JP2012508223A5 - - Google Patents
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- Publication number
- JP2012508223A5 JP2012508223A5 JP2011535182A JP2011535182A JP2012508223A5 JP 2012508223 A5 JP2012508223 A5 JP 2012508223A5 JP 2011535182 A JP2011535182 A JP 2011535182A JP 2011535182 A JP2011535182 A JP 2011535182A JP 2012508223 A5 JP2012508223 A5 JP 2012508223A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- triazin
- alkyl
- pyridin
- unsubstituted
- 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
- 125000000217 alkyl group Chemical group 0.000 claims 25
- 125000000623 heterocyclic group Chemical group 0.000 claims 23
- 150000001875 compounds Chemical class 0.000 claims 21
- 125000003118 aryl group Chemical group 0.000 claims 19
- 125000001072 heteroaryl group Chemical group 0.000 claims 19
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 16
- 125000004452 carbocyclyl group Chemical group 0.000 claims 14
- 229910052739 hydrogen Inorganic materials 0.000 claims 11
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 10
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 10
- 229910052794 bromium Inorganic materials 0.000 claims 9
- 229910052801 chlorine Inorganic materials 0.000 claims 9
- 229910052731 fluorine Inorganic materials 0.000 claims 9
- 229910052740 iodine Inorganic materials 0.000 claims 9
- 239000001257 hydrogen Substances 0.000 claims 7
- 125000005647 linker group Chemical group 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 208000035475 disorder Diseases 0.000 claims 6
- 229910052736 halogen Inorganic materials 0.000 claims 6
- 150000002367 halogens Chemical class 0.000 claims 6
- 229910052760 oxygen Inorganic materials 0.000 claims 6
- 125000000304 alkynyl group Chemical group 0.000 claims 5
- 230000003796 beauty Effects 0.000 claims 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims 5
- 150000003839 salts Chemical class 0.000 claims 5
- 239000012453 solvate Substances 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 4
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 230000003463 hyperproliferative effect Effects 0.000 claims 4
- 239000000126 substance Substances 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 239000003937 drug carrier Substances 0.000 claims 3
- 230000000694 effects Effects 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 201000001320 Atherosclerosis Diseases 0.000 claims 2
- 208000023275 Autoimmune disease Diseases 0.000 claims 2
- 208000032791 BCR-ABL1 positive chronic myelogenous leukemia Diseases 0.000 claims 2
- 208000020084 Bone disease Diseases 0.000 claims 2
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims 2
- 206010007572 Cardiac hypertrophy Diseases 0.000 claims 2
- 208000006029 Cardiomegaly Diseases 0.000 claims 2
- 208000024172 Cardiovascular disease Diseases 0.000 claims 2
- 208000035473 Communicable disease Diseases 0.000 claims 2
- 201000003883 Cystic fibrosis Diseases 0.000 claims 2
- 206010061218 Inflammation Diseases 0.000 claims 2
- 241001465754 Metazoa Species 0.000 claims 2
- 208000019695 Migraine disease Diseases 0.000 claims 2
- 208000012902 Nervous system disease Diseases 0.000 claims 2
- 208000002193 Pain Diseases 0.000 claims 2
- 201000004681 Psoriasis Diseases 0.000 claims 2
- 208000006011 Stroke Diseases 0.000 claims 2
- 230000006044 T cell activation Effects 0.000 claims 2
- 108090000190 Thrombin Proteins 0.000 claims 2
- 230000000172 allergic effect Effects 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 208000010668 atopic eczema Diseases 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 230000030833 cell death Effects 0.000 claims 2
- 208000015114 central nervous system disease Diseases 0.000 claims 2
- 230000001066 destructive effect Effects 0.000 claims 2
- 206010012601 diabetes mellitus Diseases 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 206010073071 hepatocellular carcinoma Diseases 0.000 claims 2
- 239000005556 hormone Substances 0.000 claims 2
- 229940088597 hormone Drugs 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 208000033065 inborn errors of immunity Diseases 0.000 claims 2
- 230000004054 inflammatory process Effects 0.000 claims 2
- 208000019423 liver disease Diseases 0.000 claims 2
- 206010027599 migraine Diseases 0.000 claims 2
- 230000004770 neurodegeneration Effects 0.000 claims 2
- 210000000056 organ Anatomy 0.000 claims 2
- 230000001575 pathological effect Effects 0.000 claims 2
- 208000028529 primary immunodeficiency disease Diseases 0.000 claims 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims 2
- 208000037803 restenosis Diseases 0.000 claims 2
- 125000006413 ring segment Chemical group 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 208000010110 spontaneous platelet aggregation Diseases 0.000 claims 2
- 229940124530 sulfonamide Drugs 0.000 claims 2
- 150000003456 sulfonamides Chemical class 0.000 claims 2
- 229960004072 thrombin Drugs 0.000 claims 2
- 238000002054 transplantation Methods 0.000 claims 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 1
- 102000010400 1-phosphatidylinositol-3-kinase activity proteins Human genes 0.000 claims 1
- WMHAVCWMHYZXHG-UHFFFAOYSA-N 3-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)phenol Chemical compound OC1=CC=CC(C=2N=C(N=C(N=2)N2CCOCC2)N2CCOCC2)=C1 WMHAVCWMHYZXHG-UHFFFAOYSA-N 0.000 claims 1
- CONLCFVHCYLZKW-UHFFFAOYSA-N 3-[4-morpholin-4-yl-6-(pyridin-2-ylmethylamino)-1,3,5-triazin-2-yl]phenol Chemical compound OC1=CC=CC(C=2N=C(N=C(NCC=3N=CC=CC=3)N=2)N2CCOCC2)=C1 CONLCFVHCYLZKW-UHFFFAOYSA-N 0.000 claims 1
- KAMYTFFDGJCUCA-UHFFFAOYSA-N 4-(1h-benzimidazol-4-yl)-6-morpholin-4-yl-n-(pyridin-2-ylmethyl)-1,3,5-triazin-2-amine Chemical compound C=1C=CC=NC=1CNC(N=C(N=1)C=2C=3N=CNC=3C=CC=2)=NC=1N1CCOCC1 KAMYTFFDGJCUCA-UHFFFAOYSA-N 0.000 claims 1
- NNOOIRJOIGXMEE-UHFFFAOYSA-N 4-(1h-indazol-5-yl)-6-morpholin-4-yl-n-(pyridin-2-ylmethyl)-1,3,5-triazin-2-amine Chemical compound C=1C=CC=NC=1CNC(N=C(N=1)C=2C=C3C=NNC3=CC=2)=NC=1N1CCOCC1 NNOOIRJOIGXMEE-UHFFFAOYSA-N 0.000 claims 1
- AZIIYUJTCFFXTJ-UHFFFAOYSA-N 4-(1h-indol-4-yl)-6-morpholin-4-yl-n-(pyridin-2-ylmethyl)-1,3,5-triazin-2-amine Chemical compound C=1C=CC=NC=1CNC(N=C(N=1)C=2C=3C=CNC=3C=CC=2)=NC=1N1CCOCC1 AZIIYUJTCFFXTJ-UHFFFAOYSA-N 0.000 claims 1
- WRVPFLBQQXTMEU-UHFFFAOYSA-N 4-(1h-indol-5-yl)-6-morpholin-4-yl-n-(pyridin-2-ylmethyl)-1,3,5-triazin-2-amine Chemical compound C=1C=CC=NC=1CNC(N=C(N=1)C=2C=C3C=CNC3=CC=2)=NC=1N1CCOCC1 WRVPFLBQQXTMEU-UHFFFAOYSA-N 0.000 claims 1
- MDHMXHNFPXWJEG-UHFFFAOYSA-N 4-(2-aminopyrimidin-5-yl)-6-morpholin-4-yl-n-(pyridin-2-ylmethyl)-1,3,5-triazin-2-amine Chemical compound C1=NC(N)=NC=C1C1=NC(NCC=2N=CC=CC=2)=NC(N2CCOCC2)=N1 MDHMXHNFPXWJEG-UHFFFAOYSA-N 0.000 claims 1
- VMXPZMLXTHXGLQ-UHFFFAOYSA-N 4-(3h-benzimidazol-5-yl)-6-morpholin-4-yl-n-(pyridin-2-ylmethyl)-1,3,5-triazin-2-amine Chemical compound C=1C=CC=NC=1CNC(N=C(N=1)C=2C=C3N=CNC3=CC=2)=NC=1N1CCOCC1 VMXPZMLXTHXGLQ-UHFFFAOYSA-N 0.000 claims 1
- CAVNILDGKKVJSJ-UHFFFAOYSA-N 4-(6-aminopyridin-3-yl)-6-morpholin-4-yl-n-(pyridin-2-ylmethyl)-1,3,5-triazin-2-amine Chemical compound C1=NC(N)=CC=C1C1=NC(NCC=2N=CC=CC=2)=NC(N2CCOCC2)=N1 CAVNILDGKKVJSJ-UHFFFAOYSA-N 0.000 claims 1
- BBDMJQBDNFISIX-UHFFFAOYSA-N 4-[4-(1h-benzimidazol-4-yl)-6-(pyridin-2-ylmethoxy)-1,3,5-triazin-2-yl]morpholine Chemical compound C=1C=CC=NC=1COC(N=C(N=1)C=2C=3N=CNC=3C=CC=2)=NC=1N1CCOCC1 BBDMJQBDNFISIX-UHFFFAOYSA-N 0.000 claims 1
- UPZKDZOZSLCPDX-UHFFFAOYSA-N 4-[4-(1h-indazol-4-yl)-6-(pyridin-2-ylmethoxy)-1,3,5-triazin-2-yl]morpholine Chemical compound C=1C=CC=NC=1COC(N=C(N=1)C=2C=3C=NNC=3C=CC=2)=NC=1N1CCOCC1 UPZKDZOZSLCPDX-UHFFFAOYSA-N 0.000 claims 1
- AYCPQGCCBNIKNU-UHFFFAOYSA-N 4-[4-(1h-indazol-5-yl)-6-(pyridin-2-ylmethoxy)-1,3,5-triazin-2-yl]morpholine Chemical compound C=1C=CC=NC=1COC(N=C(N=1)C=2C=C3C=NNC3=CC=2)=NC=1N1CCOCC1 AYCPQGCCBNIKNU-UHFFFAOYSA-N 0.000 claims 1
- BWHGEHLHWRIFSI-UHFFFAOYSA-N 4-[4-(1h-indol-4-yl)-6-(pyridin-2-ylmethoxy)-1,3,5-triazin-2-yl]morpholine Chemical compound C=1C=CC=NC=1COC(N=C(N=1)C=2C=3C=CNC=3C=CC=2)=NC=1N1CCOCC1 BWHGEHLHWRIFSI-UHFFFAOYSA-N 0.000 claims 1
- DDQOBEBNFDEMIW-UHFFFAOYSA-N 4-[4-(1h-indol-5-yl)-6-(pyridin-2-ylmethoxy)-1,3,5-triazin-2-yl]morpholine Chemical compound C=1C=CC=NC=1COC(N=C(N=1)C=2C=C3C=CNC3=CC=2)=NC=1N1CCOCC1 DDQOBEBNFDEMIW-UHFFFAOYSA-N 0.000 claims 1
- ADGGYDAFIHSYFI-UHFFFAOYSA-N 5-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyridin-2-amine Chemical compound C1=NC(N)=CC(C(F)(F)F)=C1C1=NC(N2CCOCC2)=NC(N2CCOCC2)=N1 ADGGYDAFIHSYFI-UHFFFAOYSA-N 0.000 claims 1
- IFPHRQQBRZZIOQ-UHFFFAOYSA-N 5-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)-4-(trifluoromethyl)pyrimidin-2-amine Chemical compound FC(F)(F)C1=NC(N)=NC=C1C1=NC(N2CCOCC2)=NC(N2CCOCC2)=N1 IFPHRQQBRZZIOQ-UHFFFAOYSA-N 0.000 claims 1
- OCKCSFKWKYZXKV-UHFFFAOYSA-N 5-(4,6-dimorpholin-4-yl-1,3,5-triazin-2-yl)-6-(trifluoromethyl)pyridin-2-amine Chemical compound FC(F)(F)C1=NC(N)=CC=C1C1=NC(N2CCOCC2)=NC(N2CCOCC2)=N1 OCKCSFKWKYZXKV-UHFFFAOYSA-N 0.000 claims 1
- WIVHSFPCDNBXSB-UHFFFAOYSA-N 5-[4-morpholin-4-yl-6-(pyridin-2-ylmethoxy)-1,3,5-triazin-2-yl]pyridin-2-amine Chemical compound C1=NC(N)=CC=C1C1=NC(OCC=2N=CC=CC=2)=NC(N2CCOCC2)=N1 WIVHSFPCDNBXSB-UHFFFAOYSA-N 0.000 claims 1
- HGNGQAXXKVMOMI-UHFFFAOYSA-N 5-[4-morpholin-4-yl-6-(pyridin-2-ylmethoxy)-1,3,5-triazin-2-yl]pyrimidin-2-amine Chemical compound C1=NC(N)=NC=C1C1=NC(OCC=2N=CC=CC=2)=NC(N2CCOCC2)=N1 HGNGQAXXKVMOMI-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- VEFTXXDQMDONGC-UHFFFAOYSA-N C1COCCN1C2N=CN=C(N2C3=CC4=C(C=C3)N=CN4)OCC5=CC=CC=N5 Chemical compound C1COCCN1C2N=CN=C(N2C3=CC4=C(C=C3)N=CN4)OCC5=CC=CC=N5 VEFTXXDQMDONGC-UHFFFAOYSA-N 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 108091007960 PI3Ks Proteins 0.000 claims 1
- 102000013530 TOR Serine-Threonine Kinases Human genes 0.000 claims 1
- 108010065917 TOR Serine-Threonine Kinases Proteins 0.000 claims 1
- 229960002685 biotin Drugs 0.000 claims 1
- 235000020958 biotin Nutrition 0.000 claims 1
- 239000011616 biotin Substances 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 210000004027 cell Anatomy 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000012636 effector Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 1
- 125000005549 heteroarylene group Chemical group 0.000 claims 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 239000002952 polymeric resin Substances 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 claims 1
- 108090000623 proteins and genes Proteins 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims 1
- 150000003457 sulfones Chemical class 0.000 claims 1
- 229920003002 synthetic resin Polymers 0.000 claims 1
- 125000003831 tetrazolyl group Chemical group 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
- 0 *C(*1)C(C2N=C(N3C(*)C(*)OC(*)C3*)N=C(*)C2)=C(*)N=C1N* Chemical compound *C(*1)C(C2N=C(N3C(*)C(*)OC(*)C3*)N=C(*)C2)=C(*)N=C1N* 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB08211219.3 | 2008-11-10 | ||
| GB0821219A GB2465405A (en) | 2008-11-10 | 2008-11-10 | Triazine, pyrimidine and pyridine analogues and their use in therapy |
| PCT/IB2009/007404 WO2010052569A2 (en) | 2008-11-10 | 2009-11-10 | Triazine, pyrimidine and pyridine analogs and their use as therapeutic agents and diagnostic probes |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015020319A Division JP6047184B2 (ja) | 2008-11-10 | 2015-02-04 | トリアジン、ピリミジン、及びピリジン類似体、並びに、治療薬及び診断プローブとしてのそれらの使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012508223A JP2012508223A (ja) | 2012-04-05 |
| JP2012508223A5 true JP2012508223A5 (enExample) | 2012-12-27 |
| JP5738768B2 JP5738768B2 (ja) | 2015-06-24 |
Family
ID=40230564
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011535182A Active JP5738768B2 (ja) | 2008-11-10 | 2009-11-10 | トリアジン、ピリミジン、及びピリジン類似体、並びに、治療薬及び診断プローブとしてのそれらの使用 |
| JP2015020319A Active JP6047184B2 (ja) | 2008-11-10 | 2015-02-04 | トリアジン、ピリミジン、及びピリジン類似体、並びに、治療薬及び診断プローブとしてのそれらの使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015020319A Active JP6047184B2 (ja) | 2008-11-10 | 2015-02-04 | トリアジン、ピリミジン、及びピリジン類似体、並びに、治療薬及び診断プローブとしてのそれらの使用 |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8921361B2 (enExample) |
| EP (1) | EP2364302B1 (enExample) |
| JP (2) | JP5738768B2 (enExample) |
| KR (1) | KR101749192B1 (enExample) |
| CN (1) | CN102209714B (enExample) |
| AU (1) | AU2009312464B2 (enExample) |
| BR (1) | BRPI0921709B1 (enExample) |
| CA (1) | CA2741990C (enExample) |
| CY (1) | CY1118438T1 (enExample) |
| DK (1) | DK2364302T3 (enExample) |
| ES (1) | ES2609296T3 (enExample) |
| GB (1) | GB2465405A (enExample) |
| HR (1) | HRP20161769T1 (enExample) |
| IL (1) | IL212726A (enExample) |
| LT (1) | LT2364302T (enExample) |
| MX (1) | MX2011004889A (enExample) |
| NZ (1) | NZ592617A (enExample) |
| RU (1) | RU2537945C2 (enExample) |
| SI (1) | SI2364302T1 (enExample) |
| SM (1) | SMT201700006B (enExample) |
| WO (1) | WO2010052569A2 (enExample) |
| ZA (1) | ZA201104298B (enExample) |
Families Citing this family (117)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3086695B2 (ja) | 1990-07-20 | 2000-09-11 | 株式会社東芝 | ガスタービン制御装置 |
| GB2465405A (en) * | 2008-11-10 | 2010-05-19 | Univ Basel | Triazine, pyrimidine and pyridine analogues and their use in therapy |
| CA2756067A1 (en) | 2009-03-27 | 2010-09-30 | Pathway Therapeutics, Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy |
| UY32582A (es) | 2009-04-28 | 2010-11-30 | Amgen Inc | Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero |
| CA2767008C (en) | 2009-07-07 | 2018-01-30 | Pathway Therapeutics, Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy |
| NZ597983A (en) | 2009-08-20 | 2014-05-30 | Karus Therapeutics Ltd | Tricyclic heterocyclic compounds as phosphoinositide 3-kinase inhibitors |
| EP2343294A1 (en) | 2009-11-30 | 2011-07-13 | Bayer Schering Pharma AG | Substituted triazolopyridines |
| EP2542536B1 (en) | 2010-03-04 | 2015-01-21 | Cellzome Limited | Morpholino substituted urea derivatives as mtor inhibitors |
| EP2616441B1 (en) | 2010-09-17 | 2019-08-07 | Purdue Pharma L.P. | Pyridine compounds and the uses thereof |
| EA026134B1 (ru) * | 2010-12-16 | 2017-03-31 | Ф. Хоффманн-Ля Рош Аг | Трициклические ингибиторы pi3k и способы их применения |
| AU2015268776B2 (en) * | 2010-12-16 | 2017-04-13 | Genentech, Inc. | Tricyclic PI3k inhibitor compounds and methods of use |
| US9656959B2 (en) * | 2010-12-22 | 2017-05-23 | Purdue Pharma L.P. | Substituted pyridines as sodium channel blockers |
| EP2667874A4 (en) * | 2011-01-27 | 2014-07-30 | Univ Princeton | MTOR KINASE HEMMER AS ANTIVIRUS AGENT |
| CN103501610A (zh) * | 2011-03-09 | 2014-01-08 | 西建阿维拉米斯研究公司 | Pi3激酶抑制剂和其用途 |
| CN107501241B (zh) | 2011-03-28 | 2020-10-13 | 梅制药公司 | 化合物、含有其的药物组合物以及它们在治疗增生性疾病中的用途 |
| CN102389430B (zh) * | 2011-09-07 | 2013-08-28 | 苏州大学 | 一种小分子化合物在制备抗肺癌药物中的应用 |
| BR112014006743A8 (pt) | 2011-09-21 | 2018-01-09 | Cellzome Ltd | composto, uso de um composto, e, método para tratar, controlar, retardar ou impedir uma ou mais condições |
| MX342326B (es) | 2011-09-27 | 2016-09-26 | Novartis Ag | 3-pirimidin-4-il-oxazolidin-2-onas como inhibidoras de idh mutante. |
| MX341577B (es) * | 2011-10-07 | 2016-08-25 | Cellzome Ltd | Derivados biciclicos de pirimidin-urea o carbamato sustituidos con morfolino como inhibidores del blanco de rapamicina de mamifero. |
| UY34632A (es) | 2012-02-24 | 2013-05-31 | Novartis Ag | Compuestos de oxazolidin- 2- ona y usos de los mismos |
| GB201204125D0 (en) | 2012-03-08 | 2012-04-25 | Karus Therapeutics Ltd | Compounds |
| WO2013140417A1 (en) * | 2012-03-19 | 2013-09-26 | Council Of Scientific & Industrial Research | BORONIC ACID BEARING LIPHAGANE COMPOUNDS AS INHIBITORS OF PI3K-α AND/OR β |
| EP2874632B1 (en) * | 2012-07-23 | 2020-06-17 | Sphaera Pharma Pte. Ltd | Triazine compound having pi3k-alpha and mtor inhibiting activity |
| CN113943306A (zh) | 2012-09-20 | 2022-01-18 | Udc 爱尔兰有限责任公司 | 供电子应用的氮杂二苯并呋喃和包含氮杂二苯并呋喃的电子器件 |
| CN102875558A (zh) * | 2012-11-05 | 2013-01-16 | 贵州大学 | 2-氯-4-取代-8-硝基苯并呋喃[3,2-d]嘧啶类化合物及其制备方法和用途 |
| US9676765B2 (en) | 2012-11-07 | 2017-06-13 | Karus Therapeutics Limited | Histone deacetylase inhibitors and their use in therapy |
| US9296733B2 (en) | 2012-11-12 | 2016-03-29 | Novartis Ag | Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases |
| CN105050602B (zh) * | 2013-01-12 | 2018-05-25 | 张大为 | 作为pi3激酶抑制剂的吡啶化合物 |
| CA2903979A1 (en) | 2013-03-14 | 2014-09-18 | Novartis Ag | 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh |
| TWI710558B (zh) * | 2013-05-01 | 2020-11-21 | 瑞士商赫孚孟拉羅股份公司 | 二雜芳基化合物及其用途 |
| SI2994465T1 (sl) | 2013-05-10 | 2018-10-30 | Karus Therapeutics Limited | Novi inhibitorji histon deacetilaze |
| CN103483345B (zh) * | 2013-09-25 | 2016-07-06 | 中山大学 | Pi3k激酶抑制剂、包含其的药物组合物及其应用 |
| WO2015088564A1 (en) * | 2013-12-13 | 2015-06-18 | Sunovion Pharmaceuticals Inc. | P2x4 receptor modulating compounds |
| WO2015088565A1 (en) * | 2013-12-13 | 2015-06-18 | Sunovion Pharmaceuticals Inc. | P2x4 receptor modulating compounds and methods of use thereof |
| GB201402431D0 (en) | 2014-02-12 | 2014-03-26 | Karus Therapeutics Ltd | Compounds |
| CN106459541B (zh) | 2014-04-02 | 2020-06-23 | 英力士苯领集团股份公司 | 用于制备具有改良机械性能的热塑性成型组合物的方法 |
| BR112016023811B8 (pt) | 2014-04-22 | 2023-01-10 | Piqur Therapeutics Ag | Método para fabricação para derivados de triazina, pirimidina e piridina, seus intermediários e seus métodos de fabricação |
| KR102287012B1 (ko) * | 2014-05-28 | 2021-08-09 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
| MY195016A (en) | 2014-08-04 | 2023-01-03 | Nuevolution As | Optionally Fused Heterocyclyl-Substituted Derivatives of Pyrimidine Useful for The Treatment of Inflammatory, Metabolic, Oncologic and Autoimmune Diseases |
| CN104151256B (zh) * | 2014-08-14 | 2016-08-24 | 西安交通大学 | 二取代苯甲酰胺类化合物及其合成方法和应用 |
| GB201419228D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| GB201419264D0 (en) | 2014-10-29 | 2014-12-10 | Karus Therapeutics Ltd | Compounds |
| MA40933A (fr) * | 2014-11-11 | 2017-09-19 | Piqur Therapeutics Ag | Difluorométhyl-aminopyridines et difluorométhyl-aminopyrimidines |
| CN104473923B (zh) * | 2014-12-29 | 2016-08-17 | 巩春智 | 一种防治慢性心力衰竭的药物组合物及其应用 |
| WO2016126726A1 (en) | 2015-02-02 | 2016-08-11 | Forma Therapeutics, Inc. | Bicyclic [4,6,0] hydroxamic acids as hdac6 inhibitors |
| TW201629026A (zh) | 2015-02-02 | 2016-08-16 | 佛瑪治療公司 | 作為ｈｄａｃ抑制劑的３－烷基雙環［４，５，０］異羥肟酸 |
| CN104860956B (zh) * | 2015-04-30 | 2017-05-10 | 华南师范大学 | 一种荧光多功能单体及其合成方法与应用 |
| CN106279211B (zh) * | 2015-06-03 | 2020-09-15 | 北京大学 | 一种噻唑并嘧啶酮化合物及其制备方法和应用 |
| GB201514758D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Formulation |
| GB201514751D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
| GB201514754D0 (en) * | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds |
| GB201514760D0 (en) | 2015-08-19 | 2015-09-30 | Karus Therapeutics Ltd | Compounds and method of use |
| CA3119019C (en) | 2015-12-10 | 2024-06-11 | Ptc Therapeutics, Inc. | Compounds and methods for treating huntington's disease |
| HRP20220227T1 (hr) * | 2015-12-16 | 2022-04-29 | Genentech, Inc. | Postupak priprave tricikličnih spojeva inhibitora p13k i postupci upotrebe navedenih spojeva u liječenju raka |
| GB201602527D0 (en) * | 2016-02-12 | 2016-03-30 | Glaxosmithkline Ip Dev Ltd | Chemical compounds |
| KR101919189B1 (ko) * | 2016-02-18 | 2018-11-15 | 경북대학교 산학협력단 | 다중치환 4H-티아졸로[4,5-e][1,4]다이아제핀-5,8-다이온 유도체 및 이의 용도 |
| PL3416945T3 (pl) | 2016-02-19 | 2020-12-28 | Sprint Bioscience Ab | Związki 6-arylo-4-(morfolin-4-ylo)-1h-pirydyn-2-onu przydatne w leczeniu nowotworu i cukrzycy |
| PT3416957T (pt) | 2016-02-19 | 2020-09-25 | Sprint Bioscience Ab | Compostos 6-heterociclil-4-morfolin-4-ilpiridin-2-ona úteis para o tratamento do cancro e da diabetes |
| US10722484B2 (en) | 2016-03-09 | 2020-07-28 | K-Gen, Inc. | Methods of cancer treatment |
| KR102483630B1 (ko) * | 2016-05-18 | 2023-01-02 | 토르쿠르 아게 | 피부 병변의 치료 |
| LT3458067T (lt) * | 2016-05-18 | 2021-04-26 | Torqur Ag | Neurologinių sutrikimų gydymas |
| EP3458035B1 (en) * | 2016-05-18 | 2026-08-19 | Torqur AG | Bimiralisib and derivatives thereof for use in the treatment of actinic keratosis |
| WO2017210545A1 (en) | 2016-06-02 | 2017-12-07 | Cadent Therapeutics, Inc. | Potassium channel modulators |
| US10555935B2 (en) | 2016-06-17 | 2020-02-11 | Forma Therapeutics, Inc. | 2-spiro-5- and 6-hydroxamic acid indanes as HDAC inhibitors |
| WO2018009899A1 (en) * | 2016-07-07 | 2018-01-11 | Cardurion Pharmaceuticals, Llc | Methods for treatment of heart failure |
| EP3548035A4 (en) | 2016-11-30 | 2020-07-22 | Case Western Reserve University | COMBINATIONS OF 15-PGDH INHIBITORS WITH CORCOSTEROIDS AND / OR TNF INHIBITORS AND THEIR USES |
| EP4063358B1 (en) | 2016-12-22 | 2024-05-22 | Global Blood Therapeutics, Inc. | Histone methyltransferase inhibitors |
| EP3571193B1 (en) | 2017-01-23 | 2021-12-01 | Cadent Therapeutics, Inc. | Potassium channel modulators |
| CN110573154A (zh) | 2017-02-06 | 2019-12-13 | 卡斯西部储备大学 | 调节短链脱氢酶活性的组合物和方法 |
| GB201702938D0 (en) | 2017-02-23 | 2017-04-12 | Univ Southampton | Methods of generating and screening compartmentalised peptides libraries |
| EP3630118A4 (en) | 2017-05-23 | 2021-03-31 | MEI Pharma, Inc. | COMBINATION THERAPY |
| CN107216344B (zh) * | 2017-05-27 | 2019-06-21 | 无锡捷化医药科技有限公司 | 一种5-溴-噻唑并[4,5-d]嘧啶的制备方法 |
| EP4151627A1 (en) | 2017-06-05 | 2023-03-22 | PTC Therapeutics, Inc. | Compounds for treating huntington's disease |
| MX2019014759A (es) * | 2017-06-09 | 2020-02-12 | Global Blood Therapeutics Inc | Compuestos de azaindol como inhibidores de metiltransferasa de histona. |
| CN107266422A (zh) * | 2017-06-12 | 2017-10-20 | 西安交通大学 | 2‑（5‑嘧啶基）‑4‑吗啉基‑6‑取代均三嗪类化合物及其盐、制备方法和应用 |
| CN111182898B (zh) | 2017-06-28 | 2024-04-16 | Ptc医疗公司 | 用于治疗亨廷顿氏病的方法 |
| CN111163838B (zh) | 2017-06-28 | 2023-03-28 | Ptc医疗公司 | 用于治疗亨廷顿氏病的方法 |
| MX2020001727A (es) | 2017-08-14 | 2020-03-20 | Mei Pharma Inc | Terapia de combinacion. |
| CN109651341A (zh) * | 2017-10-11 | 2019-04-19 | 上海医药工业研究院 | 二吗啉氰基嘧(吡)啶类衍生物及作为抗肿瘤药物应用 |
| BR112020009855A8 (pt) * | 2017-11-23 | 2023-01-10 | Piqur Therapeutics Ag | Tratamento de distúrbios de pele |
| JP7290651B2 (ja) | 2018-02-07 | 2023-06-13 | ウーシー・バイオシティ・バイオファーマシューティクス・カンパニー・リミテッド | Ａｔｒ阻害剤及びその応用 |
| BR112020019373A2 (pt) * | 2018-03-27 | 2020-12-29 | Ptc Therapeutics, Inc. | Compostos para o tratamento da doença de hutington |
| CN112189012B (zh) | 2018-04-10 | 2024-02-13 | 神经孔疗法股份有限公司 | 作为pi3激酶和自噬途径的调节剂的三取代芳基和杂芳基衍生物 |
| US10822346B2 (en) | 2018-04-17 | 2020-11-03 | Cardurion Pharmaceuticals, Llc | Meglumine salts of thienopyrimidines |
| KR20210038845A (ko) | 2018-06-27 | 2021-04-08 | 피티씨 테라퓨틱스, 인크. | 헌팅턴병 치료를 위한 헤테로아릴 화합물 |
| IL279688B2 (en) | 2018-06-27 | 2025-01-01 | Ptc Therapeutics Inc | Heterocyclic and heteroaryl compounds for the treatment of Huntington's disease |
| WO2020005882A1 (en) | 2018-06-27 | 2020-01-02 | Ptc Therapeutics, Inc. | Heteroaryl compounds for treating huntington's disease |
| EP4671385A3 (en) | 2018-08-07 | 2026-03-18 | Torqur AG | Treatment of squamous cell carcinoma |
| MX2021004647A (es) | 2018-10-22 | 2021-08-16 | Novartis Ag | Formas cristalinas de moduladores de los canales de potasio. |
| WO2020106998A1 (en) | 2018-11-21 | 2020-05-28 | Case Western Reserve University | Compositions and methods of modulating short-chain dehydrogenase activity |
| ES2974634T3 (es) | 2018-12-21 | 2024-06-28 | Celgene Corp | Inhibidores de tienopiridinas de RIPK2 |
| WO2020142729A1 (en) * | 2019-01-04 | 2020-07-09 | BellBrook Labs | Inhibitors of cgas activity as therapeutic agents |
| SG11202108274SA (en) | 2019-02-06 | 2021-08-30 | Venthera Inc | Topical phosphoinositide 3-kinase inhibitors |
| CN109942562B (zh) * | 2019-02-27 | 2022-02-08 | 江西科技师范大学 | 含芳基结构的五元杂环联三嗪类化合物及其制备方法和应用 |
| CA3139821A1 (en) | 2019-05-13 | 2020-11-19 | Ptc Therapeutics, Inc. | Compounds for treating huntington's disease |
| GB201909468D0 (en) | 2019-07-01 | 2019-08-14 | Karus Therapeutics Ltd | Compounds for treating cancer |
| EP3994142A4 (en) * | 2019-07-03 | 2023-09-06 | Borah, Inc. | CHEMICAL COMPOUNDS |
| BR112022012205A2 (pt) | 2019-12-20 | 2022-09-13 | Nuevolution As | Compostos ativos para receptores nucleares |
| AU2020405446A1 (en) | 2019-12-20 | 2022-05-26 | Nuevolution A/S | Compounds active towards nuclear receptors |
| US12486274B2 (en) | 2020-01-13 | 2025-12-02 | Verge Analytics, Inc. | Substituted pyrazolo-pyrimidines and uses thereof |
| AU2021224268A1 (en) | 2020-02-21 | 2022-09-15 | Case Western Reserve University | Compositions and methods for treating renal injury |
| JP7713954B2 (ja) | 2020-03-31 | 2025-07-28 | ヌエヴォリューション・アクティーゼルスカブ | 核内受容体に対して活性な化合物 |
| CA3174252A1 (en) | 2020-03-31 | 2021-10-07 | Nuevolution A/S | Compounds active towards nuclear receptors |
| JP2023550638A (ja) | 2020-11-25 | 2023-12-04 | デシフェラ・ファーマシューティカルズ，エルエルシー | ウイルス感染症の処置に使用するための、ｖｓｐ３４阻害剤としてのモルホリノ誘導体 |
| WO2022159981A1 (en) * | 2021-01-25 | 2022-07-28 | Athos Therapeutics, Inc. | Triazine compounds and methods of making and using the same |
| CN117396470A (zh) * | 2021-04-09 | 2024-01-12 | 巴塞尔大学 | 作为pi3k的可逆和不可逆共价抑制剂的三嗪衍生物 |
| MX2023011865A (es) * | 2021-04-09 | 2024-01-08 | Univ Basel | Derivados de triazina como inhibidores de pi3k covalentes reversibles e irreversibles. |
| EP4320110A1 (en) * | 2021-04-09 | 2024-02-14 | Universität Basel | Triazine derivative as covalent inhibitors of pi3k |
| GB202108249D0 (en) * | 2021-06-09 | 2021-07-21 | Univ Of Sussex | Compounds |
| CN117751127B (zh) * | 2021-08-20 | 2026-07-03 | 南京大美生物制药有限公司 | 一种五元含氮杂环并杂芳基类衍生物及其用途 |
| US20250197375A1 (en) * | 2021-12-08 | 2025-06-19 | Kineta, Inc. | Pyrimidines and methods of their use |
| WO2024015531A2 (en) * | 2022-07-13 | 2024-01-18 | University Of Kentucky Research Foundation | Triazine lipids, lipid synthesis, and methods for inhibiting canonical nf kb transcriptional activity |
| CN114933594A (zh) * | 2022-07-20 | 2022-08-23 | 北京科翔中升医药科技有限公司 | 一种氟代三嗪类化合物、药物组合物及用途 |
| CN116003448B (zh) * | 2022-11-07 | 2024-06-11 | 淮阴工学院 | 一种含吲哚啉多烯键识别Aβ纤维的BODIPY近红外荧光探针及其制备方法 |
| EP4682143A1 (en) * | 2023-03-10 | 2026-01-21 | Convalife Pharmaceuticals Co., Ltd. | Pharmaceutical composition containing egfr inhibitor, and preparation method therefor and use thereof |
| WO2025137105A1 (en) * | 2023-12-22 | 2025-06-26 | Deciphera Pharmaceuticals, Llc | Dual raf and tubulin inhibitors and methods of use thereof |
| WO2025181366A1 (en) * | 2024-03-01 | 2025-09-04 | Torqur Ag | Topical formulations of dual pi3k/mtor inhibitors |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1670550B2 (de) * | 1967-02-17 | 1973-04-26 | Deutsche Gold und Silber Scheide anstalt vormals Roessler, 6000 Frank fürt | Substituierte 2-amino-4-hydrazino6-piperazino-s-triazine |
| DE2013357A1 (en) * | 1970-03-20 | 1971-10-07 | Farbenfabriken Bayer AG,5O9O Lever kusen | Iminocarboxylic acid derivs in prepn of s-triazines |
| DE2712686C2 (de) * | 1977-03-23 | 1986-09-04 | Bayer Ag, 5090 Leverkusen | 4-Triazinyl-4'-benzoxazolyl- bzw. 4'-phenyl-stilben-derivate |
| JPS59145250A (ja) * | 1983-02-04 | 1984-08-20 | Mitsubishi Chem Ind Ltd | アントラキノン化合物及びアントラキノン染料 |
| GB8612062D0 (en) * | 1986-05-17 | 1986-06-25 | Fbc Ltd | Herbicides |
| AU665238B2 (en) * | 1992-02-28 | 1995-12-21 | Zenyaku Kogyo Kabushiki Kaisha | S-triazine derivative and remedy for estrogen-dependent diseases containing the same as active ingredient |
| MX9700928A (es) * | 1994-08-08 | 1997-04-30 | Nippon Shinyaku Co Ltd | Derivado de triazian y medicina que lo contiene. |
| AU764479B2 (en) * | 1998-10-29 | 2003-08-21 | Bristol-Myers Squibb Company | Compounds derived from an amine nucleus that are inhibitors of IMPDH enzyme |
| JP4709388B2 (ja) * | 1999-01-25 | 2011-06-22 | 全薬工業株式会社 | 複素環式化合物及びそれを有効成分とする抗腫瘍剤 |
| US6608053B2 (en) * | 2000-04-27 | 2003-08-19 | Yamanouchi Pharmaceutical Co., Ltd. | Fused heteroaryl derivatives |
| KR100833371B1 (ko) * | 2001-04-27 | 2008-05-28 | 젠야쿠코교가부시키가이샤 | 헤테로시클릭 화합물 및 이를 유효 성분으로 하는 항종양제 |
| US20040009981A1 (en) * | 2002-03-15 | 2004-01-15 | David Bebbington | Compositions useful as inhibitors of protein kinases |
| BR0304925A (pt) * | 2002-05-30 | 2004-09-28 | Solvay Pharm Bv | Compostos, composições farmacêuticas, e, uso dos compostos |
| AU2003245669A1 (en) * | 2002-06-21 | 2004-01-06 | Cellular Genomics, Inc. | Certain aromatic monocycles as kinase modulators |
| CA2515132C (en) * | 2003-02-07 | 2012-01-03 | Vertex Pharmaceuticals Incorporated | Heteroaryl substituted pyrroles useful as inhibitors of protein kinases |
| WO2005011703A1 (en) * | 2003-08-04 | 2005-02-10 | Akzo Nobel N.V. | 2-cyano-1,3,5-triazine-4,6-diamine derivatives |
| PE20050952A1 (es) * | 2003-09-24 | 2005-12-19 | Novartis Ag | Derivados de isoquinolina como inhibidores de b-raf |
| SI1864665T1 (sl) * | 2005-03-11 | 2012-09-28 | Zenyaku Kogyo Kk | Imunosupresivno sredstvo, ki obsega heterociklično spojino kot učinkovino |
| CN101801971A (zh) * | 2005-09-30 | 2010-08-11 | 沃泰克斯药物股份有限公司 | 可用作janus激酶抑制剂的脱氮嘌呤 |
| GB0520657D0 (en) * | 2005-10-11 | 2005-11-16 | Ludwig Inst Cancer Res | Pharmaceutical compounds |
| PL2041139T3 (pl) * | 2006-04-26 | 2012-05-31 | Hoffmann La Roche | Związki farmaceutyczne |
| AU2007282535B9 (en) * | 2006-08-08 | 2013-06-20 | Chugai Seiyaku Kabushiki Kaisha | Pyrimidine derivative as PI3K inhibitor and use thereof |
| WO2008032033A1 (en) * | 2006-09-14 | 2008-03-20 | Astrazeneca Ab | 4-benzimidazolyl-2-morpholino-6-piperazinylpyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders |
| WO2008072850A1 (en) * | 2006-12-11 | 2008-06-19 | Amorepacific Corporation | Triazine derivatives having inhibitory activity against acetyl-coa carboxylase |
| CA2675558A1 (en) * | 2007-02-06 | 2008-08-14 | Novartis Ag | Pi 3-kinase inhibitors and methods of their use |
| WO2009093981A1 (en) | 2008-01-23 | 2009-07-30 | S Bio Pte Ltd | Triazine compounds as kinase inhibitors |
| EP2082777A1 (en) * | 2008-01-27 | 2009-07-29 | Oncotherm Kft. | Flexible and porous large-area electrode for heating |
| DE202008001253U1 (de) * | 2008-01-28 | 2008-04-10 | Mirror Image Ag | Bildanzeigegerät |
| MY155653A (en) * | 2008-05-23 | 2015-11-13 | Wyeth Llc | Triazine compounds as p13 kinase and mtor inhibitors |
| GB2465405A (en) * | 2008-11-10 | 2010-05-19 | Univ Basel | Triazine, pyrimidine and pyridine analogues and their use in therapy |
-
2008
- 2008-11-10 GB GB0821219A patent/GB2465405A/en not_active Withdrawn
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