SG187795A1 - Heteroaryls and uses thereof - Google Patents
Heteroaryls and uses thereof Download PDFInfo
- Publication number
- SG187795A1 SG187795A1 SG2013009964A SG2013009964A SG187795A1 SG 187795 A1 SG187795 A1 SG 187795A1 SG 2013009964 A SG2013009964 A SG 2013009964A SG 2013009964 A SG2013009964 A SG 2013009964A SG 187795 A1 SG187795 A1 SG 187795A1
- Authority
- SG
- Singapore
- Prior art keywords
- ring
- nitrogen
- membered
- sulfur
- oxygen
- Prior art date
Links
- 125000001072 heteroaryl group Chemical group 0.000 title description 30
- 150000001875 compounds Chemical class 0.000 claims abstract description 295
- 108091007960 PI3Ks Proteins 0.000 claims abstract description 24
- 208000024172 Cardiovascular disease Diseases 0.000 claims abstract description 13
- 208000027866 inflammatory disease Diseases 0.000 claims abstract description 13
- 230000002757 inflammatory effect Effects 0.000 claims abstract description 12
- 230000002062 proliferating effect Effects 0.000 claims abstract description 10
- 102000010400 1-phosphatidylinositol-3-kinase activity proteins Human genes 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 357
- 229910052757 nitrogen Inorganic materials 0.000 claims description 348
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 332
- 229910052717 sulfur Inorganic materials 0.000 claims description 314
- 229910052760 oxygen Inorganic materials 0.000 claims description 309
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 306
- 239000011593 sulfur Substances 0.000 claims description 305
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 301
- 239000001301 oxygen Substances 0.000 claims description 301
- 125000005842 heteroatom Chemical group 0.000 claims description 293
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 286
- 125000001931 aliphatic group Chemical group 0.000 claims description 182
- 229910052739 hydrogen Inorganic materials 0.000 claims description 181
- 239000001257 hydrogen Substances 0.000 claims description 181
- 125000000623 heterocyclic group Chemical group 0.000 claims description 180
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 143
- 125000000217 alkyl group Chemical group 0.000 claims description 142
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 132
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 131
- 229910052736 halogen Inorganic materials 0.000 claims description 90
- 150000002367 halogens Chemical class 0.000 claims description 85
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 69
- 125000001188 haloalkyl group Chemical group 0.000 claims description 55
- 239000000203 mixture Substances 0.000 claims description 44
- 229910052799 carbon Inorganic materials 0.000 claims description 29
- 125000001624 naphthyl group Chemical group 0.000 claims description 27
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 17
- 239000003814 drug Substances 0.000 claims description 11
- 208000035475 disorder Diseases 0.000 claims description 10
- 229940124597 therapeutic agent Drugs 0.000 claims description 8
- 239000003937 drug carrier Substances 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 6
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 5
- 206010002198 Anaphylactic reaction Diseases 0.000 claims description 3
- 206010007572 Cardiac hypertrophy Diseases 0.000 claims description 3
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- 230000007815 allergy Effects 0.000 claims description 3
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- 208000003455 anaphylaxis Diseases 0.000 claims description 3
- 230000005784 autoimmunity Effects 0.000 claims description 3
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- 230000006020 chronic inflammation Effects 0.000 claims description 3
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- 208000003174 Brain Neoplasms Diseases 0.000 claims description 2
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- 208000026310 Breast neoplasm Diseases 0.000 claims description 2
- 206010008342 Cervix carcinoma Diseases 0.000 claims description 2
- 206010009944 Colon cancer Diseases 0.000 claims description 2
- 206010014733 Endometrial cancer Diseases 0.000 claims description 2
- 206010014759 Endometrial neoplasm Diseases 0.000 claims description 2
- 208000000461 Esophageal Neoplasms Diseases 0.000 claims description 2
- 208000008839 Kidney Neoplasms Diseases 0.000 claims description 2
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 2
- 206010030155 Oesophageal carcinoma Diseases 0.000 claims description 2
- 206010033128 Ovarian cancer Diseases 0.000 claims description 2
- 206010061535 Ovarian neoplasm Diseases 0.000 claims description 2
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims description 2
- 206010060862 Prostate cancer Diseases 0.000 claims description 2
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims description 2
- 206010038389 Renal cancer Diseases 0.000 claims description 2
- 208000005718 Stomach Neoplasms Diseases 0.000 claims description 2
- 208000024770 Thyroid neoplasm Diseases 0.000 claims description 2
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims description 2
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims description 2
- 201000010881 cervical cancer Diseases 0.000 claims description 2
- 208000029742 colonic neoplasm Diseases 0.000 claims description 2
- 229940127089 cytotoxic agent Drugs 0.000 claims description 2
- 201000004101 esophageal cancer Diseases 0.000 claims description 2
- 206010017758 gastric cancer Diseases 0.000 claims description 2
- 206010073071 hepatocellular carcinoma Diseases 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims description 2
- 201000010982 kidney cancer Diseases 0.000 claims description 2
- 208000014018 liver neoplasm Diseases 0.000 claims description 2
- 201000005202 lung cancer Diseases 0.000 claims description 2
- 208000020816 lung neoplasm Diseases 0.000 claims description 2
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 2
- 201000002528 pancreatic cancer Diseases 0.000 claims description 2
- 208000008443 pancreatic carcinoma Diseases 0.000 claims description 2
- 201000011549 stomach cancer Diseases 0.000 claims description 2
- 201000002510 thyroid cancer Diseases 0.000 claims description 2
- 201000005112 urinary bladder cancer Diseases 0.000 claims description 2
- 101000605630 Homo sapiens Phosphatidylinositol 3-kinase catalytic subunit type 3 Proteins 0.000 claims 1
- 102100038329 Phosphatidylinositol 3-kinase catalytic subunit type 3 Human genes 0.000 claims 1
- 239000002246 antineoplastic agent Substances 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 abstract description 9
- 229910052721 tungsten Inorganic materials 0.000 abstract description 3
- -1 ATR Proteins 0.000 description 116
- 239000002904 solvent Substances 0.000 description 84
- 125000004093 cyano group Chemical group *C#N 0.000 description 66
- 230000015572 biosynthetic process Effects 0.000 description 62
- 238000007429 general method Methods 0.000 description 60
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 58
- 238000003786 synthesis reaction Methods 0.000 description 55
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 53
- 125000002947 alkylene group Chemical group 0.000 description 49
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 44
- 125000004429 atom Chemical group 0.000 description 44
- 150000003557 thiazoles Chemical class 0.000 description 40
- 125000003118 aryl group Chemical group 0.000 description 39
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 39
- 239000002585 base Substances 0.000 description 38
- 125000004433 nitrogen atom Chemical group N* 0.000 description 35
- 150000003577 thiophenes Chemical class 0.000 description 35
- 229930192474 thiophene Natural products 0.000 description 32
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 28
- 150000002431 hydrogen Chemical group 0.000 description 28
- 235000002639 sodium chloride Nutrition 0.000 description 28
- 150000003839 salts Chemical class 0.000 description 26
- 206010028980 Neoplasm Diseases 0.000 description 25
- 238000012552 review Methods 0.000 description 25
- 125000001424 substituent group Chemical group 0.000 description 25
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 24
- 150000001412 amines Chemical class 0.000 description 24
- 239000003153 chemical reaction reagent Substances 0.000 description 24
- 239000002253 acid Substances 0.000 description 23
- 235000019441 ethanol Nutrition 0.000 description 23
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 23
- 201000011510 cancer Diseases 0.000 description 22
- 239000000543 intermediate Substances 0.000 description 22
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 150000002148 esters Chemical class 0.000 description 21
- 125000000524 functional group Chemical group 0.000 description 21
- 238000010276 construction Methods 0.000 description 20
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 description 19
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 description 19
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 18
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 18
- 125000005843 halogen group Chemical group 0.000 description 18
- 239000003054 catalyst Substances 0.000 description 17
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 16
- 239000003795 chemical substances by application Substances 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 150000001408 amides Chemical group 0.000 description 15
- 230000009466 transformation Effects 0.000 description 15
- 238000007876 drug discovery Methods 0.000 description 14
- 150000004820 halides Chemical class 0.000 description 14
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 14
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 238000002360 preparation method Methods 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 12
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
- 229910001868 water Inorganic materials 0.000 description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 11
- 150000007513 acids Chemical class 0.000 description 11
- 238000005859 coupling reaction Methods 0.000 description 11
- 150000002460 imidazoles Chemical class 0.000 description 11
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 10
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 10
- 150000002576 ketones Chemical class 0.000 description 10
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 9
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 9
- 230000008878 coupling Effects 0.000 description 9
- 238000010168 coupling process Methods 0.000 description 9
- 229920006395 saturated elastomer Polymers 0.000 description 9
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 8
- 102000007493 Class III Phosphatidylinositol 3-Kinases Human genes 0.000 description 8
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- 150000001299 aldehydes Chemical class 0.000 description 8
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- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 7
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- 239000000243 solution Substances 0.000 description 7
- 150000008648 triflates Chemical class 0.000 description 7
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- 150000001345 alkine derivatives Chemical class 0.000 description 6
- 125000000304 alkynyl group Chemical group 0.000 description 6
- XMIIGOLPHOKFCH-UHFFFAOYSA-N beta-phenylpropanoic acid Natural products OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 6
- 229910052794 bromium Inorganic materials 0.000 description 6
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- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 6
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- HERSKCAGZCXYMC-UHFFFAOYSA-N thiophen-3-ol Chemical class OC=1C=CSC=1 HERSKCAGZCXYMC-UHFFFAOYSA-N 0.000 description 6
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- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 1
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- CESUXLKAADQNTB-UHFFFAOYSA-N tert-butanesulfinamide Chemical compound CC(C)(C)S(N)=O CESUXLKAADQNTB-UHFFFAOYSA-N 0.000 description 1
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- CFOAUYCPAUGDFF-UHFFFAOYSA-N tosmic Chemical compound CC1=CC=C(S(=O)(=O)C[N+]#[C-])C=C1 CFOAUYCPAUGDFF-UHFFFAOYSA-N 0.000 description 1
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- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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| JP6073464B2 (ja) | 2012-04-26 | 2017-02-01 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 血小板凝集を治療するためのプロテアーゼ活性化受容体4(par4)阻害剤としてのイミダゾチアジアゾールおよびイミダゾピラジン誘導体 |
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| CN105916503B (zh) | 2014-01-14 | 2020-04-14 | 米伦纽姆医药公司 | 杂芳基化合物和其用途 |
| JP2017502092A (ja) | 2014-01-14 | 2017-01-19 | ミレニアム ファーマシューティカルズ, インコーポレイテッドMillennium Pharmaceuticals, Inc. | ヘテロアリール及びその使用 |
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- 2011-08-11 MX MX2013001660A patent/MX2013001660A/es not_active Application Discontinuation
- 2011-08-11 WO PCT/US2011/047407 patent/WO2012021696A1/en not_active Ceased
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- 2011-08-11 TW TW100128796A patent/TW201217365A/zh unknown
- 2011-08-11 JP JP2013524226A patent/JP2013536193A/ja active Pending
- 2011-08-11 KR KR1020137006232A patent/KR20130098334A/ko not_active Withdrawn
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- 2011-08-11 EA EA201390214A patent/EA201390214A1/ru unknown
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- 2011-08-11 SG SG10201506238SA patent/SG10201506238SA/en unknown
- 2011-08-11 MA MA35714A patent/MA34797B1/fr unknown
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| MA34797B1 (fr) | 2014-01-02 |
| US20150175593A1 (en) | 2015-06-25 |
| CO6690755A2 (es) | 2013-06-17 |
| WO2012021696A1 (en) | 2012-02-16 |
| SG10201506238SA (en) | 2015-09-29 |
| AU2011289377A1 (en) | 2013-03-07 |
| US20120172345A1 (en) | 2012-07-05 |
| PH12013500274A1 (en) | 2013-03-04 |
| UY33554A (es) | 2012-02-29 |
| KR20130098334A (ko) | 2013-09-04 |
| JP2013536193A (ja) | 2013-09-19 |
| TW201217365A (en) | 2012-05-01 |
| DOP2013000034A (es) | 2013-03-31 |
| US8796271B2 (en) | 2014-08-05 |
| US20150175563A1 (en) | 2015-06-25 |
| NZ607087A (en) | 2015-05-29 |
| AR082665A1 (es) | 2012-12-26 |
| CN103153300A (zh) | 2013-06-12 |
| EA201390214A1 (ru) | 2013-07-30 |
| CR20130084A (es) | 2013-05-29 |
| PE20131304A1 (es) | 2013-11-14 |
| CA2807971A1 (en) | 2012-02-16 |
| ECSP13012485A (es) | 2015-02-28 |
| CL2013000417A1 (es) | 2014-01-10 |
| EP2603214A1 (en) | 2013-06-19 |
| MX2013001660A (es) | 2013-06-03 |
| EP2603214A4 (en) | 2013-12-18 |
| US20120178723A1 (en) | 2012-07-12 |
| US8796268B2 (en) | 2014-08-05 |
| BR112013003358A2 (pt) | 2016-07-12 |
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