EA200900244A1 - Модуляторы активности хемокиновых рецепторов, их кристаллические формы и способ их получения - Google Patents
Модуляторы активности хемокиновых рецепторов, их кристаллические формы и способ их полученияInfo
- Publication number
- EA200900244A1 EA200900244A1 EA200900244A EA200900244A EA200900244A1 EA 200900244 A1 EA200900244 A1 EA 200900244A1 EA 200900244 A EA200900244 A EA 200900244A EA 200900244 A EA200900244 A EA 200900244A EA 200900244 A1 EA200900244 A1 EA 200900244A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- compounds
- crystalline forms
- receptor activity
- reception
- chemokine receptor
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/273—2-Pyrrolidones 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 other ring carbon atoms
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- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/72—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 spiro-condensed with carbocyclic rings
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Abstract
Настоящее изобретение включает новый антагонист или частичные агонисты/антагонисты МСР-1 рецепторной активности: N-((1R,2S,5R)-5-(изопропил(метил)амино)-2-((S)-2-оксо-3-(6-трифторметил)хиназолин-4-иламино)пирролидин-1-ил)циклогексил)ацетамид или его фармацевтически приемлемую соль, сольват или пролекарство, проявляющие неожиданное сочетание нужных фармакологических характеристик. Также охватываются кристаллические формы соединений по настоящему изобретению. Также целью данного изобретения являются фармацевтические композиции, содержащие эти соединения, и способы их применения в качестве агентов для лечения воспалительных заболеваний, аллергических, аутоиммунных, метаболических, раковых и/или сердечно-сосудистых заболеваний. Настоящее раскрытие также включает способ получения соединений формулы (I), включая N-((1R,2S,5R)-5-(изопропил(метил)амино)-2-((S)-2-оксо-3-(6-трифторметил)хиназолин-4-иламино)пирролидин-1-ил)циклогексил)ацетамид, где R, R, R, Rи структура (а) представлены в данном описании. Также в данное описание включаются соединения, применимые в способе получения в качестве интермедиатов.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83423506P | 2006-07-28 | 2006-07-28 | |
US89602607P | 2007-03-21 | 2007-03-21 | |
US11/782,704 US7671062B2 (en) | 2006-07-28 | 2007-07-25 | Modulators of chemokine receptor activity, crystalline forms and process |
PCT/US2007/074438 WO2008014381A2 (en) | 2006-07-28 | 2007-07-26 | Modulators of chemokine receptor activity, crystalline forms and process |
Publications (2)
Publication Number | Publication Date |
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EA200900244A1 true EA200900244A1 (ru) | 2009-08-28 |
EA014960B1 EA014960B1 (ru) | 2011-04-29 |
Family
ID=38823540
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200900244A EA014960B1 (ru) | 2006-07-28 | 2007-07-26 | Модуляторы активности хемокиновых рецепторов, их кристаллические формы и способ их получения |
Country Status (30)
Country | Link |
---|---|
US (1) | US7671062B2 (ru) |
EP (2) | EP2049477B1 (ru) |
JP (1) | JP2009544758A (ru) |
KR (1) | KR20090035036A (ru) |
CN (1) | CN101511822A (ru) |
AR (1) | AR062114A1 (ru) |
AT (1) | ATE471928T1 (ru) |
AU (1) | AU2007279256A1 (ru) |
BR (1) | BRPI0715066A2 (ru) |
CA (1) | CA2659259A1 (ru) |
CL (3) | CL2007002194A1 (ru) |
CO (1) | CO6190527A2 (ru) |
CY (1) | CY1110785T1 (ru) |
DE (1) | DE602007007335D1 (ru) |
DK (1) | DK2049477T3 (ru) |
EA (1) | EA014960B1 (ru) |
ES (1) | ES2346591T3 (ru) |
HK (1) | HK1125931A1 (ru) |
HR (1) | HRP20100371T1 (ru) |
IL (1) | IL196518A0 (ru) |
MX (1) | MX2009000803A (ru) |
NO (1) | NO20090256L (ru) |
NZ (1) | NZ574656A (ru) |
PE (1) | PE20080838A1 (ru) |
PL (1) | PL2049477T3 (ru) |
PT (1) | PT2049477E (ru) |
SG (1) | SG158925A1 (ru) |
SI (1) | SI2049477T1 (ru) |
TW (1) | TW200823203A (ru) |
WO (1) | WO2008014381A2 (ru) |
Families Citing this family (9)
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US7687508B2 (en) * | 2006-07-28 | 2010-03-30 | Bristol-Myers Squibb Company | Cyclic derivatives as modulators of chemokine receptor activity |
US8383812B2 (en) | 2009-10-13 | 2013-02-26 | Bristol-Myers Squibb Company | N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-3-(7-tert-butylpyrazolo[1,5-A][1,3,5]triazin-4-ylamino)-2-oxopyrrolidin-1-yl)cyclohexyl)acetamide, a dual modulator of chemokine receptor activity, crystalline forms and processes |
EP2567959B1 (en) | 2011-09-12 | 2014-04-16 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
RU2726206C2 (ru) * | 2015-05-21 | 2020-07-09 | Кемосентрикс, Инк. | Модуляторы ccr2 |
JP2020527576A (ja) * | 2017-07-20 | 2020-09-10 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | N−((1R,2S,5R)−5−(tert−ブチルアミノ)−2−((S)−3−(7−tert−ブチルピラゾロ[1,5−A][1,3,5]トリアジン−4−イルアミノ)−2−オキソピロリジン−1−イル)シクロヘキシル)アセトアミドの製造方法 |
US11304952B2 (en) | 2017-09-25 | 2022-04-19 | Chemocentryx, Inc. | Combination therapy using a chemokine receptor 2 (CCR2) antagonist and a PD-1/PD-L1 inhibitor |
US20190269664A1 (en) | 2018-01-08 | 2019-09-05 | Chemocentryx, Inc. | Methods of treating solid tumors with ccr2 antagonists |
EP3737367A4 (en) | 2018-01-08 | 2022-11-09 | ChemoCentryx, Inc. | METHODS OF TREATING SOLID TUMORS USING CCR2 ANTAGONISTS |
CN115494184B (zh) * | 2022-05-09 | 2023-07-28 | 浙江海正药业股份有限公司 | 一种同时检测药物中异丙苯磺酸甲酯、异丙苯磺酸乙酯的方法 |
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