BR0305717A - Inibidores da protease do hiv 2-amino-benzotiazol sulfonamida de amplo espectro - Google Patents

Inibidores da protease do hiv 2-amino-benzotiazol sulfonamida de amplo espectro

Info

Publication number
BR0305717A
BR0305717A BR0305717-8A BR0305717A BR0305717A BR 0305717 A BR0305717 A BR 0305717A BR 0305717 A BR0305717 A BR 0305717A BR 0305717 A BR0305717 A BR 0305717A
Authority
BR
Brazil
Prior art keywords
alkyl
amino
protease inhibitors
hydrogen
broad
Prior art date
Application number
BR0305717-8A
Other languages
English (en)
Inventor
Dominique Louis Nest Surleraux
Piet Tom Bert Paul Wigerinck
Daniel P Getman
Original Assignee
Tibotec Pharm Ltd
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 Tibotec Pharm Ltd filed Critical Tibotec Pharm Ltd
Publication of BR0305717A publication Critical patent/BR0305717A/pt

Links

Classifications

    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/428Thiazoles condensed with carbocyclic rings
    • 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/60Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D277/62Benzothiazoles
    • C07D277/68Benzothiazoles 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 in position 2
    • C07D277/82Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Virology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

"INIBIDORES DA PROTEASE DO HIV 2-AMINO-BENZOTIAZOL SULFONAMIDA DE AMPLO ESPECTRO". A presente invenção refere-se à aplicação de 2-amino-benzotiazóis, tendo a fórmula (I), em que R~ 1~ é hexahidrofuro[2,3-b]furanila, tetrahidrofuranila, oxozolila, tiazolila, piridinila, ou fenila, opcionalmente substituída com um ou mais substituintes selecionados de modo independente entre C~ 1-6 alquila, hidróxi, amino, halogênio, aminoC~ 1-4~ alquila e mono- ou di(C~ 1-4~ alquil)amino; R~ 2~ é hidrogênio OU C~ 1-6~ alquila; L é uma ligação direta, -O-, C~ 1-6~ alcanodiil-O- ou -O-C~ 1-6~ alcanodiila; R~ 3~ é fenilC~ 1-4~ alquila; R~ 4~ é C~ 1-6~ alquila; R~ 5~ é hidrogênio ou C~ 1-6~ alquila; R~ 6~ é hidrogênio ou C~ 1-6~ alquila; na fabricação de um medicamento útila para inibir a protease de HIV mutante em um mamífero infectado com a referida protease de HIV mutante. Além disso, refere-se a novos compostos de fórmula (I).
BR0305717-8A 2002-08-02 2003-08-04 Inibidores da protease do hiv 2-amino-benzotiazol sulfonamida de amplo espectro BR0305717A (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP02078231 2002-08-02
US42786202P 2002-11-20 2002-11-20
PCT/EP2003/050359 WO2004014371A1 (en) 2002-08-02 2003-08-04 Broadspectrum 2-amino-benzothiazole sulfonamide hiv protease inhibitors

Publications (1)

Publication Number Publication Date
BR0305717A true BR0305717A (pt) 2004-09-28

Family

ID=31716850

Family Applications (1)

Application Number Title Priority Date Filing Date
BR0305717-8A BR0305717A (pt) 2002-08-02 2003-08-04 Inibidores da protease do hiv 2-amino-benzotiazol sulfonamida de amplo espectro

Country Status (16)

Country Link
US (2) US20050267156A1 (pt)
EP (1) EP1545518A1 (pt)
KR (1) KR20050025647A (pt)
CN (1) CN1671380B (pt)
AP (1) AP1878A (pt)
AU (1) AU2003262561B2 (pt)
BR (1) BR0305717A (pt)
CA (1) CA2492832C (pt)
EA (1) EA008594B1 (pt)
HR (1) HRP20050605A2 (pt)
IL (1) IL166257A (pt)
MX (1) MXPA05001275A (pt)
NO (1) NO20051089L (pt)
NZ (1) NZ538488A (pt)
PL (1) PL374948A1 (pt)
WO (1) WO2004014371A1 (pt)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5073480B2 (ja) * 2004-05-07 2012-11-14 セコイア、ファーマシューティカルズ、インコーポレイテッド 耐性防止レトロウイルスプロテアーゼ阻害薬
JO2841B1 (en) * 2006-06-23 2014-09-15 تيبوتيك فارماسيوتيكالز ليمتد 2-(substituted-amino) -benzothiazole sulfonamide as protease inhibitors HIV (HIV)
US8267163B2 (en) * 2008-03-17 2012-09-18 Visteon Global Technologies, Inc. Radiator tube dimple pattern
WO2011061590A1 (en) 2009-11-17 2011-05-26 Hetero Research Foundation Novel carboxamide derivatives as hiv inhibitors
MX2012015293A (es) 2010-07-02 2013-05-30 Gilead Sciences Inc Derivados de acido 2-quinolinil-acetico como compuestos antivirales.
BR112013000043A2 (pt) 2010-07-02 2019-09-24 Gilead Sciences Inc derivados de ácido naft-2-ilacético para tratar aids
US9024038B2 (en) * 2010-12-27 2015-05-05 Purdue Research Foundation Compunds and methods for treating HIV
ES2707997T3 (es) 2011-04-21 2019-04-08 Gilead Sciences Inc Compuestos de benzotiazol y su uso farmacéutico
WO2013103724A1 (en) 2012-01-04 2013-07-11 Gilead Sciences, Inc. 2- (tert - butoxy) -2- (7 -methylquinolin- 6 - yl) acetic acid derivatives for treating aids
WO2013103738A1 (en) 2012-01-04 2013-07-11 Gilead Sciences, Inc. Napthalene acetic acid derivatives against hiv infection
ES2571479T3 (es) 2012-04-20 2016-05-25 Gilead Sciences Inc Derivados del ácido benzotiazol-6-il acético y su uso para tratar una infección por VIH

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5968942A (en) * 1992-08-25 1999-10-19 G. D. Searle & Co. α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
EP0715618B1 (en) * 1993-08-24 1998-12-16 G.D. Searle & Co. Hydroxyethylamino sulphonamides useful as retroviral protease inhibitors
WO1999067254A2 (en) * 1998-06-23 1999-12-29 The United States Of America Represented By The Secretary, Department Of Health And Human Services Multi-drug resistant retroviral protease inhibitors and use thereof
CA2438304C (en) * 2001-02-14 2011-04-12 Dominique Louis Nestor Ghislain Surleraux Broadspectrum 2-(substituted-amino)-benzothiazole sulfonamide hiv protease inhibitors

Also Published As

Publication number Publication date
AP1878A (en) 2008-08-13
NO20051089L (no) 2005-05-02
US20050267156A1 (en) 2005-12-01
IL166257A0 (en) 2006-01-15
MXPA05001275A (es) 2005-04-28
CA2492832A1 (en) 2004-02-19
KR20050025647A (ko) 2005-03-14
HRP20050605A2 (en) 2006-02-28
AU2003262561A1 (en) 2004-02-25
PL374948A1 (en) 2005-11-14
CN1671380A (zh) 2005-09-21
IL166257A (en) 2013-04-30
EA200500298A1 (ru) 2005-08-25
EP1545518A1 (en) 2005-06-29
AP2005003242A0 (en) 2005-03-31
WO2004014371A1 (en) 2004-02-19
NZ538488A (en) 2007-10-26
CN1671380B (zh) 2010-05-26
CA2492832C (en) 2012-05-22
EA008594B1 (ru) 2007-06-29
AU2003262561B2 (en) 2008-10-16
US20090203742A1 (en) 2009-08-13

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Legal Events

Date Code Title Description
B25G Requested change of headquarter approved

Owner name: TIBOTEC PHARMACEUTICALS LTD. (IE)

Free format text: SEDE ALTERADA CONFORME SOLICITADO NA PETICAO NO 020070001806/RJ DE 05/01/2007.

B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B09B Patent application refused [chapter 9.2 patent gazette]
B09B Patent application refused [chapter 9.2 patent gazette]

Free format text: MANTIDO O INDEFERIMENTO UMA VEZ QUE NAO FOI APRESENTADO RECURSO DENTRO DO PRAZO LEGAL.