JP2015503571A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2015503571A5 JP2015503571A5 JP2014550627A JP2014550627A JP2015503571A5 JP 2015503571 A5 JP2015503571 A5 JP 2015503571A5 JP 2014550627 A JP2014550627 A JP 2014550627A JP 2014550627 A JP2014550627 A JP 2014550627A JP 2015503571 A5 JP2015503571 A5 JP 2015503571A5
- Authority
- JP
- Japan
- Prior art keywords
- alkylene
- alkyl
- ring
- phenyl
- optionally substituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 100
- 150000001875 compounds Chemical class 0.000 claims description 86
- -1 CF 3 Chemical group 0.000 claims description 75
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 56
- 230000035772 mutation Effects 0.000 claims description 51
- 101000599886 Homo sapiens Isocitrate dehydrogenase [NADP], mitochondrial Proteins 0.000 claims description 31
- 102100037845 Isocitrate dehydrogenase [NADP], mitochondrial Human genes 0.000 claims description 31
- 125000005843 halogen group Chemical group 0.000 claims description 30
- 125000002947 alkylene group Chemical group 0.000 claims description 28
- 125000001424 substituent group Chemical group 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 206010028980 Neoplasm Diseases 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
- 125000000623 heterocyclic group Chemical group 0.000 claims description 16
- 201000011510 cancer Diseases 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 12
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 12
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 10
- 125000004452 carbocyclyl group Chemical group 0.000 claims description 10
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
- 125000004076 pyridyl group Chemical group 0.000 claims description 10
- 102200116484 rs121913502 Human genes 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- ICNPHUJONLGYDI-UHFFFAOYSA-N 4-butyl-2-n-(4-methylphenyl)-6-phenyl-1h-1,3,5-triazine-2,4-diamine Chemical compound N1C(C=2C=CC=CC=2)=NC(CCCC)(N)N=C1NC1=CC=C(C)C=C1 ICNPHUJONLGYDI-UHFFFAOYSA-N 0.000 claims description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 125000002971 oxazolyl group Chemical group 0.000 claims description 8
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 8
- HWXBTNAVRSUOJR-UHFFFAOYSA-N 2-hydroxyglutaric acid Chemical compound OC(=O)C(O)CCC(O)=O HWXBTNAVRSUOJR-UHFFFAOYSA-N 0.000 claims description 7
- KPGXRSRHYNQIFN-UHFFFAOYSA-N 2-oxoglutaric acid Chemical compound OC(=O)CCC(=O)C(O)=O KPGXRSRHYNQIFN-UHFFFAOYSA-N 0.000 claims description 7
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 7
- 230000001419 dependent effect Effects 0.000 claims description 7
- 239000003814 drug Substances 0.000 claims description 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 6
- 102000004190 Enzymes Human genes 0.000 claims description 6
- 108090000790 Enzymes Proteins 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 201000003793 Myelodysplastic syndrome Diseases 0.000 claims description 6
- 201000007224 Myeloproliferative neoplasm Diseases 0.000 claims description 6
- 208000015914 Non-Hodgkin lymphomas Diseases 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 6
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 6
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 229940124597 therapeutic agent Drugs 0.000 claims description 5
- CLBHAIBDFNDDJP-MEFGMAGPSA-N (e)-3-[4-[[4-[3-(diethylamino)propylamino]-6-phenyl-1,3,5-triazin-2-yl]amino]-2-methoxyphenyl]-2-phenylprop-2-enenitrile Chemical compound N=1C(C=2C=CC=CC=2)=NC(NCCCN(CC)CC)=NC=1NC(C=C1OC)=CC=C1\C=C(\C#N)C1=CC=CC=C1 CLBHAIBDFNDDJP-MEFGMAGPSA-N 0.000 claims description 4
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 claims description 4
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 4
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 4
- BKLDIEBDLYULCF-UHFFFAOYSA-N 3-[4-(5-aminopentylamino)-6-(3-fluoroanilino)-1,3,5-triazin-2-yl]phenol Chemical compound N=1C(C=2C=C(O)C=CC=2)=NC(NCCCCCN)=NC=1NC1=CC=CC(F)=C1 BKLDIEBDLYULCF-UHFFFAOYSA-N 0.000 claims description 4
- MUVWXGCFCZGJAL-MRXNPFEDSA-N 3-[[4-(3-chlorophenyl)-6-[[(3r)-pyrrolidin-3-yl]amino]-1,3,5-triazin-2-yl]amino]-4-methylbenzamide Chemical compound CC1=CC=C(C(N)=O)C=C1NC1=NC(N[C@H]2CNCC2)=NC(C=2C=C(Cl)C=CC=2)=N1 MUVWXGCFCZGJAL-MRXNPFEDSA-N 0.000 claims description 4
- QTSZJXMCNWRULJ-UHFFFAOYSA-N 4,6-bis(3-fluorophenyl)-2-piperidin-3-ylimino-1,3-dihydro-1,3,5-triazin-4-amine Chemical compound FC=1C=C(C=CC=1)C1(NC(=NC(=N1)NC1CNCCC1)C1=CC(=CC=C1)F)N QTSZJXMCNWRULJ-UHFFFAOYSA-N 0.000 claims description 4
- VPVZLIPBRXHMGH-UHFFFAOYSA-N 4-(furan-2-ylmethyl)-6-phenyl-2-N-[3-(trifluoromethyl)phenyl]-1H-1,3,5-triazine-2,4-diamine Chemical compound O1C(=CC=C1)CC1(NC(=NC(=N1)NC1=CC(=CC=C1)C(F)(F)F)C1=CC=CC=C1)N VPVZLIPBRXHMGH-UHFFFAOYSA-N 0.000 claims description 4
- RXQOFEFFFQEPEF-UHFFFAOYSA-N 4-[[4-(furan-2-ylmethylamino)-6-pyridin-4-yl-1,3,5-triazin-2-yl]amino]phenol Chemical compound C1=CC(O)=CC=C1NC1=NC(NCC=2OC=CC=2)=NC(C=2C=CN=CC=2)=N1 RXQOFEFFFQEPEF-UHFFFAOYSA-N 0.000 claims description 4
- OSRCRCDGQNLBNM-UHFFFAOYSA-N 4-cyclohexyl-2-N,6-diphenyl-1H-1,3,5-triazine-2,4-diamine Chemical compound C1(CCCCC1)C1(NC(=NC(=N1)NC1=CC=CC=C1)C1=CC=CC=C1)N OSRCRCDGQNLBNM-UHFFFAOYSA-N 0.000 claims description 4
- TXYRXGLQBFUCPR-UHFFFAOYSA-N 6-(3-methoxyphenyl)-4-n-methyl-2-n-(3-nitrophenyl)-1,3,5-triazine-2,4-diamine Chemical compound N=1C(C=2C=C(OC)C=CC=2)=NC(NC)=NC=1NC1=CC=CC([N+]([O-])=O)=C1 TXYRXGLQBFUCPR-UHFFFAOYSA-N 0.000 claims description 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 4
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical class CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims description 4
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Chemical class CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims description 4
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 4
- 206010039491 Sarcoma Diseases 0.000 claims description 4
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 4
- 125000000304 alkynyl group Chemical group 0.000 claims description 4
- BVCRERJDOOBZOH-UHFFFAOYSA-N bicyclo[2.2.1]heptanyl Chemical group C1C[C+]2CC[C-]1C2 BVCRERJDOOBZOH-UHFFFAOYSA-N 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 4
- 235000018417 cysteine Nutrition 0.000 claims description 4
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 4
- VYFOAVADNIHPTR-UHFFFAOYSA-N isatoic anhydride Chemical compound NC1=CC=CC=C1CO VYFOAVADNIHPTR-UHFFFAOYSA-N 0.000 claims description 4
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 4
- 150000004702 methyl esters Chemical class 0.000 claims description 4
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 4
- VJKPSOVHUPAUDR-UHFFFAOYSA-N n-(4-anilino-6-pyridin-2-yl-1,3,5-triazin-2-yl)-2-chloro-4-methylsulfonylbenzamide Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)NC1=NC(NC=2C=CC=CC=2)=NC(C=2N=CC=CC=2)=N1 VJKPSOVHUPAUDR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000003566 oxetanyl group Chemical group 0.000 claims description 4
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 4
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 claims description 4
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 4
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 claims description 4
- 125000000335 thiazolyl group Chemical group 0.000 claims description 4
- 208000031261 Acute myeloid leukaemia Diseases 0.000 claims description 3
- 208000032612 Glial tumor Diseases 0.000 claims description 3
- 206010018338 Glioma Diseases 0.000 claims description 3
- 208000006990 cholangiocarcinoma Diseases 0.000 claims description 3
- 208000005017 glioblastoma Diseases 0.000 claims description 3
- 201000001441 melanoma Diseases 0.000 claims description 3
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- 125000003107 substituted aryl group Chemical group 0.000 claims description 3
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims description 3
- 230000002792 vascular Effects 0.000 claims description 3
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 claims description 2
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 2
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 2
- 125000004208 3-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(*)=C1[H] 0.000 claims description 2
- 125000004917 3-methyl-2-butyl group Chemical group CC(C(C)*)C 0.000 claims description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 2
- 125000002393 azetidinyl group Chemical group 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 125000004284 isoxazol-3-yl group Chemical group [H]C1=C([H])C(*)=NO1 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000002757 morpholinyl group Chemical group 0.000 claims description 2
- 125000006299 oxetan-3-yl group Chemical group [H]C1([H])OC([H])([H])C1([H])* 0.000 claims description 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 2
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims description 2
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims description 2
- 208000005243 Chondrosarcoma Diseases 0.000 claims 2
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000003145 oxazol-4-yl group Chemical group O1C=NC(=C1)* 0.000 claims 1
- 150000002993 phenylalanine derivatives Chemical class 0.000 claims 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 238000000034 method Methods 0.000 description 10
- 125000001072 heteroaryl group Chemical group 0.000 description 6
- XJLXINKUBYWONI-DQQFMEOOSA-N [[(2r,3r,4r,5r)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2s,3r,4s,5s)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate Chemical compound NC(=O)C1=CC=C[N+]([C@@H]2[C@H]([C@@H](O)[C@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](OP(O)(O)=O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 XJLXINKUBYWONI-DQQFMEOOSA-N 0.000 description 5
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 description 5
- 108700028369 Alleles Proteins 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 150000002994 phenylalanines Chemical class 0.000 description 3
- KZKRRZFCAYOXQE-UHFFFAOYSA-N 1$l^{2}-azinane Chemical group C1CC[N]CC1 KZKRRZFCAYOXQE-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 235000001014 amino acid Nutrition 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 150000004677 hydrates Chemical class 0.000 description 2
- 0 *C(*)(*)Nc1nc(N/C2=C/C=C/C=C/C=C2)nc(C2=CC=CC=CC=CC2)n1 Chemical compound *C(*)(*)Nc1nc(N/C2=C/C=C/C=C/C=C2)nc(C2=CC=CC=CC=CC2)n1 0.000 description 1
- JNYLMODTPLSLIF-UHFFFAOYSA-N 6-(trifluoromethyl)pyridine-3-carboxylic acid Chemical group OC(=O)C1=CC=C(C(F)(F)F)N=C1 JNYLMODTPLSLIF-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000036952 cancer formation Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 210000000845 cartilage Anatomy 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 125000004498 isoxazol-4-yl group Chemical group O1N=CC(=C1)* 0.000 description 1
- 230000000869 mutational effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261584214P | 2012-01-06 | 2012-01-06 | |
| US61/584,214 | 2012-01-06 | ||
| PCT/CN2013/000009 WO2013102431A1 (en) | 2012-01-06 | 2013-01-05 | Therapeutically active compounds and their methods of use |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017019547A Division JP6409081B2 (ja) | 2012-01-06 | 2017-02-06 | 治療活性化合物およびその使用方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015503571A JP2015503571A (ja) | 2015-02-02 |
| JP2015503571A5 true JP2015503571A5 (enExample) | 2018-02-01 |
| JP6411895B2 JP6411895B2 (ja) | 2018-10-24 |
Family
ID=48744984
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014550627A Active JP6411895B2 (ja) | 2012-01-06 | 2013-01-05 | 治療活性化合物およびその使用方法 |
| JP2017019547A Active JP6409081B2 (ja) | 2012-01-06 | 2017-02-06 | 治療活性化合物およびその使用方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017019547A Active JP6409081B2 (ja) | 2012-01-06 | 2017-02-06 | 治療活性化合物およびその使用方法 |
Country Status (39)
Families Citing this family (101)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2010223919B2 (en) | 2009-03-13 | 2016-03-31 | Les Laboratoires Servier | Methods and compositions for cell-proliferation-related disorders |
| CR20170071A (es) | 2009-06-29 | 2017-03-28 | Agios Pharmaceuticals Inc | Compuestos terapeuticos y composiciones |
| CA2793835C (en) | 2009-10-21 | 2021-07-20 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
| CA2793836C (en) | 2009-10-21 | 2020-03-24 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
| PH12013502241A1 (en) | 2011-05-03 | 2014-01-06 | Agios Pharmaceuticals Inc | Pyruvate kinase activators for use in therapy |
| CN102827073A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
| CN102827170A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
| HUE038403T2 (hu) * | 2012-01-06 | 2018-10-29 | Agios Pharmaceuticals Inc | Terápiásan alkalmazható vegyületek és alkalmazási módszereik |
| KR101653473B1 (ko) | 2012-01-06 | 2016-09-01 | 어바이드 테라퓨틱스, 인크. | 카르바메이트 화합물 및 그의 제조 및 이용 방법 |
| US9474779B2 (en) | 2012-01-19 | 2016-10-25 | Agios Pharmaceuticals, Inc. | Therapeutically active compositions and their methods of use |
| AU2013331626B2 (en) | 2012-10-15 | 2018-08-02 | Agios Pharmaceuticals, Inc. | Therapeutic compounds and compositions |
| WO2015003355A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| CN105473560B (zh) * | 2013-07-11 | 2020-01-17 | 安吉奥斯医药品有限公司 | 治疗活性化合物及其使用方法 |
| WO2015003360A2 (en) * | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| CN105593215B (zh) | 2013-07-11 | 2019-01-15 | 安吉奥斯医药品有限公司 | 用于治疗癌症的作为idh2突变体抑制剂的2,4-或4,6-二氨基嘧啶化合物 |
| KR102302091B1 (ko) * | 2013-07-11 | 2021-09-16 | 아지오스 파마슈티컬스 아이엔씨. | 암 치료용의 ｉｄｈ２ 돌연변이체 억제제로서의 ｎ,６-비스(아릴 또는 헤테로아릴)-１，３，５-트리아진-２,４-디아민 화합물 |
| US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
| US20150031627A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
| KR102316886B1 (ko) * | 2013-08-02 | 2021-10-19 | 아지오스 파마슈티컬스 아이엔씨. | 치료학적 활성 화합물 및 이의 사용방법 |
| WO2015018060A1 (en) * | 2013-08-09 | 2015-02-12 | Agios Pharmaceuticals, Inc. | Crystalline forms of therapeutically active compounds and use thereof |
| MX389250B (es) | 2013-08-02 | 2025-03-20 | Agios Pharmaceuticals Inc | Compuestos inhibidores de isocitrato deshidrogenasa 2 (idh2) y el uso de los mismos |
| TWI651310B (zh) * | 2014-02-20 | 2019-02-21 | 日商日本煙草產業股份有限公司 | 三化合物及其醫藥用途 |
| HUE055209T2 (hu) * | 2014-03-14 | 2021-11-29 | Les Laboratoires Servier Sas | Terápiásan aktív vegyületek gyógyszerészeti készítményei |
| UA121211C2 (uk) | 2014-03-14 | 2020-04-27 | Аджіос Фармасьютикалз, Інк. | Фармацевтична композиція, що містить тверду дисперсію, та спосіб лікування гострої мієлогенної/мієлоїдної лейкемії (гмл) |
| WO2015144881A1 (en) * | 2014-03-28 | 2015-10-01 | Basf Se | Diaminotriazine derivatives as herbicides |
| WO2015155129A1 (en) * | 2014-04-07 | 2015-10-15 | Basf Se | Diaminotriazine compound |
| EP2930174A1 (en) * | 2014-04-07 | 2015-10-14 | Basf Se | Diaminotriazine derivatives as herbicides |
| JP6751081B2 (ja) * | 2014-09-19 | 2020-09-02 | フォーマ セラピューティクス，インコーポレイテッド | 変異イソクエン酸デヒドロゲナーゼ阻害剤としてのピリジニルキノリノン誘導体 |
| EP3194383B1 (en) | 2014-09-19 | 2019-11-06 | Forma Therapeutics, Inc. | Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors |
| DK3447050T3 (da) * | 2014-09-19 | 2020-03-09 | Forma Therapeutics Inc | Pyridin-2(1h)-on-quinolinderivater som mutant-isocitrat dehydrogenaseinhibitorer |
| ES2706888T3 (es) * | 2014-09-19 | 2019-04-01 | Forma Therapeutics Inc | Referencia cruzada a aplicaciones relacionadas |
| AU2015324158A1 (en) * | 2014-09-29 | 2017-04-13 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| WO2016126798A1 (en) | 2015-02-04 | 2016-08-11 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| CA2979537C (en) | 2015-03-18 | 2023-08-29 | Abide Therapeutics, Inc. | Piperazine carbamates and methods of making and using same |
| US10294206B2 (en) | 2015-04-21 | 2019-05-21 | Forma Tm2, Inc. | Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors |
| US10407419B2 (en) | 2015-04-21 | 2019-09-10 | Forma Therapeutics, Inc. | Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors |
| EA038574B1 (ru) * | 2015-04-21 | 2021-09-16 | Форма Терапьютикс, Инк. | Хинолиноновые производные пиридин-2(1h)-она и фармацевтические композиции на их основе |
| WO2016177347A1 (en) * | 2015-05-07 | 2016-11-10 | Teligene Ltd | Heterocyclic compounds as idh2 inhibitors |
| WO2016183097A1 (en) | 2015-05-11 | 2016-11-17 | Abide Therapeutics, Inc. | Methods of treating inflammation or neuropathic pain |
| MA44392B1 (fr) | 2015-06-11 | 2023-10-31 | Agios Pharmaceuticals Inc | Procédés d'utilisation d'activateurs de la pyruvate kinase |
| CN113307794A (zh) * | 2015-07-30 | 2021-08-27 | 正大天晴药业集团股份有限公司 | 1,3,5-三嗪衍生物及其使用方法 |
| AU2016303614A1 (en) * | 2015-08-05 | 2018-02-15 | Agios Pharmaceuticals, Inc. | Methods of preparing 6-(aryl or heteroaryl)-1,3,5-triazine-2,4-diols and 6-(aryl or heteroaryl)-1,3,5-triazine-2,4-diamines |
| AU2016340087C1 (en) | 2015-10-15 | 2022-08-18 | Les Laboratoires Servier | Combination therapy for treating malignancies |
| KR102701893B1 (ko) | 2015-10-15 | 2024-09-03 | 셀진 코포레이션 | 악성종양을 치료하기 위한 조합 요법 |
| US10653710B2 (en) | 2015-10-15 | 2020-05-19 | Agios Pharmaceuticals, Inc. | Combination therapy for treating malignancies |
| HUE067449T2 (hu) | 2015-10-15 | 2024-10-28 | Servier Lab | Ivozidenib, citarabin és daunorubicin vagy idarubicin kombinációs terápa akut mielogén leukémia kezelésére |
| WO2017069878A1 (en) * | 2015-10-21 | 2017-04-27 | NeuForm Pharmaceuticals, Inc. | Deuterated compounds for treating hematologic malignancies, and compositions and methods thereof |
| US20200268726A1 (en) * | 2015-12-04 | 2020-08-27 | Agios Pharmaceuticals, Inc. | Methods of treatment of malignancies |
| CN105384702B (zh) * | 2015-12-11 | 2018-04-10 | 浙江大学 | 三取代均三嗪类化合物及其制备方法 |
| CN105399695B (zh) * | 2015-12-11 | 2019-04-19 | 浙江大学 | 三嗪类化合物及其制备方法和用途 |
| CN105503754B (zh) * | 2015-12-11 | 2017-11-17 | 浙江大学 | 2‑氨基‑4‑苄基‑6‑吗啉‑1,3,5‑三嗪及其制备和应用 |
| WO2017143283A1 (en) | 2016-02-19 | 2017-08-24 | Abide Therapeutics, Inc. | Radiolabeled monoacylglycerol lipase occupancy probe |
| WO2017140758A1 (en) | 2016-02-19 | 2017-08-24 | Debiopharm International S.A. | Derivatives of 2-amino-4-(2-oxazolidinon-3-yl)-pyrimidine fused with a five-membered heteroaromatic ring in 5,6-position which are useful for the treatment of various cancers |
| CA3015757A1 (en) | 2016-02-26 | 2017-08-31 | Agios Pharmaceuticals, Inc. | Idh1 inhibitors for the treatment of haematological malignancies and solid tumours |
| CN105820133B (zh) * | 2016-03-25 | 2018-06-05 | 浙江工业大学 | 多取代均三嗪类化合物及其制备方法和应用 |
| CN105753801B (zh) * | 2016-03-25 | 2018-06-01 | 浙江工业大学 | 一种均三嗪类化合物的制备方法 |
| KR102232614B1 (ko) * | 2016-07-21 | 2021-03-29 | 난징 산홈 팔마세우티칼 컴퍼니 리미티드 | 이소시트레이트 탈수소효소 억제제의 화학적 화합물 및 이의 적용 |
| WO2018026894A1 (en) | 2016-08-03 | 2018-02-08 | Celgene Corporation | Methods of treatment of myelodysplastic syndrome |
| JP2019529534A (ja) | 2016-09-07 | 2019-10-17 | セルジーン コーポレイション | 錠剤組成物 |
| CN109996790B (zh) | 2016-09-19 | 2023-05-16 | H.隆德贝克有限公司 | 哌嗪氨基甲酸酯及其制备和使用方法 |
| JOP20190106A1 (ar) | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
| JOP20190105A1 (ar) | 2016-11-16 | 2019-05-09 | Lundbeck La Jolla Research Center Inc | مثبطات أحادي أسيل جليسرول ليباز (magl) |
| CN113549056A (zh) | 2017-01-22 | 2021-10-26 | 正大天晴药业集团股份有限公司 | 1,3,5-三嗪衍生物的盐及其晶体、它们的制备方法、药物组合物和用途 |
| ES2968376T3 (es) * | 2017-05-05 | 2024-05-09 | Memorial Sloan Kettering Cancer Center | Métodos de tratamiento de neoplasia mieloproliferativa |
| HRP20230210T1 (hr) | 2017-06-30 | 2023-04-14 | Celgene Corporation | Pripravci i postupci upotrebe 2-(4-klorofenil)-n-((2-(2,6-dioksopiperidin-3-il)-1-oksoizoindolin-5-il)metil)-2,2-difluoroacetamida |
| CN109265444B (zh) * | 2017-07-17 | 2022-03-11 | 南京圣和药业股份有限公司 | 取代的三嗪类idh抑制剂的光学异构体及其应用 |
| 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 |
| CN110051673B (zh) * | 2018-01-19 | 2022-03-11 | 南京圣和药业股份有限公司 | 一种包含三嗪类idh抑制剂的药物组合物及其用途 |
| CN110054616B (zh) * | 2018-01-19 | 2021-11-23 | 南京圣和药业股份有限公司 | 三嗪类idh抑制剂的制备方法 |
| CN110054615B (zh) * | 2018-01-19 | 2021-06-15 | 南京圣和药业股份有限公司 | 三嗪类idh抑制剂甲磺酸盐的晶型 |
| CN110054617A (zh) * | 2018-01-19 | 2019-07-26 | 南京圣和药业股份有限公司 | 三嗪类化合物、其制备方法及用途 |
| US11332453B2 (en) | 2018-05-15 | 2022-05-17 | H. Lundbeck A/S | MAGL inhibitors |
| US11311527B2 (en) | 2018-05-16 | 2022-04-26 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1) |
| US11013733B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1) |
| EP3720442B1 (en) | 2018-05-16 | 2022-12-28 | Forma Therapeutics, Inc. | Inhibiting mutant idh-1 |
| US11013734B2 (en) | 2018-05-16 | 2021-05-25 | Forma Therapeutics, Inc. | Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation |
| WO2019222551A1 (en) | 2018-05-16 | 2019-11-21 | Forma Therapeutics, Inc. | Solid forms of ((s)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile |
| US10980788B2 (en) | 2018-06-08 | 2021-04-20 | Agios Pharmaceuticals, Inc. | Therapy for treating malignancies |
| KR102328682B1 (ko) * | 2018-08-27 | 2021-11-18 | 주식회사 대웅제약 | 신규한 헤테로사이클릭아민 유도체 및 이를 포함하는 약학 조성물 |
| WO2020092894A1 (en) | 2018-11-02 | 2020-05-07 | Celgene Corporation | Solid forms of 2-methyl-1-[(4-[6-(trifluoromethyl) pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl]amino}-1,3,5-triazin-2-yl) amino]propan-2-ol |
| WO2020092906A1 (en) | 2018-11-02 | 2020-05-07 | Celgene Corporation | Co-crystals of 2-methyl-1 -[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl) pyridin-4-yl]amino}-1,3,5-triazin-2-yl)amino]propan-2-ol, compositions and methods of use thereof |
| US20220017489A1 (en) | 2018-11-02 | 2022-01-20 | Celgene Corporation | Solid dispersions for treatment of cancer |
| CN111662271B (zh) * | 2019-03-08 | 2023-11-14 | 中国药科大学 | 具有idh突变体抑制活性的化合物及其制备方法与应用 |
| CN111662275B (zh) * | 2019-03-08 | 2023-08-22 | 中国药科大学 | 苯磺酰胺类idh突变体抑制剂、其制备方法和用途 |
| WO2020239759A1 (en) | 2019-05-27 | 2020-12-03 | Sandoz Ag | Amorphous enasidenib in a stabilized form |
| CN114502537A (zh) * | 2019-09-29 | 2022-05-13 | 贝达药业股份有限公司 | 突变型idh2抑制剂及其应用 |
| KR102333854B1 (ko) | 2019-10-24 | 2021-12-06 | 한국과학기술연구원 | 단백질 키나아제 저해 활성을 갖는 신규한 피리디닐트리아진 유도체 및 이를 포함하는 암의 예방, 개선 또는 치료용 약학 조성물 |
| EP4058028B1 (en) | 2019-11-14 | 2025-03-05 | Celgene Corporation | Pediatric formulations for treatment of cancer |
| CA3175210A1 (en) | 2020-04-21 | 2021-10-28 | Cheryl A. Grice | Synthesis of a monoacylglycerol lipase inhibitor |
| CN111592524B (zh) * | 2020-05-20 | 2023-11-17 | 温州市天聚万迅信息科技有限公司 | 恩西德尼的制备方法 |
| WO2022074587A1 (en) * | 2020-10-06 | 2022-04-14 | Kures, Inc. | Mu-opioid receptor agonists and uses therefor |
| US11865079B2 (en) | 2021-02-12 | 2024-01-09 | Servier Pharmaceuticals Llc | Therapeutically active compounds and their methods of use |
| EP4291198A4 (en) * | 2021-02-12 | 2024-12-25 | Les Laboratoires Servier | THERAPEUTICALLY ACTIVE COMPOUNDS AND METHODS OF USE THEREOF |
| CN113461660B (zh) * | 2021-06-11 | 2022-08-02 | 浙江大学 | 2,4,6-三取代-1,3,5-均三嗪类化合物及制备和应用 |
| WO2023174235A1 (zh) * | 2022-03-15 | 2023-09-21 | 贝达药业股份有限公司 | 突变型idh1和idh2抑制剂及其应用 |
| AU2023241042A1 (en) | 2022-03-24 | 2024-10-10 | A2A Pharmaceuticals, Inc. | Compositions and methods for treating cancer |
| CN114773320A (zh) * | 2022-05-29 | 2022-07-22 | 重庆医科大学 | 1,3,5-三嗪化合物及其制备方法和用途 |
| CN115536637B (zh) * | 2022-10-24 | 2025-03-18 | 陕西中医药大学 | 一种均三嗪类衍生物及其合成方法与用途 |
| CN115819363B (zh) * | 2022-12-16 | 2025-04-01 | 浙江工业大学 | 酮酰胺类化合物及其制备方法和应用 |
| TW202530204A (zh) * | 2023-09-27 | 2025-08-01 | 美商Ａ２Ａ製藥公司 | 用於治療與轉化酸性捲曲螺旋蛋白相關的癌症的方法 |
| CN118745158A (zh) * | 2024-06-06 | 2024-10-08 | 四川省医学科学院·四川省人民医院 | 三嗪环衍生物、其制备方法及其应用和pdgfr激酶抑制剂 |
Family Cites Families (93)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2390529A (en) | 1942-02-03 | 1945-12-11 | Ernst A H Friedheim | Hydrazino-1,3,5-triazino derivatives of substituted phenylarsenic compounds |
| BE754242A (fr) | 1970-07-15 | 1971-02-01 | Geigy Ag J R | Diamino-s-triazines et dinitro-s-triazines |
| US3867383A (en) | 1971-03-29 | 1975-02-18 | Ciba Geigy Corp | Monoanthranilatoanilino-s-triazines |
| CH606334A5 (enExample) | 1974-06-21 | 1978-10-31 | Ciba Geigy Ag | |
| JPS58186682A (ja) | 1982-04-27 | 1983-10-31 | 日本化薬株式会社 | セルロ−ス又はセルロ−ス含有繊維材料の染色法 |
| DE3512630A1 (de) | 1985-04-06 | 1986-10-23 | Hoechst Ag, 6230 Frankfurt | Verfahren zum faerben oder bedrucken von cellulosefasern oder cellulosemischfasern |
| US5041443A (en) | 1989-02-21 | 1991-08-20 | Dainippon Pharmaceutical Co., Ltd. | Medicament for treating cerebral insufficiency diseases, novel 2-(1-piperazinyl)-4-phenylcycloalkanopyrimidine derivatives, and process for the production thereof |
| EP0385237B1 (en) | 1989-03-03 | 1994-06-29 | Dainippon Pharmaceutical Co., Ltd. | 2-(1-piperazinyl)-4-phenylcycloalkanopyridine derivatives, processes for the production thereof, and pharmaceutical composition containing the same |
| ATE130882T1 (de) * | 1990-07-12 | 1995-12-15 | Ciba Geigy Ag | Verfahren zur photochemischen und thermischen stabilisierung von polyamid-fasermaterialien. |
| JPH0499768A (ja) | 1990-08-17 | 1992-03-31 | Dainippon Pharmaceut Co Ltd | ４―（４―フェニルピリジン―２―イル）ピペラジン―１―オキシド誘導体 |
| US5489591A (en) | 1992-02-28 | 1996-02-06 | Zenyaku Kogyo Kabushiki Kaisha | S-triazine derivative and remedy for estrogen-dependent disease containing said derivative as effective component |
| IL115420A0 (en) | 1994-09-26 | 1995-12-31 | Zeneca Ltd | Aminoheterocyclic derivatives |
| WO1998021191A1 (en) | 1995-05-16 | 1998-05-22 | Nissan Chemical Industries, Ltd. | Cyanoethylmelamine derivatives and process for producing the same |
| FR2735127B1 (fr) | 1995-06-09 | 1997-08-22 | Pf Medicament | Nouvelles piperazines heteroaromatiques utiles comme medicaments. |
| GB9602166D0 (en) | 1996-02-02 | 1996-04-03 | Zeneca Ltd | Aminoheterocyclic derivatives |
| JPH09291034A (ja) | 1996-02-27 | 1997-11-11 | Yoshitomi Pharmaceut Ind Ltd | 縮合ピリジン化合物およびその医薬としての用途 |
| WO1997044322A1 (en) | 1996-05-20 | 1997-11-27 | Darwin Discovery Limited | Quinoline sulfonamides as tnf inhibitors and as pde-iv inhibitors |
| US5984882A (en) | 1996-08-19 | 1999-11-16 | Angiosonics Inc. | Methods for prevention and treatment of cancer and other proliferative diseases with ultrasonic energy |
| US6399358B1 (en) | 1997-03-31 | 2002-06-04 | Thomas Jefferson University | Human gene encoding human chondroitin 6-sulfotransferase |
| JPH11158073A (ja) * | 1997-09-26 | 1999-06-15 | Takeda Chem Ind Ltd | アデノシンａ３拮抗剤 |
| US7517880B2 (en) | 1997-12-22 | 2009-04-14 | Bayer Pharmaceuticals Corporation | Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas |
| UY25842A1 (es) | 1998-12-16 | 2001-04-30 | Smithkline Beecham Corp | Antagonistas de receptores de il-8 |
| EP1187825A1 (en) | 1999-06-07 | 2002-03-20 | Shire Biochem Inc. | Thiophene integrin inhibitors |
| ATE309207T1 (de) | 1999-08-27 | 2005-11-15 | Sugen Inc | Phosphat-mimetika sowie behandlungsmethoden unter verwendung von phosphatase-inhibitoren |
| TWI285155B (en) | 2000-07-03 | 2007-08-11 | Kansai Paint Co Ltd | Gas barrier film |
| AU8066701A (en) | 2000-07-20 | 2002-02-05 | Neurogen Corp | Capsaicin receptor ligands |
| JP2005500294A (ja) | 2001-06-19 | 2005-01-06 | ブリストル−マイヤーズ スクイブ カンパニー | ホスホジエステラーゼ７に対するピリミジン阻害剤 |
| ATE485281T1 (de) | 2001-08-17 | 2010-11-15 | Basf Se | Triazinderivate und deren verwendung als sonnenschutzmittel |
| JP4753336B2 (ja) | 2001-09-04 | 2011-08-24 | 日本化薬株式会社 | 新規アリル化合物及びその製法 |
| US7291616B2 (en) * | 2001-10-31 | 2007-11-06 | Cell Therapeutics, Inc. | Aryl triazines as LPAAT-β inhibitors and uses thereof |
| US6878196B2 (en) | 2002-01-15 | 2005-04-12 | Fuji Photo Film Co., Ltd. | Ink, ink jet recording method and azo compound |
| US20040067234A1 (en) | 2002-07-11 | 2004-04-08 | Paz Einat | Isocitrate dehydrogenase and uses thereof |
| DK2256108T3 (en) | 2002-07-18 | 2016-04-11 | Janssen Pharmaceutica Nv | Substituted triazinkinaseinhibitorer |
| JP2004107220A (ja) | 2002-09-13 | 2004-04-08 | Mitsubishi Pharma Corp | ＴＮＦ−α産生抑制剤 |
| AR042052A1 (es) | 2002-11-15 | 2005-06-08 | Vertex Pharma | Diaminotriazoles utiles como inhibidores de proteinquinasas |
| US7361691B2 (en) | 2002-12-02 | 2008-04-22 | Arqule, Inc. | Method of treating cancers using β-lapachone or analogs or derivatives thereof |
| ES2373947T3 (es) | 2002-12-16 | 2012-02-10 | Genmab A/S | Anticuerpos monoclonales humanos contra interleucina 8 (il-8). |
| AU2004204778B2 (en) | 2003-01-10 | 2008-05-22 | Threshold Pharmaceuticals, Inc. | Treatment of cancer with 2-deoxyglucose |
| US7358262B2 (en) | 2003-01-29 | 2008-04-15 | Whitehead Institute For Biomedical Research | Identification of genotype-selective anti-tumor agents |
| WO2004073619A2 (en) | 2003-02-14 | 2004-09-02 | Smithkline Beecham Corporation | Ccr8 antagonists |
| WO2004074438A2 (en) | 2003-02-14 | 2004-09-02 | Smithkline Beecham Corporation | Ccr8 antagonists |
| JP4948173B2 (ja) | 2003-10-10 | 2012-06-06 | ニツポネツクス・インコーポレーテツド | 過剰増殖性疾患治療用ピリミジン誘導体 |
| US20070196395A1 (en) | 2003-12-12 | 2007-08-23 | Mackerell Alexander | Immunomodulatory compounds that target and inhibit the py'binding site of tyrosene kinase p56 lck sh2 domain |
| JP2007517046A (ja) | 2003-12-24 | 2007-06-28 | サイオス・インコーポレーテツド | Ｔｇｆ−ベータ阻害剤による悪性神経膠腫の治療 |
| CA2581623A1 (en) | 2004-09-23 | 2006-03-30 | Reddy Us Therapeutics, Inc. | Novel pyridine compounds, process for their preparation and compositions containing them |
| WO2006070198A1 (en) | 2004-12-30 | 2006-07-06 | Astex Therapeutics Limited | Pyrazole derivatives as that modulate the activity of cdk, gsk and aurora kinases |
| MX2007008924A (es) | 2005-01-25 | 2007-08-21 | Astrazeneca Ab | Compuestos quimicos. |
| CA2611728A1 (en) | 2005-06-08 | 2006-12-14 | Millennium Pharmaceuticals, Inc. | Methods for the identification, assessment, and treatment of patients with cancer therapy |
| BRPI0615233A2 (pt) | 2005-08-26 | 2011-05-10 | Serono Lab | derivados de pirazina e uso dos mesmos como inibidores p13k |
| US8133900B2 (en) | 2005-11-01 | 2012-03-13 | Targegen, Inc. | Use of bi-aryl meta-pyrimidine inhibitors of kinases |
| TW200815426A (en) | 2006-06-28 | 2008-04-01 | Astrazeneca Ab | New pyridine analogues II 333 |
| EP2121662A1 (en) | 2006-12-04 | 2009-11-25 | Neurocrine Biosciences, Inc. | Substituted pyrimidines as adenosine receptor antagonists |
| WO2008076883A2 (en) | 2006-12-15 | 2008-06-26 | Abraxis Bioscience, Inc. | Triazine derivatives and their therapeutical applications |
| MX2009011850A (es) | 2007-04-30 | 2010-02-11 | Prometic Biosciences Inc | Derivados de triazina, composiciones que contienen dichos derivados, y metodos para el tratamiento de cancer y enfermedades autoinmunes utilizando dichos derivados. |
| JP2010529193A (ja) | 2007-06-11 | 2010-08-26 | ミイカナ セラピューティクス インコーポレイテッド | 置換ピラゾール化合物 |
| CA2693901C (en) | 2007-07-20 | 2015-12-29 | Nerviano Medical Sciences S.R.L. | Substituted indazole derivatives active as kinase inhibitors |
| WO2009027736A2 (en) * | 2007-08-27 | 2009-03-05 | Astrazeneca Ab | 2,4 diaminopyrimid'lnes for the treatment of myeloproliferative disorders and cancer |
| CA2702171A1 (en) | 2007-10-10 | 2009-04-16 | Takeda Pharmaceutical Company Limited | Amide compound |
| EP2219646A4 (en) | 2007-12-21 | 2010-12-22 | Univ Rochester | PROCESS FOR EXTENDING THE LIFE OF EUKARYOTIC ORGANISMS |
| GB0805477D0 (en) | 2008-03-26 | 2008-04-30 | Univ Nottingham | Pyrimidines triazines and their use as pharmaceutical agents |
| JP5277685B2 (ja) | 2008-03-26 | 2013-08-28 | 富士ゼロックス株式会社 | 電子写真感光体、画像形成装置、プロセスカートリッジ及び画像形成方法 |
| CN101575408B (zh) | 2008-05-09 | 2013-10-30 | Mca技术有限公司 | 用作阻燃剂和光稳定剂的聚三嗪基化合物 |
| FR2932483A1 (fr) | 2008-06-13 | 2009-12-18 | Cytomics Systems | Composes utiles pour le traitement des cancers. |
| WO2010007756A1 (ja) | 2008-07-14 | 2010-01-21 | 塩野義製薬株式会社 | Ｔｔｋ阻害作用を有するピリジン誘導体 |
| WO2010028179A1 (en) | 2008-09-03 | 2010-03-11 | Dr. Reddy's Laboratories Ltd. | Heterocyclic compounds as gata modulators |
| EP2326735B1 (en) | 2008-09-03 | 2016-11-16 | The Johns Hopkins University | Genetic alterations in isocitrate dehydrogenase and other genes in malignant glioma |
| JP2010079130A (ja) | 2008-09-29 | 2010-04-08 | Fuji Xerox Co Ltd | 電子写真感光体、プロセスカートリッジ、及び画像形成装置 |
| JP2010181540A (ja) | 2009-02-04 | 2010-08-19 | Fuji Xerox Co Ltd | 電子写真感光体、プロセスカートリッジ、及び画像形成装置 |
| JP5263304B2 (ja) | 2009-02-06 | 2013-08-14 | 日本新薬株式会社 | アミノピラジン誘導体及び医薬 |
| AU2010223919B2 (en) | 2009-03-13 | 2016-03-31 | Les Laboratoires Servier | Methods and compositions for cell-proliferation-related disorders |
| AU2010259002B2 (en) * | 2009-06-08 | 2014-03-20 | Nantbio, Inc. | Triazine derivatives and their therapeutical applications |
| US8261872B2 (en) * | 2009-06-08 | 2012-09-11 | Clark Equipment Company | Work machine having modular ignition switch keypad with latching output |
| US20120202818A1 (en) | 2009-06-09 | 2012-08-09 | California Capital Equity, Llc | Ureidophenyl substituted triazine derivatives and their therapeutical applications |
| CA2765047A1 (en) | 2009-06-09 | 2010-12-16 | California Capital Equity, Llc | Pyridyl-triazine inhibitors of hedgehog signaling |
| EP2451402B1 (en) | 2009-07-10 | 2016-04-27 | Kirk Promotion LTD. | Knee joint device |
| JP5473851B2 (ja) | 2009-09-30 | 2014-04-16 | 富士フイルム株式会社 | 高分子フィルム、位相差フィルム、偏光板及び液晶表示装置 |
| CA2793836C (en) | 2009-10-21 | 2020-03-24 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
| CA2793835C (en) | 2009-10-21 | 2021-07-20 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
| ES2642109T3 (es) | 2009-12-09 | 2017-11-15 | Agios Pharmaceuticals, Inc. | Compuestos terapéuticamente activos para su uso en el tratamiento de cáncer caracterizados por tener una mutación de IDH |
| EP2553116A4 (en) | 2010-04-01 | 2013-10-23 | Agios Pharmaceuticals Inc | METHOD FOR IDENTIFYING A CANDIDATE COMPOUND |
| CN103097340B (zh) | 2010-07-16 | 2018-03-16 | 安吉奥斯医药品有限公司 | 治疗活性组合物及其使用方法 |
| SG190921A1 (en) | 2010-11-29 | 2013-07-31 | Galleon Pharmaceuticals Inc | Novel compounds as respiratory stimulants for treatment of breathing control disorders or diseases |
| TWI555737B (zh) | 2011-05-24 | 2016-11-01 | 拜耳知識產權公司 | 含有硫醯亞胺基團之４－芳基－ｎ－苯基－１，３，５－三氮雜苯－２－胺 |
| CN102827073A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
| CN102827170A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
| CN102659765B (zh) | 2011-12-31 | 2014-09-10 | 沈阳药科大学 | 嘧啶及三嗪类化合物的制备方法和应用 |
| HUE038403T2 (hu) * | 2012-01-06 | 2018-10-29 | Agios Pharmaceuticals Inc | Terápiásan alkalmazható vegyületek és alkalmazási módszereik |
| KR101653473B1 (ko) | 2012-01-06 | 2016-09-01 | 어바이드 테라퓨틱스, 인크. | 카르바메이트 화합물 및 그의 제조 및 이용 방법 |
| ES2698625T3 (es) | 2012-01-19 | 2019-02-05 | Agios Pharmaceuticals Inc | Compuestos terapéuticamente activos y sus métodos de uso |
| US9474779B2 (en) | 2012-01-19 | 2016-10-25 | Agios Pharmaceuticals, Inc. | Therapeutically active compositions and their methods of use |
| IN2014MN01897A (enExample) | 2012-03-09 | 2015-07-10 | Carna Biosciences Inc | |
| US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
| US20150031627A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
-
2013
- 2013-01-05 HU HUE13733752A patent/HUE038403T2/hu unknown
- 2013-01-05 SM SM20180334T patent/SMT201800334T1/it unknown
- 2013-01-05 MX MX2014008350A patent/MX358940B/es active IP Right Grant
- 2013-01-05 CN CN201710083141.8A patent/CN107417667B/zh active Active
- 2013-01-05 DK DK13733752.3T patent/DK2800743T3/en active
- 2013-01-05 CN CN201380009314.1A patent/CN104114543B/zh active Active
- 2013-01-05 EP EP25191184.8A patent/EP4647076A2/en active Pending
- 2013-01-05 EP EP13733752.3A patent/EP2800743B1/en active Active
- 2013-01-05 SG SG10201602862RA patent/SG10201602862RA/en unknown
- 2013-01-05 LT LTEP13733752.3T patent/LT2800743T/lt unknown
- 2013-01-05 JP JP2014550627A patent/JP6411895B2/ja active Active
- 2013-01-05 WO PCT/CN2013/000009 patent/WO2013102431A1/en not_active Ceased
- 2013-01-05 ES ES18164959T patent/ES2901430T3/es active Active
- 2013-01-05 CN CN202210260669.9A patent/CN114933585A/zh active Pending
- 2013-01-05 SG SG11201403878QA patent/SG11201403878QA/en unknown
- 2013-01-05 EA EA201491330A patent/EA030187B1/ru not_active IP Right Cessation
- 2013-01-05 BR BR112014016805-9A patent/BR112014016805B1/pt active IP Right Grant
- 2013-01-05 HR HRP20180844TT patent/HRP20180844T1/hr unknown
- 2013-01-05 NZ NZ722582A patent/NZ722582A/en unknown
- 2013-01-05 KR KR1020147021897A patent/KR101893112B1/ko active Active
- 2013-01-05 RS RS20180756A patent/RS57401B1/sr unknown
- 2013-01-05 MY MYPI2014002013A patent/MY185206A/en unknown
- 2013-01-05 AU AU2013207289A patent/AU2013207289B2/en active Active
- 2013-01-05 UA UAA201408870A patent/UA117451C2/uk unknown
- 2013-01-05 PL PL13733752T patent/PL2800743T3/pl unknown
- 2013-01-05 NZ NZ627096A patent/NZ627096A/en unknown
- 2013-01-05 CN CN202210633951.7A patent/CN115521264A/zh active Pending
- 2013-01-05 ES ES21194846T patent/ES3043635T3/es active Active
- 2013-01-05 EP EP18164959.1A patent/EP3406608B8/en active Active
- 2013-01-05 SI SI201331050T patent/SI2800743T1/en unknown
- 2013-01-05 CN CN202210634094.2A patent/CN115536635A/zh active Pending
- 2013-01-05 PE PE2014001077A patent/PE20142098A1/es active IP Right Grant
- 2013-01-05 PT PT137337523T patent/PT2800743T/pt unknown
- 2013-01-05 EP EP21194846.8A patent/EP3984997B1/en active Active
- 2013-01-05 ES ES13733752.3T patent/ES2675760T3/es active Active
- 2013-01-05 TR TR2018/09228T patent/TR201809228T4/tr unknown
- 2013-01-05 CN CN201810599955.1A patent/CN108912066B/zh active Active
- 2013-01-05 CA CA2860623A patent/CA2860623A1/en not_active Abandoned
- 2013-01-07 TW TW102100378A patent/TWI653228B/zh active
- 2013-01-07 US US13/735,467 patent/US9732062B2/en active Active
- 2013-01-07 AR ARP130100062A patent/AR090411A1/es active IP Right Grant
- 2013-09-20 NO NO13838217A patent/NO2897546T3/no unknown
-
2014
- 2014-07-03 IL IL233503A patent/IL233503B/en active IP Right Grant
- 2014-07-04 PH PH12014501561A patent/PH12014501561A1/en unknown
- 2014-07-04 CL CL2014001793A patent/CL2014001793A1/es unknown
- 2014-07-04 NI NI201400073A patent/NI201400073A/es unknown
- 2014-07-15 ZA ZA2014/05163A patent/ZA201405163B/en unknown
- 2014-08-06 CO CO14171766A patent/CO7030962A2/es unknown
- 2014-08-06 EC ECIEPI201412726A patent/ECSP14012726A/es unknown
- 2014-08-08 CR CR20140377A patent/CR20140377A/es unknown
-
2016
- 2016-06-03 US US15/173,519 patent/US9512107B2/en active Active
- 2016-10-28 US US15/337,683 patent/US9656999B2/en active Active
-
2017
- 2017-02-06 JP JP2017019547A patent/JP6409081B2/ja active Active
- 2017-06-29 US US15/638,279 patent/US10294215B2/en active Active
- 2017-11-23 AU AU2017265096A patent/AU2017265096B9/en active Active
-
2018
- 2018-06-29 CY CY20181100683T patent/CY1120506T1/el unknown
-
2019
- 2019-04-18 US US16/388,801 patent/US20200079755A1/en not_active Abandoned
-
2020
- 2020-06-18 US US16/905,736 patent/US11505538B1/en active Active
-
2022
- 2022-09-09 US US17/941,854 patent/US20230250078A1/en active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2015503571A5 (enExample) | ||
| JP2017075193A5 (enExample) | ||
| ES2675760T3 (es) | Compuestos terapéuticamente activos y métodos de uso de los mismos | |
| JP7450581B2 (ja) | 治療活性化合物およびそれらの使用方法 | |
| JP2016523935A5 (enExample) | ||
| JP2016523976A5 (enExample) | ||
| JP2016523977A5 (enExample) | ||
| JP2007510689A5 (enExample) | ||
| RU2016137674A (ru) | Производные пиперидиндиона | |
| JP2017525757A5 (enExample) | ||
| JP2017505794A5 (enExample) | ||
| JP2017500364A5 (enExample) | ||
| RU2015100942A (ru) | Производное пиперидинилпиразолпиридина | |
| RU2014139601A (ru) | Ингибиторы серин/треониновых киназ | |
| JP2012503018A5 (enExample) | ||
| JP2019508400A5 (enExample) | ||
| JP2014501269A5 (enExample) | ||
| HRP20180546T1 (hr) | Supstituirani benzilindazoli za uporabu kao inhibitori bub1 kinaze za liječenje hiperproliferativnih bolesti | |
| JP2015528022A5 (enExample) | ||
| JP2016522246A5 (enExample) | ||
| SI3083586T1 (en) | The new carboxamides, the process of their manufacture, the pharmaceutical preparations they contain and their use for the manufacture of medicinal products | |
| JP2013528591A5 (enExample) | ||
| JP2013537174A5 (enExample) | ||
| RU2005123484A (ru) | Новые производные пиридазин-3(2н)-она | |
| RU2015122414A (ru) | Соединения n-пирролидинилмочевины, n'-пиразолилмочевины, тиомочевины, гуанидина и цианогуанидина как ингибиторы киназы trka |