PT1660095E - Inibidores tricíclicos de parp - Google Patents

Inibidores tricíclicos de parp Download PDF

Info

Publication number
PT1660095E
PT1660095E PT04743516T PT04743516T PT1660095E PT 1660095 E PT1660095 E PT 1660095E PT 04743516 T PT04743516 T PT 04743516T PT 04743516 T PT04743516 T PT 04743516T PT 1660095 E PT1660095 E PT 1660095E
Authority
PT
Portugal
Prior art keywords
parp inhibitors
tricyclic
lactam
relates
tricyclic parp
Prior art date
Application number
PT04743516T
Other languages
English (en)
Inventor
Thomas Helleday
Nicola Curtin
Original Assignee
Pfizer
Cancer Rec Tech Ltd
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
Priority claimed from GBGB0317466.1A external-priority patent/GB0317466D0/en
Priority claimed from GB0408524A external-priority patent/GB0408524D0/en
Application filed by Pfizer, Cancer Rec Tech Ltd filed Critical Pfizer
Publication of PT1660095E publication Critical patent/PT1660095E/pt

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
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/55171,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/005Enzyme inhibitors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • 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
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1137Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against enzymes
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y204/00Glycosyltransferases (2.4)
    • C12Y204/02Pentosyltransferases (2.4.2)
    • C12Y204/0203NAD+ ADP-ribosyltransferase (2.4.2.30), i.e. tankyrase or poly(ADP-ribose) polymerase
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/14Type of nucleic acid interfering N.A.
PT04743516T 2003-07-25 2004-07-23 Inibidores tricíclicos de parp PT1660095E (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0317466.1A GB0317466D0 (en) 2003-07-25 2003-07-25 Use
GB0408524A GB0408524D0 (en) 2004-04-16 2004-04-16 Use

Publications (1)

Publication Number Publication Date
PT1660095E true PT1660095E (pt) 2010-04-19

Family

ID=34117642

Family Applications (1)

Application Number Title Priority Date Filing Date
PT04743516T PT1660095E (pt) 2003-07-25 2004-07-23 Inibidores tricíclicos de parp

Country Status (23)

Country Link
US (2) US7531530B2 (pt)
EP (1) EP1660095B1 (pt)
JP (2) JP5466814B2 (pt)
KR (1) KR101138471B1 (pt)
AT (1) ATE454893T1 (pt)
AU (1) AU2004261462B2 (pt)
BR (1) BRPI0412899B1 (pt)
CA (1) CA2533332C (pt)
CY (1) CY1110335T1 (pt)
DE (1) DE602004025123D1 (pt)
DK (1) DK1660095T3 (pt)
ES (1) ES2339663T3 (pt)
HK (1) HK1084602A1 (pt)
IL (1) IL173336A (pt)
MX (1) MXPA06000993A (pt)
NO (1) NO334610B1 (pt)
NZ (1) NZ544989A (pt)
PL (1) PL1660095T3 (pt)
PT (1) PT1660095E (pt)
RU (1) RU2404183C2 (pt)
SI (1) SI1660095T1 (pt)
WO (1) WO2005012305A2 (pt)
ZA (1) ZA200600679B (pt)

Families Citing this family (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20030020488A (ko) * 2001-08-29 2003-03-10 강정훈 대나무 추출물을 유효성분으로 하는 화상치료용 조성물
WO2004087713A1 (en) * 2003-03-31 2004-10-14 Pfizer Inc. Salts of tricyclic inhibitors of poly(adp-ribose) polymerases
GB0317466D0 (en) * 2003-07-25 2003-08-27 Univ Sheffield Use
US7531530B2 (en) 2003-07-25 2009-05-12 Cancer Research Technology Limited Therapeutic compounds
EP2305221B1 (en) * 2003-12-01 2015-05-20 Kudos Pharmaceuticals Limited DNA damage repair inhibitors for treatment of cancer
KR20070046183A (ko) * 2004-09-22 2007-05-02 화이자 인코포레이티드 폴리(에이디피-리보오스) 폴리머라제 저해제를 포함하는치료 배합물
ATE551345T1 (de) * 2004-09-22 2012-04-15 Pfizer Polymorphe formen des phosphatsalzes von 8-fluor- 2-ä4-ä(methylamino)methylüphenylü-1,3,4,5- tetrahydro-6h-azepinoä5,4,3-cdüindol-6-on
MX2007008771A (es) 2005-01-19 2007-09-11 Mgi Gp Inc Compuestos de diazabenzo [des] antracen-3-ona y metodos para inhibir parp.
BRPI0613783A2 (pt) 2005-07-18 2011-02-01 Bipar Sciences Inc tratamento de cáncer
US20100279327A1 (en) * 2006-06-12 2010-11-04 Bipar Sciences, Inc. Method of treating diseases with parp inhibitors
AU2007292387A1 (en) 2006-09-05 2008-03-13 Bipar Sciences, Inc. Treatment of cancer
AU2007292306A1 (en) 2006-09-05 2008-03-13 Bipar Sciences, Inc. Inhibition of fatty acid synthesis by PARP inhibitors and methods of treatment thereof
DK2209375T3 (da) 2007-10-03 2014-10-06 Eisai Inc Parp-inhibitorforbindelser, præparater og fremgangsmåder til anvendelse deraf
CN101918003A (zh) * 2007-11-12 2010-12-15 彼帕科学公司 单独使用parp抑制剂或与抗肿瘤剂组合治疗子宫癌和卵巢癌
AU2008321128A1 (en) 2007-11-12 2009-05-22 Bipar Sciences, Inc. Treatment of breast cancer with a PARP inhibitor alone or in combination with anti-tumor agents
MX2010008572A (es) * 2008-02-04 2010-11-30 Bipar Sciences Inc Metodos de diagnostico y tratamiento de enfermedades mediadas por poli(adp-ribosa) polimerasa.
GB0804755D0 (en) * 2008-03-14 2008-04-16 Angeletti P Ist Richerche Bio Therapeutic compounds
WO2011058367A2 (en) 2009-11-13 2011-05-19 Astrazeneca Ab Diagnostic test for predicting responsiveness to treatment with poly(adp-ribose) polymerase (parp) inhibitor
EP3150610B1 (en) 2010-02-12 2019-07-31 Pfizer Inc Salts and polymorphs of 8-fluoro-2-{4-[(methylamino}methyl]phenyl}-1,3,4,5-tetrahydro-6h-azepino[5,4,3-cd]indol-6-one
DK3327148T3 (da) 2010-06-18 2021-04-12 Myriad Genetics Inc Fremgangsmåder til forudsigelse af status for brca1- og brca2-gener i en cancercelle
AU2011293635B2 (en) 2010-08-24 2015-11-26 Children's Medical Center Corporation Methods for predicting anti-cancer response
JP5699223B2 (ja) 2010-12-02 2015-04-08 シャンハイ デュァ ノボ ファルマテック カンパニー リミテッド 複素環誘導体、その合成法および医療用途
CA2833914A1 (en) * 2011-05-10 2012-11-15 Universite Laval Methods for the treatment and diagnostic of pulmonary arterial hypertension
WO2012174378A2 (en) 2011-06-17 2012-12-20 Myriad Genetics, Inc. Methods and materials for assessing allelic imbalance
KR102164964B1 (ko) 2011-07-22 2020-10-14 페이실렉스 파마슈티컬스 인코포레이티드 암의 합성치사 및 치료
EP3660161A1 (en) 2011-12-21 2020-06-03 Myriad Genetics, Inc. Methods and materials for assessing loss of heterozygosity
ES2687024T3 (es) 2012-02-23 2018-10-23 Children's Medical Center Corporation Procedimientos para predecir la respuesta contra el cáncer
NZ630278A (en) 2012-06-07 2017-02-24 Inst Curie Methods for detecting inactivation of the homologous recombination pathway (brca1/2) in human tumors
EP2892344A1 (de) * 2012-09-05 2015-07-15 Bayer CropScience AG Verwendung substituierter benzodiazepinone und benzazepinone oder deren salze als wirkstoffe gegen abiotischen pflanzenstress
US10308986B2 (en) 2013-03-14 2019-06-04 Children's Medical Center Corporation Cancer diagnosis, treatment selection and treatment
EP3693475A1 (en) 2013-04-05 2020-08-12 Myriad Genetics, Inc. Methods and materials for assessing homologous recombination deficiency
ES2909899T3 (es) 2013-12-09 2022-05-10 Inst Curie Métodos para detectar inactivación de la ruta de recombinación homóloga (BRCA1/2) en tumores humanos
DK3686288T3 (da) 2014-08-15 2023-05-22 Myriad Genetics Inc Fremgangsmåder og materialer til analyse af homolog rekombinationsdeficiens
WO2016028689A1 (en) 2014-08-22 2016-02-25 Clovis Oncology, Inc. High dosage strength tablets of rucaparib
KR20160116831A (ko) 2015-03-31 2016-10-10 (주)아모레퍼시픽 코지산 유도체를 유효성분으로 포함하는 장수 유전자 활성화용 조성물
EP3325662B1 (en) 2015-07-17 2023-08-30 Pacylex Pharmaceuticals Inc. Epigenetic silencing of nmt2
DK3594343T3 (da) 2015-07-23 2021-06-28 Inst Curie Anvendelse af en kombination af dbait-molekyle og parp-inhibitorer til behandling af kræft
GB201519573D0 (en) 2015-11-05 2015-12-23 King S College London Combination
US10857156B2 (en) 2015-11-20 2020-12-08 Senhwa Biosciences, Inc. Combination therapy of tetracyclic quinolone analogs for treating cancer
US10722484B2 (en) 2016-03-09 2020-07-28 K-Gen, Inc. Methods of cancer treatment
CA3019132A1 (en) 2016-04-01 2017-10-05 NOHMs Technologies, Inc. Modified ionic liquids containing phosphorus
WO2018022851A1 (en) 2016-07-28 2018-02-01 Mitobridge, Inc. Methods of treating acute kidney injury
EP3534957A1 (en) 2016-11-02 2019-09-11 Immunogen, Inc. Combination treatment with antibody-drug conjugates and parp inhibitors
WO2018162439A1 (en) 2017-03-08 2018-09-13 Onxeo New predictive biomarker for the sensitivity to a treatment of cancer with a dbait molecule
WO2018165615A1 (en) 2017-03-09 2018-09-13 The Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Parp-1 and methods of use thereof
US20200129476A1 (en) 2017-04-28 2020-04-30 Akribes Biomedical Gmbh PARP Inhibitor in Combination with a Glucocorticoid and/or Ascorbic Acid and/or a Protein Growth Factor for the Treatment of Impaired Wound Healing
EP3656010A4 (en) 2017-07-17 2021-08-11 Nohms Technologies, Inc. ELECTROLYTES CONTAINING PHOSPHORUS
PE20211305A1 (es) 2018-01-05 2021-07-20 Cybrexa 1 Inc Compuestos, composiciones y metodos para tratar enfermedades que involucren tejidos con enfermedades acidas o hipoxicas
CN112334133A (zh) 2018-02-15 2021-02-05 生华生物科技股份有限公司 喹诺酮类似物及其盐、组合物及其使用方法
WO2019175132A1 (en) 2018-03-13 2019-09-19 Onxeo A dbait molecule against acquired resistance in the treatment of cancer
US11874276B2 (en) 2018-04-05 2024-01-16 Dana-Farber Cancer Institute, Inc. STING levels as a biomarker for cancer immunotherapy
CN114341162A (zh) 2019-07-10 2022-04-12 赛博克萨2公司 作为治疗剂的细胞毒素的肽缀合物
KR20220051332A (ko) 2019-07-10 2022-04-26 싸이브렉사 3, 인크. 치료제로서의 미세소관 표적화제의 펩티드 접합체
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
WO2021041532A1 (en) 2019-08-26 2021-03-04 Dana-Farber Cancer Institute, Inc. Use of heparin to promote type 1 interferon signaling
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
CN115485271A (zh) 2020-04-28 2022-12-16 理森制药股份公司 用作聚(adp-核糖)聚合酶(parp)抑制剂的新型化合物
WO2022090938A1 (en) 2020-10-31 2022-05-05 Rhizen Pharmaceuticals Ag Phthalazinone derivatives useful as parp inhibitors
CN117321044A (zh) 2021-04-08 2023-12-29 理森制药股份公司 聚(adp-核糖)聚合酶抑制剂
EP4141127A1 (en) 2021-08-30 2023-03-01 Zentrum Familiärer Brust- und Eierstockkrebs Universitätsklinik Köln Method for assessing homologous recombination deficiency in ovarian cancer cells
WO2023201338A1 (en) 2022-04-15 2023-10-19 Ideaya Biosciences, Inc. Combination therapy comprising a mat2a inhibitor and a parp inhibitor
WO2023233295A1 (en) 2022-06-01 2023-12-07 Ideaya Biosciences, Inc. Thiadiazolyl derivatives as dna polymerase theta inhibitors and uses thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SK287338B6 (sk) * 1999-01-11 2010-07-07 Agouron Pharmaceuticals, Inc. Tricyklická zlúčenina, jej použitie a farmaceutická kompozícia s jej obsahom
ECSP003637A (es) 1999-08-31 2002-03-25 Agouron Pharma Inhibidores triciclicos de poli (adp-ribosa) polimerasas
US7449464B2 (en) 2003-03-12 2008-11-11 Kudos Pharmaceuticals Limited Phthalazinone derivatives
WO2004087713A1 (en) 2003-03-31 2004-10-14 Pfizer Inc. Salts of tricyclic inhibitors of poly(adp-ribose) polymerases
GB0317466D0 (en) 2003-07-25 2003-08-27 Univ Sheffield Use
US7531530B2 (en) 2003-07-25 2009-05-12 Cancer Research Technology Limited Therapeutic compounds
EP2305221B1 (en) 2003-12-01 2015-05-20 Kudos Pharmaceuticals Limited DNA damage repair inhibitors for treatment of cancer
KR20070046183A (ko) 2004-09-22 2007-05-02 화이자 인코포레이티드 폴리(에이디피-리보오스) 폴리머라제 저해제를 포함하는치료 배합물

Also Published As

Publication number Publication date
EP1660095A2 (en) 2006-05-31
US20050143370A1 (en) 2005-06-30
AU2004261462A1 (en) 2005-02-10
AU2004261462B2 (en) 2010-04-22
BRPI0412899A (pt) 2006-10-03
NZ544989A (en) 2009-10-30
NO334610B1 (no) 2014-04-22
US20070072841A1 (en) 2007-03-29
RU2404183C2 (ru) 2010-11-20
IL173336A0 (en) 2006-06-11
NO20060928L (no) 2006-02-24
PL1660095T3 (pl) 2010-07-30
JP2007533601A (ja) 2007-11-22
WO2005012305A2 (en) 2005-02-10
CA2533332A1 (en) 2005-02-10
DK1660095T3 (da) 2010-05-25
US7531530B2 (en) 2009-05-12
ZA200600679B (en) 2011-08-31
IL173336A (en) 2014-02-27
JP5580280B2 (ja) 2014-08-27
SI1660095T1 (sl) 2010-05-31
DE602004025123D1 (en) 2010-03-04
JP5466814B2 (ja) 2014-04-09
BRPI0412899B1 (pt) 2021-10-05
JP2012087135A (ja) 2012-05-10
HK1084602A1 (en) 2006-08-04
KR101138471B1 (ko) 2012-04-25
WO2005012305A3 (en) 2005-04-07
CY1110335T1 (el) 2015-01-14
MXPA06000993A (es) 2006-08-31
ATE454893T1 (de) 2010-01-15
US7351701B2 (en) 2008-04-01
KR20060066067A (ko) 2006-06-15
CA2533332C (en) 2012-01-10
RU2006105652A (ru) 2006-08-10
EP1660095B1 (en) 2010-01-13
ES2339663T3 (es) 2010-05-24

Similar Documents

Publication Publication Date Title
HK1084602A1 (en) Tricyclic parp inhibitors
WO2002044183A3 (en) Benzoazepine and benzodiazepine derivatives and their use as parp inhibitors
TW200407322A (en) Novel imidazopyridines as cyclin dependent kinase inhibitors
HUP0500574A3 (en) Acridone inhibitors of impdh enzyme, pharmaceutical compositions containing them and their use
TW200740803A (en) Heterocyclic derivatives as modulators of ion channels
IL181700A0 (en) Quinazoline derivatives and pharmaceutical compositions containing the same
SG145695A1 (en) Pyridyl derivatives and their use as therapeutic agents
SG145700A1 (en) Pyridyl derivatives and their use as therapeutic agents
ZA200710332B (en) Bicyclic derivatives as modulators of ion channels
HK1093064A1 (en) Thienopyrimidine derivatives as potassium channel inhibitors
MXPA04003668A (es) Inhibidores de fosfodiesteresa de tipo 4 y usos de los mismos.
ZA200706029B (en) Tricyclic &-opioid domulators
MXPA03008045A (es) Nuevas composiciones de medicamentos en base a agentes anticolinergicos e inhibidores de pde-iv.
HUP0501182A3 (en) Aza spiro alkane derivatives as inhibitors of metallproteases and pharmaceutical compositions containing them
HUP0203288A3 (en) Pyrrole derivatives as phosphodiesterase vii inhibitors, pharmaceutical compositions containing them and their use
AU2003226724A8 (en) Quinoline and aza-indole derivatives and their use as 5-ht6 ligands
HUP0203245A3 (en) Imidazopyridine derivatives as phosphodiesterase vii inhibitors and pharmaceutical compositions containing them
EP1244452A4 (en) UROTENSIN II RECEPTOR ANTAGONISTS
MY136840A (en) Pyrazolopyridines as cyclin dependent kinase inhibitors
MXPA05012953A (es) Benzo[b]tiofenos 3-arilsulfanil y 3-heteroarilsulfanil sustituidos como agentes terapeuticos.
PL2185561T3 (pl) Pochodne 1,2,3,4-tetrahydropirolo(1,2-a)pirazyno-6-karboksamidów i 2,3,4,5-tetrahydropirolo(1,2-a)-diazepino-7-karboksamidów, ich wytwarzanie i zastosowanie terapeutyczne
WO2002011732A8 (en) Novel bicyclic and tricyclic pyrrolidine derivatives as gnrh antagonists
MX2007007627A (es) Moduladores delta-opioides triciclicos.
HUP0301173A3 (en) Quinazoline derivatives and their use for the preparation of pharmaceutical compositions inhibiting parp enzyme
HUP0400546A3 (en) Tricyclic derivatives of indole with antiangiogenic activity and pharmaceutical compositions containing them