JP2006517912A5 - - Google Patents

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Publication number
JP2006517912A5
JP2006517912A5 JP2004564205A JP2004564205A JP2006517912A5 JP 2006517912 A5 JP2006517912 A5 JP 2006517912A5 JP 2004564205 A JP2004564205 A JP 2004564205A JP 2004564205 A JP2004564205 A JP 2004564205A JP 2006517912 A5 JP2006517912 A5 JP 2006517912A5
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JP
Japan
Prior art keywords
heteroaryl
unsubstituted
substituted
alkyl
twice
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2004564205A
Other languages
English (en)
Japanese (ja)
Other versions
JP4764009B2 (ja
JP2006517912A (ja
Filing date
Publication date
Priority claimed from DE10300015A external-priority patent/DE10300015A1/de
Application filed filed Critical
Publication of JP2006517912A publication Critical patent/JP2006517912A/ja
Publication of JP2006517912A5 publication Critical patent/JP2006517912A5/ja
Application granted granted Critical
Publication of JP4764009B2 publication Critical patent/JP4764009B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2004564205A 2003-01-03 2003-12-19 マトリックスメタロプロテイナーゼ阻害剤として使用するためのイミノ酸誘導体 Expired - Fee Related JP4764009B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE10300015.1 2003-01-03
DE10300015A DE10300015A1 (de) 2003-01-03 2003-01-03 Iminosäurederivate als Inhibitoren von Matrix-Metallproteinasen
PCT/EP2003/014611 WO2004060874A1 (de) 2003-01-03 2003-12-19 Iminosäurederivate als inhibitoren von matrix-metalloproteinasen

Publications (3)

Publication Number Publication Date
JP2006517912A JP2006517912A (ja) 2006-08-03
JP2006517912A5 true JP2006517912A5 (https=) 2007-01-25
JP4764009B2 JP4764009B2 (ja) 2011-08-31

Family

ID=32519590

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004564205A Expired - Fee Related JP4764009B2 (ja) 2003-01-03 2003-12-19 マトリックスメタロプロテイナーゼ阻害剤として使用するためのイミノ酸誘導体

Country Status (14)

Country Link
US (2) US20050004166A1 (https=)
EP (1) EP1585728B1 (https=)
JP (1) JP4764009B2 (https=)
AT (1) ATE458721T1 (https=)
AU (1) AU2003300535B2 (https=)
BR (1) BR0317894A (https=)
CA (1) CA2512346A1 (https=)
DE (2) DE10300015A1 (https=)
DK (1) DK1585728T3 (https=)
ES (1) ES2341612T3 (https=)
IL (1) IL169496A0 (https=)
MX (1) MXPA05006054A (https=)
PT (1) PT1585728E (https=)
WO (1) WO2004060874A1 (https=)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10344936A1 (de) * 2003-09-27 2005-04-21 Aventis Pharma Gmbh Bicyclische Iminosäurederivate als Inhibitoren von Matrix-Metalloproteinasen
DE102005015040A1 (de) * 2005-03-31 2006-10-05 Sanofi-Aventis Deutschland Gmbh Substituierte Tetrahydroisochinoline als MMP-Inhibitoren, Verfahren zu ihrer Herstellung und ihre Verwendung als Medikament
JP2009505962A (ja) * 2005-07-29 2009-02-12 バイエル・ヘルスケア・エルエルシー 肥満を治療するためのビフェニルアミノ酸誘導体の製造および使用
ES2549187T3 (es) 2008-07-14 2015-10-23 Novartis Ag Inhibidores selectivos de MMP-12 y MMP-13 basados en ácido hidroxámico
RU2646752C2 (ru) * 2016-02-25 2018-03-07 Федеральное государственное бюджетное научное учреждение "Научно-исследовательский институт фармакологии имени В.В. Закусова" Ингибиторы цинк-зависимых металлопротеиназ (ММП-2 и ММП-9) в ряду бензоиламино(фенилсульфонил)-замещенных циклических аминокислот как потенциальные лекарственные средства, препятствующие постинфарктному ремоделированию левого желудочка сердца

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5455258A (en) 1993-01-06 1995-10-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
IT1264447B1 (it) 1993-05-14 1996-09-23 Ist Naz Stud Cura Dei Tumori Espressione di oncogeni derivati da ntrki in cellule di feocromocitoma pc12 ed utilizzo di questo sistema come screening di sostanze di
US5863949A (en) 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
KR100266467B1 (ko) * 1995-09-27 2000-10-02 우에노 도시오 설폰아미드 유도체
RU2164914C2 (ru) * 1995-11-13 2001-04-10 Хехст Акциенгезелльшафт ЦИКЛИЧЕСКИЕ И ГЕТЕРОЦИКЛИЧЕСКИЕ N-ЗАМЕЩЕННЫЕ α-ИМИНОГИДРОКСАМОВЫЕ И КАРБОНОВЫЕ КИСЛОТЫ
WO2000058304A1 (en) * 1999-03-26 2000-10-05 Shionogi & Co., Ltd. Heterocyclic sulfonamide derivatives
AR027943A1 (es) * 2000-02-25 2003-04-16 Wyeth Corp Acidos orto-sulfonamido aril hidroxamicos como inhibidores de metaloproteinasa de matriz y preparacion de los mismos
US6855708B2 (en) 2001-03-20 2005-02-15 Merck & Co., Inc. N-arylsulfonyl aza-bicyclic derivatives as potent cell adhesion inhibitors

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