AR073740A1 - Compuestos para el tratamiento de la hepatitis c - Google Patents

Compuestos para el tratamiento de la hepatitis c

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Publication number
AR073740A1
AR073740A1 ARP090103514A ARP090103514A AR073740A1 AR 073740 A1 AR073740 A1 AR 073740A1 AR P090103514 A ARP090103514 A AR P090103514A AR P090103514 A ARP090103514 A AR P090103514A AR 073740 A1 AR073740 A1 AR 073740A1
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AR
Argentina
Prior art keywords
alkyl
hydroxyalkyl
amino
phenyl
hydrogen
Prior art date
Application number
ARP090103514A
Other languages
English (en)
Inventor
Ying Han
John F Kadow
John A Bender
Kap-Sun Yeung
Piyasena Hewawasam
Kyle E Parcella
Katharine A Grant-Young
Brett R Beno
Andrew Nickel
Original Assignee
Bristol Myers Squibb Co
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Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41226922&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR073740(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of AR073740A1 publication Critical patent/AR073740A1/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans 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 to carbon atoms of the hetero ring
    • C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/02—Heterocyclic 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
    • C07D417/10—Heterocyclic 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 carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic 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
    • C07D417/02—Heterocyclic 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
    • C07D417/12—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10—Spiro-condensed systems

Abstract

Reivindicacion 1: Un compuesto caracterizado por tener la formula 1: R1 es R5R6N; alcoxi; (alcoxicarbonilamino)alcoxi; (alquilfenil)alcoxi; (carboxi)alquenilo; (alcoxicarbonil)alquenilo; (benciloxicarbonil)alquenilo; ((N-dimetilbencil)aminocarbonil)alquenilo; o fenilo donde dicho fenilo está sustituido con 1-2 sustituyentes que se seleccionan a partir del grupo constituido por halo, ciano, alquilo, haloalquilo, hidroxialquilo, alcoxialquilo, (carboxi)alquilo, alcoxi, hidroxialquiloxi, alcoxialquiloxi, benciloxi, tetrahidropiraniloxi, carboxi, alcoxicarbonilo, alquilsulfonilo, (carboxi)alquenilo, (alcoxicarbonil)alquenilo, alquilcarboxamido, alcoxicarboxamido, alquilsulfamido, (alquilsulfamido)alquilo, Ar5, SO2NR15R16, y CONR7R8: y donde dicho fenilo también está sustituido con 0-2 sustituyentes que se seleccionan a partir del grupo constituido por halo; nitro; alquilo; cicloalquilo; haloalquilo; aminoalquilo; hidroxialquilo; alcoxialquilo; hidroxi; alcoxi; OR17 cicloalcoxi; amino; alquilamino; dialquilamino; alquilcarboxamido; alcoxicarboxamido; alcoxialquilcarboxamido; furanilo, tienilo, o pirazolilo sustituido con 0-2 sustituyentes alquilo; piridinilo sustituido con 0-2 sustituyentes halo, ciano, alquilo, hidroxi, alcoxi, amino, o alquilaminocarbonilo; pirimidinilo; pirimidindionilo; aminopirimidinilo; indolilo; isoquinolinilo; y fenilo sustituido con 0-2 sustituyentes que se seleccionan a partir del grupo constituido por halo, alquilo, cianoalquilo, hidroxialquilo, alcoxialquilo, hidroxi, alcoxi, amino, carboxi, alcoxicarbonilo, aminocarbonilo, alquilaminocarbonilo, dialquilaminocarbonilo, alquilcarboxamido, carboxialquenilo, y fenilo; R2 es hidrogeno, halo, nitro, amino, fenilo, o R5R6N; R3 es ciano, alcoxicarbonilo, (cicloalquil)oxicarbonilo, (alquilsulfonil)aminocarbonilo, CONR11R12, (R11)(R12)NCONH, triazolilo, tiazolilo, o tetrazolilo; R4 es fenilo sustituido con 0-2 sustituyentes halo; R5 es hidrogeno, alquilo, o alquilsulfonilo; R6 es hidrogeno, alquilo, hidroxialquilo, alcoxialquilo, o alquilsulfonilo; R7 es hidrogeno, alquilo, alquenilo, alquinilo, cianoalquilo, haloalquilo, hidroxialquilo, dihidroxialquilo, alcoxialquilo, oxoalquilo, aminoalquilo, (alquilamino)alquilo, (dialquilamino)alquilo, (cicloalquil)alquilo, cicloalquilo, (alquil)cicloalquilo, (hidroxialquil)cicloalquilo, (tetrahidrofuranil)alquilo, (tetrahidropiranil)alquilo, (carboxi)alquilo, (alcoxicarbonil)alquilo, (alqueniloxicarbonil)alquilo, (alcoxicarbonil)hidroxialquilo, (CONR13R14)alquilo, (CONR1314)(hidroxialquil)alquilo, (CONR13R14)cicloalquilo, (alquilcarbonil)aminoalquilo, (fenil)alquilo, (piridinil)alquilo, alquilsulfonilo, fenilsulfonilo, Ar2, Ar3, y el grupo de formulas 2; R8 es hidrogeno, alquilo, hidroxialquilo, o alcoxialquilo; o R7R8N tomado conjuntamente es azetidinilo, pirrolidinilo, piperidinilo, piperazinilo, morfolinilo, dihidroindolilo, o isoindolinilo, y está sustituido con 0-2 sustituyentes que se seleccionan a partir de alquilo, hidroxialquilo, alcoxialquilo, hidroxi, alcoxi, carboxi, alcoxicarbonilo, dialquilcarboxamido, alquilcarbonilamino, alcoxicarbonilamino, piridinilo, y fenilo donde dicho fenilo está sustituido con 0-2 sustituyentes halo o alquilo; o donde R7R8N tomado conjuntamente es, la formula 3, (quinuclidinil)amino, (quinuclidinil)(alquil)amino, (metilpirrolidinil)(alquil)amino, ((imidazolil)alquil)(hidroxialquil)amino, (alquiltiazolil)amino, ((carboxamido)ciclopentanil)amino, ((halofenil)ciclopentanil)amino, 3H-espiro(isobenzofuranil)piperidinilo, (hidroxiindanil)amino, o la formula 4;R9 es hidrogeno, alquilo, hidroxialquilo, o alcoxialquilo; R10 es hidrogeno, alquilo, hidroxialquilo, o alcoxialquilo; o y R10 tomados conjuntamente son etileno, propileno, butileno, pentileno, o hexileno; R11 es hidrogeno, alquilo, o cicloalquilo; R12 es hidrogeno, alquilo, o cicloalquilo; o R11 y R12 tomados conjuntamente con el nitrogeno al que están unidos son azetidinilo, pirrolidinilo, piperidinilo, piperazinilo, o morfolinilo; R13 es hidrogeno, alquilo, cianoalquilo, haloalquilo, alquenilo, alquinilo, o tiazolilo; R14 es hidrogeno o alquilo; R15 es hidrogeno, alquilo, hidroxialquilo, cicloalquilo, o bencilo; R16 es hidrogeno o alquilo; o R15 y R16 tomados conjuntamente con el nitrogeno al que están unidos son azetidinilo, pirrolidinilo, piperidinilo, piperazinilo, o morfolinilo; R17 es haloalquilo, cianoalquilo, (cicloalquil)alquilo, hidroxialquilo, alcoxialquilo, aminoalquilo, (R18)alquilo, (Ar4)alquilo, alquinilo, o aminocicloalquilo; R18 es CONH2, H2NCONH, dibencilamino, ftalimido, amino, alquilamino, dialquilamino, azetidinilo, pirrolidinilo, piperidinilo, piperazinilo, o morfolinilo donde azetidinilo, pirrolidinilo, piperidinilo, piperazinilo, o morfolinilo están sustituidos con 0-3 sustituyentes alquilo o alcoxicarbonilo; R19 es ciano, hidroxialquilo, morfolinilalquilo, carboxi, alcoxicarbonilo, cicloalquilsulfoxamido, ((alquil)pirazolil)amino, ((alquil)isoxazolil)amino, (tiadiazolil)amino, (triazinil)amino, o alquinilaminocarbonilo; R20 es hidrogeno, halo, alquilo, o alcoxi; R21 es hidrogeno, halo, alquilo, o alcoxi; Ar1 es fenilo, naftalenilo, piridinilo, furanilo, tienilo, pirrolilo, pirazolilo, isoxazolilo, isotiazolilo, imidazolilo, oxazolilo, tiazolilo, oxadiazolilo, oxadiatiazolilo, triazolilo, tetrazolilo, pirazinilo, pirimidinilo, o benzotiazolilo, y está sustituido con 0-2 sustituyentes que se seleccionan a partir de halo, alquilo, cicloalquilo, haloalquilo, alcoxialquilo, hidroxi, alcoxi, amino, alquilamino, dialquilamino, aminocarbonilo, piridinilo, fenilo, halofenilo, alquilfenilo, y alcoxifenilo; Ar2 es fenilo. bifenilo, o piridinilo, y está sustituido con 0-2 sustituyentes que se seleccionan a partir de halo, alquilo, ciano, hidroxi, alcoxi, y carboxi; Ar3 es pirazolilo, isoxazolilo, isotiazolilo, imidazolilo, oxazolilo, tiazolilo, triazolilo, oxadiazolilo, oxatiadiazolilo, pirimidinilo, o pirizinilo, y está sustituido con 0-2 sustituyentes que se seleccionan a partir de hidroxi, alquilo, hidroxialquilo, y CONR13R14; Ar4 es furanilo, tienilo, pirrolilo, pirazolilo, isoxazolilo, isotiazolilo, imidazolilo, oxadiazolilo, tiadiazolilo, triazolilo, piridinilo, indolilo, o fenilo, y está sustituido con 0-2 sustituyentes que se seleccionan a partir de halo, alquilo, haloalquilo, hidroxilo, y alcoxi; y Ar5 es pirrozolilo, imidazolilo, u oxadiazolilo, y está sustituido con 0-2 sustituyentes que se seleccionan a partir de alquilo, carboxi, alcoxicarbonilo, bencilo, y fenilo; o una sal farmacéuticamente aceptable del mismo.
ARP090103514A 2008-09-11 2009-09-11 Compuestos para el tratamiento de la hepatitis c AR073740A1 (es)

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US (1) US8048887B2 (es)
EP (1) EP2326633B1 (es)
JP (1) JP5685191B2 (es)
KR (1) KR20110059875A (es)
CN (1) CN102209717B (es)
AR (1) AR073740A1 (es)
AU (1) AU2009291966B2 (es)
BR (1) BRPI0918174A2 (es)
CA (1) CA2736988A1 (es)
CL (2) CL2011000527A1 (es)
CO (1) CO6382110A2 (es)
EA (1) EA019185B1 (es)
IL (1) IL211509A0 (es)
MX (1) MX2011002410A (es)
NZ (1) NZ591172A (es)
PE (1) PE20110806A1 (es)
TW (2) TW201124403A (es)
WO (1) WO2010030592A1 (es)
ZA (2) ZA201101739B (es)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8198449B2 (en) * 2008-09-11 2012-06-12 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
US7994171B2 (en) * 2008-09-11 2011-08-09 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
WO2010043721A1 (en) 2008-10-17 2010-04-22 Oryzon Genomics, S.A. Oxidase inhibitors and their use
JP2012507539A (ja) * 2008-10-30 2012-03-29 メルク・シャープ・エンド・ドーム・コーポレイション ２，５−二置換フェニルカルボキサミド・オレキシン受容体アンタゴニスト
WO2010084160A1 (en) 2009-01-21 2010-07-29 Oryzon Genomics S.A. Phenylcyclopropylamine derivatives and their medical use
ES2450891T3 (es) * 2009-06-22 2014-03-25 F. Hoffmann-La Roche Ag Bifenilamidas útiles como moduladores de receptores P2X3 y/o P2X2/3
CA2812683C (en) 2009-09-25 2017-10-10 Oryzon Genomics S.A. Lysine specific demethylase-1 inhibitors and their use
EP2486002B1 (en) 2009-10-09 2019-03-27 Oryzon Genomics, S.A. Substituted heteroaryl- and aryl- cyclopropylamine acetamides and their use
WO2011106105A2 (en) 2010-02-24 2011-09-01 Oryzon Genomics, S.A. Inhibitors for antiviral use
US9186337B2 (en) 2010-02-24 2015-11-17 Oryzon Genomics S.A. Lysine demethylase inhibitors for diseases and disorders associated with Hepadnaviridae
US8324212B2 (en) * 2010-02-25 2012-12-04 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
AR080433A1 (es) * 2010-03-02 2012-04-11 Merck Sharp & Dohme Derivados de benzofurancarboxamidas utiles para tratar o prevenir infecciones por vhc y composiciones farmaceuticas que los contienen.
JP2013522192A (ja) * 2010-03-11 2013-06-13 ブリストル−マイヤーズ スクイブ カンパニー Ｃ型肝炎の処置のための化合物
US8354410B2 (en) * 2010-03-11 2013-01-15 Bristol-Meyers Squibb Company Compounds for the treatment of hepatitis C
BR112012026694A2 (pt) 2010-04-19 2016-07-12 Oryzon Genomics Sa inibidores da desmetilase específica para lisina 1 e seu uso
AR082453A1 (es) 2010-04-21 2012-12-12 Novartis Ag Compuestos de furopiridina, composiciones farmaceuticas que los contienen y usos de los mismos
WO2011140333A1 (en) 2010-05-07 2011-11-10 The Board Of Trustees Of The Leland Stanford Junior University Identification of stabilizers of multimeric proteins
US8445497B2 (en) * 2010-06-30 2013-05-21 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
WO2012013727A1 (en) 2010-07-29 2012-02-02 Oryzon Genomics S.A. Cyclopropylamine derivatives useful as lsd1 inhibitors
SI2598482T1 (sl) 2010-07-29 2018-09-28 Oryzon Genomics, S.A. Inhibitorji demetilaze lsd1 na osnovi arilciklopropilamina in njihova medicinska uporaba
EP2963034A1 (en) 2010-08-26 2016-01-06 RFS Pharma, LLC. Potent and selective inhibitors of hepatitis c virus
WO2012045883A1 (en) 2010-10-08 2012-04-12 Oryzon Genomics S.A. Cyclopropylamine inhibitors of oxidases
WO2012058125A1 (en) 2010-10-26 2012-05-03 Presidio Pharmaceuticals, Inc. Inhibitors of hepatitis c virus
WO2012072713A2 (en) * 2010-11-30 2012-06-07 Oryzon Genomics, S.A. Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae
US8507683B2 (en) * 2010-12-09 2013-08-13 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
US9173887B2 (en) 2010-12-22 2015-11-03 Abbvie Inc. Hepatitis C inhibitors and uses thereof
EP2712315B1 (en) 2011-02-08 2021-11-24 Oryzon Genomics, S.A. Lysine demethylase inhibitors for myeloproliferative disorders
WO2013033900A1 (en) * 2011-09-08 2013-03-14 Merck Sharp & Dohme Corp. Tetracyclic heterocycle compounds and methods of use thereof for the treatment of viral diseases
WO2013033901A1 (en) 2011-09-08 2013-03-14 Merck Sharp & Dohme Corp. Heterocyclic-substituted benzofuran derivatives and methods of use thereof for the treatment of viral diseases
WO2013033899A1 (en) * 2011-09-08 2013-03-14 Merck Sharp & Dohme Corp. Substituted benzofuran compounds and methods of use thereof for the treatment of viral diseases
BR112014009238B1 (pt) 2011-10-20 2022-08-09 Oryzon Genomics S.A. Compostos de (hetero)aril ciclopropilamina, seus usos e composições farmacêuticas
JP6215212B2 (ja) 2011-10-20 2017-10-18 オリゾン・ジェノミックス・ソシエダッド・アノニマＯｒｙｚｏｎ Ｇｅｎｏｍｉｃｓ Ｓ．Ａ． Ｌｓｄ１阻害剤としての（ヘテロ）アリールシクロプロピルアミン化合物
US9303020B2 (en) 2012-02-08 2016-04-05 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
US9096580B2 (en) 2012-03-27 2015-08-04 Bristol-Myers Squibb Company Benzofuran derivatives for the treatment of hepatitis C
WO2013163466A1 (en) * 2012-04-25 2013-10-31 Presidio Pharmaceuticals, Inc. Inhibitors of hepatitis c virus
US9169214B2 (en) 2012-12-21 2015-10-27 The Board Of Trustees Of The Leland Stanford Junior University Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions
CN104884459A (zh) * 2013-01-10 2015-09-02 百时美施贵宝公司 用于治疗丙型肝炎的大环苯并呋喃和氮杂苯并呋喃化合物
WO2014121416A1 (en) * 2013-02-07 2014-08-14 Merck Sharp & Dohme Corp. Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis c
US8962651B2 (en) 2013-03-13 2015-02-24 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
US9738653B2 (en) 2013-03-14 2017-08-22 Bristol-Myers Squibb Company Fused furans for the treatment of hepatitis C
WO2014205593A1 (en) * 2013-06-24 2014-12-31 Merck Sharp & Dohme Corp. Substituted benzofuran compounds and methods of use thereof for treatment of viral diseases
WO2015088958A1 (en) * 2013-12-13 2015-06-18 Bristol-Myers Squibb Company A novel compound for the treatment of hepatitis c
EP3119769A1 (en) * 2014-03-21 2017-01-25 Bristol-Myers Squibb Pharma Company Cyanoamino (aza)benzofuran compounds for the treatment of hepatitis c
US9249152B2 (en) * 2014-03-21 2016-02-02 Bristol-Myers Squibb Company Cyano containing azabenzofuran compounds for the treatment of hepatitis C
WO2016025129A1 (en) 2014-08-14 2016-02-18 Alhamadsheh Mamoun M Conjugation of pharmaceutically active agents with transthyretin ligands through adjustable linkers to increase serum half-life
WO2016133963A1 (en) * 2015-02-19 2016-08-25 Bristol-Myers Squibb Company Benzofurans substituted with secondary benzamide as hcv inhibitors
US10570108B2 (en) 2015-02-19 2020-02-25 Bristol-Myers Squibb Company Substituted benzofuran compounds for the treatment of hepatitis C
US10131645B2 (en) 2015-02-19 2018-11-20 Bristol-Myers Squibb Company Benzofurans substituted with primary benzamide as HCV inhibitors
US10125137B2 (en) 2015-02-19 2018-11-13 Bristol-Myers Squibb Company Benzofurans substituted with bicyclic secondary benzamide as HCV inhibitors
CN107406435A (zh) * 2015-02-23 2017-11-28 百时美施贵宝公司 新的治疗丙型肝炎的化合物
WO2017165233A1 (en) * 2016-03-21 2017-09-28 Bristol-Myers Squibb Company Benzofuran derivatives for the treatment of hepatitis c
CN116730921A (zh) 2017-02-17 2023-09-12 文涵治疗有限公司 Ag-10的制备方法、其中间体及其盐
KR102512548B1 (ko) 2017-12-22 2023-03-22 삼성디스플레이 주식회사 유기 전계 발광 소자 및 유기 전계 발광 소자용 함질소 화합물
MX2020009844A (es) 2018-03-23 2021-01-15 Eidos Therapeutics Inc Metodos para tratar amiloidosis por transtiretina (ttr) usando ag10.
BR112020026493A2 (pt) 2018-08-17 2021-03-23 Eidos Therapeutics, Inc. Formulações de ag10
US11034669B2 (en) 2018-11-30 2021-06-15 Nuvation Bio Inc. Pyrrole and pyrazole compounds and methods of use thereof
WO2021008512A1 (zh) * 2019-07-18 2021-01-21 石药集团中奇制药技术（石家庄）有限公司 作为nmt抑制剂的化合物及其应用

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57123181A (en) 1981-01-23 1982-07-31 Mitsubishi Paper Mills Ltd Preparation of pyrazolo (1,5-a) pyridine derivative
PE20020506A1 (es) 2000-08-22 2002-07-09 Glaxo Group Ltd Derivados de pirazol fusionados como inhibidores de la proteina cinasa
WO2002078701A1 (en) 2001-03-30 2002-10-10 Smithkline Beecham Corporation Use of pyrazolopyridines as therapeutic compounds
AU2003290584B2 (en) 2002-11-01 2009-07-16 Viropharma Incorporated Benzofuran compounds, compositions and methods for treatment and prophylaxis of hepatitis C viral infections and associated diseases
US7868037B2 (en) 2004-07-14 2011-01-11 Ptc Therapeutics, Inc. Methods for treating hepatitis C
TW200815384A (en) * 2006-08-25 2008-04-01 Viropharma Inc Combination therapy method for treating hepatitis C virus infection and pharmaceutical compositions for use therein
WO2008100867A2 (en) * 2007-02-12 2008-08-21 Intermune, Inc. Novel inhibitors hepatitis c virus replication
GB0707000D0 (en) 2007-04-12 2007-05-30 Istituto Di Ricerche D Biolog Antiviral agents
EP2245023B1 (en) 2008-02-14 2011-12-28 F. Hoffmann-La Roche AG Heterocyclic antiviral compounds
WO2009137500A1 (en) 2008-05-05 2009-11-12 Wyeth 6-substituted benzofuran compounds to treat infection with hepatitis c virus
WO2009137493A1 (en) 2008-05-05 2009-11-12 Wyeth 2-substituted benzofuran compounds to treat infection with hepatitis c virus

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