JP2017528515A5 - - Google Patents
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- JP2017528515A5 JP2017528515A5 JP2017526014A JP2017526014A JP2017528515A5 JP 2017528515 A5 JP2017528515 A5 JP 2017528515A5 JP 2017526014 A JP2017526014 A JP 2017526014A JP 2017526014 A JP2017526014 A JP 2017526014A JP 2017528515 A5 JP2017528515 A5 JP 2017528515A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- methyl
- disorders
- phenyl
- dihydropyrazolo
- 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 description 95
- 150000001875 compounds Chemical class 0.000 claims description 34
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 32
- 208000035475 disorder Diseases 0.000 claims description 21
- 150000003839 salts Chemical class 0.000 claims description 21
- 239000012453 solvate Substances 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 18
- 125000001475 halogen functional group Chemical group 0.000 claims description 16
- -1 —C 1-4 alkyl-OH Chemical group 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 150000001204 N-oxides Chemical class 0.000 claims description 13
- 201000000980 schizophrenia Diseases 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 201000010099 disease Diseases 0.000 claims description 11
- 239000008194 pharmaceutical composition Substances 0.000 claims description 11
- 210000003169 central nervous system Anatomy 0.000 claims description 10
- 208000020016 psychiatric disease Diseases 0.000 claims description 10
- 125000004076 pyridyl group Chemical group 0.000 claims description 10
- 206010012289 Dementia Diseases 0.000 claims description 8
- 208000007590 Disorders of Excessive Somnolence Diseases 0.000 claims description 8
- 208000027626 Neurocognitive disease Diseases 0.000 claims description 8
- 206010020765 hypersomnia Diseases 0.000 claims description 8
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 8
- 208000020401 Depressive disease Diseases 0.000 claims description 6
- 208000029726 Neurodevelopmental disease Diseases 0.000 claims description 6
- 125000004414 alkyl thio group Chemical group 0.000 claims description 6
- 208000015114 central nervous system disease Diseases 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 230000002265 prevention Effects 0.000 claims description 6
- 238000001228 spectrum Methods 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 208000037490 Medically Unexplained Symptoms Diseases 0.000 claims description 5
- 208000028552 Treatment-Resistant Depressive disease Diseases 0.000 claims description 5
- 208000000044 Amnesia Diseases 0.000 claims description 4
- 208000031091 Amnestic disease Diseases 0.000 claims description 4
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims description 4
- 206010012218 Delirium Diseases 0.000 claims description 4
- 208000019022 Mood disease Diseases 0.000 claims description 4
- 208000012902 Nervous system disease Diseases 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 230000006986 amnesia Effects 0.000 claims description 4
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims description 4
- 208000010877 cognitive disease Diseases 0.000 claims description 4
- 208000024714 major depressive disease Diseases 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- 208000011117 substance-related disease Diseases 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 3
- 239000003937 drug carrier Substances 0.000 claims description 3
- 208000019116 sleep disease Diseases 0.000 claims description 3
- 230000000392 somatic effect Effects 0.000 claims description 3
- YPWPMEWGXVVJHI-VIFPVBQESA-N (7S)-3-(3-amino-1,2-oxazol-5-yl)-7-methyl-5-[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound NC1=NOC(=C1)C=1C=NN2C=1C(N(C[C@@H]2C)C1=CC=C(C=C1)C(F)(F)F)=O YPWPMEWGXVVJHI-VIFPVBQESA-N 0.000 claims description 2
- FYWDNACZTNFJLU-LBPRGKRZSA-N (7S)-3-[3-(5-fluoropyridin-3-yl)-1,2-oxazol-5-yl]-7-methyl-5-[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C2=CC=C(C=C2)C(F)(F)F)C(=O)C2=C(C=NN12)C1=CC(=NO1)C1=CC(F)=CN=C1 FYWDNACZTNFJLU-LBPRGKRZSA-N 0.000 claims description 2
- UCYHZCHUWNVYPL-LBPRGKRZSA-N (7S)-3-[3-(6-aminopyridin-3-yl)-1,2-oxazol-5-yl]-7-methyl-5-[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C2=CC=C(C=C2)C(F)(F)F)C(=O)C2=C(C=NN12)C1=CC(=NO1)C1=CC=C(N)N=C1 UCYHZCHUWNVYPL-LBPRGKRZSA-N 0.000 claims description 2
- XHFSEKAOKOVTCW-NSHDSACASA-N (7S)-5-[3-chloro-4-(trifluoromethyl)phenyl]-3-[3-(5-fluoropyridin-3-yl)-1,2-oxazol-5-yl]-7-methyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound ClC=1C=C(C=CC=1C(F)(F)F)N1C(C=2N([C@H](C1)C)N=CC=2C1=CC(=NO1)C=1C=NC=C(C=1)F)=O XHFSEKAOKOVTCW-NSHDSACASA-N 0.000 claims description 2
- DOOARMJHRBZQMZ-JTQLQIEISA-N (7S)-5-[3-chloro-4-(trifluoromethyl)phenyl]-7-methyl-3-(3-methyl-1,2-oxazol-5-yl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound ClC=1C=C(C=CC=1C(F)(F)F)N1C(C=2N([C@H](C1)C)N=CC=2C1=CC(=NO1)C)=O DOOARMJHRBZQMZ-JTQLQIEISA-N 0.000 claims description 2
- MHAFNMKYKWIWGH-NSHDSACASA-N (7S)-5-[3-chloro-4-(trifluoromethyl)phenyl]-7-methyl-3-(3-pyrazin-2-yl-1,2-oxazol-5-yl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C2=CC(Cl)=C(C=C2)C(F)(F)F)C(=O)C2=C(C=NN12)C1=CC(=NO1)C1=CN=CC=N1 MHAFNMKYKWIWGH-NSHDSACASA-N 0.000 claims description 2
- BLCIZIGYXYSJDK-LBPRGKRZSA-N (7S)-5-[3-chloro-4-(trifluoromethyl)phenyl]-7-methyl-3-(3-pyridin-2-yl-1,2-oxazol-5-yl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C2=CC(Cl)=C(C=C2)C(F)(F)F)C(=O)C2=C(C=NN12)C1=CC(=NO1)C1=NC=CC=C1 BLCIZIGYXYSJDK-LBPRGKRZSA-N 0.000 claims description 2
- DWSCDNCIDYDVCW-LBPRGKRZSA-N (7S)-5-[3-chloro-4-(trifluoromethyl)phenyl]-7-methyl-3-(3-pyridin-3-yl-1,2-oxazol-5-yl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C2=CC(Cl)=C(C=C2)C(F)(F)F)C(=O)C2=C(C=NN12)C1=CC(=NO1)C1=CC=CN=C1 DWSCDNCIDYDVCW-LBPRGKRZSA-N 0.000 claims description 2
- KZHAFIONCJZPJZ-ZDUSSCGKSA-N (7S)-5-[3-chloro-4-(trifluoromethyl)phenyl]-7-methyl-3-[3-(4-methylpyridin-3-yl)-1,2-oxazol-5-yl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C2=CC(Cl)=C(C=C2)C(F)(F)F)C(=O)C2=C(C=NN12)C1=CC(=NO1)C1=C(C)C=CN=C1 KZHAFIONCJZPJZ-ZDUSSCGKSA-N 0.000 claims description 2
- XPGBNSLUXWDXTO-NSHDSACASA-N (7S)-7-methyl-3-(3-methyl-1,2-oxazol-5-yl)-5-[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C)=O)C1=CC=C(C=C1)C(F)(F)F XPGBNSLUXWDXTO-NSHDSACASA-N 0.000 claims description 2
- WNFUQCDVIBNSQR-AWEZNQCLSA-N (7S)-7-methyl-3-(3-phenyl-1,2-oxazol-5-yl)-5-[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C1=CC=CC=C1)=O)C1=CC=C(C=C1)C(F)(F)F WNFUQCDVIBNSQR-AWEZNQCLSA-N 0.000 claims description 2
- DQNIUZKUPJKRDS-LBPRGKRZSA-N (7S)-7-methyl-3-(3-pyrazin-2-yl-1,2-oxazol-5-yl)-5-[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C1=NC=CN=C1)=O)C1=CC=C(C=C1)C(F)(F)F DQNIUZKUPJKRDS-LBPRGKRZSA-N 0.000 claims description 2
- AFIZZRIFMYCMET-ZDUSSCGKSA-N (7S)-7-methyl-3-(3-pyridin-2-yl-1,2-oxazol-5-yl)-5-[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C1=NC=CC=C1)=O)C1=CC=C(C=C1)C(F)(F)F AFIZZRIFMYCMET-ZDUSSCGKSA-N 0.000 claims description 2
- AYFYXSDJSXRLFM-ZDUSSCGKSA-N (7S)-7-methyl-3-(3-pyridin-3-yl-1,2-oxazol-5-yl)-5-[4-(trifluoromethyl)phenyl]-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C=1C=NC=CC=1)=O)C1=CC=C(C=C1)C(F)(F)F AYFYXSDJSXRLFM-ZDUSSCGKSA-N 0.000 claims description 2
- DUJSVSFDLRQQND-ZDUSSCGKSA-N (7S)-7-methyl-5-[3-methyl-4-(trifluoromethyl)phenyl]-3-(3-pyrazin-2-yl-1,2-oxazol-5-yl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4-one Chemical compound C[C@H]1CN(C2=CC(C)=C(C=C2)C(F)(F)F)C(=O)C2=C(C=NN12)C1=CC(=NO1)C1=CN=CC=N1 DUJSVSFDLRQQND-ZDUSSCGKSA-N 0.000 claims description 2
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 2
- GLQXAHBYDJPCHG-UHFFFAOYSA-N 6,7-dihydro-5h-pyrazolo[1,5-a]pyrazin-4-one Chemical group O=C1NCCN2N=CC=C12 GLQXAHBYDJPCHG-UHFFFAOYSA-N 0.000 claims description 2
- DMJHXKFDGPPVCA-AWEZNQCLSA-N C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C1=NC=CC=C1)=O)C1=CC(=C(C=C1)C(F)(F)F)C Chemical compound C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C1=NC=CC=C1)=O)C1=CC(=C(C=C1)C(F)(F)F)C DMJHXKFDGPPVCA-AWEZNQCLSA-N 0.000 claims description 2
- IKSLNXSACFFORO-AWEZNQCLSA-N C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C=1C=NC=CC=1)=O)C1=CC(=C(C=C1)C(F)(F)F)C Chemical compound C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C=1C=NC=CC=1)=O)C1=CC(=C(C=C1)C(F)(F)F)C IKSLNXSACFFORO-AWEZNQCLSA-N 0.000 claims description 2
- VYDUDGLULPYNPC-AWEZNQCLSA-N C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C=1C=NC=CC=1C)=O)C1=CC=C(C=C1)C(F)(F)F Chemical compound C[C@H]1CN(C(C=2N1N=CC=2C1=CC(=NO1)C=1C=NC=CC=1C)=O)C1=CC=C(C=C1)C(F)(F)F VYDUDGLULPYNPC-AWEZNQCLSA-N 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 230000007170 pathology Effects 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- SIUMSSQBTSGWKB-ZDUSSCGKSA-N FC=1C=C(C=NC=1)C1=NOC(=C1)C=1C=NN2C=1C(N(C[C@@H]2C)C1=CC(=C(C=C1)C(F)(F)F)C)=O Chemical compound FC=1C=C(C=NC=1)C1=NOC(=C1)C=1C=NN2C=1C(N(C[C@@H]2C)C1=CC(=C(C=C1)C(F)(F)F)C)=O SIUMSSQBTSGWKB-ZDUSSCGKSA-N 0.000 claims 1
- 229910052571 earthenware Inorganic materials 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 125000004499 isoxazol-5-yl group Chemical group O1N=CC=C1* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 201000000417 schizophrenia 15 Diseases 0.000 claims 1
- 208000012201 sexual and gender identity disease Diseases 0.000 claims 1
- 208000015891 sexual disease Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 230000006735 deficit Effects 0.000 description 2
- BTAXDTHTWCJURC-HNNXBMFYSA-N C[C@H]1CN(C(=O)C2=C(C=NN12)C3=CC(=NO3)C4=C(C=COC4)C)C5=CC(=C(C=C5)C(F)(F)F)C Chemical compound C[C@H]1CN(C(=O)C2=C(C=NN12)C3=CC(=NO3)C4=C(C=COC4)C)C5=CC(=C(C=C5)C(F)(F)F)C BTAXDTHTWCJURC-HNNXBMFYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14179601.1 | 2014-08-01 | ||
| EP14179601 | 2014-08-01 | ||
| PCT/EP2015/067534 WO2016016382A1 (en) | 2014-08-01 | 2015-07-30 | 6,7-dihydropyrazolo[1,5-a]pyrazin-4(5h)-one compounds and their use as negative allosteric modulators of mglur2 receptors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017528515A JP2017528515A (ja) | 2017-09-28 |
| JP2017528515A5 true JP2017528515A5 (enExample) | 2018-08-23 |
| JP6517340B2 JP6517340B2 (ja) | 2019-05-22 |
Family
ID=51257440
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017526014A Expired - Fee Related JP6517340B2 (ja) | 2014-08-01 | 2015-07-30 | ６，７−ジヒドロピラゾロ［１，５−ａ］ピラジン−４（５Ｈ）−オン化合物およびＭＧＬＵＲ２受容体の負のアロステリック調節因子としてのそれらの使用 |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US10220032B2 (enExample) |
| EP (1) | EP3174882B1 (enExample) |
| JP (1) | JP6517340B2 (enExample) |
| CN (1) | CN107018661B (enExample) |
| AU (1) | AU2015295300B2 (enExample) |
| CA (1) | CA2954091C (enExample) |
| ES (1) | ES2707525T3 (enExample) |
| RU (1) | RU2708391C2 (enExample) |
| WO (1) | WO2016016382A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JO3601B1 (ar) * | 2014-08-01 | 2020-07-05 | Janssen Pharmaceutica Nv | مركبات 6 ، 7 ثاني هيدرو بيرازولو [ 1، 5 الفا ] بيرازين – 4 (5 يد) – اون واستخدامها كمنظمات الوسترية سلبية لمستقبلات ملجور 2 |
| JOP20150179B1 (ar) | 2014-08-01 | 2021-08-17 | Janssen Pharmaceutica Nv | مركبات 6 ، 7 ثاني هيدرو بيرازولو [ 1، 5 الفا ] بيرازين – 4 (5 يد) – اون واستخدامها كمنظمات الوسترية سلبية لمستقبلات ملجور 2 |
| JOP20150177B1 (ar) | 2014-08-01 | 2021-08-17 | Janssen Pharmaceutica Nv | مركبات 6 ، 7 ثاني هيدرو بيرازولو [ 1، 5 الفا ] بيرازين – 4 (5 يد) – اون واستخدامها كمنظمات الوسترية سلبية لمستقبلات ملجور 2 |
| RU2696135C2 (ru) * | 2014-08-01 | 2019-07-31 | Янссен Фармацевтика Нв | 6,7-ДИГИДРОПИРАЗОЛО[1,5-α]ПИРАЗИН-4(5Н)-ОНОВЫЕ СОЕДИНЕНИЯ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ОТРИЦАТЕЛЬНЫХ АЛЛОСТЕРИЧЕСКИХ МОДУЛЯТОРОВ РЕЦЕПТОРОВ MGLUR2 |
| AU2015357169B2 (en) | 2014-12-03 | 2021-03-04 | Janssen Pharmaceutica Nv | Radiolabelled mGluR2 PET ligands |
| ES2727379T3 (es) * | 2014-12-03 | 2019-10-15 | Janssen Pharmaceutica Nv | Compuestos de 6,7-dihidropirazolo[1,5-a]pirazin-4(5H)-ona y su uso como moduladores alostéricos negativos de receptores de mGlu2 |
| RS60981B1 (sr) | 2015-12-18 | 2020-11-30 | Janssen Pharmaceutica Nv | Radiooznačeni mglur2/3 pet ligandi |
| EA037941B1 (ru) | 2015-12-18 | 2021-06-09 | Янссен Фармацевтика Нв | ЛИГАНДЫ mGluR2/3 ДЛЯ PET, МЕЧЕННЫЕ РАДИОАКТИВНЫМИ ИЗОТОПАМИ |
| SG11202004484UA (en) | 2017-11-24 | 2020-06-29 | Sumitomo Dainippon Pharma Co Ltd | 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZINONE DERIVATIVE AND MEDICAL USE THEREOF |
| JP7266010B2 (ja) * | 2019-05-30 | 2023-04-27 | 住友ファーマ株式会社 | ６，７－ジヒドロピラゾロ［１，５－ａ］ピラジノン誘導体又はその塩を含有する医薬 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7329662B2 (en) * | 2003-10-03 | 2008-02-12 | Hoffmann-La Roche Inc. | Pyrazolo-pyridine |
| DE602006013493D1 (de) * | 2005-09-27 | 2010-05-20 | Hoffmann La Roche | Oxadiazolylpyrazolopyrimidine als mglur2-antagonisten |
| GB0625827D0 (en) * | 2006-12-22 | 2007-02-07 | Astex Therapeutics Ltd | New compounds |
| JO2907B1 (en) | 2009-05-12 | 2015-09-15 | اديكس فرما اس ايه | Pyridine derivatives 1, 2, 4 trisolo [4, 3-A] and their uses as positive LLs for 2MGLUR receptors |
| JP2013529643A (ja) * | 2010-06-23 | 2013-07-22 | バーテックス ファーマシューティカルズ インコーポレイテッド | Ａｔｒキナーゼ阻害剤として有用なピロロピラジン誘導体 |
| US8592422B2 (en) * | 2010-12-17 | 2013-11-26 | Vanderbilt University | Bicyclic triazole and pyrazole lactams as allosteric modulators of mGluR5 receptors |
| CA2853923A1 (en) | 2011-11-03 | 2013-05-10 | Merck Sharp & Dohme Corp. | Quinoline carboxamide and quinoline carbonitrile derivatives as mglur2-negative allosteric modulators, compositions, and their use |
| EP2666775A1 (en) | 2012-05-21 | 2013-11-27 | Domain Therapeutics | Substituted pyrazoloquinazolinones and pyrroloquinazolinones as allosteric modulators of group II metabotropic glutamate receptors |
| US20130345204A1 (en) | 2012-06-20 | 2013-12-26 | Vanderbilt University | Substituted bicyclic cycloalkyl pyrazole lactam analogs as allosteric modulators of mglur5 receptors |
| EP2863922A4 (en) * | 2012-06-20 | 2015-11-04 | Univ Vanderbilt | SUBSTITUTED BICYCLIC ALKOXYPYRAZOL ANALOGUES AS ALLOSTERIC MODULATORS OF MGLUR5 RECEPTORS |
| WO2013192350A1 (en) * | 2012-06-20 | 2013-12-27 | Vanderbilt University | Substituted bicyclic aralkyl pyrazole lactam analogs as allosteric modulators of mglur5 receptors |
| AR093077A1 (es) | 2012-10-23 | 2015-05-20 | Hoffmann La Roche | ANTAGONISTAS DE mGlu2/3 PARA EL TRATAMIENTO DE LOS TRASTORNOS AUTISTAS |
-
2015
- 2015-07-30 US US15/500,234 patent/US10220032B2/en active Active
- 2015-07-30 RU RU2017106489A patent/RU2708391C2/ru active
- 2015-07-30 ES ES15744568T patent/ES2707525T3/es active Active
- 2015-07-30 CN CN201580041302.6A patent/CN107018661B/zh not_active Expired - Fee Related
- 2015-07-30 JP JP2017526014A patent/JP6517340B2/ja not_active Expired - Fee Related
- 2015-07-30 AU AU2015295300A patent/AU2015295300B2/en not_active Ceased
- 2015-07-30 WO PCT/EP2015/067534 patent/WO2016016382A1/en not_active Ceased
- 2015-07-30 EP EP15744568.5A patent/EP3174882B1/en active Active
- 2015-07-30 CA CA2954091A patent/CA2954091C/en active Active
-
2019
- 2019-01-31 US US16/263,731 patent/US10668065B2/en not_active Expired - Fee Related
-
2020
- 2020-05-04 US US16/865,685 patent/US20200261450A1/en not_active Abandoned
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