EA200300947A1 - Арил и гетероарил мочевины в качестве ингибиторов chk1 для использования в качестве радиосенсибилизаторов и химиосенсибилизаторов - Google Patents
Арил и гетероарил мочевины в качестве ингибиторов chk1 для использования в качестве радиосенсибилизаторов и химиосенсибилизаторовInfo
- Publication number
- EA200300947A1 EA200300947A1 EA200300947A EA200300947A EA200300947A1 EA 200300947 A1 EA200300947 A1 EA 200300947A1 EA 200300947 A EA200300947 A EA 200300947A EA 200300947 A EA200300947 A EA 200300947A EA 200300947 A1 EA200300947 A1 EA 200300947A1
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- EA
- Eurasian Patent Office
- Prior art keywords
- sensitivers
- aryl
- chk1
- inhibitors
- radio
- Prior art date
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- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
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- A61K31/33—Heterocyclic compounds
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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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Abstract
Настоящее изобретение относится к сильнодействующим и селективным химиосенсибилизирующим агентам, полезным при лечении заболеваний и состояний, относящихся к повреждению ДНК или повреждениям в репликации ДНК. Настоящие соединения являются ингибиторами киназы точки контроля Chk1. Конкретно, арил- и гетероарилзамещенные производные мочевины демонстрируют значительную активность в ингибировании Chk1.Международная заявка была опубликована вместе с отчетом о международном поиске.
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US27312401P | 2001-03-02 | 2001-03-02 | |
PCT/US2002/006452 WO2002070494A1 (en) | 2001-03-02 | 2002-03-01 | Aryl and heteroaryl urea chk1 inhibitors for use as radiosensitizers and chamosensitizers |
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EA014954B1 EA014954B1 (ru) | 2011-04-29 |
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EA200300947A EA014954B1 (ru) | 2001-03-02 | 2002-03-01 | Арил и гетероарил мочевины в качестве ингибиторов chk1 для использования в качестве радиосенсибилизаторов и химиосенсибилизаторов |
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US6211164B1 (en) * | 2000-03-10 | 2001-04-03 | Abbott Laboratories | Antisense oligonucleotides of the human chk1 gene and uses thereof |
UA76977C2 (en) * | 2001-03-02 | 2006-10-16 | Icos Corp | Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers |
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