MX2016004014A - Derivados de 4-azaindol. - Google Patents
Derivados de 4-azaindol.Info
- Publication number
- MX2016004014A MX2016004014A MX2016004014A MX2016004014A MX2016004014A MX 2016004014 A MX2016004014 A MX 2016004014A MX 2016004014 A MX2016004014 A MX 2016004014A MX 2016004014 A MX2016004014 A MX 2016004014A MX 2016004014 A MX2016004014 A MX 2016004014A
- Authority
- MX
- Mexico
- Prior art keywords
- azaindole derivatives
- azaindole
- dementia
- derivatives
- machr
- Prior art date
Links
- XWIYUCRMWCHYJR-UHFFFAOYSA-N 1h-pyrrolo[3,2-b]pyridine Chemical class C1=CC=C2NC=CC2=N1 XWIYUCRMWCHYJR-UHFFFAOYSA-N 0.000 title abstract 3
- 208000024827 Alzheimer disease Diseases 0.000 abstract 2
- 206010067889 Dementia with Lewy bodies Diseases 0.000 abstract 2
- 201000002832 Lewy body dementia Diseases 0.000 abstract 2
- 102000014415 Muscarinic acetylcholine receptor Human genes 0.000 abstract 2
- 108050003473 Muscarinic acetylcholine receptor Proteins 0.000 abstract 2
- 208000012902 Nervous system disease Diseases 0.000 abstract 1
- 208000025966 Neurological disease Diseases 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 230000007278 cognition impairment Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 238000002636 symptomatic treatment Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Se proporcionan derivados de 4-azaindol que son moduladores del receptor de acetilcolina muscarínico (mAChR, por sus siglas en inglés) M1 y que pueden ser eficaces para la prevención o la modificación de la enfermedad o el tratamiento sintomático de los déficits cognitivos asociados con trastornos neurológicos tales como demencia de tipo Alzheimer (AID, por sus siglas en inglés) o la demencia con cuerpos de Lewy (DLB, por sus siglas en inglés), y una composición farmacéutica que comprende un derivado de 4-azaindol como un componente activo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1317363.8A GB201317363D0 (en) | 2013-10-01 | 2013-10-01 | Novel compounds |
PCT/IB2014/001978 WO2015049574A1 (en) | 2013-10-01 | 2014-09-30 | 4-azaindole derivatives |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2016004014A true MX2016004014A (es) | 2016-09-21 |
MX368956B MX368956B (es) | 2019-10-23 |
Family
ID=49585123
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2016004014A MX368956B (es) | 2013-10-01 | 2014-09-30 | Derivados de 4-azaindol. |
Country Status (21)
Country | Link |
---|---|
US (3) | US20150094328A1 (es) |
EP (2) | EP3489237B1 (es) |
JP (3) | JP6517790B2 (es) |
KR (1) | KR102248559B1 (es) |
CN (1) | CN105873927B (es) |
AR (1) | AR097866A1 (es) |
AU (1) | AU2014330880B2 (es) |
BR (1) | BR112016007016A8 (es) |
CA (1) | CA2924619C (es) |
CL (1) | CL2016000726A1 (es) |
ES (2) | ES2807221T3 (es) |
GB (1) | GB201317363D0 (es) |
HK (1) | HK1223090A1 (es) |
IL (1) | IL244609B (es) |
MX (1) | MX368956B (es) |
PE (1) | PE20160839A1 (es) |
PH (1) | PH12016500529A1 (es) |
RU (1) | RU2688938C2 (es) |
SG (1) | SG11201602052YA (es) |
TW (1) | TW201546070A (es) |
WO (1) | WO2015049574A1 (es) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2592078A1 (en) | 2011-11-11 | 2013-05-15 | Almirall, S.A. | New cyclohexylamine derivatives having beta2 adrenergic agonist and M3 muscarinic antagonist activities |
TW201517906A (zh) | 2013-07-25 | 2015-05-16 | Almirall Sa | 含有maba化合物和皮質類固醇之組合 |
GB201317363D0 (en) | 2013-10-01 | 2013-11-13 | Eisai Ltd | Novel compounds |
PL3134386T3 (pl) | 2014-04-23 | 2020-11-16 | Takeda Pharmaceutical Company Limited | Pochodne izoindolin-1-onu jako dodatnia aktywność allosterycznego modulatora cholinergicznego receptora muskarynowego m1 do leczenia choroby alzheimera |
JP6531093B2 (ja) | 2014-05-16 | 2019-06-12 | 武田薬品工業株式会社 | 含窒素複素環化合物 |
TW201617343A (zh) | 2014-09-26 | 2016-05-16 | 阿爾米雷爾有限公司 | 具有β2腎上腺素促效劑及M3蕈毒拮抗劑活性之新穎雙環衍生物 |
DK3303331T3 (en) | 2015-06-08 | 2019-04-23 | Suven Life Sciences Ltd | MUSCARIN M1 RECEPTOR-POSITIVE ALLOSTER MODULATORS |
BR112018004719B1 (pt) * | 2015-09-10 | 2022-11-29 | Suven Life Sciences Limited | Composto fluoroindola e composição farmacêutica |
EP3416639B1 (en) * | 2016-02-16 | 2022-06-08 | Vanderbilt University | Positive allosteric modulators of the muscarinic acetylcholine receptor m1 |
US10899759B2 (en) | 2016-09-30 | 2021-01-26 | Vanderbilt University | Positive allosteric modulators of the muscarinic acetylcholine receptor M1 |
KR102438588B1 (ko) * | 2017-10-18 | 2022-08-31 | 수벤 라이프 사이언시스 리미티드 | 무스카린 m1 수용체 양성 알로스테릭 조절제로서 헤테로아릴 화합물 |
AU2018354969B2 (en) * | 2017-10-27 | 2020-09-17 | Suven Life Sciences Limited | Polycyclic amides as muscarinic M1 receptor positive allosteric modulators |
WO2020086864A1 (en) | 2018-10-24 | 2020-04-30 | Vanderbilt University | Positive allosteric modulators of the muscarinic acetylcholine receptor m1 |
KR102347368B1 (ko) * | 2020-11-03 | 2022-01-07 | (주)케이메디켐 | 신규한 아자인돌 유도체, 이의 제조방법 및 이를 포함하는 인지기능 개선용 조성물 |
Family Cites Families (55)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9420521D0 (en) | 1994-10-12 | 1994-11-30 | Smithkline Beecham Plc | Novel compounds |
US6063930A (en) | 1996-04-03 | 2000-05-16 | Merck & Co., Inc. | Substituted imidazole compounds useful as farnesyl-protein transferase inhibitors |
US7868204B2 (en) | 2001-09-14 | 2011-01-11 | Methylgene Inc. | Inhibitors of histone deacetylase |
MXPA04004711A (es) | 2001-11-19 | 2005-08-16 | Neurogen Corp | Amidas del acido 1h-pirrolo(3,2-b(piridin-3-carboxilico. |
GB0222743D0 (en) | 2002-10-01 | 2002-11-06 | Celltech R&D Ltd | Chemical compounds |
AR043633A1 (es) | 2003-03-20 | 2005-08-03 | Schering Corp | Ligandos de receptores de canabinoides |
WO2004089415A2 (en) | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | COMBINATIONS OF AN 11β-HYDROXYSTEROID DEHYDROGENASE TYPE 1 INHIBITOR AND A GLUCOCORTICOID RECEPTOR AGONIST |
JP2006522750A (ja) | 2003-04-11 | 2006-10-05 | ノボ ノルディスク アクティーゼルスカブ | 代謝性症候群ならびに関連の疾患および障害を治療するために、11β−ヒドロキシステロイドデヒドロゲナーゼ1型阻害剤および抗高血圧剤を使用する併用療法 |
ATE482747T1 (de) | 2003-04-11 | 2010-10-15 | High Point Pharmaceuticals Llc | Neue amide derivate und deren pharmazeutische verwendungen |
EP1853261B1 (de) | 2005-03-03 | 2017-01-11 | Universität des Saarlandes | Selektive hemmstoffe humaner corticoidsynthasen |
FR2890072A1 (fr) * | 2005-09-01 | 2007-03-02 | Fournier S A Sa Lab | Nouveaux composesde pyrrolopyridine |
WO2007084667A2 (en) | 2006-01-19 | 2007-07-26 | Osi Pharmaceutical, Inc. | Fused heterobicyclic kinase inhibitors |
US7964728B2 (en) | 2006-07-06 | 2011-06-21 | Solvay Pharmaceuticals B.V. | Azaindole derivatives with a combination of partial nicotinic acetyl-choline receptor agonism and dopamine reuptake inhibition |
WO2008067566A1 (en) | 2006-11-30 | 2008-06-05 | Amira Pharmaceuticals, Inc. | Compositions and treatments comprising 5-lipoxygenase-activating protein inhibitors and nitric oxide modulators |
BRPI0812594A2 (pt) | 2007-08-10 | 2015-06-23 | Lundbeck & Co As H | Composto ou sal ou hidrato do mesmo, composição farmacêutica, métodos para modulação da atividade de um receptor p2x7, para tratamento de uma condição responsiva á modulação do receptor p2x7 em um paciente, para inibição de morte de células gangliônicas retinais em um paciente, para determinação da presença ou ausência de receptor p2x7 em uma amostra, preparação farmacêutica acondicionada, e, uso de um composto ou sal ou hidrato do mesmo. |
AU2008295485B2 (en) | 2007-08-29 | 2013-09-05 | Merck Sharp & Dohme Corp. | 2,3-substituted azaindole derivatives for treating viral infections |
US8273737B2 (en) * | 2008-01-25 | 2012-09-25 | Merck Sharp & Dohme Corp. | Quinolizidinone M1 receptor positive allosteric modulators |
PT2240482E (pt) | 2008-01-31 | 2013-09-06 | Sanofi Sa | Azaindole-3-carboxamidas cíclicas, sua preparação e sua utilização como fármacos |
US20090247766A1 (en) | 2008-03-27 | 2009-10-01 | University Of Southern California | Substituted Nitrogen Heterocycles and Synthesis and Uses Thereof |
CA2685716A1 (en) | 2008-04-04 | 2009-10-08 | Summit Corporation Plc | Compounds for treating muscular dystrophy |
US8012992B2 (en) | 2008-06-30 | 2011-09-06 | Allergan, Inc. | Aza-indoles and related compounds having sphingosine-1-phosphate (S1P) receptor antagonist biological activity |
US20120040974A1 (en) | 2008-08-18 | 2012-02-16 | Yale University | Mif modulators |
WO2010033980A2 (en) | 2008-09-22 | 2010-03-25 | Isis Innovation Ltd. | 4-azaindole bisphosphonates |
US8557832B2 (en) | 2008-11-20 | 2013-10-15 | Merck Sharp & Dohme Corp. | Aryl methyl benzoquinazolinine M1 receptor positive allosteric modulators |
AU2009324210A1 (en) | 2008-12-05 | 2010-06-10 | F. Hoffmann-La Roche Ag | Pyrrolopyrazinyl urea kinase inhibitors |
EP2370407B1 (en) | 2008-12-19 | 2014-06-18 | Bristol-Myers Squibb Company | Carbazole and carboline kinase inhibitors |
JP2012518640A (ja) | 2009-02-23 | 2012-08-16 | メルク・シャープ・エンド・ドーム・コーポレイション | ピラゾロ[4,3−c]シンノリン−3−オンM1受容体陽性アロステリックモジュレーター |
WO2010123716A1 (en) | 2009-04-20 | 2010-10-28 | Merck Sharp & Dohme Corp. | Heterocyclic fused cinnoline m1 receptor positive allosteric modulators |
JP2012211085A (ja) | 2009-08-12 | 2012-11-01 | Kyowa Hakko Kirin Co Ltd | ヘッジホッグシグナル阻害剤 |
EP2470531A1 (en) * | 2009-08-26 | 2012-07-04 | Nycomed GmbH | Methylpyrrolopyridinecarboxamides |
MY160075A (en) | 2009-08-31 | 2017-02-15 | Merck Sharp & Dohme | Pyranyl aryl methyl benzoquinazolinone m1 receptor positive allosteric modulators |
US8664387B2 (en) | 2009-12-14 | 2014-03-04 | Merck Sharp & Dohme Corp. | Pyridoquinazolinone M1 receptor positive allosteric modulators |
JP5651708B2 (ja) * | 2009-12-17 | 2015-01-14 | メルク・シャープ・エンド・ドーム・コーポレイション | キノリンアミド化合物m1受容体陽性アロステリックモデュレータ |
US8383638B2 (en) | 2009-12-21 | 2013-02-26 | Merck Sharp & Dohme | Aminobenzoquinazolinone M1 receptor positive allosteric modulators |
SG181594A1 (en) | 2009-12-23 | 2012-07-30 | Sanofi Sa | [4[4-(5-aminomethyl-2-fluoro-phenyl)-piperidin-1-yl]-(1h-pyrrolo-pyridin-yl)-methanones and synthesis thereof |
EP2575454B1 (en) | 2010-05-28 | 2018-08-29 | Merck Sharp & Dohme Corp. | Naphthalene carboxamide m1 receptor positive allosteric modulators |
US8815902B2 (en) * | 2010-06-15 | 2014-08-26 | Merck Sharp & Dohme Corp. | Tetrahydroquinoline amide M1 receptor positive allosteric modulators |
US8557992B2 (en) * | 2010-06-15 | 2013-10-15 | Merck Sharp & Dohme Corp. | Heterocyclic fused phenanthrolinone M1 receptor positive allosteric modulators |
EP2588104B1 (en) | 2010-07-01 | 2014-12-10 | Merck Sharp & Dohme Corp. | Isoindolone m1 receptor positive allosteric modulators |
WO2012016133A2 (en) | 2010-07-29 | 2012-02-02 | President And Fellows Of Harvard College | Ros1 kinase inhibitors for the treatment of glioblastoma and other p53-deficient cancers |
US8664234B2 (en) | 2010-10-04 | 2014-03-04 | Merck Sharp & Dohme Corp. | Dihydrobenzoquinazolinone M1 receptor positive allosteric modulators |
AR084433A1 (es) | 2010-12-22 | 2013-05-15 | Ironwood Pharmaceuticals Inc | Inhibidores de la faah y composiciones farmaceuticas que los contienen |
EP3502236B1 (en) | 2011-02-18 | 2023-08-23 | The Scripps Research Institute | Directed differentiation of oligodendrocyte precursor cells to a myelinating cell fate |
US9464065B2 (en) | 2011-03-24 | 2016-10-11 | The Scripps Research Institute | Compounds and methods for inducing chondrogenesis |
WO2012154888A1 (en) | 2011-05-09 | 2012-11-15 | Proteostasis Therapeutics, Inc. | Compounds for treating protein folding disorders |
WO2012158475A1 (en) | 2011-05-17 | 2012-11-22 | Merck Sharp & Dohme Corp. | N-linked lactam m1 receptor positive allosteric modulators |
WO2012158474A1 (en) | 2011-05-17 | 2012-11-22 | Merck Sharp & Dohme Corp. | N-linked quinolineamide m1 receptor positive allosteric modulators |
WO2012158473A1 (en) | 2011-05-17 | 2012-11-22 | Merck Sharp & Dohme Corp. | N-methyl tetrahydroquinoline m1 receptor positive allosteric modulators |
AU2012328476B2 (en) | 2011-10-28 | 2017-03-30 | Vanderbilt University | Substituted 2-(4-heterocyclylbenzyl)isoindolin-1-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M1 |
JP6112316B2 (ja) | 2011-12-22 | 2017-04-12 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | テトラアザ−シクロペンタ[a]インデニル及び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 |
US9012445B2 (en) * | 2012-01-12 | 2015-04-21 | Vanderbilt University | Substituted 4-(1H-pyrazol-4-yl)benzyl analogues as positive allosteric modulators of mAChR M1 receptors |
EA028611B1 (ru) * | 2013-07-17 | 2017-12-29 | Глоубал Элаенс Фор Тб Драг Дивелопмент | Азаиндольные соединения, их получение и способы их применения |
TW201512197A (zh) * | 2013-08-30 | 2015-04-01 | Hoffmann La Roche | 吡咯并吡啶或吡唑并吡啶衍生物 |
RU2016112952A (ru) * | 2013-09-27 | 2017-10-30 | Ф. Хоффманн-Ля Рош Аг | Производные индола и индазола |
GB201317363D0 (en) | 2013-10-01 | 2013-11-13 | Eisai Ltd | Novel compounds |
-
2013
- 2013-10-01 GB GBGB1317363.8A patent/GB201317363D0/en not_active Ceased
-
2014
- 2014-09-30 EP EP18204685.4A patent/EP3489237B1/en active Active
- 2014-09-30 PE PE2016000374A patent/PE20160839A1/es not_active Application Discontinuation
- 2014-09-30 BR BR112016007016A patent/BR112016007016A8/pt active Search and Examination
- 2014-09-30 KR KR1020167011471A patent/KR102248559B1/ko active IP Right Grant
- 2014-09-30 JP JP2016519874A patent/JP6517790B2/ja not_active Expired - Fee Related
- 2014-09-30 EP EP14799529.4A patent/EP3052496B1/en active Active
- 2014-09-30 CN CN201480062539.8A patent/CN105873927B/zh not_active Expired - Fee Related
- 2014-09-30 CA CA2924619A patent/CA2924619C/en not_active Expired - Fee Related
- 2014-09-30 RU RU2016116775A patent/RU2688938C2/ru active
- 2014-09-30 WO PCT/IB2014/001978 patent/WO2015049574A1/en active Application Filing
- 2014-09-30 ES ES18204685T patent/ES2807221T3/es active Active
- 2014-09-30 SG SG11201602052YA patent/SG11201602052YA/en unknown
- 2014-09-30 AU AU2014330880A patent/AU2014330880B2/en not_active Ceased
- 2014-09-30 US US14/501,355 patent/US20150094328A1/en not_active Abandoned
- 2014-09-30 ES ES14799529T patent/ES2710190T3/es active Active
- 2014-09-30 US US15/025,996 patent/US9926312B2/en active Active
- 2014-09-30 MX MX2016004014A patent/MX368956B/es active IP Right Grant
- 2014-10-01 AR ARP140103638A patent/AR097866A1/es unknown
- 2014-10-01 TW TW103134194A patent/TW201546070A/zh unknown
-
2016
- 2016-03-15 IL IL244609A patent/IL244609B/en active IP Right Grant
- 2016-03-17 PH PH12016500529A patent/PH12016500529A1/en unknown
- 2016-03-29 CL CL2016000726A patent/CL2016000726A1/es unknown
- 2016-09-23 HK HK16111182.7A patent/HK1223090A1/zh unknown
-
2018
- 2018-01-19 US US15/875,069 patent/US10072005B2/en active Active
-
2019
- 2019-03-01 JP JP2019037299A patent/JP2019112433A/ja active Pending
-
2020
- 2020-05-08 JP JP2020082404A patent/JP6899944B2/ja active Active
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