[go: up one dir, main page]

AR095263A1 - Derivados de pirrolo[2,3-b]piridina útiles para el tratamiento del cáncer - Google Patents

Derivados de pirrolo[2,3-b]piridina útiles para el tratamiento del cáncer

Info

Publication number
AR095263A1
AR095263A1 ARP140100875A ARP140100875A AR095263A1 AR 095263 A1 AR095263 A1 AR 095263A1 AR P140100875 A ARP140100875 A AR P140100875A AR P140100875 A ARP140100875 A AR P140100875A AR 095263 A1 AR095263 A1 AR 095263A1
Authority
AR
Argentina
Prior art keywords
methyl
dimethylcyclohex
piperazin
pyrrolo
yloxy
Prior art date
Application number
ARP140100875A
Other languages
English (en)
Inventor
Souers Andrew
Tao Zhi
Fu - Wang Xilu
Wendt Michael
Judd Andrew
Kunzer Aaron
Sullivan Gerard
Original Assignee
Abbvie Inc
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=51529947&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR095263(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Abbvie Inc filed Critical Abbvie Inc
Publication of AR095263A1 publication Critical patent/AR095263A1/es

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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

Reivindicación 1: Un compuesto caracterizado porque se selecciona del grupo que consiste de: 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(2R)-1,4-dioxan-2-ilmetil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(3-nitro-4-{[(1S)-1-(tetrahidro-2H-piran-4-iI)etil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(3-nitro-4-{[(1R)-1-(tetrahidro-2H-piran-4-il)etil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(3-nitro-4-{[(5s,8s)-1-oxaspiro[4,5]dec-8-ilmetil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(3-nitro-4-{[(5r,8r)-1-oxaspiro[4,5]dec-8-ilmetil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(4-hidroxitetrahidro-2H-piran-4-iI)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-({4-[(1,4-dioxaspiro[4,5]dec-8-ilmetil)amino]-3-nitrofenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-{[4-(morfolin-4-iI)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(2S)-1,4-dioxan-2-ilmetil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-{[4-({[4-(hidroximetil)tetrahidro-2H-piran-4-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-{[4-({[3-(hidroximetil)oxetan-3-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-({4-[(3-hidroxi-3-metilbutil)amino]-3-nitrofenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-({4-[(3-hidroxitriciclo[3,3,1,1³,⁷]dec-1-il)amino]-3-nitrofenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(3-nitro-4-{[(1R,5S,6s)-3-oxabiciclo[3,1,0]hex-6-ilmetil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(3-hidroxioxetan-3-iI)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-{[4-(morfolin-4-ilamino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-{[(4-{[4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzoil]sulfamoil}-2-nitrofenil)amino]metil}tetrahidro-2H-piran-4-carboxilato de metilo; 4-(4-{[2--(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-({3-nitro-4-[2-(tetrahidro-2H-piran-4-il)hidrazinil]fenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-[(3-nitro-4-{[(4R)-oxepan-4-ilmetil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(3-nitro-4-{[(4S)-oxepan-4-ilmetil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(4-metiltetrahidro-2H-piran-4-iI)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-({3-nitro-4-[(tetrahidro-2H-tiopiran-4-ilmetil)amino]fenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-({3-nitro-4-[(oxetan-3-ilmetil)amino]fenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-{[4-({[(2R,5R)-5-metil-1,4-dioxan-2-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(6-hidroxi-1,4-dioxepan-6-iI)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-[(4-{[(4,4-difluoro-1-hidroxiciclohexil)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(4-metoxitetrahidro-2H-piran-4-il)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(3,3-difluorociclobutil)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-({3-nitro-4-[({1-[(trifluorometil)sulfonil]piperidin-4-il}metil)amino]fenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-{[4-({[1-(metilsulfonil)piperidin-4-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-{[4-({[(2R,4R,6S)-2,6-dimetiltetrahidro-2H-piran-4-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-[(3-nitro-4-{[(1-oxidotetrahidro-2H-tiopiran-4-iI)metil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-{[4-({[(4S)-2,2-dimetiltetrahidro-2H-piran-4-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-{[4-({[(4R)-2,2-dimetiltetrahidro-2H-piran-4-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-{[4-({[(2S,6R)-6-metil-1,4-dioxan-2-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(3-nitro-4-{[(3S)-tetrahidrofurano-3-ilmetil]amino}fenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-{[4-({[(2S)-6,6-dimetil-1,4-dioxan-2-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(3-metiloxetan-3-il)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(6-fluoro-1,4-dioxepan-6-il)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-[(4-{[(6-metoxi-1,4-dioxepan-6-iI)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-iI)-N-[(4-{[(trans-3-cianociclobutil)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-[(4-{[(cis-3-cianociclobutil)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-[(4-{[(1,1-dioxidotetrahidro-2H-tiopiran-4-iI)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-{[4-({[(2S,5R)-5-metil-1,4-dioxan-2-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-{[4-({[(2S,5S)-5-metil-1,4-dioxan-2-il]metil}amino)-3-nitrofenil]sulfonil}-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-[(4-{[(4-cianotetrahidro-2H-piran-4-iI)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; N-[(4-{[(1-acetiipiperidin-4-il)metil]amino}-3-nitrofenil)sulfonil]-4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-cloro-2-fluorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-({3-nitro-4-[(tetrahidro-2H-piran-4-ilmetil)amino]fenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-cloro-3-fluorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-({3-nitro-4-[(tetrahidro-2H-piran-4-ilmetil)amino]fenil}sulfonil)-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-[(4-{[(4-etiltetrahidro-2H-piran-4-il)metil]amino}-3-nitrofenil)sulfonil]-2-(1H-pirrolo[2,3-b]piridin-5-iloxi)benzamida; 4-(4-{[2-(4-clorofenil)-4,4-dimetilciclohex-1-en-1-il]metil}piperazin-1-il)-N-({4-[(1
ARP140100875A 2013-03-14 2014-03-12 Derivados de pirrolo[2,3-b]piridina útiles para el tratamiento del cáncer AR095263A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201361781070P 2013-03-14 2013-03-14

Publications (1)

Publication Number Publication Date
AR095263A1 true AR095263A1 (es) 2015-09-30

Family

ID=51529947

Family Applications (2)

Application Number Title Priority Date Filing Date
ARP140100875A AR095263A1 (es) 2013-03-14 2014-03-12 Derivados de pirrolo[2,3-b]piridina útiles para el tratamiento del cáncer
ARP200100026A AR117768A2 (es) 2013-03-14 2020-01-06 Agentes inductores de la apoptosis para tratar el cáncer y enfermedades inmunes y autoinmunes

Family Applications After (1)

Application Number Title Priority Date Filing Date
ARP200100026A AR117768A2 (es) 2013-03-14 2020-01-06 Agentes inductores de la apoptosis para tratar el cáncer y enfermedades inmunes y autoinmunes

Country Status (36)

Country Link
US (6) US20140275082A1 (es)
EP (2) EP3415514A1 (es)
JP (4) JP6449222B2 (es)
KR (2) KR20210021613A (es)
CN (2) CN107987075B (es)
AR (2) AR095263A1 (es)
AU (2) AU2014242104B2 (es)
BR (1) BR112015021115B1 (es)
CA (2) CA3110552A1 (es)
CL (2) CL2015002640A1 (es)
CR (1) CR20150510A (es)
CY (1) CY1120862T1 (es)
DK (1) DK2970257T3 (es)
DO (1) DOP2018000026A (es)
ES (1) ES2689679T3 (es)
GT (1) GT201500248A (es)
HK (1) HK1220189A1 (es)
HR (1) HRP20181403T8 (es)
HU (1) HUE038983T2 (es)
IL (3) IL240010B (es)
LT (1) LT2970257T (es)
MX (1) MX360541B (es)
MY (1) MY178821A (es)
NZ (1) NZ631701A (es)
PE (2) PE20191555A1 (es)
PL (1) PL2970257T4 (es)
PT (1) PT2970257T (es)
RS (1) RS57750B1 (es)
RU (2) RU2662812C2 (es)
SG (2) SG10201908388UA (es)
SI (1) SI2970257T1 (es)
TW (2) TWI675835B (es)
UA (1) UA120035C2 (es)
UY (1) UY35406A (es)
WO (1) WO2014158528A1 (es)
ZA (1) ZA201505203B (es)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120156134A1 (en) 2007-12-20 2012-06-21 Shayne Squires Compositions and methods for detecting or eliminating senescent cells to diagnose or treat disease
US20140189897A1 (en) 2011-06-21 2014-07-03 Mayo Foundation For Medical Education And Research Transgenic animals capable of being induced to delete senescent cells
CN104125836A (zh) 2011-12-13 2014-10-29 巴克老龄化研究所 改善医疗治疗的方法
WO2013158664A2 (en) 2012-04-17 2013-10-24 Kythera Biopharmaceuticals, Inc. Use of engineered viruses to specifically kill senescent cells
US9901080B2 (en) 2012-08-23 2018-02-27 Buck Institute For Research On Aging Transgenic mouse having a transgene that converts a prodrug into a cytotoxic compound in senescent cells
US9901081B2 (en) 2012-08-23 2018-02-27 Buck Institute For Research On Aging Transgenic mouse for determining the role of senescent cells in cancer
ES2845473T3 (es) 2013-03-14 2021-07-26 Boehringer Ingelheim Int (Bencil-ciano-metil)-amidas sustituidas de ácido 2-aza-biciclo[2.2.1]heptano-3-carboxílico inhibidores de la catepsina- C
US20140275082A1 (en) * 2013-03-14 2014-09-18 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
EP3964507A1 (en) 2013-10-04 2022-03-09 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
EP3669881B1 (en) 2014-01-28 2022-03-30 Buck Institute for Research on Aging Compositions for use in the treatment of senescence-assiocated eye disease and disorders
US10328058B2 (en) 2014-01-28 2019-06-25 Mayo Foundation For Medical Education And Research Treating atherosclerosis by removing senescent foam cell macrophages from atherosclerotic plaques
US20170216286A1 (en) 2014-01-28 2017-08-03 Mayo Foundation For Medical Education And Research Killing senescent cells and treating senescence-associated conditions using a src inhibitor and a flavonoid
JP6701088B2 (ja) 2014-03-19 2020-05-27 インフィニティー ファーマシューティカルズ, インコーポレイテッド Pi3k−ガンマ媒介障害の治療で使用するための複素環式化合物
RS59444B1 (sr) 2014-09-12 2019-11-29 Boehringer Ingelheim Int Spirociklični inhibitori katepsina c
WO2016054491A1 (en) 2014-10-03 2016-04-07 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
CN104370905B (zh) * 2014-10-22 2016-06-01 南京友杰医药科技有限公司 Bcl-2抑制剂ABT-199的合成
US10799574B2 (en) 2014-10-24 2020-10-13 Hpvvax. Llc Method and composition for treating cancer or skin lesion using a vaccine
IL251825B2 (en) 2014-10-24 2023-09-01 Hpvvax Llc Treatment of cancer and skin damage
US10195213B2 (en) 2015-03-13 2019-02-05 Unity Biotechnology, Inc. Chemical entities that kill senescent cells for use in treating age-related disease
EP3350183B1 (en) 2015-09-14 2025-04-02 Twelve Therapeutics, Inc. Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same
MA43372A (fr) 2015-12-04 2018-10-10 Novartis Ag Compositions à greffe de cytokine-anticorps et procédés d'utilisation pour l'immunorégulation
TWI726969B (zh) 2016-01-11 2021-05-11 比利時商健生藥品公司 用作雄性激素受體拮抗劑之經取代之硫尿囊素衍生物
WO2017147475A1 (en) * 2016-02-27 2017-08-31 Hpvvax, Llc Method and composition for treating cancer or skin lesion using a vaccine
WO2017161116A1 (en) 2016-03-17 2017-09-21 Infinity Pharmaceuticals, Inc. Isotopologues of isoquinolinone and quinazolinone compounds and uses thereof as pi3k kinase inhibitors
WO2017214269A1 (en) 2016-06-08 2017-12-14 Infinity Pharmaceuticals, Inc. Heterocyclic compounds and uses thereof
CN109641897B (zh) * 2016-09-01 2021-12-07 北京赛林泰医药技术有限公司 Bcl-2选择性抑制剂及其制备和用途
CN110177788B (zh) * 2017-01-07 2023-03-24 重庆复创医药研究有限公司 作为bcl-2选择性凋亡诱导剂的化合物
PL3612531T3 (pl) 2017-04-18 2022-12-19 Shanghai Fochon Pharmaceutical Co., Ltd. Środki wywołujące apoptozę
JP7374496B2 (ja) * 2017-06-26 2023-11-07 深▲チェン▼市塔吉瑞生物医薬有限公司 Bcl-2タンパク質を阻害するためのN-ベンゼンスルホニルベンズアミド系化合物、その組成物および使用
AU2019207608B2 (en) 2018-01-10 2024-03-28 Recurium Ip Holdings, Llc Benzamide compounds
KR102738032B1 (ko) 2018-04-29 2024-12-05 베이진 엘티디 Bcl-2 억제제
CN110577525A (zh) * 2018-06-11 2019-12-17 北京万全德众医药生物技术有限公司 一种维奈妥拉中间体的制备方法
IL282632B2 (en) * 2018-10-29 2024-06-01 Chia Tai Tianqing Pharmaceutical Group Co Ltd Trifluoromethyl-substituted sulfonamide as bcl-2-selective inhibitor
EP3978494A4 (en) 2019-05-24 2023-04-19 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. METHYL AND TRFLUOROMETHYL CONTAINING DISUBSTITUTED SULFONAMIDE SELECTIVE BCL-2 INHIBITORS
CN114057728A (zh) * 2020-08-06 2022-02-18 北京诺诚健华医药科技有限公司 作为bcl-2抑制剂的杂环化合物
EP4199924A4 (en) * 2020-08-21 2024-08-28 Ascentage Pharma (Suzhou) Co., Ltd. COMPOSITIONS AND METHODS FOR TREATING SYSTEMIC LUPUS ERYTHEMATOSUS
US20240166644A1 (en) * 2021-02-01 2024-05-23 Ascentage Pharma (Suzhou) Co., Ltd. Sulfonyl benzamide derivatives as bcl-2 inhibitors
CN113046433B (zh) * 2021-03-19 2022-12-02 武汉大学 细胞因子il1f9在制备检测、预防和治疗肿瘤的产品中的应用
CN115260191B (zh) * 2022-09-29 2022-12-27 上海睿跃生物科技有限公司 哌啶类化合物及其制备方法和应用

Family Cites Families (79)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY115155A (en) 1993-09-09 2003-04-30 Upjohn Co Substituted oxazine and thiazine oxazolidinone antimicrobials.
FR2736550B1 (fr) 1995-07-14 1998-07-24 Sandoz Sa Composition pharmaceutique sous la forme d'une dispersion solide comprenant un macrolide et un vehicule
WO1997010223A1 (en) 1995-09-15 1997-03-20 Pharmacia & Upjohn Company Aminoaryl oxazolidinone n-oxides
BRPI9707379C8 (pt) 1996-02-09 2017-12-12 Abbott Biotech Ltd composições farmacêuticas compreendendo anticorpo humano recombinante geneticamente engenheirado, e anticorpo humano recombinante geneticamente engenheirado.
US20030220234A1 (en) 1998-11-02 2003-11-27 Selvaraj Naicker Deuterated cyclosporine analogs and their use as immunodulating agents
ID26984A (id) 1998-07-06 2001-02-22 Bristol Myers Squibb Co Senyawa-senyawa sulfonamida sebagai antagonis reseptor angiotensin endotelin ganda
DE19913692A1 (de) 1999-03-25 2000-09-28 Basf Ag Mechanisch stabile pharmazeutische Darreichungsformen, enthaltend flüssige oder halbfeste oberflächenaktive Substanzen
DE19929361A1 (de) 1999-06-25 2001-01-04 Basf Ag Mechanisch stabile pharmazeutische Darreichungsformen, enthaltend flüssige oder halbfeste oberflächenaktive Substanzen
US20030236236A1 (en) 1999-06-30 2003-12-25 Feng-Jing Chen Pharmaceutical compositions and dosage forms for administration of hydrophobic drugs
GB9918037D0 (en) 1999-07-30 1999-09-29 Biochemie Gmbh Organic compounds
US6787534B2 (en) 1999-12-28 2004-09-07 Eisai Co., Ltd. Sulfonamide-containing heterocyclic compounds
US6720338B2 (en) 2000-09-20 2004-04-13 Abbott Laboratories N-acylsulfonamide apoptosis promoters
US20020055631A1 (en) 2000-09-20 2002-05-09 Augeri David J. N-acylsulfonamide apoptosis promoters
UY26942A1 (es) 2000-09-20 2002-04-26 Abbott Lab N-acilsulfonamidas promotoras de la apoptosis
US6995162B2 (en) 2001-01-12 2006-02-07 Amgen Inc. Substituted alkylamine derivatives and methods of use
KR100880760B1 (ko) 2001-06-06 2009-02-02 일라이 릴리 앤드 캄파니 항종양제로서 사용하기 위한 벤조일술폰아미드 및술포닐벤즈아미딘
GB0123400D0 (en) 2001-09-28 2001-11-21 Novartis Ag Organic compounds
DE60332322D1 (de) 2002-02-26 2010-06-10 Astrazeneca Ab Neue kristalline formen der krebsbekämpfenden verbindung zd1839
PL208114B1 (pl) 2002-02-26 2011-03-31 Astrazeneca Ab Kompozycja farmaceutyczna, sposób jej wytwarzania i zastosowanie
FR2836914B1 (fr) 2002-03-11 2008-03-14 Aventis Pharma Sa Indazoles substitues, compositions les contenant, procede de fabrication et utilisation
MY129850A (en) 2002-04-29 2007-05-31 Merck Sharp & Dohme Tetrahydropyranyl cyclopentyl tetrahydropyridopyridine modulators of chemokine receptor activity
US7642260B2 (en) 2003-11-13 2010-01-05 Abbott Laboratories, Inc. Apoptosis promoters
US7973161B2 (en) 2003-11-13 2011-07-05 Abbott Laboratories Apoptosis promoters
WO2005049593A2 (en) 2003-11-13 2005-06-02 Abbott Laboratories N-acylsulfonamide apoptosis promoters
US8614318B2 (en) 2003-11-13 2013-12-24 Abbvie Inc. Apoptosis promoters
US7767684B2 (en) 2003-11-13 2010-08-03 Abbott Laboratories Apoptosis promoters
US7790190B2 (en) 2004-03-20 2010-09-07 Yasoo Health, Inc. Aqueous emulsions of lipophile solubilized with vitamin E TPGS and linoleic acid
WO2005099353A2 (en) 2004-04-19 2005-10-27 Symed Labs Limited A novel process for the preparation of linezolid and related compounds
ATE429423T1 (de) 2004-07-20 2009-05-15 Symed Labs Ltd Neue zwischenprodukte für linezolid und verwandte verbindungen
ES2306216T3 (es) 2004-08-27 2008-11-01 Bayer Pharmaceuticals Corporation Composiciones farmaceuticas en forma de dispersiones solidas para el tratamiento de cancer.
US7511013B2 (en) 2004-09-29 2009-03-31 Amr Technology, Inc. Cyclosporin analogues and their pharmaceutical uses
FR2884821B1 (fr) 2005-04-26 2007-07-06 Aventis Pharma Sa Pyrrolopyridines substitues, compositions les contenant, procede de fabrication et utilisation
DK1888550T3 (da) 2005-05-12 2014-09-29 Abbvie Bahamas Ltd Apoptosepromotorer
US8624027B2 (en) 2005-05-12 2014-01-07 Abbvie Inc. Combination therapy for treating cancer and diagnostic assays for use therein
ATE469151T1 (de) 2005-05-16 2010-06-15 Irm Llc Pyrrolopyridinderivate als proteinkinaseinhibitoren
TW200716636A (en) 2005-05-31 2007-05-01 Speedel Experimenta Ag Heterocyclic spiro-compounds
HUE027370T2 (en) 2005-06-22 2016-10-28 Plexxikon Inc Pyrrolo [2,3-b] pyridine derivatives as protein kinase inhibitors
US7514068B2 (en) 2005-09-14 2009-04-07 Concert Pharmaceuticals Inc. Biphenyl-pyrazolecarboxamide compounds
EP1880715A1 (en) 2006-07-19 2008-01-23 Abbott GmbH & Co. KG Pharmaceutically acceptable solubilizing composition and pharmaceutical dosage form containing same
WO2008030836A2 (en) 2006-09-05 2008-03-13 Abbott Laboratories Bcl inhibitors treating platelet excess
US8796267B2 (en) 2006-10-23 2014-08-05 Concert Pharmaceuticals, Inc. Oxazolidinone derivatives and methods of use
US20080182845A1 (en) 2006-11-16 2008-07-31 Abbott Laboratories Method of preventing or treating organ, hematopoietic stem cell or bone marrow transplant rejection
RU2460725C2 (ru) 2007-02-15 2012-09-10 Ф. Хоффманн-Ля Рош Аг Новые 2-аминооксазолины в качестве лигандов taar1
WO2008124878A1 (en) 2007-04-13 2008-10-23 Cryptopharma Pty Ltd Non-steroidal compounds
CA2686545C (en) 2007-04-19 2010-11-02 Concert Pharmaceuticals Inc. Deuterated morpholinyl compounds
US7531685B2 (en) 2007-06-01 2009-05-12 Protia, Llc Deuterium-enriched oxybutynin
US20090131485A1 (en) 2007-09-10 2009-05-21 Concert Pharmaceuticals, Inc. Deuterated pirfenidone
US20090118238A1 (en) 2007-09-17 2009-05-07 Protia, Llc Deuterium-enriched alendronate
US20090088416A1 (en) 2007-09-26 2009-04-02 Protia, Llc Deuterium-enriched lapaquistat
US20090082471A1 (en) 2007-09-26 2009-03-26 Protia, Llc Deuterium-enriched fingolimod
US20110123482A1 (en) 2007-10-01 2011-05-26 The Johns Hopkins University Methods of Treating Neurological Autoimmune Disorders with Cyclophosphamide
US20090137457A1 (en) 2007-10-02 2009-05-28 Concert Pharmaceuticals, Inc. Pyrimidinedione derivatives
EP2212298B1 (en) 2007-10-18 2013-03-27 Concert Pharmaceuticals Inc. Deuterated etravirine
US20090105338A1 (en) 2007-10-18 2009-04-23 Protia, Llc Deuterium-enriched gabexate mesylate
AU2008317375B2 (en) 2007-10-26 2013-02-28 Concert Pharmaceuticals, Inc. Deuterated darunavir
NZ601350A (en) 2007-11-16 2013-08-30 Abbvie Inc Method of treating arthritis
MX2010006260A (es) 2007-12-06 2010-08-23 Abbott Lab Composiciones orales de abt-263 para tratar cancer.
US8187836B2 (en) 2008-01-15 2012-05-29 Abbott Laboratories Mammalian expression vectors and uses thereof
NZ592719A (en) 2008-10-07 2012-09-28 Astrazeneca Uk Ltd PHARMACEUTICAL FORMULATION 514 comprising 4-[3-( 4-cyclopropanecarbonyl-piperazine-1-carbonyl)-4-fluoro-benzyl]-2H-phthalazin-1-one
UA108193C2 (uk) 2008-12-04 2015-04-10 Апоптозіндукуючий засіб для лікування раку і імунних і аутоімунних захворювань
US8557983B2 (en) 2008-12-04 2013-10-15 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US20100160322A1 (en) 2008-12-04 2010-06-24 Abbott Laboratories Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US8586754B2 (en) 2008-12-05 2013-11-19 Abbvie Inc. BCL-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
BRPI0922771A2 (pt) 2008-12-05 2018-11-06 Abbott Lab agentes indutores de apoptose seletivos para bcl-2 para o tratamento de câncer e doenças imunes
US8563735B2 (en) 2008-12-05 2013-10-22 Abbvie Inc. Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
WO2010077740A2 (en) 2008-12-09 2010-07-08 Cytokine Pharmasciences, Inc. Novel antiviral compounds, compositions, and methods of use
GB2466622A (en) * 2008-12-23 2010-06-30 Trinity College Dublin Alpha2-Adrenoceptor Ligands
US20120094963A1 (en) 2008-12-23 2012-04-19 of Queen Elizabeth near Dublin Targeting prodrugs and compositions for the treatment of gastrointestinal diseases
WO2010083441A2 (en) 2009-01-19 2010-07-22 Abbott Laboratories Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
CN102282128B (zh) 2009-01-19 2015-06-17 Abbvie公司 用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂
US20100297194A1 (en) 2009-04-30 2010-11-25 Nathaniel Catron Formulation for oral administration of apoptosis promoter
IL299019A (en) 2009-05-26 2023-02-01 Abbvie Ireland Unlimited Co Process for preparing 2-(1h-pyrrolo[2,3-b]pyridin-5-yloxy)-4-(4-((9-(4-chlorophenyl)-3-isopropyl-3-azaspiro[5.5]undec-8-en-8-yl)methyl)piperazin-1-yl)benzoic acid
US8546399B2 (en) 2009-05-26 2013-10-01 Abbvie Inc. Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases
TWI540132B (zh) 2009-06-08 2016-07-01 亞培公司 Bcl-2族群抑制劑之口服醫藥劑型
US20120277210A1 (en) * 2010-10-29 2012-11-01 Abbott Laboratories Solid dispersions containing an apoptosis-inducing agent
UA113500C2 (xx) 2010-10-29 2017-02-10 Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб
US20120129853A1 (en) * 2010-11-23 2012-05-24 Abbott Laboratories Methods of treatment using selective bcl-2 inhibitors
SI2643322T1 (en) 2010-11-23 2018-01-31 Abbvie Inc. Salts and crystalline forms of an apoptosis induction agent
US20140275082A1 (en) * 2013-03-14 2014-09-18 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases

Also Published As

Publication number Publication date
HRP20181403T1 (hr) 2018-11-30
KR102260645B1 (ko) 2021-06-08
JP2020180145A (ja) 2020-11-05
CA3110552A1 (en) 2014-10-02
BR112015021115A2 (pt) 2017-10-10
UA120035C2 (uk) 2019-09-25
AU2018226476C1 (en) 2020-01-16
IL287315A (en) 2021-12-01
TWI675835B (zh) 2019-11-01
CL2015002640A1 (es) 2016-03-18
SG11201507363UA (en) 2015-10-29
EP3415514A1 (en) 2018-12-19
EP2970257B1 (en) 2018-05-30
EP2970257A1 (en) 2016-01-20
US20200331907A1 (en) 2020-10-22
PL2970257T3 (pl) 2018-11-30
MY178821A (en) 2020-10-20
IL265296A (en) 2019-05-30
CN105026394B (zh) 2017-12-29
MX360541B (es) 2018-10-19
AU2014242104B2 (en) 2018-07-05
CL2018000353A1 (es) 2018-07-13
TWI717662B (zh) 2021-02-01
ES2689679T3 (es) 2018-11-15
TW201524976A (zh) 2015-07-01
CN107987075A (zh) 2018-05-04
MX2015011641A (es) 2015-12-16
TW201908316A (zh) 2019-03-01
PL2970257T4 (pl) 2019-01-31
JP2016517406A (ja) 2016-06-16
RS57750B1 (sr) 2018-12-31
HRP20181403T8 (hr) 2018-12-28
AU2014242104A1 (en) 2015-07-30
AU2018226476B2 (en) 2019-10-10
US20210403467A1 (en) 2021-12-30
KR20210021613A (ko) 2021-02-26
PE20191555A1 (es) 2019-10-24
PE20151555A1 (es) 2015-12-06
LT2970257T (lt) 2018-09-25
KR20150130486A (ko) 2015-11-23
DOP2018000026A (es) 2018-10-31
RU2018127315A (ru) 2019-03-13
CY1120862T1 (el) 2019-12-11
BR112015021115B1 (pt) 2022-05-03
PT2970257T (pt) 2018-10-25
RU2015143917A (ru) 2017-04-18
UY35406A (es) 2014-09-30
JP6449222B2 (ja) 2019-01-09
AR117768A2 (es) 2021-08-25
SG10201908388UA (en) 2019-10-30
CN105026394A (zh) 2015-11-04
JP2019038820A (ja) 2019-03-14
GT201500248A (es) 2017-09-14
SI2970257T1 (sl) 2018-10-30
ZA201505203B (en) 2016-07-27
HK1220189A1 (zh) 2017-04-28
US20170008891A1 (en) 2017-01-12
JP2021167330A (ja) 2021-10-21
US20150299197A1 (en) 2015-10-22
RU2662812C2 (ru) 2018-07-31
DK2970257T3 (en) 2018-09-10
AU2018226476A1 (en) 2018-09-27
CN107987075B (zh) 2020-12-01
IL240010B (en) 2019-09-26
HUE038983T2 (hu) 2018-12-28
IL240010A0 (en) 2015-09-24
US10081628B2 (en) 2018-09-25
US20140275082A1 (en) 2014-09-18
CA2899041A1 (en) 2014-10-02
NZ631701A (en) 2017-05-26
RU2018127315A3 (es) 2021-10-05
WO2014158528A1 (en) 2014-10-02
US20180354952A1 (en) 2018-12-13
CR20150510A (es) 2015-12-11

Similar Documents

Publication Publication Date Title
AR095263A1 (es) Derivados de pirrolo[2,3-b]piridina útiles para el tratamiento del cáncer
JP2016517406A5 (es)
RU2012127760A (ru) Bcl-2-селективные апоптоз-индуцирующие средства для лечения рака и иммунных заболеваний
NZ610746A (en) Methods of treatment using selective bcl-2 inhibitors
RU2331642C2 (ru) Новые ингибиторы киназ
RU2481336C2 (ru) Циклопента(d)пиримидины в качестве ингибиторов протеинкиназ акт
IL288243B1 (en) Heteroaryl-substituted pyridines and methods of use
ME02205B (me) INDUKUJUĆI AGENSI APOPTOZE ZA LEČENJE KANCERA I IMUNIH l AUTOIMUNIH OBOLJENJA
AR097388A1 (es) Beneficio de supervivencia en pacientes con tumores sólidos con niveles elevados de proteína c reactiva
FI3672976T3 (fi) Bcl-2-inhibiittoreita
EA201491943A1 (ru) ТРИАЗОЛЫ, ЗАМЕЩЕННЫЕ КАРБОКСАМИДОМ ИЛИ СУЛЬФОНАМИДОМ, И РОДСТВЕННЫЕ ПРОИЗВОДНЫЕ В КАЧЕСТВЕ МОДУЛЯТОРОВ ДЛЯ ОРФАННОГО ЯДЕРНОГО РЕЦЕПТОРА RORγ
RU2012116207A (ru) Производные индола в качестве модуляторов crac
ES2668380T3 (es) Moduladores de receptores de andrógenos y sus usos
AR072900A1 (es) Agentes terapeuticos derivados de pirazolo[3,4-d]pirimidina
RU2393156C2 (ru) Замещенные гидантоины для лечения рака
PE20161315A1 (es) Compuestos de pirazolona y usos de los mismos
JP2014523851A5 (es)
AR035626A1 (es) Compuestos de indol inhibidores de tirosina quinasa, composicion farmaceutica, procedimiento para prepararla,y, uso de los compuestos en la preparación de medicamentos
JP2013528204A5 (es)
MA52424A (fr) Compositions pharmaceutiques comprenant du (2s)--((1s)-1-cyano-2-[4-(3-methyl-2-oxo-2,3-dihydro-1,3-benzoxazol-5-yl)phenyl]ethyl)-1,4-oxazepane-2-carboxamide
SV2017005530A (es) Combinaciones que contienen 2,3- dihidroimidazo[1,2-c]quinazolina sustituida
AR092045A1 (es) Combinaciones farmaceuticas
RU2013157374A (ru) Производное индазола и пирролопиридина и его фармацевтическое применение
PE20191792A1 (es) Derivados de isoxazol como agonistas del receptor nuclear y usos de los mismos
AR056645A1 (es) Compuestos de urea sustituida inhibidores de enzimas chk1 .

Legal Events

Date Code Title Description
FC Refusal