EA200601982A1 - Производные аминопиридина в качестве селективных агонистов d3 - дофаминовых рецепторов - Google Patents

Производные аминопиридина в качестве селективных агонистов d3 - дофаминовых рецепторов

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Publication number
EA200601982A1
EA200601982A1 EA200601982A EA200601982A EA200601982A1 EA 200601982 A1 EA200601982 A1 EA 200601982A1 EA 200601982 A EA200601982 A EA 200601982A EA 200601982 A EA200601982 A EA 200601982A EA 200601982 A1 EA200601982 A1 EA 200601982A1
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EA
Eurasian Patent Office
Prior art keywords
disorder
disorders
sexual dysfunction
sex
selective
Prior art date
Application number
EA200601982A
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English (en)
Inventor
Шарлотта Мойра Норфор Аллертон
Эндрю Саймон Кук
Дейвид Хепуорт
Дункан Чарльз Миллер
Original Assignee
Пфайзер Инк.
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34970000&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EA200601982(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from GB0411891A external-priority patent/GB0411891D0/en
Priority claimed from GB0412463A external-priority patent/GB0412463D0/en
Application filed by Пфайзер Инк. filed Critical Пфайзер Инк.
Publication of EA200601982A1 publication Critical patent/EA200601982A1/ru

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    • 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
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    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

В настоящем изобретении предложены соединения формулы (I), которые представляют собой класс агонистов дофамина, более конкретно, класс агонистов, которые являются более селективными в отношении D3 по сравнению с D2. Эти соединения являются полезными для лечения и/или предотвращения сексуальной дисфункции, например женской сексуальной дисфункции (FSD), в частности расстройства женского полового возбуждения (FSAD), гипоактивного расстройства полового влечения (HSDD; отсутствие интереса к сексу), женского оргазмического расстройства (FOD; неспособность достижения оргазма); и мужской сексуальной дисфункции, в частности мужской эректильной дисфункции (MED). Мужская сексуальная дисфункция при упоминании здесь означает, что она включает эякуляторные расстройства, такие как преждевременная эякуляция, аноргазмия (неспособность достижения оргазма) или расстройства влечения, такие как гипоактивное расстройство полового влечения (HSDD; отсутствие интереса к сексу). Эти соединения также являются полезными в лечении нейропсихиатрических расстройств и нейродегенеративных расстройств.
EA200601982A 2004-05-27 2005-05-17 Производные аминопиридина в качестве селективных агонистов d3 - дофаминовых рецепторов EA200601982A1 (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0411891A GB0411891D0 (en) 2004-05-27 2004-05-27 New aminopyridine derivatives and their use as pharmaceuticals
GB0412463A GB0412463D0 (en) 2004-06-03 2004-06-03 New aminopyridine derivatives and their use as pharmaceuticals
PCT/IB2005/001554 WO2005115985A1 (en) 2004-05-27 2005-05-17 Aminopyridine derivatives as selective dopamine d3 agonists

Publications (1)

Publication Number Publication Date
EA200601982A1 true EA200601982A1 (ru) 2007-04-27

Family

ID=34970000

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200601982A EA200601982A1 (ru) 2004-05-27 2005-05-17 Производные аминопиридина в качестве селективных агонистов d3 - дофаминовых рецепторов

Country Status (21)

Country Link
EP (1) EP1758862A1 (ru)
JP (1) JP4198183B2 (ru)
AP (1) AP2006003824A0 (ru)
AR (1) AR049548A1 (ru)
AU (1) AU2005247699A1 (ru)
BR (1) BRPI0511571A (ru)
CA (1) CA2567935C (ru)
EA (1) EA200601982A1 (ru)
EC (1) ECSP067029A (ru)
GT (1) GT200500125A (ru)
IL (1) IL179314A0 (ru)
MA (1) MA28607B1 (ru)
MX (1) MXPA06013786A (ru)
NL (1) NL1029139C2 (ru)
NO (1) NO20065326L (ru)
PA (1) PA8635101A1 (ru)
PE (1) PE20060366A1 (ru)
SV (1) SV2005002129A (ru)
TW (1) TW200609216A (ru)
UY (1) UY28925A1 (ru)
WO (1) WO2005115985A1 (ru)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0502509D0 (en) * 2005-02-07 2005-03-16 Pfizer Ltd Novel salt form of a dopamine agonist
MX2011008583A (es) * 2009-02-13 2011-12-12 Bayer Pharma AG Pirimidinas fusionadas.
EP2558437B1 (en) * 2010-04-12 2015-08-05 Supernus Pharmaceuticals, Inc. Methods for producing viloxazine salts and novel polymorphs thereof
EP2726171B1 (en) 2011-06-30 2017-05-17 Donaldson Company, Inc. Air/oil separator assemblies
GB2543296A (en) * 2015-10-13 2017-04-19 Indivior Uk Ltd Dopamine D3 receptor antagonists having a morpholine moiety
EA037520B1 (ru) 2016-07-20 2021-04-07 Новартис Аг Производные аминопиридина и их применение в качестве селективных ингибиторов alk–2
EP3953350A1 (en) * 2019-04-12 2022-02-16 The United States of America, as Represented by The Department of Health and Human Services D3 receptor agonist compounds; methods of preparation; intermediates thereof; and methods of use thereof
EP4061367A1 (en) 2019-11-22 2022-09-28 Incyte Corporation Combination therapy comprising an alk2 inhibitor and a jak2 inhibitor
WO2021257532A1 (en) 2020-06-16 2021-12-23 Incyte Corporation Alk2 inhibitors for the treatment of anemia

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5077290A (en) * 1990-10-11 1991-12-31 Merck & Co., Inc. Morpholine derivatives compositions and use
GB0130219D0 (en) * 2001-12-18 2002-02-06 Pfizer Ltd Compounds for the treatment of sexual dysfunction
SI1572214T1 (sl) * 2002-12-10 2010-07-30 Pfizer Ltd Derivati morfolina za uporabo kot dopaminski agonisti pri zdravljenju med drugim spolne disfunkcije

Also Published As

Publication number Publication date
AU2005247699A1 (en) 2005-12-08
EP1758862A1 (en) 2007-03-07
CA2567935A1 (en) 2005-12-08
PA8635101A1 (es) 2006-05-16
GT200500125A (es) 2006-01-10
UY28925A1 (es) 2005-12-30
MXPA06013786A (es) 2007-01-25
PE20060366A1 (es) 2006-05-15
JP4198183B2 (ja) 2008-12-17
IL179314A0 (en) 2007-03-08
TW200609216A (en) 2006-03-16
NL1029139C2 (nl) 2006-06-19
MA28607B1 (fr) 2007-05-02
CA2567935C (en) 2009-10-27
AR049548A1 (es) 2006-08-16
BRPI0511571A (pt) 2008-01-02
JP2008500331A (ja) 2008-01-10
NO20065326L (no) 2006-12-19
ECSP067029A (es) 2006-12-29
NL1029139A1 (nl) 2005-11-30
SV2005002129A (es) 2005-12-13
AP2006003824A0 (en) 2006-12-31
WO2005115985A1 (en) 2005-12-08

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