JP2016513696A5 - - Google Patents

Download PDF

Info

Publication number
JP2016513696A5
JP2016513696A5 JP2016502433A JP2016502433A JP2016513696A5 JP 2016513696 A5 JP2016513696 A5 JP 2016513696A5 JP 2016502433 A JP2016502433 A JP 2016502433A JP 2016502433 A JP2016502433 A JP 2016502433A JP 2016513696 A5 JP2016513696 A5 JP 2016513696A5
Authority
JP
Japan
Prior art keywords
optionally substituted
substituted
optionally
compound
branched
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
JP2016502433A
Other languages
English (en)
Japanese (ja)
Other versions
JP6534650B2 (ja
JP2016513696A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/027428 external-priority patent/WO2014152518A2/en
Publication of JP2016513696A publication Critical patent/JP2016513696A/ja
Publication of JP2016513696A5 publication Critical patent/JP2016513696A5/ja
Application granted granted Critical
Publication of JP6534650B2 publication Critical patent/JP6534650B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2016502433A 2013-03-14 2014-03-14 ロイコトリエンa4加水分解酵素の阻害剤 Active JP6534650B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361781193P 2013-03-14 2013-03-14
US61/781,193 2013-03-14
PCT/US2014/027428 WO2014152518A2 (en) 2013-03-14 2014-03-14 Inhibitors of leukotriene a4 hydrolase

Publications (3)

Publication Number Publication Date
JP2016513696A JP2016513696A (ja) 2016-05-16
JP2016513696A5 true JP2016513696A5 (US20080131398A1-20080605-C00009.png) 2017-04-13
JP6534650B2 JP6534650B2 (ja) 2019-06-26

Family

ID=51581716

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016502433A Active JP6534650B2 (ja) 2013-03-14 2014-03-14 ロイコトリエンa4加水分解酵素の阻害剤

Country Status (10)

Country Link
US (2) US9777006B2 (US20080131398A1-20080605-C00009.png)
EP (1) EP2970309A4 (US20080131398A1-20080605-C00009.png)
JP (1) JP6534650B2 (US20080131398A1-20080605-C00009.png)
KR (1) KR20150127246A (US20080131398A1-20080605-C00009.png)
AU (1) AU2014239567B2 (US20080131398A1-20080605-C00009.png)
BR (1) BR112015022864A8 (US20080131398A1-20080605-C00009.png)
CA (1) CA2906084A1 (US20080131398A1-20080605-C00009.png)
MX (1) MX2015011678A (US20080131398A1-20080605-C00009.png)
RU (1) RU2678196C2 (US20080131398A1-20080605-C00009.png)
WO (1) WO2014152518A2 (US20080131398A1-20080605-C00009.png)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2905340C (en) 2013-03-12 2022-05-31 Celtaxsys, Inc. Low dose oral formulations of acebilustat
AU2014240042C1 (en) 2013-03-14 2019-09-05 Celltaxis, Llc Inhibitors of leukotriene A4 hydrolase
WO2014152536A2 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase
CN104530153A (zh) * 2015-01-15 2015-04-22 佛山市赛维斯医药科技有限公司 一类苯基s-葡萄糖苷衍生物、其制备方法和在医药上的用途
CN104530152A (zh) * 2015-01-15 2015-04-22 佛山市赛维斯医药科技有限公司 一种含丙烯腈基和三氟甲氧苯基o-葡萄糖苷结构化合物及用途
CN104530151A (zh) * 2015-01-15 2015-04-22 佛山市赛维斯医药科技有限公司 一种含硝基苯s-葡萄糖苷结构的化合物及其用途
AU2017371353B2 (en) 2016-12-09 2022-02-03 Celltaxis, Llc Monamine and monoamine derivatives as inhibitors of leukotriene A4 hydrolase
US11498903B2 (en) 2017-08-17 2022-11-15 Bristol-Myers Squibb Company 2-(1,1′-biphenyl)-1H-benzodimidazole derivatives and related compounds as apelin and APJ agonists for treating cardiovascular diseases
WO2019222265A1 (en) * 2018-05-15 2019-11-21 Alkahest, Inc. Treatment of aging-associated disease with modulators of leukotriene a4 hydrolase
EP3801559A4 (en) 2018-05-31 2022-03-02 Celltaxis, LLC METHOD FOR REDUCING LUNG EXACERBATIONS IN PATIENTS SUFFERING FROM RESPIRATORY DISEASE
US11155560B2 (en) 2018-10-30 2021-10-26 Kronos Bio, Inc. Substituted pyrazolo[1,5-a]pyrimidines for modulating CDK9 activity
US11708366B2 (en) 2020-08-14 2023-07-25 Novartis Ag Heteroaryl substituted spiropiperidinyl derivatives and pharmaceutical uses thereof
US11957671B2 (en) 2021-11-01 2024-04-16 Alkahest, Inc. Benzodioxane modulators of leukotriene A4 hydrolase (LTA4H) for prevention and treatment of aging-associated diseases

Family Cites Families (70)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL6815872A (US20080131398A1-20080605-C00009.png) 1967-11-22 1969-05-27
JPS5614663B2 (US20080131398A1-20080605-C00009.png) 1971-08-21 1981-04-06
US4582833A (en) 1984-04-16 1986-04-15 American Cyanamid Company 2-(substituted-1-piperazinyl)[1,2,4]triazolo[1,5-a]pyrimidines
US4576943A (en) 1984-10-09 1986-03-18 American Cyanamid Company Pyrazolo[1,5-a]pyrimidines
US5308852A (en) 1992-06-29 1994-05-03 Merck Frosst Canada, Inc. Heteroarylnaphthalenes as inhibitors of leukotriene biosynthesis
US6506876B1 (en) 1994-10-11 2003-01-14 G.D. Searle & Co. LTA4 hydrolase inhibitor pharmaceutical compositions and methods of use
WO1997029774A1 (en) 1996-02-13 1997-08-21 G.D. Searle & Co. Combinations, having immunosuppressive effects, containing a cyclooxygenase-2 inhibitor and a leukotriene a4 hydrolase inhibitor
US5952349A (en) 1996-07-10 1999-09-14 Schering Corporation Muscarinic antagonists for treating memory loss
US6309561B1 (en) 1997-12-24 2001-10-30 3M Innovative Properties Company Liquid crystal compounds having a chiral fluorinated terminal portion
US6380203B1 (en) * 1998-01-14 2002-04-30 Merck & Co., Inc. Angiogenesis inhibitors
GB9815880D0 (en) 1998-07-21 1998-09-16 Pfizer Ltd Heterocycles
GB9919776D0 (en) 1998-08-31 1999-10-27 Zeneca Ltd Compoujnds
AR023659A1 (es) 1998-09-18 2002-09-04 Vertex Pharma Un compuesto inhibidor de p38, una composicion farmaceutica que lo comprende y el uso de dicha composicion en el tratamiento y prevencion de estados patologicos
US6699873B1 (en) 1999-08-04 2004-03-02 Millennium Pharmaceuticals, Inc. Melanocortin-4 receptor binding compounds and methods of use thereof
US6924313B1 (en) 1999-09-23 2005-08-02 Pfizer Inc. Substituted tertiary-heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity
US6800651B2 (en) 2000-02-03 2004-10-05 Eli Lilly And Company Potentiators of glutamate receptors
US6552023B2 (en) 2000-02-22 2003-04-22 Cv Therapeutics, Inc. Aralkyl substituted piperazine compounds
US6451798B2 (en) 2000-02-22 2002-09-17 Cv Therapeutics, Inc. Substituted alkyl piperazine derivatives
JP2001354657A (ja) 2000-06-09 2001-12-25 Sds Biotech:Kk 置換ピペラジン誘導体及び農園芸用殺菌剤
DE60114518T2 (de) 2000-07-06 2006-08-10 Fuji Photo Film Co. Ltd., Minamiashigara Flüssigkristallzusammensetzung, die Flüssigkristallmoleküle und Ausrichtungsmittel enthält
WO2002064211A1 (en) 2001-02-09 2002-08-22 Merck & Co., Inc. Thrombin inhibitors
JP4365094B2 (ja) 2001-03-02 2009-11-18 メルク フロスト カナダ リミテツド カテプシンシステインプロテアーゼ阻害薬
AUPR362001A0 (en) 2001-03-08 2001-04-05 Fujisawa Pharmaceutical Co., Ltd. New compound
FR2826011B1 (fr) 2001-06-14 2004-12-10 Oreal Nouveaux derives de la 7-oxo-dhea et utilisation cosmetique
SE0102616D0 (sv) 2001-07-25 2001-07-25 Astrazeneca Ab Novel compounds
CA2460313C (en) 2001-09-14 2011-03-08 Tularik Inc. Bisphenylsulfanyl and sulphonate compounds and use thereof for elevating hdl cholesterol levels
AU2002363236A1 (en) 2001-10-30 2003-05-12 Millennium Pharmaceuticals, Inc. Compounds, pharmaceutical compositions and methods of use therefor
EP1562973A4 (en) 2002-10-17 2007-01-03 Decode Genetics Ehf RECOMMENDATIONS FOR MYOKARDINFARKT
US7851486B2 (en) 2002-10-17 2010-12-14 Decode Genetics Ehf. Susceptibility gene for myocardial infarction, stroke, and PAOD; methods of treatment
US20040198777A1 (en) 2002-12-20 2004-10-07 Mitokor, Inc. Ligands of adenine nucleotide translocase (ANT) and compositions and methods related thereto
JPWO2004089410A1 (ja) 2003-04-03 2006-07-06 協和醗酵工業株式会社 神経因性疼痛の予防及び/または治療剤
WO2004099164A1 (en) 2003-05-02 2004-11-18 Rigel Pharmaceuticals, Inc. Substituted diphenyl isoxazoles, pyrazoles and oxadiazoles useful for treating hcv infection
JP2005008581A (ja) * 2003-06-20 2005-01-13 Kissei Pharmaceut Co Ltd 新規なピラゾロ[1,5−a]ピリミジン誘導体、それを含有する医薬組成物およびそれらの用途
AU2004261628B2 (en) 2003-07-28 2011-05-12 Janssen Pharmaceutica N.V. Benzimidazole, benzthiazole and benzoxazole derivatives and their use as LTA4H modulators
US20050272051A1 (en) 2003-09-17 2005-12-08 Decode Genetics Ehf. Methods of preventing or treating recurrence of myocardial infarction
DE10356579A1 (de) * 2003-12-04 2005-07-07 Merck Patent Gmbh Aminderivate
SE0303480D0 (sv) 2003-12-19 2003-12-19 Biovitrum Ab Benzofuranes
ATE437880T1 (de) 2004-02-04 2009-08-15 Neurosearch As Dimere azacyclische verbindungen und deren verwendung
WO2006033795A2 (en) * 2004-09-17 2006-03-30 Wyeth Substituted pyrazolo [1, 5-a] pyrimidines for inhibiting abnormal cell growth
MX2007012235A (es) 2005-03-31 2008-03-18 Johnson & Johnson Moduladores de leucotrieno a4 hidrolasa de fenilo y piridilo.
GB0514018D0 (en) 2005-07-07 2005-08-17 Ionix Pharmaceuticals Ltd Chemical compounds
KR101328306B1 (ko) 2005-09-21 2013-11-11 디코드 제네틱스 이에이치에프 염증 치료를 위한 lta4h의 바이아릴 치환된헤테로사이클 억제제
CN1947717B (zh) 2005-10-14 2012-09-26 卓敏 选择性抑制腺苷酸环化酶1的化合物在制备用于治疗神经性疼痛和炎性疼痛的药物中的应用
DE102005049954A1 (de) 2005-10-19 2007-05-31 Sanofi-Aventis Deutschland Gmbh Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen
DK1976828T3 (en) 2005-12-29 2017-03-06 Celtaxsys Inc DIAMINE DERIVATIVES AS INhibitors of Leukotriene A4 HYDROLASE
EP2295432A1 (en) 2006-02-10 2011-03-16 TransTech Pharma Inc. Process for the preparation of aminobenzimidazole derivatives
WO2008016131A1 (fr) * 2006-08-04 2008-02-07 Takeda Pharmaceutical Company Limited Composé hétérocyclique à cycles fusionnés
RU2009112495A (ru) 2006-10-19 2010-11-27 Ф. Хоффманн-Ля Рош Аг (Ch) Аминометил-2-имидазолы со сродством к рецепторам, ассоциированным со следовыми аминами
ES2620818T3 (es) 2006-12-14 2017-06-29 Janssen Pharmaceutica N.V. Procedimiento para la preparación de derivados de piperazinil y diazepanil benzamida
FR2911139A1 (fr) 2007-01-05 2008-07-11 Sanofi Aventis Sa Nouveaux derives de phenyl-(4-phenyl-pyrimidin-2-yl)amines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
FR2911138B1 (fr) 2007-01-05 2009-02-20 Sanofi Aventis Sa Nouveaux derives de n, n'-2,4-dianilinopyrimidines, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
FR2911140B1 (fr) 2007-01-05 2009-02-20 Sanofi Aventis Sa Nouveaux derives de 2-anilino 4-heteroaryle pyrimides, leur preparation a titre de medicaments, compositions pharmaceutiques et notamment comme inhibiteurs de ikk
JP5431316B2 (ja) 2007-07-02 2014-03-05 エフ.ホフマン−ラ ロシュ アーゲー Ccr2受容体アンタゴニストとしてのイミダゾール誘導体
AU2008334444B2 (en) 2007-12-12 2011-12-15 Astrazeneca Ab Peptidyl nitriles and use thereof as dipeptidyl peptidase I inhibitors
MX2010009416A (es) * 2008-02-26 2010-09-24 Novartis Ag Compuestos heterociclicos como inhibidores de cxcr2.
US20100029657A1 (en) 2008-02-29 2010-02-04 Wyeth Bridged, Bicyclic Heterocyclic or Spiro Bicyclic Heterocyclic Derivatives of Pyrazolo[1, 5-A]Pyrimidines, Methods for Preparation and Uses Thereof
EP2110374A1 (en) 2008-04-18 2009-10-21 Merck Sante Benzofurane, benzothiophene, benzothiazol derivatives as FXR modulators
WO2010011912A1 (en) 2008-07-25 2010-01-28 Smithkline Beecham Corporation Trpv4 antagonists
CN102030700B (zh) 2009-09-30 2016-06-01 中国医学科学院药物研究所 苯甲酰胺基羧酸类化合物及其制法和药物用途
CA2779108C (en) 2009-10-30 2018-01-02 Janssen Pharmaceutica Nv 4-substituted-2-phenoxy-phenylamine delta opioid receptor modulators
MX2012006484A (es) 2009-12-07 2012-08-01 Targacept Inc 3,6-diazabiciclo [3.1.1] heptanos como ligandos de receptores nicotinicos neuronales de acetilcolina.
JP5889895B2 (ja) 2010-07-29 2016-03-22 ライジェル ファーマシューティカルズ, インコーポレイテッド Ampk活性化複素環化合物およびその使用方法
WO2012067822A1 (en) * 2010-11-16 2012-05-24 Abbott Laboratories Pyrazolo [1, 5 -a] pyrimidin potassium channel modulators
SG193424A1 (en) 2011-03-15 2013-10-30 Rib X Pharmaceuticals Inc Antimicrobial agents
JP2014515370A (ja) 2011-05-23 2014-06-30 ヤンセン ファーマシューティカ エヌ.ベー. グルカゴン受容体拮抗薬として有用なピコリンアミド−プロパン酸誘導体
CN103159742B (zh) 2011-12-16 2015-08-12 北京韩美药品有限公司 5-氯嘧啶类化合物及其作为egfr酪氨酸激酶抑制剂的应用
US9006235B2 (en) * 2012-03-06 2015-04-14 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
CA2905340C (en) 2013-03-12 2022-05-31 Celtaxsys, Inc. Low dose oral formulations of acebilustat
AU2014240042C1 (en) 2013-03-14 2019-09-05 Celltaxis, Llc Inhibitors of leukotriene A4 hydrolase
WO2014152536A2 (en) 2013-03-14 2014-09-25 Celtaxsys, Inc. Inhibitors of leukotriene a4 hydrolase

Similar Documents

Publication Publication Date Title
JP2016513696A5 (US20080131398A1-20080605-C00009.png)
JP2016516043A5 (US20080131398A1-20080605-C00009.png)
JP2016506962A5 (US20080131398A1-20080605-C00009.png)
JP2016513681A5 (US20080131398A1-20080605-C00009.png)
CY1118721T1 (el) Παραγωγα 2,3 διϋδρο-1η-ινδεν-1-υλ-2,7-διαζασπειρο[3.6]εννεανιου και η χρηση αυτων ως ανταγωνιστες ή αντιστροφοι αγωνιστες του υποδοχεα γκρελινης
JP2015522650A5 (US20080131398A1-20080605-C00009.png)
JP2015537020A5 (US20080131398A1-20080605-C00009.png)
JP2017509586A5 (US20080131398A1-20080605-C00009.png)
MX2017010477A (es) Compuestos triciclicos y usos de los mismos en medicina.
JP2016506961A5 (US20080131398A1-20080605-C00009.png)
JP2014503574A5 (US20080131398A1-20080605-C00009.png)
WO2015200481A8 (en) Mnk inhibitors and methods related thereto
EA201692095A1 (ru) Имидазо[4,5-c]хинолин-2-оновые соединения и их применение в лечении рака
EA201490418A1 (ru) Новые макроциклические соединения в качестве ингибиторов фактора xia
TN2013000434A1 (en) Novel imidazole derivatives useful for the treatment of arthritis
EA201390969A1 (ru) Модуляторы глюкагонового рецептора
EA201391263A1 (ru) Комбинированные терапии гематологических опухолей
EA201391486A1 (ru) Способы и композиции для лечения болезни паркинсона
EA201500298A1 (ru) Алкоксипиразолы в качестве активаторов растворимой гуанилатциклазы
RU2015147447A (ru) Производные доластатина 10 и ауристатинов
MX2021006544A (es) Inhibidores de cinasa dependiente de ciclina 9 (cdk9) y polimorfos de los mismos para uso como agentes para el tratamiento de cancer.
JP2015521195A5 (US20080131398A1-20080605-C00009.png)
CY1124251T1 (el) Παραγωγα καρβοξαμιδιου
JP2019535723A5 (US20080131398A1-20080605-C00009.png)
RU2013136895A (ru) Новое бициклическое соединение или его соль