IL194340A0 - Combination therapy of(2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4-yl)-1-oxo-2,6-dihydro-1h[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide - Google Patents

Combination therapy of(2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4-yl)-1-oxo-2,6-dihydro-1h[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide

Info

Publication number
IL194340A0
IL194340A0 IL194340A IL19434008A IL194340A0 IL 194340 A0 IL194340 A0 IL 194340A0 IL 194340 A IL194340 A IL 194340A IL 19434008 A IL19434008 A IL 19434008A IL 194340 A0 IL194340 A0 IL 194340A0
Authority
IL
Israel
Prior art keywords
diazepino
indol
pyrazol
acetamide
dihydro
Prior art date
Application number
IL194340A
Other languages
English (en)
Original Assignee
Pfizer Prod 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 Prod Inc filed Critical Pfizer Prod Inc
Publication of IL194340A0 publication Critical patent/IL194340A0/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/337—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having four-membered rings, e.g. taxol
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • 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
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic 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
    • A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/5517—1,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • 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
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
    • 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
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Molecular Biology (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
IL194340A 2006-04-04 2008-09-25 Combination therapy of(2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4-yl)-1-oxo-2,6-dihydro-1h[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide IL194340A0 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US78927606P 2006-04-04 2006-04-04
PCT/IB2007/000928 WO2007113671A1 (en) 2006-04-04 2007-03-26 Combination therapy of (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4-yl)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide

Publications (1)

Publication Number Publication Date
IL194340A0 true IL194340A0 (en) 2009-08-03

Family

ID=38421777

Family Applications (1)

Application Number Title Priority Date Filing Date
IL194340A IL194340A0 (en) 2006-04-04 2008-09-25 Combination therapy of(2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4-yl)-1-oxo-2,6-dihydro-1h[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide

Country Status (14)

Country Link
US (1) US20090312280A1 (enExample)
EP (1) EP2007375A1 (enExample)
JP (1) JP2007277240A (enExample)
KR (1) KR20080100838A (enExample)
CN (1) CN101415417A (enExample)
AR (1) AR060284A1 (enExample)
AU (1) AU2007232279B2 (enExample)
BR (1) BRPI0709731A2 (enExample)
CA (1) CA2648371A1 (enExample)
IL (1) IL194340A0 (enExample)
MX (1) MX2008012791A (enExample)
RU (1) RU2409361C2 (enExample)
TW (1) TW200806301A (enExample)
WO (1) WO2007113671A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2009113436A1 (ja) * 2008-03-14 2011-07-21 国立大学法人 千葉大学 Fgfr3遺伝子阻害剤の放射線照射併用による放射線の抗癌作用増強法および副作用軽減法
EP2258378A4 (en) * 2008-03-27 2012-01-04 Taiho Pharmaceutical Co Ltd ANTICROBIAL AGENTS WITH A CYTIDINE DERIVATIVE AND CARBOPLATIN
KR101676062B1 (ko) * 2009-04-11 2016-11-14 어레이 바이오파마 인크. Dna 손상제를 강화시키기 위한 체크포인트 키나제 1 억제제
US8481557B2 (en) 2009-04-11 2013-07-09 Array Biopharma Inc. Method of treatment using checkpoint kinase 1 inhibitors
CN108721284A (zh) 2010-11-16 2018-11-02 阵列生物制药公司 检测点激酶1抑制剂和wee1激酶抑制剂的组合
KR101716012B1 (ko) 2011-12-31 2017-03-13 베이진 엘티디 Parp 저해제로서의 융합된 테트라 또는 펜타-사이클릭 다이하이드로다이아제피노카르바졸론
KR101684039B1 (ko) 2011-12-31 2016-12-07 베이진 엘티디 Parp 저해제로서의 융합된 테트라 또는 펜타-사이클릭 피리도프탈라지논
AU2014293013A1 (en) 2013-07-26 2016-03-17 Race Oncology Ltd. Combinatorial methods to improve the therapeutic benefit of bisantrene
EP3461480A1 (en) 2017-09-27 2019-04-03 Onxeo Combination of a dna damage response cell cycle checkpoint inhibitors and belinostat for treating cancer

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE9704545D0 (sv) * 1997-12-05 1997-12-05 Astra Pharma Prod Novel compounds
EA009337B1 (ru) * 2003-01-09 2007-12-28 Пфайзер Инк. Трициклические соединения, представляющие собой ингибиторы протеинкиназ, для увеличения эффективности противоопухолевых агентов и лучевой терапии

Also Published As

Publication number Publication date
AU2007232279B2 (en) 2010-05-06
US20090312280A1 (en) 2009-12-17
AU2007232279A1 (en) 2007-10-11
RU2008139406A (ru) 2010-04-10
JP2007277240A (ja) 2007-10-25
RU2409361C2 (ru) 2011-01-20
TW200806301A (en) 2008-02-01
WO2007113671A1 (en) 2007-10-11
BRPI0709731A2 (pt) 2011-07-26
CN101415417A (zh) 2009-04-22
CA2648371A1 (en) 2007-10-11
KR20080100838A (ko) 2008-11-19
AR060284A1 (es) 2008-06-04
MX2008012791A (es) 2008-10-15
EP2007375A1 (en) 2008-12-31

Similar Documents

Publication Publication Date Title
IL201691A0 (en) 9-(pyrazol-3-yl)-9h-purine-2-amine and 3-(pyrazol-3-yl)-3h- imidazo [4,5-b]pyridin-5-amine derivatives and their use for the treatment of cancer
SI2069342T1 (sl) Derivati aril fenil imidazo a piridinov njihova priprava in njihova terapevtska uporaba
IL201471A0 (en) Triazolopyridine carboxamide derivatives and triazolopyrimidine carboxamide derivatives, preparation thereof and therapeutic use thereof
IL196517A (en) Use of (12r, 10s, 9s) –– 10– Hydroxy – 10 – Hydroxymethyl –– 9 – Methyl – 12,11,10,9,3,2 – Hexahydro-12,9-Epoxy-H1-Diindolo [1 , 2,3 – fg: 3 ′, 2 ′, 1′ – kl] pyrrolo [3,4– i] –6,1– benzodiazomine-1-one for the preparation of a drug for the treatment of myelo-proliferative diseases associated with jak2 activation
ZA200703999B (en) Imidazo[4,5-B]Pyridin-2-One and Oxazolo [4,5-B]Pyridin-2- One compounds and analogs thereof as therapeutic compounds
PL2010536T3 (pl) Imidazo[1,2-b]pirydazyny, sposoby ich otrzymywania oraz ich zastosowanie jako ligandów receptora GABA
IL191160A (en) Use of pyrido [3,2- b] pyrazine-6-yl urine urine for the preparation of drugs to treat diseases caused by the enzyme pi3k inhibition.
IL201450A0 (en) Triazolopyridine carboxamide derivatives and triazolopyrimidine carboxamide derivatives, preparation thereof and therapeutic use thereof
IL196700A0 (en) Compositions, suitable for oral administration, comprising a triazolo [4,5-d]pyrimidin derivate
ZA200808025B (en) Dimers of artemisinin derivatives, preparation thereof and therapeutic use thereof
TW200806301A (en) Combination therapy of (2R,Z)-2-amino-2-cyclohexyl-N-(5-(1-methyl-1H-pyrazol-4-YL)-1-OXO-2,6-dihydro-1H-[1,2]diazepino[4,5,6-CD]indol-8-YL)acetamide
IL218443A0 (en) Pharmaceutical compositions comprising 7-(2,5-dihydro-4-imidazo[1,2-a]pyridine-3-yl-2,5-dioxo-1h-pyrrol-3-yl)-9-fluoro-1,2,3,4 tetrahydro-2-(1-piperidinyl-carbonyl)pyrrolo[3,2,1-jk][1,4]benzodiazepine, and process for their preparation
IL206673A0 (en) Imidazo[1,2-a]pyridine-2-carboxamide derivatives, their preparation and their therapeutic application
IL197500A0 (en) Derivatives of pyrrolizine, indolizine and quinolizine, preparation thereof and therapeutic use thereof
IL206671A0 (en) N-HETEROCYCLIC-IMIDAZO[1,2-a]PYRIDINE-2-CARBOXAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION
IL198481A0 (en) Pyrrole derivatives, preparation use of the same in therapy
ZA201008178B (en) Imidazo [2,1-b]quinazolin-2-one derivatives and their use as platelet anti-aggregative agents
IL206669A0 (en) 6-HETEROCYCLIC IMIDAZO[1,2-a]PYRIDINE-2-CARBOXAMIDE DERIVATIVES, PREPARATION AND THERAPEUTIC USE THEREOF
ZA200705035B (en) Imidazo[1,2-a]pyrazin-8-ylamines useful as modulators of kinase activity
IL213208A0 (en) 6-cycloamino-3-(1h-pyrrolo[2,3-b]pyridin-4-yl)imidazo[1,2-b]pyridazine derivatives, preparation thereof and therapeutic use thereof
ZA200809016B (en) 4, 5-Dihydro-[1,2,4] Triazolo [4,3-F] PteridinesS as protein kinase PLK1 inhibitors for the treatment of proliferative disorders
AR060348A1 (es) Formas polimorficas de (2r,z)-2-amino-2-ciclohexil-n-(5-(1-metil-1h-pirazol-4-il)-1-oxo-2,6-dihidro-1h-(1,2)diazepino(4,5,6-cd)indol-8-il)acetamida (2r,z)-2--amino-2-ciclohexil-n-(5-(1-metil-1h-pirazol-4-il)-1-oxo-2,6-dihidro-1h-[1,2]diazepino[4,5,6-cd]indol-8-il)acetamida (2r,z)-2--amino-2-ciclohex
ZA200904148B (en) Pyrrolo [1,2-A]imidazoledione effective in the treatment of peripheral neurotoxicity induced by chemotherapeutic agents
IL176824A0 (en) Tricyclic benzazepine derivatives as squalene synthase inhibitors used for the treatment of cardiovascular diseases
IL212473A0 (en) Use of 7-chloro-n,n,5-trimethyl-4-oxo-3-phenyl-3,5-dihydro-4h-pyridazino [4,5-b]indole-1-acetamide as a biomarker of peripheral benzodiazepine receptor levels