MXPA05012129A - Haloalquilo que contiene compuestos como inhibidores de la proteasa de cisteina. - Google Patents

Haloalquilo que contiene compuestos como inhibidores de la proteasa de cisteina.

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Publication number
MXPA05012129A
MXPA05012129A MXPA05012129A MXPA05012129A MXPA05012129A MX PA05012129 A MXPA05012129 A MX PA05012129A MX PA05012129 A MXPA05012129 A MX PA05012129A MX PA05012129 A MXPA05012129 A MX PA05012129A MX PA05012129 A MXPA05012129 A MX PA05012129A
Authority
MX
Mexico
Prior art keywords
containing compounds
protease inhibitors
cysteine protease
haloalkyl containing
haloalkyl
Prior art date
Application number
MXPA05012129A
Other languages
English (en)
Inventor
Sheila M Zippel
Original Assignee
Axys Pharm 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 Axys Pharm Inc filed Critical Axys Pharm Inc
Publication of MXPA05012129A publication Critical patent/MXPA05012129A/es

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    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/20Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
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    • C07C317/00Sulfones; Sulfoxides
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    • C07C317/48Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
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    • C07C323/51Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C323/60Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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Abstract

La presente invencion se dirige a compuestos que son inhibidores de las proteasas de cisteina, en particular, las catepsinas B, K, L, F y S y por lo tanto son utiles en el tratamiento de enfermedades mediadas por estas proteasas. La presente invencion se dirige a composiciones farmaceuticas que comprenden estos compuestos y procesos para prepararlos.
MXPA05012129A 2003-09-18 2004-09-17 Haloalquilo que contiene compuestos como inhibidores de la proteasa de cisteina. MXPA05012129A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US50468003P 2003-09-18 2003-09-18
US56106204P 2004-04-09 2004-04-09
PCT/US2004/030442 WO2005028429A2 (en) 2003-09-18 2004-09-17 Haloalkyl containing compounds as cysteine protease inhibitors

Publications (1)

Publication Number Publication Date
MXPA05012129A true MXPA05012129A (es) 2006-02-08

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ID=34381124

Family Applications (1)

Application Number Title Priority Date Filing Date
MXPA05012129A MXPA05012129A (es) 2003-09-18 2004-09-17 Haloalquilo que contiene compuestos como inhibidores de la proteasa de cisteina.

Country Status (19)

Country Link
US (1) US7547701B2 (es)
EP (1) EP1663958B1 (es)
JP (1) JP4991295B2 (es)
KR (1) KR20060079143A (es)
AU (1) AU2004274471A1 (es)
BR (1) BRPI0410979A (es)
CA (1) CA2521811A1 (es)
DK (1) DK1663958T3 (es)
EA (1) EA011855B1 (es)
ES (1) ES2534222T3 (es)
LV (1) LV13440B (es)
MX (1) MXPA05012129A (es)
NO (1) NO20061627L (es)
NZ (1) NZ542865A (es)
PT (1) PT1663958E (es)
RU (1) RU2007114127A (es)
SG (1) SG146658A1 (es)
TW (1) TW200524851A (es)
WO (1) WO2005028429A2 (es)

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PT1482924E (pt) * 2002-03-05 2008-08-27 Axys Pharm Inc Inibidores de proteases da cisteína catepsina
SG146658A1 (en) 2003-09-18 2008-10-30 Schering Ag Haloalkyl containing compounds as cysteine protease inhibitors
JP2007513972A (ja) * 2003-12-11 2007-05-31 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 低分子治療剤または生物製剤の投与によって引き起こされる免疫応答を治療するためのカテプシンsインヒビターの使用
EP1697355A2 (en) * 2003-12-23 2006-09-06 Axys Pharmaceuticals, Inc. Amidino compounds as cysteine protease inhibitors
JP2007519744A (ja) * 2004-01-30 2007-07-19 バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト システインプロテアーゼインヒビターとしてのシリナン化合物。
JP2008513473A (ja) * 2004-09-17 2008-05-01 バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト システインプロテアーゼインヒビターn−(1−シアノシクロプロピル)−3−シクロプロピルメタンスルホニル−2(r)−[2,2,2−トリフルオロ−1(s)−(4−フルオロフェニル)エチルアミノ]−プロピオンアミドの多形体
AR055283A1 (es) * 2004-11-23 2007-08-15 Merck Frosst Canada Ltd Inhibidores de cisteinproteasa de catepsina
EP1817275A1 (en) * 2004-12-01 2007-08-15 Schering Aktiengesellschaft Haloalkyl containing compounds as cysteine protease inhibitors
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 (en) * 2005-03-22 2006-09-28 Celera Genomics Sulfonyl containing compounds as cysteine protease inhibitors
CA2610014A1 (en) 2005-06-02 2006-12-07 Merck Frosst Canada Ltd. Fluoroalkylamine derivatives as cathepsin inhibitors
GB0611654D0 (en) * 2006-06-13 2006-07-19 Medivir Ab Compounds
WO2008028301A1 (en) * 2006-09-08 2008-03-13 Merck Frosst Canada Ltd. Prodrugs of inhibitors of cathepsin s
WO2008037072A1 (en) 2006-09-25 2008-04-03 Merck Frosst Canada Ltd. Cathepsin b inhibitors
CA2664878A1 (en) * 2006-10-04 2008-04-10 Virobay, Inc. Di-fluoro containing compounds as cysteine protease inhibitors
US7893112B2 (en) 2006-10-04 2011-02-22 Virobay, Inc. Di-fluoro containing compounds as cysteine protease inhibitors
WO2008070994A1 (en) 2006-12-14 2008-06-19 Nps Pharmaceuticals, Inc. Use of d-serine derivatives for the treatment of anxiety disorders
WO2009123623A1 (en) * 2008-04-01 2009-10-08 Virobay, Inc. Di-fluoro containing compounds as cysteine protease inhibitors
JP5198220B2 (ja) * 2008-11-13 2013-05-15 東ソ−・エフテック株式会社 アミノ酸誘導体の製造方法
WO2010069069A1 (en) * 2008-12-17 2010-06-24 Merck Frosst Canada Ltd. Cathepsin b inhibitors
US20120101053A1 (en) * 2009-06-22 2012-04-26 Cameron Black Cathepsin cysteine protease inhibitors for the treatment of various diseases
US8324417B2 (en) * 2009-08-19 2012-12-04 Virobay, Inc. Process for the preparation of (S)-2-amino-5-cyclopropyl-4,4-difluoropentanoic acid and alkyl esters and acid salts thereof
EP2681188A4 (en) * 2011-03-02 2015-04-15 Merck Sharp & Dohme amidation
WO2012119941A1 (en) 2011-03-04 2012-09-13 Prozymex A/S Peptidyl nitrilcompounds as peptidase inhibitors
JP5951650B2 (ja) 2011-03-18 2016-07-13 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH N−(3−カルバモイルフェニル)−1h−ピラゾール−5−カルボキサミド誘導体及び害虫を防除するためのそれらの使用
WO2017036357A1 (zh) 2015-08-29 2017-03-09 广东东阳光药业有限公司 组织蛋白酶k抑制剂及其用途
WO2020201572A1 (en) 2019-04-05 2020-10-08 Université De Bretagne Occidentale Protease-activated receptor-2 inhibitors for the treatment of sensory neuropathy induced by a marine neurotoxic poisoning

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JP2007505920A (ja) 2007-03-15
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NZ542865A (en) 2009-04-30
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LV13440B (en) 2006-10-20
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