ME01488B - Derivati oksadiazola i njihovo korišćenje kao potencijatora metabotropnih glutamatnih receptora-842 - Google Patents
Derivati oksadiazola i njihovo korišćenje kao potencijatora metabotropnih glutamatnih receptora-842Info
- Publication number
- ME01488B ME01488B MEP-2012-131A MEP13112A ME01488B ME 01488 B ME01488 B ME 01488B ME P13112 A MEP13112 A ME P13112A ME 01488 B ME01488 B ME 01488B
- Authority
- ME
- Montenegro
- Prior art keywords
- compound
- salt
- methyl
- pharmaceutically acceptable
- oxadiazol
- Prior art date
Links
- 102000016193 Metabotropic glutamate receptors Human genes 0.000 title 1
- 108010010914 Metabotropic glutamate receptors Proteins 0.000 title 1
- 150000004866 oxadiazoles Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 22
- 150000003839 salts Chemical class 0.000 claims abstract 20
- 238000002360 preparation method Methods 0.000 claims abstract 2
- 230000003287 optical effect Effects 0.000 claims 7
- 208000012902 Nervous system disease Diseases 0.000 claims 4
- 230000000926 neurological effect Effects 0.000 claims 4
- 208000020016 psychiatric disease Diseases 0.000 claims 4
- -1 trifluoromethoxyl Chemical group 0.000 claims 3
- IDLSDBFWSRXGLF-UHFFFAOYSA-N 2-[(4-chlorophenyl)methyl]-7-methyl-5-[3-[(2-methylpiperazin-1-yl)methyl]-1,2,4-oxadiazol-5-yl]-3h-isoindol-1-one Chemical compound CC1CNCCN1CC1=NOC(C=2C=C(C)C=3C(=O)N(CC=4C=CC(Cl)=CC=4)CC=3C=2)=N1 IDLSDBFWSRXGLF-UHFFFAOYSA-N 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 208000019901 Anxiety disease Diseases 0.000 claims 2
- 208000020925 Bipolar disease Diseases 0.000 claims 2
- 208000011688 Generalised anxiety disease Diseases 0.000 claims 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 2
- 206010026749 Mania Diseases 0.000 claims 2
- 208000019022 Mood disease Diseases 0.000 claims 2
- 208000025966 Neurological disease Diseases 0.000 claims 2
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 claims 2
- 208000028017 Psychotic disease Diseases 0.000 claims 2
- 206010041250 Social phobia Diseases 0.000 claims 2
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 claims 2
- 230000036506 anxiety Effects 0.000 claims 2
- 230000002490 cerebral effect Effects 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 230000006735 deficit Effects 0.000 claims 2
- 230000004064 dysfunction Effects 0.000 claims 2
- 208000029364 generalized anxiety disease Diseases 0.000 claims 2
- 229930195712 glutamate Natural products 0.000 claims 2
- 208000019906 panic disease Diseases 0.000 claims 2
- 208000028173 post-traumatic stress disease Diseases 0.000 claims 2
- 230000002035 prolonged effect Effects 0.000 claims 2
- 201000000980 schizophrenia Diseases 0.000 claims 2
- 208000005809 status epilepticus Diseases 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 208000024891 symptom Diseases 0.000 claims 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 2
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 1
- BTXFSYKEPWTYTB-UHFFFAOYSA-N 2-[(4-chlorophenyl)methyl]-5-[3-(2,5-diazabicyclo[2.2.1]heptan-2-ylmethyl)-1,2,4-oxadiazol-5-yl]-7-methyl-3h-isoindol-1-one Chemical compound O=C1C=2C(C)=CC(C=3ON=C(CN4C5CC(NC5)C4)N=3)=CC=2CN1CC1=CC=C(Cl)C=C1 BTXFSYKEPWTYTB-UHFFFAOYSA-N 0.000 claims 1
- QKSTZJGOYWJNSO-UHFFFAOYSA-N 2-[(4-chlorophenyl)methyl]-7-methyl-5-[3-(piperazin-1-ylmethyl)-1,2,4-oxadiazol-5-yl]-3h-isoindol-1-one Chemical compound O=C1C=2C(C)=CC(C=3ON=C(CN4CCNCC4)N=3)=CC=2CN1CC1=CC=C(Cl)C=C1 QKSTZJGOYWJNSO-UHFFFAOYSA-N 0.000 claims 1
- IPCYZQQFECEHLI-UHFFFAOYSA-N 7-methyl-5-[3-(piperazin-1-ylmethyl)-1,2,4-oxadiazol-5-yl]-2-[[4-(trifluoromethoxy)phenyl]methyl]-3h-isoindol-1-one Chemical compound O=C1C=2C(C)=CC(C=3ON=C(CN4CCNCC4)N=3)=CC=2CN1CC1=CC=C(OC(F)(F)F)C=C1 IPCYZQQFECEHLI-UHFFFAOYSA-N 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 229940095064 tartrate Drugs 0.000 claims 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
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Abstract
Jedinjenja sa formulom (I) pri cemu su R1 i Q kako је opisano i specifikaciji, njihove farmaceutski prihvatljive soli, postupci dobijanja, farmaceutske smješe koje ih sadrže i metode za njihovo korišćenje.
Claims (15)
1.Jedinjenje prema Formuli I: naznačeno time. što R1 predstavlja halo ili C1-3haloalkoksil; Q predstavlja i R2 predstavlja vodonik ili C1-3alkil; ili farmaceutski prihvatljiva so, optički izomer, ili kombinacija navedenog jedinjenja ili soli.
2.Jedinjenje prema zahtevu 1, naznačeno time što R1 predstavlja hloro, ili farmaceutski prihvatljiva so, ili optički izomer navedenog jedinjenja ili soli.
3.Jedinjenje prema zahtevu 1. naznačeno time što R1 predstavlja trifluorometoksil, ili farmaceutski prihvatljiva so, ili optički izomer navedenog jedinjenja ili soli.
4.Jedinjenje prema zahtevu 1, naznačeno time što Q predstavlja ili farmaceutski prihvatljiva so, ili optički izomer navedenog jedinjenja ili soli.
5.Jedinjenje prema zahtevu 4, naznačeno time što Q predstavlja i R2 predstavlja H; ili farmaceutski prihvatljiva so, ili optički izomer navedenog jedinjenja ili soli.
6.Jedinjenje prema zahtevu 1, naznačeno time što R1 predstavlja hloro i Q predstavlja ili farmaceutski prihvatljiva so, ili optički izomer navedenog jedinjenja ili soli.
7.Jedinjenje prema zahtevu 1, naznačeno time što R1 predstavlja trifluorometoksil i Q predstavlja ili farmaceutski prihvatljiva so, ili optički izomer navedenog jedinjenja ili soli.
8.Jedinjenje ili njegova farmaceutski prihvatljiva so prema zahtevu 1, naznačeni time što se jedinjenje bira između: 7-metil-5-(3-piperazin-l-ilmetil-[l,2,4]oksadiazol-5-il)-2-(4-trifluorometoksi benzil)- 2.3-dihidroizoindol-l-ona; 2-(4-hloro-benzil)-5-[3-(2,5-diaza-biciklo[2.2.1]hept-2-ilmetil)-[l,2,4]oksadiazol-5- il]-7-metil-2,3-dihidro-izoindol-l-ona; 2-(4-hloro-benzil)-7-metil-5-[3-(3-metil-piperazin-l-ilmetil)-[l,2,4]oksadiazol-5-il]- 2.3-dihidro-izoindol-1 -ona; 2-(4-hloro-benzil)-7-metil-5-(3-piperazin-l-ilmetil-[l,2,4]oksađiazol-5-il)-2,3- dihidro-izoindol-1 -ona; 2-(4-hloro-benzil)-7-metil-5-[3-(2-metil-piperazin-l-ilmetil)-[l,2,4]oksadiazol-5-il]- 2.3-dihidro-izoindol-1-ona, ili 2-(4-hIoro-benzil)-7-metil-5-[3-(2-metil-piperazin-l-ilmetil)-[l,2,4]oksadiazol-5-il]- 2,3-dihidro-izoindol-1 -ona.
9.Jedinjenje ili njegova farmaceutski prihvatljiva so prema zahtevu 1, naznačeno time daje 7-metil-5-(3-piperazin-l-ilmetil-[l,2,4]oksadiazol-5-il)-2-(4- trifluorometoksibenzil)-2,3-dihidroizoindol-1 -on.
10.Farmaceutski prihvatljiva so 7-metil-5-(3-piperazin-l-ilmetil-[l,2,4]oksadiazol-5-il)- 2-(4-trifluorometoksibenzil)-2,3-dihidroizoindol-l-ona prema zahtevu 9, naznačena time da je odabrana od soli hidrohlorida, hidrobromida, fosfata, acetata, fumarata, maleata, tartrata, citrata, metansulfonata ili p-toluensulfonata.
11.Farmaceutska smeša, naznačena time što sadrži jedinjenje ili so prema bilo kojem od zahteva 1-10 i farmaceutski prihvatljiv nosač ili ekscipijent.
12.Jedinjenje ili so prema bilo kojem od zahteva 1-10, naznačeni time što se koriste u tretmanu subjekta koji boluje od neuroloških ili psihijatrijskih poremećaja vezanih sa disfunkcijom glutamata.
13.Jedinjenje za korišćenje prema zahtevu 12, naznačeno time što se neurološki ili psihijatrijski poremećaj odabire između Alchajmerove bolesti, cerebralnih deficita nakon prolongiranog statusa epileptikusa, tolerancije na supstance, simptoma odvikavanja od supstanci, psihoze, šizofrenije, anksioznosti, generalizovanog anksioznog poremećaja, paničnog poremećaja, društvene fobije, opsesivno kompulzivnog poremećaja i post traumatskog stresnog poremećaja, poremećaja raspoloženja, depresije, manije ili bipolarnih poremećaja.
14.Korišćenje jedinjenja ili soli prema bilo kojem od zahteva 1-10, naznačeno time što mu je namena priređivanje medikamenta za terapiju neuroloških ili psihijatrijskih poremećaja povezanih sa disfunkcijom glutamata.
15.Korišćenje prema zahtevu 14, naznačeno time što se neurološki ili psihijatrijski poremećaj odabire između Alchajmerove bolesti, cerebralnih deficita nakon prolongiranog statusa epileptikusa, tolerancije na supstance, simptome odvikavanja od supstanci, psihoze, šizofrenije, anksioznosti, generalizovanog anksioznog poremećaja, paničnog poremećaja, društvene fobije, opsesivno kompulzivnog poremećaja i post traumatskog stresnog poremećaja, poremećaja raspoloženja, depresije, manije ili bipolarnih poremećaja.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US94255307P | 2007-06-07 | 2007-06-07 | |
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Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7807706B2 (en) * | 2005-08-12 | 2010-10-05 | Astrazeneca Ab | Metabotropic glutamate-receptor-potentiating isoindolones |
| US7868008B2 (en) * | 2005-08-12 | 2011-01-11 | Astrazeneca Ab | Substituted isoindolones and their use as metabotropic glutamate receptor potentiators |
| TW200804281A (en) * | 2006-02-16 | 2008-01-16 | Astrazeneca Ab | New metabotropic glutamate receptor-potentiating isoindolones |
| AR059898A1 (es) | 2006-03-15 | 2008-05-07 | Janssen Pharmaceutica Nv | Derivados de 3-ciano-piridona 1,4-disustituida y su uso como moduladores alostericos de los receptores mglur2 |
| TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
| TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
| TW200911255A (en) | 2007-06-07 | 2009-03-16 | Astrazeneca Ab | Metabotropic glutamate receptor oxadiazole ligands and their use as potentiators-841 |
| TWI417100B (zh) | 2007-06-07 | 2013-12-01 | Astrazeneca Ab | 二唑衍生物及其作為代謝型麩胺酸受體增效劑-842之用途 |
| NZ584152A (en) | 2007-09-14 | 2011-11-25 | Ortho Mcneil Janssen Pharm | 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones |
| SI2203439T1 (sl) | 2007-09-14 | 2011-05-31 | Ortho Mcneil Janssen Pharm | 1',3'-disubstituirani 4-fenil-3,4,5,6-tetrahidro-2H-1'H-(1,4')bipiridinil-2'-oni |
| US8722894B2 (en) | 2007-09-14 | 2014-05-13 | Janssen Pharmaceuticals, Inc. | 1,3-disubstituted-4-phenyl-1H-pyridin-2-ones |
| RU2492170C9 (ru) * | 2007-11-14 | 2013-12-27 | Орто-Макнейл-Янссен Фармасьютикалз, Инк. | Имидазо[1,2-а]пиридиновые производные и их применение в качестве положительных аллостерических модуляторов рецепторов mglur2 |
| US7790760B2 (en) * | 2008-06-06 | 2010-09-07 | Astrazeneca Ab | Metabotropic glutamate receptor isoxazole ligands and their use as potentiators 286 |
| RS52703B (sr) | 2008-06-20 | 2013-08-30 | Astrazeneca Ab | Derivat dibenzotiazepina i njegova upotreba |
| AU2009289784B2 (en) | 2008-09-02 | 2012-03-22 | Addex Pharma S.A. | 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors |
| US8697689B2 (en) | 2008-10-16 | 2014-04-15 | Janssen Pharmaceuticals, Inc. | Indole and benzomorpholine derivatives as modulators of metabotropic glutamate receptors |
| WO2010060589A1 (en) | 2008-11-28 | 2010-06-03 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors |
| BRPI1010831A2 (pt) | 2009-05-12 | 2016-04-05 | Addex Pharmaceuticals Sa | derivados de 1,2,4-triazolo[4,3-a]piridina e seu como moduladores alostéricos positivos de receptores de mglur2 |
| MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| CN102439008B (zh) | 2009-05-12 | 2015-04-29 | 杨森制药有限公司 | 1,2,4-三唑并[4,3-a]吡啶衍生物及其用于治疗或预防神经和精神病症的用途 |
| WO2011084098A1 (en) * | 2010-01-07 | 2011-07-14 | Astrazeneca Ab | Process for making a metabotropic glutamate receptor positive allosteric modulator - 874 |
| AU2011245737A1 (en) * | 2010-04-30 | 2012-12-20 | Astrazeneca Ab | Polymorphs of a metabotropic glutamate receptor positive allosteric modulator |
| WO2012062759A1 (en) | 2010-11-08 | 2012-05-18 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
| PT2649069E (pt) | 2010-11-08 | 2015-11-20 | Janssen Pharmaceuticals Inc | Derivados de 1,2,4-triazolo[4,3-a]piridina e sua utilização como moduladores alostéricos positivos de recetores mglur2 |
| JP5852665B2 (ja) | 2010-11-08 | 2016-02-03 | ジヤンセン・フアーマシユーチカルズ・インコーポレーテツド | 1,2,4−トリアゾロ[4,3−a]ピリジン誘導体およびmGluR2受容体のポジティブアロステリックモジュレーターとしてのそれらの使用 |
| CN102180872B (zh) * | 2011-04-01 | 2014-04-02 | 华中科技大学 | [1,3,4]噁二唑类衍生物及其应用 |
| JO3368B1 (ar) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2 |
| JO3367B1 (ar) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2 |
| AU2015208233B2 (en) | 2014-01-21 | 2019-08-29 | Janssen Pharmaceutica Nv | Combinations comprising positive allosteric modulators or orthosteric agonists of metabotropic glutamatergic receptor subtype 2 and their use |
| ES2860298T3 (es) | 2014-01-21 | 2021-10-04 | Janssen Pharmaceutica Nv | Combinaciones que comprenden moduladores alostéricos positivos del receptor glutamatérgico metabotrópico de subtipo 2 y su uso |
| WO2017014170A1 (ja) * | 2015-07-17 | 2017-01-26 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2017014321A1 (en) | 2015-07-17 | 2017-01-26 | Takeda Pharmaceutical Company Limited | Oxadiazole derivatives useful as hdac inhibitors |
| JPWO2017033946A1 (ja) | 2015-08-25 | 2018-06-07 | 武田薬品工業株式会社 | 複素環化合物 |
| WO2020102150A1 (en) | 2018-11-13 | 2020-05-22 | Incyte Corporation | Heterocyclic derivatives as pi3k inhibitors |
| US11078204B2 (en) | 2018-11-13 | 2021-08-03 | Incyte Corporation | Heterocyclic derivatives as PI3K inhibitors |
| WO2020102216A1 (en) | 2018-11-13 | 2020-05-22 | Incyte Corporation | Substituted heterocyclic derivatives as pi3k inhibitors |
| MX2022000693A (es) * | 2019-07-18 | 2022-05-26 | Abaxys Therapeutics | Formulacion solida de un derivado de 1,2,4-oxadiazol. |
| GB2621323A (en) * | 2022-08-03 | 2024-02-14 | Sirgartan Holdings Ltd | Treatments for obsessive compulsive disorder |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2008803A (en) * | 1932-04-18 | 1935-07-23 | Stephan Engineering Corp | Fuel atomizing and igniting means |
| US3993617A (en) | 1975-10-30 | 1976-11-23 | Morton-Norwich Products, Inc. | Antifungal 2-substituted phthalimidines |
| US5175157A (en) | 1985-11-27 | 1992-12-29 | Boehringer Ingelheim Gmbh | Cyclic amine derivatives, pharmaceutical compositions containing these compounds and methods for preparing them |
| WO1992017448A1 (fr) | 1991-04-01 | 1992-10-15 | Kyowa Hakko Kogyo Co., Ltd. | Derive de 3-methylenisoindolin-1-one |
| TW219935B (me) | 1991-12-25 | 1994-02-01 | Mitsubishi Chemicals Co Ltd | |
| EP0602814A1 (en) | 1992-12-18 | 1994-06-22 | Takeda Chemical Industries, Ltd. | Crystal forms of optically active isoindolines and their use |
| US5681954A (en) | 1993-05-14 | 1997-10-28 | Daiichi Pharmaceutical Co., Ltd. | Piperazine derivatives |
| RU2124511C1 (ru) * | 1993-05-14 | 1999-01-10 | Фармасьютикал Ко., Лтд | Производные пиперазина |
| WO1997029079A1 (en) | 1996-02-06 | 1997-08-14 | Japan Tobacco Inc. | Novel compounds and pharmaceutical use thereof |
| US6417362B1 (en) | 1997-05-30 | 2002-07-09 | Meiji Seika Kaisha, Ltd. | Nitrogenous heterocyclic compounds and hyperlipemia remedy containing the same |
| CN1158264C (zh) | 1997-11-21 | 2004-07-21 | Nps药物有限公司 | 用于治疗中枢神经系统疾病的代谢性谷氨酸受体拮抗剂 |
| PT1260512E (pt) | 2000-02-29 | 2007-10-10 | Mitsubishi Pharma Corp | ''novos derivados de amida cíclicos'' |
| IL153645A0 (en) | 2000-07-31 | 2003-07-06 | Smithkline Beecham Plc | Carboxamide compounds and their use as antagonists of a human 11cby receptor |
| US7476688B2 (en) * | 2001-04-19 | 2009-01-13 | Eisai R&D Management Co., Ltd. | Cyclic amidine derivatives |
| EP1431267A4 (en) | 2001-08-09 | 2004-12-22 | Ono Pharmaceutical Co | COMPOUNDS DERIVED FROM CARBOXYLIC ACID AND MEDICAMENTS COMPRISING SUCH COMPOUNDS AS ACTIVE INGREDIENT |
| WO2003087044A2 (en) | 2002-04-09 | 2003-10-23 | 7Tm Pharma A/S | Novel carboxamide compounds for use in mch receptor related disorders |
| FR2840302B1 (fr) | 2002-06-03 | 2004-07-16 | Aventis Pharma Sa | Derives d'isoindolones, procede de preparation et intermediaire de ce procede a titre de medicaments et compositions pharmaceutiques les renfermant |
| DE10238865A1 (de) | 2002-08-24 | 2004-03-11 | Boehringer Ingelheim International Gmbh | Neue Carbonsäureamid-Verbindungen mit MCH-antagonistischer Wirkung, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung |
| GB0223232D0 (en) | 2002-10-07 | 2002-11-13 | Pfizer Ltd | Chemical compounds |
| RU2343145C2 (ru) * | 2002-11-26 | 2009-01-10 | Маруиси Фармасьютикал Ко., Лтд. | Производные изоиндолина |
| AU2004226450A1 (en) | 2003-03-26 | 2004-10-14 | Merck & Co. Inc. | Benzamide modulators of metabotropic glutamate receptors |
| GB0308025D0 (en) | 2003-04-07 | 2003-05-14 | Glaxo Group Ltd | Compounds |
| US7129260B2 (en) | 2003-06-02 | 2006-10-31 | Abbott Laboratories | Isoindolinone kinase inhibitors |
| JP2007510629A (ja) | 2003-10-22 | 2007-04-26 | イーライ リリー アンド カンパニー | 新規mch受容体アンタゴニスト |
| JP2007519754A (ja) | 2004-01-30 | 2007-07-19 | スミスクライン ビーチャム コーポレーション | 化合物 |
| BRPI0507495A (pt) * | 2004-02-18 | 2007-07-10 | Astrazeneca Ab | composto, composição farmacêutica, uso do composto método para o tratamento de distúrbios mediados por mglur5, e, método para inibir a ativação de receptores de mglur5 |
| JP4883296B2 (ja) | 2004-03-05 | 2012-02-22 | 日産化学工業株式会社 | イソキサゾリン置換ベンズアミド化合物及び有害生物防除剤 |
| CN1934094A (zh) | 2004-03-05 | 2007-03-21 | 万有制药株式会社 | 二芳基取代杂环5元环衍生物 |
| SE0400970D0 (sv) | 2004-04-14 | 2004-04-14 | Astrazeneca Ab | Nicotinic acetylcholine receptor ligands |
| TW200613272A (en) | 2004-08-13 | 2006-05-01 | Astrazeneca Ab | Isoindolone compounds and their use as metabotropic glutamate receptor potentiators |
| AU2005299797A1 (en) | 2004-10-25 | 2006-05-04 | Merck & Co., Inc. | Heterocyclic indanone potentiators of metabotropic glutamate receptors |
| EP1855670A4 (en) | 2005-02-24 | 2010-05-05 | Merck Sharp & Dohme | BENZAZOLE AMPLIFIERS OF METABOTROPIC GLUTAMATE RECEPTORS |
| GB0510142D0 (en) * | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds A1 |
| CA2608014A1 (en) | 2005-05-18 | 2006-11-23 | Addex Pharma Sa | Substituted oxadiazole derivatives as positive allosteric modulators of metabotropic glutamate receptors |
| TW200728277A (en) | 2005-06-29 | 2007-08-01 | Palau Pharma Sa | Bicyclic derivatives as P38 inhibitors |
| US7807706B2 (en) | 2005-08-12 | 2010-10-05 | Astrazeneca Ab | Metabotropic glutamate-receptor-potentiating isoindolones |
| US7868008B2 (en) | 2005-08-12 | 2011-01-11 | Astrazeneca Ab | Substituted isoindolones and their use as metabotropic glutamate receptor potentiators |
| EP1912940A1 (en) * | 2005-08-12 | 2008-04-23 | AstraZeneca AB | Substituted isoindolones and their use as metabotropic glutamate receptor potentiators |
| BRPI0616571A2 (pt) * | 2005-09-27 | 2011-06-21 | Hoffmann La Roche | oxadiazolil pirazol-piridiminas como antagonistas de mglur2, processo para sua preparação, composição farmacêutica que os contém e uso dos mesmo |
| TW200804281A (en) | 2006-02-16 | 2008-01-16 | Astrazeneca Ab | New metabotropic glutamate receptor-potentiating isoindolones |
| TW200911255A (en) | 2007-06-07 | 2009-03-16 | Astrazeneca Ab | Metabotropic glutamate receptor oxadiazole ligands and their use as potentiators-841 |
| TWI417100B (zh) | 2007-06-07 | 2013-12-01 | Astrazeneca Ab | 二唑衍生物及其作為代謝型麩胺酸受體增效劑-842之用途 |
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