BRPI0408704A - benzil-piridazinonas como inibidores de transcriptase reversa - Google Patents

benzil-piridazinonas como inibidores de transcriptase reversa

Info

Publication number
BRPI0408704A
BRPI0408704A BRPI0408704-6A BRPI0408704A BRPI0408704A BR PI0408704 A BRPI0408704 A BR PI0408704A BR PI0408704 A BRPI0408704 A BR PI0408704A BR PI0408704 A BRPI0408704 A BR PI0408704A
Authority
BR
Brazil
Prior art keywords
reverse transcriptase
formula
compounds
transcriptase inhibitors
pyridazinones
Prior art date
Application number
BRPI0408704-6A
Other languages
English (en)
Inventor
James Patrick Dunn
Brian William Dymock
Taraneh Mirzadegan
Eric Brian Sjogren
Steven Swallow
Zachary Kevin Sweeney
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of BRPI0408704A publication Critical patent/BRPI0408704A/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom 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
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/14Oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D237/00Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/22Nitrogen and oxygen atoms
    • 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
    • C07D405/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • 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
    • C07D409/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms

Abstract

"BENZIL-PIRIDAZINONAS COMO INIBIDORES DE TRANSCRIPTASE REVERSA". Esta invenção refere-se a derivados de piridazinonas inusitados, da fórmula I, onde R¬ 1¬-R¬ 4¬, R¬ 7¬, R¬ 8¬ e X¬ 1¬ são como definidos no sumário, e seus sais e solvatos farmaceuticamente aceitáveis, e métodos para inibir ou modular a trasncriptase reversa do Vírus da Imunodeficiência Humana (HIV) com compostos da fórmula I, composições farmacêuticas que contêm os compostos da fórmula I misturados com pelo menos um solvente, veículo ou excipiente, e processos para preparar compostos da fórmula I. Os compostos são úteis para tratar distúrbios nos quais HIV e vírus geneticamente relacionados estão implicados.
BRPI0408704-6A 2003-03-24 2004-03-17 benzil-piridazinonas como inibidores de transcriptase reversa BRPI0408704A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US45714403P 2003-03-24 2003-03-24
PCT/EP2004/002736 WO2004085406A1 (en) 2003-03-24 2004-03-17 Benzyl-pyridazinons as reverse transcriptase inhibitors

Publications (1)

Publication Number Publication Date
BRPI0408704A true BRPI0408704A (pt) 2006-03-07

Family

ID=33098202

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0408704-6A BRPI0408704A (pt) 2003-03-24 2004-03-17 benzil-piridazinonas como inibidores de transcriptase reversa

Country Status (13)

Country Link
US (1) US7189718B2 (pt)
EP (1) EP1608629A1 (pt)
JP (1) JP4485520B2 (pt)
KR (1) KR20050119652A (pt)
CN (1) CN100469769C (pt)
AR (1) AR043674A1 (pt)
AU (1) AU2004224191A1 (pt)
BR (1) BRPI0408704A (pt)
CA (1) CA2518823A1 (pt)
MX (1) MXPA05010081A (pt)
RU (1) RU2344128C2 (pt)
TW (1) TW200505453A (pt)
WO (1) WO2004085406A1 (pt)

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JO2849B1 (en) 2007-02-13 2015-03-15 جانسين فارماسوتيكا ان. في Dopamine 2 receptor antagonists are rapidly hydrolyzed
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ES2524787T3 (es) * 2007-11-15 2014-12-12 Msd Italia S.R.L. Derivados de piridazinona como inhibidores de PARP
JP5539216B2 (ja) 2007-11-20 2014-07-02 メルク・シャープ・アンド・ドーム・コーポレーション 非ヌクレオシド系逆転写酵素阻害剤
US8877816B2 (en) * 2007-11-21 2014-11-04 Decode Genetics Ehf 4-(or 5-) substituted catechol derivatives
RU2495878C2 (ru) * 2007-12-21 2013-10-20 Ф.Хоффманн-Ля Рош Аг Гетероциклические антивирусные соединения
JP5457450B2 (ja) 2008-07-31 2014-04-02 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 迅速解離性ドーパミン2受容体拮抗薬としてのピペラジン−1−イル−トリフルオロメチル−置換−ピリジン
CN102171204B (zh) 2008-10-02 2014-08-20 旭化成制药株式会社 8位取代异喹啉衍生物及其用途
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Also Published As

Publication number Publication date
AU2004224191A1 (en) 2004-10-07
JP4485520B2 (ja) 2010-06-23
RU2344128C2 (ru) 2009-01-20
AR043674A1 (es) 2005-08-03
US7189718B2 (en) 2007-03-13
JP2006521310A (ja) 2006-09-21
US20040198736A1 (en) 2004-10-07
TW200505453A (en) 2005-02-16
RU2005132630A (ru) 2006-07-27
WO2004085406A1 (en) 2004-10-07
CN100469769C (zh) 2009-03-18
CN1764649A (zh) 2006-04-26
CA2518823A1 (en) 2004-10-07
EP1608629A1 (en) 2005-12-28
MXPA05010081A (es) 2005-11-23
KR20050119652A (ko) 2005-12-21

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Legal Events

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

Free format text: REFERENTE AS 7A E 8A ANUIDADES.

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: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2159 DE 22/05/2012.