ATE462708T1 - Zur behandlung von hyperproliferationserkrankungen und mit angiogenese assoziierten krankheiten geeignete pyrrolotriazinderivate - Google Patents

Zur behandlung von hyperproliferationserkrankungen und mit angiogenese assoziierten krankheiten geeignete pyrrolotriazinderivate

Info

Publication number
ATE462708T1
ATE462708T1 AT05758135T AT05758135T ATE462708T1 AT E462708 T1 ATE462708 T1 AT E462708T1 AT 05758135 T AT05758135 T AT 05758135T AT 05758135 T AT05758135 T AT 05758135T AT E462708 T1 ATE462708 T1 AT E462708T1
Authority
AT
Austria
Prior art keywords
diseases
angiogenesis
treatment
hyperproliferation
derivatives suitable
Prior art date
Application number
AT05758135T
Other languages
English (en)
Inventor
Julie Dixon
Catherine Brennan
Karl Miranda
Brent Chandler
Barton Phillips
Jianmei Fan
Michael Brands
Andrea Mcclure
Benjamin Jones
Wenlang Fu
Donald Bierer
Steven Magnuson
Harold Kluender
Original Assignee
Bayer Pharmaceuticals Corp
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34971944&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ATE462708(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bayer Pharmaceuticals Corp filed Critical Bayer Pharmaceuticals Corp
Application granted granted Critical
Publication of ATE462708T1 publication Critical patent/ATE462708T1/de

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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—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
    • 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
    • C07D491/10—Spiro-condensed systems
    • C07D491/113—Spiro-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
    • 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
    • A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
AT05758135T 2004-06-03 2005-06-03 Zur behandlung von hyperproliferationserkrankungen und mit angiogenese assoziierten krankheiten geeignete pyrrolotriazinderivate ATE462708T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US57665204P 2004-06-03 2004-06-03
US62653104P 2004-11-09 2004-11-09
PCT/US2005/019472 WO2005121147A1 (en) 2004-06-03 2005-06-03 Pyrrolotriazine derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis

Publications (1)

Publication Number Publication Date
ATE462708T1 true ATE462708T1 (de) 2010-04-15

Family

ID=34971944

Family Applications (1)

Application Number Title Priority Date Filing Date
AT05758135T ATE462708T1 (de) 2004-06-03 2005-06-03 Zur behandlung von hyperproliferationserkrankungen und mit angiogenese assoziierten krankheiten geeignete pyrrolotriazinderivate

Country Status (30)

Country Link
US (3) US7563791B2 (de)
EP (1) EP1765823B1 (de)
JP (1) JP4958772B2 (de)
KR (1) KR101235602B1 (de)
CN (1) CN1993361B (de)
AR (1) AR049138A1 (de)
AT (1) ATE462708T1 (de)
AU (1) AU2005252217B2 (de)
BR (1) BRPI0510848A (de)
CA (1) CA2569396C (de)
DE (1) DE602005020293D1 (de)
EC (1) ECSP067043A (de)
ES (1) ES2342722T3 (de)
GT (1) GT200500137A (de)
HN (1) HN2005000255A (de)
IL (1) IL179264A0 (de)
MA (1) MA28689B1 (de)
MX (1) MX279139B (de)
MY (1) MY145077A (de)
NO (1) NO20070049L (de)
NZ (1) NZ551742A (de)
PE (1) PE20060243A1 (de)
PH (1) PH12006502386B1 (de)
RU (1) RU2401269C2 (de)
SG (1) SG127661A1 (de)
SV (1) SV2006002134A (de)
TW (1) TW200608979A (de)
UY (1) UY28931A1 (de)
WO (1) WO2005121147A1 (de)
ZA (1) ZA200700011B (de)

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GB0512324D0 (en) 2005-06-16 2005-07-27 Novartis Ag Organic compounds
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US7514435B2 (en) * 2005-11-18 2009-04-07 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
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PE20070855A1 (es) * 2005-12-02 2007-10-14 Bayer Pharmaceuticals Corp Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
WO2007071752A2 (en) 2005-12-21 2007-06-28 Novartis Ag Pyrimidinyl aryl urea derivatives being fgf inhibitors
EP1882475A1 (de) * 2006-07-26 2008-01-30 Novartis AG Methoden zur Behandlung von Erkrankungen, die durch den Fibroblastwachstumsfaktorrezeptor vermittelt werden
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KR101553211B1 (ko) 2007-09-10 2015-09-15 씨아이피엘에이 엘티디. Ｒａｆ 키나아제 저해제의 제조방법 및 상기 제조방법에 사용되는 중간체
MX2010003269A (es) * 2007-09-25 2010-08-02 Bayer Healthcare Llc Derivados de pirrolotriazina utiles para tratar cancer a traves de la inhibicion de la aurora quinasa.
EP2085397A1 (de) * 2008-01-21 2009-08-05 Esteve Quimica, S.A. Kristalline Form von Abacavir
EP2376491B1 (de) 2008-12-19 2015-03-04 Cephalon, Inc. Pyrrolotriazine als alk- und jak2-inhibitoren
CA2877474A1 (en) * 2011-06-20 2012-12-27 Myrexis, Inc. Compounds and therapeutic uses thereof
JP5955953B2 (ja) 2011-07-01 2016-07-20 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ Ａｌｋ１阻害剤としてのヒドロキシメチルアリール−置換ピロロトリアジン
JP6047582B2 (ja) * 2011-12-15 2016-12-21 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ 置換ベンゾチエニル−ピロロトリアジンおよび癌の処置におけるその使用
UY34484A (es) 2011-12-15 2013-07-31 Bayer Ip Gmbh Benzotienilo-pirrolotriazinas disustituidas y sus usos
CA2865021C (en) * 2012-02-23 2020-06-30 Bayer Intellectual Property Gmbh Substituted benzothienyl-pyrrolotriazines and uses thereof
BR112016028845B1 (pt) 2014-06-17 2023-04-04 Chiesi Farmaceutici S.P.A. Composto, composição farmacêutica e uso de um composto
US10053465B2 (en) 2015-08-26 2018-08-21 Incyte Corporation Pyrrolopyrimidine derivatives as TAM inhibitors
JP7114076B2 (ja) 2015-12-22 2022-08-08 シャイ・セラピューティクス・エルエルシー がん及び炎症性疾患の処置のための化合物
WO2017152117A1 (en) 2016-03-03 2017-09-08 Cornell University Small molecule ire1-alpha inhibitors
CN114456176B (zh) * 2016-03-28 2024-08-30 因赛特公司 作为tam抑制剂的吡咯并三嗪化合物
WO2018161033A1 (en) * 2017-03-02 2018-09-07 Wright, Adrian Small molecule ire1-alpha inhibitors
CA3066939A1 (en) 2017-06-21 2018-12-27 SHY Therapeutics LLC Compounds that interact with the ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease
KR102739325B1 (ko) 2017-09-27 2024-12-09 인사이트 코포레이션 Tam 억제제로서 유용한 피롤로트리아진 유도체의 염
US11241438B2 (en) 2018-06-29 2022-02-08 Incyte Corporation Formulations of an AXL/MER inhibitor
EP3898609A1 (de) 2018-12-19 2021-10-27 Shy Therapeutics LLC Mit der ras-superfamilie interagierende verbindungen zur behandlung von krebs, entzündlichen erkrankungen, rasopathien und fibrotischen erkrankungen
JP7536767B2 (ja) 2018-12-31 2024-08-20 バイオメア フュージョン，インコーポレイテッド メニン－ｍｌｌ相互作用の不可逆的阻害剤
US11174263B2 (en) 2018-12-31 2021-11-16 Biomea Fusion, Inc. Inhibitors of menin-MLL interaction
EP4424312A3 (de) 2019-04-12 2025-01-08 Blueprint Medicines Corporation Pyrrolotriazinderivate zur behandlung von kit- und pdgfra-vermittelten erkrankungen
CN114126620B (zh) * 2019-05-13 2024-12-31 传达治疗有限公司 Fgfr抑制剂和其使用方法
WO2021057877A1 (zh) * 2019-09-26 2021-04-01 深圳市塔吉瑞生物医药有限公司 取代的芳香稠合环衍生物及其组合物及用途
PH12022552347A1 (en) 2020-03-06 2024-01-29 Incyte Corp Combination therapy comprising axl/mer and pd-1/pd-l1 inhibitors
US12534479B2 (en) * 2020-07-10 2026-01-27 Findcure Biosciences (Zhongshan) Co., Ltd. Triazine compound and composition and use thereof
WO2022109577A1 (en) 2020-11-18 2022-05-27 Relay Therapeutics, Inc. Fgfr inhibitors and methods of making and using the same
CA3228627A1 (en) 2021-08-11 2023-02-16 Thomas Butler Covalent inhibitors of menin-mll interaction for diabetes mellitus
KR20240087693A (ko) 2021-08-20 2024-06-19 바이오메아 퓨전, 인크. 암 치료를 위한 비가역적 메닌-mll 억제제인 n-[4-[4-(4-모르폴리닐)-7h-피롤로[2,3-d]피리미딘-6-일]페닐]-4-[[3(r)-[(1-옥소-2-프로펜-1-일)아미노]-1-피페리디닐]메틸]-2-피리딘카르복스아미드의 결정질 형태
TW202430528A (zh) 2023-01-18 2024-08-01 美商拜歐米富士恩股份有限公司 Ｎ－［４－［４－（４－嗎啉基）－７ｈ－吡咯並［２，３－ｄ］嘧啶－６－基］苯基］－４－［［３（ｒ）－［（１－氧代－２－丙烯－１－基）氨基］－１－哌啶基］甲基］－２－吡啶甲醯胺的結晶形式作為ｍｅｎｉｎ－ｍｌｌ相互作用的共價抑制劑

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PE20070855A1 (es) * 2005-12-02 2007-10-14 Bayer Pharmaceuticals Corp Derivados de 4-amino-pirrolotriazina sustituida como inhibidores de quinasas
MX2010003269A (es) * 2007-09-25 2010-08-02 Bayer Healthcare Llc Derivados de pirrolotriazina utiles para tratar cancer a traves de la inhibicion de la aurora quinasa.

Also Published As

Publication number Publication date
CA2569396C (en) 2011-12-20
MA28689B1 (fr) 2007-06-01
HK1109141A1 (en) 2008-05-30
CN1993361B (zh) 2010-05-26
CA2569396A1 (en) 2005-12-22
KR101235602B1 (ko) 2013-02-21
KR20070035028A (ko) 2007-03-29
UY28931A1 (es) 2005-12-30
MX279139B (es) 2010-09-21
US20070208013A1 (en) 2007-09-06
MXPA06013457A (es) 2007-03-01
TW200608979A (en) 2006-03-16
EP1765823A1 (de) 2007-03-28
HN2005000255A (es) 2010-09-17
RU2401269C2 (ru) 2010-10-10
US20130225809A1 (en) 2013-08-29
AU2005252217A1 (en) 2005-12-22
SG127661A1 (en) 2007-01-30
NZ551742A (en) 2010-08-27
JP2008501703A (ja) 2008-01-24
SV2006002134A (es) 2006-10-04
NO20070049L (no) 2007-01-30
JP4958772B2 (ja) 2012-06-20
GT200500137A (es) 2006-05-18
BRPI0510848A (pt) 2007-11-27
DE602005020293D1 (de) 2010-05-12
EP1765823B1 (de) 2010-03-31
AR049138A1 (es) 2006-06-28
MY145077A (en) 2011-12-15
RU2006147237A (ru) 2008-07-20
US20100075958A1 (en) 2010-03-25
ZA200700011B (en) 2008-11-26
US8338595B2 (en) 2012-12-25
AU2005252217B2 (en) 2011-05-12
ES2342722T3 (es) 2010-07-13
IL179264A0 (en) 2007-03-08
US7563791B2 (en) 2009-07-21
WO2005121147A1 (en) 2005-12-22
PE20060243A1 (es) 2006-04-21
CN1993361A (zh) 2007-07-04
PH12006502386B1 (en) 2010-12-23
ECSP067043A (es) 2006-12-29

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