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AR053561A1 - Compuestos novedosos, isomeros de los mismos o las sales farmaceuticamente aceptables de los mismos como el antagonista del receptor vaniloide y las composiciones farmaceuticas que contienen los mismos - Google Patents

Compuestos novedosos, isomeros de los mismos o las sales farmaceuticamente aceptables de los mismos como el antagonista del receptor vaniloide y las composiciones farmaceuticas que contienen los mismos

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Publication number
AR053561A1
AR053561A1 ARP060101059A ARP060101059A AR053561A1 AR 053561 A1 AR053561 A1 AR 053561A1 AR P060101059 A ARP060101059 A AR P060101059A AR P060101059 A ARP060101059 A AR P060101059A AR 053561 A1 AR053561 A1 AR 053561A1
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AR
Argentina
Prior art keywords
alkoxy
alkyl
haloc1
alkenyl
phenyl
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Application number
ARP060101059A
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English (en)
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Amorepacific Corp
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Publication date
Application filed by Amorepacific Corp filed Critical Amorepacific Corp
Publication of AR053561A1 publication Critical patent/AR053561A1/es

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    • C07C275/04Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms
    • C07C275/20Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to acyclic carbon atoms of an unsaturated carbon skeleton
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    • A61K31/17Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/14Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D295/155Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
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Abstract

La presente se refiere a los compuestos novedosos, los isomeros de los mismos o las sales farmacéuticamente aceptables de los mismos como el antagonista del receptor vaniloide (Receptor Vaniloide 1; VR1; TRPV1), y una composicion farmacéutica que contiene a los mismos. La presente proporciona una composicion farmacéutica para prevenir o tratar una enfermedad tal como dolor, migrana, artralgia, neuralgia, neuropatías, herida en los nervios, skin disorder, hipersensibilidad de la vejiga urinaria, síndrome del intestino irritable, urgencia fecal, a desorden respiratorio, irritacion de la piel, membrana del ojo o mucosa, ulcera duodenal-estomacal, la enfermedad inflamatoria s, ear disease, y heart disease. Reivindicacion 1: Un compuesto de la formula (1), un isomero del mismo, o una sal farmacéuticamente aceptable del mismo en donde: X es NHCH2, CR11=CR12, NH, CHR11CHR12, o C:::C, en donde R11 y R12 son independientemente H, halogeno, alquilo C1-5, alcoxi C1-5, halo C1-5- alquilo o fenilo; R1 es alquenilo C2-5 o alquinilo C2-5; R2 es H, halogeno, nitro, ciano, alquilo C1-5, alcoxi C1-5, haloC1-5-alquilo, alquenilo C2-5, alquinilo C2-5, carboxi, alcoxicarbonilo C1-5, alquiltio C1-5, fenilo, o fenilC1-3alquilo, en donde, cada fenilo puede estar sustituido o no sustituido con uno o más sustituyentes seleccionados de carboxi, alquilo C1-5, halogeno, nitro, alquenilo C2-5, alcoxi C1-5, haloC1-5alquilo, alquilcarbonilo C1-5, alquiltio C1-5, alquilsulfonilo C1-5 y alcoxicarbonilo C1-5; R3 es H, alquilo C1-5, alcoxi C1-5, o haloC1-5alquilo; R4, R5, R6, R7, y R8 son independientemente H, carboxi, alquilo C1-5, nitro, alquenilo C2-5, alcoxi C1-5, alquinilo C2-5, haloC1-5alquilo, alquiltio C1-5, alquilsulfonilo C1-5, alquilcarbonilo C1-5, alcoxicarbonilo C1-5, hidroxi, alqueniloxi C2-5, alcoxi C1-5-alcoxi C1-5, alcoxi C1-5-alcoxiC1-5-alquilo C1-5, alquilpiperazinilo C1-3, piperazinilo C1-5alcoxi, piperidiniloC1-5alcoxi, alcoxi C1-5-alquilamino C1-5, alquilamino C1-7, morfolinilo, morfoliniloC1-5alquiloxi, tetrahidropiraniloxi, fenilo o halogeno, en donde fenilo puede estar sustituido o no sustituido con uno o más sustituyentes seleccionados de carboxi, alquilo C1-5, halogeno, nitro, alquenilo C2-5, alcoxi C1-5, haloC1-5alquilo, alquilcarbonilo C1-5, alquiltio C1-5, alquilsulfonilo C1-5, alcoxicarbonilo C1-5, o piperidiniloxi no sustituido o sustituido con alcoxicarbonilo C1-5, y R9 y 10 son independientemente H, -SO2R13, -SOR13, alquilo C1-5, alcoxi C1-5, haloC1-5alquilo, alquenilo C2-5, alcoxicarbonilo C1-5, alquiltio C1-5, fenilo, o fenilC1-3alquilo, en donde, cada fenilo puede estar sustituido o no sustituido con uno o más sustituyentes seleccionados de carboxi alquilo C1-5, halogeno, nitro, alquenilo C2-5, alcoxi C1-5, haloC1-5alquilo, alquilcarbonilo C1-5, alquiltio C1-5, alquilsulfonilo C1-5 y alcoxicarbonilo C1-5, y R13 es H, amino, alquilo C1-5, alquenilo C2-5, alcoxi C1-5, haloC1-5alquilo, trifluormetilo, fenilo o fenilC1-3alquilo.
ARP060101059A 2005-03-19 2006-03-17 Compuestos novedosos, isomeros de los mismos o las sales farmaceuticamente aceptables de los mismos como el antagonista del receptor vaniloide y las composiciones farmaceuticas que contienen los mismos AR053561A1 (es)

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KR20050022986 2005-03-19
US66326905P 2005-03-21 2005-03-21

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AR053561A1 true AR053561A1 (es) 2007-05-09

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ARP060101059A AR053561A1 (es) 2005-03-19 2006-03-17 Compuestos novedosos, isomeros de los mismos o las sales farmaceuticamente aceptables de los mismos como el antagonista del receptor vaniloide y las composiciones farmaceuticas que contienen los mismos
ARP060101058A AR056943A1 (es) 2005-03-19 2006-03-17 DERIVADOS DE AMIDAS, ISoMEROS DE LOS MISMOS O LAS SALES FARMACÉUTICAMENTE ACEPTABLES DE LOS MISMOS COMO EL ANTAGONISTA DEL RECEPTOR VANILOIDE Y LAS COMPOSICIONES FARMACÉUTICAS QUE CONTIENEN LOS MISMOS

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ARP060101058A AR056943A1 (es) 2005-03-19 2006-03-17 DERIVADOS DE AMIDAS, ISoMEROS DE LOS MISMOS O LAS SALES FARMACÉUTICAMENTE ACEPTABLES DE LOS MISMOS COMO EL ANTAGONISTA DEL RECEPTOR VANILOIDE Y LAS COMPOSICIONES FARMACÉUTICAS QUE CONTIENEN LOS MISMOS

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US (2) US7763657B2 (es)
EP (2) EP1861357B1 (es)
JP (2) JP5159604B2 (es)
KR (2) KR101304981B1 (es)
AR (2) AR053561A1 (es)
AU (2) AU2006225496A1 (es)
BR (2) BRPI0608714A2 (es)
CA (2) CA2601871A1 (es)
EA (2) EA200702020A1 (es)
IL (2) IL185892A0 (es)
MX (2) MX2007011466A (es)
NO (2) NO20075354L (es)
TW (2) TW200716523A (es)
WO (2) WO2006101318A1 (es)

Families Citing this family (19)

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Publication number Priority date Publication date Assignee Title
JP5159604B2 (ja) 2005-03-19 2013-03-06 アモーレパシフィック コーポレイション バニロイド受容体拮抗薬としての新規な化合物、その異性体又はその薬剤学的に許容される塩、及びこれを含む医薬組成物
PL2054411T3 (pl) 2006-07-27 2015-02-27 Amorepacific Corp Nowe związki, ich izomery lub ich farmaceutycznie dopuszczalne sole jako antagoniści receptora waniloidowego oraz zawierające je kompozycje farmaceutyczne
DE102007017884A1 (de) 2007-04-13 2008-10-16 Grünethal GmbH Neue Vanilloid-Rezeptor Liganden und ihre Verwendung zur Herstellung von Arzneimitteln
US20110160279A1 (en) * 2007-08-13 2011-06-30 Board Of Trustees Of Southern Illinois University METHODS FOR TREATMENT AND PREVENTION OF OTOTOXICITY BY siRNA
KR101619341B1 (ko) 2008-01-28 2016-05-11 (주)아모레퍼시픽 바닐로이드 수용체 길항체로서의 신규 화합물, 이의 이성질체 또는 약제학적으로 허용가능한 염, 및 이를 함유하는 약학 조성물
WO2009136625A1 (ja) * 2008-05-07 2009-11-12 大日本住友製薬株式会社 環状アミン-1-カルボン酸エステル誘導体およびそれを含有する医薬組成物
US8691855B2 (en) 2008-07-02 2014-04-08 Amorepacific Corporation Compounds, isomer thereof, or pharmaceutically acceptable salts thereof as vanilloid receptor antagonist and pharmaceutical compositions containing the same
EP2635281B1 (en) 2010-11-03 2018-03-14 University Of Hawaii Methods and compositions for prevention and treatment of cardiac hypertrophy
AR085509A1 (es) 2011-03-09 2013-10-09 Bayer Cropscience Ag Indol- y bencimidazolcarboxamidas como insecticidas y acaricidas
WO2013102145A1 (en) 2011-12-28 2013-07-04 Global Blood Therapeutics, Inc. Substituted heteroaryl aldehyde compounds and methods for their use in increasing tissue oxygenation
AP2014007805A0 (en) 2011-12-28 2014-07-31 Cytokinetics Inc The Regents Of The University Of California Substituted benzaldehyde compounds and methods fortheir use in increasing tissue oxygenation
CN107573275A (zh) * 2012-12-28 2018-01-12 日本脏器制药株式会社 肉桂酰胺衍生物
PE20151900A1 (es) 2013-03-15 2016-01-20 Global Blood Therapeutics Inc Compuestos y sus usos para modular la hemoglobina
AP2015008718A0 (en) 2013-03-15 2015-09-30 Global Blood Therapeutics Inc Compounds and uses thereof for the modulation of hemoglobin
ES2852054T3 (es) 2013-03-15 2021-09-10 Global Blood Therapeutics Inc Compuestos y usos de los mismos para la modulación de hemoglobina
US8952171B2 (en) 2013-03-15 2015-02-10 Global Blood Therapeutics, Inc. Compounds and uses thereof for the modulation of hemoglobin
WO2015120133A1 (en) 2014-02-07 2015-08-13 Global Blood Therapeutics, Inc. Crystalline polymorphs of the free base of 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde
SG10201912511WA (en) 2015-12-04 2020-02-27 Global Blood Therapeutics Inc Dosing regimens for 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde
US11014884B2 (en) 2018-10-01 2021-05-25 Global Blood Therapeutics, Inc. Modulators of hemoglobin

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6087254A (ja) * 1983-10-19 1985-05-16 Japan Carlit Co Ltd:The 新規尿素化合物及びそれを含有する除草剤
WO2000050387A1 (en) * 1999-02-22 2000-08-31 Pacific Corporation Vanilloid analogues containing resiniferatoxin pharmacophores as potent vanilloid receptor agonists and analgesics, compositions and uses thereof
AU8022901A (en) 2000-08-21 2002-03-04 Pacific Corp Novel thiourea derivatives and the pharmaceutical compositions containing the same
JP2004506714A (ja) * 2000-08-21 2004-03-04 パシフィック コーポレーション 新規チオ尿素化合物及びこれを含有する薬学的組成物
GB0105895D0 (en) * 2001-03-09 2001-04-25 Smithkline Beecham Plc Novel compounds
PL373484A1 (en) 2001-12-10 2005-09-05 Amgen Inc. Vanilloid receptor ligands and their use in treatments
PL210288B1 (pl) * 2002-05-08 2011-12-30 Bayer Healthcare Ag Pochodne hydroksytetrahydro-naftalenylomocznika, leki je zawierające i ich zastosowanie do wytwarzania leków
AU2003251828A1 (en) * 2002-07-12 2004-02-02 Janssen Pharmaceutica N.V. Naphthol, quinoline and isoquinoline-derivatives as modulators of vanilloid vr1 receptor
KR100707123B1 (ko) 2003-07-02 2007-04-16 그뤼넨탈 게엠베하 바닐로이드 수용체의 길항제로서 강력한 진통효과를나타내는 4-(메틸설포닐아미노)페닐 동족체 및 이를함유하는 약학적 조성물
CA2571133C (en) * 2004-07-15 2011-04-19 Japan Tobacco Inc. Fused benzamide compound and vanilloid receptor 1 (vr1) activity inhibitor
ITMI20042042A1 (it) * 2004-10-26 2005-01-26 Pharmeste Srl Derivati solfonammidici antagonisti del recettore dei vanilloidi trpv1
WO2006095263A1 (en) * 2005-03-10 2006-09-14 Pfizer Japan Inc. Substituted n-sulfonylaminophenylethyl-2-phenoxy acetamide compounds
JP5159604B2 (ja) 2005-03-19 2013-03-06 アモーレパシフィック コーポレイション バニロイド受容体拮抗薬としての新規な化合物、その異性体又はその薬剤学的に許容される塩、及びこれを含む医薬組成物

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