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PE20160040A1 - Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a - Google Patents

Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a

Info

Publication number
PE20160040A1
PE20160040A1 PE2015001893A PE2015001893A PE20160040A1 PE 20160040 A1 PE20160040 A1 PE 20160040A1 PE 2015001893 A PE2015001893 A PE 2015001893A PE 2015001893 A PE2015001893 A PE 2015001893A PE 20160040 A1 PE20160040 A1 PE 20160040A1
Authority
PE
Peru
Prior art keywords
new type
inhibiting compounds
phosphodiesterase inhibiting
cyc3
cyc1
Prior art date
Application number
PE2015001893A
Other languages
English (en)
Inventor
Jurgen Dinges
Karla Drescher
Jayne Froggett
Michael Ochse
Clarissa Jakob
Katja Jantos
Herve Geneste
Original Assignee
AbbVie Deutschland GmbH and Co KG
Abbvie Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=50241454&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20160040(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by AbbVie Deutschland GmbH and Co KG, Abbvie Inc filed Critical AbbVie Deutschland GmbH and Co KG
Publication of PE20160040A1 publication Critical patent/PE20160040A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Psychology (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Epidemiology (AREA)

Abstract

Compuestos de la formula I, los N-oxidos, tautomeros, y las sales farmaceuticamente aceptables de los mismos; que son inhibidores de la fosfodiesterasa tipo 10. Donde Q es O o S; X1 es N o CH; X2 es O o S; R1 es Y1-Cyc1; R2 es hidrogeno, halogeno, etc.; R3 es Y3-Cyc3, R4 es C1-C4 alquilo, etc.; Y1 , Y3 es enlace, CH2, etc.; Cyc1; Cyc3 son fenilo, etc. Compuestos preferidos son: 5-metil-3-(oxetan-3-ilamino)-7-(piridin-4-il)tieno[2,3-d]piridazin-4(5H)-ona; 5-metil-3-(morfolin-4-il)-7-(piridin-4-il)tieno[2,3-d]piridazin-4(5H)-ona
PE2015001893A 2013-03-13 2014-03-12 Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a PE20160040A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201361779141P 2013-03-13 2013-03-13

Publications (1)

Publication Number Publication Date
PE20160040A1 true PE20160040A1 (es) 2016-02-11

Family

ID=50241454

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2015001893A PE20160040A1 (es) 2013-03-13 2014-03-12 Nuevos compuestos inhibidores de la fosfodiesterasa del tipo 10a

Country Status (22)

Country Link
US (1) US9200005B2 (es)
EP (1) EP2970328B1 (es)
JP (1) JP2016510786A (es)
KR (1) KR20150127724A (es)
CN (1) CN105358561A (es)
AR (1) AR095267A1 (es)
AU (1) AU2014230825A1 (es)
BR (1) BR112015022094A2 (es)
CA (1) CA2902654A1 (es)
CL (1) CL2015002545A1 (es)
CR (1) CR20150496A (es)
DO (1) DOP2015000214A (es)
HK (1) HK1219273A1 (es)
IL (1) IL240593A0 (es)
MX (1) MX2015012389A (es)
PE (1) PE20160040A1 (es)
PH (1) PH12015501962A1 (es)
RU (1) RU2015143536A (es)
SG (1) SG11201507380PA (es)
TW (1) TW201441230A (es)
UY (1) UY35393A (es)
WO (1) WO2014140086A1 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2852054T3 (es) 2013-03-15 2021-09-10 Global Blood Therapeutics Inc Compuestos y usos de los mismos para la modulación de hemoglobina
EA202092627A1 (ru) 2013-11-18 2021-09-30 Глобал Блад Терапьютикс, Инк. Соединения и их применения для модуляции гемоглобина
JP6767969B2 (ja) 2014-09-05 2020-10-14 ジェネンテック, インコーポレイテッド がんの処置における使用のためのpcafおよびgcn5阻害剤としての式(i)のフタラジン誘導体
CN107074823B (zh) 2014-09-05 2021-05-04 基因泰克公司 治疗性化合物及其用途
CN107406429B (zh) 2015-01-09 2021-07-06 基因泰克公司 哒嗪酮衍生物及其在治疗癌症中的用途
CN111182898B (zh) * 2017-06-28 2024-04-16 Ptc医疗公司 用于治疗亨廷顿氏病的方法
CN115838364A (zh) * 2022-12-20 2023-03-24 河南沁朋科技有限公司 一种3,3-双噻吩的合成方法
TW202506660A (zh) * 2023-04-27 2025-02-16 美商塞普特納公司 Mrgprx2拮抗劑及其使用方法

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US20030032579A1 (en) 2001-04-20 2003-02-13 Pfizer Inc. Therapeutic use of selective PDE10 inhibitors
SE0300120D0 (sv) * 2003-01-17 2003-01-17 Astrazeneca Ab Novel compounds
CA2534432A1 (en) 2003-07-31 2005-02-10 Bayer Pharmaceuticals Corporation Methods for treating diabetes and related disorders using pde10a inhibitors
MXPA06014236A (es) 2004-06-07 2007-02-14 Pfizer Prod Inc Inhibicion de la fosfodiesterasa 10 como tratamiento para las afecciones relacionadas con el sindrome metabolico y con la obesidad.
AU2005282721A1 (en) 2004-09-03 2006-03-16 Memory Pharmaceuticals Corporation 4-substituted 4, 6-dialkoxy-cinnoline derivatives as phospodiesterase 10 inhibitors for the treatment of psychiatric or neurological syndroms
AU2006279548A1 (en) 2005-08-16 2007-02-22 Amgen, Inc. Phosphodiesterase 10 inhibitors
NL2000397C2 (nl) 2006-01-05 2007-10-30 Pfizer Prod Inc Bicyclische heteroarylverbindingen als PDE10 inhibitoren.
WO2007082546A1 (en) 2006-01-20 2007-07-26 H. Lundbeck A/S Use of tofisopam as a pde10a inhibitor
US20100222353A1 (en) 2006-01-27 2010-09-02 Pfizer Products Inc. Aminophthalazine derivative compounds
MX2008010668A (es) 2006-02-21 2008-10-01 Amgen Inc Derivados de cinolina como inhibidores de fosfodiesterasa 10.
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EP1996587A1 (en) 2006-02-23 2008-12-03 Pfizer Products Incorporated Substituted quinazolines as pde10 inhibitors
US20070287707A1 (en) 2006-02-28 2007-12-13 Arrington Mark P Phosphodiesterase 10 inhibitors
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Also Published As

Publication number Publication date
US20140275069A1 (en) 2014-09-18
MX2015012389A (es) 2016-03-03
IL240593A0 (en) 2015-09-24
KR20150127724A (ko) 2015-11-17
PH12015501962A1 (en) 2016-01-11
BR112015022094A2 (pt) 2018-06-12
WO2014140086A1 (en) 2014-09-18
AR095267A1 (es) 2015-09-30
SG11201507380PA (en) 2015-10-29
CR20150496A (es) 2016-02-19
HK1219273A1 (zh) 2017-03-31
CN105358561A (zh) 2016-02-24
JP2016510786A (ja) 2016-04-11
AU2014230825A1 (en) 2015-09-03
RU2015143536A (ru) 2017-04-18
TW201441230A (zh) 2014-11-01
CA2902654A1 (en) 2014-09-18
EP2970328A1 (en) 2016-01-20
CL2015002545A1 (es) 2016-07-22
DOP2015000214A (es) 2015-12-31
UY35393A (es) 2014-10-31
EP2970328B1 (en) 2017-04-26
US9200005B2 (en) 2015-12-01

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