PE20120136A1 - Compuestos derivados de n-acilsulfonamidas como inhibidores de bcl-2 - Google Patents

Compuestos derivados de n-acilsulfonamidas como inhibidores de bcl-2

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Publication number
PE20120136A1
PE20120136A1 PE2011001147A PE2011001147A PE20120136A1 PE 20120136 A1 PE20120136 A1 PE 20120136A1 PE 2011001147 A PE2011001147 A PE 2011001147A PE 2011001147 A PE2011001147 A PE 2011001147A PE 20120136 A1 PE20120136 A1 PE 20120136A1
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PE
Peru
Prior art keywords
fused
benzene
phenyl
methyl
bcl
Prior art date
Application number
PE2011001147A
Other languages
English (en)
Inventor
Milan Bruncko
Yujia Dai
Hong Ding
George A Doherty
Steven W Elmore
Lisa A Hasvold
Laura Hexamer
Aaron R Kunzer
Robert A Mantei
William J Mcclellan
Chang H Park
Cheol-Min Park
Andrew M Petros
Xiaohong Song
Andrew J Souers
Gerard M Sullivan
Zhi-Fu Tao
Gary T Wang
Le Wang
Xilu Wang
Michael D Wendt
Peter Edward Czabotar
Guillaume Laurent Lessene
Peter Malcom Colman
Original Assignee
Abbvie Inc
Inst Medical W & E Hall
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.)
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41809142&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20120136(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Abbvie Inc, Inst Medical W & E Hall filed Critical Abbvie Inc
Publication of PE20120136A1 publication Critical patent/PE20120136A1/es

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    • 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
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07D209/04Indoles; Hydrogenated indoles
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    • C07D471/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
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  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Indole Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Pyrane Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Quinoline Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyrrole Compounds (AREA)

Abstract

SE REFIERE A COMPUESTOS HETEROCICLICOS DE FORMULA (I) DONDE A1 ES C(A2) O N, EN DONDE A2 ES H, NHC(O)NH2, SO2NH2, ENTRE OTROS; B1 ES H, C(O)NHNOH, C(NH)NH2, CN, ENTRE OTROS; D1 ES H, SO2NH2, CF3, C(O)OH, ENTRE OTROS; E1 ES H, C(NH)NH2, F, CN, ENTRE OTROS; Y1 ES H, NO2, CN, OCF3, ENTRE OTROS; Z1 ES R26 O R27, EN DONDE R26 ES FENILENO NO FUSIONADO O FUSIONADO CON BENCENO, ENTRE OTROS; R27 ES HETEROARILENO NO FUSIONADO O FUSIONADO CON BENCENO, ENTRE OTROS; Z2 ES R28, R29, ENTRE OTROS, EN DONDE R28 ES FENILENO NO FUSIONADO O FUSIONADO CON BENCENO, ENTRE OTROS; R29 ES HETEROARILENO NO FUSIONADO O FUSIONADO CON BENCENO, ENTRE OTROS; Z1A Y Z2A ESTAN AMBOS AUSENTES O FORMAN JUNTOS CH2, CH2CH2, ENTRE OTROS; L1 ES C(O)NH, SO2NH, C(N)NH, ENTRE OTROS; Z3 ES R38, R39, ENTRE OTROS, EN DONDE R38 ES FENILO NO FUSIONADO O FUSIONADO CON BENCENO, ENTRE OTROS; R39 ES HETEROARILO NO FUSIONADO O FUSIONADO CON BENCENO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 4-(4-((4'-CLORO-1,1'-BIFENIL-2-IL)METIL)PIPERAZIN-1-IL)-2-(3-((DIMETILAMINO)METIL)FENOXI)-N-((3-NITRO-4-((TETRAHIDRO-2H-PIRAN-4-ILMETIL)AMINO)FENIL)SULFONIL)BENZAMIDA; 2-(3-(ACETILAMINO)FENOXI)-4-(4-((4'-CLORO-1,1'-BIFENIL-2-IL)METIL)PIPERAZIN-1-IL)-N-((3-NITRO-4-((TETRAHIDRO-2H-PIRAN-4-ILMETIL)AMINO)FENIL)SULFONIL)BENZAMIDA; ENTRE OTROS. DICHOS COMPUESTOS INHIBEN LA ACTIVIDAD DE PROTEINAS ANTI-APOPTOTICAS Bcl-2 SIENDO UTILES EN EL TRATAMIENTO DE CANCER DE VEJIGA, LEUCEMIA LINFOBLASTICA, MELANOMA
PE2011001147A 2008-12-04 2009-12-04 Compuestos derivados de n-acilsulfonamidas como inhibidores de bcl-2 PE20120136A1 (es)

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US11984408P 2008-12-04 2008-12-04

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ID=41809142

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PE2015001179A PE20151091A1 (es) 2008-12-04 2009-12-04 Agentes inductores de apoptosis para el tratamiento de cancer y enfermedades inmunes y autoinmunes
PE2011001147A PE20120136A1 (es) 2008-12-04 2009-12-04 Compuestos derivados de n-acilsulfonamidas como inhibidores de bcl-2

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EP (2) EP2376197B1 (es)
JP (2) JP5699306B2 (es)
KR (2) KR101683561B1 (es)
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AU (1) AU2009322269B2 (es)
BR (1) BRPI0922314A2 (es)
CA (1) CA2744708C (es)
CL (1) CL2011001281A1 (es)
CO (1) CO6382143A2 (es)
CR (2) CR20170289A (es)
DO (2) DOP2011000155A (es)
EC (1) ECSP11011173A (es)
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MY (2) MY179077A (es)
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PE (2) PE20151091A1 (es)
PH (1) PH12015502017A1 (es)
RU (1) RU2527450C2 (es)
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TW (2) TWI600643B (es)
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UY (1) UY32681A (es)
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