JP2013518040A5 - - Google Patents

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Publication number
JP2013518040A5
JP2013518040A5 JP2012549412A JP2012549412A JP2013518040A5 JP 2013518040 A5 JP2013518040 A5 JP 2013518040A5 JP 2012549412 A JP2012549412 A JP 2012549412A JP 2012549412 A JP2012549412 A JP 2012549412A JP 2013518040 A5 JP2013518040 A5 JP 2013518040A5
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JP
Japan
Prior art keywords
piperidino
asthma
alkyl
independently
formula
Prior art date
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Application number
JP2012549412A
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English (en)
Japanese (ja)
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JP5859980B2 (ja
JP2013518040A (ja
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Publication date
Priority claimed from GBGB1001070.0A external-priority patent/GB201001070D0/en
Application filed filed Critical
Publication of JP2013518040A publication Critical patent/JP2013518040A/ja
Publication of JP2013518040A5 publication Critical patent/JP2013518040A5/ja
Application granted granted Critical
Publication of JP5859980B2 publication Critical patent/JP5859980B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2012549412A 2010-01-22 2011-01-21 チリダニグループ1ペプチダーゼアレルゲン阻害物質としてのピルブアミド化合物及びその使用 Expired - Fee Related JP5859980B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1001070.0A GB201001070D0 (en) 2010-01-22 2010-01-22 Theraputic compounds and their use
GB1001070.0 2010-01-22
PCT/GB2011/000079 WO2011089396A2 (en) 2010-01-22 2011-01-21 Pyruvamide compounds as inhibitors of dust mite group 1 peptidase allergen and their use.

Publications (3)

Publication Number Publication Date
JP2013518040A JP2013518040A (ja) 2013-05-20
JP2013518040A5 true JP2013518040A5 (enExample) 2014-03-06
JP5859980B2 JP5859980B2 (ja) 2016-02-16

Family

ID=42045942

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012549412A Expired - Fee Related JP5859980B2 (ja) 2010-01-22 2011-01-21 チリダニグループ1ペプチダーゼアレルゲン阻害物質としてのピルブアミド化合物及びその使用

Country Status (27)

Country Link
US (2) US8541363B2 (enExample)
EP (1) EP2526116B1 (enExample)
JP (1) JP5859980B2 (enExample)
KR (1) KR101798676B1 (enExample)
CN (1) CN102822192B (enExample)
AU (1) AU2011208510B2 (enExample)
BR (1) BR112012017476B8 (enExample)
CA (1) CA2786690C (enExample)
CY (1) CY1116824T1 (enExample)
DK (1) DK2526116T3 (enExample)
ES (1) ES2544732T3 (enExample)
GB (1) GB201001070D0 (enExample)
HR (1) HRP20150844T1 (enExample)
HU (1) HUE025340T2 (enExample)
IL (1) IL220665A (enExample)
ME (1) ME02218B (enExample)
MX (1) MX2012007711A (enExample)
NZ (1) NZ601155A (enExample)
PL (1) PL2526116T3 (enExample)
PT (1) PT2526116E (enExample)
RS (1) RS54148B1 (enExample)
RU (1) RU2586215C2 (enExample)
SG (1) SG182535A1 (enExample)
SI (1) SI2526116T1 (enExample)
SM (1) SMT201500215B (enExample)
WO (1) WO2011089396A2 (enExample)
ZA (1) ZA201204764B (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201001070D0 (en) 2010-01-22 2010-03-10 St George's Hospital Medical School Theraputic compounds and their use
RU2015117578A (ru) * 2012-10-11 2016-11-27 Ф. Хоффманн-Ля Рош Аг Кетоамидные ингибиторы иммунопротеасом
CN103724334A (zh) * 2013-10-02 2014-04-16 张惠琳 新的抗变态反应的苯并环庚并噻吩类化合物
WO2015106240A1 (en) 2014-01-13 2015-07-16 The General Hospital Corporation Heteroaryl disulfide compounds as allosteric effectors for increasing the oxygen-binding affinity of hemoglobin
US20160331783A1 (en) * 2014-01-13 2016-11-17 The General Hospital Corporation Bisamide compounds as allosteric effectors for reducing the oxygen-binding affinity of hemoglobin
GB201908511D0 (en) 2019-06-13 2019-07-31 Adorx Therapeutics Ltd Hydroxamate compounds
US20240317801A1 (en) * 2020-12-17 2024-09-26 Disc Medicine, Inc. Peptidomimetic matriptase 2 inhibitors and uses thereof
WO2023165334A1 (zh) * 2022-03-01 2023-09-07 成都威斯克生物医药有限公司 酮酰胺类衍生物及其制药用途
WO2024028417A1 (en) 2022-08-03 2024-02-08 Institut National de la Santé et de la Recherche Médicale New composition for the treatment and/or prevention of vitiligo

Family Cites Families (25)

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Publication number Priority date Publication date Assignee Title
US3149159A (en) 1962-04-16 1964-09-15 Smith Kline French Lab Substituted 7-aminoalkylbicyclo-[4. 2. 0] octa-1, 3, 5-trienes
EP0100673A2 (en) 1982-08-02 1984-02-15 The Research Foundation Of State University Of New York A method of enhancing neurofiber regrowth
US5066785A (en) 1988-11-15 1991-11-19 City Of Hope Carboxyl terminal peptide and protein sequencing
WO1990012805A1 (fr) 1989-04-15 1990-11-01 Zaidan Hojin Biseibutsu Kagaku Kenkyu Kai Postostatine et son compose connexe, ou leurs sels
US6235929B1 (en) * 1991-12-27 2001-05-22 Georgia Tech Research Corporation Tripeptide α-ketoamides
DE4331135A1 (de) 1993-09-14 1995-03-16 Bayer Ag Neue antiviral wirksame valinhaltige Pseudopeptide
US5580854A (en) 1994-03-04 1996-12-03 Mount Sinai School Of Medicine Of The City University Of New York Substrate-related peptidyl-aldehyde inhibitors of the proteolytic activity of the multicatalytic proteinase complex
JPH08208462A (ja) * 1994-11-24 1996-08-13 Takeda Chem Ind Ltd カテプシンl阻害剤
AU3935895A (en) 1994-11-24 1996-06-17 Takeda Chemical Industries Ltd. Alpha-ketoamide derivatives as cathepsin l inhibitor
EP0820464A2 (en) 1995-03-31 1998-01-28 Takeda Chemical Industries, Ltd. Cysteine protease inhibitor
AU716716B2 (en) 1995-07-17 2000-03-02 Medivir Uk Ltd Cysteine protease inhibitors for use in treatment of IgE mediated allergic diseases
AU728373B2 (en) 1995-12-07 2001-01-11 Scripps Research Institute, The HIV protease inhibitors
AU1599497A (en) 1996-02-16 1997-09-02 Bayer Aktiengesellschaft Oxime- and nitron-substituted pseudopeptides with an anti-viral action
CA2225325A1 (en) 1997-12-19 1999-06-19 The University Of British Columbia Hemiasterlin analogs
TR200103406T2 (tr) 1998-03-19 2002-06-21 Vertex Pharmaceuticals Incorporated Kaspaz inhibitörleri.
US7521068B2 (en) 1998-11-12 2009-04-21 Elan Pharma International Ltd. Dry powder aerosols of nanoparticulate drugs
WO2001040262A1 (en) 1999-12-03 2001-06-07 Bristol-Myers Squibb Pharma Company Alpha-ketoamide inhibitors of hepatitis c virus ns3 protease
JP2002030053A (ja) * 2000-07-13 2002-01-29 Senju Pharmaceut Co Ltd α−ケトアミド誘導体の製造法
CZ2003195A3 (cs) 2000-07-21 2003-04-16 Schering Corporation Peptidové inhibitory serinové proteázy NS3 a farmaceutický prostředek
EP1553964A4 (en) * 2002-09-25 2009-08-12 Georgia Tech Res Inst INHIBITORS OF CETOAMIDES IN CHRONIC NERVOUS DISEASES
US20080108593A1 (en) 2003-11-12 2008-05-08 Shinshu Tlo Co., Ltd Allergen Decomposer and Antiallergenic Feathers
CA2617294A1 (en) 2005-08-03 2007-02-08 Boehringer Ingelheim International Gmbh Substituted ethane-1,2-diamines for the treatment of alzheimer's disease ii
WO2007041775A1 (en) 2005-10-10 2007-04-19 The University Of Queensland Cysteine protease inhibitors incorporating azide groups
GB201001070D0 (en) 2010-01-22 2010-03-10 St George's Hospital Medical School Theraputic compounds and their use
GB201011411D0 (en) 2010-07-06 2010-08-18 St Georges Hosp Medical School Therapeutic compounds and their use

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