JP2003522768A5 - - Google Patents

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Publication number
JP2003522768A5
JP2003522768A5 JP2001558442A JP2001558442A JP2003522768A5 JP 2003522768 A5 JP2003522768 A5 JP 2003522768A5 JP 2001558442 A JP2001558442 A JP 2001558442A JP 2001558442 A JP2001558442 A JP 2001558442A JP 2003522768 A5 JP2003522768 A5 JP 2003522768A5
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JP
Japan
Prior art keywords
signs
administered
makovec
bronchoconstriction
ovalbumin
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2001558442A
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English (en)
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JP2003522768A (ja
JP4817577B2 (ja
Filing date
Publication date
Priority claimed from IT2000TO000127A external-priority patent/IT1320162B1/it
Application filed filed Critical
Publication of JP2003522768A publication Critical patent/JP2003522768A/ja
Publication of JP2003522768A5 publication Critical patent/JP2003522768A5/ja
Application granted granted Critical
Publication of JP4817577B2 publication Critical patent/JP4817577B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

これらの特性の両方、すなわち、インビトロ試験で示された最適バイオアベイラビリティおよび効力は、本発明化合物の幾つかのインビボにおける高活性を明白にする。すなわち、例えば、Makovecらが記載した方法[J.Med.Chem.35(1992)、3633−3640]に従って予め感作したモルモットにおいて、オボアルブミン(食塩水中、0.5%w/v)をエーロゾル投与して行なう攻撃の30分前に化合物17を0.3mg/Kgの用量で投与すると、気管支収縮の微候が完全に阻害され、該微候を腹収縮の第1出現として記録した。
JP2001558442A 2000-02-09 2001-02-07 抗ロイコトリエン活性を持つチロシン誘導体 Expired - Fee Related JP4817577B2 (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
ITTO2000A000127 2000-02-09
IT2000A000127 2000-02-09
IT2000TO000127A IT1320162B1 (it) 2000-02-09 2000-02-09 Derivati della tirosina ad attivita' anti leucotrienica, procedimentoper la loro preparazione e loro uso farmaceutico.
PCT/EP2001/001315 WO2001058892A1 (en) 2000-02-09 2001-02-07 Tyrosine derivatives with anti-leukotriene activity

Publications (3)

Publication Number Publication Date
JP2003522768A JP2003522768A (ja) 2003-07-29
JP2003522768A5 true JP2003522768A5 (ja) 2011-09-08
JP4817577B2 JP4817577B2 (ja) 2011-11-16

Family

ID=11457397

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001558442A Expired - Fee Related JP4817577B2 (ja) 2000-02-09 2001-02-07 抗ロイコトリエン活性を持つチロシン誘導体

Country Status (11)

Country Link
US (1) US6605722B2 (ja)
EP (1) EP1255749B1 (ja)
JP (1) JP4817577B2 (ja)
AT (1) ATE354571T1 (ja)
AU (1) AU776214B2 (ja)
CA (1) CA2399451C (ja)
DE (1) DE60126745T2 (ja)
ES (1) ES2282234T3 (ja)
IT (1) IT1320162B1 (ja)
PT (1) PT1255749E (ja)
WO (1) WO2001058892A1 (ja)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001261654A (ja) * 2000-03-21 2001-09-26 Mitsui Chemicals Inc キノリン誘導体およびそれを有効成分として含有する核内レセプター作動薬
AU2003284001A1 (en) * 2002-10-07 2004-05-04 Bristol-Myers Squibb Company Triazolone and triazolethione derivatives
PL1644336T3 (pl) 2003-06-06 2011-07-29 Fibrogen Inc Związki heteroarylowe zawierające azot i ich zastosowanie w zwiększaniu poziomu endogennej erytropoetyny
MX2008009581A (es) 2006-01-27 2009-01-07 Fibrogen Inc Compuestos de cianoisoquinolina que estabilizan el factor inducible hipoxia (fih).
MX2008012734A (es) 2006-04-04 2009-01-29 Fibrogen Inc Compuestos pirrolo- y tiazolo-piridina como moduladores del factor inducible de hipoxia (hif).
US7687705B2 (en) * 2006-04-10 2010-03-30 Alabama A&M University Institute Efficient thermoelectric device
US8927591B2 (en) 2008-11-14 2015-01-06 Fibrogen, Inc. Thiochromene derivatives as HIF hydroxylase inhibitors
US9409892B2 (en) 2012-03-09 2016-08-09 Fibrogen, Inc. 4-hydroxy-isoquinoline compounds as HIF hydroxylase inhibitors
ES2631655T3 (es) 2012-07-16 2017-09-01 Fibrogen, Inc. Procedimiento para fabricar compuestos de isoquinolina
SI3470397T1 (sl) 2012-07-16 2022-07-29 Fibrogen, Inc. Kristalinične oblike zaviralca prolil hidroksilaze
US8883823B2 (en) 2012-07-16 2014-11-11 Fibrogen, Inc. Crystalline forms of a prolyl hydroxylase inhibitor
KR102233081B1 (ko) 2013-01-24 2021-03-29 피브로겐, 인크. 〔[1-시아노-5-(4-클로로페녹시)-4-하이드록시-아이소퀴놀린-3-카보닐]-아미노〕-아세트산의 결정 형태
EP3509590A4 (en) 2016-09-07 2020-12-02 Pliant Therapeutics, Inc. N-ACYL AMINO ACID COMPOUNDS AND METHOD OF USING

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1261835A (en) 1984-08-20 1989-09-26 Masaaki Toda (fused) benz(thio)amides
GB8607294D0 (en) 1985-04-17 1986-04-30 Ici America Inc Heterocyclic amide derivatives
FI94342C (fi) 1988-03-29 1995-08-25 Ciba Geigy Ag Menetelmä uusien alkanofenonien valmistamiseksi
EP0480717B1 (en) 1990-10-12 1998-04-15 Merck Frosst Canada Inc. Unsaturated hydroxyalkylquinoline acids as leukotriene antagonists
US5508408A (en) 1993-09-10 1996-04-16 Ciba-Geigy Corporation Quinoline compound
ES2103180B1 (es) * 1994-08-01 1998-04-01 Menarini Lab Fenilacetamidas con accion antagonista de los leucotrienos.
JPH11506425A (ja) 1995-04-21 1999-06-08 第一製薬株式会社 エチニルチアゾール誘導体
DE19823722A1 (de) * 1998-05-27 1999-12-02 Merckle Gmbh Chinolinylmethoxyaryl-Verbindungen als duale Inhibitoren der Cyclooxygenase und 5-Lipoxygenase

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