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EA200501122A1 - Замещенные алкиламидопиперидины - Google Patents

Замещенные алкиламидопиперидины

Info

Publication number
EA200501122A1
EA200501122A1 EA200501122A EA200501122A EA200501122A1 EA 200501122 A1 EA200501122 A1 EA 200501122A1 EA 200501122 A EA200501122 A EA 200501122A EA 200501122 A EA200501122 A EA 200501122A EA 200501122 A1 EA200501122 A1 EA 200501122A1
Authority
EA
Eurasian Patent Office
Prior art keywords
subject
relates
pharmaceutically acceptable
pharmaceutical composition
acceptable carrier
Prior art date
Application number
EA200501122A
Other languages
English (en)
Other versions
EA009818B1 (ru
Inventor
Мохаммад Р. Марзабади
Джон М. Ветцель
Чиен-Ан Чен
Ю Дзианг
Каи Лу
Original Assignee
Х. Лундбекк А/С
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.)
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Publication date
Application filed by Х. Лундбекк А/С filed Critical Х. Лундбекк А/С
Publication of EA200501122A1 publication Critical patent/EA200501122A1/ru
Publication of EA009818B1 publication Critical patent/EA009818B1/ru

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
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    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/26Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P25/00Drugs for disorders of the nervous system
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    • A61P3/00Drugs for disorders of the metabolism
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    • A61P7/12Antidiuretics, e.g. drugs for diabetes insipidus
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    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/26Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms
    • C07D211/28Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms to which a second hetero atom is attached
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    • C07D211/80Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D211/84Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
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    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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    • C07D401/02Heterocyclic 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
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Animal Behavior & Ethology (AREA)
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  • Neurology (AREA)
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  • Diabetes (AREA)
  • Biomedical Technology (AREA)
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  • Obesity (AREA)
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  • Pain & Pain Management (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Данное изобретение относится к соединениям, которые представляют собой селективные антагонисты рецепторов меланин-концентрирующего гормона-1 (MCH1). Изобретение относится к фармацевтической композиции, включающей терапевтически эффективное количество соединения по изобретению и фармацевтически приемлемый носитель. Изобретение относится к фармацевтической композиции, полученной объединением терапевтически эффективного количества соединения по данному изобретению и фармацевтически приемлемого носителя. Данное изобретение дополнительно относится к способу получения фармацевтической композиции, включающему объединение терапевтически эффективного количества соединения по данному изобретению и фармацевтически приемлемого носителя. Данное изобретение также относится к способу снижения массы тела у субъекта, включающему введение субъекту соединения по изобретению в количестве, эффективном для снижения массы тела субъекта, данное изобретение дополнительно относится к способу лечения субъекта, страдающего от депрессии и/или тревожного состояния, включающему введение субъекту соединения по изобретению в количестве, эффективном для лечения депрессии и/или тревожного состояния у субъекта.Отчет о международном поиске был опубликован 2005.01.13.
EA200501122A 2003-01-14 2004-01-06 Замещенные алкиламидопиперидины EA009818B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/345,063 US7105544B2 (en) 2001-07-05 2003-01-14 Substituted alkyl amido piperidines
PCT/US2004/000175 WO2004064764A2 (en) 2003-01-14 2004-01-06 Substituted alkyl amido piperidines

Publications (2)

Publication Number Publication Date
EA200501122A1 true EA200501122A1 (ru) 2006-02-24
EA009818B1 EA009818B1 (ru) 2008-04-28

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EA200501122A EA009818B1 (ru) 2003-01-14 2004-01-06 Замещенные алкиламидопиперидины

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US (2) US7105544B2 (ru)
EP (1) EP1590326A4 (ru)
JP (1) JP2006515618A (ru)
KR (1) KR20060002747A (ru)
CN (1) CN1735595A (ru)
AR (1) AR042839A1 (ru)
AU (1) AU2004206794A1 (ru)
BR (1) BRPI0406725A (ru)
CA (1) CA2509456A1 (ru)
CL (1) CL2004000064A1 (ru)
CO (1) CO5590901A2 (ru)
EA (1) EA009818B1 (ru)
IL (1) IL169637A0 (ru)
IS (1) IS7860A (ru)
MX (1) MXPA05006956A (ru)
NO (1) NO20053838L (ru)
NZ (1) NZ540366A (ru)
PL (1) PL378394A1 (ru)
UA (1) UA79659C2 (ru)
WO (1) WO2004064764A2 (ru)
ZA (1) ZA200504218B (ru)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7105544B2 (en) * 2001-07-05 2006-09-12 Synaptic Pharmaceutical Corporation Substituted alkyl amido piperidines
WO2003099266A2 (en) * 2002-05-23 2003-12-04 Abbott Laboratories Acetamides and benzamides that are useful in treating sexual dysfunction
US20040029887A1 (en) * 2002-05-23 2004-02-12 Bhatia Pramila A. Acetamides and benzamides that are useful in treating sexual dysfunction
US20060009461A1 (en) * 2002-05-23 2006-01-12 Bhatia Pramila A Acetamides and benzamides that are useful in treating sexual dysfunction
AU2004209505B2 (en) * 2003-02-10 2009-07-23 Banyu Pharmaceutical Co., Ltd. Melanin-concentrating hormone receptor antagonists containing piperidine derivatives as the active ingredient
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IL169637A0 (en) 2007-07-04
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US20060217418A1 (en) 2006-09-28
UA79659C2 (en) 2007-07-10
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