[go: up one dir, main page]

BRPI0513777A - composto ou um sal do mesmo, composição farmacêutica, e, uso de um composto ou de um sal do mesmo - Google Patents

composto ou um sal do mesmo, composição farmacêutica, e, uso de um composto ou de um sal do mesmo

Info

Publication number
BRPI0513777A
BRPI0513777A BRPI0513777-2A BRPI0513777A BRPI0513777A BR PI0513777 A BRPI0513777 A BR PI0513777A BR PI0513777 A BRPI0513777 A BR PI0513777A BR PI0513777 A BRPI0513777 A BR PI0513777A
Authority
BR
Brazil
Prior art keywords
nitrogen
formula
salt
compound
ring
Prior art date
Application number
BRPI0513777-2A
Other languages
English (en)
Inventor
Lisa Selsam Beavers
Serge Louis Boulet
Terry Patrick Finn
Robert Alan Gadski
William Joseph Hornback
Cynthia Darshini Jesudason
Richard Todd Pickard
Freddie Craig Stevens
Grant Mattews Vaught
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of BRPI0513777A publication Critical patent/BRPI0513777A/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity 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
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/32Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

COMPOSTO OU UM SAL DO MESMO, COMPOSIçãO FARMACêUTICA, E, USO DE UM COMPOSTO OU DE UM SAL DO MESMO A presente invenção revela compostos inéditos de aril oxazol de Fórmula I (I), ou seus sais farmaceuticamente aceitáveis, que apresentam atividade antagonista ou agonista inversa de receptor de histamina-H3, e também métodos para preparar e usar referidos compostos. Em outra concretização, a invenção revela composições farmacêuticas compreendendo compostos de Fórmula I, e também métodos de usar estas composições para tratar obesidade, deficiências cognitivas, narcolepsia e outras doenças relacionadas com receptor de histamina H3. Fórmula I (I) ou um sal farmaceuticamente aceitável da mesma, em que: m é, independentemente, em cada ocorrência, 1, 2 ou 3, Z representa independentemente carbono (substituído com hidrogênio ou pelos substituintes opcionais aqui indicados) ou nitrogênio, desde que, quando Z for nitrogênio, então R6 não seja ligado a Z; R1 e R2 são independentemente -(Cl-C7) alquila (opcionalmente substituído com de um a três halogênios), ou R1 e R2 e o nitrogênio a que estão ligados formam um anel azetidinila, um anel pirrolidinila, ou um anel piperidinila, sendo que, adicionalmente, um anel pirrolidinila ou anel piperidinila, sendo que, adicionalmente, o anel azetidinila, pirrolidinila, ou piperidinila assim formado pode ser opcionalmente substituído de uma a três vezes com R5; R6 é, independentemente, em cada ocorrência, -H, -halogênio, ou -CH~ 3~.
BRPI0513777-2A 2004-07-26 2005-07-14 composto ou um sal do mesmo, composição farmacêutica, e, uso de um composto ou de um sal do mesmo BRPI0513777A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US59119104P 2004-07-26 2004-07-26
PCT/US2005/024883 WO2006019833A1 (en) 2004-07-26 2005-07-14 Oxazole derivatives as histamine h3 receptor agents, preparation and therapeutic uses

Publications (1)

Publication Number Publication Date
BRPI0513777A true BRPI0513777A (pt) 2008-05-13

Family

ID=35134220

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0513777-2A BRPI0513777A (pt) 2004-07-26 2005-07-14 composto ou um sal do mesmo, composição farmacêutica, e, uso de um composto ou de um sal do mesmo

Country Status (17)

Country Link
US (1) US7666871B2 (pt)
EP (1) EP1786790B1 (pt)
JP (1) JP4982367B2 (pt)
CN (1) CN1989115B (pt)
AT (1) ATE432926T1 (pt)
AU (1) AU2005275183B2 (pt)
BR (1) BRPI0513777A (pt)
CA (1) CA2575081C (pt)
CY (1) CY1109493T1 (pt)
DE (1) DE602005014786D1 (pt)
DK (1) DK1786790T3 (pt)
ES (1) ES2325865T3 (pt)
MX (1) MX2007001029A (pt)
PL (1) PL1786790T3 (pt)
PT (1) PT1786790E (pt)
SI (1) SI1786790T1 (pt)
WO (1) WO2006019833A1 (pt)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8008301B2 (en) * 2004-04-01 2011-08-30 Eli Lilly And Company Histamine H3 receptor agents, preparation and therapeutic uses
WO2006089076A2 (en) 2005-02-18 2006-08-24 Neurogen Corporation Thiazole amides, imidazole amides and related analogues
JP2008534542A (ja) 2005-03-31 2008-08-28 ユセベ ファルマ ソシエテ アノニム オキサゾール部分又はチアゾール部分を含む化合物、それらの製造方法及びそれらの使用
RU2418793C2 (ru) 2005-11-15 2011-05-20 Оцука Фармасьютикал Ко., Лтд. Соединение оксазола и фармацевтическая композиция
AU2007227681A1 (en) 2006-03-15 2007-09-27 Wyeth N-substituted-azacyclylamines as histamine-3 antagonists
WO2007136668A2 (en) 2006-05-19 2007-11-29 Wyeth N-benzoyl-and n-benzylpyrrolidin-3-ylamines as histamine-3 antagonists
EP2024327A1 (de) * 2006-05-19 2009-02-18 Basf Se Benzoylsubstituierte alanine
US8329159B2 (en) * 2006-08-11 2012-12-11 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
PE20081152A1 (es) 2006-10-06 2008-08-10 Wyeth Corp Azaciclilaminas n-sustituidas como antagonistas de histamina-3
US7803825B2 (en) 2007-07-16 2010-09-28 Wyeth Llc Aminoalkylazole derivatives as histamine-3 antagonists
WO2009126782A1 (en) * 2008-04-11 2009-10-15 High Point Pharmaceuticals, Llc Histamine h3 receptor ligands
US8383829B2 (en) * 2008-04-15 2013-02-26 Konica Minolta Holdings, Inc. Electrochromic compound, electrode, and display element
SA110310332B1 (ar) * 2009-05-01 2013-12-10 Astrazeneca Ab مركبات ميثانون (3 استبدال -ازيتيدين -1-يل )(5- فينيل -1، 3، 4- أوكساديازول -2-يل )
JP5827683B2 (ja) 2010-07-06 2015-12-02 アストラゼネカ アクチボラグ 療法薬976
UY34194A (es) 2011-07-15 2013-02-28 Astrazeneca Ab ?(3-(4-(espiroheterocíclico)metil)fenoxi)azetidin-1-il)(5-(fenil)-1,3,4-oxadiazol-2-il)metanona en el tratamiento de la obesidad?
WO2013151982A1 (en) 2012-04-03 2013-10-10 Arena Pharmaceuticals, Inc. Methods and compounds useful in treating pruritus, and methods for identifying such compounds
BR112015017331B1 (pt) 2013-01-23 2022-01-11 Astrazeneca Ab Compostos de formula i, forma cristalina, uso dos compostos, combinação e composição
WO2016097071A1 (en) * 2014-12-18 2016-06-23 F. Hoffmann-La Roche Ag Estrogen receptor modulators and uses thereof
MA41562B1 (fr) 2015-06-03 2019-05-31 Bristol Myers Squibb Co Agonistes d'apj 4-hydroxy-3-(heteroaryl)pyridine-2-one a utiliser dans le traitement de troubles cardio-vasculaires
HRP20211864T1 (hr) 2015-07-06 2022-03-04 Alkermes, Inc. Inhibitori hetero-halo histonske deacetilaze
US10421756B2 (en) 2015-07-06 2019-09-24 Rodin Therapeutics, Inc. Heterobicyclic N-aminophenyl-amides as inhibitors of histone deacetylase
BR112019014235A2 (pt) 2017-01-11 2020-03-17 Rodin Therapeutics, Inc. Inibidores bicíclicos de histona desacetilase
AU2018313094A1 (en) 2017-08-07 2020-02-20 Rodin Therapeutics, Inc. Bicyclic inhibitors of histone deacetylase

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3819037A1 (de) * 1988-06-04 1989-12-14 Hoechst Ag 2,4-disubstituierte oxazol-derivate, verfahren zu ihrer herstellung sowie ihre verwendung als therapiemittel gegen krankheiten, die durch rhinoviren verursacht werden
KR100196356B1 (ko) * 1993-09-28 1999-06-15 오스카 아끼히꼬 당뇨병 치료제
AU3957600A (en) 1999-04-26 2000-11-10 Boehringer Ingelheim International Gmbh Piperidyl-imidazole derivatives, their preparations and therapeutic uses
JP2004532834A (ja) 2001-03-23 2004-10-28 イーライ・リリー・アンド・カンパニー ヒスタミンh3受容体アンタゴニストである非イミダゾール系アリールアルキルアミン化合物、その製造および治療的使用
EP1474419B1 (en) 2002-02-01 2007-09-05 Novo Nordisk A/S Amides of aminoalkyl-substituted azetidines, pyrrolidines, piperidines and azepanes
US7332508B2 (en) 2002-12-18 2008-02-19 Novo Nordisk A/S Substituted homopiperidine, piperidine or pyrrolidine derivatives
US7259262B2 (en) * 2003-10-24 2007-08-21 Hoffmann-La Roche Inc. Arylazole derivatives, their manufacture and use as pharmaceutical agents

Also Published As

Publication number Publication date
MX2007001029A (es) 2007-04-12
US20070197604A1 (en) 2007-08-23
US7666871B2 (en) 2010-02-23
JP2008507579A (ja) 2008-03-13
CY1109493T1 (el) 2014-08-13
DK1786790T3 (da) 2009-07-20
CN1989115B (zh) 2012-03-21
CA2575081C (en) 2013-05-07
JP4982367B2 (ja) 2012-07-25
AU2005275183A1 (en) 2006-02-23
EP1786790B1 (en) 2009-06-03
ES2325865T3 (es) 2009-09-22
DE602005014786D1 (de) 2009-07-16
SI1786790T1 (sl) 2009-10-31
WO2006019833A1 (en) 2006-02-23
CA2575081A1 (en) 2006-02-23
EP1786790A1 (en) 2007-05-23
CN1989115A (zh) 2007-06-27
PL1786790T3 (pl) 2009-10-30
AU2005275183B2 (en) 2011-03-17
PT1786790E (pt) 2009-08-18
ATE432926T1 (de) 2009-06-15

Similar Documents

Publication Publication Date Title
BRPI0513777A (pt) composto ou um sal do mesmo, composição farmacêutica, e, uso de um composto ou de um sal do mesmo
NZ588121A (en) Novel estrogen receptor ligands
BRPI0608732A2 (pt) composto ou um sal, hidrato, solvato, complexo ou pró-droga farmaceuticamente aceitável do mesmo, sal de um composto, processo para a preparação de um composto, uso de um composto, composição farmacêutica, e, produto
TWI262917B (en) 2-Furancarboxylic hydrazides and pharmaceutical compositions containing the same
TW200716528A (en) Cyclopropanecarboxamide derivatives
TW200637550A (en) Thiazole-4-carboxamide derivatives as mGluR5 antagonists
EA201101398A1 (ru) Замещенные пиперидины в качестве антагонистов ccr3
NO20064579L (no) Bifenylforbindelser anvendelige som muskariniske receptorantagonister
ATE457988T1 (de) A2a-adenosin-rezeptor-antagonisten
EA200970705A1 (ru) Новые фармацевтические композиции
ATE325796T1 (de) Derivate von triazolyl-imidazopyridine und von triazolylpurine als ligande des adenosine a2a rezeptoren und ihre verwendung als medicamente
MXPA05007115A (es) Nuevos agonistas inversos del receptor cb 1.
GB0701366D0 (en) Novel pharmaceutical compositions
BRPI0512058A (pt) composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, uso de um composto
AR046085A1 (es) Agonistas etilamino amino sustituidos del receptor beta 2 adrenergico
MY139612A (en) Benzoxazine derivatives as 5-th6 modulators and uses thereof
CY1109694T1 (el) Παραγωγα πυρρολιδινης ως ανταγωνιστες υποδοχεα η3 ισταμινης
MX2007005709A (es) Compuestos de n-sulfonilaminobencil-2-fenoxiacetamida sustituidos.
ES2197003A1 (es) Nuevos compuestos antagonistas de integrinas alfa.
BRPI0415109A (pt) compostos de 1-[2-(4-hidroxifenil)-2-hidroxietil]-piperidin-4-ol como antagonistas de receptor de nmda
DE602005007064D1 (de) Chromanderivate und ihre verwendung als liganden des 5-ht-rezeptors
EA200401077A1 (ru) 2-оксазоламины и их применение в качестве антагонистов рецептора 5-ht2b
PH12022550860A1 (en) 5-oxa-2-azaspiro[3.4]octane derivatives as m4 agonists
NO20065323L (no) 6-substituerte pyridoindolonderivater, fremstilling og anvendelse derav
EA201071259A1 (ru) Спиро(пиперидин-4,2-пирролидин)-1-(3,5-трифторметилфенил)метилкарбоксамиды в качестве антагонистов рецептора nk1 тахикинина

Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 11A ANUIDADE.

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: EM VIRTUDE DO ARQUIVAMENTO PUBLICADO NA RPI 2384 DE 13-09-2016 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDO O ARQUIVAMENTO DO PEDIDO DE PATENTE, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013.