MX2012001064A - Inhibidores de la fosfolipasa d selectivos de isoforma. - Google Patents

Inhibidores de la fosfolipasa d selectivos de isoforma.

Info

Publication number
MX2012001064A
MX2012001064A MX2012001064A MX2012001064A MX2012001064A MX 2012001064 A MX2012001064 A MX 2012001064A MX 2012001064 A MX2012001064 A MX 2012001064A MX 2012001064 A MX2012001064 A MX 2012001064A MX 2012001064 A MX2012001064 A MX 2012001064A
Authority
MX
Mexico
Prior art keywords
inhibitors
disclosed
isoform selective
compounds
selective phospholipase
Prior art date
Application number
MX2012001064A
Other languages
English (en)
Spanish (es)
Inventor
Craig W Lindsley
Brown H Alex
Alex G Waterson
Sarah A Scott
Original Assignee
Univ Vanderbilt
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 Univ Vanderbilt filed Critical Univ Vanderbilt
Publication of MX2012001064A publication Critical patent/MX2012001064A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/10Spiro-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
    • A61K31/435Heterocyclic 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
    • A61K31/438The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (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)
MX2012001064A 2009-07-24 2010-07-23 Inhibidores de la fosfolipasa d selectivos de isoforma. MX2012001064A (es)

Applications Claiming Priority (2)

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

Publications (1)

Publication Number Publication Date
MX2012001064A true MX2012001064A (es) 2012-07-17

Family

ID=43499428

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2012001064A MX2012001064A (es) 2009-07-24 2010-07-23 Inhibidores de la fosfolipasa d selectivos de isoforma.

Country Status (14)

Country Link
US (1) US9127005B2 (cg-RX-API-DMAC7.html)
EP (1) EP2456307B1 (cg-RX-API-DMAC7.html)
JP (1) JP2013500260A (cg-RX-API-DMAC7.html)
KR (1) KR20120090034A (cg-RX-API-DMAC7.html)
CN (1) CN102573474A (cg-RX-API-DMAC7.html)
AU (1) AU2010275526A1 (cg-RX-API-DMAC7.html)
BR (1) BR112012001586A2 (cg-RX-API-DMAC7.html)
CA (1) CA2768940C (cg-RX-API-DMAC7.html)
IL (1) IL217720A0 (cg-RX-API-DMAC7.html)
IN (1) IN2012DN01661A (cg-RX-API-DMAC7.html)
MX (1) MX2012001064A (cg-RX-API-DMAC7.html)
RU (1) RU2012106657A (cg-RX-API-DMAC7.html)
SG (1) SG178102A1 (cg-RX-API-DMAC7.html)
WO (1) WO2011011680A1 (cg-RX-API-DMAC7.html)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9127005B2 (en) 2009-07-24 2015-09-08 Vanderbilt University Isoform selective phospholipase D inhibitors
US9453017B2 (en) 2011-09-30 2016-09-27 Vanderbilt University Antiviral therapies with phospholipase D inhibitors

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2013359311A1 (en) * 2012-12-11 2015-07-23 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
CN119365445A (zh) * 2022-06-16 2025-01-24 日本烟草产业株式会社 二氢噁二嗪酮化合物及其药物用途

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
US20040029244A1 (en) 2000-05-25 2004-02-12 Ben-Tsion 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
KR101144889B1 (ko) 2002-09-18 2012-05-14 학교법인 포항공과대학교 포스포리파제 d를 포함하는 펩티드 복합체
WO2006071730A1 (en) * 2004-12-27 2006-07-06 Astrazeneca Ab Pyrazolone compounds as metabotropic glutamate receptor agonists for the treatment of neurological and psychiatric disorders
WO2006107451A2 (en) 2005-02-23 2006-10-12 Univ Emory Honokiol derivatives for the treatment of proliferative disorders
CN101448844B (zh) * 2006-05-18 2012-07-25 霍夫曼-拉罗奇有限公司 作为腺苷a2b受体拮抗剂的噻唑并嘧啶/吡啶脲衍生物
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
WO2010112560A1 (en) 2009-03-31 2010-10-07 Sanofi-Aventis Deutschland Gmbh Drug delivery device body
CA2764038A1 (en) 2009-05-29 2010-12-02 The Trustees Of Columiba University In The City Of New York Modulation of phospholipase d for the treatment of neurodegenerative disorders
AU2010275526A1 (en) 2009-07-24 2012-03-15 Vanderbilt University Isoform selective Phospholipase D inhibitors
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
CA2850597A1 (en) 2011-09-30 2013-04-04 Vanderbilt University Antiviral therapies with phospholipase d inhibitors
AU2013359311A1 (en) 2012-12-11 2015-07-23 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

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9127005B2 (en) 2009-07-24 2015-09-08 Vanderbilt University Isoform selective phospholipase D inhibitors
US9453017B2 (en) 2011-09-30 2016-09-27 Vanderbilt University Antiviral therapies with phospholipase D inhibitors

Also Published As

Publication number Publication date
SG178102A1 (en) 2012-03-29
KR20120090034A (ko) 2012-08-16
IL217720A0 (en) 2012-03-29
IN2012DN01661A (cg-RX-API-DMAC7.html) 2015-06-05
WO2011011680A1 (en) 2011-01-27
EP2456307A4 (en) 2013-01-16
US9127005B2 (en) 2015-09-08
BR112012001586A2 (pt) 2015-09-01
EP2456307B1 (en) 2016-11-02
CA2768940A1 (en) 2011-01-27
EP2456307A1 (en) 2012-05-30
AU2010275526A1 (en) 2012-03-15
JP2013500260A (ja) 2013-01-07
RU2012106657A (ru) 2013-08-27
CA2768940C (en) 2018-03-13
US20120214832A1 (en) 2012-08-23
CN102573474A (zh) 2012-07-11

Similar Documents

Publication Publication Date Title
MY150542A (en) Cmet inhibitors
PT2470546E (pt) Compostos de hexa-hidrooxazinopteridina para serem utilizados como inibidores de mtor
MY150596A (en) Hsp90 inhibitors
EA201190227A1 (ru) Оксазолзамещенные индазолы в качестве ингибиторов pi3-киназ
TR201203989T1 (tr) Ksantin oksidaz inhibitörleri olarak etkin olan yeni bileşikler, bunları hazırlamaya yönelik yöntem ve bunları içeren farmasötik bileşim.
MX2012006805A (es) Indolil-piperidinil bencilaminas como inhibidores de beta-triptasa.
WO2013003298A3 (en) Inhibitors of pde10
NZ704662A (en) Crystalline forms of the prolyl hydroxylase inhibitor [(4-hydroxy-1-methyl-7-phenoxy-isoquinoline-3-carbonyl)-amino]-acetic acid
BRPI1009333B8 (pt) compostos inibidores de beta-secretase, seus usos, bem como composição farmacêutica
MX336381B (es) Boronatos como inhibidores de arginasa.
WO2013067349A9 (en) Novel chemistry used in biosensors
EA201490912A1 (ru) Производные [1,2,3]триазоло[4,5-d]пиримидина в качестве агонистов каннабиноидного рецептора 2
ECSP12011581A (es) Inhibidores de bace
MX2009003834A (es) Derivados de pirrolidina como inhibidores de iap.
BR112013031405A2 (pt) piridopirazinas substituídas como novos inibidores de syk
UA111198C2 (uk) Похідні 1-феніл-2-піридинілалкільних спиртів як інгібітори фосфодіестерази
PH12013500554A1 (en) Process for preparing pan-cdk inhibitors of the formula (i) and intermediates in the preparation
CY1112829T1 (el) Νεα μεθοδος συνθεσης για την αγομελατινη
EA201270302A1 (ru) Безводные формы производных пиридина
EA201391481A1 (ru) Аналоги эпоксиэйкозатриеновой кислоты и способы их получения и использования
MX2012007341A (es) Inhibidores de proteasoma y procesos para su preparacion, purificacion y uso.
IN2012DN01661A (cg-RX-API-DMAC7.html)
EA200900090A1 (ru) Бензиламины, способ их получения и их применение в качестве противовоспалительных средств
PH12015501175A1 (en) Substituted pyridopyrazines as syk inhibitors
MX391837B (es) Composiciones depuradoras de oxigeno.

Legal Events

Date Code Title Description
FA Abandonment or withdrawal