EE200200132A - Uudsed spiroheterotsüklilised ühendid, mis on kasulikud tsüsteiinproteaaside pöörduvate inhibiitoritena - Google Patents

Uudsed spiroheterotsüklilised ühendid, mis on kasulikud tsüsteiinproteaaside pöörduvate inhibiitoritena

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Publication number
EE200200132A
EE200200132A EEP200200132A EEP200200132A EE200200132A EE 200200132 A EE200200132 A EE 200200132A EE P200200132 A EEP200200132 A EE P200200132A EE P200200132 A EEP200200132 A EE P200200132A EE 200200132 A EE200200132 A EE 200200132A
Authority
EE
Estonia
Prior art keywords
compounds useful
cysteine proteases
reversible inhibitors
spiroheterocyclic compounds
novel
Prior art date
Application number
EEP200200132A
Other languages
English (en)
Estonian (et)
Inventor
J. Emmanuel Michel
L. Frye Leah
R. Hickey Eugene
Liu Weimin
M. Morwick Tina
M. Spero Denice
Sun Sanxing
S. Thomson David
D. Ward Yancey
R. R. Young Erick
Original Assignee
Boehringer Ingelheim Pharmaceuticals, Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Boehringer Ingelheim Pharmaceuticals, Inc. filed Critical Boehringer Ingelheim Pharmaceuticals, Inc.
Publication of EE200200132A publication Critical patent/EE200200132A/xx

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    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • 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
    • AHUMAN NECESSITIES
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • AHUMAN NECESSITIES
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    • C07D207/04Heterocyclic 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 no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic 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 no double bonds between ring members or between ring members and non-ring members 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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    • C07D207/04Heterocyclic 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 no double bonds between ring members or between ring members and non-ring members
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    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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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    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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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  • Psychiatry (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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EEP200200132A 1999-09-13 2000-08-28 Uudsed spiroheterotsüklilised ühendid, mis on kasulikud tsüsteiinproteaaside pöörduvate inhibiitoritena EE200200132A (et)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US15373899P 1999-09-13 1999-09-13
US22290000P 2000-08-03 2000-08-03
PCT/US2000/023584 WO2001019816A1 (fr) 1999-09-13 2000-08-28 Composes spiroheterocycliques utiles comme inhibiteurs reversibles de cysteine protease

Publications (1)

Publication Number Publication Date
EE200200132A true EE200200132A (et) 2003-12-15

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ID=26850810

Family Applications (1)

Application Number Title Priority Date Filing Date
EEP200200132A EE200200132A (et) 1999-09-13 2000-08-28 Uudsed spiroheterotsüklilised ühendid, mis on kasulikud tsüsteiinproteaaside pöörduvate inhibiitoritena

Country Status (30)

Country Link
EP (1) EP1218372B1 (fr)
JP (1) JP2003529546A (fr)
KR (1) KR20030024651A (fr)
CN (1) CN100410250C (fr)
AR (1) AR032136A1 (fr)
AT (1) ATE244235T1 (fr)
AU (1) AU782246B2 (fr)
BG (1) BG106483A (fr)
BR (1) BR0013966A (fr)
CA (1) CA2385130C (fr)
CZ (1) CZ2002844A3 (fr)
DE (1) DE60003702T2 (fr)
DK (1) DK1218372T3 (fr)
EE (1) EE200200132A (fr)
ES (1) ES2199856T3 (fr)
HK (1) HK1048807A1 (fr)
HR (1) HRP20020221A2 (fr)
HU (1) HUP0302380A2 (fr)
IL (2) IL148184A0 (fr)
MY (1) MY122696A (fr)
NO (1) NO323354B1 (fr)
NZ (1) NZ518255A (fr)
PL (1) PL364045A1 (fr)
PT (1) PT1218372E (fr)
RU (1) RU2255937C2 (fr)
SA (1) SA00210456B1 (fr)
SK (1) SK286463B6 (fr)
TW (1) TWI230159B (fr)
WO (1) WO2001019816A1 (fr)
YU (1) YU17402A (fr)

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Publication number Priority date Publication date Assignee Title
JP2002539192A (ja) 1999-03-15 2002-11-19 アクシス・ファーマシューティカルズ・インコーポレイテッド プロテアーゼ阻害剤としての新規な化合物及び組成物
US6420364B1 (en) * 1999-09-13 2002-07-16 Boehringer Ingelheim Pharmaceuticals, Inc. Compound useful as reversible inhibitors of cysteine proteases
US7030116B2 (en) 2000-12-22 2006-04-18 Aventis Pharmaceuticals Inc. Compounds and compositions as cathepsin inhibitors
AR036375A1 (es) * 2001-08-30 2004-09-01 Novartis Ag Compuestos pirrolo [2,3-d] pirimidina -2- carbonitrilo, un proceso para su preparacion, una composicion farmaceutica y el uso de dichos compuestos para la preparacion de medicamentos
CN1324008C (zh) 2001-09-14 2007-07-04 安万特药物公司 作为组织蛋白酶抑制剂的新化合物和组合物
EP1434769A2 (fr) 2001-10-02 2004-07-07 Boehringer Ingelheim Pharmaceuticals Inc. Composes utiles comme inhibiteurs reversibles de cysteine protease
WO2003037892A1 (fr) * 2001-10-29 2003-05-08 Boehringer Ingelheim Pharmaceuticals, Inc. Composes convenant comme inhibiteurs reversibles de proteases de la cysteine
WO2003042197A1 (fr) 2001-11-14 2003-05-22 Aventis Pharmaceuticals Inc. Nouveaux composes et compositions jouant le role d'inhibiteurs de cathepsine s
WO2003075853A2 (fr) 2002-03-08 2003-09-18 Bristol-Myers Squibb Company Derives cycliques servant de modulateurs de l'activite du recepteur de la chimiokine
US7101880B2 (en) 2002-06-24 2006-09-05 Schering Aktiengesellschaft Peptidic compounds as cysteine protease inhibitors
ATE555087T1 (de) 2002-11-27 2012-05-15 Incyte Corp 3-aminopyrrolidinderivate als modulatoren von chemokinrezeptoren
WO2004052921A1 (fr) * 2002-12-05 2004-06-24 Axys Pharmaceuticals, Inc. Derives de cyanomethyle en tant qu'inhibiteurs de la protease a cysteine
US7109243B2 (en) 2003-03-24 2006-09-19 Irm Llc Inhibitors of cathepsin S
US7384970B2 (en) 2003-03-24 2008-06-10 Irm Llc Inhibitors of cathepsin S
CA2526694A1 (fr) * 2003-06-04 2004-12-16 John W. Patterson Composes amidino servant d'inhibiteurs de proteases a cysteine
US7173051B2 (en) 2003-06-13 2007-02-06 Irm, Llc Inhibitors of cathepsin S
US7256207B2 (en) 2003-08-20 2007-08-14 Irm Llc Inhibitors of cathepsin S
SG146658A1 (en) * 2003-09-18 2008-10-30 Schering Ag Haloalkyl containing compounds as cysteine protease inhibitors
US7297714B2 (en) * 2003-10-21 2007-11-20 Irm Llc Inhibitors of cathepsin S
US8163735B2 (en) 2004-12-02 2012-04-24 Virobay, Inc. Sulfonamide compounds as cysteine protease inhibitors
BRPI0609695A2 (pt) 2005-03-21 2011-10-18 Applera Corp composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, método para tratar uma doença e uma paciente sofrendo uma terapia
WO2006102535A2 (fr) 2005-03-22 2006-09-28 Celera Genomics Composes contenant du sulfonyle en tant qu'inhibiteurs de cysteine proteases
BRPI0612545A2 (pt) * 2005-06-14 2010-11-23 Schering Corp compostos inibidores de protease, composições farmacêuticas e uso dos mesmos
US8067457B2 (en) 2005-11-01 2011-11-29 Millennium Pharmaceuticals, Inc. Compounds useful as antagonists of CCR2
WO2007053499A2 (fr) 2005-11-01 2007-05-10 Millennium Pharmaceuticals, Inc. Composés pouvant être employés en tant qu'antagonistes de ccr2
UY30090A1 (es) * 2006-01-16 2007-08-31 Syngenta Participations Ag Insecticidas novedosos
WO2007137738A1 (fr) * 2006-06-01 2007-12-06 Sanofi-Aventis Nitriles spirocycliques en tant qu'inhibiteurs de protéase
CA2664878A1 (fr) 2006-10-04 2008-04-10 Virobay, Inc. Composes contenant un di-fluoro en tant qu'inhibiteurs de cysteine-protease
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HRP20020221A2 (en) 2005-10-31
NO20021207L (no) 2002-03-12
EP1218372A1 (fr) 2002-07-03
CA2385130C (fr) 2009-10-20
YU17402A (sh) 2004-11-25
EP1218372B1 (fr) 2003-07-02
AU7081800A (en) 2001-04-17
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TWI230159B (en) 2005-04-01
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ATE244235T1 (de) 2003-07-15
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