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

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

Info

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
Authority
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.)
Filing date
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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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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
    • 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)
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  • 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)
  • Peptides Or Proteins (AREA)
  • Indole Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyrane Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Quinoline Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Thiazole And Isothizaole 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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Application Number Priority Date Filing Date Title
US11984408P 2008-12-04 2008-12-04

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PE20120136A1 true PE20120136A1 (es) 2012-03-25

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ID=41809142

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

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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

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EP (2) EP3112361A1 (es)
JP (2) JP5699306B2 (es)
KR (2) KR101792640B1 (es)
CN (2) CN106008466B (es)
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)
ES (1) ES2622344T3 (es)
IL (2) IL212879B (es)
MX (2) MX362778B (es)
MY (2) MY166546A (es)
NZ (1) NZ592802A (es)
PE (2) PE20120136A1 (es)
PH (1) PH12015502017A1 (es)
RU (1) RU2527450C2 (es)
SG (1) SG10201500678RA (es)
TW (2) TWI600650B (es)
UA (1) UA108193C2 (es)
UY (1) UY32681A (es)
WO (1) WO2010065824A2 (es)
ZA (1) ZA201103807B (es)

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ME02642B (me) * 2008-12-05 2017-06-20 Abbvie Inc Sulfonamid derivati i kao BCL- 2 selektivni agensi za induciranje apoptoze namijenjeni liječenju raka i imunih bolesti
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TWI520960B (zh) * 2010-05-26 2016-02-11 艾伯維有限公司 用於治療癌症及免疫及自體免疫疾病之細胞凋亡誘導劑
MX387728B (es) 2010-06-03 2025-03-18 Pharmacyclics Llc El uso de inhibidores de la tirosina quinasa de bruton (btk).
UA113500C2 (xx) * 2010-10-29 2017-02-10 Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб
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