PL378372A1 - Tricykliczne związki jako inhibitory kinaz białkowych do wzmacniania skuteczności środków przeciwnowotworowych i radioterapii - Google Patents

Tricykliczne związki jako inhibitory kinaz białkowych do wzmacniania skuteczności środków przeciwnowotworowych i radioterapii

Info

Publication number
PL378372A1
PL378372A1 PL378372A PL37837204A PL378372A1 PL 378372 A1 PL378372 A1 PL 378372A1 PL 378372 A PL378372 A PL 378372A PL 37837204 A PL37837204 A PL 37837204A PL 378372 A1 PL378372 A1 PL 378372A1
Authority
PL
Poland
Prior art keywords
efectivenes
terapeutic
radiation
increasing
protein kinase
Prior art date
Application number
PL378372A
Other languages
English (en)
Inventor
Sacha Ninkovic
Michael John Bennett
Yuanjin Rui
Fen Wang
Suzanne Pritchett Benedict
Min Teng
Yong Wang
Jinjiang Zhu
Original Assignee
Pfizer 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 Pfizer Inc. filed Critical Pfizer Inc.
Publication of PL378372A1 publication Critical patent/PL378372A1/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/06Peri-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • 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
    • 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
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/06Peri-condensed systems
PL378372A 2003-01-09 2004-01-05 Tricykliczne związki jako inhibitory kinaz białkowych do wzmacniania skuteczności środków przeciwnowotworowych i radioterapii PL378372A1 (pl)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US43939603P 2003-01-09 2003-01-09

Publications (1)

Publication Number Publication Date
PL378372A1 true PL378372A1 (pl) 2006-04-03

Family

ID=32713475

Family Applications (1)

Application Number Title Priority Date Filing Date
PL378372A PL378372A1 (pl) 2003-01-09 2004-01-05 Tricykliczne związki jako inhibitory kinaz białkowych do wzmacniania skuteczności środków przeciwnowotworowych i radioterapii

Country Status (35)

Country Link
US (3) US6967198B2 (pl)
EP (2) EP1585749B1 (pl)
JP (1) JP3990718B2 (pl)
KR (1) KR100697746B1 (pl)
CN (1) CN1759118B (pl)
AP (1) AP2048A (pl)
AT (1) ATE404564T1 (pl)
AU (1) AU2004203977B2 (pl)
BR (1) BRPI0406701A (pl)
CA (1) CA2512683C (pl)
CR (1) CR7899A (pl)
CY (1) CY1108408T1 (pl)
DE (1) DE602004015724D1 (pl)
DK (1) DK1585749T3 (pl)
EA (1) EA009337B1 (pl)
EC (1) ECSP055911A (pl)
ES (1) ES2309484T3 (pl)
GE (1) GEP20084367B (pl)
HK (1) HK1086257A1 (pl)
HR (1) HRP20050624A2 (pl)
IL (1) IL169082A (pl)
IS (1) IS7884A (pl)
MA (1) MA27703A1 (pl)
MX (1) MXPA05007352A (pl)
NO (1) NO20053775L (pl)
NZ (1) NZ540638A (pl)
OA (1) OA13017A (pl)
PL (1) PL378372A1 (pl)
PT (1) PT1585749E (pl)
RS (1) RS20050522A (pl)
SI (1) SI1585749T1 (pl)
TN (1) TNSN05176A1 (pl)
UA (1) UA80733C2 (pl)
WO (1) WO2004063198A1 (pl)
ZA (1) ZA200504674B (pl)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2003214879B2 (en) * 2002-01-22 2008-02-07 The Regents Of The University Of California Non-steroidal ligands for the glucocorticoid receptor, compositions and uses thereof
ATE404564T1 (de) * 2003-01-09 2008-08-15 Pfizer Diazepinoindolderivate als kinaseinhibitoren
BRPI0607798A2 (pt) * 2005-02-18 2010-06-22 Astrazeneca Ab método para prognosticar uma responsividade do paciente a um inibidor de chk1, uso de um inibidor de chk1, e, kit para prognosticar uma resposta do paciente a um inibidor de chk1
SI1869020T1 (sl) 2005-03-29 2011-02-28 Icos Corp Derivati heteroaril uree, ki so uporabni za inhibicijo chk1
GB0510390D0 (en) * 2005-05-20 2005-06-29 Novartis Ag Organic compounds
JP5180824B2 (ja) 2005-06-29 2013-04-10 スレッシュホールド ファーマシューティカルズ, インコーポレイテッド ホスホルアミデートアルキル化剤プロドラッグ
US8324169B2 (en) * 2005-08-15 2012-12-04 The Regents Of The University Of California VEGF-activated ligands
JP4935675B2 (ja) 2005-08-25 2012-05-23 宇部興産株式会社 光学活性(S又はR)−α−アミノ酸及び光学活性(R又はS)−α−アミノ酸エステルの製造方法
AU2006282767A1 (en) * 2005-08-26 2007-03-01 The Regents Of The University Of California Non-steroidal antiandrogens
CA2648369A1 (en) * 2006-04-04 2007-10-11 Pfizer Products Inc. Polymorphic forms of (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4?l)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide
CN101415417A (zh) * 2006-04-04 2009-04-22 辉瑞产品公司 (2r,z)-2-氨基-2-环己基-n-(5-(1-甲基-1h-吡唑-4-基)-1-氧代-2,6-二氢-1h-[1,2]二氮杂卓并[4,5,6-cd]吲哚-8-基)乙酰胺的组合疗法
JP2010510222A (ja) * 2006-11-17 2010-04-02 シェーリング コーポレイション 増殖性障害に対する併用療法
US8158656B2 (en) * 2008-05-16 2012-04-17 Shenzhen Chipscreen Biosciences Ltd. 2-indolinone derivatives as multi-target protein kinase inhibitors and histone deacetylase inhibitors
JP5576370B2 (ja) * 2008-08-06 2014-08-20 ファイザー・インク Chk−1阻害剤としての6置換2−ヘテロシクリルアミノピラジン化合物
EP2346881A1 (en) * 2008-10-10 2011-07-27 Priaxon AG Novel compounds which modulate kinase activity
US8314108B2 (en) 2008-12-17 2012-11-20 Eli Lilly And Company 5-(5-(2-(3-aminopropoxy)-6-methoxyphenyl)-1H-pyrazol-3-ylamino)pyrazine-2-carbonitrile, pharmaceutically acceptable salts thereof, or solvate of salts
US8663210B2 (en) 2009-05-13 2014-03-04 Novian Health, Inc. Methods and apparatus for performing interstitial laser therapy and interstitial brachytherapy
US8211901B2 (en) 2009-05-22 2012-07-03 Shenzhen Chipscreen Biosciences Ltd. Naphthamide derivatives as multi-target protein kinase inhibitors and histone deacetylase inhibitors
CN101906076B (zh) 2009-06-04 2013-03-13 深圳微芯生物科技有限责任公司 作为蛋白激酶抑制剂和组蛋白去乙酰化酶抑制剂的萘酰胺衍生物、其制备方法及应用
BR112013028665A2 (pt) 2011-05-06 2016-09-06 Zafgen Inc compostos de sulfonamida tricíclicos e métodos para fazer e usar os mesmos
EP2793882A4 (en) 2011-12-22 2015-04-29 Threshold Pharmaceuticals Inc ADMINISTRATION OF HYPOXIA ACTIVATED DRUGS IN COMBINATION WITH CHK1 INHIBITORS FOR THE TREATMENT OF CANCER
MX2014008071A (es) 2011-12-31 2015-07-06 Beigene Ltd Tetra o penta-piridoftalazinonas ciclicas fusionadas como inhibidores de poli(adenosin-difosfato-ribosa)polimerasas.
NO2797921T3 (pl) * 2011-12-31 2018-02-03
CN102746211B (zh) * 2012-06-27 2015-05-27 上海泰坦化学有限公司 一种取代吲哚-3-甲醛类化合物的制备方法
TWI633107B (zh) * 2013-05-22 2018-08-21 開曼群島商百濟神州生物科技有限公司 作為parp抑制劑的稠合四或五環二氫二氮呯并咔唑酮
CN112472699A (zh) 2013-07-26 2021-03-12 种族肿瘤学公司 改善比生群及衍生物的治疗益处的组合方法
WO2015069489A1 (en) 2013-11-06 2015-05-14 Merck Patent Gmbh Predictive biomarker for hypoxia-activated prodrug therapy
PT3157566T (pt) 2014-06-17 2019-07-11 Vertex Pharma Método para tratamento de cancro utilizando uma combinação de inibidores chk1 e atr
MX2018002322A (es) 2015-08-25 2018-04-11 Beigene Ltd Procedimiento para la preparacion de un inhibidor de poli(adp-ribosa)polimerasa, formas cristalinas, y usos del mismo.
CA3000684A1 (en) 2015-09-30 2017-04-06 Vertex Pharmaceuticals Incorporated Method for treating cancer using a combination of dna damaging agents and atr inhibitors
WO2018059437A1 (en) 2016-09-27 2018-04-05 Beigene, Ltd. Treatment cancers using combination comprising parp inhibitors
JP6541635B2 (ja) * 2016-10-28 2019-07-10 ベイジーン リミテッド Parp阻害剤としての縮合四環式または縮合五環式ジヒドロジアゼピノカルバゾロン
WO2018157794A1 (en) 2017-02-28 2018-09-07 Beigene, Ltd. Crystalline forms of salts of fused tera or penta-cyclic dihydrodiazepinocarazolones, and uses thereof
US11661581B2 (en) * 2017-05-25 2023-05-30 University Of Massachusetts Use of CDK inhibitors to enhance growth and self-renewal of progenitor cells
NZ762985A (en) * 2017-09-22 2024-03-22 Jubilant Epipad LLC Heterocyclic compounds as pad inhibitors
EP3461480A1 (en) 2017-09-27 2019-04-03 Onxeo Combination of a dna damage response cell cycle checkpoint inhibitors and belinostat for treating cancer
CN113631179A (zh) * 2019-01-25 2021-11-09 努梅迪公司 用于治疗特发性肺纤维化的方法
WO2021018298A1 (zh) * 2019-08-01 2021-02-04 南京明德新药研发有限公司 作为parp抑制剂吲哚并七元酰肟化合物
CN114746413B (zh) 2019-11-29 2024-02-23 南京明德新药研发有限公司 二氮杂吲哚类衍生物及其作为Chk1抑制剂的应用
CA3184988A1 (en) * 2020-07-13 2022-01-20 Ahmed Mamai Nicotinamide phosphoribosyltransferase (nampt) inhibitor-conjugates and uses thereof
US20230331739A1 (en) * 2020-07-31 2023-10-19 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Indolo heptamyl oxime analog crystal as parp inhibitor and method for preparing same

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9722320D0 (en) 1997-10-22 1997-12-17 Janssen Pharmaceutica Nv Human cell cycle checkpoint proteins
US6383744B1 (en) 1998-07-10 2002-05-07 Incyte Genomics, Inc. Human checkpoint kinase
EP1135135A4 (en) 1998-09-18 2006-08-09 Smithkline Beecham Corp CHK1 KINASE INHIBITORS
SI20691B (sl) * 1999-01-11 2008-10-31 Agouron Pharma Triciklični inhibitorji poli(ADP-riboza) polimeraz
ES2302699T3 (es) 1999-08-27 2008-08-01 Novartis Vaccines And Diagnostics, Inc. Oligonucleotidos quimericos antisentido y formulaciones de transfeccion celular de los mismos.
ECSP003637A (es) 1999-08-31 2002-03-25 Agouron Pharma Inhibidores triciclicos de poli (adp-ribosa) polimerasas
US6670167B1 (en) 1999-11-01 2003-12-30 Agouron Pharmaceuticals, Inc. Catalytic domain of the human effector cell cycle checkpoint protein kinase materials and methods for identification of inhibitors thereof
DK1218494T3 (da) 1999-09-22 2005-08-08 Canbas Co Ltd Præparater og fremgangsmåder til inhibering af C2-cellecyklusstandsning og sensibilisering af celler til DNA-beskadigende midler
US6211164B1 (en) 2000-03-10 2001-04-03 Abbott Laboratories Antisense oligonucleotides of the human chk1 gene and uses thereof
WO2002044183A2 (en) 2000-12-01 2002-06-06 Guilford Pharmaceuticals Inc. Benzoazepine and benzodiazepine derivatives and their use as parp inhibitors
UA76977C2 (en) 2001-03-02 2006-10-16 Icos Corp Aryl- and heteroaryl substituted chk1 inhibitors and their use as radiosensitizers and chemosensitizers
ATE404564T1 (de) * 2003-01-09 2008-08-15 Pfizer Diazepinoindolderivate als kinaseinhibitoren

Also Published As

Publication number Publication date
US20050075499A1 (en) 2005-04-07
JP2006516274A (ja) 2006-06-29
NO20053775D0 (no) 2005-08-08
US7132533B2 (en) 2006-11-07
DE602004015724D1 (de) 2008-09-25
IS7884A (is) 2005-06-09
ZA200504674B (en) 2006-07-26
EA200500893A1 (ru) 2006-02-24
AP2005003353A0 (en) 2005-09-30
US20070135415A1 (en) 2007-06-14
AU2004203977A1 (en) 2004-07-29
EP1585749B1 (en) 2008-08-13
HRP20050624A2 (en) 2006-02-28
MA27703A1 (fr) 2006-01-02
IL169082A (en) 2011-02-28
CN1759118A (zh) 2006-04-12
ECSP055911A (es) 2005-11-22
DK1585749T3 (da) 2008-09-22
NO20053775L (no) 2005-09-16
WO2004063198A1 (en) 2004-07-29
EA009337B1 (ru) 2007-12-28
NZ540638A (en) 2007-12-21
CR7899A (es) 2005-08-05
UA80733C2 (en) 2007-10-25
EP1585749A1 (en) 2005-10-19
MXPA05007352A (es) 2006-02-17
KR20050092397A (ko) 2005-09-21
CA2512683C (en) 2010-03-16
CA2512683A1 (en) 2004-07-29
KR100697746B1 (ko) 2007-03-22
CN1759118B (zh) 2010-12-08
BRPI0406701A (pt) 2005-12-20
TNSN05176A1 (fr) 2007-06-11
OA13017A (en) 2006-11-10
ATE404564T1 (de) 2008-08-15
US7462713B2 (en) 2008-12-09
AU2004203977B2 (en) 2010-06-17
ES2309484T3 (es) 2008-12-16
AP2048A (en) 2009-09-24
GEP20084367B (en) 2008-05-13
US6967198B2 (en) 2005-11-22
CY1108408T1 (el) 2014-02-12
PT1585749E (pt) 2008-10-23
HK1086257A1 (en) 2006-09-15
RS20050522A (en) 2007-12-31
EP1947102A1 (en) 2008-07-23
SI1585749T1 (sl) 2008-10-31
JP3990718B2 (ja) 2007-10-17
US20060004052A1 (en) 2006-01-05

Similar Documents

Publication Publication Date Title
PL378372A1 (pl) Tricykliczne związki jako inhibitory kinaz białkowych do wzmacniania skuteczności środków przeciwnowotworowych i radioterapii
HK1088332A1 (en) Pyrrolotriazine compounds as kinase inhibitors
HK1199254A1 (en) Process for the preparation of aurora kinase inhibitors
IL172132A0 (en) Thienopyridone derivatives as kinase inhibitors
IL173380A0 (en) Pyridinylamino-pyrimidine derivatives as protein kinase inhibitors
IL167088A (en) Pyrazolopyrimidine derivatives as cyclin dependent kinase inhibitors
PL373338A1 (pl) Związki pirolo-triazynoaniliny użyteczne jako inhibitory kinazy
EP1673343A4 (en) COMPOUNDS AND COMPOSITIONS AS PROTEIN KINASE INHIBITORS
AP2114A (en) Aminoheteroaryl compounds as protein kinase inhibitors
IL183188A0 (en) Pyrrolidyl derivatives of heteroaromatic compounds as phosphodiesterase inhibitors
IL165515A0 (en) Bisindolyl-maleimid derivatives as kinase inhibitors
EP1670771A4 (en) COMPOUNDS AND COMPOSITIONS INHIBITING PROTEIN-KINASES
HK1071757A1 (en) Imidazopyridines as cyclin dependent kinase inhibitors
IL173381A0 (en) 2-aminophenyl-4-phenylpyrimidines as kinase inhibitors
EP1613595A4 (en) NOVEL COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF PROTEIN KINASE
HK1096385A1 (en) Indazole compounds useful as protein kinase inhibitors
EP1503996A4 (en) AS KINASE INHIBITORS SUITABLE ARYLKETONE PYRROLOTRIAZIN COMPOUNDS
IL173200A0 (en) Piperidyl-quinazoline derivatives as tyrosine kinase inhibitors
SI2039685T1 (sl) Heterobiciklične spojine kot P38 inhibitorji
EP1957078A4 (en) PYRROLOTRIAZINE DERIVATIVES USEFUL FOR TREATING CANCER BY INHIBITING AURORA KINASE
IL172375A0 (en) Chinazoline derivatives as aurora kinase inhibitors
HK1071758A1 (en) Pyrazolopyridines as cyclin dependent kinase inhibitors
EP1778693A4 (en) AS KINASEINHIBITORS USEFUL COMPOUNDS OF TRICYCLIC HETEROARYL
EP1713793A4 (en) PYRIMIDINONE COMPOUNDS SUITED AS KINASEINHIBITORS
AU2003254051A8 (en) Pyrazolopyrimidines as kinase inhibitors

Legal Events

Date Code Title Description
REFS Decisions on refusal to grant patents (taken after the publication of the particulars of the applications)