BRPI0418306B8 - composto n-[(1s,1ar,7br)-4,7-difluoro-1,1a,2,7b-tetraidrociclopropa[c]cromen-1-il]-n’-[5-(4-(sulfonamido)fenoxi)-2-piridinil]ureia, composição farmacêutica e uso do dito composto para profilaxia ou tratamento de infecções por hiv-1 - Google Patents

composto n-[(1s,1ar,7br)-4,7-difluoro-1,1a,2,7b-tetraidrociclopropa[c]cromen-1-il]-n’-[5-(4-(sulfonamido)fenoxi)-2-piridinil]ureia, composição farmacêutica e uso do dito composto para profilaxia ou tratamento de infecções por hiv-1

Info

Publication number
BRPI0418306B8
BRPI0418306B8 BRPI0418306A BRPI0418306A BRPI0418306B8 BR PI0418306 B8 BRPI0418306 B8 BR PI0418306B8 BR PI0418306 A BRPI0418306 A BR PI0418306A BR PI0418306 A BRPI0418306 A BR PI0418306A BR PI0418306 B8 BRPI0418306 B8 BR PI0418306B8
Authority
BR
Brazil
Prior art keywords
alkyl
compound
orx
nrxrx
hiv
Prior art date
Application number
BRPI0418306A
Other languages
English (en)
Inventor
Sahlberg Christer
Sund Christian
Antonov Dmitry
Jansson Katarina
Roue Nathalie
Lindström Stefan
Original Assignee
Medivir Ab
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
Priority claimed from SE0400021A external-priority patent/SE0400021D0/xx
Priority claimed from SE0400585A external-priority patent/SE0400585D0/xx
Application filed by Medivir Ab filed Critical Medivir Ab
Publication of BRPI0418306A publication Critical patent/BRPI0418306A/pt
Publication of BRPI0418306B1 publication Critical patent/BRPI0418306B1/pt
Publication of BRPI0418306B8 publication Critical patent/BRPI0418306B8/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • 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
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Virology (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • AIDS & HIV (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)
  • Enzymes And Modification Thereof (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

inibidores de transcriptase reserva não nucleotídicos compostos de fórmula z: (z) onde; a é ch ou n; r1 é um sustituinte para um átomo de carbono no anel contendo a selecionado de -s(=o) pra, onde ra é -alquil c1-c4- orx, -nrxrx, -nhnrxrx, -nhnhc (=o) orx, -nrxoh; -c(=o) -rb, onde rb é -alquil c1-c4-, -orx -nrxrx, -nhnrxrx, -nh-alquil c1-c3-c (=o) orx, -nrxrc, onde rc é h, alquil c1-c4, -nrxrx; -c(=o) rd, -cn, s (=o) prx onde rd é rd é alquil c1-c4, -orx, -nrxrx, -alquil c1-c3-o-alquil c1-c3-c (=o) orx, -alquil c1-c3-coorx; éteres ou ésteres -alquil c1-c3-oh ou alquil c1-c4 dos mesmos -(o-alquil c1-c3) q-o-rx; um anel aromático de 5 ou 6 membros tendo de 1-3 heteroátomos; p é 1 ou 2; rx é independentemente selecionado de h, alquil c1-c4 ou acetil; ou um par de rx que pode junto com o átomo de n adjacente formar um anel; l é -o-, -s(=o)r- ou -ch2-, onde r é 0, 1 ou 2; r3-r7 são substituintes como definido na especificiação; x é - (cr8r'8) n-d- (cr8r8) m-; d é uma ligação, -nr9-, -o-, -s-, -s(=o) - ou -s(=o)2-; e sais farmaceuticamente aceitáveis e pró-fármacos dos mesmos, tendo utilidade como anti-virais para hiv.
BRPI0418306A 2004-01-08 2004-12-30 composto n-[(1s,1ar,7br)-4,7-difluoro-1,1a,2,7b-tetraidrociclopropa[c]cromen-1-il]-n’-[5-(4-(sulfonamido)fenoxi)-2-piridinil]ureia, composição farmacêutica e uso do dito composto para profilaxia ou tratamento de infecções por hiv-1 BRPI0418306B8 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE0400021A SE0400021D0 (sv) 2004-01-08 2004-01-08 Non-nucleoside reverse transcriptase inhibitors
SE0400585A SE0400585D0 (sv) 2004-03-09 2004-03-09 NNRTI Antivirals
PCT/SE2004/002034 WO2005066131A1 (en) 2004-01-08 2004-12-30 Non-nucleotide reverse transcriptase inhibitors

Publications (3)

Publication Number Publication Date
BRPI0418306A BRPI0418306A (pt) 2007-05-02
BRPI0418306B1 BRPI0418306B1 (pt) 2018-09-18
BRPI0418306B8 true BRPI0418306B8 (pt) 2021-05-25

Family

ID=34752289

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0418306A BRPI0418306B8 (pt) 2004-01-08 2004-12-30 composto n-[(1s,1ar,7br)-4,7-difluoro-1,1a,2,7b-tetraidrociclopropa[c]cromen-1-il]-n’-[5-(4-(sulfonamido)fenoxi)-2-piridinil]ureia, composição farmacêutica e uso do dito composto para profilaxia ou tratamento de infecções por hiv-1

Country Status (16)

Country Link
US (1) US7915295B2 (pt)
EP (1) EP1701942B1 (pt)
JP (1) JP4762917B2 (pt)
AT (1) ATE451357T1 (pt)
AU (1) AU2004312284B2 (pt)
BR (1) BRPI0418306B8 (pt)
CA (1) CA2550187C (pt)
DE (1) DE602004024584D1 (pt)
DK (1) DK1701942T3 (pt)
EA (1) EA009700B1 (pt)
ES (1) ES2337794T3 (pt)
HK (1) HK1101400A1 (pt)
IL (1) IL176740A (pt)
NZ (1) NZ548367A (pt)
SG (1) SG149070A1 (pt)
WO (1) WO2005066131A1 (pt)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1534276B1 (en) * 2002-09-05 2008-11-05 Medivir AB Non-nucleoside reverse transcriptase inhibitors
US7388008B2 (en) 2004-08-02 2008-06-17 Ambrilia Biopharma Inc. Lysine based compounds
ES2539527T3 (es) * 2005-04-27 2015-07-01 Taimed Biologics, Inc. Método para mejorar la farmacocinética de los inhibidores de las proteasas y de los precursores de los inhibidores de las proteasas
EP1971615B1 (en) 2005-11-30 2014-01-01 TaiMed Biologics, Inc. Lysme-based prodrugs of aspartyl protease inhibitors and processes for their preparation
GB0608876D0 (en) * 2006-05-05 2006-06-14 Medivir Ab Combination therapy
EP2021327B1 (en) * 2006-05-15 2012-04-04 Merck Sharp & Dohme Corp. Antidiabetic bicyclic compounds
WO2008078200A2 (en) 2006-09-21 2008-07-03 Ambrilia Biopharma Inc. Protease inhibitors
JP6636031B2 (ja) * 2015-01-30 2020-01-29 ジェネンテック, インコーポレイテッド 治療用化合物およびその使用

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TR200002058T2 (tr) * 1998-01-16 2001-05-21 Medivir Ab Antiviraller
WO1999051613A1 (en) * 1998-04-03 1999-10-14 Medivir Ab Prodrugs of phosphorous-containing pharmaceuticals
SE0100733D0 (sv) * 2001-03-05 2001-03-05 Medivir Ab Non-nucleoside reverse transcriptase inhibitors
SE0102867D0 (sv) * 2001-08-28 2001-08-28 Medivir Ab Non-nucleoside reverse transcriptase inhibitors
EP1534276B1 (en) * 2002-09-05 2008-11-05 Medivir AB Non-nucleoside reverse transcriptase inhibitors

Also Published As

Publication number Publication date
DK1701942T3 (da) 2010-04-06
NZ548367A (en) 2010-06-25
EP1701942A1 (en) 2006-09-20
SG149070A1 (en) 2009-01-29
ES2337794T3 (es) 2010-04-29
HK1101400A1 (en) 2007-10-18
AU2004312284A1 (en) 2005-07-21
BRPI0418306B1 (pt) 2018-09-18
IL176740A0 (en) 2006-10-31
DE602004024584D1 (de) 2010-01-21
JP4762917B2 (ja) 2011-08-31
BRPI0418306A (pt) 2007-05-02
EA009700B1 (ru) 2008-02-28
AU2004312284A2 (en) 2005-07-21
CA2550187C (en) 2012-08-07
AU2004312284B2 (en) 2010-08-05
JP2007519640A (ja) 2007-07-19
US20080070951A1 (en) 2008-03-20
WO2005066131A1 (en) 2005-07-21
EP1701942B1 (en) 2009-12-09
EA200601289A1 (ru) 2006-12-29
CA2550187A1 (en) 2005-07-21
ATE451357T1 (de) 2009-12-15
IL176740A (en) 2011-09-27
US7915295B2 (en) 2011-03-29

Similar Documents

Publication Publication Date Title
RU2008112691A (ru) Азотсодержащее гетероциклическое соединение и его фармацевтическое применение
MA54327B1 (fr) Inhibiteurs de kras g12c
AR062109A1 (es) Derivados sustituidos de espirocetal y uso de los mismos como farmacos terapeuticos para la diabetes. composiciones farmaceuticas.
EA200970461A1 (ru) ЗАМЕЩЕННЫЕ ПРОИЗВОДНЫЕ 3-ИЗОБУТИЛ-9,10-ДИМЕТОКСИ-1,3,4,6,7,11b-ГЕКСАГИДРО-2Н-ПИРИДО[2,1-a]ИЗОХИНОЛИН-2-ОЛА И СВЯЗАННЫЕ С НИМИ СПОСОБЫ
JP2007533741A5 (ja) Bace阻害剤として有用なピロリジン誘導体
JP2013531029A5 (pt)
EA201791254A1 (ru) Кристаллические сольваты и комплексы производных (1s)-1,5-ангидро-1-c-(3-((фенил)метил)фенил)-d-глюцитола с аминокислотами в качестве ингибиторов sglt2 для лечения диабета
GEP20156250B (en) 1,3-disubstituted imidazolidin-2-one derivatives as inhibitors of cyp 17
NO20070258L (no) Benzyltriazolonforbindelser som ikke-nukleoside revers transkriptase inhibitorer
MA33240B1 (fr) Inhibiteurs de bêta-sécrétase
NO20065613L (no) 3-karbamoyl-2-pyridonderivat.
DK1119567T3 (da) Quinazolinderivater
RU2010126105A (ru) Производные пиридина, замещенные гетероциклическим кольцом и фосфоноксиметильной группой, и содержащие их противогрибковые средства
DE602005016297D1 (de) Antithrombotische diamide
AR069789A1 (es) Pirazoles condensados, una composicion farmaceutica que los contiene y su uso en la preparacion de un medicamento para el tratamiento del sida o el arc.
EA200900135A1 (ru) Производные пиразола в качестве ингибиторов цитохрома р450
EA201000702A1 (ru) Некоторые производные 2-пиразинона и их применение в качестве ингибиторов нейтрофильной эластазы
RU2012137501A (ru) Сигма-лиганды для применения при профилактике и/или лечении послеоперационной боли
EA200501075A1 (ru) Лекарственное средство для профилактики и лечения артериосклероза и гипертензии
BRPI0418306B8 (pt) composto n-[(1s,1ar,7br)-4,7-difluoro-1,1a,2,7b-tetraidrociclopropa[c]cromen-1-il]-n’-[5-(4-(sulfonamido)fenoxi)-2-piridinil]ureia, composição farmacêutica e uso do dito composto para profilaxia ou tratamento de infecções por hiv-1
RU2012106822A (ru) Индольное производное или его фармацевтически приемлемая соль
JP2005503435A5 (pt)
RU2009102270A (ru) Производные тиазолилмочевины в качестве ингибиторов фосфатидилинозитол-3-киназы
ATE308540T1 (de) Antithrombosemittel
WO2005100322A8 (en) Sulphur-linked imidazole compounds for the treament of hiv

Legal Events

Date Code Title Description
B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B07D Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]
B07E Notification of approval relating to section 229 industrial property law [chapter 7.5 patent gazette]
B06A Patent application procedure suspended [chapter 6.1 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]

Free format text: PRAZO DE VALIDADE: 10 (DEZ) ANOS CONTADOS A PARTIR DE 18/09/2018, OBSERVADAS AS CONDICOES LEGAIS.

B16C Correction of notification of the grant [chapter 16.3 patent gazette]

Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 30/12/2004 OBSERVADAS AS CONDICOES LEGAIS. PATENTE CONCEDIDA CONFORME ADI 5.529/DF

B21F Lapse acc. art. 78, item iv - on non-payment of the annual fees in time

Free format text: REFERENTE A 17A ANUIDADE.

B24J Lapse because of non-payment of annual fees (definitively: art 78 iv lpi, resolution 113/2013 art. 12)

Free format text: EM VIRTUDE DA EXTINCAO PUBLICADA NA RPI 2651 DE 26-10-2021 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDA A EXTINCAO DA PATENTE E SEUS CERTIFICADOS, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013.