[go: up one dir, main page]

PE20120184A1 - Derivados del pirrolo[2,3-b]piridina para la inhibicion de las proteinas quinasas raf - Google Patents

Derivados del pirrolo[2,3-b]piridina para la inhibicion de las proteinas quinasas raf

Info

Publication number
PE20120184A1
PE20120184A1 PE2011001620A PE2011001620A PE20120184A1 PE 20120184 A1 PE20120184 A1 PE 20120184A1 PE 2011001620 A PE2011001620 A PE 2011001620A PE 2011001620 A PE2011001620 A PE 2011001620A PE 20120184 A1 PE20120184 A1 PE 20120184A1
Authority
PE
Peru
Prior art keywords
pyridine
pyrrolo
difluoro
carbonyl
phenyl
Prior art date
Application number
PE2011001620A
Other languages
English (en)
Inventor
Prabha N Ibrahim
Wayne Spevak
Hanna Cho
Hongyao Zhu
Original Assignee
Plexxikon Inc
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 Plexxikon Inc filed Critical Plexxikon Inc
Publication of PE20120184A1 publication Critical patent/PE20120184A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE PIRROLO[2,3-b]PIRIDINA TAL COMO: ACIDO PROPANO-1-SULFONICO DE {2,4-DIFLUORO-3-[5-(2-METOXI-PIRIMIDIN-5-IL)-1H-PIRROLO[2,3-b]PIRIDINA-3-CARBONIL]-FENIL}-AMIDA; ACIDO PROPANO-1-SULFONICO DE [3-(5-CIANO-1H-PIRROLO[2,3-b]PIRIDINA-3-CARBONIL)-2,4-DIFLUORO-FENIL]-AMIDA; ACIDO PROPANO-1-SULFONICO DE [3-(5-CIANO-1H-PIRROLO[2,3-b]PIRIDINA-3-CARBONIL)-2-FLUORO-FENIL]-AMIDA; N-[3-(5-CIANO-1H-PIRROLO[2,3-b]PIRIDINA-3-CARBONIL)-2,4-DIFLUORO-FENIL]-2,5-DIFLUORO-BENCENOSULFONAMIDA; N-[3-(5-CIANO-1H-PIRROLO[2,3-b]PIRIDINA-3-CARBONIL)-2,4-DIFLUORO-FENIL]-3-FLUORO-BENCENO-SULFONAMIDA; ACIDO PIRROLIDINA-1-SULFONICO DE [3-(5-CIANO-1H-PIRROLO[2,3-b]PIRIDINA-3-CARBONIL)-2,4-DIFLUORO-FENIL]-AMIDA; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LAS PROTEINA QUINASAS RAF COMO A-RAF, B-RAF Y c-RAF-1 SIENDO UTILES EN EL TRATAMIENTO DE MELANOMA, GLIOMA, CANCER COLORRECTAL, CANCER DE TIROIDES
PE2011001620A 2009-03-11 2010-03-10 Derivados del pirrolo[2,3-b]piridina para la inhibicion de las proteinas quinasas raf PE20120184A1 (es)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
US15939609P 2009-03-11 2009-03-11
US15940209P 2009-03-11 2009-03-11
US15939009P 2009-03-11 2009-03-11
US15939509P 2009-03-11 2009-03-11
US15940009P 2009-03-11 2009-03-11
US15940609P 2009-03-11 2009-03-11
US15939209P 2009-03-11 2009-03-11

Publications (1)

Publication Number Publication Date
PE20120184A1 true PE20120184A1 (es) 2012-03-28

Family

ID=42199540

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2011001620A PE20120184A1 (es) 2009-03-11 2010-03-10 Derivados del pirrolo[2,3-b]piridina para la inhibicion de las proteinas quinasas raf

Country Status (23)

Country Link
US (1) US8901301B2 (es)
EP (1) EP2406259A1 (es)
JP (1) JP2012520307A (es)
KR (1) KR101663339B1 (es)
CN (1) CN102421776A (es)
AR (1) AR075812A1 (es)
AU (1) AU2010224245B2 (es)
BR (1) BRPI1011515A2 (es)
CA (1) CA2755045A1 (es)
CO (1) CO6620074A2 (es)
CR (1) CR20110476A (es)
EC (1) ECSP11011313A (es)
MA (1) MA33181B1 (es)
MX (1) MX2011009489A (es)
MY (1) MY161861A (es)
NI (1) NI201100168A (es)
NO (1) NO20111241A1 (es)
PE (1) PE20120184A1 (es)
RU (1) RU2011141123A (es)
SG (2) SG10201402977WA (es)
TW (1) TW201036973A (es)
WO (1) WO2010104945A1 (es)
ZA (1) ZA201106599B (es)

Families Citing this family (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008063888A2 (en) 2006-11-22 2008-05-29 Plexxikon, Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor
SG183036A1 (en) 2007-07-17 2012-08-30 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
WO2009143018A2 (en) 2008-05-19 2009-11-26 Plexxikon, Inc. Compounds and methods for kinase modulation, and indications therefor
JP2012509342A (ja) 2008-11-20 2012-04-19 オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド 置換ピロロ[2,3−b]−ピリジンおよび−ピラジン
CN102361870B (zh) 2009-04-03 2015-11-25 豪夫迈罗氏公司 丙烷-1-磺酸{3-[5-(4-氯-苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基]-2,4-二氟-苯基}-酰胺组合物及其用途
MX2012005284A (es) 2009-11-06 2012-06-28 Plexxikon Inc Compuestos y metodos para la modulacion de cinasas. e indicaciones para ello.
BR112012011792A2 (pt) 2009-11-18 2015-10-13 Plexxikon Inc "compostos e métodos para modulação de quinases, e indicações para os mesmos"
CA2784393A1 (en) 2009-12-23 2011-06-30 Plexxikon, Inc. Compounds and methods for kinase modulation, and indications therefor
TWI619713B (zh) 2010-04-21 2018-04-01 普雷辛肯公司 用於激酶調節的化合物和方法及其適應症
WO2011143646A1 (en) 2010-05-14 2011-11-17 OSI Pharmaceuticals, LLC Fused bicyclic kinase inhibitors
AR081039A1 (es) 2010-05-14 2012-05-30 Osi Pharmaceuticals Llc Inhibidores biciclicos fusionados de quinasa
WO2012075324A1 (en) 2010-12-02 2012-06-07 University Of Pittsburgh - Of The Commonwealth System Of Higher Education Methods for treating a tumor using an antibody that specifically binds hmw-maa
JP5941069B2 (ja) * 2011-02-07 2016-06-29 プレキシコン インコーポレーテッドPlexxikon Inc. キナーゼ調節のための化合物および方法、ならびにそれに対する適応症
WO2012149547A1 (en) * 2011-04-28 2012-11-01 Duke University Methods of treating hemoglobinopathies
CN103917235A (zh) 2011-05-17 2014-07-09 普莱希科公司 激酶调节及其适应症
US9988687B2 (en) * 2011-09-20 2018-06-05 The George Washington Univeristy Companion diagnostics for cancer and screening methods to identify companion diagnostics for cancer based on splicing variants
US9249110B2 (en) 2011-09-21 2016-02-02 Neupharma, Inc. Substituted quinoxalines as B-raf kinase inhibitors
US20130172375A1 (en) 2011-12-13 2013-07-04 Hoffmann-La Roche Inc. Pharmaceutical composition
US9358235B2 (en) 2012-03-19 2016-06-07 Plexxikon Inc. Kinase modulation, and indications therefor
US9150570B2 (en) 2012-05-31 2015-10-06 Plexxikon Inc. Synthesis of heterocyclic compounds
BR112014032346A2 (pt) 2012-06-26 2017-06-27 Del Mar Pharmaceuticals métodos para tratamento de malignidades resistentes ao inibidor de tirosina-quinase em pacientes com polimorfismos genéticos ou desregulações de ahi1 mutações empregando dianidrogalactitol, diacetildianidrogalactitol, dibromodulcitol, ou análogos ou derivados destes
TWI601725B (zh) 2012-08-27 2017-10-11 加拓科學公司 取代的氮雜吲哚化合物及其鹽、組合物和用途
CA2883894C (en) 2012-09-06 2020-08-18 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
WO2014081760A1 (en) 2012-11-20 2014-05-30 Duke University Methods of treating hemoglobinopathies
RS57117B1 (sr) 2012-12-21 2018-06-29 Plexxikon Inc Jedinjenja i metode modulacije kinaze i povezane indikacije
SG11201506687RA (en) 2013-03-15 2015-09-29 Plexxikon Inc Heterocyclic compounds and uses thereof
US20140303121A1 (en) 2013-03-15 2014-10-09 Plexxikon Inc. Heterocyclic compounds and uses thereof
CN105492011A (zh) 2013-04-08 2016-04-13 丹尼斯·M·布朗 不理想给药化学化合物的治疗增效
RU2015149937A (ru) 2013-05-30 2017-07-06 Плексксикон Инк. Соединения для модулирования киназы и показания к их применению
EP3094736A4 (en) 2014-01-14 2017-10-25 Dana-Farber Cancer Institute, Inc. Compositions and methods for identification, assessment, prevention, and treatment of melanoma using pd-l1 isoforms
WO2015134536A1 (en) 2014-03-04 2015-09-11 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
JP6832846B2 (ja) 2014-09-15 2021-02-24 プレキシコン インコーポレーテッドPlexxikon Inc. ヘテロ環化合物およびその用途
WO2016057367A1 (en) 2014-10-06 2016-04-14 Dana-Farber Cancer Institute, Inc. Angiopoietin-2 biomarkers predictive of anti-immune checkpoint response
WO2016164641A1 (en) 2015-04-08 2016-10-13 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
MX386963B (es) 2015-05-06 2025-03-19 Daiichi Sankyo Inc Formas sólidas de quinasas que modulan un compuesto.
CN107531706A (zh) 2015-05-06 2018-01-02 普莱希科公司 调节激酶的1H‑吡咯并[2,3‑b]吡啶衍生物的合成
WO2017019804A2 (en) 2015-07-28 2017-02-02 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
MY195977A (en) 2015-09-21 2023-02-27 Plexxikon Inc Heterocyclic Compounds and uses Thereof
SG11201804711RA (en) 2015-12-07 2018-07-30 Plexxikon Inc Compounds and methods for kinase modulation, and indications therefor
US10160747B2 (en) 2016-03-16 2018-12-25 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
TW201815766A (zh) 2016-09-22 2018-05-01 美商普雷辛肯公司 用於ido及tdo調節之化合物及方法以及其適應症
CA3047580A1 (en) 2016-12-23 2018-07-26 Plexxikon Inc. Compounds and methods for cdk8 modulation and indications therefor
MX393780B (es) 2017-01-17 2025-03-24 Heparegenix Gmbh Inhibidores de proteina cinasa para promover la regeneracion hepatica o reducir o prevenir la muerte de hepatocitos
US10577366B2 (en) 2017-03-20 2020-03-03 Plexxikon Inc. Crystalline forms of a compound that inhibits bromodomain
US10428067B2 (en) 2017-06-07 2019-10-01 Plexxikon Inc. Compounds and methods for kinase modulation
US10435404B2 (en) 2017-07-25 2019-10-08 Plexxikon Inc. Formulations of a compound modulating kinases
WO2019075243A1 (en) 2017-10-13 2019-04-18 Plexxikon Inc. SOLID FORMS OF A COMPOUND FOR MODULATING KINASES
AU2018354423B2 (en) 2017-10-27 2024-11-07 Plexxikon Inc. Formulations of a compound modulating kinases
ES3000465T3 (en) 2018-01-31 2025-02-28 Heparegenix Gmbh Protein kinase mkk4 inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death
CA3094336A1 (en) 2018-03-20 2019-09-26 Plexxikon Inc. Compounds and methods for ido and tdo modulation, and indications therefor
GB201809460D0 (en) * 2018-06-08 2018-07-25 Crt Pioneer Fund Lp Salt form
US11731968B2 (en) 2018-06-21 2023-08-22 Heparegenix Gmbh Tricyclic protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death
CN112424201B (zh) 2018-07-16 2024-04-02 海帕瑞吉尼克斯股份有限公司 促进肝再生或者减少或预防肝细胞死亡的蛋白激酶抑制剂
JP7636646B2 (ja) 2019-04-09 2025-02-27 オプナ バイオ ソシエテ アノニム Ep300またはcbpの調節のための縮合アジンおよびその適応
AU2021207236A1 (en) 2020-01-15 2022-08-11 Heparegenix Gmbh 3-benzoyl-1h-pyrrolo[2,3-b]pyridine derivatives as MKK4 inhibitors for treating liver diseases
AU2021261383A1 (en) 2020-04-23 2022-11-17 Opna Bio SA Compounds and methods for CD73 modulation and indications therefor
CN115605460A (zh) 2020-04-29 2023-01-13 普莱希科公司(Us) 杂环化合物的合成
TW202227068A (zh) 2020-08-21 2022-07-16 美商普雷辛肯公司 組合藥物療法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT1534340E (pt) * 2002-09-06 2012-03-13 Cerulean Pharma Inc Polímeros à base de ciclodextrina para a administração de medicamentos ligados por ligação covalente
DK2395004T3 (en) * 2005-06-22 2016-03-21 Plexxikon Inc Pyrrolo [2,3-b] pyridine derivatives as protein kinase inhibitors
PE20081581A1 (es) 2006-12-21 2008-11-12 Plexxikon Inc COMPUESTOS PIRROLO[2,3-b]PIRIDINAS COMO MODULADORES DE QUINASA

Also Published As

Publication number Publication date
ECSP11011313A (es) 2011-10-31
CN102421776A (zh) 2012-04-18
ZA201106599B (en) 2014-02-26
CO6620074A2 (es) 2013-02-15
CR20110476A (es) 2012-01-04
WO2010104945A1 (en) 2010-09-16
KR20110125670A (ko) 2011-11-21
NO20111241A1 (no) 2011-09-28
EP2406259A1 (en) 2012-01-18
US8901301B2 (en) 2014-12-02
AU2010224245B2 (en) 2016-07-21
KR101663339B1 (ko) 2016-10-06
AR075812A1 (es) 2011-04-27
MA33181B1 (fr) 2012-04-02
MY161861A (en) 2017-05-15
CA2755045A1 (en) 2010-09-16
BRPI1011515A2 (pt) 2016-03-29
AU2010224245A1 (en) 2011-09-29
RU2011141123A (ru) 2013-04-20
TW201036973A (en) 2010-10-16
US20100286178A1 (en) 2010-11-11
SG10201402977WA (en) 2014-09-26
MX2011009489A (es) 2011-10-11
JP2012520307A (ja) 2012-09-06
NI201100168A (es) 2012-01-11
SG174257A1 (en) 2011-10-28

Similar Documents

Publication Publication Date Title
PE20120184A1 (es) Derivados del pirrolo[2,3-b]piridina para la inhibicion de las proteinas quinasas raf
EA201200951A1 (ru) Определенные триазолопиридины и триазолопиразины, их композиции и способы их применения
EA201101585A1 (ru) 3-(1,2,3-триазол-4-ил)пирроло[2,3-b]пиридинпроизводные
PE20120518A1 (es) Compuestos derivados de pirrolopiridina como moduladores de quinasas
EA201101192A1 (ru) Фармацевтическая композиция, включающая производные глюкопиранозилдифенилметана, фармацевтическая дозированная форма, содержащая указанные производные, способ их получения и применения для улучшения гликемического контроля у пациентов
CL2007001710A1 (es) Compuestos derivados de amino-pirazolopiridina sustituidos; metodo de preparacion; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como tumores, artritis reumatoide, enfermedades de crecimiento vascular desregulado, entre otras.
UY30892A1 (es) Inhibidores de la actividad akt
CL2008000670A1 (es) Compuestos derivados de tiazolidindionas y oxazolidindionas sustituidas; composicion farmaceutica; proceso de preparacion de la composicion farmaceutica; y uso en el tratamiento de enfermedades tales como artritis reumatoide, epoc, cancer, entre otras.
EA201290103A1 (ru) Гетероциклические соединения и их использование
IL206704A0 (en) Fused heterocyclic derivatives and methods of use as c-met inhibitors
IL206930A0 (en) Fused pyridines active as inhibitors of c-met
EP4406557A3 (en) Materials and methods for improving gastrointestinal function
EA201290255A1 (ru) Способы и композиции для лечения рака
EA201201081A1 (ru) Производные гетарил[1,8]нафтиридина
MY167575A (en) Heterocyclic compounds and use thereof as modulators of type iii receptor tyrosine kinases
MX352927B (es) Derivados de 1h-pirrolo [2,3-b] piridina y su uso como inhibidores de quinasa.
EA200800726A1 (ru) Введение ингибиторов дипептидилпептидазы
MX385217B (es) Antagonistas de actriib y dosificación y usos de los mismos.
HUE049886T2 (hu) Tumorspecifikus neoantigéneket tartalmazó készítmények, tumorok kezelésében történõ alkalmazásra
IL215074A0 (en) Substituted imidazo[1,2-a]pyridine derivatives, pharmaceutical compositions, and methods of use as beta-secretase inhibitors
EA201101399A1 (ru) Гетероциклические соединения в качестве ингибиторов аутотаксина
CL2010001474A1 (es) Compuestos derivados de tiofeno o tiazol sustituidos, inhibidores de pi3k; composicion farmaceutica; utiles en el tratamiento del cancer, inflamacion y en el tratamiento de trastornos cardiovasculares.
EP2617721A4 (en) NEW HETEROCYCLIC COMPOUND AND COMPOSITION FOR THE TREATMENT OF INFLAMMATORY DISORDERS THEREWITH
PH12013501754A1 (en) Triazolopyridine compounds as pim kinase inhibitors
CL2011000846A1 (es) Compuestos heterociclicos sustituidos; composicion farmaceutica; y su uso para el tratamiento de la hepatitis c.

Legal Events

Date Code Title Description
FD Application declared void or lapsed