SG11202105180PA - 9-substituted amino triazolo quinazoline derivatives as adenosine receptor antagonists, pharmaceutical compositions and their use - Google Patents

9-substituted amino triazolo quinazoline derivatives as adenosine receptor antagonists, pharmaceutical compositions and their use

Info

Publication number
SG11202105180PA
SG11202105180PA SG11202105180PA SG11202105180PA SG11202105180PA SG 11202105180P A SG11202105180P A SG 11202105180PA SG 11202105180P A SG11202105180P A SG 11202105180PA SG 11202105180P A SG11202105180P A SG 11202105180PA SG 11202105180P A SG11202105180P A SG 11202105180PA
Authority
SG
Singapore
Prior art keywords
pharmaceutical compositions
substituted amino
receptor antagonists
adenosine receptor
quinazoline derivatives
Prior art date
Application number
SG11202105180PA
Other languages
English (en)
Inventor
Matthew Larsen
Amjad Ali
Jared Cumming
Duane Demong
Qiaolin Deng
Thomas Graham
Elisabeth Hennessy
Andrew Hoover
Ping Liu
Kun Liu
Umar Faruk Mansoor
Jianping Pan
Christopher Plummer
Aaron Sather
Uma Swaminathan
Huijun Wang
Yonglian Zhang
Original Assignee
Merck Sharp & Dohme
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=69005832&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11202105180P(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of SG11202105180PA publication Critical patent/SG11202105180PA/en

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
    • 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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
    • C07K16/2818—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD28 or CD152
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Biochemistry (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
SG11202105180PA 2018-11-30 2019-11-26 9-substituted amino triazolo quinazoline derivatives as adenosine receptor antagonists, pharmaceutical compositions and their use SG11202105180PA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862774077P 2018-11-30 2018-11-30
PCT/US2019/063136 WO2020112700A1 (fr) 2018-11-30 2019-11-26 Dérivés amino triazolo quinazoline 9-substitués utiles en tant qu'antagonistes du récepteur de l'adénosine, compositions pharmaceutiques et leur utilisation

Publications (1)

Publication Number Publication Date
SG11202105180PA true SG11202105180PA (en) 2021-06-29

Family

ID=69005832

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11202105180PA SG11202105180PA (en) 2018-11-30 2019-11-26 9-substituted amino triazolo quinazoline derivatives as adenosine receptor antagonists, pharmaceutical compositions and their use

Country Status (25)

Country Link
US (2) US11312719B2 (fr)
EP (1) EP3886988A1 (fr)
JP (1) JP7241871B2 (fr)
KR (1) KR102653800B1 (fr)
CN (1) CN113329791A (fr)
AR (1) AR117164A1 (fr)
AU (1) AU2019385905B2 (fr)
BR (1) BR112021010427B1 (fr)
CA (1) CA3120862C (fr)
CL (1) CL2021001406A1 (fr)
CO (1) CO2021006888A2 (fr)
CR (1) CR20210271A (fr)
DO (1) DOP2021000104A (fr)
EA (1) EA202191498A1 (fr)
EC (1) ECSP21036982A (fr)
IL (1) IL283334A (fr)
JO (2) JOP20210116A1 (fr)
MA (1) MA54298A (fr)
MX (1) MX2021006329A (fr)
NI (1) NI202100043A (fr)
PE (1) PE20211768A1 (fr)
PH (1) PH12021551196A1 (fr)
SG (1) SG11202105180PA (fr)
TW (1) TW202039496A (fr)
WO (1) WO2020112700A1 (fr)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RS53072B (en) 2007-06-18 2014-04-30 Merck Sharp & Dohme B.V. HUMAN RECEPTOR ANTIBODIES PROGRAMMED DEATH PD-1
US11466017B2 (en) 2011-03-10 2022-10-11 Board Of Regents, The University Of Texas System Heterocyclic inhibitors of PTPN11
CN109475531B (zh) 2016-05-31 2021-08-17 得克萨斯州立大学董事会 Ptpn11的杂环抑制剂
MX2020011528A (es) 2018-05-02 2021-02-09 Navire Pharma Inc Inhibidores heterociclicos sustituidos de ptpn11.
EP4356973A3 (fr) 2018-08-10 2024-06-26 Navire Pharma, Inc. Dérivés de 6-(4-amino-3-méthyl-2-oxa-8-azaspiro[4.5!décan-8-yl)-3-(2,3-dichlorophényl)-2-méthylpyrimidin-4(3h)-one et composés apparentés en tant qu'inhibiteurs de ptpn11 (shp2)
WO2023158626A1 (fr) * 2022-02-16 2023-08-24 Merck Sharp & Dohme Llc Antagonistes du récepteur de l'adénosine, compositions pharmaceutiques et leur utilisation
WO2023201267A1 (fr) 2022-04-13 2023-10-19 Gilead Sciences, Inc. Polythérapie pour le traitement de cancers exprimant trop-2

Family Cites Families (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2109577A1 (de) 1971-03-01 1972-09-14 Boehringer Mannheim Gmbh Antimikrobiell wirksame Nitrofuran Derivate und Verfahren zur Herstellung derselben
US3957766A (en) 1970-06-19 1976-05-18 Boehringer Mannheim G.M.B.H. Novel nitrofuran compounds and pharmaceutical compositions
US4713383A (en) 1984-10-01 1987-12-15 Ciba-Geigy Corporation Triazoloquinazoline compounds, and their methods of preparation, pharmaceutical compositions, and uses
GB9524395D0 (en) 1995-11-29 1996-01-31 Nickerson Biocem Ltd Promoters
US6759759B2 (en) 2000-08-29 2004-07-06 Tamagawa Seiki Kabushiki Kaisha Rotary contactless connector and non-rotary contactless connector
KR100687954B1 (ko) 2001-10-15 2007-02-27 쉐링 코포레이션 아데노신 Ａ2ａ 수용체 길항제로서의이미다조（4,3-ｅ）-1,2,4-트리아졸로（1,5-ｃ） 피리미딘
AR038366A1 (es) 2001-11-30 2005-01-12 Schering Corp Compuestos de 1,2,4-triazolo [1,5-c] pirimidinas sustituidas, antagonistas del receptor de adenosina a2a, composiciones farmaceuticas, el uso de dichos compuestos para la manufactura de un medicamento para el tratamiento de enfermedades del sistema nervioso central y un kit que comprende combinacion
EP1448565B1 (fr) 2001-11-30 2009-12-30 Schering Corporation Antagonistes du recepteur adenosine a 2a
PT2206517T (pt) 2002-07-03 2023-11-07 Tasuku Honjo Composições de imunopotenciação contendo anticorpos anti-pd-l1
AU2003272886A1 (en) 2002-09-24 2004-04-19 Kyowa Hakko Kogyo Co., Ltd. (1,2,4)-TRIAZOLO(1,5-c)PYRIMIDINE DERIVATIVE
ES2367430T3 (es) 2002-12-23 2011-11-03 Wyeth Llc Anticuerpos contra pd-1 y sus usos.
EP1591527B1 (fr) 2003-01-23 2015-08-26 Ono Pharmaceutical Co., Ltd. Substance specifique a pd-1 humain
US7674791B2 (en) 2003-04-09 2010-03-09 Biogen Idec Ma Inc. Triazolopyrazines and methods of making and using the same
PT1678182E (pt) 2003-10-28 2007-04-30 Schering Corp Processo para preparar 5-amino-pirazolo-[4,3-e]-1,2,4-triazolo[1,5-c]pirimidinas
NZ550591A (en) 2004-04-21 2010-10-29 Schering Corp Pyrazolo-[4,3-e]-1,2,4-triazolo-[1,5-c]-pyrimidine adenosine A2A receptor antagonists
US7472383B2 (en) 2004-08-13 2008-12-30 Sun Microsystems, Inc. System and method for providing exceptional flow control in protected code through memory layers
CA2591125A1 (fr) 2004-12-21 2006-06-29 Schering Corporation Antagonistes de recepteur a2a de pyrazolo [1,5-a]pyrimidine adenosine
ES2427646T5 (es) 2005-05-09 2017-08-22 Ono Pharmaceutical Co., Ltd. Anticuerpos monoclonales humanos contra muerte programada 1 (PD1) y métodos para el tratamiento del cáncer mediante el uso de anticuerpos anti-PD-1 solos o combinados con otros agentes inmunoterapéuticos
MX2007015942A (es) 2005-07-01 2008-03-07 Medarex Inc Anticuerpos monoclonales humanos para ligandos 1 (pd-l1) de muerte programada.
CN101312978A (zh) 2005-09-19 2008-11-26 先灵公司 作为腺苷A2a受体拮抗剂的2－杂芳基－吡唑并－[4,3－e]－1,2,4－三唑并－[1,5－c]－嘧啶
DE602007004851D1 (de) 2006-06-26 2010-04-01 Schering Corp A2a-adenosin-rezeptor-antagonisten
RS53072B (en) 2007-06-18 2014-04-30 Merck Sharp & Dohme B.V. HUMAN RECEPTOR ANTIBODIES PROGRAMMED DEATH PD-1
PE20091101A1 (es) 2007-12-18 2009-07-26 Pharminox Ltd AMIDAS DE ACIDO 3-SUBSTITUIDO-4-OXO-3,4-DIHIDRO-IMIDAZO[5,1-d] [1,2,3,5-TETRACINA-8-CARBOXILICO Y SU EMPLEO
AU2009222040A1 (en) 2008-03-04 2009-09-11 Schering Corporation Amino-quinoxaline and amino-quinoline compounds for use as adenosine A2a receptor antagonists
EP2262837A4 (fr) 2008-03-12 2011-04-06 Merck Sharp & Dohme Protéines de liaison avec pd-1
EP2328919A2 (fr) 2008-08-25 2011-06-08 Amplimmune, Inc. Antagonistes de pd-i et procédés de traitement d'une maladie infectieuse
PL2342226T3 (pl) 2008-09-26 2017-01-31 Dana-Farber Cancer Institute, Inc. Ludzkie przeciwciała anty-PD-1, PD-L1 i PD-L2 oraz ich zastosowania
HUE034832T2 (hu) 2008-12-09 2021-12-28 Hoffmann La Roche Anti-PD-L1 antitestek és alkalmazásuk T-sejt-funkció fokozására
EP2509983B1 (fr) 2009-11-16 2014-09-17 Merck Sharp & Dohme Corp. Composés tricycliques condensés possédant une activité antagoniste des récepteurs a2a de l'adénosine
US20130017199A1 (en) 2009-11-24 2013-01-17 AMPLIMMUNE ,Inc. a corporation Simultaneous inhibition of pd-l1/pd-l2
CN103842030B (zh) 2011-08-01 2018-07-31 霍夫曼-拉罗奇有限公司 使用pd-1轴结合拮抗剂和mek抑制剂治疗癌症的方法
US9495379B2 (en) 2012-10-08 2016-11-15 Veritas Technologies Llc Locality aware, two-level fingerprint caching
WO2014101113A1 (fr) 2012-12-28 2014-07-03 Merck Sharp & Dohme Corp. Composés de 7-méthoxy-[1,2,4]triazolo[1,5-c]quinazoline-5-amine à substitution pipérazine présentant des propriétés d'antagoniste d'a2a
WO2014101120A1 (fr) 2012-12-28 2014-07-03 Merck Sharp & Dohme Corp. Composés de 7-méthoxy-[1,2,4]triazolo[1,5-c]quinazoline-5-amine à substitution hétérobicyclo présentant des propriétés d'antagoniste d'a2a
WO2015027431A1 (fr) 2013-08-29 2015-03-05 Merck Sharp & Dohme Corp. Antagonistes 2,2-difluorodioxolo du récepteur a2a
JP6779204B2 (ja) 2014-11-18 2020-11-04 メルク・シャープ・アンド・ドーム・コーポレーションＭｅｒｃｋ Ｓｈａｒｐ ＆ Ｄｏｈｍｅ Ｃｏｒｐ． Ａ２ａ拮抗薬特性を有するアミノピラジン化合物
US10085991B2 (en) 2014-12-04 2018-10-02 Merck Sharp & Dohme Corp. Formulation inhibiting effects of low acid environment
US10138212B2 (en) 2015-02-06 2018-11-27 Merck Sharp & Dohme Corp. Aminoquinazoline compounds as A2A antagonist
EP3307067B1 (fr) 2015-06-11 2022-11-02 Merck Sharp & Dohme LLC Composés d'aminopyrazine ayant des propriétés d'antagoniste a2a
EP3313187B1 (fr) 2015-06-26 2020-08-05 Merck Sharp & Dohme Corp. Formulation à libération prolongée et comprimés préparés à partir de celle-ci
WO2017008205A1 (fr) 2015-07-10 2017-01-19 Merck Sharp & Dohme Corp. Composés d'aminoquinazoline substitués a titre d'antagonistes du récepteur a2a
CN116768859A (zh) 2017-01-20 2023-09-19 艾库斯生物科学有限公司 用于治疗癌症相关疾病的唑嘧啶
EP3723754A4 (fr) 2017-12-13 2021-05-19 Merck Sharp & Dohme Corp. Composés imidazo[1,2-c]quinazolin-5-amine présentant des propriétés antagonistes du a2a
CA3100731A1 (fr) 2018-05-18 2019-11-21 Incyte Corporation Derives de pyrimidine fusionnes utilises en tant qu'inhibiteurs de a2a/a2b
WO2020106560A1 (fr) 2018-11-20 2020-05-28 Merck Sharp & Dohme Corp. Composés amino-triazolopyrimidine et amino-triazolopyrazine substitués utilisés en tant qu'antagonistes de récepteur de l'adénosine, compositions pharmaceutiques et leur utilisation
MA55142A (fr) 2018-11-20 2022-02-23 Merck Sharp & Dohme Amino-triazolopyrimidine et amino-triazolopyrazine substitués antagoniste du récepteur de l'adénosine, compositions pharmaceutiques et leur utilisation
MX2021006012A (es) 2018-11-30 2021-07-06 Merck Sharp & Dohme Derivados de amino triazolo quinazolina 7-, 8-, y 10-sustituidos como antagonistas de receptor de adenosina, composiciones farmaceuticas y su uso.

Also Published As

Publication number Publication date
MX2021006329A (es) 2021-08-11
AU2019385905B2 (en) 2023-01-12
BR112021010427A2 (pt) 2021-08-17
US20220220117A1 (en) 2022-07-14
JOP20210116A1 (ar) 2023-01-30
PH12021551196A1 (en) 2021-11-29
CA3120862A1 (fr) 2020-06-04
JP2022511441A (ja) 2022-01-31
DOP2021000104A (es) 2021-07-30
EP3886988A1 (fr) 2021-10-06
MA54298A (fr) 2022-03-09
CN113329791A (zh) 2021-08-31
US20210107904A1 (en) 2021-04-15
AR117164A1 (es) 2021-07-14
US11312719B2 (en) 2022-04-26
BR112021010427B1 (pt) 2022-09-27
JOP20210117A1 (ar) 2023-01-30
EA202191498A1 (ru) 2021-08-20
CL2021001406A1 (es) 2021-11-12
JP7241871B2 (ja) 2023-03-17
CA3120862C (fr) 2024-05-07
AU2019385905A1 (en) 2021-06-03
KR102653800B1 (ko) 2024-04-01
IL283334A (en) 2021-07-29
TW202039496A (zh) 2020-11-01
NI202100043A (es) 2021-08-13
KR20210096184A (ko) 2021-08-04
CO2021006888A2 (es) 2021-06-10
CR20210271A (es) 2021-07-14
PE20211768A1 (es) 2021-09-07
WO2020112700A1 (fr) 2020-06-04
ECSP21036982A (es) 2021-06-30

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