CA2653777A1 - 2-anilino-4-(heterocyclic)amino-pyrimidines - Google Patents
2-anilino-4-(heterocyclic)amino-pyrimidines Download PDFInfo
- Publication number
- CA2653777A1 CA2653777A1 CA002653777A CA2653777A CA2653777A1 CA 2653777 A1 CA2653777 A1 CA 2653777A1 CA 002653777 A CA002653777 A CA 002653777A CA 2653777 A CA2653777 A CA 2653777A CA 2653777 A1 CA2653777 A1 CA 2653777A1
- Authority
- CA
- Canada
- Prior art keywords
- pyrimidine
- propyl
- diamine
- phenyl
- biphenyl
- 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.)
- Abandoned
Links
- 150000005005 aminopyrimidines Chemical class 0.000 title abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 60
- 206010019280 Heart failures Diseases 0.000 claims abstract description 38
- 239000003112 inhibitor Substances 0.000 claims abstract description 34
- 238000000034 method Methods 0.000 claims abstract description 32
- 230000002107 myocardial effect Effects 0.000 claims abstract description 12
- -1 pyrrolin-1-y1 Chemical group 0.000 claims description 588
- 150000001875 compounds Chemical class 0.000 claims description 110
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 100
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 50
- 125000000623 heterocyclic group Chemical group 0.000 claims description 41
- 229910052739 hydrogen Inorganic materials 0.000 claims description 33
- 239000001257 hydrogen Substances 0.000 claims description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 26
- 125000001072 heteroaryl group Chemical group 0.000 claims description 25
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 25
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 22
- 125000004429 atom Chemical group 0.000 claims description 20
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 17
- 125000001424 substituent group Chemical group 0.000 claims description 17
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 16
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 16
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 14
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
- 150000002367 halogens Chemical class 0.000 claims description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 10
- 125000005647 linker group Chemical group 0.000 claims description 10
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 9
- 206010007556 Cardiac failure acute Diseases 0.000 claims description 9
- 241000282414 Homo sapiens Species 0.000 claims description 9
- 239000003814 drug Substances 0.000 claims description 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 8
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 7
- 201000010099 disease Diseases 0.000 claims description 7
- 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 description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 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 6
- 206010003119 arrhythmia Diseases 0.000 claims description 6
- 230000006793 arrhythmia Effects 0.000 claims description 6
- 125000006268 biphenyl-3-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])C(*)=C([H])C([H])=C1[H] 0.000 claims description 6
- 229940079593 drug Drugs 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 208000017169 kidney disease Diseases 0.000 claims description 6
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 5
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 5
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- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 5
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 5
- 230000001225 therapeutic effect Effects 0.000 claims description 5
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 4
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims description 4
- 206010007558 Cardiac failure chronic Diseases 0.000 claims description 4
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 4
- IPRJXAGUEGOFGG-UHFFFAOYSA-N N-butylbenzenesulfonamide Chemical compound CCCCNS(=O)(=O)C1=CC=CC=C1 IPRJXAGUEGOFGG-UHFFFAOYSA-N 0.000 claims description 4
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- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000000638 stimulation Effects 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- PKVDVCMRWCLXKR-UHFFFAOYSA-N 2-n-(3-chlorophenyl)-4-n-(piperidin-2-ylmethyl)pyrimidine-2,4-diamine Chemical compound ClC1=CC=CC(NC=2N=C(NCC3NCCCC3)C=CN=2)=C1 PKVDVCMRWCLXKR-UHFFFAOYSA-N 0.000 claims description 3
- WKPKDVNXMWQVKU-UHFFFAOYSA-N 2-n-(3-methoxyphenyl)-4-n-(3-pyrrolidin-1-ylpropyl)pyrimidine-2,4-diamine Chemical compound COC1=CC=CC(NC=2N=C(NCCCN3CCCC3)C=CN=2)=C1 WKPKDVNXMWQVKU-UHFFFAOYSA-N 0.000 claims description 3
- ZNFARSGNRFIBEY-UHFFFAOYSA-N 2-n-[3-(3-methylphenyl)phenyl]-4-n-(3-pyrazolidin-1-ylpropyl)pyrimidine-2,4-diamine Chemical compound CC1=CC=CC(C=2C=C(NC=3N=C(NCCCN4NCCC4)C=CN=3)C=CC=2)=C1 ZNFARSGNRFIBEY-UHFFFAOYSA-N 0.000 claims description 3
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 3
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 3
- 125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 206010002383 Angina Pectoris Diseases 0.000 claims description 3
- 201000001320 Atherosclerosis Diseases 0.000 claims description 3
- 206010007559 Cardiac failure congestive Diseases 0.000 claims description 3
- 206010007572 Cardiac hypertrophy Diseases 0.000 claims description 3
- 208000006029 Cardiomegaly Diseases 0.000 claims description 3
- 206010056370 Congestive cardiomyopathy Diseases 0.000 claims description 3
- 201000010046 Dilated cardiomyopathy Diseases 0.000 claims description 3
- 206010048554 Endothelial dysfunction Diseases 0.000 claims description 3
- 206010061216 Infarction Diseases 0.000 claims description 3
- 206010028980 Neoplasm Diseases 0.000 claims description 3
- 206010063837 Reperfusion injury Diseases 0.000 claims description 3
- 208000017442 Retinal disease Diseases 0.000 claims description 3
- 206010038923 Retinopathy Diseases 0.000 claims description 3
- 208000006011 Stroke Diseases 0.000 claims description 3
- 206010042434 Sudden death Diseases 0.000 claims description 3
- 208000015294 blood coagulation disease Diseases 0.000 claims description 3
- 201000011510 cancer Diseases 0.000 claims description 3
- 208000026106 cerebrovascular disease Diseases 0.000 claims description 3
- 208000035475 disorder Diseases 0.000 claims description 3
- 239000002934 diuretic Substances 0.000 claims description 3
- 230000008694 endothelial dysfunction Effects 0.000 claims description 3
- 230000010247 heart contraction Effects 0.000 claims description 3
- 230000007574 infarction Effects 0.000 claims description 3
- 208000027866 inflammatory disease Diseases 0.000 claims description 3
- 208000037906 ischaemic injury Diseases 0.000 claims description 3
- 208000012947 ischemia reperfusion injury Diseases 0.000 claims description 3
- 230000000302 ischemic effect Effects 0.000 claims description 3
- 239000003226 mitogen Substances 0.000 claims description 3
- 201000001119 neuropathy Diseases 0.000 claims description 3
- 230000007823 neuropathy Effects 0.000 claims description 3
- 208000030613 peripheral artery disease Diseases 0.000 claims description 3
- 208000033808 peripheral neuropathy Diseases 0.000 claims description 3
- 230000036454 renin-angiotensin system Effects 0.000 claims description 3
- 208000037803 restenosis Diseases 0.000 claims description 3
- 208000032598 susceptibility microvascular complications of diabetes Diseases 0.000 claims description 3
- 208000019553 vascular disease Diseases 0.000 claims description 3
- 125000001617 2,3-dimethoxy phenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 2
- 125000005808 2,4,6-trimethoxyphenyl group Chemical group [H][#6]-1=[#6](-[#8]C([H])([H])[H])-[#6](-*)=[#6](-[#8]C([H])([H])[H])-[#6]([H])=[#6]-1-[#8]C([H])([H])[H] 0.000 claims description 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 2
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims description 2
- PYRBBLDGJYYBKR-UHFFFAOYSA-N 2-N-[3-(1,3-benzothiazol-2-yl)phenyl]-4-N-[3-(1,3-dihydropyrazol-2-yl)propyl]pyrimidine-2,4-diamine Chemical compound S1C(=NC2=C1C=CC=C2)C=2C=C(C=CC2)NC2=NC=CC(=N2)NCCCN2NC=CC2 PYRBBLDGJYYBKR-UHFFFAOYSA-N 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
- LBRCSHJFEHRFMU-UHFFFAOYSA-N 2-n-(3-aminophenyl)-4-n-(3-morpholin-4-ylpropyl)pyrimidine-2,4-diamine Chemical compound NC1=CC=CC(NC=2N=C(NCCCN3CCOCC3)C=CN=2)=C1 LBRCSHJFEHRFMU-UHFFFAOYSA-N 0.000 claims description 2
- OFDGVGLYJNTNLR-UHFFFAOYSA-N 2-n-(3-chlorophenyl)-4-n-(2,2,6,6-tetramethylpiperidin-4-yl)pyrimidine-2,4-diamine Chemical compound C1C(C)(C)NC(C)(C)CC1NC1=CC=NC(NC=2C=C(Cl)C=CC=2)=N1 OFDGVGLYJNTNLR-UHFFFAOYSA-N 0.000 claims description 2
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- AVGYVMZYRPRURN-UHFFFAOYSA-N 2-n-(3-chlorophenyl)-4-n-[(1-methylpiperidin-2-yl)methyl]pyrimidine-2,4-diamine Chemical compound CN1CCCCC1CNC1=CC=NC(NC=2C=C(Cl)C=CC=2)=N1 AVGYVMZYRPRURN-UHFFFAOYSA-N 0.000 claims description 2
- LTGFJAODGMTKNB-UHFFFAOYSA-N 2-n-(3-chlorophenyl)-4-n-[(1-propan-2-ylpiperidin-3-yl)methyl]pyrimidine-2,4-diamine Chemical compound C1N(C(C)C)CCCC1CNC1=CC=NC(NC=2C=C(Cl)C=CC=2)=N1 LTGFJAODGMTKNB-UHFFFAOYSA-N 0.000 claims description 2
- JKXMUQDZRLBIKI-UHFFFAOYSA-N 2-n-(3-chlorophenyl)-4-n-[3-(2,5-dihydropyrrol-1-yl)propyl]pyrimidine-2,4-diamine Chemical compound ClC1=CC=CC(NC=2N=C(NCCCN3CC=CC3)C=CN=2)=C1 JKXMUQDZRLBIKI-UHFFFAOYSA-N 0.000 claims description 2
- DTJLZSSPGOXHKN-UHFFFAOYSA-N 2-n-(3-chlorophenyl)-4-n-[3-(4-methylpiperazin-1-yl)propyl]pyrimidine-2,4-diamine Chemical compound C1CN(C)CCN1CCCNC1=CC=NC(NC=2C=C(Cl)C=CC=2)=N1 DTJLZSSPGOXHKN-UHFFFAOYSA-N 0.000 claims description 2
- DMGFVZYGJUBCHC-UHFFFAOYSA-N 2-n-(3-fluorophenyl)-4-n-(3-pyrazolidin-1-ylpropyl)pyrimidine-2,4-diamine Chemical compound FC1=CC=CC(NC=2N=C(NCCCN3NCCC3)C=CN=2)=C1 DMGFVZYGJUBCHC-UHFFFAOYSA-N 0.000 claims description 2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
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- Vascular Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81395606P | 2006-06-15 | 2006-06-15 | |
| US60/813,956 | 2006-06-15 | ||
| PCT/US2007/071077 WO2007146981A2 (en) | 2006-06-15 | 2007-06-13 | 2-anilino-4-(heterocyclic)amino-pyrimidines as inhibitors of protein kinase c-alpha |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2653777A1 true CA2653777A1 (en) | 2007-12-21 |
Family
ID=38608732
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002653777A Abandoned CA2653777A1 (en) | 2006-06-15 | 2007-06-13 | 2-anilino-4-(heterocyclic)amino-pyrimidines |
Country Status (16)
| Country | Link |
|---|---|
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| EP (1) | EP2054392A2 (enExample) |
| JP (1) | JP2009540013A (enExample) |
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| CN (1) | CN101506175A (enExample) |
| AR (1) | AR061380A1 (enExample) |
| AU (1) | AU2007257650A1 (enExample) |
| BR (1) | BRPI0713696A2 (enExample) |
| CA (1) | CA2653777A1 (enExample) |
| CL (1) | CL2007001749A1 (enExample) |
| IL (1) | IL195864A0 (enExample) |
| MX (1) | MX2008016004A (enExample) |
| RU (1) | RU2008152195A (enExample) |
| TW (1) | TW200815424A (enExample) |
| WO (1) | WO2007146981A2 (enExample) |
| ZA (1) | ZA200809941B (enExample) |
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| WO2007146977A1 (en) | 2006-06-15 | 2007-12-21 | Boehringer Ingelheim International Gmbh | 2-anilino-4-aminoalkyleneaminopyrimidines |
| CN101686675A (zh) * | 2007-03-20 | 2010-03-31 | 史密丝克莱恩比彻姆公司 | 化合物 |
| WO2009012421A1 (en) * | 2007-07-17 | 2009-01-22 | Rigel Pharmaceuticals, Inc. | Cyclic amine substituted pyrimidinediamines as pkc inhibitors |
| WO2010083241A2 (en) * | 2009-01-14 | 2010-07-22 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds for treatment of inflammatory disorders |
| JP5781942B2 (ja) * | 2009-01-14 | 2015-09-24 | ライジェル ファーマシューティカルズ, インコーポレイテッド | 2,4−ピリミジンジアミン化合物を用いた炎症性障害の治療法 |
| US8394951B2 (en) | 2009-01-15 | 2013-03-12 | Rigel Pharmaceuticals Inc. | Protein kinase C inhibitors and uses thereof |
| AR076024A1 (es) * | 2009-04-03 | 2011-05-11 | Schering Corp | Derivados de heterociclos biciclicos puenteados y metodos de uso de los mismos |
| JP2013506686A (ja) | 2009-09-30 | 2013-02-28 | プレジデント アンド フェロウズ オブ ハーバード カレッジ | オートファジー阻害遺伝子産物の変調によりオートファジーを変調する方法 |
| CA2780759A1 (en) | 2009-12-01 | 2011-06-09 | Rigel Pharmaceuticals, Inc. | Protein kinase c inhibitors and uses thereof |
| JP2013517273A (ja) * | 2010-01-13 | 2013-05-16 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | 化合物および方法 |
| JP5607241B2 (ja) | 2010-05-21 | 2014-10-15 | ケミリア・エービー | 新規ピリミジン誘導体 |
| EP2688883B1 (en) | 2011-03-24 | 2016-05-18 | Noviga Research AB | Pyrimidine derivatives |
| WO2013092854A1 (en) | 2011-12-23 | 2013-06-27 | Cellzome Limited | Pyrimidine-2,4-diamine derivatives as kinase inhibitors |
| CN102746255A (zh) * | 2012-07-24 | 2012-10-24 | 安徽中医学院 | 具有抗肿瘤活性的化合物、制备方法及应用 |
| US10202356B2 (en) | 2013-03-14 | 2019-02-12 | Tolero Pharmaceuticals, Inc. | JAK2 and ALK2 inhibitors and methods for their use |
| CA2937447A1 (en) * | 2014-01-29 | 2015-08-06 | Vaxine Pty Ltd | New target for diabetes treatment and prevention. |
| WO2016060963A1 (en) * | 2014-10-14 | 2016-04-21 | Sunshine Lake Pharma Co., Ltd. | Substituted heteroaryl compounds and methods of use |
| SG11201807010PA (en) * | 2016-02-22 | 2018-09-27 | Hoffmann La Roche | Process for the manufacture of 3-piperazin-1-yl-propylamine derivatives |
| EP3421485A1 (en) | 2017-06-30 | 2019-01-02 | Université de Strasbourg | Peptides for treatment and prevention of hyperglycaemia |
| CA3096984A1 (en) | 2018-04-05 | 2019-10-10 | Sumitomo Dainippon Pharma Oncology, Inc. | Axl kinase inhibitors and use of the same |
| MX2021000977A (es) | 2018-07-26 | 2021-04-12 | Sumitomo Pharma Oncology Inc | Metodos para tratar enfermedades asociadas con expresion anormal de receptor de activina a tipo 1 (acvr1) e inhibidores de acvr1 para uso en los mismos. |
| EP4295846A3 (en) | 2019-05-10 | 2024-02-28 | Deciphera Pharmaceuticals, LLC | Heteroarylaminopyrimidine amide autophagy inhibitors and methods of use thereof |
| PE20220597A1 (es) | 2019-05-10 | 2022-04-22 | Deciphera Pharmaceuticals Llc | Inhibidores de la autofagia de fenilaminopirimidina amida y metodos de uso de estos |
| CA3143489A1 (en) | 2019-06-17 | 2020-12-24 | Deciphera Pharmaceuticals, Llc | Aminopyrimidine amide autophagy inhibitors and methods of use thereof |
| MX420195B (es) | 2019-07-22 | 2025-02-10 | Lupin Ltd | Compuestos macrocíclicos como agonistas de sting y métodos y usos de los mismos |
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| CL2009000600A1 (es) * | 2008-03-20 | 2010-05-07 | Bayer Cropscience Ag | Uso de compuestos de diaminopirimidina como agentes fitosanitarios; compuestos de diaminopirimidina; su procedimiento de preparacion; agente que los contiene; procedimiento para la preparacion de dicho agente; y procedimiento para combatir plagas de animales y/u hongos dañinos patogenos de plantas. |
| CN102089278A (zh) * | 2008-06-11 | 2011-06-08 | Irm责任有限公司 | 用于治疗疟疾的化合物和组合物 |
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-
2007
- 2007-06-13 RU RU2008152195/04A patent/RU2008152195A/ru unknown
- 2007-06-13 BR BRPI0713696-0A patent/BRPI0713696A2/pt not_active IP Right Cessation
- 2007-06-13 MX MX2008016004A patent/MX2008016004A/es not_active Application Discontinuation
- 2007-06-13 JP JP2009515622A patent/JP2009540013A/ja active Pending
- 2007-06-13 CA CA002653777A patent/CA2653777A1/en not_active Abandoned
- 2007-06-13 AU AU2007257650A patent/AU2007257650A1/en not_active Abandoned
- 2007-06-13 KR KR1020097000717A patent/KR20090019011A/ko not_active Withdrawn
- 2007-06-13 US US11/762,394 patent/US20070293494A1/en not_active Abandoned
- 2007-06-13 EP EP07798482A patent/EP2054392A2/en not_active Withdrawn
- 2007-06-13 WO PCT/US2007/071077 patent/WO2007146981A2/en not_active Ceased
- 2007-06-13 CN CNA2007800303500A patent/CN101506175A/zh active Pending
- 2007-06-14 CL CL2007001749A patent/CL2007001749A1/es unknown
- 2007-06-14 TW TW096121541A patent/TW200815424A/zh unknown
- 2007-06-15 AR ARP070102631A patent/AR061380A1/es not_active Application Discontinuation
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2008
- 2008-11-24 ZA ZA200809941A patent/ZA200809941B/xx unknown
- 2008-12-11 IL IL195864A patent/IL195864A0/en unknown
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2009
- 2009-05-14 US US12/465,704 patent/US8354407B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| JP2009540013A (ja) | 2009-11-19 |
| MX2008016004A (es) | 2009-01-16 |
| CL2007001749A1 (es) | 2008-01-25 |
| ZA200809941B (en) | 2009-07-29 |
| WO2007146981A3 (en) | 2008-02-21 |
| US20090227586A1 (en) | 2009-09-10 |
| CN101506175A (zh) | 2009-08-12 |
| AU2007257650A1 (en) | 2007-12-21 |
| RU2008152195A (ru) | 2010-07-20 |
| WO2007146981A2 (en) | 2007-12-21 |
| US20070293494A1 (en) | 2007-12-20 |
| AR061380A1 (es) | 2008-08-20 |
| BRPI0713696A2 (pt) | 2012-11-06 |
| US8354407B2 (en) | 2013-01-15 |
| EP2054392A2 (en) | 2009-05-06 |
| IL195864A0 (en) | 2009-09-01 |
| TW200815424A (en) | 2008-04-01 |
| KR20090019011A (ko) | 2009-02-24 |
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Legal Events
| Date | Code | Title | Description |
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| FZDE | Discontinued |
Effective date: 20130613 |