BG106483A - Нови спирохетероциклени съединения като инхибитори с обратимо действие на цистеин протеази - Google Patents

Нови спирохетероциклени съединения като инхибитори с обратимо действие на цистеин протеази Download PDF

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Publication number
BG106483A
BG106483A BG106483A BG10648302A BG106483A BG 106483 A BG106483 A BG 106483A BG 106483 A BG106483 A BG 106483A BG 10648302 A BG10648302 A BG 10648302A BG 106483 A BG106483 A BG 106483A
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Bulgaria
Prior art keywords
phenyl
alkyl
pyrrolidinyl
methyl
substituted
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Pending
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BG106483A
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Bulgarian (bg)
English (en)
Inventor
Michel Emmanuel
Leah FRYE
Eugene Hickey
Weimin Liu
Tina Morwick
Denice SPERO
Sanxing Sun
David Thomson
Yancey Ward
Erick Richard YOUNG
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Boehringer Ingelheim Pharma GmbH Co KG
Boehringer Ingelheim Pharmaceuticals Inc
Original Assignee
Boehringer Ingelheim Pharma GmbH Co KG
Boehringer Ingelheim Pharmaceuticals Inc
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Application filed by Boehringer Ingelheim Pharma GmbH Co KG, Boehringer Ingelheim Pharmaceuticals Inc filed Critical Boehringer Ingelheim Pharma GmbH Co KG
Publication of BG106483A publication Critical patent/BG106483A/bg
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    • 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
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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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  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
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  • Physical Education & Sports Medicine (AREA)
  • Neurology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Diabetes (AREA)
  • Rheumatology (AREA)
  • Neurosurgery (AREA)
  • Immunology (AREA)
  • Biomedical Technology (AREA)
  • Pulmonology (AREA)
  • Urology & Nephrology (AREA)
  • Endocrinology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Dermatology (AREA)
  • Vascular Medicine (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
BG106483A 1999-09-13 2002-03-05 Нови спирохетероциклени съединения като инхибитори с обратимо действие на цистеин протеази Pending BG106483A (bg)

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
BG106483A true BG106483A (bg) 2002-10-31

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BG106483A Pending BG106483A (bg) 1999-09-13 2002-03-05 Нови спирохетероциклени съединения като инхибитори с обратимо действие на цистеин протеази

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)

Families Citing this family (46)

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TR200103337T2 (tr) 1999-03-15 2002-03-21 Axys Pharmaceuticals, Inc. Protez inhibit”rleri olarak yeni bileçikler ve bileçimler
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
RU2316546C2 (ru) 2001-09-14 2008-02-10 Авентис Фармасьютикалз Инк. Новые соединения в качестве ингибиторов катепсина, фармацевтическая композиция на их основе, их применение и способ их получения
CA2459825A1 (fr) 2001-10-02 2003-04-10 Boehringer Ingelheim Pharmaceuticals, Inc. Composes utiles comme inhibiteurs reversibles de cysteine protease
US6841571B2 (en) 2001-10-29 2005-01-11 Boehringer Ingelheim Pharmaceuticals, Inc. Compounds useful as reversible inhibitors of cysteine proteases
CA2467391A1 (fr) 2001-11-14 2003-05-22 Aventis Pharmaceuticals Inc. Nouveaux composes et compositions jouant le role d'inhibiteurs de cathepsine s
AU2003218028A1 (en) 2002-03-08 2003-09-22 Bristol-Myers Squibb Company Cyclic derivatives as modulators of chemokine receptor activity
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
AU2003298740A1 (en) * 2002-12-05 2004-06-30 Axys Pharmaceuticals, Inc. Cyanomethyl derivatives as cysteine protease inhibitors
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
EP1761485A1 (fr) * 2003-06-04 2007-03-14 Schering AG 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
NZ542865A (en) * 2003-09-18 2009-04-30 Virobay Inc Haloalkyl containing compounds as cysteine protease inhibitors
US7297714B2 (en) * 2003-10-21 2007-11-20 Irm Llc Inhibitors of cathepsin S
WO2006060810A1 (fr) 2004-12-02 2006-06-08 Schering Aktiengesellschaft Composes de sulfonamide utilises comme inhibiteurs des cysteine proteases
KR101447897B1 (ko) 2005-03-21 2014-10-07 비로베이, 인코포레이티드 시스테인 단백질분해효소 억제제로서의 알파 케토아미드화합물
MX2007011739A (es) 2005-03-22 2008-03-14 Celera Genomics Compuestos que contienen sulfonilo como inhibidores de cisteina proteasa.
KR20080028881A (ko) * 2005-06-14 2008-04-02 쉐링 코포레이션 헤테로사이클릭 아스파르틸 프로테아제 억제제, 이의제조방법 및 용도
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