MX2009005194A - Derivados de purina 7-sustituidos para inmunosupresion. - Google Patents

Derivados de purina 7-sustituidos para inmunosupresion.

Info

Publication number
MX2009005194A
MX2009005194A MX2009005194A MX2009005194A MX2009005194A MX 2009005194 A MX2009005194 A MX 2009005194A MX 2009005194 A MX2009005194 A MX 2009005194A MX 2009005194 A MX2009005194 A MX 2009005194A MX 2009005194 A MX2009005194 A MX 2009005194A
Authority
MX
Mexico
Prior art keywords
immunosuppression
purine derivatives
substituted purine
purinone
prevention
Prior art date
Application number
MX2009005194A
Other languages
English (en)
Inventor
Koc-Kan Ho
Adolph Bohnstedt
Celia Kingsbury
Jorge Quintero
Michael Ohlmeyer
Original Assignee
Pharmacopeia Llc
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
Application filed by Pharmacopeia Llc filed Critical Pharmacopeia Llc
Publication of MX2009005194A publication Critical patent/MX2009005194A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • 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
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52—Purines, e.g. adenine
    • A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Pain & Pain Management (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Transplantation (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La presente invención provee nuevos derivados de purinona y derivados relacionados útiles para la prevención y tratamiento de enfermedades autoinmunes, enfermedad inflamatoria, enfermedad moderada por célula cebada y rechazo de trasplante. Los compuestos son de fórmula general (III). (ver fórmula (III)).
MX2009005194A 2006-11-16 2006-11-16 Derivados de purina 7-sustituidos para inmunosupresion. MX2009005194A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2006/061004 WO2008060301A1 (en) 2006-11-16 2006-11-16 7-substituted purine derivatives for immunosuppression

Publications (1)

Publication Number Publication Date
MX2009005194A true MX2009005194A (es) 2009-11-10

Family

ID=38578618

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009005194A MX2009005194A (es) 2006-11-16 2006-11-16 Derivados de purina 7-sustituidos para inmunosupresion.

Country Status (11)

Country Link
EP (1) EP2099800A1 (es)
JP (1) JP2010510211A (es)
KR (1) KR20100014271A (es)
CN (1) CN101595110A (es)
AU (1) AU2006350748A1 (es)
BR (1) BRPI0622030A2 (es)
CA (1) CA2669686A1 (es)
CR (1) CR10870A (es)
IL (1) IL198761A0 (es)
MX (1) MX2009005194A (es)
WO (1) WO2008060301A1 (es)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7884109B2 (en) * 2005-04-05 2011-02-08 Wyeth Llc Purine and imidazopyridine derivatives for immunosuppression
US7989459B2 (en) * 2006-02-17 2011-08-02 Pharmacopeia, Llc Purinones and 1H-imidazopyridinones as PKC-theta inhibitors
JP5647998B2 (ja) 2009-03-13 2015-01-07 カトリーケ ユニバーシテイト ルーヴェン、ケー．ユー． ルーヴェン アール アンド ディー 免疫抑制剤としてのチアゾロピリミジン調節因子
WO2010118986A1 (en) 2009-04-14 2010-10-21 Cellzome Limited Fluoro substituted pyrimidine compounds as jak3 inhibitors
EP2475648A1 (en) 2009-09-11 2012-07-18 Cellzome Limited Ortho substituted pyrimidine compounds as jak inhibitors
CN102666545B (zh) 2009-10-20 2016-04-06 塞尔卓姆有限公司 作为jak抑制剂的杂环吡唑并嘧啶类似物
TWI478714B (zh) 2009-10-29 2015-04-01 Vectura Ltd 作為Ｊａｎｕｓ激酶３（ＪＡＫ３）抑制劑之含氮雜芳基衍生物類
BR112012027803A2 (pt) 2010-04-30 2016-08-09 Cellzome Ltd compostos de pirazol como inibidores de jak
GB201012889D0 (en) 2010-08-02 2010-09-15 Univ Leuven Kath Antiviral activity of novel bicyclic heterocycles
HUE030720T2 (en) 2010-05-31 2017-06-28 Ono Pharmaceutical Co Purinone derivative as btk kinase inhibitor
US20130165426A1 (en) * 2010-07-06 2013-06-27 Université de Montréal Imidazopyridine, imidazopyrimidine and imidazopyrazine derivatives as melanocortin-4 receptor modulators
WO2012022681A2 (en) 2010-08-20 2012-02-23 Cellzome Limited Heterocyclyl pyrazolopyrimidine analogues as selective jak inhibitors
KR101227388B1 (ko) * 2010-09-09 2013-01-30 주식회사 만도 3웨이 형식의 저압 배기가스 재순환 밸브 구조
GB201015411D0 (en) 2010-09-15 2010-10-27 Univ Leuven Kath Anti-cancer activity of novel bicyclic heterocycles
US9018395B2 (en) 2011-01-27 2015-04-28 Université de Montréal Pyrazolopyridine and pyrazolopyrimidine derivatives as melanocortin-4 receptor modulators
WO2012143320A1 (en) 2011-04-18 2012-10-26 Cellzome Limited (7h-pyrrolo[2,3-d]pyrimidin-2-yl)amine compounds as jak3 inhibitors
AU2012288892B2 (en) 2011-07-28 2016-04-21 Cellzome Limited Heterocyclyl pyrimidine analogues as JAK inhibitors
WO2013017479A1 (en) 2011-07-29 2013-02-07 Cellzome Limited Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors
WO2013017480A1 (en) 2011-07-29 2013-02-07 Cellzome Limited Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors
WO2013025628A1 (en) 2011-08-15 2013-02-21 Ligand Pharmaceuticals Incorporated Janus kinase inhibitor compounds and methods
JP2014531449A (ja) 2011-09-20 2014-11-27 セルゾーム リミティッド キナーゼ阻害剤としてのピラゾロ［４，３―ｃ］ピリジン誘導体
KR20180034705A (ko) 2011-11-29 2018-04-04 오노 야꾸힝 고교 가부시키가이샤 퓨리논 유도체 염산염
WO2013092854A1 (en) 2011-12-23 2013-06-27 Cellzome Limited Pyrimidine-2,4-diamine derivatives as kinase inhibitors
US8501724B1 (en) * 2012-01-31 2013-08-06 Pharmacyclics, Inc. Purinone compounds as kinase inhibitors
WO2014013014A1 (en) 2012-07-18 2014-01-23 Fundació Privada Centre De Regulació Genòmica (Crg) Jak inhibitors for activation of epidermal stem cell populations
WO2015089218A1 (en) 2013-12-10 2015-06-18 David Wustrow Monocyclic pyrimidine/pyridine compounds as inhibitors of p97 complex
ES2819867T3 (es) 2014-01-20 2021-04-19 Cleave Biosciences Inc Pirimidinas condensadas como inhibidores del complejo p97
JP6528779B2 (ja) 2014-03-25 2019-06-12 小野薬品工業株式会社 びまん性大細胞型ｂ細胞リンパ腫の予防および／または治療剤
JP6750613B2 (ja) 2015-04-09 2020-09-02 小野薬品工業株式会社 プリノン誘導体の製造方法
AU2016356694B2 (en) 2015-11-20 2021-07-29 Forma Therapeutics, Inc. Purinones as ubiquitin-specific protease 1 inhibitors
WO2018041989A1 (en) 2016-09-02 2018-03-08 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for diagnosing and treating refractory celiac disease type 2
CN110621652A (zh) * 2017-05-17 2019-12-27 株式会社德山 二氨基苯化合物的制造方法
EP3947737A2 (en) 2019-04-02 2022-02-09 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods of predicting and preventing cancer in patients having premalignant lesions
US20220202820A1 (en) 2019-04-16 2022-06-30 INSERM (Institut National de la Santé et de la Recherche Médicale) Use of jak inhibitors for the treatment of painful conditions involving nav1.7 channels
KR102516260B1 (ko) * 2020-07-10 2023-03-31 울산과학기술원 Trap1 선택적 억제제로서의 화합물 및 이를 포함하는 암 예방 또는 치료용 조성물
KR102579424B1 (ko) * 2021-02-19 2023-09-18 울산과학기술원 미토콘드리아 내부 축적이 증가된 trap1 선택적 억제제로서의 화합물 및 이의 용도
WO2023222565A1 (en) 2022-05-16 2023-11-23 Institut National de la Santé et de la Recherche Médicale Methods for assessing the exhaustion of hematopoietic stems cells induced by chronic inflammation

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT1704145E (pt) * 2004-01-12 2012-09-04 Ym Biosciences Australia Pty Inibidores de quinase seletivos
AR054416A1 (es) * 2004-12-22 2007-06-27 Incyte Corp Pirrolo [2,3-b]piridin-4-il-aminas y pirrolo [2,3-b]pirimidin-4-il-aminas como inhibidores de las quinasas janus. composiciones farmaceuticas.
ZA200707342B (en) * 2005-02-03 2009-03-25 Vertex Pharma Pyrrolopyrimidines useful as inhibitors of protein kinase
CA2604161A1 (en) * 2005-04-05 2006-10-12 Pharmacopeia, Inc. Purine and imidazopyridine derivatives for immunosuppression

Also Published As

Publication number Publication date
AU2006350748A2 (en) 2009-08-06
CN101595110A (zh) 2009-12-02
AU2006350748A1 (en) 2008-05-22
JP2010510211A (ja) 2010-04-02
CR10870A (es) 2009-12-01
KR20100014271A (ko) 2010-02-10
CA2669686A1 (en) 2008-05-22
BRPI0622030A2 (pt) 2014-04-22
IL198761A0 (en) 2010-02-17
WO2008060301A1 (en) 2008-05-22
EP2099800A1 (en) 2009-09-16

Similar Documents

Publication Publication Date Title
MX2009005194A (es) Derivados de purina 7-sustituidos para inmunosupresion.
AR063141A1 (es) Derivados de 2- ( benzimidazolil ) purina 8- sustituida para inmunosupresion
NO20075560L (no) Purin og imidazopyridin derivater for immunsuppresjon
MX2010008198A (es) Inhibidores de cinasa de pirrolopirazina.
WO2011117145A3 (en) Pyrrolopyrazine kinase inhibitors
TW200942543A (en) Pyrrolopyrazine kinase inhibitors
MX2011012353A (es) Derivados de n-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo[2, 3-d]pirimidinas y pirrol-3-il-pirrolo[2,3-d]pirimidinas como inhibidores de la cinasa janus.
SMT201300110B (it) Processi intermedi per la preparazione di analoghidi 1'-cianocarbonucleoside
NO20071522L (no) Fremgangsmate for fremstilling av kirale 8-(3-amino-piperidin-1-yl)-xantiner
HK1152712A1 (en) Compounds including an anti-inflammatory pharmacore and methods of use
PT1827441E (pt) Combinações para o tratamento de doenças que envolvem proliferação celular
TW200942545A (en) Azetidine and cyclobutane derivatives as JAK inhibitors
TW200631583A (en) Substituted pteridines for the treatment of inflammatory diseases
NZ612909A (en) Processes for preparing isoquinolinones and solid forms of isoquinolinones
EA201270498A1 (ru) 8-этил-6-(арил)пиридо[2,3-d]пиримидин-7(8h)-оны для лечения заболеваний цнс
MX343042B (es) Compuestos heteroarilicos biciclicos.
WO2009024542A3 (en) Purin derivatives for use in the treatment of fab-related diseases
EA201390736A1 (ru) Циклобутилзамещенные производные пирролопиридина и пирролопиримидина как ингибиторы jak
NZ596571A (en) Pyrazolopyrimidines and related heterocycles as kinase inhibitors
NZ597050A (en) Pyrimidinones as pi3k inhibitors
CR20120635A (es) Compuestos heterocìclicos de nitrògeno ùtiles como inhibidores de pde10
MA31918B1 (fr) Agents et épitopes de liaison à wise
UY33801A (es) COMPUESTOS SUSTITUIDOS DE N-(1H-INDAZOL-4IL)IMIDAZO[1,2-a]PIRIDIN-3-CARBOXAMIDA COMO INHIBIDORES DE LA TIROSINA QUINASA RECEPTORA DE TIPO III
TW200740844A (en) Novel MAdCAM antibodies
WO2007120842A3 (en) Methods and compositions for targeting c-rel

Legal Events

Date Code Title Description
FA Abandonment or withdrawal