MA30360B1 - Dérivés pyrimidiniques utilisés comme inhibiteurs de la pi3k - Google Patents

Dérivés pyrimidiniques utilisés comme inhibiteurs de la pi3k

Info

Publication number
MA30360B1
MA30360B1 MA31338A MA31338A MA30360B1 MA 30360 B1 MA30360 B1 MA 30360B1 MA 31338 A MA31338 A MA 31338A MA 31338 A MA31338 A MA 31338A MA 30360 B1 MA30360 B1 MA 30360B1
Authority
MA
Morocco
Prior art keywords
group
alk
alkyl
unsubstituted
substituted
Prior art date
Application number
MA31338A
Other languages
English (en)
Inventor
Stewart James Baker
Paul John Goldsmith
Timothy Colin Hancox
Neil Anthony Pegg
Stephen Price
Stephen Joseph Shuttleworth
Sukhjit Sohal
Original Assignee
Hoffmann La Roche
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
Priority claimed from GB0608264A external-priority patent/GB0608264D0/en
Priority claimed from GB0608397A external-priority patent/GB0608397D0/en
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA30360B1 publication Critical patent/MA30360B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Immunology (AREA)
  • Hematology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Cardiology (AREA)
  • Endocrinology (AREA)
  • Oncology (AREA)
  • Obesity (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Pain & Pain Management (AREA)
  • Emergency Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Transplantation (AREA)
  • Communicable Diseases (AREA)
  • Pulmonology (AREA)
  • Virology (AREA)
  • Psychiatry (AREA)
  • Vascular Medicine (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Dermatology (AREA)
  • Gastroenterology & Hepatology (AREA)

Abstract

COMPOSES PHARMACEUTIQUES Thiénopyrimidines de formule (Ia) ou (Ib): dans laquelle R1 est un groupe de formule: R2 est un atome d'hydrogène, un halo ou un groupe alkyle en C1-C6; R3 est un groupe indole substitué ou non substitué; R4 et R5 forment, avec l'atome d'azote auquel ils sont attachés, un groupe choisi parmi la pipérazine, pipéridine et pyrrolidine, groupe substitué ou non substitué par un ou plusieurs groupe (s) choisi(s) parmi un alkyle en C1-C6, S(O)2R10, -S(O)2-(alk)q-NR11R12, oxo(=0), -alk-OR10, -(alk)q-Het, un groupe hétérocyclyle et -NR13R14 ; ou un de R4 et R5 est un alkyle en C1-C4 et l'autre un groupe pipérazine, pipéridine ou pyrrolidine, substitué ou non substitué; R10 est un atome d'hydrogène ou un alkyle en C1-C6 non substitué; R11 et R12 sont chacun choisis indépendamment parmi un atome d'hydrogène et un alkyle en C1-C4 non substitué, ou R11 et R12 forment, avec l'atome d'azote auquel ils sont attachés, un groupe hétérocyclique saturé à 5 ou 6 atomes; R13 et R14 sont chacun choisis indépendamment parmi un alkyle en C1-C6, -S(O)2 R10, alk-OR10, -(alk)q-Ph et -(alk)q-Het; Ph est un phényle; q est 0 ou 1; Het est un groupe thiazole, imidazole, pyrrole, pyridine ou pyrimidine, lequel est substitué ou non substitué ; et alk est un alkylène en C1-C6; et le sel pharmaceutiquement acceptable de ceux-ci, possèdent une activité en tant qu'inhibiteurs de la PI3K, et peuvent donc être utilisés pour traiter des maladies et des troubles résultant de la croissance, de la fonction ou du comportement cellulaire anormal(e) associé (e) à la PI3 kinase, en particulier, le sous-type p110 delta, tels que les troubles immuns, la maladie cardiovasculaire, l'infection virale, l'inflammation, les troubles du métabolisme/endocriniens ou les troubles neurologiques. Des procédés de synthèse des composés sont également décrits
MA31338A 2006-04-26 2008-10-27 Dérivés pyrimidiniques utilisés comme inhibiteurs de la pi3k MA30360B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0608264A GB0608264D0 (en) 2006-04-26 2006-04-26 Pharmaceutical compounds
GB0608397A GB0608397D0 (en) 2006-04-27 2006-04-27 Pharmaceutical compounds

Publications (1)

Publication Number Publication Date
MA30360B1 true MA30360B1 (fr) 2009-04-01

Family

ID=38110021

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31338A MA30360B1 (fr) 2006-04-26 2008-10-27 Dérivés pyrimidiniques utilisés comme inhibiteurs de la pi3k

Country Status (15)

Country Link
US (2) US8252792B2 (fr)
EP (1) EP2032582A1 (fr)
JP (1) JP5302186B2 (fr)
KR (1) KR20090021155A (fr)
AU (1) AU2007242594A1 (fr)
BR (1) BRPI0710866A2 (fr)
CA (1) CA2650196A1 (fr)
CR (1) CR10369A (fr)
EC (1) ECSP088867A (fr)
IL (1) IL194755A0 (fr)
MA (1) MA30360B1 (fr)
MX (1) MX2008013582A (fr)
NO (1) NO20084832L (fr)
RU (1) RU2008141356A (fr)
WO (1) WO2007122410A1 (fr)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI498332B (zh) 2006-04-26 2015-09-01 Hoffmann La Roche 作為pi3k抑制劑之嘧啶衍生物及相關製備方法、醫藥組合物、用途、套組及產物
MX2009005950A (es) 2006-12-07 2009-10-12 Genentech Inc Compuestos inhibidores de fosfoinositido 3-quinasas y metodos de uso.
RU2470936C2 (ru) 2006-12-07 2012-12-27 Дженентек, Инк. Соединения-ингибиторы фосфоинозитид 3-киназы и способы применения
US7893060B2 (en) 2007-06-12 2011-02-22 F. Hoffmann-La Roche Ag Thiazolopyrimidines and their use as inhibitors of phosphatidylinositol-3 kinase
EP2205242B1 (fr) 2007-09-12 2015-04-15 Genentech, Inc. Combinaisons de composés inhibiteurs des phosphoinositide 3-kinases et agents chimiothérapeutiques, et leurs procédés d'utilisation
CA2704711C (fr) 2007-09-24 2016-07-05 Genentech, Inc. Composes inhibiteurs de la pi3k a base de thiazolopyrimidine
JP5348725B2 (ja) * 2007-10-25 2013-11-20 ジェネンテック, インコーポレイテッド チエノピリミジン化合物の製造方法
GB0721095D0 (en) * 2007-10-26 2007-12-05 Piramed Ltd Pharmaceutical compounds
CA2729045A1 (fr) 2008-07-31 2010-02-04 Philippe Bergeron Composes de pyrimidine, compositions et procedes d'utilisation
CN102170873B (zh) 2008-10-01 2014-07-30 诺华股份有限公司 用于治疗与hedgehog通路有关的病症的smoothened拮抗
TWI378933B (en) 2008-10-14 2012-12-11 Daiichi Sankyo Co Ltd Morpholinopurine derivatives
EA024252B1 (ru) 2009-01-08 2016-08-31 Кьюрис, Инк. Ингибиторы фосфоинозитид-3-киназ с цинксвязывающей группой
BRPI1009022A2 (pt) 2009-05-27 2016-03-08 Hoffmann La Roche "composto, composição farmacêutica, processo para produzir uma composição farmacêutica, uso de um composto, método para tratamento de uma doença ou transtorno e kit"
US8158625B2 (en) 2009-05-27 2012-04-17 Genentech, Inc. Bicyclic indole-pyrimidine PI3K inhibitor compounds selective for P110 delta, and methods of use
LT3141252T (lt) 2009-06-17 2018-11-12 Vertex Pharmaceuticals Inc. Gripo virusų replikacijos inhibitoriai
AR077405A1 (es) 2009-07-10 2011-08-24 Sanofi Aventis Derivados del indol inhibidores de hsp90, composiciones que los contienen y utilizacion de los mismos para el tratamiento del cancer
MX2012002059A (es) * 2009-08-20 2012-04-19 Karus Therapeutics Ltd Compestos heterociclicos triciclicos como inhibidores de fosfoionositida 3-quinasa.
EP2499143B1 (fr) 2009-11-12 2016-03-16 F.Hoffmann-La Roche Ag Composés des purines n7-substituées et des pyrazolopyrimidines, compositions et les procédés pour leur utilisation
JP5579864B2 (ja) 2009-11-12 2014-08-27 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト N−9−置換プリン化合物、組成物及び使用の方法
TW201500358A (zh) 2010-12-16 2015-01-01 赫夫門羅氏藥廠股份有限公司 三環pi3k抑制劑化合物及其使用方法
UA118010C2 (uk) 2011-08-01 2018-11-12 Вертекс Фармасьютікалз Інкорпорейтед Інгібітори реплікації вірусів грипу
GB201204125D0 (en) 2012-03-08 2012-04-25 Karus Therapeutics Ltd Compounds
KR20160027219A (ko) 2012-05-23 2016-03-09 에프. 호프만-라 로슈 아게 내배엽 및 간세포를 수득하고 사용하는 조성물 및 방법
US20150258127A1 (en) 2012-10-31 2015-09-17 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for preventing antiphospholipid syndrome (aps)
IN2015DN03235A (fr) 2012-11-07 2015-10-02 Karus Therapeutics Ltd
PT2994465T (pt) 2013-05-10 2018-10-25 Karus Therapeutics Ltd Novos inibidores de histona desacetilase
US9296727B2 (en) 2013-10-07 2016-03-29 Vertex Pharmaceuticals Incorporated Methods of regioselective synthesis of 2,4-disubstituted pyrimidines
LT3068776T (lt) 2013-11-13 2019-08-12 Vertex Pharmaceuticals Incorporated Gripo virusų replikacijos inhibitoriai
JP6618901B2 (ja) 2013-11-13 2019-12-11 バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated インフルエンザウイルスの複製の阻害剤を調製する方法
GB201402431D0 (en) 2014-02-12 2014-03-26 Karus Therapeutics Ltd Compounds
GB201419264D0 (en) 2014-10-29 2014-12-10 Karus Therapeutics Ltd Compounds
GB201419228D0 (en) 2014-10-29 2014-12-10 Karus Therapeutics Ltd Compounds
JP6454419B2 (ja) * 2014-12-11 2019-01-16 ナトコ ファーマ リミテッド 抗癌剤としての7−(モルホリニル)−2−(N−ピペラジニル)メチルチエノ[2,3−c]ピリジン誘導体
WO2016147543A1 (fr) 2015-03-13 2016-09-22 Ricoh Company, Ltd. Composé électrochromique, composition électrochromique, élément électrochromique et élément d'obscurcissement électrochromique
EP3294735B8 (fr) 2015-05-13 2022-01-05 Vertex Pharmaceuticals Incorporated Inhibiteurs de la réplication des virus de la grippe
EP3294717B1 (fr) 2015-05-13 2020-07-29 Vertex Pharmaceuticals Inc. Procédés de préparation d'inhibiteurs de réplication des virus de la grippe
GB201514754D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds
GB201514758D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Formulation
GB201514760D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds and method of use
GB201514751D0 (en) 2015-08-19 2015-09-30 Karus Therapeutics Ltd Compounds
CN109414408B (zh) * 2016-05-16 2022-03-29 得克萨斯州大学系统董事会 阳离子磺酰胺氨基脂质和两亲性两性离子氨基脂质
GB201909468D0 (en) 2019-07-01 2019-08-14 Karus Therapeutics Ltd Compounds for treating cancer
WO2022224267A1 (fr) * 2021-04-21 2022-10-27 Natco Pharma Limited Procédé amélioré pour la préparation de dérivés de 7-(morpholinyl)-2-(n-pipérazinyl)méthylthiéno[2, 3-c]pyridine

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1067123B1 (fr) 1998-03-31 2011-01-19 Kyowa Hakko Kirin Co., Ltd. Composes heterocycliques azotes
US6232320B1 (en) 1998-06-04 2001-05-15 Abbott Laboratories Cell adhesion-inhibiting antiinflammatory compounds
KR100774855B1 (ko) 2000-04-27 2007-11-08 아스텔라스세이야쿠 가부시키가이샤 축합 헤테로아릴 유도체
AU2003255845A1 (en) 2002-08-22 2004-03-11 Piramed Limited Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents
GB0423653D0 (en) * 2004-10-25 2004-11-24 Piramed Ltd Pharmaceutical compounds
TWI498332B (zh) 2006-04-26 2015-09-01 Hoffmann La Roche 作為pi3k抑制劑之嘧啶衍生物及相關製備方法、醫藥組合物、用途、套組及產物

Also Published As

Publication number Publication date
IL194755A0 (en) 2009-08-03
US8252792B2 (en) 2012-08-28
NO20084832L (no) 2008-11-18
EP2032582A1 (fr) 2009-03-11
JP2009534453A (ja) 2009-09-24
US20120283257A1 (en) 2012-11-08
ECSP088867A (es) 2008-12-30
AU2007242594A1 (en) 2007-11-01
US8697693B2 (en) 2014-04-15
RU2008141356A (ru) 2010-06-10
CA2650196A1 (fr) 2007-11-01
KR20090021155A (ko) 2009-02-27
CR10369A (es) 2009-01-09
BRPI0710866A2 (pt) 2012-08-14
US20100016306A1 (en) 2010-01-21
WO2007122410A1 (fr) 2007-11-01
MX2008013582A (es) 2009-01-19
JP5302186B2 (ja) 2013-10-02

Similar Documents

Publication Publication Date Title
MA30360B1 (fr) Dérivés pyrimidiniques utilisés comme inhibiteurs de la pi3k
US8258154B2 (en) Bicyclic heteroaryl inhibitors of PDE4
US20250188074A1 (en) Ptpn11 inhibitors
US5326770A (en) Monoamine oxidase-B (MAO-B) inhibitory 5-substituted 2,4-thiazolidinediones useful in treating memory disorders of mammals
US20090275586A1 (en) Heterocyclic inhibitors of pde4
US8138205B2 (en) Heteroarylalkoxy-substituted quinolone inhibitors of PDE4
MA30412B1 (fr) Composés Pharmaceutiques
MX2009010884A (es) 2-morfolin-4-il-pirimidinas como inhibidores de fosfatidilinositol-3-cinasa (pi3k).
MX2011002825A (es) Compuestos heterociclicos de carboxamida.
MX2010004819A (es) Derivados de [1h-pirazolo[3,4-b]piridin-4-il]-fenilo o piridin-2-ilo como proteina cinasa c-theta.
TW200946522A (en) BACE inhibitors
US20130116279A1 (en) Bicyclic heteroaryl inhibitors of pde4
CZ288944B6 (cs) Derivát 5H-thiazolo[3,2-a]pyrimidinu, způsob jeho přípravy, meziprodukt pro jeho přípravu a farmaceutický prostředek, který ho obsahuje
WO2015112847A1 (fr) Inhibiteurs d'itk à base d'arylpyridinone permettant de traiter une inflammation et un cancer
EP3458063A1 (fr) Procédés d'utilisation d'activateurs de la guanylate cyclase soluble dans la triazolo-pyrazinyle pour des troubles fibrotiques
WO2024020221A1 (fr) Modulateurs de protéolyse tyk2 et leurs procédés d'utilisation
US20100105729A1 (en) Aryl-substituted heterocyclic pde4 inhibitors as anti-inflammatory agents
US6699867B2 (en) Use of 2-amino-thiazoline derivatives as inhibitors of inducible NO-synthase
WO2001035959A1 (fr) Utilisation de derives de thiazole pour traiter/prevenir les troubles induits par la kinase p38
WO1994026737A1 (fr) Derive d'imidazolylquinoxalinedione et composition pharmaceutique le contenant
AU2018447240B2 (en) Indazole kinase inhibitor and use thereof
US6699895B2 (en) 2-aminothiazoline derivatives and process for preparing the same
EP0573360B1 (fr) Composés pyrrolothiénopyraziniques comme antagonistes des récepteurs 5-HT3