BRPI1015540A2 - ''composto de 1-cianoetil-heterociclilcarboxamida substituídos 750'' - Google Patents

''composto de 1-cianoetil-heterociclilcarboxamida substituídos 750''

Info

Publication number
BRPI1015540A2
BRPI1015540A2 BRPI1015540A BRPI1015540A BRPI1015540A2 BR PI1015540 A2 BRPI1015540 A2 BR PI1015540A2 BR PI1015540 A BRPI1015540 A BR PI1015540A BR PI1015540 A BRPI1015540 A BR PI1015540A BR PI1015540 A2 BRPI1015540 A2 BR PI1015540A2
Authority
BR
Brazil
Prior art keywords
cyanoethylheterocyclylcarboxamide
substituted
compound
cyanoethylheterocyclylcarboxamide compound
Prior art date
Application number
BRPI1015540A
Other languages
English (en)
Inventor
Mather Andrew
Mete Antonio
Millichip Ian
Ford Rhonan
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of BRPI1015540A2 publication Critical patent/BRPI1015540A2/pt

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings 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
    • C07D309/14—Nitrogen atoms not forming part of a nitro radical
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/351—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/02—Nasal agents, e.g. decongestants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
BRPI1015540A 2009-05-07 2010-05-05 ''composto de 1-cianoetil-heterociclilcarboxamida substituídos 750'' BRPI1015540A2 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US17627909P 2009-05-07 2009-05-07
US18562909P 2009-06-10 2009-06-10
PCT/GB2010/050736 WO2010128324A1 (en) 2009-05-07 2010-05-05 Substituted 1-cyanoethylheterocyclylcarboxamide compounds 750

Publications (1)

Publication Number Publication Date
BRPI1015540A2 true BRPI1015540A2 (pt) 2019-09-24

Family

ID=42271991

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI1015540A BRPI1015540A2 (pt) 2009-05-07 2010-05-05 ''composto de 1-cianoetil-heterociclilcarboxamida substituídos 750''

Country Status (22)

Country Link
US (2) US8193239B2 (pt)
EP (1) EP2427445A1 (pt)
JP (1) JP2012526093A (pt)
KR (1) KR20120034639A (pt)
CN (1) CN102574830A (pt)
AR (1) AR076551A1 (pt)
AU (1) AU2010244218B2 (pt)
BR (1) BRPI1015540A2 (pt)
CA (1) CA2759581A1 (pt)
CL (1) CL2011002787A1 (pt)
CO (1) CO6450612A2 (pt)
CR (1) CR20110579A (pt)
CU (1) CU20110204A7 (pt)
EA (1) EA201190235A1 (pt)
EC (1) ECSP11011439A (pt)
IL (1) IL215615A0 (pt)
MX (1) MX2011011661A (pt)
SG (1) SG175090A1 (pt)
TW (1) TW201041889A (pt)
UY (1) UY32611A (pt)
WO (1) WO2010128324A1 (pt)
ZA (1) ZA201108962B (pt)

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KR101362589B1 (ko) 2010-08-20 2014-02-12 추가이 세이야쿠 가부시키가이샤 4환성 화합물을 포함하는 조성물
UY33905A (es) * 2011-02-11 2012-08-31 Glaxosmithkline Llc Inhibidores de la catepsina c
WO2012119941A1 (en) 2011-03-04 2012-09-13 Prozymex A/S Peptidyl nitrilcompounds as peptidase inhibitors
US10668075B2 (en) 2012-09-25 2020-06-02 Chugai Seiyaku Kabushiki Kaisha RET inhibitor
UY35391A (es) 2013-03-14 2014-09-30 Boehringer Ingelheim Int Acido 2-aza-biciclo[2.2.1]heptano-3-carboxilico (bencil-cianometil)-amidas sustituidas inhibidores de catepsina c
US8889708B2 (en) 2013-03-14 2014-11-18 Boehringer Ingelheim International Gmbh Substituted bicyclic 1-carboxylic-acid (benzyl-cyano-methyl)-amides inhibitors of cathepsin C
WO2014140078A1 (en) * 2013-03-14 2014-09-18 Boehringer Ingelheim International Gmbh Substituted 2-aza-bicyclo[2.2.1]heptane-3-carboxylic acid (cyano-methyl)-amides inhibitors of cathepsin c
JP6441831B2 (ja) 2013-03-14 2018-12-19 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング カテプシンｃの置換２−アザ−ビシクロ［２．２．２］オクタン−３−カルボン酸（ベンジル−シアノ−メチル）−アミド阻害剤
CA2914132A1 (en) 2013-06-21 2014-12-24 Lupin Limited Substituted heterocyclic compounds as crac modulators
US9790231B2 (en) 2013-06-24 2017-10-17 Lupin Limited Chromane and chromene derivatives and their use as CRAC modulators
JP6408008B2 (ja) * 2013-09-09 2018-10-17 プロザイメックス・アクティーゼルスカブＰｒｏＺｙｍｅｘ Ａ／Ｓ ジペプチジルペプチダーゼｉインヒビターとしてのペプチジルニトリル化合物
NO2699580T3 (pt) 2014-01-24 2018-02-24
AR100187A1 (es) 2014-04-25 2016-09-14 Chugai Pharmaceutical Co Ltd Composición farmacéutica que contiene un inhibidor de alk (quinasa de linfoma anaplásico)
KR20220042486A (ko) 2014-04-25 2022-04-05 추가이 세이야쿠 가부시키가이샤 4환성 화합물의 신규 결정
ES2664810T3 (es) 2014-06-12 2018-04-23 Pfizer Limited Derivados de imidazopiridazina como moduladores de la actividad del receptor GABAA
WO2016016242A1 (en) 2014-08-01 2016-02-04 Boehringer Ingelheim International Gmbh Substituted oxetanes and their use as inhibitors of cathepsin c
TWI765410B (zh) 2014-08-08 2022-05-21 日商中外製藥股份有限公司 ４環性化合物的非晶質體的用途
MX367316B (es) 2014-09-12 2019-08-15 Boehringer Ingelheim Int Inhibidores espirociclicos de catepsina c.
BR112017013982A2 (pt) 2015-01-16 2018-01-02 Chugai Seiyaku Kabushiki Kaisha fármaco de combinação
WO2016139355A1 (en) 2015-03-05 2016-09-09 Prozymex A/S N-substituted 3,3'-(biphenyl-4,4'-diyl)bis-2-aminopropanenitriles as dppi inhibitors
JP6783426B2 (ja) * 2015-03-05 2020-11-11 ニュープロザイム・セラピューティクス・アンパルトセルスカブＮｅｕｐｒｏｚｙｍｅ Ｔｈｅｒａｐｅｕｔｉｃｓ ＡｐＳ ジペプチジルペプチダーゼｉ阻害剤としてのペプチジルニトリル化合物
CN106478629A (zh) * 2015-08-24 2017-03-08 上海医药工业研究院 一种利格列汀的制备工艺
MX2018010374A (es) 2016-03-01 2019-03-28 Propellon Therapeutics Inc Inhibidores del enlace proteína-proteína de wdr5.
EP3423437A4 (en) 2016-03-01 2019-07-24 Propellon Therapeutics Inc. INHIBITORS OF THE LINK BETWEEN THE WDR5 PROTEIN AND ITS LIAISON PARTNERS
KR20190035781A (ko) * 2016-07-29 2019-04-03 인스메드 인코포레이티드 기관지확장증을 치료하기 위한 특정 (2s)-n-[(1s)-1-시아노-2-페닐에틸]-1,4-옥사제판-2-카르복스아미드
KR20210032439A (ko) * 2018-07-17 2021-03-24 인스메드 인코포레이티드 염증성 장 질환을 치료하기 위한 특정 (2s)-n-[(1s)-1-시아노-2-페닐에틸]-1,4-옥사제판-2-카복스아미드
KR20210032431A (ko) * 2018-07-17 2021-03-24 인스메드 인코포레이티드 루푸스 신염을 치료하기 위한 특정 (2s)-n-[(1s)-1-시아노-2-페닐에틸]-1,4-옥사제판-2-카복스아미드
JP7167171B2 (ja) 2018-09-04 2022-11-08 中外製薬株式会社 ４環性化合物の製造方法
TW202214616A (zh) 2020-08-26 2022-04-16 大陸商四川海思科製藥有限公司 一種作為二肽基肽酶1抑制劑的腈衍生物及其用途
JP2023551488A (ja) 2020-12-04 2023-12-08 瑞石生物医薬有限公司 カテプシンｃの小分子阻害剤及びその医薬的使用
JP2024505715A (ja) * 2021-02-05 2024-02-07 メッドシャイン ディスカバリー インコーポレイテッド １，４－オキサゼパンを含む縮合環誘導体
WO2023160541A1 (zh) * 2022-02-22 2023-08-31 四川海思科制药有限公司 一种含氮杂环化合物的制备方法
WO2024008680A1 (en) 2022-07-06 2024-01-11 Chiesi Farmaceutici S.P.A. Azetidine derivatives and use thereof as dipeptidyl peptidase 1 inhibitors

Family Cites Families (8)

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CO5150173A1 (es) 1998-12-10 2002-04-29 Novartis Ag Compuestos n-(glicilo sustituido)-2-cianopirrolidinas inhibidores de peptidasa de dipeptidilo-iv (dpp-iv) los cuales son efectivos en el tratamiento de condiciones mediadas por la inhibicion de dpp-iv
ES2264937T3 (es) 1999-07-30 2007-02-01 Boehringer Ingelheim Pharmaceuticals Inc. Nuevos compuestos derivados de succinato, utiles como inhibidores de cisteina-proteasa.
CA2395179A1 (en) 1999-12-24 2001-07-05 F. Hoffmann-La Roche Ag Nitrile derivatives as cathepsin k inhibitors
PL367527A1 (en) 2001-06-27 2005-02-21 Smithkline Beecham Corporation Fluoropyrrolidines as dipeptidyl peptidase inhibitors
JP4357293B2 (ja) 2001-06-27 2009-11-04 スミスクライン ビーチャム コーポレーション ジペプチジルペプチダーゼ阻害剤としてのフルオロピロリジン類
US6995180B2 (en) * 2002-10-23 2006-02-07 Bristol Myers Squibb Company Glycinenitrile-based inhibitors of dipeptidyl peptidase IV and methods
US20070099958A1 (en) * 2003-06-18 2007-05-03 Prozymex A/S Protease inhibitors
US7504413B2 (en) * 2004-05-06 2009-03-17 Cytokinetics, Inc. N-(4-(imidazo[1,2A]pyridin-YL)phenethyl)benzamide inhibitors of the mitotic kinesin CENP-E for treating certain cellular proliferation diseases

Also Published As

Publication number Publication date
CO6450612A2 (es) 2012-05-31
EP2427445A1 (en) 2012-03-14
US20100286118A1 (en) 2010-11-11
UY32611A (es) 2010-12-31
CU20110204A7 (es) 2012-03-15
CR20110579A (es) 2012-01-09
MX2011011661A (es) 2011-11-18
TW201041889A (en) 2010-12-01
ZA201108962B (en) 2012-08-29
US20120329775A1 (en) 2012-12-27
US8193239B2 (en) 2012-06-05
CA2759581A1 (en) 2010-11-11
IL215615A0 (en) 2011-12-29
EA201190235A1 (ru) 2012-05-30
AU2010244218B2 (en) 2012-07-19
WO2010128324A1 (en) 2010-11-11
AU2010244218A1 (en) 2011-11-03
ECSP11011439A (es) 2011-12-30
JP2012526093A (ja) 2012-10-25
CL2011002787A1 (es) 2012-06-22
AR076551A1 (es) 2011-06-22
CN102574830A (zh) 2012-07-11
KR20120034639A (ko) 2012-04-12
SG175090A1 (en) 2011-11-28

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Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]
B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: EM VIRTUDE DO ARQUIVAMENTO PUBLICADO NA RPI 2543 DE 01-10-2019 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDO O ARQUIVAMENTO DO PEDIDO DE PATENTE, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013.