CA2768940C - Isoform selective phospholipase d inhibitors - Google Patents

Isoform selective phospholipase d inhibitors Download PDF

Info

Publication number
CA2768940C
CA2768940C CA2768940A CA2768940A CA2768940C CA 2768940 C CA2768940 C CA 2768940C CA 2768940 A CA2768940 A CA 2768940A CA 2768940 A CA2768940 A CA 2768940A CA 2768940 C CA2768940 C CA 2768940C
Authority
CA
Canada
Prior art keywords
optionally substituted
cycloalkyl
alkyl
compound
amino
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
CA2768940A
Other languages
English (en)
French (fr)
Other versions
CA2768940A1 (en
Inventor
H. Alex Brown
Craig W. Lindsley
Alex G. Waterson
Sarah A. Scott
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Vanderbilt University
Original Assignee
Vanderbilt University
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 Vanderbilt University filed Critical Vanderbilt University
Publication of CA2768940A1 publication Critical patent/CA2768940A1/en
Application granted granted Critical
Publication of CA2768940C publication Critical patent/CA2768940C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10—Spiro-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
    • A61K31/435—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
    • A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
CA2768940A 2009-07-24 2010-07-23 Isoform selective phospholipase d inhibitors Expired - Fee Related CA2768940C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US22849209P 2009-07-24 2009-07-24
US61/228,492 2009-07-24
PCT/US2010/043045 WO2011011680A1 (en) 2009-07-24 2010-07-23 Isoform selective phospholipase d inhibitors

Publications (2)

Publication Number Publication Date
CA2768940A1 CA2768940A1 (en) 2011-01-27
CA2768940C true CA2768940C (en) 2018-03-13

Family

ID=43499428

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2768940A Expired - Fee Related CA2768940C (en) 2009-07-24 2010-07-23 Isoform selective phospholipase d inhibitors

Country Status (14)

Country Link
US (1) US9127005B2 (enExample)
EP (1) EP2456307B1 (enExample)
JP (1) JP2013500260A (enExample)
KR (1) KR20120090034A (enExample)
CN (1) CN102573474A (enExample)
AU (1) AU2010275526A1 (enExample)
BR (1) BR112012001586A2 (enExample)
CA (1) CA2768940C (enExample)
IL (1) IL217720A0 (enExample)
IN (1) IN2012DN01661A (enExample)
MX (1) MX2012001064A (enExample)
RU (1) RU2012106657A (enExample)
SG (1) SG178102A1 (enExample)
WO (1) WO2011011680A1 (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2012106657A (ru) 2009-07-24 2013-08-27 Вандербилт Юниверсити Изоформы избирательного ингибитора фосфолипазы d
US9453017B2 (en) 2011-09-30 2016-09-27 Vanderbilt University Antiviral therapies with phospholipase D inhibitors
US20140163055A1 (en) * 2012-12-11 2014-06-12 Vanderbilt University Methods and compositions of treating hiv infection
EP2931277A4 (en) * 2012-12-11 2016-07-27 Univ Vanderbilt PROCEDURE AND COMPOSITIONS WITH ACTIVE INHIBITORS AND / OR PHOSPHOLIPASE D INHIBITORS
CN114778844A (zh) * 2022-03-07 2022-07-22 天津市肿瘤医院(天津医科大学肿瘤医院) Pld1作为评估肿瘤患者对于化疗药物敏感性的分子标志物的用途
EP4541791A4 (en) * 2022-06-16 2026-06-24 Shionogi & Co Dihydrooxadiazinone compound and pharmaceutical use thereof

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1281502B1 (it) 1995-06-13 1998-02-18 Sardinian Antiviral Research C Impiego di un inibitore non nucleosidico della trascrittasi inversa in associazione con inibitori nucleosidici per il trattamento della
US6187559B1 (en) 1997-08-28 2001-02-13 Novartis Ag Phospholipase D gene
AU6262601A (en) 2000-05-25 2001-12-03 Ben Williger Phospholipase d effectors for therapy and screening
US6482829B2 (en) * 2000-06-08 2002-11-19 Hoffmann-La Roche Inc. Substituted heterocyclic siprodecane compound active as an antagonist of neurokinin 1 receptor
US20060172363A1 (en) 2002-09-18 2006-08-03 Postech Foundation Peptide complexes containing phospholipase d
BRPI0517423A (pt) * 2004-12-27 2008-10-07 Astrazeneca Ab composto, composição farmacêutica, método para o tratamento ou prevenção de distúrbios neurológicos e psiquiátricos associados com disfunção do glutamato em um animal, e, uso em um composto
AU2006233101B2 (en) 2005-02-23 2011-09-01 Arbiser, Jack Honokiol derivatives for the treatment of proliferative disorders
KR101077295B1 (ko) * 2006-05-18 2011-10-26 에프. 호프만-라 로슈 아게 아데노신 a2b 수용체 길항물질로서의 티아졸로-피라미딘/피리딘 우레아 유도체
US20100009970A1 (en) 2008-03-19 2010-01-14 Combinatorx (Singapore) Pte. Ltd. Compositions and methods for treatment of viral diseases
WO2010037081A1 (en) 2008-09-29 2010-04-01 Palatin Technologies, Inc. Melanocortin receptor-specific spiro-piperidine compounds
EP2413993B1 (en) 2009-03-31 2020-07-15 Sanofi-Aventis Deutschland GmbH Drug delivery device body
WO2010138869A1 (en) 2009-05-29 2010-12-02 The Trustees Of Columbia University In The City Of New York Modulation of phospholipase d for the treatment of neurodegenerative disorders
RU2012106657A (ru) 2009-07-24 2013-08-27 Вандербилт Юниверсити Изоформы избирательного ингибитора фосфолипазы d
US9149445B2 (en) 2009-07-27 2015-10-06 The Trustees Of Princeton University Inhibition of glycerol-3-phosphate acyltransferase (GPAT) and associated enzymes for treatment of viral infections
US9453017B2 (en) 2011-09-30 2016-09-27 Vanderbilt University Antiviral therapies with phospholipase D inhibitors
US20140163055A1 (en) 2012-12-11 2014-06-12 Vanderbilt University Methods and compositions of treating hiv infection
EP2931277A4 (en) 2012-12-11 2016-07-27 Univ Vanderbilt PROCEDURE AND COMPOSITIONS WITH ACTIVE INHIBITORS AND / OR PHOSPHOLIPASE D INHIBITORS

Also Published As

Publication number Publication date
EP2456307A1 (en) 2012-05-30
US20120214832A1 (en) 2012-08-23
WO2011011680A1 (en) 2011-01-27
IL217720A0 (en) 2012-03-29
CN102573474A (zh) 2012-07-11
US9127005B2 (en) 2015-09-08
EP2456307B1 (en) 2016-11-02
MX2012001064A (es) 2012-07-17
EP2456307A4 (en) 2013-01-16
SG178102A1 (en) 2012-03-29
JP2013500260A (ja) 2013-01-07
IN2012DN01661A (enExample) 2015-06-05
CA2768940A1 (en) 2011-01-27
BR112012001586A2 (pt) 2015-09-01
KR20120090034A (ko) 2012-08-16
RU2012106657A (ru) 2013-08-27
AU2010275526A1 (en) 2012-03-15

Similar Documents

Publication Publication Date Title
CN113365988B (zh) Shp2抑制剂及其应用
CN116888108B (zh) 新型egfr降解剂
US10399940B2 (en) Substituted pyrrolidines and methods of use
CN111440189B (zh) 稠环嘧啶氨基衍生物、其制备方法、中间体、药物组合物及应用
CN106188138B (zh) 一种二氨基嘧啶化合物及包含该化合物的组合物
TW201823249A (zh) Menin-mll相互作用之稠合二環抑制劑
WO2013038386A1 (en) Heterocyclic compounds for the treatment of cystic fibrosis
CN110382495B (zh) Cdk4/6抑制剂
EP2456307B1 (en) Isoform selective phospholipase d inhibitors
KR102359707B1 (ko) 아미노피리딘 유도체 및 이의 선택적 alk-2 억제제로서의 용도
KR20110028367A (ko) 치환된 n-옥시드 피라진 유도체
CN117510463A (zh) Kif18a抑制剂化合物、药物组合物及其制备方法和应用
JP2022511236A (ja) 置換キナゾリノン誘導体、及びmGluR4のポジティブアロステリック調節剤としてのその使用
EP2575461A1 (en) Substituted-6-methylnicotinamides as mglur5 positive allosteric modulators
CN116964061A (zh) 作为细胞周期蛋白依赖性激酶7(cdk7)抑制剂的三环嘧啶
CN121532384A (zh) 嘧啶化合物及其作为usp1抑制剂的用途
KR20240024963A (ko) 티아졸-락탐-스피로헤테로사이클릭 화합물 및 이의 적용
CN101141959B (zh) 作为甘氨酸转运体1(GlyT-1)抑制剂用于治疗神经学和神经精神病学障碍的2,5-二取代的苯甲酮衍生物
TW202227437A (zh) 作為蛋白激酶抑制劑的取代的吡咯並[2, 3-b]吡啶及吡唑並[3,4-b]吡啶衍生物
WO2025256655A1 (zh) 一种含嘧啶多元并环类衍生物抑制剂的晶型及其制备方法
CN121646596A (zh) 吡啶酮并环类衍生物及其应用
CN113087724A (zh) 异噻唑并嘧啶酮类化合物,包含其的药物组合物及其用途
HK1230186A1 (en) Condensed-ring pyrimidylamino derivative, preparation method therefor, and intermediate, pharmaceutical composition and applications thereof
HK40015028A (en) 2-benzopyrazinyl-n-heteroaryl-2-phenyl-acetamide compounds
CN114127077A (zh) 用作Cdc7抑制剂的四并环类化合物

Legal Events

Date Code Title Description
EEER Examination request

Effective date: 20150722

MKLA Lapsed

Effective date: 20200831