-3-yl]acetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1=CC=C(C(F)(F)F)N=C1 QWLMSTZXMUMIFV-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- XVXGWZNJKSPVAQ-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=CC(=CC=1)C(F)(F)F)CN1CCC1 XVXGWZNJKSPVAQ-UHFFFAOYSA-N 0.000 claims description 3
- AVAIWPYMCQSQRB-UHFFFAOYSA-N 6-[4-[2-amino-1-(3-fluorophenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=CC(F)=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 AVAIWPYMCQSQRB-UHFFFAOYSA-N 0.000 claims description 3
- JNCDNFPUXLKIJP-UHFFFAOYSA-N 6-[4-[2-amino-1-(4-chloro-3-fluorophenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(Cl)C(F)=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 JNCDNFPUXLKIJP-UHFFFAOYSA-N 0.000 claims description 3
- VCQXACIYKXUTSF-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethoxy)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C=1C=C(OC(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C=1C=NNC=1 VCQXACIYKXUTSF-UHFFFAOYSA-N 0.000 claims description 3
- VHMVHAGZKRSNDS-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-chloropyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1Cl VHMVHAGZKRSNDS-UHFFFAOYSA-N 0.000 claims description 3
- CRRPJTULCQOFOC-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-ethenylpyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C=C CRRPJTULCQOFOC-UHFFFAOYSA-N 0.000 claims description 3
- PUDRMQRZDFNBTI-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-ethoxypyrimidin-4-amine Chemical compound CCOC1=C(N)N=CN=C1N1CCN(C(CN)C=2C=CC(=CC=2)C(F)(F)F)CC1 PUDRMQRZDFNBTI-UHFFFAOYSA-N 0.000 claims description 3
- CBGPEGDCORSVLT-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperidin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)C(CC1)CCN1C1=NC=NC(N)=C1C=1C=NNC=1 CBGPEGDCORSVLT-UHFFFAOYSA-N 0.000 claims description 3
- AINBPFACADOEBE-UHFFFAOYSA-N 6-[4-[2-amino-1-[6-(trifluoromethyl)pyridin-3-yl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)N=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 AINBPFACADOEBE-UHFFFAOYSA-N 0.000 claims description 3
- WOHMLWSICHUZCI-UHFFFAOYSA-N 6-[4-[3-(azetidin-1-yl)-1-(4-chlorophenyl)propyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=CC(Cl)=CC=1)CCN1CCC1 WOHMLWSICHUZCI-UHFFFAOYSA-N 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 239000013256 coordination polymer Substances 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 16
- 201000010099 disease Diseases 0.000 abstract description 13
- 230000003463 hyperproliferative effect Effects 0.000 abstract description 6
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 264
- 239000000543 intermediate Substances 0.000 description 65
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 57
- 239000000203 mixture Substances 0.000 description 55
- 238000004808 supercritical fluid chromatography Methods 0.000 description 41
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 30
- 239000011541 reaction mixture Substances 0.000 description 30
- 239000000243 solution Substances 0.000 description 25
- AHDGSOPLHGSLPK-UHFFFAOYSA-N 4-amino-1-(6-amino-5-cyanopyrimidin-4-yl)piperidine-4-carboxylic acid Chemical compound NC1=NC=NC(N2CCC(N)(CC2)C(O)=O)=C1C#N AHDGSOPLHGSLPK-UHFFFAOYSA-N 0.000 description 22
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 22
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
- 239000007787 solid Substances 0.000 description 19
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 18
- 239000000651 prodrug Substances 0.000 description 18
- 229940002612 prodrug Drugs 0.000 description 18
- QFKBMLPAZPBJOE-UHFFFAOYSA-N 4-amino-1-(6-amino-5-chloropyrimidin-4-yl)piperidine-4-carboxylic acid Chemical compound NC1=NC=NC(N2CCC(N)(CC2)C(O)=O)=C1Cl QFKBMLPAZPBJOE-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
- 238000002953 preparative HPLC Methods 0.000 description 15
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Substances N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 14
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 14
- KDVZJCYZKUTIHP-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-bromopyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1Br KDVZJCYZKUTIHP-UHFFFAOYSA-N 0.000 description 13
- 241000124008 Mammalia Species 0.000 description 13
- OYRRZWATULMEPF-UHFFFAOYSA-N pyrimidin-4-amine Chemical compound NC1=CC=NC=N1 OYRRZWATULMEPF-UHFFFAOYSA-N 0.000 description 13
- 150000001412 amines Chemical class 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 12
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 11
- 102000001253 Protein Kinase Human genes 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 11
- 239000002244 precipitate Substances 0.000 description 11
- 108060006633 protein kinase Proteins 0.000 description 11
- 108090000623 proteins and genes Proteins 0.000 description 11
- MMMSSXLSEGSDHS-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 MMMSSXLSEGSDHS-UHFFFAOYSA-N 0.000 description 10
- 102000004190 Enzymes Human genes 0.000 description 10
- 108090000790 Enzymes Proteins 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 10
- 238000003786 synthesis reaction Methods 0.000 description 10
- LBUNNMJLXWQQBY-UHFFFAOYSA-N 4-fluorophenylboronic acid Chemical compound OB(O)C1=CC=C(F)C=C1 LBUNNMJLXWQQBY-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- 239000012043 crude product Substances 0.000 description 9
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 9
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 9
- 239000003112 inhibitor Substances 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 239000012044 organic layer Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 8
- 210000004027 cell Anatomy 0.000 description 8
- 230000002401 inhibitory effect Effects 0.000 description 8
- 230000005764 inhibitory process Effects 0.000 description 8
- 102000004169 proteins and genes Human genes 0.000 description 8
- DQSBRYJETNYGCI-UHFFFAOYSA-N 5-bromo-6-chloropyrimidin-4-amine Chemical compound NC1=NC=NC(Cl)=C1Br DQSBRYJETNYGCI-UHFFFAOYSA-N 0.000 description 7
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 7
- 150000007513 acids Chemical class 0.000 description 7
- 239000002246 antineoplastic agent Substances 0.000 description 7
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 7
- 239000012267 brine Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 7
- 229910000027 potassium carbonate Inorganic materials 0.000 description 7
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 7
- MZGSRODYXJPWKE-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-piperazin-1-ylpyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N1CCNCC1 MZGSRODYXJPWKE-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 6
- 229910000024 caesium carbonate Inorganic materials 0.000 description 6
- 230000010261 cell growth Effects 0.000 description 6
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- 239000003826 tablet Substances 0.000 description 6
- 230000014616 translation Effects 0.000 description 6
- RXLYPPSAPOEZIY-UHFFFAOYSA-N 2-[[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]methyl]-4,5-dichlorophenol Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1CC1=CC(Cl)=C(Cl)C=C1O RXLYPPSAPOEZIY-UHFFFAOYSA-N 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 102000038030 PI3Ks Human genes 0.000 description 5
- 108091007960 PI3Ks Proteins 0.000 description 5
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 235000011054 acetic acid Nutrition 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 230000022131 cell cycle Effects 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 150000002576 ketones Chemical class 0.000 description 5
- 230000026731 phosphorylation Effects 0.000 description 5
- 238000006366 phosphorylation reaction Methods 0.000 description 5
- 238000001959 radiotherapy Methods 0.000 description 5
- 238000006722 reduction reaction Methods 0.000 description 5
- 238000004007 reversed phase HPLC Methods 0.000 description 5
- 239000000741 silica gel Substances 0.000 description 5
- 229910002027 silica gel Inorganic materials 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 5
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical class ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 5
- 238000013519 translation Methods 0.000 description 5
- OEAXBXCYSAIWDD-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-[3-(trifluoromethyl)phenyl]acetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1=CC=CC(C(F)(F)F)=C1 OEAXBXCYSAIWDD-UHFFFAOYSA-N 0.000 description 4
- DPGSPRJLAZGUBQ-UHFFFAOYSA-N 2-ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Chemical compound CC1(C)OB(C=C)OC1(C)C DPGSPRJLAZGUBQ-UHFFFAOYSA-N 0.000 description 4
- RWLZSQDGEYWUSU-UHFFFAOYSA-N 5-bromo-6-[4-[2-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN(C)C)N(CC1)CCN1C1=NC=NC(N)=C1Br RWLZSQDGEYWUSU-UHFFFAOYSA-N 0.000 description 4
- IVIHGYDROQUEOM-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperidin-1-yl]-5-bromopyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)C(CC1)CCN1C1=NC=NC(N)=C1Br IVIHGYDROQUEOM-UHFFFAOYSA-N 0.000 description 4
- 208000026310 Breast neoplasm Diseases 0.000 description 4
- 102000002278 Ribosomal Proteins Human genes 0.000 description 4
- 108010000605 Ribosomal Proteins Proteins 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 238000006069 Suzuki reaction reaction Methods 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 230000003321 amplification Effects 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 239000002775 capsule Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 238000003818 flash chromatography Methods 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 230000014759 maintenance of location Effects 0.000 description 4
- 208000030159 metabolic disease Diseases 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 230000035772 mutation Effects 0.000 description 4
- 238000003199 nucleic acid amplification method Methods 0.000 description 4
- 108090000765 processed proteins & peptides Proteins 0.000 description 4
- 230000035755 proliferation Effects 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- ZAHRKKWIAAJSAO-UHFFFAOYSA-N rapamycin Natural products COCC(O)C(=C/C(C)C(=O)CC(OC(=O)C1CCCCN1C(=O)C(=O)C2(O)OC(CC(OC)C(=CC=CC=CC(C)CC(C)C(=O)C)C)CCC2C)C(C)CC3CCC(O)C(C3)OC)C ZAHRKKWIAAJSAO-UHFFFAOYSA-N 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 150000003335 secondary amines Chemical class 0.000 description 4
- 230000011664 signaling Effects 0.000 description 4
- 229960002930 sirolimus Drugs 0.000 description 4
- 239000012279 sodium borohydride Substances 0.000 description 4
- 229910000033 sodium borohydride Inorganic materials 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 229940124597 therapeutic agent Drugs 0.000 description 4
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 3
- PZJIROPGHLJDJY-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-[4-[1-(3-fluorophenyl)-2-piperidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(F)C=CC=1)CN1CCCCC1 PZJIROPGHLJDJY-UHFFFAOYSA-N 0.000 description 3
- SMCAESWMRAHOKB-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-[4-[2-pyrrolidin-1-yl-1-[3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(C=CC=1)C(F)(F)F)CN1CCCC1 SMCAESWMRAHOKB-UHFFFAOYSA-N 0.000 description 3
- KODBGGCHGJZJNY-UHFFFAOYSA-N 5-bromo-6-[4-[1-(4-fluorophenyl)-2-pyrrolidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound NC1=NC=NC(N2CCN(CC2)C(CN2CCCC2)C=2C=CC(F)=CC=2)=C1Br KODBGGCHGJZJNY-UHFFFAOYSA-N 0.000 description 3
- FVFJADZFRVBXGA-UHFFFAOYSA-N 5-bromo-6-[4-[2-piperidin-1-yl-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound NC1=NC=NC(N2CCN(CC2)C(CN2CCCCC2)C=2C=CC(=CC=2)C(F)(F)F)=C1Br FVFJADZFRVBXGA-UHFFFAOYSA-N 0.000 description 3
- UWRGCDQCHNMPRC-UHFFFAOYSA-N 6-[4-[[2-(azetidin-3-yloxy)-4,5-dichlorophenyl]methyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1CC1=CC(Cl)=C(Cl)C=C1OC1CNC1 UWRGCDQCHNMPRC-UHFFFAOYSA-N 0.000 description 3
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 239000005711 Benzoic acid Substances 0.000 description 3
- 206010061218 Inflammation Diseases 0.000 description 3
- 208000008839 Kidney Neoplasms Diseases 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 230000033115 angiogenesis Effects 0.000 description 3
- 235000010233 benzoic acid Nutrition 0.000 description 3
- 230000033228 biological regulation Effects 0.000 description 3
- 150000001649 bromium compounds Chemical class 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 150000001805 chlorine compounds Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 208000035475 disorder Diseases 0.000 description 3
- 239000002552 dosage form Substances 0.000 description 3
- 239000012458 free base Substances 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 230000004054 inflammatory process Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 108020004999 messenger RNA Proteins 0.000 description 3
- 150000002825 nitriles Chemical class 0.000 description 3
- 210000000496 pancreas Anatomy 0.000 description 3
- 230000037361 pathway Effects 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- IDXKTTNFXPPXJY-UHFFFAOYSA-N pyrimidin-1-ium;chloride Chemical compound Cl.C1=CN=CN=C1 IDXKTTNFXPPXJY-UHFFFAOYSA-N 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- 238000004366 reverse phase liquid chromatography Methods 0.000 description 3
- 238000005070 sampling Methods 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- QFJCIRLUMZQUOT-HPLJOQBZSA-N sirolimus Chemical compound C1C[C@@H](O)[C@H](OC)C[C@@H]1C[C@@H](C)[C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@](O)(O2)[C@H](C)CC[C@H]2C[C@H](OC)/C(C)=C/C=C/C=C/[C@@H](C)C[C@@H](C)C(=O)[C@H](OC)[C@H](O)/C(C)=C/[C@@H](C)C(=O)C1 QFJCIRLUMZQUOT-HPLJOQBZSA-N 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 238000000825 ultraviolet detection Methods 0.000 description 3
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 2
- ULTHEAFYOOPTTB-UHFFFAOYSA-N 1,4-dibromobutane Chemical compound BrCCCCBr ULTHEAFYOOPTTB-UHFFFAOYSA-N 0.000 description 2
- UIUKIJNFQRBIPO-UHFFFAOYSA-N 1-(3-fluorophenyl)-2-piperidin-1-ylethanol Chemical compound C=1C=CC(F)=CC=1C(O)CN1CCCCC1 UIUKIJNFQRBIPO-UHFFFAOYSA-N 0.000 description 2
- AFEAWYLBSVKOAY-UHFFFAOYSA-N 1-[(2-methylpropan-2-yl)oxycarbonyl]-4-[(2-methylpropan-2-yl)oxycarbonylamino]piperidine-4-carboxylic acid Chemical compound CC(C)(C)OC(=O)NC1(C(O)=O)CCN(C(=O)OC(C)(C)C)CC1 AFEAWYLBSVKOAY-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- RAHWENZDXQYASY-UHFFFAOYSA-N 2-[1-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]ethyl]-5-chlorophenol Chemical compound C=1C=C(Cl)C=C(O)C=1C(C)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 RAHWENZDXQYASY-UHFFFAOYSA-N 0.000 description 2
- UWPDXHHXHOYKOI-UHFFFAOYSA-N 2-[4-(6-amino-5-bromopyrimidin-4-yl)piperazin-1-yl]-2-[3-(trifluoromethyl)phenyl]acetonitrile Chemical compound NC1=NC=NC(N2CCN(CC2)C(C#N)C=2C=C(C=CC=2)C(F)(F)F)=C1Br UWPDXHHXHOYKOI-UHFFFAOYSA-N 0.000 description 2
- DMBXRYJQQGGYHD-UHFFFAOYSA-N 2-[4-(6-amino-5-bromopyrimidin-4-yl)piperazin-1-yl]-2-[4-(trifluoromethyl)phenyl]acetonitrile Chemical compound NC1=NC=NC(N2CCN(CC2)C(C#N)C=2C=CC(=CC=2)C(F)(F)F)=C1Br DMBXRYJQQGGYHD-UHFFFAOYSA-N 0.000 description 2
- QNKOCFJZJWOXDE-UHFFFAOYSA-N 2-[4-(trifluoromethyl)phenyl]acetonitrile Chemical compound FC(F)(F)C1=CC=C(CC#N)C=C1 QNKOCFJZJWOXDE-UHFFFAOYSA-N 0.000 description 2
- RNGNQFSTMTXKET-UHFFFAOYSA-N 2-[4-[4-amino-6-[4-[2-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-5-yl]phenyl]propan-2-ol Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN(C)C)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(C(C)(C)O)C=C1 RNGNQFSTMTXKET-UHFFFAOYSA-N 0.000 description 2
- YWOISVBWYNAERO-UHFFFAOYSA-N 2-[4-[6-amino-5-(1H-pyrazol-4-yl)pyrimidin-4-yl]piperazin-1-yl]-2-(4-methylsulfonylphenyl)acetonitrile Chemical compound CS(=O)(=O)c1ccc(cc1)C(C#N)N1CCN(CC1)c1ncnc(N)c1-c1cn[nH]c1 YWOISVBWYNAERO-UHFFFAOYSA-N 0.000 description 2
- MHHGRUQUGVEDCC-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(3,4-dichlorophenyl)acetonitrile Chemical compound Nc1ncnc(N2CCN(CC2)C(C#N)c2ccc(Cl)c(Cl)c2)c1-c1ccc(F)cc1 MHHGRUQUGVEDCC-UHFFFAOYSA-N 0.000 description 2
- TZUGACGKOBAAFX-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(3-chloro-4-fluorophenyl)acetonitrile Chemical compound Nc1ncnc(N2CCN(CC2)C(C#N)c2ccc(F)c(Cl)c2)c1-c1ccc(F)cc1 TZUGACGKOBAAFX-UHFFFAOYSA-N 0.000 description 2
- VGWUOKNMQVXNLZ-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(4-chloro-3-fluorophenyl)acetonitrile Chemical compound Nc1ncnc(N2CCN(CC2)C(C#N)c2ccc(Cl)c(F)c2)c1-c1ccc(F)cc1 VGWUOKNMQVXNLZ-UHFFFAOYSA-N 0.000 description 2
- PZGCLZNIYNHOLQ-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(4-chlorophenyl)acetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1=CC=C(Cl)C=C1 PZGCLZNIYNHOLQ-UHFFFAOYSA-N 0.000 description 2
- PNELMSYEUNNHCE-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(4-fluorophenyl)acetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1=CC=C(F)C=C1 PNELMSYEUNNHCE-UHFFFAOYSA-N 0.000 description 2
- PARUIZNDUVDJJH-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(6-chloropyridin-3-yl)acetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1=CC=C(Cl)N=C1 PARUIZNDUVDJJH-UHFFFAOYSA-N 0.000 description 2
- DVBGLZQXRFQYFW-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(6-methoxypyridin-3-yl)acetonitrile Chemical compound C1=NC(OC)=CC=C1C(C#N)N1CCN(C=2C(=C(N)N=CN=2)C=2C=CC(F)=CC=2)CC1 DVBGLZQXRFQYFW-UHFFFAOYSA-N 0.000 description 2
- HDIBSDAVXUHPHM-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-[4-(trifluoromethyl)phenyl]acetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1=CC=C(C(F)(F)F)C=C1 HDIBSDAVXUHPHM-UHFFFAOYSA-N 0.000 description 2
- GZBACRMFEDHLMQ-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-[4-fluoro-3-(trifluoromethyl)phenyl]acetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1=CC=C(F)C(C(F)(F)F)=C1 GZBACRMFEDHLMQ-UHFFFAOYSA-N 0.000 description 2
- LWNCMOYGNIEUBB-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-cyclohexylacetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1CCCCC1 LWNCMOYGNIEUBB-UHFFFAOYSA-N 0.000 description 2
- ZDOIQVOXFFGYHB-UHFFFAOYSA-N 2-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-pyridin-3-ylacetonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C#N)C1=CC=CN=C1 ZDOIQVOXFFGYHB-UHFFFAOYSA-N 0.000 description 2
- MPCXCKXGCBIQNZ-UHFFFAOYSA-N 2-piperazin-1-yl-2-[4-(trifluoromethyl)phenyl]ethanamine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N1CCNCC1 MPCXCKXGCBIQNZ-UHFFFAOYSA-N 0.000 description 2
- UUEKUOCQTDOUTP-UHFFFAOYSA-N 2-piperazin-1-yl-2-[4-(trifluoromethyl)phenyl]ethanamine;hydrochloride Chemical compound Cl.C=1C=C(C(F)(F)F)C=CC=1C(CN)N1CCNCC1 UUEKUOCQTDOUTP-UHFFFAOYSA-N 0.000 description 2
- FOKXJBAOYOERDP-UHFFFAOYSA-N 3-[[2-[4-[6-amino-5-(1-methylpyrazol-3-yl)pyrimidin-4-yl]piperazin-1-yl]-2-[4-(trifluoromethyl)phenyl]ethyl]amino]-2,3-dimethylbutan-2-ol Chemical compound CN1C=CC(C=2C(=NC=NC=2N)N2CCN(CC2)C(CNC(C)(C)C(C)(C)O)C=2C=CC(=CC=2)C(F)(F)F)=N1 FOKXJBAOYOERDP-UHFFFAOYSA-N 0.000 description 2
- RGNUWPUTQXUXQZ-UHFFFAOYSA-N 4,6-dichloro-5-ethylpyrimidine Chemical compound CCC1=C(Cl)N=CN=C1Cl RGNUWPUTQXUXQZ-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- UDEZVIRHXVCHLL-UHFFFAOYSA-N 4-[1-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(azetidin-1-yl)ethyl]benzonitrile Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=CC(=CC=1)C#N)CN1CCC1 UDEZVIRHXVCHLL-UHFFFAOYSA-N 0.000 description 2
- BRDKKWWMEGAFFW-UHFFFAOYSA-N 4-[4-amino-6-[4-[2-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-5-yl]benzoic acid Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN(C)C)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(C(O)=O)C=C1 BRDKKWWMEGAFFW-UHFFFAOYSA-N 0.000 description 2
- ZIJPAZBDDUXIIX-UHFFFAOYSA-N 4-amino-6-[3-amino-3-[[(2,4-difluorobenzoyl)amino]methyl]pyrrolidin-1-yl]pyrimidine-5-carboxamide Chemical compound NC(=O)C1=C(N)N=CN=C1N1CC(N)(CNC(=O)C=2C(=CC(F)=CC=2)F)CC1 ZIJPAZBDDUXIIX-UHFFFAOYSA-N 0.000 description 2
- MMBATPFOMXPRKJ-UHFFFAOYSA-N 4-amino-6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-5-ol Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1O MMBATPFOMXPRKJ-UHFFFAOYSA-N 0.000 description 2
- BNDTXUGXLYTVHW-UHFFFAOYSA-N 4-amino-6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidine-5-carbonitrile Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C#N BNDTXUGXLYTVHW-UHFFFAOYSA-N 0.000 description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 2
- CKOVQFRNHWIDIS-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-[4-[1-(4-fluorophenyl)-2-piperidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=CC(F)=CC=1)CN1CCCCC1 CKOVQFRNHWIDIS-UHFFFAOYSA-N 0.000 description 2
- GGRDNSPVEJQBBQ-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-[4-[1-(4-fluorophenyl)-2-pyrrolidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=CC(F)=CC=1)CN1CCCC1 GGRDNSPVEJQBBQ-UHFFFAOYSA-N 0.000 description 2
- WJKBZYILJASKEE-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-[4-[2-piperidin-1-yl-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=CC(=CC=1)C(F)(F)F)CN1CCCCC1 WJKBZYILJASKEE-UHFFFAOYSA-N 0.000 description 2
- WWDOLCUGSDRCRP-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-[4-[[4-(trifluoromethyl)phenyl]methyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1CC1=CC=C(C(F)(F)F)C=C1 WWDOLCUGSDRCRP-UHFFFAOYSA-N 0.000 description 2
- HHECCAZZKIBWLT-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-[4-[[4-(trifluoromethyl)phenyl]methyl]piperidin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCC1CC1=CC=C(C(F)(F)F)C=C1 HHECCAZZKIBWLT-UHFFFAOYSA-N 0.000 description 2
- OSKPKUBBIPVDEA-UHFFFAOYSA-N 5-(6-aminopyridin-3-yl)-6-[4-[2-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN(C)C)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(N)N=C1 OSKPKUBBIPVDEA-UHFFFAOYSA-N 0.000 description 2
- JWNMQRWPSZBIRR-UHFFFAOYSA-N 5-bromo-6-[4-[1-(3-fluorophenyl)-2-piperidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound NC1=NC=NC(N2CCN(CC2)C(CN2CCCCC2)C=2C=C(F)C=CC=2)=C1Br JWNMQRWPSZBIRR-UHFFFAOYSA-N 0.000 description 2
- YNHZEHYABFDFDO-UHFFFAOYSA-N 5-bromo-6-[4-[1-(4-fluorophenyl)-2-piperidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound NC1=NC=NC(N2CCN(CC2)C(CN2CCCCC2)C=2C=CC(F)=CC=2)=C1Br YNHZEHYABFDFDO-UHFFFAOYSA-N 0.000 description 2
- MPBVVWFECAGLKU-UHFFFAOYSA-N 5-bromo-6-[4-[2-piperidin-1-yl-1-[3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound Nc1ncnc(N2CCN(CC2)C(CN2CCCCC2)c2cccc(c2)C(F)(F)F)c1Br MPBVVWFECAGLKU-UHFFFAOYSA-N 0.000 description 2
- KXPXVCMLCFWFJW-UHFFFAOYSA-N 5-bromo-6-[4-[2-pyrrolidin-1-yl-1-[3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound NC1=NC=NC(N2CCN(CC2)C(CN2CCCC2)C=2C=C(C=CC=2)C(F)(F)F)=C1Br KXPXVCMLCFWFJW-UHFFFAOYSA-N 0.000 description 2
- DUEWGVGSNWEHTC-UHFFFAOYSA-N 5-cyclopropyl-6-[4-[2-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN(C)C)N(CC1)CCN1C1=NC=NC(N)=C1C1CC1 DUEWGVGSNWEHTC-UHFFFAOYSA-N 0.000 description 2
- XODZVALGKSETDI-UHFFFAOYSA-N 6-[4-(2-amino-1-cyclohexylethyl)piperazin-1-yl]-5-ethylpyrimidin-4-amine Chemical compound CCC1=C(N)N=CN=C1N1CCN(C(CN)C2CCCCC2)CC1 XODZVALGKSETDI-UHFFFAOYSA-N 0.000 description 2
- DIAQYSLZMGCMGJ-UHFFFAOYSA-N 6-[4-(2-amino-1-phenylethyl)piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=CC=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 DIAQYSLZMGCMGJ-UHFFFAOYSA-N 0.000 description 2
- PFRJJWWPORNTLC-UHFFFAOYSA-N 6-[4-(2-amino-1-phenylethyl)piperazin-1-yl]-5-bromopyrimidin-4-amine Chemical compound C=1C=CC=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1Br PFRJJWWPORNTLC-UHFFFAOYSA-N 0.000 description 2
- LZEIZJWSDOAMHN-UHFFFAOYSA-N 6-[4-(2-amino-1-pyridin-3-ylethyl)piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=CN=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 LZEIZJWSDOAMHN-UHFFFAOYSA-N 0.000 description 2
- ONSMSGSUCWAFJE-UHFFFAOYSA-N 6-[4-[(4-chlorophenyl)methyl]piperidin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCC1CC1=CC=C(Cl)C=C1 ONSMSGSUCWAFJE-UHFFFAOYSA-N 0.000 description 2
- JZSKKZDAVFEUKI-UHFFFAOYSA-N 6-[4-[(cyclopentylamino)-(4-fluorophenyl)methyl]piperidin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCC1C(C=1C=CC(F)=CC=1)NC1CCCC1 JZSKKZDAVFEUKI-UHFFFAOYSA-N 0.000 description 2
- QYFWKAAHEMXBJV-UHFFFAOYSA-N 6-[4-[1-(3-fluorophenyl)-2-piperidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C1=NC(N)=CC(N2CCN(CC2)C(CN2CCCCC2)C=2C=C(F)C=CC=2)=N1 QYFWKAAHEMXBJV-UHFFFAOYSA-N 0.000 description 2
- YBTRLRWHXNZKMS-UHFFFAOYSA-N 6-[4-[1-(4-fluorophenyl)-2-piperidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C1=NC(N)=CC(N2CCN(CC2)C(CN2CCCCC2)C=2C=CC(F)=CC=2)=N1 YBTRLRWHXNZKMS-UHFFFAOYSA-N 0.000 description 2
- QTNXQGPDTJDWLZ-UHFFFAOYSA-N 6-[4-[1-(4-fluorophenyl)-2-pyrrolidin-1-ylethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C1=NC(N)=CC(N2CCN(CC2)C(CN2CCCC2)C=2C=CC(F)=CC=2)=N1 QTNXQGPDTJDWLZ-UHFFFAOYSA-N 0.000 description 2
- ZEDLSCZYQROHLE-UHFFFAOYSA-N 6-[4-[1-[2-(azetidin-3-yloxy)-4-chlorophenyl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(Cl)C=C(OC2CNC2)C=1C(C)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 ZEDLSCZYQROHLE-UHFFFAOYSA-N 0.000 description 2
- ZVYNXNWMPJPQGX-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(2,3-dichlorophenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C(=C(Cl)C=CC=1)Cl)CN1CCC1 ZVYNXNWMPJPQGX-UHFFFAOYSA-N 0.000 description 2
- DZBIXVFNNIYAMP-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(2,3-difluoro-4-methylphenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound FC1=C(F)C(C)=CC=C1C(N1CCN(CC1)C=1C(=C(N)N=CN=1)C1=CNN=C1)CN1CCC1 DZBIXVFNNIYAMP-UHFFFAOYSA-N 0.000 description 2
- DFZMVCDBKCYXSH-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(2,3-difluorophenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C(=C(F)C=CC=1)F)CN1CCC1 DFZMVCDBKCYXSH-UHFFFAOYSA-N 0.000 description 2
- QZBZINLUZLQNLE-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(3,4-dichlorophenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(Cl)C(Cl)=CC=1)CN1CCC1 QZBZINLUZLQNLE-UHFFFAOYSA-N 0.000 description 2
- IPUUHKGPQVPFGC-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(3,4-dichlorophenyl)ethyl]piperazin-1-yl]-5-(6-piperazin-1-ylpyridin-3-yl)pyrimidin-4-amine Chemical compound C=1C=C(N2CCNCC2)N=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(Cl)C(Cl)=CC=1)CN1CCC1 IPUUHKGPQVPFGC-UHFFFAOYSA-N 0.000 description 2
- GXYWKLODYORGKX-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(3-fluoro-4-methoxyphenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C1=C(F)C(OC)=CC=C1C(N1CCN(CC1)C=1C(=C(N)N=CN=1)C=1C=CC(F)=CC=1)CN1CCC1 GXYWKLODYORGKX-UHFFFAOYSA-N 0.000 description 2
- WRRZJSQJDSGTQB-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(3-fluorophenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(F)C=CC=1)CN1CCC1 WRRZJSQJDSGTQB-UHFFFAOYSA-N 0.000 description 2
- WSKDMHDDEWWFCX-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(3-fluorophenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(F)C=CC=1)CN1CCC1 WSKDMHDDEWWFCX-UHFFFAOYSA-N 0.000 description 2
- ITXFJWAJRISIAO-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(4-imidazol-1-ylphenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=CC(=CC=1)N1C=NC=C1)CN1CCC1 ITXFJWAJRISIAO-UHFFFAOYSA-N 0.000 description 2
- RRCLHLQPBHVAGJ-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(4-methylsulfonylphenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C(N1CCN(CC1)C=1C(=C(N)N=CN=1)C=1C=CC(F)=CC=1)CN1CCC1 RRCLHLQPBHVAGJ-UHFFFAOYSA-N 0.000 description 2
- GMQLYFYAIMCLAF-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(5,6,7,8-tetrahydronaphthalen-2-yl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C2CCCCC2=CC=1)CN1CCC1 GMQLYFYAIMCLAF-UHFFFAOYSA-N 0.000 description 2
- ADIULAYLFWZSLV-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(5,6,7,8-tetrahydronaphthalen-2-yl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C2CCCCC2=CC=1)CN1CCC1 ADIULAYLFWZSLV-UHFFFAOYSA-N 0.000 description 2
- JXBMYCSYZAIJTH-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(5,6,7,8-tetrahydronaphthalen-2-yl)ethyl]piperazin-1-yl]-5-(6-piperazin-1-ylpyridin-3-yl)pyrimidin-4-amine Chemical compound C=1C=C(N2CCNCC2)N=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C2CCCCC2=CC=1)CN1CCC1 JXBMYCSYZAIJTH-UHFFFAOYSA-N 0.000 description 2
- CGTQFSMDHAESNJ-UHFFFAOYSA-N 6-[4-[2-(dimethylamino)ethoxy-(4-fluorophenyl)methyl]piperidin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C(OCCN(C)C)C(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 CGTQFSMDHAESNJ-UHFFFAOYSA-N 0.000 description 2
- CMWLCHSTVVYTFM-UHFFFAOYSA-N 6-[4-[2-amino-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl]piperazin-1-yl]-5-ethylpyrimidin-4-amine Chemical compound CCC1=C(N)N=CN=C1N1CCN(C(CN)C=2C=C3OCCOC3=CC=2)CC1 CMWLCHSTVVYTFM-UHFFFAOYSA-N 0.000 description 2
- KCMBQENQXWWXDX-UHFFFAOYSA-N 6-[4-[2-amino-1-(3,4-dichlorophenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(Cl)C(Cl)=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 KCMBQENQXWWXDX-UHFFFAOYSA-N 0.000 description 2
- RZLQNDVONYRFCZ-UHFFFAOYSA-N 6-[4-[2-amino-1-(3-chloro-4-fluorophenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C(Cl)=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 RZLQNDVONYRFCZ-UHFFFAOYSA-N 0.000 description 2
- XJTDLSUUILSBSQ-UHFFFAOYSA-N 6-[4-[2-amino-1-(4-chloro-3-fluorophenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C=1C=C(Cl)C(F)=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C=1C=NNC=1 XJTDLSUUILSBSQ-UHFFFAOYSA-N 0.000 description 2
- VQYYPVPZRSOPHE-UHFFFAOYSA-N 6-[4-[2-amino-1-(4-chlorophenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(Cl)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 VQYYPVPZRSOPHE-UHFFFAOYSA-N 0.000 description 2
- WZQPDUPNWNYRGZ-UHFFFAOYSA-N 6-[4-[2-amino-1-(4-chlorophenyl)ethyl]piperazin-1-yl]-5-ethylpyrimidin-4-amine Chemical compound CCC1=C(N)N=CN=C1N1CCN(C(CN)C=2C=CC(Cl)=CC=2)CC1 WZQPDUPNWNYRGZ-UHFFFAOYSA-N 0.000 description 2
- QOAJNEZEOFGNDX-UHFFFAOYSA-N 6-[4-[2-amino-1-(4-fluorophenyl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 QOAJNEZEOFGNDX-UHFFFAOYSA-N 0.000 description 2
- AFLROXNDLUFCMR-UHFFFAOYSA-N 6-[4-[2-amino-1-(4-methylsulfonylphenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=CC(S(=O)(=O)C)=CC=C1C(CN)N1CCN(C=2C(=C(N)N=CN=2)C2=CNN=C2)CC1 AFLROXNDLUFCMR-UHFFFAOYSA-N 0.000 description 2
- HRDNQTRURDVWED-UHFFFAOYSA-N 6-[4-[2-amino-1-(6-chloropyridin-3-yl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(Cl)N=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 HRDNQTRURDVWED-UHFFFAOYSA-N 0.000 description 2
- GQBFYQDLMHVDBC-UHFFFAOYSA-N 6-[4-[2-amino-1-(6-chloropyridin-3-yl)ethyl]piperazin-1-yl]-5-ethylpyrimidin-4-amine Chemical compound CCC1=C(N)N=CN=C1N1CCN(C(CN)C=2C=NC(Cl)=CC=2)CC1 GQBFYQDLMHVDBC-UHFFFAOYSA-N 0.000 description 2
- XJTLKGSNWAMFGV-UHFFFAOYSA-N 6-[4-[2-amino-1-(6-methoxypyridin-3-yl)ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C1=NC(OC)=CC=C1C(CN)N1CCN(C=2C(=C(N)N=CN=2)C=2C=CC(F)=CC=2)CC1 XJTLKGSNWAMFGV-UHFFFAOYSA-N 0.000 description 2
- PEXYGWVOMRGCMP-UHFFFAOYSA-N 6-[4-[2-amino-1-[2-fluoro-4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=C(F)C=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 PEXYGWVOMRGCMP-UHFFFAOYSA-N 0.000 description 2
- NHLVVBQVYVWDTO-UHFFFAOYSA-N 6-[4-[2-amino-1-[2-fluoro-5-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C(C(F)(F)F)=CC=C(F)C=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 NHLVVBQVYVWDTO-UHFFFAOYSA-N 0.000 description 2
- KPARNPNYKLSWPR-UHFFFAOYSA-N 6-[4-[2-amino-1-[3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=CC(C(F)(F)F)=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 KPARNPNYKLSWPR-UHFFFAOYSA-N 0.000 description 2
- NMRPZLNVYXFBDQ-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1,2-oxazol-4-yl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C=1C=NOC=1 NMRPZLNVYXFBDQ-UHFFFAOYSA-N 0.000 description 2
- GUOQUSRFPFKBCC-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1-ethylpyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NN(CC)C=C1C1=C(N)N=CN=C1N1CCN(C(CN)C=2C=CC(=CC=2)C(F)(F)F)CC1 GUOQUSRFPFKBCC-UHFFFAOYSA-N 0.000 description 2
- CDDICJBFDYJQKQ-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1-methylpyrazol-3-yl)pyrimidin-4-amine Chemical compound CN1C=CC(C=2C(=NC=NC=2N)N2CCN(CC2)C(CN)C=2C=CC(=CC=2)C(F)(F)F)=N1 CDDICJBFDYJQKQ-UHFFFAOYSA-N 0.000 description 2
- VAIFBJMSMMVFMV-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1-methylpyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NN(C)C=C1C1=C(N)N=CN=C1N1CCN(C(CN)C=2C=CC(=CC=2)C(F)(F)F)CC1 VAIFBJMSMMVFMV-UHFFFAOYSA-N 0.000 description 2
- LRVNLSGZICUQLS-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C=1C=NNC=1 LRVNLSGZICUQLS-UHFFFAOYSA-N 0.000 description 2
- NRDMRJFTTDZUJO-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrrol-3-yl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C=1C=CNC=1 NRDMRJFTTDZUJO-UHFFFAOYSA-N 0.000 description 2
- DTRSWGDSVFJRDN-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(2,2,2-trifluoroethoxy)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1OCC(F)(F)F DTRSWGDSVFJRDN-UHFFFAOYSA-N 0.000 description 2
- ZUPODOQBOLVNJM-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-[(3-fluoroazetidin-1-yl)methyl]pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1CN1CC(F)C1 ZUPODOQBOLVNJM-UHFFFAOYSA-N 0.000 description 2
- IRHPCOFQAKQMKZ-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-fluoropyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1F IRHPCOFQAKQMKZ-UHFFFAOYSA-N 0.000 description 2
- PZMJEFZKUHGWCU-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-methoxypyrimidin-4-amine Chemical compound COC1=C(N)N=CN=C1N1CCN(C(CN)C=2C=CC(=CC=2)C(F)(F)F)CC1 PZMJEFZKUHGWCU-UHFFFAOYSA-N 0.000 description 2
- YMMQCIOYDSVEKE-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-phenylmethoxypyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1OCC1=CC=CC=C1 YMMQCIOYDSVEKE-UHFFFAOYSA-N 0.000 description 2
- LTYBCYMWIJYVDA-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperidin-1-yl]-5-(1,2-oxazol-4-yl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)C(CC1)CCN1C1=NC=NC(N)=C1C=1C=NOC=1 LTYBCYMWIJYVDA-UHFFFAOYSA-N 0.000 description 2
- ZFRRPTYEXATFLA-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperidin-1-yl]-5-(1-methylpyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NN(C)C=C1C1=C(N)N=CN=C1N1CCC(C(CN)C=2C=CC(=CC=2)C(F)(F)F)CC1 ZFRRPTYEXATFLA-UHFFFAOYSA-N 0.000 description 2
- NEIPIANQJOZZOB-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperidin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(CN)C(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 NEIPIANQJOZZOB-UHFFFAOYSA-N 0.000 description 2
- AAUFNNMZNJHJBR-UHFFFAOYSA-N 6-[4-[2-amino-1-[4-fluoro-3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C(C(F)(F)F)=CC=1C(CN)N(CC1)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 AAUFNNMZNJHJBR-UHFFFAOYSA-N 0.000 description 2
- XRPOQCMAHIABMN-UHFFFAOYSA-N 6-[4-[2-piperidin-1-yl-1-[3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C1=NC(N)=CC(N2CCN(CC2)C(CN2CCCCC2)C=2C=C(C=CC=2)C(F)(F)F)=N1 XRPOQCMAHIABMN-UHFFFAOYSA-N 0.000 description 2
- KURLDNSCOYEODU-UHFFFAOYSA-N 6-[4-[2-pyrrolidin-1-yl-1-[3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound C1=NC(N)=CC(N2CCN(CC2)C(CN2CCCC2)C=2C=C(C=CC=2)C(F)(F)F)=N1 KURLDNSCOYEODU-UHFFFAOYSA-N 0.000 description 2
- HIQODPYGJGGRPJ-UHFFFAOYSA-N 6-[4-[4-(azetidin-1-yl)-1-(4-chlorophenyl)butyl]piperazin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=CC(Cl)=CC=1)CCCN1CCC1 HIQODPYGJGGRPJ-UHFFFAOYSA-N 0.000 description 2
- HHTBUHOCANWNHD-UHFFFAOYSA-N 6-[4-amino-2-[(4-chlorophenyl)methyl]piperidin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C1C(N)CCN(C=2C(=C(N)N=CN=2)C=2C=CC(F)=CC=2)C1CC1=CC=C(Cl)C=C1 HHTBUHOCANWNHD-UHFFFAOYSA-N 0.000 description 2
- DARCAFFNPMBQIS-UHFFFAOYSA-N 6-[4-amino-2-[(4-fluorophenyl)methyl]piperidin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C1C(N)CCN(C=2C(=C(N)N=CN=2)C=2C=CC(F)=CC=2)C1CC1=CC=C(F)C=C1 DARCAFFNPMBQIS-UHFFFAOYSA-N 0.000 description 2
- CYIGOQPXGBDEMI-UHFFFAOYSA-N 6-[4-amino-2-[[4-(4-fluorophenyl)phenyl]methyl]piperidin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound C1C(N)CCN(C=2C(=C(N)N=CN=2)C=2C=CC(F)=CC=2)C1CC(C=C1)=CC=C1C1=CC=C(F)C=C1 CYIGOQPXGBDEMI-UHFFFAOYSA-N 0.000 description 2
- GFQGRBHYPKIIRV-UHFFFAOYSA-N 6-chloro-5-ethylpyrimidin-4-amine Chemical compound CCC1=C(N)N=CN=C1Cl GFQGRBHYPKIIRV-UHFFFAOYSA-N 0.000 description 2
- ZKHQWZAMYRWXGA-UHFFFAOYSA-N Adenosine triphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C(O)C1O ZKHQWZAMYRWXGA-UHFFFAOYSA-N 0.000 description 2
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 206010006187 Breast cancer Diseases 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- JGLMVXWAHNTPRF-CMDGGOBGSA-N CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O Chemical compound CCN1N=C(C)C=C1C(=O)NC1=NC2=CC(=CC(OC)=C2N1C\C=C\CN1C(NC(=O)C2=CC(C)=NN2CC)=NC2=CC(=CC(OCCCN3CCOCC3)=C12)C(N)=O)C(N)=O JGLMVXWAHNTPRF-CMDGGOBGSA-N 0.000 description 2
- PGTJVBDIWBKSEC-UHFFFAOYSA-N COC(N=C1)=CC=C1C1=C(N)N=CN=C1N(CC1)CC1(CC(C(F)=C(C=C1)C(N)=O)=C1F)N Chemical compound COC(N=C1)=CC=C1C1=C(N)N=CN=C1N(CC1)CC1(CC(C(F)=C(C=C1)C(N)=O)=C1F)N PGTJVBDIWBKSEC-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 206010009944 Colon cancer Diseases 0.000 description 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 206010022489 Insulin Resistance Diseases 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- SSIJBBZLXHCINJ-UHFFFAOYSA-N NC(CC(C(F)=C(C=C1)C(N)=O)=C1F)(CC1)CN1C1=NC=NC(N)=C1C1=CC=C(C(F)(F)F)C=C1 Chemical compound NC(CC(C(F)=C(C=C1)C(N)=O)=C1F)(CC1)CN1C1=NC=NC(N)=C1C1=CC=C(C(F)(F)F)C=C1 SSIJBBZLXHCINJ-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- 208000008589 Obesity Diseases 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 206010038389 Renal cancer Diseases 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- IIHHUIMHJFWTKF-UHFFFAOYSA-N [1-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperidin-4-yl]-[4-(4-fluorophenyl)phenyl]methanol Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCC1C(O)C(C=C1)=CC=C1C1=CC=C(F)C=C1 IIHHUIMHJFWTKF-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 229960002684 aminocaproic acid Drugs 0.000 description 2
- 230000006907 apoptotic process Effects 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- GHWVXCQZPNWFRO-UHFFFAOYSA-N butane-2,3-diamine Chemical compound CC(N)C(C)N GHWVXCQZPNWFRO-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000004296 chiral HPLC Methods 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000002648 combination therapy Methods 0.000 description 2
- 229940125898 compound 5 Drugs 0.000 description 2
- 239000008120 corn starch Substances 0.000 description 2
- 229940127089 cytotoxic agent Drugs 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000010511 deprotection reaction Methods 0.000 description 2
- 206010012601 diabetes mellitus Diseases 0.000 description 2
- 230000004069 differentiation Effects 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 235000003599 food sweetener Nutrition 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 230000014509 gene expression Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000003102 growth factor Substances 0.000 description 2
- 229940088597 hormone Drugs 0.000 description 2
- 239000005556 hormone Substances 0.000 description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 2
- 208000013403 hyperactivity Diseases 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000001990 intravenous administration Methods 0.000 description 2
- TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Chemical compound OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-UHFFFAOYSA-N 0.000 description 2
- 201000010982 kidney cancer Diseases 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 238000004811 liquid chromatography Methods 0.000 description 2
- SIAPCJWMELPYOE-UHFFFAOYSA-N lithium hydride Chemical compound [LiH] SIAPCJWMELPYOE-UHFFFAOYSA-N 0.000 description 2
- 229910000103 lithium hydride Inorganic materials 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000001630 malic acid Substances 0.000 description 2
- 235000011090 malic acid Nutrition 0.000 description 2
- 238000004949 mass spectrometry Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 230000002503 metabolic effect Effects 0.000 description 2
- DEQQYNWWAKOCIZ-UHFFFAOYSA-N methyl 4-[1-[4-[6-amino-5-(1H-pyrazol-4-yl)pyrimidin-4-yl]piperazin-1-yl]-2-(azetidin-1-yl)ethyl]benzoate Chemical class COC(=O)c1ccc(cc1)C(CN1CCC1)N1CCN(CC1)c1ncnc(N)c1-c1cn[nH]c1 DEQQYNWWAKOCIZ-UHFFFAOYSA-N 0.000 description 2
- ZLHKITOOTQYHQW-UHFFFAOYSA-N methyl 4-[4-amino-6-[4-[2-(dimethylamino)-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-5-yl]benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1C1=C(N)N=CN=C1N1CCN(C(CN(C)C)C=2C=CC(=CC=2)C(F)(F)F)CC1 ZLHKITOOTQYHQW-UHFFFAOYSA-N 0.000 description 2
- 244000005700 microbiome Species 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 235000020824 obesity Nutrition 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000002018 overexpression Effects 0.000 description 2
- MXQOYLRVSVOCQT-UHFFFAOYSA-N palladium;tritert-butylphosphane Chemical compound [Pd].CC(C)(C)P(C(C)(C)C)C(C)(C)C.CC(C)(C)P(C(C)(C)C)C(C)(C)C MXQOYLRVSVOCQT-UHFFFAOYSA-N 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 230000002062 proliferating effect Effects 0.000 description 2
- 210000002307 prostate Anatomy 0.000 description 2
- 230000002685 pulmonary effect Effects 0.000 description 2
- QDXGKRWDQCEABB-UHFFFAOYSA-N pyrimidine-5-carboxamide Chemical compound NC(=O)C1=CN=CN=C1 QDXGKRWDQCEABB-UHFFFAOYSA-N 0.000 description 2
- 238000006268 reductive amination reaction Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 230000019491 signal transduction Effects 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
- 239000012321 sodium triacetoxyborohydride Substances 0.000 description 2
- VNFWTIYUKDMAOP-UHFFFAOYSA-N sphos Chemical compound COC1=CC=CC(OC)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 VNFWTIYUKDMAOP-UHFFFAOYSA-N 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 235000000346 sugar Nutrition 0.000 description 2
- 239000003765 sweetening agent Substances 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 238000003419 tautomerization reaction Methods 0.000 description 2
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 2
- HAMPKJFJUJORMC-UHFFFAOYSA-N tert-butyl 4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCN1C(CN)C1=CC=C(C(F)(F)F)C=C1 HAMPKJFJUJORMC-UHFFFAOYSA-N 0.000 description 2
- HUTHFQDPGGVEMM-UHFFFAOYSA-N tert-butyl 4-amino-4-[[(2,4-difluorobenzoyl)amino]methyl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1(N)CNC(=O)C1=CC=C(F)C=C1F HUTHFQDPGGVEMM-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- LEIMLDGFXIOXMT-UHFFFAOYSA-N trimethylsilyl cyanide Chemical compound C[Si](C)(C)C#N LEIMLDGFXIOXMT-UHFFFAOYSA-N 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical compound C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- DNISEZBAYYIQFB-PHDIDXHHSA-N (2r,3r)-2,3-diacetyloxybutanedioic acid Chemical compound CC(=O)O[C@@H](C(O)=O)[C@H](C(O)=O)OC(C)=O DNISEZBAYYIQFB-PHDIDXHHSA-N 0.000 description 1
- IYGWDOXHCPQXKN-UHFFFAOYSA-N (4-chlorophenyl)-piperidin-4-ylmethanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCNCC1 IYGWDOXHCPQXKN-UHFFFAOYSA-N 0.000 description 1
- NPJBPJIQMCHZLJ-UHFFFAOYSA-N (6-aminopyridin-3-yl)boronic acid Chemical compound NC1=CC=C(B(O)O)C=N1 NPJBPJIQMCHZLJ-UHFFFAOYSA-N 0.000 description 1
- GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 1
- IBODDUNKEPPBKW-UHFFFAOYSA-N 1,5-dibromopentane Chemical compound BrCCCCCBr IBODDUNKEPPBKW-UHFFFAOYSA-N 0.000 description 1
- FSNGFFWICFYWQC-UHFFFAOYSA-N 1-(2-chloroethyl)pyrrolidine;hydron;chloride Chemical compound Cl.ClCCN1CCCC1 FSNGFFWICFYWQC-UHFFFAOYSA-N 0.000 description 1
- SKMPCOWKGMSVJC-UHFFFAOYSA-N 1-(3-fluorophenyl)-2-piperidin-1-ylethanone Chemical compound FC1=CC=CC(C(=O)CN2CCCCC2)=C1 SKMPCOWKGMSVJC-UHFFFAOYSA-N 0.000 description 1
- QCVSDCHNBNFJDQ-UHFFFAOYSA-N 1-(4-chloro-2-hydroxyphenyl)ethanone Chemical compound CC(=O)C1=CC=C(Cl)C=C1O QCVSDCHNBNFJDQ-UHFFFAOYSA-N 0.000 description 1
- BISLYFJHPWWIIU-UHFFFAOYSA-N 1-[(1-methylimidazol-2-yl)-phenylmethyl]piperazine Chemical compound CN1C=CN=C1C(C=1C=CC=CC=1)N1CCNCC1 BISLYFJHPWWIIU-UHFFFAOYSA-N 0.000 description 1
- LGHIKTWGKIFAEI-UHFFFAOYSA-N 1-[2-(3-fluorophenyl)ethyl]piperidine Chemical compound Fc1cccc(CCN2CCCCC2)c1 LGHIKTWGKIFAEI-UHFFFAOYSA-N 0.000 description 1
- IFPBLWCGTIRCQN-UHFFFAOYSA-N 1-[2-chloro-2-(3-fluorophenyl)ethyl]piperidine Chemical compound FC1=CC=CC(C(Cl)CN2CCCCC2)=C1 IFPBLWCGTIRCQN-UHFFFAOYSA-N 0.000 description 1
- CHBUQROGENLOCG-UHFFFAOYSA-N 1-[2-chloro-2-[4-(trifluoromethyl)phenyl]ethyl]azetidine Chemical compound C1=CC(C(F)(F)F)=CC=C1C(Cl)CN1CCC1 CHBUQROGENLOCG-UHFFFAOYSA-N 0.000 description 1
- KYPLPMHPUCDRNO-UHFFFAOYSA-N 1-[2-piperidin-1-yl-1-[4-(trifluoromethyl)phenyl]ethyl]piperazine;hydrochloride Chemical compound Cl.C1=CC(C(F)(F)F)=CC=C1C(N1CCNCC1)CN1CCCCC1 KYPLPMHPUCDRNO-UHFFFAOYSA-N 0.000 description 1
- OTGQJUWMOCXVKZ-UHFFFAOYSA-N 1-[2-pyrrolidin-1-yl-1-[4-(trifluoromethyl)phenyl]ethyl]piperazine;hydrochloride Chemical compound Cl.C1=CC(C(F)(F)F)=CC=C1C(N1CCNCC1)CN1CCCC1 OTGQJUWMOCXVKZ-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- 125000006334 2,4-difluoro benzoyl group Chemical group [H]C1=C([H])C(C(*)=O)=C(F)C([H])=C1F 0.000 description 1
- QACNLSWHYNYFJS-UHFFFAOYSA-N 2-(cyclohexen-1-yl)-4-ethyl-4,5,5-trimethyl-1,3,2-dioxaborolane Chemical compound O1C(C)(C)C(CC)(C)OB1C1=CCCCC1 QACNLSWHYNYFJS-UHFFFAOYSA-N 0.000 description 1
- JFTZVYKESKQING-UHFFFAOYSA-N 2-(cyclopenten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Chemical compound O1C(C)(C)C(C)(C)OB1C1=CCCC1 JFTZVYKESKQING-UHFFFAOYSA-N 0.000 description 1
- UZYQSNQJLWTICD-UHFFFAOYSA-N 2-(n-benzoylanilino)-2,2-dinitroacetic acid Chemical compound C=1C=CC=CC=1N(C(C(=O)O)([N+]([O-])=O)[N+]([O-])=O)C(=O)C1=CC=CC=C1 UZYQSNQJLWTICD-UHFFFAOYSA-N 0.000 description 1
- OXQGTIUCKGYOAA-UHFFFAOYSA-N 2-Ethylbutanoic acid Chemical compound CCC(CC)C(O)=O OXQGTIUCKGYOAA-UHFFFAOYSA-N 0.000 description 1
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 1
- UVVBTHYPMAWWCK-UHFFFAOYSA-N 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propan-2-ol Chemical compound C1=CC(C(C)(O)C)=CC=C1B1OC(C)(C)C(C)(C)O1 UVVBTHYPMAWWCK-UHFFFAOYSA-N 0.000 description 1
- IARZIPYMYCXENR-UHFFFAOYSA-N 2-[4-(6-amino-5-ethylpyrimidin-4-yl)piperazin-1-yl]-2-cyclohexylacetonitrile Chemical compound CCC1=C(N)N=CN=C1N1CCN(C(C#N)C2CCCCC2)CC1 IARZIPYMYCXENR-UHFFFAOYSA-N 0.000 description 1
- HXJDWNPRUKQYIQ-UHFFFAOYSA-N 2-[[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]methyl]-5-chlorophenol Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1CC1=CC=C(Cl)C=C1O HXJDWNPRUKQYIQ-UHFFFAOYSA-N 0.000 description 1
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical class NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 description 1
- KMGUEILFFWDGFV-UHFFFAOYSA-N 2-benzoyl-2-benzoyloxy-3-hydroxybutanedioic acid Chemical compound C=1C=CC=CC=1C(=O)C(C(C(O)=O)O)(C(O)=O)OC(=O)C1=CC=CC=C1 KMGUEILFFWDGFV-UHFFFAOYSA-N 0.000 description 1
- ITAQNNGDCNFGID-UHFFFAOYSA-N 2-bromo-1-(3-fluorophenyl)ethanone Chemical compound FC1=CC=CC(C(=O)CBr)=C1 ITAQNNGDCNFGID-UHFFFAOYSA-N 0.000 description 1
- OYFKMXOQLFOOFW-UHFFFAOYSA-N 2-piperidin-4-yl-2-[4-(trifluoromethyl)phenyl]ethanamine;hydrochloride Chemical compound Cl.C=1C=C(C(F)(F)F)C=CC=1C(CN)C1CCNCC1 OYFKMXOQLFOOFW-UHFFFAOYSA-N 0.000 description 1
- NMTUHPSKJJYGML-UHFFFAOYSA-N 3-(trifluoromethyl)benzaldehyde Chemical compound FC(F)(F)C1=CC=CC(C=O)=C1 NMTUHPSKJJYGML-UHFFFAOYSA-N 0.000 description 1
- PXFUWRWCKSLCLS-UHFFFAOYSA-N 3-fluoroazetidine;hydron;chloride Chemical compound Cl.FC1CNC1 PXFUWRWCKSLCLS-UHFFFAOYSA-N 0.000 description 1
- XFHHSKSQYRYYTN-UHFFFAOYSA-N 3-iodoazetidine-1-carboxylic acid Chemical compound OC(=O)N1CC(I)C1 XFHHSKSQYRYYTN-UHFFFAOYSA-N 0.000 description 1
- RZVJTHXDHLQJIK-UHFFFAOYSA-N 4,5-dichloro-2-hydroxybenzaldehyde Chemical compound OC1=CC(Cl)=C(Cl)C=C1C=O RZVJTHXDHLQJIK-UHFFFAOYSA-N 0.000 description 1
- PLOZXUFHBRJLFX-UHFFFAOYSA-N 4-amino-6-chloropyrimidin-5-ol Chemical compound NC1=NC=NC(Cl)=C1O PLOZXUFHBRJLFX-UHFFFAOYSA-N 0.000 description 1
- MAVMFCKRFRCMLE-UHFFFAOYSA-N 4-amino-6-chloropyrimidine-5-carbonitrile Chemical compound NC1=NC=NC(Cl)=C1C#N MAVMFCKRFRCMLE-UHFFFAOYSA-N 0.000 description 1
- 102100036009 5'-AMP-activated protein kinase catalytic subunit alpha-2 Human genes 0.000 description 1
- ZZYCMROJUJXVIM-UHFFFAOYSA-N 5-(4-fluorophenyl)-6-[4-[(4-fluorophenyl)-pyrrolidin-1-ylmethyl]piperidin-1-yl]pyrimidin-4-amine Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCC1C(C=1C=CC(F)=CC=1)N1CCCC1 ZZYCMROJUJXVIM-UHFFFAOYSA-N 0.000 description 1
- DIHUPOFZOKWNBR-UHFFFAOYSA-N 5-bromo-6-[4-[2-pyrrolidin-1-yl-1-[4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]pyrimidin-4-amine Chemical compound NC1=NC=NC(N2CCN(CC2)C(CN2CCCC2)C=2C=CC(=CC=2)C(F)(F)F)=C1Br DIHUPOFZOKWNBR-UHFFFAOYSA-N 0.000 description 1
- PYZFNSYJSDPLHL-UHFFFAOYSA-N 5-ethyl-4-hydroxy-1h-pyrimidin-6-one Chemical compound CCC1=C(O)N=CNC1=O PYZFNSYJSDPLHL-UHFFFAOYSA-N 0.000 description 1
- URRWCJHKBVTGSL-UHFFFAOYSA-N 6-[1-[4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazin-1-yl]-2-(azetidin-1-yl)ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C=1C=C(F)C=CC=1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C2SC(=O)NC2=CC=1)CN1CCC1 URRWCJHKBVTGSL-UHFFFAOYSA-N 0.000 description 1
- WYONQEKTSMEJPL-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(2-chloro-4-fluorophenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C(=CC(F)=CC=1)Cl)CN1CCC1 WYONQEKTSMEJPL-UHFFFAOYSA-N 0.000 description 1
- KXARHIHVFZCNJC-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(3-chloro-4-fluorophenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(Cl)C(F)=CC=1)CN1CCC1 KXARHIHVFZCNJC-UHFFFAOYSA-N 0.000 description 1
- NTFDLPTYWXUGAT-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(3-fluoro-4-methoxyphenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=C(F)C(OC)=CC=C1C(N1CCN(CC1)C=1C(=C(N)N=CN=1)C1=CNN=C1)CN1CCC1 NTFDLPTYWXUGAT-UHFFFAOYSA-N 0.000 description 1
- HDTQVEYELPMKHE-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(4-chloro-3-fluorophenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(F)C(Cl)=CC=1)CN1CCC1 HDTQVEYELPMKHE-UHFFFAOYSA-N 0.000 description 1
- JIKUATYMHWIKIR-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-(4-chloro-3-methylphenyl)ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=C(Cl)C(C)=CC(C(CN2CCC2)N2CCN(CC2)C=2C(=C(N)N=CN=2)C2=CNN=C2)=C1 JIKUATYMHWIKIR-UHFFFAOYSA-N 0.000 description 1
- FSPFMSRTXKXWCZ-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-[2-chloro-3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C(=C(C=CC=1)C(F)(F)F)Cl)CN1CCC1 FSPFMSRTXKXWCZ-UHFFFAOYSA-N 0.000 description 1
- QKOUTCCVXKYURA-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-[2-fluoro-3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C(=C(C=CC=1)C(F)(F)F)F)CN1CCC1 QKOUTCCVXKYURA-UHFFFAOYSA-N 0.000 description 1
- ZWUJBLYDNLAFPW-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-[2-fluoro-4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1H-pyrazol-4-yl)pyrimidin-4-amine Chemical compound Nc1ncnc(N2CCN(CC2)C(CN2CCC2)c2ccc(cc2F)C(F)(F)F)c1-c1cn[nH]c1 ZWUJBLYDNLAFPW-UHFFFAOYSA-N 0.000 description 1
- CGFBMTJBBPMPGY-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-[3-fluoro-4-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(F)C(=CC=1)C(F)(F)F)CN1CCC1 CGFBMTJBBPMPGY-UHFFFAOYSA-N 0.000 description 1
- FNJRSYLAQNXXSO-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-[4-chloro-3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(C(Cl)=CC=1)C(F)(F)F)CN1CCC1 FNJRSYLAQNXXSO-UHFFFAOYSA-N 0.000 description 1
- XJNYPDNKMRUJKI-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-[4-fluoro-3-(trifluoromethoxy)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(OC(F)(F)F)C(F)=CC=1)CN1CCC1 XJNYPDNKMRUJKI-UHFFFAOYSA-N 0.000 description 1
- HYVUUZDNESHEAW-UHFFFAOYSA-N 6-[4-[2-(azetidin-1-yl)-1-[4-fluoro-3-(trifluoromethyl)phenyl]ethyl]piperazin-1-yl]-5-(1h-pyrazol-4-yl)pyrimidin-4-amine Chemical compound C1=NNC=C1C=1C(N)=NC=NC=1N(CC1)CCN1C(C=1C=C(C(F)=CC=1)C(F)(F)F)CN1CCC1 HYVUUZDNESHEAW-UHFFFAOYSA-N 0.000 description 1
- FIECZQTZWMPKCU-UHFFFAOYSA-N 6-[4-[chloro-(4-fluorophenyl)methyl]piperidin-1-yl]-5-(4-fluorophenyl)pyrimidin-4-amine Chemical compound ClC(C1CCN(CC1)C1=C(C(=NC=N1)N)C1=CC=C(C=C1)F)C1=CC=C(C=C1)F FIECZQTZWMPKCU-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- 208000031261 Acute myeloid leukaemia Diseases 0.000 description 1
- 208000010507 Adenocarcinoma of Lung Diseases 0.000 description 1
- 108700028369 Alleles Proteins 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 102100033972 Amyloid protein-binding protein 2 Human genes 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 201000001320 Atherosclerosis Diseases 0.000 description 1
- 208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 206010005003 Bladder cancer Diseases 0.000 description 1
- 241000167854 Bourreria succulenta Species 0.000 description 1
- NYHBYEUKXSXHHH-UHFFFAOYSA-N C1CNCCN1NC1=CC=NC=N1 Chemical compound C1CNCCN1NC1=CC=NC=N1 NYHBYEUKXSXHHH-UHFFFAOYSA-N 0.000 description 1
- 102100033029 Carbonic anhydrase-related protein 11 Human genes 0.000 description 1
- 229940123587 Cell cycle inhibitor Drugs 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 208000010833 Chronic myeloid leukaemia Diseases 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 201000004624 Dermatitis Diseases 0.000 description 1
- 206010012689 Diabetic retinopathy Diseases 0.000 description 1
- 235000019739 Dicalciumphosphate Nutrition 0.000 description 1
- 101000785279 Dictyostelium discoideum Calcium-transporting ATPase PAT1 Proteins 0.000 description 1
- 206010061818 Disease progression Diseases 0.000 description 1
- 101100520660 Drosophila melanogaster Poc1 gene Proteins 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 241000854350 Enicospilus group Species 0.000 description 1
- 208000000461 Esophageal Neoplasms Diseases 0.000 description 1
- 108090000371 Esterases Proteins 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 230000005526 G1 to G0 transition Effects 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 208000032612 Glial tumor Diseases 0.000 description 1
- 206010018338 Glioma Diseases 0.000 description 1
- 102000009465 Growth Factor Receptors Human genes 0.000 description 1
- 108010009202 Growth Factor Receptors Proteins 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 101000783681 Homo sapiens 5'-AMP-activated protein kinase catalytic subunit alpha-2 Proteins 0.000 description 1
- 101000779309 Homo sapiens Amyloid protein-binding protein 2 Proteins 0.000 description 1
- 101000867841 Homo sapiens Carbonic anhydrase-related protein 11 Proteins 0.000 description 1
- 101001075218 Homo sapiens Gastrokine-1 Proteins 0.000 description 1
- 101000713296 Homo sapiens Proton-coupled amino acid transporter 1 Proteins 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 208000031226 Hyperlipidaemia Diseases 0.000 description 1
- 206010020751 Hypersensitivity Diseases 0.000 description 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 description 1
- 102000004310 Ion Channels Human genes 0.000 description 1
- 208000007766 Kaposi sarcoma Diseases 0.000 description 1
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 208000001145 Metabolic Syndrome Diseases 0.000 description 1
- 206010027476 Metastases Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 1
- 208000034578 Multiple myelomas Diseases 0.000 description 1
- 208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 description 1
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 description 1
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-diisopropylethylamine Substances CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 1
- JKVUCYISRXVULH-UHFFFAOYSA-N N-[1-(4-chlorophenyl)-3-hydroxypropyl]piperidine-4-carboxamide Chemical compound N1CCC(CC1)C(=O)NC(CCO)C1=CC=C(C=C1)Cl JKVUCYISRXVULH-UHFFFAOYSA-N 0.000 description 1
- 206010029260 Neuroblastoma Diseases 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 206010030155 Oesophageal carcinoma Diseases 0.000 description 1
- 206010061902 Pancreatic neoplasm Diseases 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 1
- 206010035226 Plasma cell myeloma Diseases 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 description 1
- 102000009516 Protein Serine-Threonine Kinases Human genes 0.000 description 1
- 108010009341 Protein Serine-Threonine Kinases Proteins 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
- 208000015634 Rectal Neoplasms Diseases 0.000 description 1
- 206010038933 Retinopathy of prematurity Diseases 0.000 description 1
- 101100520662 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) PBA1 gene Proteins 0.000 description 1
- 208000016780 Scleredema Diseases 0.000 description 1
- 206010055953 Scleroedema Diseases 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 208000005718 Stomach Neoplasms Diseases 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 208000024313 Testicular Neoplasms Diseases 0.000 description 1
- 206010057644 Testis cancer Diseases 0.000 description 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- 208000024770 Thyroid neoplasm Diseases 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 102000040945 Transcription factor Human genes 0.000 description 1
- 108091023040 Transcription factor Proteins 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 102000001742 Tumor Suppressor Proteins Human genes 0.000 description 1
- 108010040002 Tumor Suppressor Proteins Proteins 0.000 description 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 description 1
- 208000002495 Uterine Neoplasms Diseases 0.000 description 1
- 241000256856 Vespidae Species 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- BDMZVTZYYPRKRF-UHFFFAOYSA-N [1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl]-(4-chlorophenyl)methanone Chemical compound NC1=C(C(=NC=N1)N1CCC(CC1)C(=O)C1=CC=C(C=C1)Cl)Br BDMZVTZYYPRKRF-UHFFFAOYSA-N 0.000 description 1
- OJEZAYUDOOGICH-UHFFFAOYSA-N [1-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperidin-4-yl]-(4-chlorophenyl)methanone Chemical compound NC1=C(C(=NC=N1)N1CCC(CC1)C(=O)C1=CC=C(C=C1)Cl)C1=CC=C(C=C1)F OJEZAYUDOOGICH-UHFFFAOYSA-N 0.000 description 1
- CTCBPRXHVPZNHB-VQFZJOCSSA-N [[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate;(2r,3r,4s,5r)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O.C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O CTCBPRXHVPZNHB-VQFZJOCSSA-N 0.000 description 1
- 201000000690 abdominal obesity-metabolic syndrome Diseases 0.000 description 1
- 230000001594 aberrant effect Effects 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 206010064930 age-related macular degeneration Diseases 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 230000007815 allergy Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000004037 angiogenesis inhibitor Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000002280 anti-androgenic effect Effects 0.000 description 1
- 230000000340 anti-metabolite Effects 0.000 description 1
- 230000001028 anti-proliverative effect Effects 0.000 description 1
- 239000000051 antiandrogen Substances 0.000 description 1
- 229940030495 antiandrogen sex hormone and modulator of the genital system Drugs 0.000 description 1
- 239000013059 antihormonal agent Substances 0.000 description 1
- 239000002256 antimetabolite Substances 0.000 description 1
- 229940100197 antimetabolite Drugs 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 208000006673 asthma Diseases 0.000 description 1
- 239000000305 astragalus gummifer gum Substances 0.000 description 1
- 208000010668 atopic eczema Diseases 0.000 description 1
- 239000005441 aurora Substances 0.000 description 1
- 230000035578 autophosphorylation Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- JVVOXDMXZKLGIE-UHFFFAOYSA-N benzyl n-[2-[4-(6-amino-5-formylpyrimidin-4-yl)piperazin-1-yl]-2-[4-(trifluoromethyl)phenyl]ethyl]carbamate Chemical compound NC1=NC=NC(N2CCN(CC2)C(CNC(=O)OCC=2C=CC=CC=2)C=2C=CC(=CC=2)C(F)(F)F)=C1C=O JVVOXDMXZKLGIE-UHFFFAOYSA-N 0.000 description 1
- 229960000397 bevacizumab Drugs 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000008827 biological function Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- MIOPJNTWMNEORI-UHFFFAOYSA-N camphorsulfonic acid Chemical class C1CC2(CS(O)(=O)=O)C(=O)CC1C2(C)C MIOPJNTWMNEORI-UHFFFAOYSA-N 0.000 description 1
- 150000001719 carbohydrate derivatives Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000004663 cell proliferation Effects 0.000 description 1
- 230000036755 cellular response Effects 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 150000001793 charged compounds Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 235000019693 cherries Nutrition 0.000 description 1
- 239000007958 cherry flavor Substances 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 210000000349 chromosome Anatomy 0.000 description 1
- 208000037976 chronic inflammation Diseases 0.000 description 1
- 208000037893 chronic inflammatory disorder Diseases 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 210000004292 cytoskeleton Anatomy 0.000 description 1
- 210000000172 cytosol Anatomy 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 229960001251 denosumab Drugs 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 description 1
- 229940038472 dicalcium phosphate Drugs 0.000 description 1
- 229910000390 dicalcium phosphate Inorganic materials 0.000 description 1
- VQAZCUCWHIIFGE-UHFFFAOYSA-N diethyl 2-ethylpropanedioate Chemical compound CCOC(=O)C(CC)C(=O)OCC VQAZCUCWHIIFGE-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000005750 disease progression Effects 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- VHJLVAABSRFDPM-QWWZWVQMSA-N dithiothreitol Chemical compound SC[C@@H](O)[C@H](O)CS VHJLVAABSRFDPM-QWWZWVQMSA-N 0.000 description 1
- CETRZFQIITUQQL-UHFFFAOYSA-N dmso dimethylsulfoxide Chemical compound CS(C)=O.CS(C)=O CETRZFQIITUQQL-UHFFFAOYSA-N 0.000 description 1
- 229960001776 edrecolomab Drugs 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 150000002085 enols Chemical group 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- 201000004101 esophageal cancer Diseases 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- PQVSTLUFSYVLTO-UHFFFAOYSA-N ethyl n-ethoxycarbonylcarbamate Chemical compound CCOC(=O)NC(=O)OCC PQVSTLUFSYVLTO-UHFFFAOYSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 210000002950 fibroblast Anatomy 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- MHMNJMPURVTYEJ-UHFFFAOYSA-N fluorescein-5-isothiocyanate Chemical compound O1C(=O)C2=CC(N=C=S)=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 MHMNJMPURVTYEJ-UHFFFAOYSA-N 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- HLXVERDKKMHKLD-UHFFFAOYSA-N formylazanium;acetate Chemical compound NC=O.CC(O)=O HLXVERDKKMHKLD-UHFFFAOYSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 102000034356 gene-regulatory proteins Human genes 0.000 description 1
- 108091006104 gene-regulatory proteins Proteins 0.000 description 1
- 208000005017 glioblastoma Diseases 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000003979 granulating agent Substances 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 239000007902 hard capsule Substances 0.000 description 1
- 210000003128 head Anatomy 0.000 description 1
- 230000002489 hematologic effect Effects 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 201000001421 hyperglycemia Diseases 0.000 description 1
- 230000028993 immune response Effects 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 239000000367 immunologic factor Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 229940060367 inert ingredients Drugs 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 239000012444 intercalating antibiotic Substances 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 229940043355 kinase inhibitor Drugs 0.000 description 1
- TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 1
- 229950002950 lintuzumab Drugs 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 229940040692 lithium hydroxide monohydrate Drugs 0.000 description 1
- GLXDVVHUTZTUQK-UHFFFAOYSA-M lithium hydroxide monohydrate Substances [Li+].O.[OH-] GLXDVVHUTZTUQK-UHFFFAOYSA-M 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 208000020816 lung neoplasm Diseases 0.000 description 1
- 208000002780 macular degeneration Diseases 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 230000036210 malignancy Effects 0.000 description 1
- 229960002510 mandelic acid Drugs 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 201000001441 melanoma Diseases 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000002207 metabolite Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 230000009401 metastasis Effects 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- REIZEQZILPXYKS-UHFFFAOYSA-N methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1B1OC(C)(C)C(C)(C)O1 REIZEQZILPXYKS-UHFFFAOYSA-N 0.000 description 1
- 235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
- 239000008108 microcrystalline cellulose Substances 0.000 description 1
- 229940016286 microcrystalline cellulose Drugs 0.000 description 1
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 1
- 239000003226 mitogen Substances 0.000 description 1
- 230000008747 mitogenic response Effects 0.000 description 1
- 230000011278 mitosis Effects 0.000 description 1
- 230000004899 motility Effects 0.000 description 1
- 210000000066 myeloid cell Anatomy 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- SPVCHERKDBLNPJ-UHFFFAOYSA-N n-[(3-aminopyrrolidin-3-yl)methyl]-2,4-difluorobenzamide;dihydrochloride Chemical compound Cl.Cl.C=1C=C(F)C=C(F)C=1C(=O)NCC1(N)CCNC1 SPVCHERKDBLNPJ-UHFFFAOYSA-N 0.000 description 1
- ABTCIXPAKHAJMG-UHFFFAOYSA-N n-[[3-amino-1-(6-amino-5-bromopyrimidin-4-yl)pyrrolidin-3-yl]methyl]-2,4-difluorobenzamide Chemical compound NC1=NC=NC(N2CC(N)(CNC(=O)C=3C(=CC(F)=CC=3)F)CC2)=C1Br ABTCIXPAKHAJMG-UHFFFAOYSA-N 0.000 description 1
- YZMHQCWXYHARLS-UHFFFAOYSA-N naphthalene-1,2-disulfonic acid Chemical class C1=CC=CC2=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC=C21 YZMHQCWXYHARLS-UHFFFAOYSA-N 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- 210000003061 neural cell Anatomy 0.000 description 1
- 239000002858 neurotransmitter agent Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 239000007968 orange flavor Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 210000001672 ovary Anatomy 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- RFIOZSIHFNEKFF-UHFFFAOYSA-N piperazine-1-carboxylic acid Chemical compound OC(=O)N1CCNCC1 RFIOZSIHFNEKFF-UHFFFAOYSA-N 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 108091033319 polynucleotide Proteins 0.000 description 1
- 102000040430 polynucleotide Human genes 0.000 description 1
- 239000002157 polynucleotide Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000010837 poor prognosis Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- 201000001514 prostate carcinoma Diseases 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 230000009822 protein phosphorylation Effects 0.000 description 1
- 238000001243 protein synthesis Methods 0.000 description 1
- 230000004850 protein–protein interaction Effects 0.000 description 1
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 description 1
- WHYQCQRHPQBZHM-UHFFFAOYSA-N pyrazole-1-carboxylic acid Chemical compound OC(=O)N1C=CC=N1 WHYQCQRHPQBZHM-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 206010038038 rectal cancer Diseases 0.000 description 1
- 201000001275 rectum cancer Diseases 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000024122 regulation of cell motility Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- 210000003705 ribosome Anatomy 0.000 description 1
- 229960004641 rituximab Drugs 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 208000007754 scleredema adultorum Diseases 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007901 soft capsule Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 206010041823 squamous cell carcinoma Diseases 0.000 description 1
- 208000017572 squamous cell neoplasm Diseases 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 201000000498 stomach carcinoma Diseases 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- NOVUBWBKZLPMFG-UHFFFAOYSA-N tert-butyl 4-(2-amino-1-phenylethyl)piperazine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCN1C(CN)C1=CC=CC=C1 NOVUBWBKZLPMFG-UHFFFAOYSA-N 0.000 description 1
- IPISOFJLWYBCAV-UHFFFAOYSA-N tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole-1-carboxylate Chemical compound C1=NN(C(=O)OC(C)(C)C)C=C1B1OC(C)(C)C(C)(C)O1 IPISOFJLWYBCAV-UHFFFAOYSA-N 0.000 description 1
- YEPQVWSKCYHOBU-UHFFFAOYSA-N tert-butyl 4-(6-amino-5-bromopyrimidin-4-yl)piperazine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCN1C1=NC=NC(N)=C1Br YEPQVWSKCYHOBU-UHFFFAOYSA-N 0.000 description 1
- ZSDGACHAFZDZLZ-UHFFFAOYSA-N tert-butyl 4-[2-amino-1-[4-(trifluoromethyl)phenyl]ethyl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1C(CN)C1=CC=C(C(F)(F)F)C=C1 ZSDGACHAFZDZLZ-UHFFFAOYSA-N 0.000 description 1
- UCSFEUQDMPZQAW-UHFFFAOYSA-N tert-butyl 4-[6-amino-5-(4-fluorophenyl)pyrimidin-4-yl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCN1C1=NC=NC(N)=C1C1=CC=C(F)C=C1 UCSFEUQDMPZQAW-UHFFFAOYSA-N 0.000 description 1
- VZUDEIWBRDTYNS-UHFFFAOYSA-N tert-butyl 4-[cyano-[4-(trifluoromethyl)phenyl]methyl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCC1C(C#N)C1=CC=C(C(F)(F)F)C=C1 VZUDEIWBRDTYNS-UHFFFAOYSA-N 0.000 description 1
- XYNSZNYCTLOTBZ-UHFFFAOYSA-N tert-butyl 4-[cyano-[4-(trifluoromethyl)phenyl]methylidene]piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(CC1)=C(C#N)c1ccc(cc1)C(F)(F)F XYNSZNYCTLOTBZ-UHFFFAOYSA-N 0.000 description 1
- GFRZXIHYVYRFPV-UHFFFAOYSA-N tert-butyl 4-amino-4-(aminomethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(N)(CN)CC1 GFRZXIHYVYRFPV-UHFFFAOYSA-N 0.000 description 1
- ROUYFJUVMYHXFJ-UHFFFAOYSA-N tert-butyl 4-oxopiperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(=O)CC1 ROUYFJUVMYHXFJ-UHFFFAOYSA-N 0.000 description 1
- ZRGABVGIJOGXGJ-UHFFFAOYSA-N tert-butyl N-[2-[1-(6-amino-5-bromopyrimidin-4-yl)piperidin-4-yl]-2-[4-(trifluoromethyl)phenyl]ethyl]carbamate Chemical compound CC(C)(C)OC(=O)NCC(C1CCN(CC1)c1ncnc(N)c1Br)c1ccc(cc1)C(F)(F)F ZRGABVGIJOGXGJ-UHFFFAOYSA-N 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
- CWXPZXBSDSIRCS-UHFFFAOYSA-N tert-butyl piperazine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCNCC1 CWXPZXBSDSIRCS-UHFFFAOYSA-N 0.000 description 1
- 201000003120 testicular cancer Diseases 0.000 description 1
- SYZCZDCAEVUSPM-UHFFFAOYSA-M tetrahexylazanium;bromide Chemical compound [Br-].CCCCCC[N+](CCCCCC)(CCCCCC)CCCCCC SYZCZDCAEVUSPM-UHFFFAOYSA-M 0.000 description 1
- WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
- 230000004797 therapeutic response Effects 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 201000002510 thyroid cancer Diseases 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 230000017423 tissue regeneration Effects 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- 230000002103 transcriptional effect Effects 0.000 description 1
- 229960000575 trastuzumab Drugs 0.000 description 1
- PBIMIGNDTBRRPI-UHFFFAOYSA-N trifluoro borate Chemical compound FOB(OF)OF PBIMIGNDTBRRPI-UHFFFAOYSA-N 0.000 description 1
- 230000005747 tumor angiogenesis Effects 0.000 description 1
- 210000004881 tumor cell Anatomy 0.000 description 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 201000005112 urinary bladder cancer Diseases 0.000 description 1
- 206010046766 uterine cancer Diseases 0.000 description 1
- 230000004862 vasculogenesis Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- QDLHCMPXEPAAMD-QAIWCSMKSA-N wortmannin Chemical compound C1([C@]2(C)C3=C(C4=O)OC=C3C(=O)O[C@@H]2COC)=C4[C@@H]2CCC(=O)[C@@]2(C)C[C@H]1OC(C)=O QDLHCMPXEPAAMD-QAIWCSMKSA-N 0.000 description 1
- QDLHCMPXEPAAMD-UHFFFAOYSA-N wortmannin Natural products COCC1OC(=O)C2=COC(C3=O)=C2C1(C)C1=C3C2CCC(=O)C2(C)CC1OC(C)=O QDLHCMPXEPAAMD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
- C07D239/49—Two nitrogen atoms with an aralkyl radical, or substituted aralkyl radical, attached in position 5, e.g. trimethoprim
-
- 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
- C07D401/04—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
-
- 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
-
- 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
- C07D401/14—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
-
- C—CHEMISTRY; METALLURGY
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- 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
- C07D403/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D405/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D405/14—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
-
- 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
- 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
- C07D413/06—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 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
- C07D413/14—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161533606P | 2011-09-12 | 2011-09-12 | |
| PCT/US2012/054877 WO2013040044A1 (en) | 2011-09-12 | 2012-09-12 | Aminopyrimidine derivatives for use as modulators of kinase activity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA201400338A1 EA201400338A1 (ru) | 2014-12-30 |
| EA028057B1 true EA028057B1 (ru) | 2017-10-31 |
Family
ID=46964039
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201400338A EA028057B1 (ru) | 2011-09-12 | 2012-09-12 | Производные аминопиримидина для применения в качестве модуляторов киназной активности |
Country Status (24)
| Country | Link |
|---|---|
| US (3) | US9321760B2 (enExample) |
| EP (1) | EP2755958B9 (enExample) |
| JP (1) | JP6082011B2 (enExample) |
| KR (1) | KR101992505B1 (enExample) |
| CN (2) | CN106946796B (enExample) |
| AU (2) | AU2012308681B2 (enExample) |
| BR (1) | BR112014005468A2 (enExample) |
| CA (1) | CA2844704C (enExample) |
| DK (1) | DK2755958T3 (enExample) |
| EA (1) | EA028057B1 (enExample) |
| ES (1) | ES2646759T3 (enExample) |
| HR (1) | HRP20171655T1 (enExample) |
| HU (1) | HUE034979T2 (enExample) |
| IL (2) | IL231381B (enExample) |
| LT (1) | LT2755958T (enExample) |
| MX (1) | MX347241B (enExample) |
| NO (1) | NO2639780T3 (enExample) |
| PL (1) | PL2755958T3 (enExample) |
| PT (1) | PT2755958T (enExample) |
| RS (1) | RS56486B1 (enExample) |
| SG (1) | SG2014009260A (enExample) |
| SI (1) | SI2755958T1 (enExample) |
| WO (1) | WO2013040044A1 (enExample) |
| ZA (1) | ZA201401007B (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG10201604682VA (en) | 2011-06-10 | 2016-07-28 | Merck Patent Gmbh | Compositions and methods for the production of pyrimidine and pyridine compounds with btk inhibitory activity |
| JP6082011B2 (ja) * | 2011-09-12 | 2017-02-15 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | キナーゼ活性のモジュレーターとして使用するためのアミノピリミジン誘導体 |
| ES2620119T3 (es) | 2012-11-16 | 2017-06-27 | Merck Patent Gmbh | Derivados heterocíclicos novedosos como moduladores de la actividad de quinasa |
| AR095202A1 (es) * | 2013-03-11 | 2015-09-30 | Merck Patent Gmbh | Heterociclos como moduladores de la actividad quinasa |
| JO3517B1 (ar) | 2014-01-17 | 2020-07-05 | Novartis Ag | ان-ازاسبيرو الكان حلقي كبديل مركبات اريل-ان مغايرة وتركيبات لتثبيط نشاط shp2 |
| WO2015107493A1 (en) | 2014-01-17 | 2015-07-23 | Novartis Ag | 1 -pyridazin-/triazin-3-yl-piper(-azine)/idine/pyrolidine derivatives and and compositions thereof for inhibiting the activity of shp2 |
| ES2699354T3 (es) | 2014-01-17 | 2019-02-08 | Novartis Ag | Derivados de 1-(triazin-3-il/piridazin-3-il)-piper(-azin)idina y composiciones de las mismas para inhibir la actividad de SHP2 |
| RU2690679C2 (ru) * | 2014-02-11 | 2019-06-05 | Мерк Патент Гмбх | Новые пиримидинимидазоламины в качестве модуляторов активности киназы |
| EP2939514B1 (en) | 2014-04-30 | 2018-09-05 | LG Electronics Inc. | Lawn mower robot and control method thereof |
| AU2015265696B2 (en) * | 2014-05-28 | 2018-01-18 | Astrazeneca Ab | Processes for the preparation of AZD5363 and novel intermediate used therein |
| JP6878316B2 (ja) | 2015-06-19 | 2021-05-26 | ノバルティス アーゲー | Shp2の活性を阻害するための化合物および組成物 |
| WO2016203404A1 (en) | 2015-06-19 | 2016-12-22 | Novartis Ag | Compounds and compositions for inhibiting the activity of shp2 |
| CN112625028B (zh) | 2015-06-19 | 2024-10-29 | 诺华股份有限公司 | 用于抑制shp2活性的化合物和组合物 |
| WO2017019804A2 (en) | 2015-07-28 | 2017-02-02 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| JP6921846B6 (ja) * | 2016-03-16 | 2021-09-15 | プレキシコン インコーポレーテッドPlexxikon Inc. | キナーゼ調節およびその適応症のための化合物および方法 |
| RU2744988C2 (ru) | 2016-06-14 | 2021-03-17 | Новартис Аг | Соединения и композиции для подавления активности shp2 |
| CA3048340A1 (en) | 2017-01-10 | 2018-07-19 | Novartis Ag | Pharmaceutical combination comprising an alk inhibitor and a shp2 inhibitor |
| CN109467538A (zh) | 2017-09-07 | 2019-03-15 | 和记黄埔医药(上海)有限公司 | 环烯烃取代的杂芳环类化合物及其用途 |
| WO2019084395A1 (en) | 2017-10-27 | 2019-05-02 | University Of Virginia Patent Foundation | COMPOUNDS AND METHODS FOR REGULATING, LIMITING OR INHIBITING AVIL EXPRESSION |
| EP3962485A4 (en) * | 2019-05-02 | 2022-12-28 | University Of Virginia Patent Foundation | SUBSTITUTED (PIPERIDINE-1-YL)ARYL ANALOGUES TO MODULATE AVILACTIVITY |
| US11866421B2 (en) | 2021-05-31 | 2024-01-09 | Epigen Biosciences, Inc. | Pyrimidine and pyridine amine compounds and usage thereof in disease treatment |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050130954A1 (en) * | 2003-11-21 | 2005-06-16 | Mitchell Ian S. | AKT protein kinase inhibitors |
| WO2006071819A1 (en) * | 2004-12-28 | 2006-07-06 | Exelixis, Inc. | [1h-pyrazolo[3, 4-d]pyrimidin-4-yl]-piperidine or -piperazine compounds as serine-theoronine kinase modulators (p70s6k, atk1 and atk2) for the treatment of immunological, inflammatory and proliferative diseases |
| WO2008075172A2 (en) * | 2006-12-19 | 2008-06-26 | Pfizer Products Inc. | Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020137755A1 (en) * | 2000-12-04 | 2002-09-26 | Bilodeau Mark T. | Tyrosine kinase inhibitors |
| TW200306819A (en) | 2002-01-25 | 2003-12-01 | Vertex Pharma | Indazole compounds useful as protein kinase inhibitors |
| JP2006522124A (ja) | 2003-04-03 | 2006-09-28 | バーテックス ファーマシューティカルズ インコーポレイテッド | プロテインキナーゼのインヒビターとして有用な組成物 |
| JP2007507531A (ja) | 2003-09-30 | 2007-03-29 | アイアールエム・リミテッド・ライアビリティ・カンパニー | タンパク質キナーゼ阻害剤としての化合物および組成物 |
| JP4800216B2 (ja) | 2003-10-24 | 2011-10-26 | エグゼリクシス, インコーポレイテッド | p70S6キナーゼモジュレーターおよび使用方法 |
| KR20060117329A (ko) | 2003-11-21 | 2006-11-16 | 노파르티스 아게 | 단백질 키나제 저해제로서의 1h-이미다조퀴놀린 유도체 |
| US8044057B2 (en) | 2003-12-09 | 2011-10-25 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Methods for suppressing an immune response or treating a proliferative disorder |
| AU2005249380C1 (en) | 2004-04-23 | 2012-09-20 | Exelixis, Inc. | Kinase modulators and methods of use |
| CN101107245A (zh) | 2005-01-19 | 2008-01-16 | 神经能质公司 | 经杂芳基取代的哌嗪-吡啶类似物 |
| GB0501999D0 (en) | 2005-02-01 | 2005-03-09 | Sentinel Oncology Ltd | Pharmaceutical compounds |
| WO2006136821A1 (en) | 2005-06-22 | 2006-12-28 | Astex Therapeutics Limited | Pharmaceutical compounds |
| FI3719018T3 (fi) * | 2006-04-25 | 2025-10-07 | Astex Therapeutics Ltd | Puriini- ja deatsapuriinijohdannaisia farmaseuttisina yhdisteinä |
| WO2008012635A2 (en) * | 2006-07-26 | 2008-01-31 | Pfizer Products Inc. | Amine derivatives useful as anticancer agents |
| EP2131656A4 (en) * | 2006-11-15 | 2011-12-07 | Forest Lab Holdings Ltd | phthalazine |
| UA99284C2 (ru) | 2007-05-11 | 2012-08-10 | Елі Ліллі Енд Компані | ИНГИБИТОРЫ р70 S6-КИНАЗЫ |
| AR074072A1 (es) | 2008-11-11 | 2010-12-22 | Lilly Co Eli | Compuesto de imidazol -piperidin -pirrol-pirimidin-6-ona, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para tratar el glioblastoma multiforme |
| CN102317269B (zh) | 2009-02-11 | 2015-06-17 | 默克专利有限公司 | 新氨基氮杂杂环甲酰胺类 |
| US9029359B2 (en) * | 2009-09-04 | 2015-05-12 | Biogen Idec Ma, Inc. | Heteroaryl Btk inhibitors |
| UA110113C2 (xx) | 2010-07-29 | 2015-11-25 | Біциклічні азагетероциклічні карбоксаміди | |
| WO2012016001A1 (en) | 2010-07-29 | 2012-02-02 | Merck Patent Gmbh | Cyclic amine azaheterocyclic carboxamides |
| CA2818706C (en) | 2010-11-24 | 2019-07-23 | Merck Patent Gmbh | Quinazoline carboxamide azetidines |
| ES2644536T3 (es) * | 2011-09-12 | 2017-11-29 | Merck Patent Gmbh | Imidazol-aminas novedosas como moduladores de la actividad cinasa |
| JP6082011B2 (ja) * | 2011-09-12 | 2017-02-15 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | キナーゼ活性のモジュレーターとして使用するためのアミノピリミジン誘導体 |
| ES2807539T3 (es) * | 2012-11-16 | 2021-02-23 | Merck Patent Gmbh | Derivados de imidazol-piperidinilo como moduladores de la actividad de quinasa |
| RU2690679C2 (ru) * | 2014-02-11 | 2019-06-05 | Мерк Патент Гмбх | Новые пиримидинимидазоламины в качестве модуляторов активности киназы |
-
2012
- 2012-09-12 JP JP2014530756A patent/JP6082011B2/ja not_active Expired - Fee Related
- 2012-09-12 AU AU2012308681A patent/AU2012308681B2/en not_active Ceased
- 2012-09-12 ES ES12766773.1T patent/ES2646759T3/es active Active
- 2012-09-12 MX MX2014002836A patent/MX347241B/es active IP Right Grant
- 2012-09-12 BR BR112014005468A patent/BR112014005468A2/pt not_active IP Right Cessation
- 2012-09-12 HU HUE12766773A patent/HUE034979T2/en unknown
- 2012-09-12 CA CA2844704A patent/CA2844704C/en not_active Expired - Fee Related
- 2012-09-12 RS RS20171130A patent/RS56486B1/sr unknown
- 2012-09-12 HR HRP20171655TT patent/HRP20171655T1/hr unknown
- 2012-09-12 WO PCT/US2012/054877 patent/WO2013040044A1/en not_active Ceased
- 2012-09-12 SG SG2014009260A patent/SG2014009260A/en unknown
- 2012-09-12 CN CN201710022892.9A patent/CN106946796B/zh not_active Expired - Fee Related
- 2012-09-12 EA EA201400338A patent/EA028057B1/ru not_active IP Right Cessation
- 2012-09-12 US US14/236,405 patent/US9321760B2/en not_active Expired - Fee Related
- 2012-09-12 SI SI201231118T patent/SI2755958T1/sl unknown
- 2012-09-12 DK DK12766773.1T patent/DK2755958T3/en active
- 2012-09-12 EP EP12766773.1A patent/EP2755958B9/en active Active
- 2012-09-12 LT LTEP12766773.1T patent/LT2755958T/lt unknown
- 2012-09-12 PT PT127667731T patent/PT2755958T/pt unknown
- 2012-09-12 KR KR1020147007739A patent/KR101992505B1/ko not_active Expired - Fee Related
- 2012-09-12 CN CN201280054959.2A patent/CN103930407B/zh not_active Expired - Fee Related
- 2012-09-12 PL PL12766773T patent/PL2755958T3/pl unknown
-
2013
- 2013-03-15 NO NO13001311A patent/NO2639780T3/no unknown
-
2014
- 2014-02-10 ZA ZA2014/01007A patent/ZA201401007B/en unknown
- 2014-03-06 IL IL231381A patent/IL231381B/en active IP Right Grant
-
2016
- 2016-03-03 US US15/060,050 patent/US9662330B2/en not_active Expired - Fee Related
-
2017
- 2017-04-18 US US15/490,370 patent/US10080750B2/en active Active
- 2017-10-09 AU AU2017245469A patent/AU2017245469B2/en not_active Ceased
-
2019
- 2019-05-07 IL IL266510A patent/IL266510B/en active IP Right Grant
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050130954A1 (en) * | 2003-11-21 | 2005-06-16 | Mitchell Ian S. | AKT protein kinase inhibitors |
| WO2006071819A1 (en) * | 2004-12-28 | 2006-07-06 | Exelixis, Inc. | [1h-pyrazolo[3, 4-d]pyrimidin-4-yl]-piperidine or -piperazine compounds as serine-theoronine kinase modulators (p70s6k, atk1 and atk2) for the treatment of immunological, inflammatory and proliferative diseases |
| WO2008075172A2 (en) * | 2006-12-19 | 2008-06-26 | Pfizer Products Inc. | Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases |
Non-Patent Citations (1)
| Title |
|---|
| C. BARILLARI, ET AL.: "Solid Phase Synthesis of Diamino-Substituted Pyrimidines", EUR. J. ORG. CHEM., 1 January 2001 (2001-01-01), pages 4737 - 4741, XP055044047, DOI: 10.1002/1099-0690(200112)2001:24<4737::AID-EJOC4737>3.0.CO;2-1 * |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EA028057B1 (ru) | Производные аминопиримидина для применения в качестве модуляторов киназной активности | |
| US20220162203A1 (en) | Heteroaryl derivative, method for producing same, and pharmaceutical composition comprising same as effective component | |
| US9145392B2 (en) | Imidazole amines as modulators of kinase activity | |
| EP2598497B1 (en) | Cyclic amine azaheterocyclic carboxamides | |
| EA023821B1 (ru) | Хиназолинкарбоксамидазетидины, их применение в лечении гиперпролиферативных заболеваний и содержащие их композиции | |
| US11446287B2 (en) | Compounds and methods for EP300 or CBP modulation and indications therefor | |
| RU2674261C2 (ru) | Производные 6-[4-(1н-имидазол-2-ил)пиперидин-1-ил]пиримидин-4-амина в качестве модуляторов активности киназ | |
| US20240150337A1 (en) | Heteroaryl derivative, method for producing same, and pharmaceutical composition comprising same as effective component | |
| WO2020187292A1 (zh) | 2-取代吡唑氨基-4-取代氨基-5-嘧啶甲酰胺类化合物、组合物及其应用 | |
| HK1240220A1 (en) | Aminopyrimidine derivatives for use as modulators of kinase activity | |
| EP4399202A1 (en) | Substituted quinolines as improved nf-kb-inducing kinase (nik) inhibitors | |
| WO2013062071A1 (ja) | ピペラジン誘導体及びその塩 | |
| HK1198168B (zh) | 用作激酶活性调节剂的氨基嘧啶衍生物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG TJ TM |
|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): RU |