[go: up one dir, main page]

AR087700A1 - Inhibidores de aldh-2 en el tratamiento de adicciones - Google Patents

Inhibidores de aldh-2 en el tratamiento de adicciones

Info

Publication number
AR087700A1
AR087700A1 ARP120103172A ARP120103172A AR087700A1 AR 087700 A1 AR087700 A1 AR 087700A1 AR P120103172 A ARP120103172 A AR P120103172A AR P120103172 A ARP120103172 A AR P120103172A AR 087700 A1 AR087700 A1 AR 087700A1
Authority
AR
Argentina
Prior art keywords
optionally substituted
alkyl
hydrogen
aldh
inhibitors
Prior art date
Application number
ARP120103172A
Other languages
English (en)
Original Assignee
Gilead Sciences 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
Application filed by Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of AR087700A1 publication Critical patent/AR087700A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/22Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
    • C07D311/26Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3
    • C07D311/34Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 3 only
    • C07D311/36Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 3 only not hydrogenated in the hetero ring, e.g. isoflavones
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/32Alcohol-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/34Tobacco-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/06Heterocyclic 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 linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/10Heterocyclic 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 linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/06Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Addiction (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Psychiatry (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Reivindicación 1: Un compuesto de la fórmula (1) donde: R¹ es alquilo opcionalmente sustituido, cicloalquilo opcionalmente sustituido, heterociclilo opcionalmente sustituido, heteroarilo opcionalmente sustituido o fenilo opcionalmente sustituido; R² es hidrógeno, alquilo opcionalmente sustituido, cicloalquilo opcionalmente sustituido o fenilo opcionalmente sustituido; R³ es hidrógeno, ciano, amino opcionalmente sustituido, alquilo, alcoxi o halo; y X, Y y Z se seleccionan de -CR⁴- y -N-, en el cual R⁴ es hidrógeno, alquilo, alcoxi inferior o halo; o una de sus sales farmacéuticamente aceptables. Reivindicación 10: Una composición farmacéutica que comprende una cantidad terapéuticamente eficaz del compuesto de la reivindicación 1 y uno o más vehículos farmacéuticamente aceptables.
ARP120103172A 2011-08-30 2012-08-28 Inhibidores de aldh-2 en el tratamiento de adicciones AR087700A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161529164P 2011-08-30 2011-08-30

Publications (1)

Publication Number Publication Date
AR087700A1 true AR087700A1 (es) 2014-04-09

Family

ID=46982916

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP120103172A AR087700A1 (es) 2011-08-30 2012-08-28 Inhibidores de aldh-2 en el tratamiento de adicciones

Country Status (15)

Country Link
US (1) US8673966B2 (es)
EP (1) EP2751090A1 (es)
JP (1) JP2014525457A (es)
KR (1) KR20140057634A (es)
CN (1) CN103764640A (es)
AR (1) AR087700A1 (es)
AU (1) AU2012300209B2 (es)
BR (1) BR112014004943A2 (es)
CA (1) CA2845796A1 (es)
EA (1) EA201490270A1 (es)
HK (1) HK1199729A1 (es)
IL (1) IL230746A0 (es)
MX (1) MX2014002270A (es)
TW (1) TWI468403B (es)
WO (1) WO2013033377A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL3341355T3 (pl) * 2015-10-09 2021-03-08 Northwestern University Kwas (S)-3-amino-4-(difluorometylenylo)cyklopent-1-eno-1-karboksylowy i związki pokrewne jako dezaktywatory aminotransferazy GABA do leczenia padaczki, uzależnienia oraz raka wątrobowokomórkowego
WO2023244574A1 (en) 2022-06-14 2023-12-21 Amygdala Neurosciences, Inc. Aldh-2 inhibitor compounds and methods of use
WO2023244563A1 (en) 2022-06-14 2023-12-21 Amygdala Neurosciences, Inc. Aldh-2 inhibitor compounds and methods of use

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US4326525A (en) 1980-10-14 1982-04-27 Alza Corporation Osmotic device that improves delivery properties of agent in situ
US5364620A (en) 1983-12-22 1994-11-15 Elan Corporation, Plc Controlled absorption diltiazem formulation for once daily administration
US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
US4992445A (en) 1987-06-12 1991-02-12 American Cyanamid Co. Transdermal delivery of pharmaceuticals
US5001139A (en) 1987-06-12 1991-03-19 American Cyanamid Company Enchancers for the transdermal flux of nivadipine
US4902514A (en) 1988-07-21 1990-02-20 Alza Corporation Dosage form for administering nilvadipine for treating cardiovascular symptoms
US5204369A (en) 1991-07-01 1993-04-20 The Endowment For Research In Human Biology Method for the inhibition of aldh-i useful in the treatment of alcohol dependence or alcohol abuse
WO1999058124A1 (en) * 1998-05-12 1999-11-18 The Endowment For Research In Human Biology, Inc. Methods and assays useful in the treatment of alcohol dependence or alcohol abuse
EP1645272A3 (en) * 1998-05-12 2008-11-05 The Endowment For Research In Human Biology, Inc. Daidzin derivatives for the treatment of alcohol dependence or alcohol abuse
CN1671373A (zh) * 2002-06-27 2005-09-21 人类生物研究基金公司 用于抑制aldh的化合物
JP2007297283A (ja) 2004-07-28 2007-11-15 Santen Pharmaceut Co Ltd 新規桂皮酸関連化合物
JP2011510072A (ja) * 2008-01-24 2011-03-31 ギリアード・パロ・アルト・インコーポレイテッド 嗜癖の処置におけるaldh−2インヒビター

Also Published As

Publication number Publication date
AU2012300209B2 (en) 2015-01-22
US8673966B2 (en) 2014-03-18
CN103764640A (zh) 2014-04-30
US20130231325A1 (en) 2013-09-05
TWI468403B (zh) 2015-01-11
JP2014525457A (ja) 2014-09-29
BR112014004943A2 (pt) 2017-03-21
WO2013033377A1 (en) 2013-03-07
HK1199729A1 (en) 2015-07-17
AU2012300209A1 (en) 2013-04-04
EP2751090A1 (en) 2014-07-09
CA2845796A1 (en) 2013-03-07
IL230746A0 (en) 2014-03-31
MX2014002270A (es) 2015-01-16
TW201331197A (zh) 2013-08-01
KR20140057634A (ko) 2014-05-13
EA201490270A1 (ru) 2014-10-30

Similar Documents

Publication Publication Date Title
AR108388A2 (es) Compuestos de oxazol sustituidos con indazol como inhibidores de pi3-quinasas
AR101815A1 (es) Compuestos y composiciones como inhibidores de quinasa
EA201300200A1 (ru) N-((6-аминопиридин-3-ил)метил)гетероарилкарбоксамиды в качестве ингибиторов калликреина в плазме
BR112014010407A2 (pt) compostos de azetidina, composições e seu uso como inibidores de hidrolase de epóxido solúvel
MX385616B (es) Inhibidores de cdk
AR091519A1 (es) Inhibidores pirrolopirazona de tanquirasa
UA111382C2 (uk) Інгібітори протеїнкінази
ECSP12012103A (es) Inhibidores de virus flaviviridae.
EA201400333A1 (ru) Бензонитрильные производные в качестве ингибиторов киназ
PE20140192A1 (es) Derivados de bencimidazol como inhibidores de cinasa pi3
EA201790661A3 (ru) Ингибиторы вируса гепатита c
PE20160200A1 (es) Inhibidores de bromodominios
PE20161073A1 (es) Amino-heteroaril-benzamidas como inhibidores de cinasa
AR097866A1 (es) Derivados de 4-azaindol
AR094911A1 (es) SALES DE DERIVADOS DE 2-AMINO-1-HIDROXIETIL-8-HIDROXIQUINOLIN-2(1H)-ONA QUE TIENEN ACTIVIDAD AGONISTA DEL RECEPTOR b2 ADRENÉRGICO ASÍ COMO ACTIVIDAD ANTAGONISTA DEL RECEPTOR MUSCARÍNICO M₃
ES2531056T3 (es) Espirociclos como inhibidores de 11-beta hidroxilesteroide deshidrogenasa tipo 1
PE20140863A1 (es) Compuestos de benceno sustituidos con arilo o heteroarilo
ES2662444T3 (es) Derivado de piridina
CR20110343A (es) Inhibidores de proteína cinasa
EA201490724A1 (ru) Замещенные соединения тетрагидроизохинолина в качестве ингибиторов фактора xia
AR085615A1 (es) Derivados de fluoropiridinona utiles como agentes antibacterianos y composiciones farmaceuticas que los contienen
CO6480931A2 (es) Sulfonamidas heterocíclicas, usos y composiciones farmacéuticas de las mismas.
AR094812A1 (es) Derivado de piridina monocíclico como inhibidor del fgfr
CR11483A (es) Inhibidores de peptido desformilasa
AR091271A1 (es) Pirrolopirimidona y pirrolopiridona, inhibidores de tanquirasa

Legal Events

Date Code Title Description
FB Suspension of granting procedure