JP2015505542A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015505542A5 JP2015505542A5 JP2014553655A JP2014553655A JP2015505542A5 JP 2015505542 A5 JP2015505542 A5 JP 2015505542A5 JP 2014553655 A JP2014553655 A JP 2014553655A JP 2014553655 A JP2014553655 A JP 2014553655A JP 2015505542 A5 JP2015505542 A5 JP 2015505542A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- pyrazin
- ethyl
- amino
- pyridin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 150000001875 compounds Chemical class 0.000 claims 14
- 230000001419 dependent effect Effects 0.000 claims 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 5
- 206010028980 Neoplasm Diseases 0.000 claims 4
- 125000004429 atom Chemical group 0.000 claims 4
- 201000011510 cancer Diseases 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 210000003734 kidney Anatomy 0.000 claims 4
- 229910052757 nitrogen Inorganic materials 0.000 claims 4
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 208000027866 inflammatory disease Diseases 0.000 claims 3
- 208000015122 neurodegenerative disease Diseases 0.000 claims 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- 125000004434 sulfur atom Chemical group 0.000 claims 3
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims 2
- 208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 claims 2
- 208000010833 Chronic myeloid leukaemia Diseases 0.000 claims 2
- 208000007766 Kaposi sarcoma Diseases 0.000 claims 2
- 208000034578 Multiple myelomas Diseases 0.000 claims 2
- 208000033761 Myelogenous Chronic BCR-ABL Positive Leukemia Diseases 0.000 claims 2
- 208000033776 Myeloid Acute Leukemia Diseases 0.000 claims 2
- 206010035226 Plasma cell myeloma Diseases 0.000 claims 2
- 208000024770 Thyroid neoplasm Diseases 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 125000003342 alkenyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 210000004556 brain Anatomy 0.000 claims 2
- 210000000481 breast Anatomy 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 210000004027 cell Anatomy 0.000 claims 2
- 210000001072 colon Anatomy 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 210000002615 epidermis Anatomy 0.000 claims 2
- 210000003238 esophagus Anatomy 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 210000003128 head Anatomy 0.000 claims 2
- 230000002757 inflammatory effect Effects 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 208000032839 leukemia Diseases 0.000 claims 2
- 210000004185 liver Anatomy 0.000 claims 2
- 210000004072 lung Anatomy 0.000 claims 2
- 201000001441 melanoma Diseases 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 210000000066 myeloid cell Anatomy 0.000 claims 2
- OKPBZUTXNVCBHM-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-[6-(methylaminomethyl)pyridin-3-yl]phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound C1=NC(CNC)=CC=C1C(C=C1)=CC=C1OC1=CN=CC(N(C)CCN(C)C(C)=O)=N1 OKPBZUTXNVCBHM-UHFFFAOYSA-N 0.000 claims 2
- 210000003739 neck Anatomy 0.000 claims 2
- 210000001672 ovary Anatomy 0.000 claims 2
- 125000004043 oxo group Chemical group O=* 0.000 claims 2
- 210000000496 pancreas Anatomy 0.000 claims 2
- 210000002307 prostate Anatomy 0.000 claims 2
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 2
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 2
- 210000002784 stomach Anatomy 0.000 claims 2
- -1 tert-butyloxy, neopentyl Chemical group 0.000 claims 2
- 210000001550 testis Anatomy 0.000 claims 2
- 201000002510 thyroid cancer Diseases 0.000 claims 2
- 210000003932 urinary bladder Anatomy 0.000 claims 2
- 210000004291 uterus Anatomy 0.000 claims 2
- IAYIVOHVDGNJAW-UHFFFAOYSA-N 1-[2-[[6-[4-(5-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]amino]ethyl]piperidin-2-one Chemical compound N1=CC(C)=CC=C1C(C=C1)=CC=C1OC1=CN=CC(NCCN2C(CCCC2)=O)=N1 IAYIVOHVDGNJAW-UHFFFAOYSA-N 0.000 claims 1
- MSDPXGZYQDMCRP-UHFFFAOYSA-N 1-[2-[methyl-[6-[4-(5-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]amino]ethyl]piperidin-2-one Chemical compound C=1N=CC(OC=2C=CC(=CC=2)C=2N=CC(C)=CC=2)=NC=1N(C)CCN1CCCCC1=O MSDPXGZYQDMCRP-UHFFFAOYSA-N 0.000 claims 1
- YBJHBAHKTGYVGT-UHFFFAOYSA-N 5-(2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl)pentanoic acid Chemical compound N1C(=O)NC2C(CCCCC(=O)O)SCC21 YBJHBAHKTGYVGT-UHFFFAOYSA-N 0.000 claims 1
- CMUGHZFPFWNUQT-HUBLWGQQSA-N 6-[5-(2-oxo-hexahydro-thieno[3,4-d]imidazol-4-yl)-pentanoylamino]-hexanoic acid Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)NCCCCCC(=O)O)SC[C@@H]21 CMUGHZFPFWNUQT-HUBLWGQQSA-N 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- UMWYPMUNNQMKCC-UHFFFAOYSA-N CN(CCN(C)c1cncc(Oc2ccc(cc2)-c2ccc(cn2)[N+]([O-])=O)n1)C(C)=O Chemical compound CN(CCN(C)c1cncc(Oc2ccc(cc2)-c2ccc(cn2)[N+]([O-])=O)n1)C(C)=O UMWYPMUNNQMKCC-UHFFFAOYSA-N 0.000 claims 1
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 1
- BKIOIASWRZYNMC-UHFFFAOYSA-N N-[2-[[6-[4-[6-[4-(6-aminohexanoyl)piperazin-1-yl]pyridin-3-yl]phenoxy]pyrazin-2-yl]-methylamino]ethyl]-N-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=NC(=CC=2)N2CCN(CC2)C(=O)CCCCCN)=N1 BKIOIASWRZYNMC-UHFFFAOYSA-N 0.000 claims 1
- 208000034189 Sclerosis Diseases 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 206010003246 arthritis Diseases 0.000 claims 1
- 125000004603 benzisoxazolyl group Chemical group O1N=C(C2=C1C=CC=C2)* 0.000 claims 1
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 claims 1
- 210000000988 bone and bone Anatomy 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 230000003463 hyperproliferative effect Effects 0.000 claims 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims 1
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 1
- 206010025135 lupus erythematosus Diseases 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- SXECCXUBNRDIRK-UHFFFAOYSA-N n-[2-[6-[4-(5-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]sulfanylethyl]-n-propan-2-ylacetamide Chemical compound CC(C)N(C(C)=O)CCSC1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC(C)=CC=2)=N1 SXECCXUBNRDIRK-UHFFFAOYSA-N 0.000 claims 1
- ZCSUOEYWGSYHDE-UHFFFAOYSA-N n-[2-[[6-[2-fluoro-4-(5-fluoropyridin-2-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C(=CC(=CC=2)C=2N=CC(F)=CC=2)F)=N1 ZCSUOEYWGSYHDE-UHFFFAOYSA-N 0.000 claims 1
- AMOYNRBZVPREEJ-UHFFFAOYSA-N n-[2-[[6-[2-fluoro-4-(5-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C(=CC(=CC=2)C=2N=CC(C)=CC=2)F)=N1 AMOYNRBZVPREEJ-UHFFFAOYSA-N 0.000 claims 1
- NMEYBBIHHOAULH-UHFFFAOYSA-N n-[2-[[6-[2-fluoro-4-(6-morpholin-4-ylpyridin-3-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C(=CC(=CC=2)C=2C=NC(=CC=2)N2CCOCC2)F)=N1 NMEYBBIHHOAULH-UHFFFAOYSA-N 0.000 claims 1
- LNXXFRZZOMSYFT-UHFFFAOYSA-N n-[2-[[6-[4-(2-aminopyrimidin-4-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=C(N)N=CC=2)=N1 LNXXFRZZOMSYFT-UHFFFAOYSA-N 0.000 claims 1
- BXRDLTFAIAKKNX-UHFFFAOYSA-N n-[2-[[6-[4-(2-cyanopyridin-4-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=C(N=CC=2)C#N)=N1 BXRDLTFAIAKKNX-UHFFFAOYSA-N 0.000 claims 1
- BPACBFXULSQLDW-UHFFFAOYSA-N n-[2-[[6-[4-(2-fluoropyridin-4-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=C(F)N=CC=2)=N1 BPACBFXULSQLDW-UHFFFAOYSA-N 0.000 claims 1
- CRUUFNUBDCUODT-UHFFFAOYSA-N n-[2-[[6-[4-(3-cyanopyridin-4-yl)-2-fluorophenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C(=CC(=CC=2)C=2C(=CN=CC=2)C#N)F)=N1 CRUUFNUBDCUODT-UHFFFAOYSA-N 0.000 claims 1
- LPDPCXPKZWNOGE-UHFFFAOYSA-N n-[2-[[6-[4-(3-cyanopyridin-4-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C(=CN=CC=2)C#N)=N1 LPDPCXPKZWNOGE-UHFFFAOYSA-N 0.000 claims 1
- LCAZWQCKEMBHKH-UHFFFAOYSA-N n-[2-[[6-[4-(5-aminopyrazin-2-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC(N)=NC=2)=N1 LCAZWQCKEMBHKH-UHFFFAOYSA-N 0.000 claims 1
- IICGIVPNGIVPHS-UHFFFAOYSA-N n-[2-[[6-[4-(5-azidopyridin-2-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC(=CC=2)N=[N+]=[N-])=N1 IICGIVPNGIVPHS-UHFFFAOYSA-N 0.000 claims 1
- KWESHVKSKXFOQE-UHFFFAOYSA-N n-[2-[[6-[4-(5-fluoropyridin-2-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC(F)=CC=2)=N1 KWESHVKSKXFOQE-UHFFFAOYSA-N 0.000 claims 1
- GZKZWHKTSUWIJT-UHFFFAOYSA-N n-[2-[[6-[4-(5-methoxypyridin-2-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound N1=CC(OC)=CC=C1C(C=C1)=CC=C1OC1=CN=CC(N(C)CCN(C)C(C)=O)=N1 GZKZWHKTSUWIJT-UHFFFAOYSA-N 0.000 claims 1
- JMRDBWAMAQBISE-UHFFFAOYSA-N n-[2-[[6-[4-(6-aminopyridin-2-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=C(N)C=CC=2)=N1 JMRDBWAMAQBISE-UHFFFAOYSA-N 0.000 claims 1
- AKTIYLRDMGCPSO-UHFFFAOYSA-N n-[2-[[6-[4-(6-cyanopyridin-3-yl)phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=NC(=CC=2)C#N)=N1 AKTIYLRDMGCPSO-UHFFFAOYSA-N 0.000 claims 1
- JAJIIHLFYUFSIJ-UHFFFAOYSA-N n-[2-[[6-[4-[6-(hydroxymethyl)pyridin-3-yl]phenoxy]pyrazin-2-yl]-methylamino]ethyl]-n-methylacetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=NC(CO)=CC=2)=N1 JAJIIHLFYUFSIJ-UHFFFAOYSA-N 0.000 claims 1
- NNWDBFSGOYPWIT-UHFFFAOYSA-N n-[5-[4-[6-[2-[acetyl(methyl)amino]ethyl-methylamino]pyrazin-2-yl]oxy-3-fluorophenyl]pyridin-2-yl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C(=CC(=CC=2)C=2C=NC(NC(C)=O)=CC=2)F)=N1 NNWDBFSGOYPWIT-UHFFFAOYSA-N 0.000 claims 1
- ZVIIYVVBSVBDOM-UHFFFAOYSA-N n-[5-[4-[6-[2-[acetyl(methyl)amino]ethyl-methylamino]pyrazin-2-yl]oxyphenyl]pyridin-2-yl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=NC(NC(C)=O)=CC=2)=N1 ZVIIYVVBSVBDOM-UHFFFAOYSA-N 0.000 claims 1
- SQJXWBYHQXSQKE-UHFFFAOYSA-N n-[6-[4-[6-[2-[acetyl(methyl)amino]ethyl-methylamino]pyrazin-2-yl]oxyphenyl]pyridin-2-yl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=C(NC(C)=O)C=CC=2)=N1 SQJXWBYHQXSQKE-UHFFFAOYSA-N 0.000 claims 1
- FXDUNTQJDBNYBM-UHFFFAOYSA-N n-ethyl-n-[2-[6-[4-(5-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]sulfanylethyl]acetamide Chemical compound CCN(C(C)=O)CCSC1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC(C)=CC=2)=N1 FXDUNTQJDBNYBM-UHFFFAOYSA-N 0.000 claims 1
- AHINMVOEKJEPPV-UHFFFAOYSA-N n-methyl-3-[methyl-[6-[4-(5-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]amino]propanamide Chemical compound CNC(=O)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC(C)=CC=2)=N1 AHINMVOEKJEPPV-UHFFFAOYSA-N 0.000 claims 1
- CVKLBVGHLHNKHS-UHFFFAOYSA-N n-methyl-n-[2-[6-[4-(5-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]sulfanylethyl]acetamide Chemical compound CC(=O)N(C)CCSC1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC(C)=CC=2)=N1 CVKLBVGHLHNKHS-UHFFFAOYSA-N 0.000 claims 1
- ABXORIGECMXSTH-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-(4-pyridin-2-ylphenoxy)pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC=CC=2)=N1 ABXORIGECMXSTH-UHFFFAOYSA-N 0.000 claims 1
- CLPPYFZJVJCQPD-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-(4-pyridin-4-ylphenoxy)pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=CN=CC=2)=N1 CLPPYFZJVJCQPD-UHFFFAOYSA-N 0.000 claims 1
- AIIVJLWYWWZCQE-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-(1,3-thiazol-2-yl)phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2SC=CN=2)=N1 AIIVJLWYWWZCQE-UHFFFAOYSA-N 0.000 claims 1
- LUJRZYDSQWMMHV-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-(1h-pyrrolo[2,3-c]pyridin-5-yl)phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC=3NC=CC=3C=2)=N1 LUJRZYDSQWMMHV-UHFFFAOYSA-N 0.000 claims 1
- UZEUDQHJIWFBPX-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-(5-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=CC(C)=CC=2)=N1 UZEUDQHJIWFBPX-UHFFFAOYSA-N 0.000 claims 1
- OQFALOXDLYJORL-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-(6-methylpyridin-2-yl)phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=C(C)C=CC=2)=N1 OQFALOXDLYJORL-UHFFFAOYSA-N 0.000 claims 1
- PIFVKHOMCACBMI-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-(6-methylpyridin-3-yl)phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=NC(C)=CC=2)=N1 PIFVKHOMCACBMI-UHFFFAOYSA-N 0.000 claims 1
- NYYHHCCHKYIWNC-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-(6-methylsulfonylpyridin-2-yl)phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2N=C(C=CC=2)S(C)(=O)=O)=N1 NYYHHCCHKYIWNC-UHFFFAOYSA-N 0.000 claims 1
- CMQWXGQEPJOJPC-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-(6-morpholin-4-ylpyridin-3-yl)phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=NC(=CC=2)N2CCOCC2)=N1 CMQWXGQEPJOJPC-UHFFFAOYSA-N 0.000 claims 1
- JMNKYIAQLNRPDF-UHFFFAOYSA-N n-methyl-n-[2-[methyl-[6-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)phenoxy]pyrazin-2-yl]amino]ethyl]acetamide Chemical compound CC(=O)N(C)CCN(C)C1=CN=CC(OC=2C=CC(=CC=2)C=2C=3C=CNC=3N=CN=2)=N1 JMNKYIAQLNRPDF-UHFFFAOYSA-N 0.000 claims 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 230000009885 systemic effect Effects 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12000559.0 | 2012-01-28 | ||
| EP12000559 | 2012-01-28 | ||
| PCT/EP2013/000050 WO2013110433A1 (en) | 2012-01-28 | 2013-01-10 | Azaheterocyclic compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015505542A JP2015505542A (ja) | 2015-02-23 |
| JP2015505542A5 true JP2015505542A5 (https=) | 2016-03-03 |
Family
ID=47603585
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014553655A Ceased JP2015505542A (ja) | 2012-01-28 | 2013-01-10 | アザ複素環式化合物 |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US9493444B2 (https=) |
| EP (1) | EP2807154B1 (https=) |
| JP (1) | JP2015505542A (https=) |
| KR (1) | KR20140117641A (https=) |
| CN (1) | CN104080773B (https=) |
| AU (1) | AU2013212175B2 (https=) |
| BR (1) | BR112014018341A8 (https=) |
| CA (1) | CA2862698A1 (https=) |
| HK (1) | HK1202543A1 (https=) |
| IL (1) | IL233705A0 (https=) |
| MX (1) | MX2014009133A (https=) |
| RU (1) | RU2014134909A (https=) |
| SG (1) | SG11201404217XA (https=) |
| WO (1) | WO2013110433A1 (https=) |
| ZA (1) | ZA201406322B (https=) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2865511A1 (en) | 2012-03-07 | 2013-09-12 | Institute Of Cancer Research: Royal Cancer Hospital (The) | 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use |
| WO2015035223A1 (en) | 2013-09-09 | 2015-03-12 | Peloton Therapeutics, Inc. | Aryl ethers and uses thereof |
| US9611223B2 (en) | 2013-09-11 | 2017-04-04 | Institute Of Cancer Research: Royal Cancer Hospital (The) | 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use |
| JP6694811B2 (ja) * | 2013-10-04 | 2020-05-20 | ノバルティス アーゲー | ＲＮＡ干渉に使用するためのＲＮＡｉ剤用の３’末端キャップ |
| ES2737148T3 (es) | 2013-12-16 | 2020-01-10 | Peloton Therapeutics Inc | Análogos de sulfona y sulfoximina cíclicos y usos de los mismos |
| GB201322333D0 (en) * | 2013-12-17 | 2014-01-29 | Agency Science Tech & Res | WNT pathway modulators |
| WO2016145045A1 (en) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Compositions for use in treating glioblastoma |
| US10278942B2 (en) | 2015-03-11 | 2019-05-07 | Peloton Therapeutics, Inc. | Compositions for use in treating pulmonary arterial hypertension |
| WO2016144826A1 (en) | 2015-03-11 | 2016-09-15 | Peloton Therapeutics, Inc. | Substituted pyridines and uses thereof |
| US10807948B2 (en) | 2015-03-11 | 2020-10-20 | Peloton Therapeutics, Inc. | Aromatic compounds and uses thereof |
| WO2016168510A1 (en) | 2015-04-17 | 2016-10-20 | Peloton Therapeutics, Inc. | Combination therapy of a hif-2-alpha inhibitor and an immunotherapeutic agent and uses thereof |
| US9796697B2 (en) | 2015-06-12 | 2017-10-24 | Peloton Therapeutics, Inc. | Tricyclic inhibitors of HIF-2-alpha and uses thereof |
| WO2017062688A1 (en) | 2015-10-08 | 2017-04-13 | Suzhou Yunxuan Yiyao Keji Youxian Gongsi | Wnt signaling pathway inhibitors and therapeutic applications thereof |
| EP3359154B1 (en) * | 2015-10-08 | 2021-05-26 | Suzhou Yunxuan Yiyao Keji Youxian Gongsi | Wnt signaling pathway inhibitors and therapeutic applications thereof |
| CA3081553C (en) | 2017-11-17 | 2022-11-15 | Cellix Bio Private Limited | Compositions and methods for the treatment of eye disorders |
| CA3141404A1 (en) * | 2019-06-14 | 2020-12-17 | Disarm Therapeutics, Inc. | Inhibitors of sarm1 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2726164A1 (en) * | 2008-05-27 | 2009-12-23 | The Board Of Regents Of The University Of Texas System | Wnt protein signalling inhibitors |
| GB0818241D0 (en) * | 2008-10-06 | 2008-11-12 | Cancer Res Technology | Compounds and their use |
-
2013
- 2013-01-10 HK HK15103108.6A patent/HK1202543A1/xx unknown
- 2013-01-10 US US14/375,072 patent/US9493444B2/en not_active Expired - Fee Related
- 2013-01-10 RU RU2014134909A patent/RU2014134909A/ru unknown
- 2013-01-10 BR BR112014018341A patent/BR112014018341A8/pt not_active IP Right Cessation
- 2013-01-10 WO PCT/EP2013/000050 patent/WO2013110433A1/en not_active Ceased
- 2013-01-10 MX MX2014009133A patent/MX2014009133A/es unknown
- 2013-01-10 JP JP2014553655A patent/JP2015505542A/ja not_active Ceased
- 2013-01-10 KR KR1020147023947A patent/KR20140117641A/ko not_active Withdrawn
- 2013-01-10 AU AU2013212175A patent/AU2013212175B2/en not_active Expired - Fee Related
- 2013-01-10 SG SG11201404217XA patent/SG11201404217XA/en unknown
- 2013-01-10 CN CN201380006903.4A patent/CN104080773B/zh not_active Expired - Fee Related
- 2013-01-10 CA CA2862698A patent/CA2862698A1/en not_active Abandoned
- 2013-01-10 EP EP13701200.1A patent/EP2807154B1/en not_active Not-in-force
-
2014
- 2014-07-17 IL IL233705A patent/IL233705A0/en unknown
- 2014-08-27 ZA ZA2014/06322A patent/ZA201406322B/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2015505542A5 (https=) | ||
| RU2014134909A (ru) | Азагетероциклические соединения | |
| US11028088B2 (en) | Modulators of BTK proteolysis and methods of use | |
| JP7447002B2 (ja) | ＳＨＰ２のオクタヒドロシクロペンタ［ｃ］ピロールのアロステリック阻害剤 | |
| TWI762743B (zh) | 磺醯胺化合物及其用途 | |
| US20200038513A1 (en) | Modulators of fak proteolysis and associated methods of use | |
| JP6736559B2 (ja) | トリアゾロピリミジン化合物およびその使用 | |
| KR101910720B1 (ko) | 키나제 억제제로서의 아미노헤테로아릴 벤즈아미드 | |
| JP6545199B2 (ja) | ３−アミノ−１，５，６，７−テトラヒドロ−４ｈ−インドール−４−オン類 | |
| AU2019249849A1 (en) | BRM targeting compounds and associated methods of use | |
| JP7738550B2 (ja) | Ｅｒｋ１およびｅｒｋ２の複素環式阻害剤の使用のための改善された方法、キット、組成物、ならびに投与レジメン | |
| ES2684120T3 (es) | Combinación de un inhibidor de IAP y un taxano | |
| WO2018226542A1 (en) | Modulators of proteolysis and associated methods of use | |
| JP2011513305A5 (https=) | ||
| RS57177B1 (sr) | Derivati benzamida za inhibiranje aktivnosti abl1, abl2 i bcr-abl1 | |
| JP2017532360A5 (https=) | ||
| HRP20171655T1 (hr) | Derivati aminopirimidina za upotrebu kao modulatori aktivnosti kinaze | |
| US20200121684A1 (en) | Modulators of btk proteolysis and methods of use | |
| US20220071970A1 (en) | Quinuclidine-3-one derivatives and their use in cancer treatment | |
| CA3063804A1 (en) | A class of isoindolone-imide ring-1,3-dione-2-ene compounds, composition and use thereof | |
| JP2025509965A (ja) | がんを治療するための組成物及び方法 | |
| WO2020198067A1 (en) | Pkm2 modulators and methods for their use | |
| HK1239664B (en) | Triazolopyrimidine compounds and uses thereof | |
| HK1239664A1 (en) | Triazolopyrimidine compounds and uses thereof |