AR100154A1 - Compuesto heterocíclico que contiene nitrógeno - Google Patents
Compuesto heterocíclico que contiene nitrógenoInfo
- Publication number
- AR100154A1 AR100154A1 ARP150101206A ARP150101206A AR100154A1 AR 100154 A1 AR100154 A1 AR 100154A1 AR P150101206 A ARP150101206 A AR P150101206A AR P150101206 A ARP150101206 A AR P150101206A AR 100154 A1 AR100154 A1 AR 100154A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- group
- optionally
- substituted
- alkyl group
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/46—Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
-
- 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
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
-
- 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
- A61K31/13—Amines
-
- 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
- A61K31/325—Carbamic acids; Thiocarbamic acids; Anhydrides or salts thereof
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/4035—Isoindoles, e.g. phthalimide
-
- 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
- A61K31/435—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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/24—Antidepressants
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- C07D401/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D401/10—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 linked by a carbon chain containing aromatic rings
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Anesthesiology (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
La presente proporciona un compuesto que tiene una actividad del receptor colinérgico muscarínico M1 del modulador alostérico positivo y útil como un agente para la profilaxis o el tratamiento de la enfermedad de Alzheimer, la esquizofrenia, el dolor, el trastorno del sueño, la demencia de la enfermedad de Parkinson o la demencia con cuerpos de Lewy, y similares. Reivindicación 1: Un compuesto representado por la fórmula (1), caracterizado porque R¹ un grupo cíclico de 5 o 6 miembros sustituido en forma opcional o un grupo alquilo C₁₋₆ sustituido en forma opcional; R² y R³ son iguales o diferentes y cada uno es un átomo de hidrógeno, un átomo de halógeno, un grupo ciano, un grupo alquilo C₁₋₆ sustituido en forma opcional, un grupo alcoxi C₁₋₆ sustituido en forma opcional o un grupo cicloalquilo C₃₋₆ sustituido en forma opcional; R⁴ es un átomo de halógeno, un grupo ciano, un grupo alquilo C₁₋₆ sustituido en forma opcional, un grupo alcoxi C₁₋₆ sustituido en forma opcional, un grupo carbamoilo sustituido en forma opcional o un grupo cíclico de 3 a 8 miembros sustituido en forma opcional; y el Anillo A es un anillo aromático de 6 miembros sustituido en forma opcional y adicional; o una sal del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014089585 | 2014-04-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR100154A1 true AR100154A1 (es) | 2016-09-14 |
Family
ID=53276227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP150101206A AR100154A1 (es) | 2014-04-23 | 2015-04-22 | Compuesto heterocíclico que contiene nitrógeno |
Country Status (36)
Country | Link |
---|---|
US (16) | US9868725B2 (es) |
EP (1) | EP3134386B1 (es) |
JP (1) | JP6517239B2 (es) |
KR (1) | KR102349237B1 (es) |
CN (1) | CN106536508B (es) |
AR (1) | AR100154A1 (es) |
AU (1) | AU2015250610B2 (es) |
BR (1) | BR112016024472B1 (es) |
CA (1) | CA2946519C (es) |
CL (1) | CL2016002661A1 (es) |
CR (1) | CR20160544A (es) |
CY (1) | CY1123569T1 (es) |
DK (1) | DK3134386T3 (es) |
DO (1) | DOP2016000286A (es) |
EA (1) | EA030373B1 (es) |
EC (1) | ECSP16090152A (es) |
ES (1) | ES2811088T3 (es) |
HR (1) | HRP20201171T1 (es) |
HU (1) | HUE050543T2 (es) |
IL (1) | IL248393B (es) |
LT (1) | LT3134386T (es) |
MX (1) | MX2016013810A (es) |
MY (1) | MY195742A (es) |
NZ (1) | NZ725921A (es) |
PE (1) | PE20161400A1 (es) |
PH (1) | PH12016502095A1 (es) |
PL (1) | PL3134386T3 (es) |
PT (1) | PT3134386T (es) |
RS (1) | RS60524B1 (es) |
SG (1) | SG11201608785PA (es) |
SI (1) | SI3134386T1 (es) |
TN (1) | TN2016000455A1 (es) |
TW (1) | TWI664165B (es) |
UA (1) | UA122391C2 (es) |
UY (1) | UY36091A (es) |
WO (1) | WO2015163485A1 (es) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109593096B (zh) | 2013-03-15 | 2022-01-14 | 因赛特公司 | 作为bet蛋白抑制剂的三环杂环 |
WO2015095492A1 (en) | 2013-12-19 | 2015-06-25 | Incyte Corporation | Tricyclic heterocycles as bet protein inhibitors |
ES2811088T3 (es) * | 2014-04-23 | 2021-03-10 | Takeda Pharmaceuticals Co | Derivados de isoindolin-1-ona como actividad del modulador alostérico positivo del receptor M1 muscarínico colinérgico para el tratamiento de la enfermedad de Alzheimer |
DK3134403T3 (en) | 2014-04-23 | 2020-03-09 | Incyte Corp | 1h-pyrrolo[2,3-c]pyridin-7(6h)-on og pyrazolo[3,4-c]pyridin-7(6h)-on som inhibitorer af bet-proteiner |
EP3144308B1 (en) | 2014-05-16 | 2020-06-24 | Takeda Pharmaceutical Company Limited | Nitrogen-containing heterocyclic compound |
EP3156397B1 (en) | 2014-06-13 | 2019-08-07 | Takeda Pharmaceutical Company Limited | Nitrogen-containing heterocyclic compound |
US9527864B2 (en) | 2014-09-15 | 2016-12-27 | Incyte Corporation | Tricyclic heterocycles as BET protein inhibitors |
TW201710255A (zh) | 2015-06-26 | 2017-03-16 | 武田藥品工業股份有限公司 | 雜環化合物 |
US10548899B2 (en) | 2015-10-20 | 2020-02-04 | Takeda Pharmaceutical Company Limited | Quinazolinone and benzotriazinone compounds with cholinergic muscarinin M1 receptor positive allosteric modulator activity |
US20170121347A1 (en) | 2015-10-29 | 2017-05-04 | Incyte Corporation | Amorphous solid form of a bet protein inhibitor |
WO2017107089A1 (en) * | 2015-12-23 | 2017-06-29 | Merck Sharp & Dohme Corp. | 3- (1h-pyrazol-4-yl) pyridineallosteric modulators of the m4 muscarinic acetylcholine receptor |
US10548877B2 (en) | 2016-03-11 | 2020-02-04 | Takeda Pharmaceutical Company Limited | Aromatic ring compound |
PL3472157T3 (pl) | 2016-06-20 | 2023-07-31 | Incyte Corporation | Stałe postacie krystaliczne inhibitora bet |
WO2018005249A1 (en) * | 2016-06-28 | 2018-01-04 | Merck Sharp & Dohme Corp. | Benzoisoquinolinone m1 receptor positive allosteric modulators |
CN110753689B (zh) * | 2017-02-28 | 2024-01-26 | 武田药品工业株式会社 | 用于生产杂环化合物的方法 |
WO2018194181A1 (en) | 2017-04-18 | 2018-10-25 | Takeda Pharmaceutical Company Limited | Heterocyclic compounds useful as modulators of acetylcholine receptors |
US20200182850A1 (en) | 2017-05-19 | 2020-06-11 | Takeda Pharmaceutical Company Limited | Screening method |
US10945771B2 (en) | 2017-06-09 | 2021-03-16 | Merck Sharp & Dohme Corp. | Azabicyclo[4.1.0]heptane allosteric modulators of the M4 muscarinic acetylcholine receptor |
BR112019026096A2 (pt) | 2017-06-20 | 2020-07-07 | Takeda Pharmaceutical Company Limited | composto, medicamento, métodos para modulação alostérica positiva do receptor muscarínico colinérgico m1 e para a profilaxia ou o tratamento de constipação, e, uso do composto |
PT3643718T (pt) | 2017-06-20 | 2023-10-26 | Takeda Pharmaceuticals Co | Composto heterocíclico e seu uso como modulador alostérico positivo do recetor muscarínico colinérgico m1 |
WO2019000237A1 (en) * | 2017-06-27 | 2019-01-03 | Merck Sharp & Dohme Corp. | ALLOSTERIC MODULATORS OF 3- (1H-PYRAZOL-4-YL) PYRIDINE FROM THE M4 ACETYLCHOLINE MUSCARINIC RECEPTOR |
WO2019000238A1 (en) | 2017-06-27 | 2019-01-03 | Merck Sharp & Dohme Corp. | 5- (PYRIDIN-3-YL) OXAZOLE ALLOSTERIC MODULATORS OF M4 ACETYLCHOLINE MUSCARINIC RECEPTOR |
WO2019000236A1 (en) * | 2017-06-27 | 2019-01-03 | Merck Sharp & Dohme Corp. | ALLOSTERIC MODULATORS OF 3- (1H-PYRAZOL-4-YL) PYRIDINE FROM THE M4 ACETYLCHOLINE MUSCARINIC RECEPTOR |
JP2020158392A (ja) * | 2017-07-25 | 2020-10-01 | Agc株式会社 | フルオロフェノール誘導体の製造方法及び新規なフルオロ化合物 |
CN111386270B (zh) * | 2017-11-23 | 2022-05-03 | 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经取代氮杂环 |
US12012419B2 (en) | 2018-09-28 | 2024-06-18 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
WO2020067456A1 (ja) | 2018-09-28 | 2020-04-02 | 武田薬品工業株式会社 | 複素環化合物 |
JP7446232B2 (ja) | 2018-09-28 | 2024-03-08 | 武田薬品工業株式会社 | 縮合環化合物 |
CN113329679A (zh) * | 2018-12-28 | 2021-08-31 | 卢遂显 | 检测治疗和预防神经发育障碍的方法 |
CN116234552A (zh) * | 2020-07-29 | 2023-06-06 | (株)倍宝尊 | mGluR5和5-HT2A受体的双重调节剂及其用途 |
EP4447953A1 (en) | 2021-12-13 | 2024-10-23 | Sage Therapeutics, Inc. | Combination of muscarinic receptor positive modulators and nmda positive allosteric modulators |
Family Cites Families (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4416647Y1 (es) | 1965-05-26 | 1969-07-18 | ||
JPS60172704A (ja) | 1984-02-14 | 1985-09-06 | Mitsuwa Seiki Co Ltd | 流体アクチユエ−タの制御方法 |
JP2699511B2 (ja) | 1988-01-29 | 1998-01-19 | 武田薬品工業株式会社 | 置換アミン類 |
US5538983A (en) | 1990-05-16 | 1996-07-23 | The Rockefeller University | Method of treating amyloidosis by modulation of calcium |
TW219935B (es) | 1991-12-25 | 1994-02-01 | Mitsubishi Chemicals Co Ltd | |
JPH06220044A (ja) * | 1991-12-25 | 1994-08-09 | Mitsubishi Kasei Corp | ベンズアミド誘導体 |
GB9409150D0 (en) | 1994-05-09 | 1994-06-29 | Black James Foundation | Cck and gastrin receptor ligands |
US5744476A (en) | 1994-06-27 | 1998-04-28 | Interneuron Pharmaceuticals, Inc. | Dopamine D1 agonists for the treatment of dementia |
JP2992677B2 (ja) | 1995-06-05 | 1999-12-20 | 武田薬品工業株式会社 | 骨形成促進医薬組成物 |
WO1998030243A1 (en) | 1997-01-08 | 1998-07-16 | Warner-Lambert Company | Acetylcholinesterase inhibitors in combination with muscarinic agonists for the treatment of alzheimer's disease |
US7084126B1 (en) | 2000-05-01 | 2006-08-01 | Healthpartners Research Foundation | Methods and compositions for enhancing cellular function through protection of tissue components |
CA2411386A1 (en) | 2000-06-30 | 2002-01-10 | Eli Lilly And Company | Combination therapy for treatment of psychoses |
WO2002074293A2 (en) | 2001-03-15 | 2002-09-26 | Saegis Pharmaceuticals Inc | Methods for restoring cognitive function following systemic stress |
WO2002081446A1 (en) | 2001-04-06 | 2002-10-17 | Daewoong Co., Ltd. | 3-cyclopentyloxy-4-methoxyphenyl-isoindolinone derivatives and the use thereof |
WO2002081447A1 (en) | 2001-04-06 | 2002-10-17 | Daewoong Pharmaceutical Co., Ltd. | 3-cyclopentyloxy-4-methoxyphenyl-isothiazolinone derivatives and the use thereof |
US20040023951A1 (en) | 2001-06-18 | 2004-02-05 | Bymaster Franklin Porter | Combination therapy for treatment of psychoses |
DE10137163A1 (de) | 2001-07-30 | 2003-02-13 | Bayer Ag | Substituierte Isoindole und ihre Verwendung |
US20040044023A1 (en) | 2002-08-30 | 2004-03-04 | Marc Cantillon | Compositions and methods for treating or preventing memory impairment |
WO2004073639A2 (en) | 2003-02-19 | 2004-09-02 | Merck & Co. Inc. | Treatment of psychosis with a muscarinic m1 receptor ectopic activator |
EP1613321A2 (en) | 2003-03-28 | 2006-01-11 | Acadia Pharmaceuticals Inc. | Muscarinic m1 receptor agonists for pain management |
US20040266659A1 (en) | 2003-06-27 | 2004-12-30 | Stephen LaBerge | Substances that enhance recall and lucidity during dreaming |
TW200613272A (en) * | 2004-08-13 | 2006-05-01 | Astrazeneca Ab | Isoindolone compounds and their use as metabotropic glutamate receptor potentiators |
EP1874356A2 (en) | 2005-04-15 | 2008-01-09 | Board of Trustees of Michigan State University | Aminergic pharmaceutical compositions and methods |
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 |
CA2620333A1 (en) | 2005-08-26 | 2007-03-01 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
US20110319386A1 (en) | 2005-08-26 | 2011-12-29 | Braincells Inc. | Neurogenesis by muscarinic receptor modulation |
WO2007044937A2 (en) | 2005-10-13 | 2007-04-19 | President And Fellows Of Harvard College | Compositions and methods to modulate memory |
GB0607946D0 (en) | 2006-04-21 | 2006-05-31 | Minster Res The Ltd | Mono and combination therapy |
GB0607952D0 (en) | 2006-04-21 | 2006-05-31 | Minster Res Ltd | Novel treatment |
GB0607949D0 (en) | 2006-04-21 | 2006-05-31 | Minster Res The Ltd | Mono and combination therapy |
TW200806625A (en) | 2006-05-26 | 2008-02-01 | Astrazeneca Ab | Therapeutic compounds |
US8143284B2 (en) | 2006-10-05 | 2012-03-27 | Abbott Laboratories | Poly(ADP-ribose)polymerase inhibitors |
US8618074B2 (en) | 2007-03-15 | 2013-12-31 | Board Of Regents Of The University Of Texas System | GPCR enhanced neuroprotection to treat brain injury |
CA2700332A1 (en) | 2007-09-21 | 2009-03-26 | Acadia Pharmaceuticals, Inc. | N-substituted piperidine derivatives as serotonin receptor agents |
CA2700331A1 (en) | 2007-09-21 | 2009-03-26 | Acadia Pharmaceuticals, Inc. | Co-administration of pimavanserin with other agents |
US20090082368A1 (en) * | 2007-09-24 | 2009-03-26 | Painceptor Pharma Corporation | Methods of modulating neurotrophin-mediated activity |
CA2700841A1 (en) | 2007-09-27 | 2009-04-02 | The United States Of America, As Represented By The Secretary, Departmen T Of Health And Human Services | Isoindoline compounds for the treatment of spinal muscular atrophy and other uses |
WO2010042603A1 (en) | 2008-10-08 | 2010-04-15 | Cingulate Neuro Therapeutics, Llc | Amyloid and depression |
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 |
US20120046273A1 (en) | 2009-03-05 | 2012-02-23 | Mithridion, Inc. | Compounds and compositions for cognition-enhancement, methods of making, and methods of treating |
EP2454236B1 (en) | 2009-07-14 | 2019-09-04 | Nerviano Medical Sciences S.r.l. | 3-oxo-2,3-dihydro-1h-isoindole-4-carboxamides as parp inhibitors |
EP3061821B1 (en) | 2009-07-22 | 2019-07-10 | Puretech Health LLC | Compositions for treatment of disorders ameliorated by muscarinic receptor activation |
US10265311B2 (en) | 2009-07-22 | 2019-04-23 | PureTech Health LLC | Methods and compositions for treatment of disorders ameliorated by muscarinic receptor activation |
SG181917A1 (en) | 2009-12-22 | 2012-08-30 | Vertex Pharma | Isoindolinone inhibitors of phosphatidylinositol 3-kinase |
US8314120B2 (en) * | 2010-03-30 | 2012-11-20 | Abbott Gmbh & Co. Kg | Small molecule potentiators of metabotropic glutamate receptors |
EP2588104B1 (en) | 2010-07-01 | 2014-12-10 | Merck Sharp & Dohme Corp. | Isoindolone m1 receptor positive allosteric modulators |
US9549928B2 (en) | 2011-04-29 | 2017-01-24 | The University Of Toledo | Muscarinic agonists as enhancers of cognitive flexibility |
EP2709451B1 (en) | 2011-05-17 | 2015-12-30 | Merck Sharp & Dohme Corp. | N-linked lactam m1 receptor positive allosteric modulators |
WO2012170599A1 (en) | 2011-06-10 | 2012-12-13 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
EP3639823A1 (en) * | 2011-10-28 | 2020-04-22 | Vanderbilt University Center for Technology Transfer and Commercialization | Substituted 2-(4-heterocyclylbenzyl)isoindolin-1-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m1 |
EP2821401B1 (en) | 2012-03-02 | 2020-09-09 | Takeda Pharmaceutical Company Limited | Dihydroquinolinone compounds as modulators of the muscarininc m1 receptor |
US20130289019A1 (en) | 2012-04-26 | 2013-10-31 | Amazing Grace, Inc. | Methods of treating behaviorial and/or mental disorders |
WO2014077401A1 (ja) * | 2012-11-19 | 2014-05-22 | 武田薬品工業株式会社 | 含窒素複素環化合物 |
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 |
ES2811088T3 (es) * | 2014-04-23 | 2021-03-10 | Takeda Pharmaceuticals Co | Derivados de isoindolin-1-ona como actividad del modulador alostérico positivo del receptor M1 muscarínico colinérgico para el tratamiento de la enfermedad de Alzheimer |
CA2996717A1 (en) | 2015-09-11 | 2017-03-16 | Chase Pharmaceuticals Corporation | Muscarinic combination and its use for combating hypocholinergic disorders of the central nervous system |
CN110337289A (zh) | 2016-12-29 | 2019-10-15 | Rvx疗法有限公司 | 用于增强cns药物并减轻它们的副作用的方法和组合物 |
-
2015
- 2015-04-22 ES ES15726362T patent/ES2811088T3/es active Active
- 2015-04-22 NZ NZ725921A patent/NZ725921A/en unknown
- 2015-04-22 SI SI201531316T patent/SI3134386T1/sl unknown
- 2015-04-22 CR CR20160544A patent/CR20160544A/es unknown
- 2015-04-22 MX MX2016013810A patent/MX2016013810A/es active IP Right Grant
- 2015-04-22 SG SG11201608785PA patent/SG11201608785PA/en unknown
- 2015-04-22 MY MYPI2016703862A patent/MY195742A/en unknown
- 2015-04-22 DK DK15726362.5T patent/DK3134386T3/da active
- 2015-04-22 EP EP15726362.5A patent/EP3134386B1/en active Active
- 2015-04-22 PE PE2016002118A patent/PE20161400A1/es unknown
- 2015-04-22 EA EA201692132A patent/EA030373B1/ru not_active IP Right Cessation
- 2015-04-22 JP JP2016564111A patent/JP6517239B2/ja active Active
- 2015-04-22 AR ARP150101206A patent/AR100154A1/es active IP Right Grant
- 2015-04-22 TN TN2016000455A patent/TN2016000455A1/en unknown
- 2015-04-22 PL PL15726362T patent/PL3134386T3/pl unknown
- 2015-04-22 US US15/306,012 patent/US9868725B2/en active Active
- 2015-04-22 KR KR1020167032435A patent/KR102349237B1/ko active IP Right Grant
- 2015-04-22 CA CA2946519A patent/CA2946519C/en active Active
- 2015-04-22 HU HUE15726362A patent/HUE050543T2/hu unknown
- 2015-04-22 UA UAA201611867A patent/UA122391C2/uk unknown
- 2015-04-22 UY UY0001036091A patent/UY36091A/es not_active Application Discontinuation
- 2015-04-22 LT LTEP15726362.5T patent/LT3134386T/lt unknown
- 2015-04-22 RS RS20200816A patent/RS60524B1/sr unknown
- 2015-04-22 CN CN201580034130.XA patent/CN106536508B/zh active Active
- 2015-04-22 BR BR112016024472-9A patent/BR112016024472B1/pt active IP Right Grant
- 2015-04-22 AU AU2015250610A patent/AU2015250610B2/en active Active
- 2015-04-22 PT PT157263625T patent/PT3134386T/pt unknown
- 2015-04-22 TW TW104112837A patent/TWI664165B/zh active
- 2015-04-22 WO PCT/JP2015/062912 patent/WO2015163485A1/en active Application Filing
- 2015-04-22 US US14/693,342 patent/US9315458B2/en active Active
-
2016
- 2016-02-02 US US15/013,675 patent/US9518042B2/en active Active
- 2016-02-02 US US15/013,625 patent/US9499516B2/en active Active
- 2016-10-12 US US15/291,769 patent/US9675597B2/en active Active
- 2016-10-19 CL CL2016002661A patent/CL2016002661A1/es unknown
- 2016-10-19 IL IL24839316A patent/IL248393B/en active IP Right Grant
- 2016-10-20 PH PH12016502095A patent/PH12016502095A1/en unknown
- 2016-10-20 DO DO2016000286A patent/DOP2016000286A/es unknown
- 2016-11-23 EC ECIEPI201690152A patent/ECSP16090152A/es unknown
- 2016-12-22 US US15/388,834 patent/US9655881B2/en active Active
- 2016-12-22 US US15/388,887 patent/US9662316B2/en active Active
-
2017
- 2017-04-14 US US15/488,002 patent/US9775827B2/en active Active
- 2017-05-30 US US15/608,557 patent/US9789083B2/en active Active
- 2017-05-30 US US15/608,565 patent/US9789084B2/en active Active
- 2017-08-24 US US15/685,800 patent/US20180000780A1/en not_active Abandoned
- 2017-12-04 US US15/830,634 patent/US10457670B2/en active Active
-
2018
- 2018-12-04 US US16/209,349 patent/US10865200B2/en active Active
-
2020
- 2020-07-27 HR HRP20201171TT patent/HRP20201171T1/hr unknown
- 2020-07-27 CY CY20201100688T patent/CY1123569T1/el unknown
- 2020-09-30 US US17/038,917 patent/US20210009572A1/en not_active Abandoned
-
2022
- 2022-07-25 US US17/872,680 patent/US20220411413A1/en not_active Abandoned
-
2023
- 2023-11-08 US US18/504,741 patent/US20240109874A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR100154A1 (es) | Compuesto heterocíclico que contiene nitrógeno | |
UY35377A (es) | Compuestos de 1,3-oxazin-2-amina fusionados con ciclopropilo perfluorado como inhibidores de beta-secretasa y métodos de uso | |
AR095823A1 (es) | Compuesto de ciclopropanamina y uso del mismo | |
CY1119707T1 (el) | Ενωσεις διαρυλικου αμιδιου ως αναστολεις της κινασης | |
BR112018070602A2 (pt) | composto, composição farmacêutica, uso do composto, e, método para tratar uma doença ou distúrbio | |
AR094277A1 (es) | Derivados de fumarato sustituidos con deuterio | |
CR20170568A (es) | Compuesto heterocíclico | |
EA201690044A1 (ru) | Модуляторы ядерного транспорта и их применение | |
BR112017010354A2 (pt) | compostos de triazolopirimidina e usos dos mesmos | |
CY1124022T1 (el) | Σχημα χορηγησης για νιτροκατεχολες | |
BR112015009850A2 (pt) | compostos de piridila substituídos por heteroarila úteis como moduladores de quinase | |
UY36263A (es) | Compuestos de tiazin-2-amina fusionados con ciclopropilo como inhibidores de beta-secretasa y métodos de uso | |
CO2017001178A2 (es) | Derivado de piridona que tiene un grupo tetrahidropiranil metilo | |
PE20160523A1 (es) | Derivados de arilo o heteroarilo como inhibidores de moleculas pequenas de fibrosis | |
CY1119583T1 (el) | Φαινοξυαιθυλο παραγωγα κυκλικης αμινης και η δραστικοτητα τους ως τροποποιητες του ερ4 υποδοχεα | |
CU20170007A7 (es) | Compuestos de imidazopiridazina | |
AR097932A1 (es) | Antagonista del receptor de somatostatina del subtipo 5 (sstr5) | |
SV2016005293A (es) | Compuestos de azol amido-sustituidos como inhibidores de tnks1 y/o tnks2 | |
AR104539A1 (es) | Compuestos cíclicos | |
AR099880A1 (es) | Derivados de nicotinamida como moduladores de trpa1 | |
EA201792670A1 (ru) | Производные 2-(1-гетероарилпиперазин-4-ил)метил-1,4- бензодиоксана в качестве альфа2c-антагонистов | |
AR105106A1 (es) | Derivados de 1,3-oxazin-4-ona como moduladores alostéricos del receptor muscarínico colinérgico m1 | |
AR088236A1 (es) | Derivado de sulfonamida y sus usos | |
CL2017000242A1 (es) | Compuestos de imidazopiridazina | |
AR099145A1 (es) | Compuesto de pirazolo-pirimidina con acción inhibidora de pde2a |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration |