CL2016000726A1 - Derivados de 4-azaindol - Google Patents
Derivados de 4-azaindolInfo
- Publication number
- CL2016000726A1 CL2016000726A1 CL2016000726A CL2016000726A CL2016000726A1 CL 2016000726 A1 CL2016000726 A1 CL 2016000726A1 CL 2016000726 A CL2016000726 A CL 2016000726A CL 2016000726 A CL2016000726 A CL 2016000726A CL 2016000726 A1 CL2016000726 A1 CL 2016000726A1
- Authority
- CL
- Chile
- Prior art keywords
- azaindole derivatives
- machrm1
- demence
- acetilcoline
- azaindol
- 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 2
- 206010012289 Dementia Diseases 0.000 abstract 1
- 231100000876 cognitive deterioration Toxicity 0.000 abstract 1
- 208000010877 cognitive disease Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 210000004558 lewy body Anatomy 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 230000003551 muscarinic effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 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)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (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
COMPUESTOS DERIVADOS DE 4-AZAINDOL O UNA SAL DE LOS MISMOS, MODULADORES DEL RECEPTOR DE ACETILCOLINA MUSCARINICO M1 (MACHRM1); COMPOSICION FARMACEUTICA QUE LOS COMPRENDE; Y METODOS PARA EL TRATAMIENTO SINTOMATICO DEL DETERIORO COGNITIVO EN LA DEMENCIA DE TIPO ALZHEIMER (AD) Y EN LA DEMENCIA CON CUERPOS DE LEWY (DLB).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1317363.8A GB201317363D0 (en) | 2013-10-01 | 2013-10-01 | Novel compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2016000726A1 true CL2016000726A1 (es) | 2016-09-23 |
Family
ID=49585123
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL2016000726A CL2016000726A1 (es) | 2013-10-01 | 2016-03-29 | Derivados de 4-azaindol |
Country Status (21)
Country | Link |
---|---|
US (3) | US9926312B2 (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) | ES2710190T3 (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 (13)
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 |
JP6517239B2 (ja) | 2014-04-23 | 2019-05-22 | 武田薬品工業株式会社 | アルツハイマー病治療のためのコリン作動性ムスカリンm1受容体ポジティブアロステリックモジュレーター活性としてのイソインドリン−1−オン誘導体 |
WO2015174534A1 (ja) | 2014-05-16 | 2015-11-19 | 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 |
NZ740587A (en) * | 2015-09-10 | 2019-07-26 | Suven Life Sciences Ltd | Fluoroindole derivatives as muscarinic m1 receptor positive allosteric modulators |
US11111251B2 (en) * | 2016-02-16 | 2021-09-07 | 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 |
CN111212840B (zh) * | 2017-10-18 | 2022-07-22 | 苏文生命科学有限公司 | 作为毒蕈碱m1受体正向别构调节剂的杂芳基化合物 |
CN111278814B (zh) * | 2017-10-27 | 2022-10-28 | 苏文生命科学有限公司 | 作为毒蕈碱m1受体正向别构调节剂的多环酰胺 |
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 |
WO2004089896A1 (en) | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | 11β-HYDROXYSTEROID DEHYDROGENASE TYPE 1 ACTIVE COMPOUNDS |
WO2004089416A2 (en) | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | Combination of an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent |
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 |
CA2635899A1 (en) | 2006-01-19 | 2007-07-26 | Osi Pharmaceuticals, 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 |
EA020332B1 (ru) | 2007-08-10 | 2014-10-30 | Х. Лундбекк А/С | Аналоги гетероариламидов |
JP5258889B2 (ja) | 2007-08-29 | 2013-08-07 | メルク・シャープ・アンド・ドーム・コーポレーション | ウイルス感染症の治療のための2,3−置換アザインドール誘導体 |
AU2009206580A1 (en) * | 2008-01-25 | 2009-07-30 | Merck Sharp & Dohme Corp. | Quinolizidinone M1 receptor positive allosteric modulators |
DK2240482T3 (da) | 2008-01-31 | 2013-10-21 | Sanofi Sa | Cykliske azaindol-3-carboxamider, deres fremstilling og deres anvendelse som lægemidler |
WO2009121033A2 (en) | 2008-03-27 | 2009-10-01 | University Of Southern California | Substituted nitrogen heterocycles and synthesis and uses thereof |
WO2009121623A2 (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 |
AU2009283195A1 (en) | 2008-08-18 | 2010-02-25 | Yale University | MIF modulators |
WO2010033980A2 (en) | 2008-09-22 | 2010-03-25 | Isis Innovation Ltd. | 4-azaindole bisphosphonates |
MY162502A (en) | 2008-11-20 | 2017-06-15 | Merck Sharp & Dohme | Aryl methyl benzoquinazolinone m1 receptor positive allosteric modulators |
BRPI0922937A2 (pt) | 2008-12-05 | 2019-09-24 | Hoffmann La Roche | inibidores de pirrolopirazinil uréia quinase |
EP2370407B1 (en) | 2008-12-19 | 2014-06-18 | Bristol-Myers Squibb Company | Carbazole and carboline kinase inhibitors |
US8486946B2 (en) | 2009-02-23 | 2013-07-16 | Merck Sharp & Dohme Corp. | Pyrazolo [4,3-c] cinnolin-3-one M1 receptor positive allosteric modulators |
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 |
US8816085B2 (en) * | 2009-08-26 | 2014-08-26 | Takeda Gmbh | Methylpyrrolopyridinecarboxamides |
AU2010286683B9 (en) | 2009-08-31 | 2014-09-04 | Merck Sharp & Dohme Llc | Pyranyl aryl methyl benzoquinazolinone M1 receptor positive allosteric modulators |
EP2512245B1 (en) * | 2009-12-14 | 2014-07-23 | Merck Sharp & Dohme Corp. | Pyridoquinazolinone m1 receptor positive allosteric modulators |
ES2575154T3 (es) * | 2009-12-17 | 2016-06-24 | Merck Sharp & Dohme Corp. | Moduladores alostéricos positivos del receptor M1 de quinolina amida |
EP2515656B1 (en) | 2009-12-21 | 2014-08-06 | Merck Sharp & Dohme Corp. | Aminobenzoquinazolinone m1 receptor positive allosteric modulators |
RU2012131280A (ru) | 2009-12-23 | 2014-02-10 | Санофи | [4-(5-аминометил-2-фторфенил)пиперидин-1-ил]-(1н-пирролопиридинил)метаноны и их синтез |
US8883850B2 (en) | 2010-05-28 | 2014-11-11 | Merck Sharp & Dohme Corp. | Naphthalene carboxamide M1 receptor positive allosteric modulators |
EP2582241B1 (en) * | 2010-06-15 | 2016-04-06 | Merck Sharp & Dohme Corp. | Heterocyclic fused phenanthrolinone m1 receptor positive allosteric modulators |
WO2011159554A1 (en) * | 2010-06-15 | 2011-12-22 | Merck Sharp & Dohme Corp. | Tetrahydroquinoline amide 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 |
WO2012047702A1 (en) | 2010-10-04 | 2012-04-12 | 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 |
EP2675893B1 (en) | 2011-02-18 | 2019-01-09 | 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 |
EP2709621B1 (en) | 2011-05-17 | 2016-11-02 | Merck Sharp & Dohme Corp. | N-linked quinolineamide m1 receptor positive allosteric modulators |
WO2012158475A1 (en) | 2011-05-17 | 2012-11-22 | Merck Sharp & Dohme Corp. | N-linked lactam m1 receptor positive allosteric modulators |
US9284312B2 (en) * | 2011-05-17 | 2016-03-15 | Merck Sharp & Dohme Corp. | N-methyl tetrahydroquinoline M1 receptor positive allosteric modulators |
ES2604958T3 (es) | 2011-10-28 | 2017-03-10 | Vanderbilt University | Análogos de 2-(4-heterociclilbencil)isoindolin-1-ona sustituidos como moduladores alostéricos positivos del receptor muscarínico de acetilcolina M1 |
US9403835B2 (en) | 2011-12-22 | 2016-08-02 | Ares Trading S.A. | Tetraaza-cyclopenta[a]indenyl and their use as positive allosteric modulators |
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 |
CN105636646B (zh) * | 2013-07-17 | 2017-12-19 | 全球结核病药物研发联盟 | 氮杂吲哚化合物、其合成及其使用方法 |
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 |
WO2015044072A1 (en) * | 2013-09-27 | 2015-04-02 | F. Hoffmann-La Roche Ag | Indol and indazol derivatives |
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 US US15/025,996 patent/US9926312B2/en active Active
- 2014-09-30 EP EP18204685.4A patent/EP3489237B1/en active Active
- 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 BR BR112016007016A patent/BR112016007016A8/pt active Search and Examination
- 2014-09-30 US US14/501,355 patent/US20150094328A1/en not_active Abandoned
- 2014-09-30 CN CN201480062539.8A patent/CN105873927B/zh not_active Expired - Fee Related
- 2014-09-30 WO PCT/IB2014/001978 patent/WO2015049574A1/en active Application Filing
- 2014-09-30 CA CA2924619A patent/CA2924619C/en not_active Expired - Fee Related
- 2014-09-30 MX MX2016004014A patent/MX368956B/es active IP Right Grant
- 2014-09-30 SG SG11201602052YA patent/SG11201602052YA/en unknown
- 2014-09-30 PE PE2016000374A patent/PE20160839A1/es not_active Application Discontinuation
- 2014-09-30 ES ES14799529T patent/ES2710190T3/es active Active
- 2014-09-30 ES ES18204685T patent/ES2807221T3/es active Active
- 2014-09-30 RU RU2016116775A patent/RU2688938C2/ru active
- 2014-09-30 AU AU2014330880A patent/AU2014330880B2/en not_active Ceased
- 2014-09-30 EP EP14799529.4A patent/EP3052496B1/en active Active
- 2014-10-01 TW TW103134194A patent/TW201546070A/zh unknown
- 2014-10-01 AR ARP140103638A patent/AR097866A1/es 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
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CL2016000726A1 (es) | Derivados de 4-azaindol | |
CY1123645T1 (el) | Δικυκλικα παραγωγα, μεθοδος για παρασκευη αυτων και φαρμακευτικες συνθεσεις που περιεχουν αυτα | |
CL2015001733A1 (es) | Compuestos derivados de lactamas fusionadas de arilo y heteroarilo, moduladores de ezh2; composicion farmaceutica que los comprende; uso del compuesto para el tratamiento del cancer. | |
CL2016003246A1 (es) | Compuestos de dihidroisoquinolinona sustituida | |
ECSP20025899A (es) | Compuestos útiles para inhibir a cdk7 | |
CL2018001217A1 (es) | Antagonistas del receptor muscarinico 4 y metodos de uso. | |
DK3313838T3 (da) | Polycykliske amidderivater som cdk9-inhibitorer | |
EA201891209A1 (ru) | Модуляторы хемокиновых рецепторов | |
CR20180564A (es) | Nuevos derivados piperidinilo, un proceso para su preparación y composiciones farmacéuticas que lo contienen | |
CL2014001793A1 (es) | Compuestos derivados de 1,3,5-triazinas sustituidas y sus sales, como inhibidores de la idh2 mutante; composicion farmaceutica que los comprende; y su uso para el tratamiento del cancer. | |
CL2015003147A1 (es) | Compuestos de biheteroarilo y usos de los mismos | |
CL2015002855A1 (es) | Derivados de oxopiridina sustituida. | |
CL2017003127A1 (es) | Derivados de 2,3-dihidro-4h-1,3-benzoxazin-4-ona como moduladores de receptor muscarinico m1 colinergico. | |
CR20160296A (es) | Benzamidas sustituidas y métodos para usarlas | |
DK3357919T3 (da) | Aromatiske heterocykliske forbindelser som antiinflammatoriske forbindelser | |
CL2018002335A1 (es) | Moduladores alostéricos positivos del receptor de acetilcolina muscarínico m1 | |
CO2019005059A2 (es) | Inhibidores de magl | |
BR112016021962A2 (pt) | Compostos, composição farmacêutica e seus usos como moduladores de ror gama | |
CL2018000696A1 (es) | Derivados de indol mono - o disustituidos como inhibidores de la replicación viral del dengue. | |
GT201700023A (es) | Derivados de heterociclico opcionalmente condensados de piridimina útiles para el tratamiento de enfermedades inflamatorias, metabolicas, oncológicas y autoinmunitarias | |
CO2019005038A2 (es) | Inhibidores de magl | |
CL2019001336A1 (es) | Inhibidores de la magl. | |
CL2016001587A1 (es) | Derivado basado en 1,2-naftoquinona y método de preparación del mismo. | |
CL2015003635A1 (es) | Compuestos de tetrahidrocarbazol y carbazol carboxamida sustituidos útiles como inhibidores de quinasa. | |
UY36654A (es) | Azabenzimidazoles con propiedades moduladoras del receptor ampa y composiciones farmacéuticas que los contienen |