MA35404B1 - Composés pour le traitement de la toxicomanie - Google Patents

Composés pour le traitement de la toxicomanie

Info

Publication number
MA35404B1
MA35404B1 MA36629A MA36629A MA35404B1 MA 35404 B1 MA35404 B1 MA 35404B1 MA 36629 A MA36629 A MA 36629A MA 36629 A MA36629 A MA 36629A MA 35404 B1 MA35404 B1 MA 35404B1
Authority
MA
Morocco
Prior art keywords
treatment
compounds
formula
drug addiction
dopamine
Prior art date
Application number
MA36629A
Other languages
English (en)
French (fr)
Inventor
Carina E Cannizzaro
Michael Graupe
Juan A Guerrero
Yafan Lu
Robert G Strickley
Chandrasekar Venkataramani
Jeff Zablocki
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 MA35404B1 publication Critical patent/MA35404B1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/66Phosphorus compounds
    • A61K31/675Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/64One oxygen atom attached in position 2 or 6
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4418Non condensed pyridines; Hydrogenated derivatives thereof having a carbocyclic group directly attached to the heterocyclic ring, e.g. cyproheptadine
    • 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
    • A61P25/30Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/553Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
    • C07F9/576Six-membered rings
    • C07F9/58Pyridine rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Addiction (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Psychiatry (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
MA36629A 2011-07-01 2013-12-30 Composés pour le traitement de la toxicomanie MA35404B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161503923P 2011-07-01 2011-07-01
PCT/US2012/044809 WO2013006400A1 (en) 2011-07-01 2012-06-29 Compounds for the treatment of addiction

Publications (1)

Publication Number Publication Date
MA35404B1 true MA35404B1 (fr) 2014-09-01

Family

ID=46513858

Family Applications (1)

Application Number Title Priority Date Filing Date
MA36629A MA35404B1 (fr) 2011-07-01 2013-12-30 Composés pour le traitement de la toxicomanie

Country Status (32)

Country Link
US (6) US8558001B2 (enExample)
EP (2) EP2993170B1 (enExample)
JP (1) JP5943998B2 (enExample)
KR (2) KR20160106207A (enExample)
CN (1) CN103635460B (enExample)
AP (1) AP3544A (enExample)
AR (1) AR086792A1 (enExample)
AU (1) AU2012279332B2 (enExample)
BR (1) BR112014000033A2 (enExample)
CA (1) CA2840763C (enExample)
CL (1) CL2013003597A1 (enExample)
CO (1) CO6821964A2 (enExample)
CR (1) CR20130659A (enExample)
DK (1) DK2993170T3 (enExample)
EA (1) EA025573B1 (enExample)
EC (1) ECSP13013087A (enExample)
ES (2) ES2553829T3 (enExample)
IL (1) IL230657B (enExample)
MA (1) MA35404B1 (enExample)
MD (1) MD4436B1 (enExample)
MX (1) MX337611B (enExample)
PE (1) PE20141067A1 (enExample)
PH (1) PH12013502674A1 (enExample)
PL (1) PL2726460T3 (enExample)
PT (1) PT2726460E (enExample)
SG (1) SG10201605355RA (enExample)
SI (1) SI2726460T1 (enExample)
TW (1) TWI567061B (enExample)
UA (1) UA109199C2 (enExample)
UY (1) UY34165A (enExample)
WO (1) WO2013006400A1 (enExample)
ZA (1) ZA201308977B (enExample)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012149106A1 (en) 2011-04-29 2012-11-01 The Board Of Trustees Of The Leland Stanford Junior University Compositions and methods for increasing proliferation of adult salivary stem cells
TWI510480B (zh) 2011-05-10 2015-12-01 Gilead Sciences Inc 充當離子通道調節劑之稠合雜環化合物
NO3175985T3 (enExample) 2011-07-01 2018-04-28
TWI549944B (zh) 2011-07-01 2016-09-21 吉李德科學股份有限公司 作為離子通道調節劑之稠合雜環化合物
TWI567061B (zh) 2011-07-01 2017-01-21 吉李德科學股份有限公司 用於治療成癮之化合物
KR20150135332A (ko) 2013-03-14 2015-12-02 더 보드 오브 트러스티스 오브 더 리랜드 스탠포드 쥬니어 유니버시티 미토콘드리아 알데히드 탈수소효소-2 조절인자들 및 이들의 사용 방법
LT3080134T (lt) * 2013-12-13 2018-11-12 Vertex Pharmaceuticals Incorporated Piridono amidų provaistai, naudotini kaip natrio kanalų moduliatoriai
US10077669B2 (en) 2014-11-26 2018-09-18 United Technologies Corporation Non-metallic engine case inlet compression seal for a gas turbine engine
US10289971B2 (en) 2015-02-13 2019-05-14 Atlassian Pty Ltd Issue and trigger rebalancing in a ranked issue management system
HUE061016T2 (hu) 2016-08-19 2023-05-28 Univ Bristol Citizin-származékok a szenvedélybetegségek kezelésére
JOP20180040A1 (ar) 2017-04-20 2019-01-30 Gilead Sciences Inc مثبطات pd-1/pd-l1
KR20200070273A (ko) * 2017-10-16 2020-06-17 아미그달라 뉴로사이언시즈, 인크. 중독을 예방하기 위한 병용 요법
SI3752501T1 (sl) 2018-02-13 2023-08-31 Gilead Sciences, Inc. Inhibitorji pd-1/pd-l1
CA3093130C (en) 2018-04-19 2023-10-17 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
DK3793565T3 (en) 2018-05-14 2022-03-07 Gilead Sciences Inc Mcl-1-inhibitorer
SI3820572T1 (sl) 2018-07-13 2023-12-29 Gilead Sciences, Inc. Inhibitorji pd-1/pd-l1
EP3829562A1 (en) * 2018-07-27 2021-06-09 Amygdala Neurosciences, Inc. Combination therapy for nicotine addiction
WO2020076974A1 (en) * 2018-10-12 2020-04-16 Amygdala Neurosciences, Inc. Addiction treatment of an alcohol-consuming patient population
JP7158577B2 (ja) 2018-10-24 2022-10-21 ギリアード サイエンシーズ, インコーポレイテッド Pd-1/pd-l1阻害剤
US12029718B2 (en) 2021-11-09 2024-07-09 Cct Sciences, Llc Process for production of essentially pure delta-9-tetrahydrocannabinol
JP2025520426A (ja) 2022-06-14 2025-07-03 アミグダラ ニューロサイエンシーズ, インコーポレイテッド Aldh-2阻害化合物及び使用方法
US20230399299A1 (en) 2022-06-14 2023-12-14 Amygdala Neurosciences, Inc. Aldh-2 inhibitor compounds and methods of use

Family Cites Families (22)

* 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
AU3899199A (en) 1998-05-12 1999-11-29 Endowment for Research in Human Biology, Inc., The Methods and assays useful in the treatment of alcohol dependence or alcohol abuse
MXPA05000122A (es) 2002-06-27 2005-12-14 Endowment For Res In Human Bio Compuestos utiles para la inhibicion de aldehido-deshidrogenasa.
JP2004182657A (ja) * 2002-12-04 2004-07-02 Eisai Co Ltd Hdlレベル上昇促進剤
US20080004260A1 (en) 2006-06-29 2008-01-03 Transcept Pharmaceuticals, Inc. Compositions of 5-HT3 antagonists and dopamine D2 antagonists for treatment of dopamine-associated chronic conditions
WO2008014497A2 (en) 2006-07-27 2008-01-31 Cv Therapeutics, Inc. Aldh-2 inhibitors in the treatment of addiction
US20080207610A1 (en) 2006-07-27 2008-08-28 Jeff Zablocki Aldh-2 inhibitors in the treatment of addiction
US8158810B2 (en) 2006-07-27 2012-04-17 Gilead Sciences, Inc. ALDH-2 inhibitors in the treatment of addiction
EP2126574B1 (en) 2007-03-08 2015-12-23 The Board of Trustees of the Leland Stanford Junior University Mitochondrial aldehyde dehydrogenase-2 modulators and methods of use thereof
CN101925590A (zh) 2008-01-24 2010-12-22 吉利德帕洛阿尔托股份有限公司 治疗成瘾的aldh-2抑制剂
JP5301563B2 (ja) 2008-05-01 2013-09-25 ヴァイティー ファーマシューティカルズ,インコーポレイテッド 11β−ヒドロキシステロイドデヒドロゲナーゼ1の環状インヒビター
ES2477552T3 (es) 2008-09-08 2014-07-17 The Board Of Trustees Of The Leland Stanford Junior University Moduladores de la actividad de la aldehidodeshidrogenasa y métodos de uso de los mismos
KR20110082180A (ko) * 2008-10-28 2011-07-18 더 보드 오브 트러스티스 오브 더 리랜드 스탠포드 쥬니어 유니버시티 알데히드 탈수소효소의 조절자 및 그것의 사용방법
UY33469A (es) * 2010-06-29 2012-01-31 Irm Llc Y Novartis Ag Composiciones y metodos para modular la via de señalizacion de wnt
TWI567061B (zh) 2011-07-01 2017-01-21 吉李德科學股份有限公司 用於治療成癮之化合物

Also Published As

Publication number Publication date
MD20140009A2 (ro) 2014-06-30
KR20140042884A (ko) 2014-04-07
WO2013006400A1 (en) 2013-01-10
KR20160106207A (ko) 2016-09-09
MD4436B1 (ro) 2016-09-30
DK2993170T3 (da) 2018-01-29
US20170266210A1 (en) 2017-09-21
MX2013014938A (es) 2014-04-30
EP2993170A1 (en) 2016-03-09
AP3544A (en) 2016-01-14
EP2726460A1 (en) 2014-05-07
US20130203704A1 (en) 2013-08-08
US9610299B2 (en) 2017-04-04
ZA201308977B (en) 2014-08-27
US9000015B2 (en) 2015-04-07
US20130005689A1 (en) 2013-01-03
NZ618537A (en) 2016-03-31
SG10201605355RA (en) 2016-08-30
PL2726460T3 (pl) 2016-03-31
AU2012279332A1 (en) 2013-04-04
EA025573B1 (ru) 2017-01-30
JP2014520809A (ja) 2014-08-25
KR101664915B1 (ko) 2016-10-11
US20140051668A1 (en) 2014-02-20
BR112014000033A2 (pt) 2019-06-18
PH12013502674A1 (en) 2014-02-10
US8558001B2 (en) 2013-10-15
EP2726460B1 (en) 2015-09-23
EA201391635A1 (ru) 2014-04-30
IL230657A0 (en) 2014-03-31
HK1217487A1 (en) 2017-01-13
US8575353B2 (en) 2013-11-05
TWI567061B (zh) 2017-01-21
CA2840763C (en) 2019-09-10
UA109199C2 (uk) 2015-07-27
PT2726460E (pt) 2015-12-07
ES2656716T3 (es) 2018-02-28
UY34165A (es) 2013-01-31
US10507215B2 (en) 2019-12-17
AP2013007282A0 (en) 2013-11-30
CN103635460A (zh) 2014-03-12
ES2553829T3 (es) 2015-12-14
HK1197236A1 (en) 2015-01-09
US20150250805A1 (en) 2015-09-10
PE20141067A1 (es) 2014-09-05
ECSP13013087A (es) 2014-01-31
AU2012279332B2 (en) 2015-02-05
CO6821964A2 (es) 2013-12-31
TW201307288A (zh) 2013-02-16
JP5943998B2 (ja) 2016-07-05
CN103635460B (zh) 2016-03-16
US9987295B2 (en) 2018-06-05
CR20130659A (es) 2014-02-18
AR086792A1 (es) 2014-01-22
SI2726460T1 (sl) 2015-11-30
EP2993170B1 (en) 2017-10-25
MX337611B (es) 2016-03-10
CA2840763A1 (en) 2013-01-10
US20180338989A1 (en) 2018-11-29
IL230657B (en) 2018-02-28
CL2013003597A1 (es) 2014-06-13

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