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RU2002113759A - Соединения имидазола в качестве ингибиторов фосфодиэстеразы VII - Google Patents

Соединения имидазола в качестве ингибиторов фосфодиэстеразы VII

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Publication number
RU2002113759A
RU2002113759A RU2002113759/04A RU2002113759A RU2002113759A RU 2002113759 A RU2002113759 A RU 2002113759A RU 2002113759/04 A RU2002113759/04 A RU 2002113759/04A RU 2002113759 A RU2002113759 A RU 2002113759A RU 2002113759 A RU2002113759 A RU 2002113759A
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formula
compounds
diseases
imidazole
solvates
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RU2002113759/04A
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Ханс Михаэль ЭГГЕНВАЙЛЕР (DE)
Ханс Михаэль ЭГГЕНВАЙЛЕР
Рохус ЙОНАС (DE)
Рохус ЙОНАС
Михаэль ВОЛЬФ (DE)
Михаэль Вольф
Михаель ГАССЕН (DE)
Михаель ГАССЕН
Томас ВЕЛЬГЕ (DE)
Томас ВЕЛЬГЕ
Original Assignee
Мерк Патент ГмбХ (DE)
Мерк Патент Гмбх
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Publication of RU2002113759A publication Critical patent/RU2002113759A/ru

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    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/06Peri-condensed systems
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P31/04Antibacterial agents
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    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
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    • A61P37/00Drugs for immunological or allergic disorders
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    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/06Peri-condensed systems

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  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Urology & Nephrology (AREA)
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Claims (7)

1. Соединения имидазола формулы
Figure 00000001
в которых R1 и R2, независимо друг от друга, обозначают А1, ОА1, SA1
или Hal;
А1 обозначает Н, А, алкенил, циклоалкил или алкиленциклоалкил;
А обозначает алкил, содержащий 1-10 атомов углерода;
Hal обозначает F, CI, Вг или I;
Х обозначает О, S, SO или SO2,
и их физиологически приемлемые соли и/или сольваты.
2. Соединения имидазола формулы I по п.1 и их физиологически приемлемые соли и сольваты в качестве медицинских препаратов.
3. Медицинские препараты по п.2 для ингибирования фосфодиэстеразы VII.
4. Медицинские препараты по п.3 для лечения аллергических заболеваний, астмы, хронического бронхита, атопического дерматита, псориаза и других кожных заболеваний, воспалительных заболеваний, аутоиммунных болезней, таких, как, например, ревматоидный артрит, рассеянный склероз, болезнь Крона, сахарный диабет или язвенный колит, остеопороз, реакции отторжения трансплантированной ткани, кахексия, рост опухолей или опухолевых метастазов, сепсис, расстройства памяти, атеросклероз и СПИД.
5. Фармацевтические препараты, содержащие, по крайней мере, один медицинский препарат по одному из пп.3 и 4, которые могут содержать также эксципиенты и/или вспомогательные вещества и другие активные ингредиенты.
6. Применение соединений формулы I по п.1 и/или их физиологически приемлемых солей или сольватов в приготовлении медицинских препаратов для лечения аллергических заболеваний, астмы, хронического бронхита, атопического дерматита, псориаза и других кожных заболеваний, воспалительных заболеваний, аутоиммунных болезней, таких, как, например, ревматоидный артрит, рассеянный склероз, болезнь Крона, сахарный диабет или язвенный колит, остеопороз, реакции отторжения трансплантированной ткани, кахексия, рост опухолей или опухолевых метастазов, сепсис, расстройства памяти, атеросклероз и СПИД.
7. Способ получения соединений формулы I по п.1 и их солей, отличающийся тем, что проводят реакцию соединений формулы II
Figure 00000002
в которой R1, R2 и Х соответствуют приведенным выше определениям;
L обозначает Cl, Br, ОН, SCH3 или активную этерифицированную группу ОН, с имидазолом,
и/или соединение формулы I преобразуют в одну из его солей.
RU2002113759/04A 1999-11-13 2000-10-31 Соединения имидазола в качестве ингибиторов фосфодиэстеразы VII RU2002113759A (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19954707.6 1999-11-13
DE19954707A DE19954707A1 (de) 1999-11-13 1999-11-13 Imidazolverbindungen als Phosphodiesterase VII-Hemmer

Publications (1)

Publication Number Publication Date
RU2002113759A true RU2002113759A (ru) 2004-01-10

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US (1) US6884800B1 (ru)
EP (1) EP1228073B1 (ru)
JP (1) JP4819272B2 (ru)
KR (1) KR20020049051A (ru)
CN (1) CN1390222A (ru)
AR (1) AR026421A1 (ru)
AT (1) ATE245653T1 (ru)
AU (1) AU775886B2 (ru)
BR (1) BR0015487A (ru)
CA (1) CA2391087A1 (ru)
CZ (1) CZ20021474A3 (ru)
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DK (1) DK1228073T3 (ru)
ES (1) ES2200968T3 (ru)
HU (1) HUP0203422A3 (ru)
MX (1) MXPA02004728A (ru)
NO (1) NO20022232D0 (ru)
PL (1) PL355098A1 (ru)
PT (1) PT1228073E (ru)
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SK (1) SK6012002A3 (ru)
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ES2217956B1 (es) * 2003-01-23 2006-04-01 Almirall Prodesfarma, S.A. Nuevos derivados de 4-aminotieno(2,3-d)pirimidin-6-carbonitrilo.
EP2258357A3 (en) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
CA2620333A1 (en) 2005-08-26 2007-03-01 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
WO2007047978A2 (en) 2005-10-21 2007-04-26 Braincells, Inc. Modulation of neurogenesis by pde inhibition
EP1942879A1 (en) 2005-10-31 2008-07-16 Braincells, Inc. Gaba receptor mediated modulation of neurogenesis
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
WO2007134077A2 (en) 2006-05-09 2007-11-22 Braincells, Inc. 5 ht receptor mediated neurogenesis
JP2009536669A (ja) 2006-05-09 2009-10-15 ブレインセルス,インコーポレイティド アンジオテンシン調節による神経新生
KR20090064418A (ko) 2006-09-08 2009-06-18 브레인셀즈 인코퍼레이션 4-아실아미노피리딘 유도체 포함 조합물
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
US8637528B2 (en) * 2007-03-27 2014-01-28 Omeros Corporation Use of PDE7 inhibitors for the treatment of movement disorders
EP2139475B1 (en) * 2007-03-27 2014-12-17 Omeros Corporation PDE7 inhibitors for use in the treatment of movement disorders
DE102007047738A1 (de) * 2007-10-05 2009-04-09 Merck Patent Gmbh Imidazolderivate
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
US20120115849A1 (en) 2010-11-08 2012-05-10 Demopulos Gregory A Treatment of Addiction and Impulse-Control Disorders Using PDE7 Inhibitors
US9220715B2 (en) 2010-11-08 2015-12-29 Omeros Corporation Treatment of addiction and impulse-control disorders using PDE7 inhibitors
WO2013106547A1 (en) 2012-01-10 2013-07-18 President And Fellows Of Harvard College Beta-cell replication promoting compounds and methods of their use
JP7213863B2 (ja) 2017-07-12 2023-01-27 ダート・ニューロサイエンス・エルエルシー Pde7阻害剤としての置換ベンゾオキサゾール及びベンゾフラン化合物
EP4572765A1 (en) 2022-08-18 2025-06-25 Mitodicure GmbH Use of a therapeutic agent with phosphodiesterase-7 inhibitory activity for the treatment and prevention of diseases associated with chronic fatigue, exhaustion and/or exertional intolerance

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JP4819272B2 (ja) 2011-11-24
EP1228073A2 (de) 2002-08-07
MXPA02004728A (es) 2002-08-30
ES2200968T3 (es) 2004-03-16
WO2001036425A3 (de) 2002-01-10
WO2001036425A2 (de) 2001-05-25
DK1228073T3 (da) 2003-11-03
BR0015487A (pt) 2002-07-02
HUP0203422A2 (hu) 2003-02-28
NO20022232L (no) 2002-05-10
AU1390701A (en) 2001-05-30
CA2391087A1 (en) 2001-05-25
CZ20021474A3 (cs) 2002-07-17
AU775886B2 (en) 2004-08-19
JP2003514821A (ja) 2003-04-22
SK6012002A3 (en) 2002-09-10
EP1228073B1 (de) 2003-07-23
DE50003036D1 (de) 2003-08-28
DE19954707A1 (de) 2001-05-17
ZA200204729B (en) 2003-11-26
NO20022232D0 (no) 2002-05-10
HUP0203422A3 (en) 2004-12-28
ATE245653T1 (de) 2003-08-15
PT1228073E (pt) 2003-12-31
KR20020049051A (ko) 2002-06-24
PL355098A1 (en) 2004-04-05
CN1390222A (zh) 2003-01-08
AR026421A1 (es) 2003-02-12
US6884800B1 (en) 2005-04-26

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