AR069595A1 - Compuestos amida como refuerzos de antivirales - Google Patents

Compuestos amida como refuerzos de antivirales

Info

Publication number
AR069595A1
AR069595A1 ARP080105313A ARP080105313A AR069595A1 AR 069595 A1 AR069595 A1 AR 069595A1 AR P080105313 A ARP080105313 A AR P080105313A AR P080105313 A ARP080105313 A AR P080105313A AR 069595 A1 AR069595 A1 AR 069595A1
Authority
AR
Argentina
Prior art keywords
optionally substituted
alkyl
compounds
nitrogen
certain drugs
Prior art date
Application number
ARP080105313A
Other languages
English (en)
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39386111&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR069595(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Tibotec Pharm Ltd filed Critical Tibotec Pharm Ltd
Publication of AR069595A1 publication Critical patent/AR069595A1/es

Links

Classifications

    • 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
    • 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
    • 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
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Virology (AREA)
  • General Health & Medical Sciences (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente se refiere a compuestos que tienen propiedades inhibidoras de CYP450 y por lo tanto son utiles como refuerzos de determinadas drogas, es decir, son capaces de aumentar por lo menos una de las variables farmacocinéticas de determinadas drogas cuando se co-administran. Proporciona además el uso de dichos compuestos como mejoradores de la biodisponibilidad de determinadas drogas. Además se proporcionan métodos para la preparacion de los compuestos de la invencion y composiciones farmaceuticas para el tratamiento del HIV. Reivindicacion 1: Un compuesto de la formula (1) las sales y formas estereoisoméricas del mismo, en el cual R es H, fenilo, piridilo, alquilo C1-6 o la formula (2) en el cual A y B son en forma independiente entre sí H alquilo C1-6 sustituido en forma opcional con alquinilo, heteroarilo o un heteroátomo seleccionado entre nitrogeno, oxígeno o azufre que está sustituido en forma opcional con alquilo C1-6; o en el cual A y B junto con el nitrogeno al cual están unidos forman un anillo heterocíclico de 5 o 6 miembros, saturado, parcialmente o totalmente insaturado, que contiene desde 1 hasta 4 heteroátomos cada uno seleccionado en forma independiente entre nitrogeno, oxígeno o azufre, donde dichos heteroátomos están sustituidos en forma opcional con alquilo C1-6; R1 está seleccionado entre el grupo que comprende el grupo de formulas (3) R2 es alquilo C1-6 sustituido en forma opcional con OH, aminoalquilo, pirrolidinilo, morfolinilo, alquinilo o cicloalquilo C3-7 sustituido en forma opcional con halogeno; R3 es OH; R4 es H o alquilo; R5 es piridilo o fenilo sustituido en forma opcional con halogeno; X es O, S o N sustituido en forma opcional con alquilo C1-6.
ARP080105313A 2007-12-06 2008-12-05 Compuestos amida como refuerzos de antivirales AR069595A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP07122468 2007-12-06

Publications (1)

Publication Number Publication Date
AR069595A1 true AR069595A1 (es) 2010-02-03

Family

ID=39386111

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080105313A AR069595A1 (es) 2007-12-06 2008-12-05 Compuestos amida como refuerzos de antivirales

Country Status (24)

Country Link
US (1) US8350048B2 (es)
EP (1) EP2235008B1 (es)
JP (1) JP5509092B2 (es)
KR (1) KR101624675B1 (es)
CN (1) CN101878210B (es)
AP (1) AP2804A (es)
AR (1) AR069595A1 (es)
AU (1) AU2008333165B2 (es)
BR (1) BRPI0821021A2 (es)
CA (1) CA2706155C (es)
CL (1) CL2008003639A1 (es)
EA (1) EA019616B1 (es)
HK (1) HK1149553A1 (es)
IL (1) IL205489A (es)
MX (1) MX2010006166A (es)
MY (1) MY151005A (es)
NZ (1) NZ585652A (es)
PA (1) PA8806801A1 (es)
PE (1) PE20091263A1 (es)
TW (1) TWI438202B (es)
UA (1) UA103013C2 (es)
UY (1) UY31513A1 (es)
WO (1) WO2009071650A2 (es)
ZA (1) ZA201004025B (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA026673B1 (ru) * 2008-10-07 2017-05-31 Янссен Сайенсиз Айрлэнд Юси Амидные соединения в качестве усилителей противовирусных препаратов
US20120172368A1 (en) * 2009-09-03 2012-07-05 Koen Vandyck Bis-Benzimidazole Derivatives
US8759535B2 (en) 2010-02-18 2014-06-24 High Point Pharmaceuticals, Llc Substituted fused imidazole derivatives, pharmaceutical compositions, and methods of use thereof
CA2833006A1 (en) * 2011-04-22 2012-10-26 Merck Sharp & Dohme Corp. Taste-masked formulations of raltegravir
WO2014194519A1 (en) 2013-06-07 2014-12-11 Merck Sharp & Dohme Corp. Imidazole derivatives and methods of use thereof for improving pharmacokinetics of drug
CN104000824B (zh) * 2014-05-28 2016-07-06 中山大学 苯并五元杂环类化合物在制备抗hiv-1病毒药物中的应用
WO2016089648A1 (en) 2014-12-01 2016-06-09 Vtv Therapeutics Llc Bach 1 inhibitors in combination with nrf2 activators and pharmaceutical compositions thereof
CN105985356B (zh) * 2015-02-05 2018-06-22 四川大学 咪唑[2,1-b]噻唑衍生物及其制备方法和用途
CA3007025A1 (en) 2015-12-22 2017-06-29 Kancera Ab Bicyclic hydroxamic acids useful as inhibitors of mammalian histone deacetylase activity
AR114136A1 (es) 2017-10-10 2020-07-29 Hoffmann La Roche Compuestos heterocíclicos

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6037157A (en) 1995-06-29 2000-03-14 Abbott Laboratories Method for improving pharmacokinetics
TWI286476B (en) 2001-12-12 2007-09-11 Tibotec Pharm Ltd Combination of cytochrome P450 dependent protease inhibitors
MY142238A (en) * 2002-03-12 2010-11-15 Tibotec Pharm Ltd Broadspectrum substituted benzimidazole sulfonamide hiv protease inhibitors
KR101327772B1 (ko) * 2002-08-02 2013-11-11 얀센 알 앤드 디 아일랜드 광범위 2-아미노-벤조티아졸 설폰아미드 hiv 프로테아제 저해제
AR053845A1 (es) * 2005-04-15 2007-05-23 Tibotec Pharm Ltd 5-tiazolilmetil[(1s,2r)-3-[[(2-amino-6-benzoxazolil)sulfonil)](2-metilpropil)amino]-2-hidroxi-1-(fenilmetil)propil]carbamato como mejorador de farmacos metabolizados por el citocromo p450
US8048871B2 (en) 2006-08-18 2011-11-01 Sequoia Pharmaceuticals, Inc. Compositions and methods for inhibiting cytochrome P450

Also Published As

Publication number Publication date
PE20091263A1 (es) 2009-08-14
ZA201004025B (en) 2011-12-28
BRPI0821021A2 (pt) 2015-06-16
KR20100092489A (ko) 2010-08-20
MX2010006166A (es) 2010-10-05
TWI438202B (zh) 2014-05-21
MY151005A (en) 2014-03-31
AU2008333165A1 (en) 2009-06-11
KR101624675B1 (ko) 2016-05-27
CA2706155A1 (en) 2009-06-11
US20100305073A1 (en) 2010-12-02
CL2008003639A1 (es) 2010-01-15
TW200938540A (en) 2009-09-16
CA2706155C (en) 2016-07-19
PA8806801A1 (es) 2009-07-23
AP2010005285A0 (en) 2010-06-30
AP2804A (en) 2013-11-30
UA103013C2 (uk) 2013-09-10
CN101878210A (zh) 2010-11-03
NZ585652A (en) 2011-10-28
EP2235008A2 (en) 2010-10-06
EA201070691A1 (ru) 2010-10-29
HK1149553A1 (en) 2011-10-07
JP2011506291A (ja) 2011-03-03
UY31513A1 (es) 2009-07-17
IL205489A (en) 2016-09-29
IL205489A0 (en) 2010-12-30
JP5509092B2 (ja) 2014-06-04
EA019616B1 (ru) 2014-05-30
US8350048B2 (en) 2013-01-08
WO2009071650A2 (en) 2009-06-11
CN101878210B (zh) 2013-07-17
WO2009071650A3 (en) 2009-09-11
EP2235008B1 (en) 2016-03-16
AU2008333165B2 (en) 2013-04-11

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