CR10870A - PURINE DERIVATIVES 7-REPLACED FOR IMMUNOSUPPRESSION - Google Patents

PURINE DERIVATIVES 7-REPLACED FOR IMMUNOSUPPRESSION

Info

Publication number
CR10870A
CR10870A CR10870A CR10870A CR10870A CR 10870 A CR10870 A CR 10870A CR 10870 A CR10870 A CR 10870A CR 10870 A CR10870 A CR 10870A CR 10870 A CR10870 A CR 10870A
Authority
CR
Costa Rica
Prior art keywords
immunosuppression
replaced
purine derivatives
derivatives
moderate
Prior art date
Application number
CR10870A
Other languages
Spanish (es)
Inventor
Michael Ohlmeyer
Adolph Bohnstedt
Celia Kingsbury
Koc-Kan Ho
Jorge Quintero
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 CR10870A publication Critical patent/CR10870A/en

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

Abstract

La presente invencion provee nuevos derivados de purinona y derivados relacionados utiles para la prevencion y tratamiento de enfermedades autoinmunes, enfermedad inflamatoria, enfermedad moderada por celula cebada y rechazo de trasplante. Los compuestos de la formula general (III).The present invention provides new purinone derivatives and related derivatives useful for the prevention and treatment of autoimmune diseases, inflammatory disease, moderate barley cell disease and transplant rejection. The compounds of the general formula (III).

CR10870A 2006-11-16 2009-06-16 PURINE DERIVATIVES 7-REPLACED FOR IMMUNOSUPPRESSION CR10870A (en)

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
CR10870A true CR10870A (en) 2009-12-01

Family

ID=38578618

Family Applications (1)

Application Number Title Priority Date Filing Date
CR10870A CR10870A (en) 2006-11-16 2009-06-16 PURINE DERIVATIVES 7-REPLACED FOR IMMUNOSUPPRESSION

Country Status (11)

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

Families Citing this family (37)

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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
ES2665277T3 (en) 2009-03-13 2018-04-25 Katholieke Universiteit Leuven K.U. Leuven R&D Purine analogues and their use as immunosuppressive agents
EP2419423A1 (en) 2009-04-14 2012-02-22 Cellzome Limited Fluoro substituted pyrimidine compounds as jak3 inhibitors
CA2771675A1 (en) 2009-09-11 2011-03-17 Cellzome Limited Ortho substituted pyrimidine compounds as jak inhibitors
MX2012004020A (en) 2009-10-20 2012-05-08 Cellzome Ltd Heterocyclyl pyrazolopyrimidine analogues as jak inhibitors.
BR112012010186B8 (en) 2009-10-29 2021-05-25 Palau Pharma Sa heteroaryl derivatives containing n as jak3 kinase inhibitors and pharmaceutical composition comprising them
SG184989A1 (en) 2010-04-30 2012-11-29 Cellzome Ltd Pyrazole compounds as jak inhibitors
GB201012889D0 (en) 2010-08-02 2010-09-15 Univ Leuven Kath Antiviral activity of novel bicyclic heterocycles
MX2012013622A (en) 2010-05-31 2013-02-01 Ono Pharmaceutical Co Purinone derivative.
WO2012003576A1 (en) * 2010-07-06 2012-01-12 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 (en) * 2010-09-09 2013-01-30 주식회사 만도 3 way type lp egr valve constitution
GB201015411D0 (en) 2010-09-15 2010-10-27 Univ Leuven Kath Anti-cancer activity of novel bicyclic heterocycles
CA2825098C (en) 2011-01-27 2020-03-10 Universite De Montreal 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
KR20140047092A (en) 2011-07-28 2014-04-21 셀좀 리미티드 Heterocyclyl pyrimidine analogues as jak inhibitors
WO2013017480A1 (en) 2011-07-29 2013-02-07 Cellzome Limited Pyrazolo[4,3-c]pyridine derivatives as jak inhibitors
WO2013017479A1 (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
WO2013041605A1 (en) 2011-09-20 2013-03-28 Cellzome Limited Pyrazolo[4,3-c]pyridine derivatives as kinase inhibitors
BR112014012727B1 (en) 2011-11-29 2022-10-25 Ono Pharmaceutical Co., Ltd 6-AMINO-9-[(3R)-1-(2-BUTINOYL)-3-PYRROLIDINYL]-7-(4-PHENOXYPHENYL)-7,9-DIHYDRO-8H-PURI-8-ONE E PHARMACEUTICAL COMPOSITION
AU2012357038B2 (en) 2011-12-23 2016-05-12 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
US9868722B2 (en) 2013-12-10 2018-01-16 Cleave Biosciences, Inc. Monocyclic pyrimidine/pyridine compounds as inhibitors of P97 complex
BR112016016421B1 (en) 2014-01-20 2022-10-18 Cleave Biosciences, Inc FUSED PYRIMIDINE COMPOUND, PHARMACEUTICAL COMPOSITION AND ITS USE
JP6528779B2 (en) 2014-03-25 2019-06-12 小野薬品工業株式会社 Preventive and / or therapeutic agent for diffuse large B cell lymphoma
US10239879B2 (en) 2015-04-09 2019-03-26 Ono Pharmaceutical Co., Ltd. Process for producing purinone derivative
RU2750151C2 (en) 2015-11-20 2021-06-22 Форма Терапьютикс, Инк. Hypoxantines as inhibitors of ubiquitin-specific protease 1
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
WO2018212162A1 (en) * 2017-05-17 2018-11-22 株式会社トクヤマ Method for producing diaminobenzene compound
US20220177978A1 (en) 2019-04-02 2022-06-09 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods of predicting and preventing cancer in patients having premalignant lesions
WO2020212395A1 (en) 2019-04-16 2020-10-22 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 (en) * 2020-07-10 2023-03-31 울산과학기술원 Compounds as a TRAP1 selective inhibitor, and composition for preventing or treating cancer comprising the same
KR102579424B1 (en) * 2021-02-19 2023-09-18 울산과학기술원 Compounds as a TRAP1 selective inhibitor with increased mitochondrial drug accumulation, and use thereof
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
CA2545427C (en) * 2004-01-12 2012-08-21 Cytopia Research Pty Ltd Selective kinase inhibitors
AR054416A1 (en) * 2004-12-22 2007-06-27 Incyte Corp PIRROLO [2,3-B] PIRIDIN-4-IL-AMINAS AND PIRROLO [2,3-B] PIRIMIDIN-4-IL-AMINAS AS INHIBITORS OF THE JANUS KINASES. PHARMACEUTICAL COMPOSITIONS.
KR20070104641A (en) * 2005-02-03 2007-10-26 버텍스 파마슈티칼스 인코포레이티드 Pyrrolopyrimidines useful as inhibitors of protein kinase
BRPI0610514A2 (en) * 2005-04-05 2016-11-16 Pharmacopeia Inc compound, pharmaceutical composition, and method of treating a disorder

Also Published As

Publication number Publication date
CN101595110A (en) 2009-12-02
EP2099800A1 (en) 2009-09-16
IL198761A0 (en) 2010-02-17
WO2008060301A1 (en) 2008-05-22
MX2009005194A (en) 2009-11-10
BRPI0622030A2 (en) 2014-04-22
AU2006350748A1 (en) 2008-05-22
JP2010510211A (en) 2010-04-02
AU2006350748A2 (en) 2009-08-06
CA2669686A1 (en) 2008-05-22
KR20100014271A (en) 2010-02-10

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Legal Events

Date Code Title Description
FA Abandonment or withdrawal (granting procedure)