MA33085B1 - Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du recepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructives - Google Patents
Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du recepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructivesInfo
- Publication number
- MA33085B1 MA33085B1 MA33952A MA33952A MA33085B1 MA 33085 B1 MA33085 B1 MA 33085B1 MA 33952 A MA33952 A MA 33952A MA 33952 A MA33952 A MA 33952A MA 33085 B1 MA33085 B1 MA 33085B1
- Authority
- MA
- Morocco
- Prior art keywords
- treatment
- asthma
- antagonists
- premedine
- copd
- Prior art date
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- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
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- A—HUMAN NECESSITIES
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- A—HUMAN NECESSITIES
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
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- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
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- Neurology (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
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- Immunology (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
CETTE INVENTION CONCERNE DE NOUVEAUX ANTAGONISTES DE CCR2 (RÉCEPTEUR 2 DE CHIMIOKINE CC) ET LEUR UTILISATION DANS DES MÉDICAMENTS DESTINÉS AU TRAITEMENT D'ÉTATS PATHOLOGIQUES ET DE MALADIES, EN PARTICULIER DE L'ASTHME ET LES BRONCHO-PNEUMOPATHIES CHRONIQUES OBSTRUCTIVES, COMME REPRÉSENTÉ DANS LA FORMULE (I), OÙ A EST PRIS DANS UNE LIAISON UNIQUE, =CH-, -CH2-, -O-, -S-, AND -NH-; N VAUT 1, 2 OU 3; Z EST C OU N, LES AUTRES VARIABLES ÉTANT COMME DÉFINIES DANS LES REVENDICATIONS, AINSI QUE LEURS FORMES DE SELS D'ADJONCTION ACIDES AVEC DES ACIDES DE QUALITÉ PHARMACOLOGIQUE.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08172336 | 2008-12-19 | ||
EP09160416 | 2009-05-15 | ||
PCT/EP2009/067378 WO2010070032A1 (fr) | 2008-12-19 | 2009-12-17 | Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du récepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructives |
Publications (1)
Publication Number | Publication Date |
---|---|
MA33085B1 true MA33085B1 (fr) | 2012-03-01 |
Family
ID=42049604
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA33952A MA33085B1 (fr) | 2008-12-19 | 2009-12-17 | Pyrimidine-4 carboxamides cycliques en tant qu'antagonistes du recepteur ccr2 pour le traitement d'inflammations, de l'asthme et des broncho-pneumopathies chroniques obstructives |
Country Status (28)
Country | Link |
---|---|
US (3) | US20120053164A1 (fr) |
EP (2) | EP2816040B1 (fr) |
JP (2) | JP2012512834A (fr) |
KR (1) | KR101754698B1 (fr) |
CN (2) | CN103724328B (fr) |
AR (1) | AR074814A1 (fr) |
AU (1) | AU2009327127C1 (fr) |
BR (1) | BRPI0923051B1 (fr) |
CA (1) | CA2747677C (fr) |
CL (1) | CL2011001322A1 (fr) |
CO (1) | CO6382124A2 (fr) |
DK (1) | DK2379525T3 (fr) |
EA (1) | EA020548B1 (fr) |
EC (1) | ECSP11011163A (fr) |
ES (1) | ES2551557T3 (fr) |
HK (1) | HK1159099A1 (fr) |
HU (1) | HUE025547T2 (fr) |
IL (1) | IL212605A (fr) |
MA (1) | MA33085B1 (fr) |
MX (1) | MX2011005150A (fr) |
NZ (1) | NZ592723A (fr) |
PE (1) | PE20120061A1 (fr) |
PL (1) | PL2379525T3 (fr) |
SG (1) | SG172289A1 (fr) |
TN (1) | TN2011000310A1 (fr) |
TW (1) | TWI478913B (fr) |
WO (1) | WO2010070032A1 (fr) |
ZA (1) | ZA201103158B (fr) |
Families Citing this family (53)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008145681A2 (fr) | 2007-05-31 | 2008-12-04 | Boehringer Ingelheim International Gmbh | Antagonistes des récepteurs ccr2 et utilisations de ceux-ci |
US8193182B2 (en) | 2008-01-04 | 2012-06-05 | Intellikine, Inc. | Substituted isoquinolin-1(2H)-ones, and methods of use thereof |
EP2240452B1 (fr) | 2008-01-04 | 2019-05-29 | Intellikine, LLC | Dérivés de 1h-pyrazolo[3,4-d]pyrimidin-4-amine en tant que modulateurs de kinase pi3, leurs compositions et utilisations |
JP5731978B2 (ja) | 2008-09-26 | 2015-06-10 | インテリカイン, エルエルシー | 複素環キナーゼ阻害剤 |
JP2012512834A (ja) | 2008-12-19 | 2012-06-07 | 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 | 炎症、喘息及びcopdの処置のためのccr2受容体アンタゴニストとしての環状ピリミジン−4−カルボキサミド |
EP2415765A4 (fr) * | 2009-03-30 | 2012-08-15 | Astellas Pharma Inc | Composé pyrimidine |
JP5789252B2 (ja) | 2009-05-07 | 2015-10-07 | インテリカイン, エルエルシー | 複素環式化合物およびその使用 |
US8338441B2 (en) | 2009-05-15 | 2012-12-25 | Gilead Sciences, Inc. | Inhibitors of human immunodeficiency virus replication |
WO2011073155A1 (fr) * | 2009-12-17 | 2011-06-23 | Boehringer Ingelheim International Gmbh | Nouveaux antagonistes du récepteur ccr2 et leurs utilisations |
PL3091012T3 (pl) * | 2009-12-17 | 2018-08-31 | Centrexion Therapeutics Corporation | Antagoniści receptora CCR2 i ich zastosowanie |
US8946218B2 (en) | 2010-05-12 | 2015-02-03 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
JP2013526507A (ja) * | 2010-05-12 | 2013-06-24 | 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 | 新規ccr2受容体アンタゴニスト、その製造方法及び薬物としてのその使用 |
WO2011144501A1 (fr) | 2010-05-17 | 2011-11-24 | Boehringer Ingelheim International Gmbh | Antagonistes du récepteur ccr2 et leurs utilisations |
AU2011255218B2 (en) | 2010-05-21 | 2015-03-12 | Infinity Pharmaceuticals, Inc. | Chemical compounds, compositions and methods for kinase modulation |
US9018212B2 (en) | 2010-05-25 | 2015-04-28 | Boehringer Ingelheim International Gmbh | Pyridazine carboxamides as CCR2 receptor antagonists |
JP5721242B2 (ja) | 2010-06-01 | 2015-05-20 | 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 | 新規ccr2アンタゴニスト |
WO2012064973A2 (fr) | 2010-11-10 | 2012-05-18 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et utilisations de ceux-ci |
NZ612909A (en) | 2011-01-10 | 2015-09-25 | Infinity Pharmaceuticals Inc | Processes for preparing isoquinolinones and solid forms of isoquinolinones |
EP2721025B1 (fr) * | 2011-06-16 | 2015-11-25 | Boehringer Ingelheim International Gmbh | Nouveaux antagonistes sélectifs de ccr2 |
EP2731941B1 (fr) | 2011-07-15 | 2019-05-08 | Boehringer Ingelheim International GmbH | Antagonistes ccr2, nouveaux et sélectifs |
MX2014000648A (es) | 2011-07-19 | 2014-09-25 | Infinity Pharmaceuticals Inc | Compuestos heterociclicos y sus usos. |
CN103930422A (zh) | 2011-07-19 | 2014-07-16 | 无限药品股份有限公司 | 杂环化合物及其用途 |
AR091790A1 (es) | 2011-08-29 | 2015-03-04 | Infinity Pharmaceuticals Inc | Derivados de isoquinolin-1-ona y sus usos |
EP2771484A1 (fr) | 2011-10-28 | 2014-09-03 | Galderma Research & Development | Nouveaux marqueurs d'infiltrat leucocytaire de rosacée et utilisations de ceux-ci |
GB2511685A (en) | 2011-11-18 | 2014-09-10 | Heptares Therapeutics Ltd | Muscarinic m1 receptor agonists |
US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
US8828998B2 (en) | 2012-06-25 | 2014-09-09 | Infinity Pharmaceuticals, Inc. | Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors |
WO2014019023A1 (fr) * | 2012-08-01 | 2014-02-06 | Bionomics Limited | Modulateurs du récepteur α7 nicotinique d'acétylcholine et leurs utilisations |
UA110688C2 (uk) | 2012-09-21 | 2016-01-25 | Пфайзер Інк. | Біциклічні піридинони |
CN105102612B (zh) | 2012-12-06 | 2020-11-17 | 恩立夫克治疗有限责任公司 | 治疗性凋亡细胞制剂、其制备方法以及其用途 |
CN103102261A (zh) * | 2013-02-06 | 2013-05-15 | 上海药明康德新药开发有限公司 | 一种螺[2.5]辛烷-5-羧酸的合成方法 |
US9481667B2 (en) | 2013-03-15 | 2016-11-01 | Infinity Pharmaceuticals, Inc. | Salts and solid forms of isoquinolinones and composition comprising and methods of using the same |
SG10201902074UA (en) | 2013-10-04 | 2019-04-29 | Infinity Pharmaceuticals Inc | Heterocyclic compounds and uses thereof |
WO2015051241A1 (fr) | 2013-10-04 | 2015-04-09 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
JOP20200052A1 (ar) * | 2013-12-19 | 2017-06-16 | Bayer Pharma AG | بيبريدينيل تتراهيدرو كوينولينات مستبدلة واستخدامها كمعضدات مستقبل أدريني ألفا- 2c |
CA2943075C (fr) | 2014-03-19 | 2023-02-28 | Infinity Pharmaceuticals, Inc. | Composes heterocycliques destines a etre utilises dans le traitement de troubles medies par pi3k-gamma |
US20150320755A1 (en) | 2014-04-16 | 2015-11-12 | Infinity Pharmaceuticals, Inc. | Combination therapies |
WO2016054491A1 (fr) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
EP3050574B1 (fr) | 2015-01-28 | 2019-10-09 | Universite De Bordeaux | Utilisation de plerixafor pour le traitement et/ou la prévention des exacerbations aiguës de la bronchopneumopathie chronique obstructive |
JP6917910B2 (ja) * | 2015-07-02 | 2021-08-11 | セントレクシオン セラピューティクス コーポレイション | (4−((3r,4r)−3−メトキシテトラヒドロ−ピラン−4−イルアミノ)ピペリジン−1−イル)(5−メチル−6−(((2r,6s)−6−(p−トリル)テトラヒドロ−2h−ピラン−2−イル)メチルアミノ)ピリミジン−4イル)メタノンクエン酸塩 |
GB201513743D0 (en) | 2015-08-03 | 2015-09-16 | Heptares Therapeutics Ltd | Muscarinic agonists |
US10160761B2 (en) | 2015-09-14 | 2018-12-25 | Infinity Pharmaceuticals, Inc. | Solid forms of isoquinolinones, and process of making, composition comprising, and methods of using the same |
GB201519194D0 (en) * | 2015-10-30 | 2015-12-16 | Heptares Therapeutics Ltd | CGRP receptor antagonists |
US10759806B2 (en) | 2016-03-17 | 2020-09-01 | Infinity Pharmaceuticals, Inc. | Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as PI3K kinase inhibitors |
MY195948A (en) | 2016-03-22 | 2023-02-27 | Merck Sharp & Dohme | Allosteric Modulators of Nicotinic Acetylcholine Receptors |
WO2017214269A1 (fr) | 2016-06-08 | 2017-12-14 | Infinity Pharmaceuticals, Inc. | Composés hétérocycliques et leurs utilisations |
SG11201811237WA (en) | 2016-06-24 | 2019-01-30 | Infinity Pharmaceuticals Inc | Combination therapies |
GB201617454D0 (en) | 2016-10-14 | 2016-11-30 | Heptares Therapeutics Limited | Pharmaceutical compounds |
CN108017599B (zh) * | 2016-11-04 | 2020-03-03 | 上海爱科百发生物医药技术有限公司 | [3-(胺甲基)-氧杂环丁烷-3-基]氨基甲酸对甲氧基苄酯对氯苯甲酸盐合成方法 |
GB201810239D0 (en) | 2018-06-22 | 2018-08-08 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
GB201819960D0 (en) | 2018-12-07 | 2019-01-23 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
GB202020191D0 (en) | 2020-12-18 | 2021-02-03 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
WO2022271982A1 (fr) * | 2021-06-23 | 2022-12-29 | Synaptive Therapeutics, Llc | Phénéthylamine substituée pour le traitement d'une inflammation et de troubles psychologiques |
Family Cites Families (122)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4032526A (en) | 1975-10-02 | 1977-06-28 | American Cyanamid Company | 1,2-dimethyl-3 or 5-piperazinyl-pyrazolium salts |
GB2068961B (en) | 1980-02-13 | 1983-11-30 | Sankyo Co | Quinazoline derivatives |
US4621305A (en) | 1984-08-22 | 1986-11-04 | General Motors Corporation | Header connector and attachment |
DE3517617A1 (de) | 1985-05-15 | 1986-11-20 | Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München | Neue pyridaziniumverbindungen, verfahren zu deren herstellung und diese enthaltende fungizide und algizide mittel |
DE3931432A1 (de) * | 1989-09-21 | 1991-04-04 | Hoechst Ag | Pyrimidin-4,6-dicarbonsaeurediamide, verfahren zu deren herstellung sowie verwendung derselben sowie arzneimittel auf basis dieser verbindungen |
US5096916A (en) * | 1990-05-07 | 1992-03-17 | Aegis Technology, Inc. | Treatment of chronic obstructive pulmonary disease (copd) by inhalation of an imidazoline |
EP0665833B1 (fr) | 1992-10-23 | 1999-07-14 | MERCK SHARP & DOHME LTD. | Ligands pour les sous-types de recepteurs de dopamine |
JP3166376B2 (ja) | 1993-02-03 | 2001-05-14 | 松下電器産業株式会社 | 熱利用装置 |
TW531537B (en) * | 1995-12-27 | 2003-05-11 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4-substituted piperidine derivatives |
US5629325A (en) | 1996-06-06 | 1997-05-13 | Abbott Laboratories | 3-pyridyloxymethyl heterocyclic ether compounds useful in controlling chemical synaptic transmission |
US6437138B1 (en) | 1996-06-06 | 2002-08-20 | Abbott Laboratories | 3-pyridyloxymethyl heterocyclic ether compounds useful in controlling chemical synaptic transmission |
US6514977B1 (en) | 1997-05-22 | 2003-02-04 | G.D. Searle & Company | Substituted pyrazoles as p38 kinase inhibitors |
US6979686B1 (en) | 2001-12-07 | 2005-12-27 | Pharmacia Corporation | Substituted pyrazoles as p38 kinase inhibitors |
EE04588B1 (et) | 1997-10-27 | 2006-02-15 | Neurosearch A/S | Heteroarüüldiasatsükloalkaanid kui atsetüülkoliini nikotiinretseptorite kolinergilised ligandid, nende kasutamine ravimitena ning neid sisaldav farmatseutiline kompositsioon |
ATE262523T1 (de) | 1998-11-20 | 2004-04-15 | Searle Llc | Verfahren zur herstellung 5-substituierter pyrazole unter verwendung von dithietane |
US6248755B1 (en) | 1999-04-06 | 2001-06-19 | Merck & Co., Inc. | Pyrrolidine modulators of chemokine receptor activity |
EP1632479B1 (fr) | 1999-05-04 | 2011-01-12 | Schering Corporation | Compositions pharmaceutiques contenant des derives de piperazine antagonistes du ccr5 |
WO2001052902A1 (fr) | 2000-01-24 | 2001-07-26 | Isis Pharmaceuticals, Inc. | Modulation antisens de l'expression de l'oxyde nitrique synthase inductible |
GB0004153D0 (en) | 2000-02-23 | 2000-04-12 | Astrazeneca Uk Ltd | Novel use |
US20020045613A1 (en) | 2000-04-27 | 2002-04-18 | Heinz Pauls | 1-aroyl-piperidinyl benzamidines |
AU5741301A (en) | 2000-05-22 | 2001-12-03 | Aventis Pharm Prod Inc | Arylmethylamine derivatives for use as tryptase inhibitors |
TR200402579T4 (tr) | 2000-10-12 | 2004-12-21 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Kristalin monohidrat, bunun imalat yöntemi ve bir ilaç maddesinin imalatında kullanımı |
AR035700A1 (es) | 2001-05-08 | 2004-06-23 | Astrazeneca Ab | Derivados de arilheteroalquilamina, composicion farmaceutica, usos de estos derivados para la fabricacion de medicamentos, metodos de tratamiento, y proceso para la preparacion de estos derivados |
SK287262B6 (sk) | 2001-06-22 | 2010-04-07 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Kryštalický bezvodný tiotropiumbromid, spôsob jeho výroby, farmaceutický prostriedok s jeho obsahom a jeho použitie |
US20050143372A1 (en) | 2001-10-30 | 2005-06-30 | Shomir Ghosh | Compounds, pharmaceutical compositions and methods of use therefor |
US6806279B2 (en) | 2001-12-17 | 2004-10-19 | Sunesis Pharmaceuticals, Inc. | Small-molecule inhibitors of interleukin-2 |
WO2003066604A2 (fr) | 2002-02-05 | 2003-08-14 | Novo Nordisk A/S | Nouvelles aryl- et heteroarylpiperazines |
HUP0200849A2 (hu) | 2002-03-06 | 2004-08-30 | Sanofi-Synthelabo | N-aminoacetil-2-ciano-pirrolidin-származékok, e vegyületeket tartalmazó gyógyszerkészítmények és eljárás előállításukra |
US20030195192A1 (en) | 2002-04-05 | 2003-10-16 | Fortuna Haviv | Nicotinamides having antiangiogenic activity |
IL164002A0 (en) | 2002-03-13 | 2005-12-18 | Janssen Pharmaceutica Nv | Sulfonyl-derivatives as novel inhibitors of histone deacetylase |
US20040014744A1 (en) | 2002-04-05 | 2004-01-22 | Fortuna Haviv | Substituted pyridines having antiangiogenic activity |
AU2003235097A1 (en) | 2002-04-24 | 2003-11-10 | Takeda Pharmaceutical Company Limited | Use of compounds having ccr antagonism |
CA2483752C (fr) | 2002-04-29 | 2011-03-29 | Merck & Co., Inc. | Modulateurs tetrahydropyranyl cyclopentyl tetrahydropyridopyridine de l'activite des recepteurs de chimiokine |
AR040442A1 (es) | 2002-06-05 | 2005-04-06 | Pharmacia Corp | Derivados de pirazol como inhibidores de la quinasa p38 |
WO2004024710A1 (fr) | 2002-09-13 | 2004-03-25 | Glaxo Group Limited | Composes a base d'uree, actifs en tant qu'antagonistes du recepteur de la vanilloide et utilises pour traiter les douleurs |
SE0203304D0 (sv) | 2002-11-07 | 2002-11-07 | Astrazeneca Ab | Novel Coumpounds |
GB0229618D0 (en) | 2002-12-19 | 2003-01-22 | Cancer Rec Tech Ltd | Pyrazole compounds |
US20040147561A1 (en) | 2002-12-27 | 2004-07-29 | Wenge Zhong | Pyrid-2-one derivatives and methods of use |
WO2004074438A2 (fr) | 2003-02-14 | 2004-09-02 | Smithkline Beecham Corporation | Antagonistes de ccr8 |
NZ542680A (en) | 2003-03-12 | 2008-08-29 | Kudos Pharm Ltd | Phthalazinone derivatives |
DK1615909T3 (da) | 2003-04-23 | 2008-11-17 | Glaxo Group Ltd | Piperazin-derivater og deres anvendelse til behandling af neurologiske og psykiatriske sygdomme |
FR2854158B1 (fr) | 2003-04-25 | 2006-11-17 | Sanofi Synthelabo | Derives de 2-acylamino-4-phenylethiazole, leur preparation et leur application en therapeutique |
TW200514781A (en) | 2003-07-18 | 2005-05-01 | Glaxo Group Ltd | Novel compounds |
KR20060054392A (ko) | 2003-07-29 | 2006-05-22 | 노보 노르디스크 에이/에스 | 피리다지닐-피페라진 및 히스타민 h3 수용체 리간드로서그들의 사용 |
AP2439A (en) | 2003-12-18 | 2012-08-31 | Incyte Corp | 3-Cycloalkylaminopyrrolidine derivatives as modulators of chemokine receptors |
GB0403155D0 (en) * | 2004-02-12 | 2004-03-17 | Vernalis Res Ltd | Chemical compounds |
EP1720545B1 (fr) | 2004-03-03 | 2014-10-29 | ChemoCentryx, Inc. | Heterocycles d'azote bicycliques et ponts |
PE20060285A1 (es) | 2004-03-30 | 2006-05-08 | Aventis Pharma Inc | Piridonas sustituidas como inhibidores de pol(adp-ribosa)-polimerasa (parp) |
US7423147B2 (en) | 2004-03-31 | 2008-09-09 | Janssen Pharmaceutical, N.V. | Pyridine compounds as histamine H3 modulators |
JP5213229B2 (ja) | 2004-04-23 | 2013-06-19 | エグゼリクシス, インコーポレイテッド | キナーゼ調節因子および使用方法 |
CA2567851A1 (fr) | 2004-05-21 | 2006-01-05 | Merck & Co., Inc. | Modulateurs heterocycliques et carbocycliques d'amino cyclopentyle de l'activite du recepteur de la chimiokine |
GEP20105024B (en) | 2004-06-02 | 2010-06-25 | Takeda Pharmaceuticals Co | Fused heterocyclic compound |
FR2871157A1 (fr) | 2004-06-04 | 2005-12-09 | Aventis Pharma Sa | Produits biaryl aromatiques, compositions les contenant et utilisation |
EA200700117A1 (ru) | 2004-06-24 | 2007-06-29 | Инсайт Корпорейшн | N-замещенные пиперидины и их применение в качестве фармацевтических препаратов |
UA85597C2 (ru) | 2004-06-25 | 2009-02-10 | Янссен Фармацевтика Н.В. | Четвертичные соли как антагонисты ccr2 |
GEP20094844B (en) | 2004-06-28 | 2009-11-25 | Incyte Corp | 3-aminocyclopentane carboxamides as modulators of chemokine receptors |
GB0419072D0 (en) * | 2004-08-26 | 2004-09-29 | Kudos Pharm Ltd | Phthalazinone derivatives |
BRPI0514632A (pt) * | 2004-08-26 | 2008-06-17 | Kudos Pharm Ltd | derivados de ftalazinona 4-heteroarilmetila substituìdos |
GB0420831D0 (en) | 2004-09-17 | 2004-10-20 | Glaxo Group Ltd | Novel compounds |
EP2266569A3 (fr) | 2004-09-20 | 2011-03-09 | Xenon Pharmaceuticals Inc. | Dérivés hétérocycliques et leur utilisation en tant qu'inhibiteurs de la stearoyl-coa desaturase |
GB0421525D0 (en) * | 2004-09-28 | 2004-10-27 | Novartis Ag | Inhibitors of protein kineses |
WO2006038734A1 (fr) | 2004-10-08 | 2006-04-13 | Astellas Pharma Inc. | Dérivés de la pyridazinone inhibiteurs de cytokines |
ES2441718T3 (es) | 2004-11-02 | 2014-02-06 | Northwestern University | Compuestos de piridazina, composiciones y métodos |
UY29219A1 (es) | 2004-11-22 | 2006-04-28 | Incyte Corp | Sales de la n-(2- (((3r)-1-(trans-4-hidroxi-4-(6-metoxipiridin-3-il)-cilohexil) pirrolidin-3-il)amino)-2-oxoetil)-3- (trifluorometil) benzamida |
DE102004061751A1 (de) | 2004-12-22 | 2006-07-06 | Bayer Healthcare Ag | Cyanoguanidin-substituierte Pyrazoline |
BRPI0608205B8 (pt) | 2005-02-17 | 2021-05-25 | Astellas Pharma Inc | derivado heterocíclico-1-carboxilato de piridila não-aromático nitrogenado, composição farmacêutica e uso do dito composto para o tratamento de frequência urinária, incontinência urinária, bexiga hiperativa e dor |
EP1879881A2 (fr) | 2005-04-14 | 2008-01-23 | Bristol-Myers Squibb Company | Inhibiteurs de la 11-beta hydroxysteroide deshydrogenase de type i |
WO2006113140A2 (fr) | 2005-04-15 | 2006-10-26 | Elan Pharmaceuticals, Inc. | Nouveaux composes s'utilisant dans l'antagonisme du recepteur de bradykinine b1 |
AU2006236387A1 (en) | 2005-04-18 | 2006-10-26 | Neurogen Corporation | Subtituted heteroaryl CB1 antagonists |
US20080221111A1 (en) | 2005-05-11 | 2008-09-11 | Nycomed Gmbh | Combination of a Pd4 Inhibitor and a Tetrahydrobiopterin Derivative |
CN101228161B (zh) | 2005-05-20 | 2012-10-10 | 沃泰克斯药物股份有限公司 | 适用作蛋白激酶抑制剂的吡咯并吡啶类 |
CN103110635A (zh) | 2005-07-04 | 2013-05-22 | 海波因特制药有限责任公司 | 组胺h3受体拮抗剂 |
AU2006275568A1 (en) | 2005-08-02 | 2007-02-08 | Neurogen Corporation | Dipiperazinyl ketones and related analogues |
GB0517184D0 (en) | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
AR055203A1 (es) * | 2005-08-31 | 2007-08-08 | Otsuka Pharma Co Ltd | Derivados de benzotiofeno con propiedades antipsicoticas |
TW200800999A (en) | 2005-09-06 | 2008-01-01 | Astrazeneca Ab | Novel compounds |
WO2007038669A2 (fr) | 2005-09-27 | 2007-04-05 | Irm Llc | Composes et compositions contenant de la diarylamine, et utilisation en tant que modulateurs de recepteurs de c-kit |
JO2769B1 (en) | 2005-10-26 | 2014-03-15 | جانسين فارماسوتيكا ان. في | Rapid decomposition of physiologically antagonistic agents of the 2-dopamine receptor |
US20100016289A1 (en) | 2005-11-01 | 2010-01-21 | Kevin Sprott | Compounds Useful as Antagonists of CCR2 |
US8067457B2 (en) | 2005-11-01 | 2011-11-29 | Millennium Pharmaceuticals, Inc. | Compounds useful as antagonists of CCR2 |
AU2006337682A1 (en) | 2005-11-14 | 2007-08-16 | Irm Llc | Compounds and compositions as LXR modulators |
BRPI0620066A2 (pt) * | 2005-12-20 | 2011-11-01 | Novartis Ag | derivados de ácido nicotìnico como moduladores do receptor de glutamato metabotrópico, processo para preparação dos mesmos, composição farmacêutica e uso dos referidos derivados |
WO2007084868A2 (fr) | 2006-01-17 | 2007-07-26 | Kalypsys, Inc. | Traitement d'une inflammation et de troubles associes par l'activation de la reponse upr (proteine depliee) |
JO2660B1 (en) | 2006-01-20 | 2012-06-17 | نوفارتيس ايه جي | Pi-3 inhibitors and methods of use |
NZ595571A (en) | 2006-02-28 | 2013-04-26 | Helicon Therapeutics Inc | Pyrazole compounds and uses thereof |
CA2643066A1 (fr) | 2006-03-16 | 2007-09-20 | Pfizer Products Inc. | Pyrazoles |
CN101466677A (zh) | 2006-04-11 | 2009-06-24 | 默克公司 | 二芳基取代的烷烃 |
US7807671B2 (en) | 2006-04-25 | 2010-10-05 | Bristol-Myers Squibb Company | Diketo-piperazine and piperidine derivatives as antiviral agents |
CA2650704A1 (fr) | 2006-04-28 | 2007-11-08 | Northwestern University | Sels de composes de pyridazine |
JP2009541268A (ja) | 2006-06-22 | 2009-11-26 | ビオヴィトルム・アクチボラゲット(プブリクト) | Mnkキナーゼ阻害剤としてのピリジンおよびピラジン誘導体 |
GB0617575D0 (en) | 2006-09-06 | 2006-10-18 | Syngenta Ltd | Herbicidal compounds and compositions |
JP2010510224A (ja) * | 2006-11-17 | 2010-04-02 | アボット・ラボラトリーズ | ケモカイン受容体拮抗薬としてのアミノピロリジン類 |
SG193664A1 (en) | 2006-12-28 | 2013-10-30 | Abbott Lab | Inhibitors of poly(adp-ribose)polymerase |
CA2676715A1 (fr) | 2007-02-12 | 2008-08-21 | Merck & Co., Inc. | Derives de piperazine pour le traitement de la maladie d'alzheimer et des conditions apparentees |
JP4785881B2 (ja) | 2007-02-27 | 2011-10-05 | 大塚製薬株式会社 | 医薬 |
FR2915552B1 (fr) | 2007-04-27 | 2009-11-06 | Technip France | Conduite tubulaire flexible pour le transport d'hydrocarbures gazeux. |
WO2008145681A2 (fr) | 2007-05-31 | 2008-12-04 | Boehringer Ingelheim International Gmbh | Antagonistes des récepteurs ccr2 et utilisations de ceux-ci |
EP2173735B1 (fr) | 2007-07-02 | 2012-01-11 | F. Hoffmann-La Roche AG | Dérivés imidazolés comme antagonistes du récepteur ccr2 |
US7977358B2 (en) | 2007-07-26 | 2011-07-12 | Hoffmann-La Roche Inc. | Pyrazol derivatives |
EP2042516A1 (fr) | 2007-09-27 | 2009-04-01 | Protaffin Biotechnologie AG | Mutants de MCP-1 capable d'antagonisé des glycosaminoglycans et leurs procédés d'utilisation |
EP2190836B1 (fr) | 2007-08-22 | 2011-08-17 | Irm Llc | Derives de 2-heteroarylamino-pyrimidine en tant qu'inhibiteurs de kinase |
KR20100050570A (ko) | 2007-10-01 | 2010-05-13 | 에프. 호프만-라 로슈 아게 | Ccr 수용체 길항제로서의 n-헤테로사이클릭 바이아릴 카복스아마이드 |
EP2200470A4 (fr) | 2007-10-12 | 2013-11-20 | Jong O Whang | Outil de serrage pour lacet de chaussure |
US20090131417A1 (en) | 2007-11-20 | 2009-05-21 | Letavic Michael A | Substituted pyridyl amide compounds as modulators of the histamine h3 receptor |
WO2009066084A1 (fr) * | 2007-11-21 | 2009-05-28 | F. Hoffmann-La Roche Ag | 2-morpholinopyrimidines et leur utilisation en tant qu'inhibiteurs de kinase pi3 |
JP5385297B2 (ja) * | 2007-11-22 | 2014-01-08 | 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 | 新規化合物 |
EP2062889A1 (fr) * | 2007-11-22 | 2009-05-27 | Boehringer Ingelheim Pharma GmbH & Co. KG | Composés |
WO2009153182A1 (fr) | 2008-06-18 | 2009-12-23 | F. Hoffmann-La Roche Ag | Nouveaux dérivés de carboxamide d’hétéroaryle |
NZ601483A (en) * | 2008-08-04 | 2013-10-25 | Chdi Foundation Inc | Certain kynurenine-3-monooxygenase inhibitors, pharmaceutical compositions, and methods of use thereof |
GB0815369D0 (en) * | 2008-08-22 | 2008-10-01 | Summit Corp Plc | Compounds for treatment of duchenne muscular dystrophy |
NZ591226A (en) * | 2008-09-02 | 2012-11-30 | Boehringer Ingelheim Int | Benzoic acid amides, production thereof, and use thereof as medicaments |
JP2012512834A (ja) | 2008-12-19 | 2012-06-07 | 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 | 炎症、喘息及びcopdの処置のためのccr2受容体アンタゴニストとしての環状ピリミジン−4−カルボキサミド |
CA2750635A1 (fr) | 2009-02-23 | 2010-08-26 | Merck Canada Inc. | Derives heterocycliques comme inhibiteurs de la stearoyl-coenzyme a delta-9 desaturase |
PL3091012T3 (pl) * | 2009-12-17 | 2018-08-31 | Centrexion Therapeutics Corporation | Antagoniści receptora CCR2 i ich zastosowanie |
WO2011073155A1 (fr) | 2009-12-17 | 2011-06-23 | Boehringer Ingelheim International Gmbh | Nouveaux antagonistes du récepteur ccr2 et leurs utilisations |
JP2013526507A (ja) | 2010-05-12 | 2013-06-24 | 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 | 新規ccr2受容体アンタゴニスト、その製造方法及び薬物としてのその使用 |
US8946218B2 (en) | 2010-05-12 | 2015-02-03 | Boehringer Ingelheim International Gmbh | CCR2 receptor antagonists, method for producing the same, and use thereof as medicaments |
WO2011144501A1 (fr) | 2010-05-17 | 2011-11-24 | Boehringer Ingelheim International Gmbh | Antagonistes du récepteur ccr2 et leurs utilisations |
US9018212B2 (en) | 2010-05-25 | 2015-04-28 | Boehringer Ingelheim International Gmbh | Pyridazine carboxamides as CCR2 receptor antagonists |
JP5721242B2 (ja) | 2010-06-01 | 2015-05-20 | 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 | 新規ccr2アンタゴニスト |
EP2721025B1 (fr) | 2011-06-16 | 2015-11-25 | Boehringer Ingelheim International Gmbh | Nouveaux antagonistes sélectifs de ccr2 |
EP2731941B1 (fr) | 2011-07-15 | 2019-05-08 | Boehringer Ingelheim International GmbH | Antagonistes ccr2, nouveaux et sélectifs |
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