JP5518076B2 - 三環式カルバメートｊａｋ阻害剤 - Google Patents
三環式カルバメートｊａｋ阻害剤 Download PDFInfo
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- JP5518076B2 JP5518076B2 JP2011528087A JP2011528087A JP5518076B2 JP 5518076 B2 JP5518076 B2 JP 5518076B2 JP 2011528087 A JP2011528087 A JP 2011528087A JP 2011528087 A JP2011528087 A JP 2011528087A JP 5518076 B2 JP5518076 B2 JP 5518076B2
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- JP
- Japan
- Prior art keywords
- oxo
- substituted
- pyrimidinediamine
- indeno
- tetrahydro
- 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.)
- Expired - Fee Related
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- 229940122245 Janus kinase inhibitor Drugs 0.000 title description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 284
- -1 amino, substituted amino, carboxyl Chemical group 0.000 claims description 132
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 100
- 125000001072 heteroaryl group Chemical group 0.000 claims description 97
- 125000000623 heterocyclic group Chemical group 0.000 claims description 93
- 238000000034 method Methods 0.000 claims description 91
- 102000042838 JAK family Human genes 0.000 claims description 84
- 108091082332 JAK family Proteins 0.000 claims description 84
- 201000010099 disease Diseases 0.000 claims description 84
- 125000003118 aryl group Chemical group 0.000 claims description 69
- 125000000217 alkyl group Chemical group 0.000 claims description 68
- 150000003839 salts Chemical class 0.000 claims description 59
- 229910052739 hydrogen Inorganic materials 0.000 claims description 53
- 230000000694 effects Effects 0.000 claims description 48
- 239000001257 hydrogen Substances 0.000 claims description 48
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 41
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 41
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 36
- 125000003107 substituted aryl group Chemical group 0.000 claims description 36
- 239000008194 pharmaceutical composition Substances 0.000 claims description 34
- 125000005843 halogen group Chemical group 0.000 claims description 32
- 125000003342 alkenyl group Chemical group 0.000 claims description 31
- 125000000304 alkynyl group Chemical group 0.000 claims description 31
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 30
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 30
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 28
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 27
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 25
- 101000997832 Homo sapiens Tyrosine-protein kinase JAK2 Proteins 0.000 claims description 24
- 102100033444 Tyrosine-protein kinase JAK2 Human genes 0.000 claims description 24
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 23
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 22
- 206010052779 Transplant rejections Diseases 0.000 claims description 21
- 125000004104 aryloxy group Chemical group 0.000 claims description 21
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 21
- 125000003545 alkoxy group Chemical group 0.000 claims description 20
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 20
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 20
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 238000000338 in vitro Methods 0.000 claims description 15
- 125000002252 acyl group Chemical group 0.000 claims description 14
- 230000002401 inhibitory effect Effects 0.000 claims description 14
- 208000032839 leukemia Diseases 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 12
- 208000017733 acquired polycythemia vera Diseases 0.000 claims description 12
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 12
- 208000037244 polycythemia vera Diseases 0.000 claims description 12
- 125000004429 atom Chemical group 0.000 claims description 11
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 11
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 11
- 208000003476 primary myelofibrosis Diseases 0.000 claims description 11
- 208000023275 Autoimmune disease Diseases 0.000 claims description 10
- 208000032027 Essential Thrombocythemia Diseases 0.000 claims description 10
- 206010028537 myelofibrosis Diseases 0.000 claims description 10
- 125000005338 substituted cycloalkoxy group Chemical group 0.000 claims description 10
- 125000001153 fluoro group Chemical group F* 0.000 claims description 9
- 206010025323 Lymphomas Diseases 0.000 claims description 8
- 208000014767 Myeloproliferative disease Diseases 0.000 claims description 8
- 125000002619 bicyclic group Chemical group 0.000 claims description 8
- 125000004304 oxazol-5-yl group Chemical group O1C=NC=C1* 0.000 claims description 8
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims description 7
- 125000003282 alkyl amino group Chemical group 0.000 claims description 6
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 6
- 208000034578 Multiple myelomas Diseases 0.000 claims description 5
- 206010035226 Plasma cell myeloma Diseases 0.000 claims description 5
- 230000004054 inflammatory process Effects 0.000 claims description 5
- 229910052700 potassium Inorganic materials 0.000 claims description 5
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- HIDWGGVLNMQJDI-YADHBBJMSA-N (3ar,8bs)-7-[[4-[(4-ethyl-2,2-dimethyl-3-oxo-1,4-benzoxazin-6-yl)amino]-5-methylpyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C1=C2N(CC)C(=O)C(C)(C)OC2=CC=C1NC(C(=CN=1)C)=NC=1NC(C=C12)=CC=C1C[C@@H]1[C@H]2NC(=O)O1 HIDWGGVLNMQJDI-YADHBBJMSA-N 0.000 claims description 4
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- POOVTNBASOLYTF-UXHICEINSA-N (3ar,8bs)-7-[[5-chloro-4-[(2,2,4-trimethyl-3-oxo-1,4-benzoxazin-6-yl)amino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C1=C2N(C)C(=O)C(C)(C)OC2=CC=C1NC(C(=CN=1)Cl)=NC=1NC(C=C12)=CC=C1C[C@@H]1[C@H]2NC(=O)O1 POOVTNBASOLYTF-UXHICEINSA-N 0.000 claims description 4
- QBUTXIWMTYTWAG-CVEARBPZSA-N (3ar,8bs)-7-[[5-chloro-4-[(2,2-difluoro-1,3-benzodioxol-4-yl)amino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C=12OC(F)(F)OC2=CC=CC=1NC(C(=CN=1)Cl)=NC=1NC(C=C12)=CC=C1C[C@@H]1[C@H]2NC(=O)O1 QBUTXIWMTYTWAG-CVEARBPZSA-N 0.000 claims description 4
- QHNRSODSZAPMJQ-RTWAWAEBSA-N (3ar,8bs)-7-[[5-chloro-4-[(4-ethyl-2,2-dimethyl-3-oxo-1,4-benzoxazin-6-yl)amino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C1=C2N(CC)C(=O)C(C)(C)OC2=CC=C1NC(C(=CN=1)Cl)=NC=1NC(C=C12)=CC=C1C[C@@H]1[C@H]2NC(=O)O1 QHNRSODSZAPMJQ-RTWAWAEBSA-N 0.000 claims description 4
- LRYHYBJLHRJMRV-RPWUZVMVSA-N (3ar,8bs)-7-[[5-fluoro-4-[4-(2-pyridin-4-ylethyl)anilino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound FC1=CN=C(NC=2C=C3[C@@H]4NC(=O)O[C@@H]4CC3=CC=2)N=C1NC(C=C1)=CC=C1CCC1=CC=NC=C1 LRYHYBJLHRJMRV-RPWUZVMVSA-N 0.000 claims description 4
- WJNZUEHGXCVNMT-PKTZIBPZSA-N (3ar,8bs)-7-[[5-fluoro-4-[4-(pyridin-2-ylmethoxy)anilino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound FC1=CN=C(NC=2C=C3[C@@H]4NC(=O)O[C@@H]4CC3=CC=2)N=C1NC(C=C1)=CC=C1OCC1=CC=CC=N1 WJNZUEHGXCVNMT-PKTZIBPZSA-N 0.000 claims description 4
- ILZRWQGBCDRMTM-YADHBBJMSA-N (3ar,8bs)-7-[[5-methyl-4-(5,6,7,8-tetrahydronaphthalen-1-ylamino)pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C1CCCC2=C1C=CC=C2NC1=NC(NC=2C=C3[C@@H]4NC(=O)O[C@@H]4CC3=CC=2)=NC=C1C ILZRWQGBCDRMTM-YADHBBJMSA-N 0.000 claims description 4
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- LFXYNDJMAWSNCO-RPWUZVMVSA-N (3ar,8bs)-7-[[5-methyl-4-[4-(pyridin-2-ylmethoxy)anilino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound CC1=CN=C(NC=2C=C3[C@@H]4NC(=O)O[C@@H]4CC3=CC=2)N=C1NC(C=C1)=CC=C1OCC1=CC=CC=N1 LFXYNDJMAWSNCO-RPWUZVMVSA-N 0.000 claims description 4
- JJFVYFFGUVGGBG-RPWUZVMVSA-N (3ar,8bs)-7-[[5-methyl-4-[4-(pyridin-3-ylmethoxy)anilino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound CC1=CN=C(NC=2C=C3[C@@H]4NC(=O)O[C@@H]4CC3=CC=2)N=C1NC(C=C1)=CC=C1OCC1=CC=CN=C1 JJFVYFFGUVGGBG-RPWUZVMVSA-N 0.000 claims description 4
- UVJVCQQMPSMBQV-VQTJNVASSA-N (3as,8br)-7-[[4-[(2,2-dimethyl-3-oxo-4h-1,4-benzoxazin-6-yl)amino]-5-methylpyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound O1C(C)(C)C(=O)NC2=CC(NC3=NC(NC=4C=C5[C@H]6NC(=O)O[C@H]6CC5=CC=4)=NC=C3C)=CC=C21 UVJVCQQMPSMBQV-VQTJNVASSA-N 0.000 claims description 4
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- GNBCSICJCDWIIX-LEWJYISDSA-N (3as,8br)-7-[[5-chloro-4-(5,6,7,8-tetrahydronaphthalen-1-ylamino)pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C1CCCC2=C1C=CC=C2NC1=NC(NC=2C=C3[C@H]4NC(=O)O[C@H]4CC3=CC=2)=NC=C1Cl GNBCSICJCDWIIX-LEWJYISDSA-N 0.000 claims description 4
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- ILZRWQGBCDRMTM-FCHUYYIVSA-N (3as,8br)-7-[[5-methyl-4-(5,6,7,8-tetrahydronaphthalen-1-ylamino)pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C1CCCC2=C1C=CC=C2NC1=NC(NC=2C=C3[C@H]4NC(=O)O[C@H]4CC3=CC=2)=NC=C1C ILZRWQGBCDRMTM-FCHUYYIVSA-N 0.000 claims description 4
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- QDEZKIPXCZIJQK-LEWJYISDSA-N (3as,8br)-7-[[5-methyl-4-[(2,2,4-trimethyl-3-oxo-1,4-benzoxazin-6-yl)amino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C1=C2N(C)C(=O)C(C)(C)OC2=CC=C1NC(C(=CN=1)C)=NC=1NC(C=C12)=CC=C1C[C@H]1[C@@H]2NC(=O)O1 QDEZKIPXCZIJQK-LEWJYISDSA-N 0.000 claims description 4
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- MIOFWJOSEYOEBR-GHTZIAJQSA-N (3as,8br)-7-[[5-methyl-4-[(4-methyl-3-oxo-1,4-benzothiazin-6-yl)amino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound C1=C2N(C)C(=O)CSC2=CC=C1NC(C(=CN=1)C)=NC=1NC(C=C12)=CC=C1C[C@H]1[C@@H]2NC(=O)O1 MIOFWJOSEYOEBR-GHTZIAJQSA-N 0.000 claims description 4
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- JJFVYFFGUVGGBG-BJKOFHAPSA-N (3as,8br)-7-[[5-methyl-4-[4-(pyridin-3-ylmethoxy)anilino]pyrimidin-2-yl]amino]-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-2-one Chemical compound CC1=CN=C(NC=2C=C3[C@H]4NC(=O)O[C@H]4CC3=CC=2)N=C1NC(C=C1)=CC=C1OCC1=CC=CN=C1 JJFVYFFGUVGGBG-BJKOFHAPSA-N 0.000 claims description 4
- ZRGUAWDZNKYUTB-UXHICEINSA-N 3-[[2-[[(3ar,8bs)-2-oxo-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-7-yl]amino]-5-chloropyrimidin-4-yl]amino]-n-tert-butylbenzenesulfonamide Chemical compound CC(C)(C)NS(=O)(=O)C1=CC=CC(NC=2C(=CN=C(NC=3C=C4[C@@H]5NC(=O)O[C@@H]5CC4=CC=3)N=2)Cl)=C1 ZRGUAWDZNKYUTB-UXHICEINSA-N 0.000 claims description 4
- 206010061218 Inflammation Diseases 0.000 claims description 4
- YZIAXLQCWQGICF-FCHUYYIVSA-N n-[2-[4-[[2-[[(3as,8br)-2-oxo-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-7-yl]amino]-5-chloropyrimidin-4-yl]amino]phenyl]ethyl]cyclopropanesulfonamide Chemical compound ClC1=CN=C(NC=2C=C3[C@H]4NC(=O)O[C@H]4CC3=CC=2)N=C1NC(C=C1)=CC=C1CCNS(=O)(=O)C1CC1 YZIAXLQCWQGICF-FCHUYYIVSA-N 0.000 claims description 4
- ZAXFOQPUHRVKIE-YADHBBJMSA-N n-[[4-[[2-[[(3ar,8bs)-2-oxo-1,3a,4,8b-tetrahydroindeno[1,2-d][1,3]oxazol-7-yl]amino]-5-chloropyrimidin-4-yl]amino]-3-methylphenyl]methyl]cyclopropanesulfonamide Chemical compound C=1C=C(NC=2C(=CN=C(NC=3C=C4[C@@H]5NC(=O)O[C@@H]5CC4=CC=3)N=2)Cl)C(C)=CC=1CNS(=O)(=O)C1CC1 ZAXFOQPUHRVKIE-YADHBBJMSA-N 0.000 claims description 4
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Classifications
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/62—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems having two or more ring systems containing condensed 1,3-oxazole rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/34—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
- C07D265/36—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings condensed with one six-membered ring
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- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Epidemiology (AREA)
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- Diabetes (AREA)
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- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Oncology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9950708P | 2008-09-23 | 2008-09-23 | |
| US61/099,507 | 2008-09-23 | ||
| PCT/US2009/057972 WO2010039518A2 (en) | 2008-09-23 | 2009-09-23 | Tricyclic carbamate jak inhibitors |
Publications (3)
| Publication Number | Publication Date |
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| JP2012503604A JP2012503604A (ja) | 2012-02-09 |
| JP2012503604A5 JP2012503604A5 (https=) | 2013-05-30 |
| JP5518076B2 true JP5518076B2 (ja) | 2014-06-11 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2011528087A Expired - Fee Related JP5518076B2 (ja) | 2008-09-23 | 2009-09-23 | 三環式カルバメートｊａｋ阻害剤 |
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| Country | Link |
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| US (2) | US8846908B2 (https=) |
| EP (1) | EP2344476B1 (https=) |
| JP (1) | JP5518076B2 (https=) |
| CA (1) | CA2736258C (https=) |
| ES (1) | ES2542884T3 (https=) |
| WO (1) | WO2010039518A2 (https=) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2792278C (en) * | 2010-04-13 | 2019-05-14 | Rigel Pharmaceuticals, Inc. | 2,4-pyrimidinediamine compounds and prodrugs thereof and their uses |
| EP2951590A1 (en) | 2013-02-04 | 2015-12-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for assaying jak2 activity in red blood cells and uses thereof |
| KR101665301B1 (ko) | 2013-08-07 | 2016-10-11 | 카딜라 핼쓰캐어 리미티드 | 야누스 키나제의 억제제로서 n-시아노메틸아미드 |
| WO2018167283A1 (en) | 2017-03-17 | 2018-09-20 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the diagnosis and treatment of pancreatic ductal adenocarcinoma associated neural remodeling |
| WO2018189335A1 (en) | 2017-04-13 | 2018-10-18 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the diagnosis and treatment of pancreatic ductal adenocarcinoma |
| WO2020092015A1 (en) | 2018-11-02 | 2020-05-07 | University Of Rochester | Therapeutic mitigation of epithelial infection |
| KR20210131316A (ko) * | 2019-02-27 | 2021-11-02 | 밀레니엄 파머슈티컬스 인코퍼레이티드 | Sumo-활성화 효소 저해제 및 관문 저해제의 투여 |
| CN114761013A (zh) | 2019-09-27 | 2022-07-15 | 迪斯克医药公司 | 治疗骨髓纤维化和相关病症的方法 |
| WO2021231798A1 (en) | 2020-05-13 | 2021-11-18 | Disc Medicine, Inc. | Anti-hemojuvelin (hjv) antibodies for treating myelofibrosis |
| WO2021257857A1 (en) | 2020-06-19 | 2021-12-23 | Incyte Corporation | Naphthyridinone compounds as jak2 v617f inhibitors |
| WO2021257863A1 (en) | 2020-06-19 | 2021-12-23 | Incyte Corporation | Pyrrolotriazine compounds as jak2 v617f inhibitors |
| SMT202500271T1 (it) | 2020-07-02 | 2025-09-12 | Incyte Corp | Composti di urea triciclici come inibitori di v617f di jak2 |
| US11767323B2 (en) | 2020-07-02 | 2023-09-26 | Incyte Corporation | Tricyclic pyridone compounds as JAK2 V617F inhibitors |
| US11661422B2 (en) | 2020-08-27 | 2023-05-30 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
| WO2022140231A1 (en) | 2020-12-21 | 2022-06-30 | Incyte Corporation | Deazaguaine compounds as jak2 v617f inhibitors |
| AR125273A1 (es) | 2021-02-25 | 2023-07-05 | Incyte Corp | Lactamas espirocíclicas como inhibidores de jak2 v617f |
| CN119173514A (zh) | 2022-03-17 | 2024-12-20 | 因赛特公司 | 作为jak2 v617f抑制剂的三环脲化合物 |
| CN119431398A (zh) * | 2023-07-31 | 2025-02-14 | 中国科学院上海有机化学研究所 | R406及其衍生物协同trail的抗肿瘤应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
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| TWI329105B (en) * | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| ES2445208T3 (es) * | 2002-07-29 | 2014-02-28 | Rigel Pharmaceuticals, Inc. | Compuestos de 2,4-pirimidindiamina para uso en métodos para tratar o prevenir enfermedades autoinmunitarias |
| EP1883302A4 (en) * | 2005-05-03 | 2009-05-20 | Rigel Pharmaceuticals Inc | JAK KINASE HEMMER AND ITS USE |
| WO2006133426A2 (en) * | 2005-06-08 | 2006-12-14 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| CA2642229C (en) * | 2006-02-24 | 2015-05-12 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
| EP2089369B1 (en) * | 2006-10-19 | 2011-02-02 | Rigel Pharmaceuticals, Inc. | 2,4 -pyrimidinediamine derivatives as inhibitors of jak kinases for the treatment of autoimmune diseases |
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2009
- 2009-09-23 ES ES09818261.1T patent/ES2542884T3/es active Active
- 2009-09-23 JP JP2011528087A patent/JP5518076B2/ja not_active Expired - Fee Related
- 2009-09-23 WO PCT/US2009/057972 patent/WO2010039518A2/en not_active Ceased
- 2009-09-23 US US13/119,950 patent/US8846908B2/en active Active
- 2009-09-23 EP EP20090818261 patent/EP2344476B1/en not_active Not-in-force
- 2009-09-23 CA CA2736258A patent/CA2736258C/en active Active
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2014
- 2014-08-22 US US14/466,697 patent/US20140363443A1/en not_active Abandoned
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| Publication number | Publication date |
|---|---|
| ES2542884T3 (es) | 2015-08-12 |
| EP2344476B1 (en) | 2015-04-29 |
| US8846908B2 (en) | 2014-09-30 |
| CA2736258C (en) | 2016-11-29 |
| EP2344476A2 (en) | 2011-07-20 |
| CA2736258A1 (en) | 2010-04-08 |
| WO2010039518A3 (en) | 2010-07-22 |
| EP2344476A4 (en) | 2012-08-15 |
| JP2012503604A (ja) | 2012-02-09 |
| US20140363443A1 (en) | 2014-12-11 |
| WO2010039518A2 (en) | 2010-04-08 |
| US20110269749A1 (en) | 2011-11-03 |
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