ECSP10010476A - Derivados de arilsulfonil pirazolin carboxamidina como antagonistas de 5-ht6 - Google Patents

Derivados de arilsulfonil pirazolin carboxamidina como antagonistas de 5-ht6

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Publication number
ECSP10010476A
ECSP10010476A EC2010010476A ECSP10010476A ECSP10010476A EC SP10010476 A ECSP10010476 A EC SP10010476A EC 2010010476 A EC2010010476 A EC 2010010476A EC SP10010476 A ECSP10010476 A EC SP10010476A EC SP10010476 A ECSP10010476 A EC SP10010476A
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EC
Ecuador
Prior art keywords
disorders
compounds
disorder
disease
attention deficit
Prior art date
Application number
EC2010010476A
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English (en)
Inventor
Loevezijn Arnold Van
Bakker Wouter I Iwema
Axel Stoit
Agatha A M Rensink
Jennifer Venhorst
Der Neut Martina A W Van
Haan Martin De
Cornelis G Kruse
Original Assignee
Abbott Healthcare Products Bv
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Publication date
Application filed by Abbott Healthcare Products Bv filed Critical Abbott Healthcare Products Bv
Publication of ECSP10010476A publication Critical patent/ECSP10010476A/es

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    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41551,2-Diazoles non condensed and containing further heterocyclic rings
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
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    • 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
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    • A61K31/635Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
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    • C07D231/06Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
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    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
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    • 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
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    • C07D491/02Heterocyclic 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
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    • C07D491/02Heterocyclic 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
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring

Abstract

Esta invención se refiere a derivados de arilsulfonil pirazolin carboxamidina como antagonistas de receptores 5-HT6, a métodos para la preparación de estos compuestos y a novedosos intermediarios útiles para su síntesis. La invención también se refiere a los usos de tales compuestos y composiciones particularmente su uso en la administración de los mismos a pacientes para lograr un efecto terapéutico en la enfermedad de Parkinson, corea de Huntington, esquizofrenia, ansiedad, depresión, depresión maníaca, psicosis, epilepsia, trastornos obsesivos compulsivos, trastornos del ánimo, migraña, enfermedad de Alzheimer, declinación cognitiva relacionada con la edad, deterioro cognitivo leve, trastornos del sueño, trastornos de la alimentación, anorexia, bulimia, trastornos de atracones en la alimentación , ataques de pánico, acatisia, trastorno de hiperactividad y déficit de atención, trastorno de déficit de atención, abstinencia del abuso de cocaína, etanol, nicotina o benzodiazepinas, dolor, trastornos asociados con trauma espinal o daño en la cabeza, hidrocefalia, trastorno funcional del intestino, Síndrome de Intestino Irritable, obesidad y diabetes tipo 2. Los compuestos tienen la fórmula general (1): en donde los símbolos tienen los significados dados en la descripción.
EC2010010476A 2008-03-18 2010-09-13 Derivados de arilsulfonil pirazolin carboxamidina como antagonistas de 5-ht6 ECSP10010476A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US3746308P 2008-03-18 2008-03-18
EP08152873 2008-03-18

Publications (1)

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ECSP10010476A true ECSP10010476A (es) 2010-10-30

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US (3) US8563723B2 (es)
EP (2) EP2265589B1 (es)
JP (1) JP5504252B2 (es)
KR (1) KR101623357B1 (es)
CN (2) CN104003937A (es)
AR (1) AR070898A1 (es)
AU (1) AU2009226956C1 (es)
BR (1) BRPI0908738A8 (es)
CA (1) CA2717922A1 (es)
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CR (1) CR11742A (es)
DK (2) DK2265589T3 (es)
DO (2) DOP2010000276A (es)
EA (1) EA023176B1 (es)
EC (1) ECSP10010476A (es)
ES (2) ES2565184T3 (es)
HK (2) HK1201823A1 (es)
IL (1) IL207846A0 (es)
MX (1) MX2010010299A (es)
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PH (1) PH12013502376A1 (es)
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AR079935A1 (es) * 2010-01-29 2012-02-29 Abbott Healthcare Products Bv Sintesis de derivados de pirazolin carboxamidina sustituida
HUE050962T2 (hu) * 2011-08-15 2021-01-28 Univ Utah Res Found Hiszton demetiláz inhibitor szubsztituált (E)-N'-(1-feniletilidén)-benzohidrazid származékok
SI2920165T1 (sl) * 2012-11-16 2017-02-28 Bristol-Myers Squibb Company Modulatorji dihidropirazola GPR40
CA2891551A1 (en) * 2012-11-16 2014-05-22 Bristol-Myers Squibb Company Dihydropyrazole gpr40 modulators
BR112015010791A2 (pt) 2012-11-16 2017-07-11 Bristol Myers Squibb Co moduladores de gpr40 de di-hidropirazol
CA2948349C (en) * 2014-05-09 2023-03-28 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Pyrazole derivatives and their use as cannabinoid receptor mediators
EP3180312B1 (en) 2014-08-12 2019-10-16 Loyola University Of Chicago Indoline sulfonamide inhibitors of dape and ndm-1 and use of the same
EP3109237A1 (en) * 2015-06-22 2016-12-28 AnaMar AB Novel 5-ht2 antagonists
CN107460160A (zh) * 2017-08-23 2017-12-12 世贸天阶制药(江苏)有限责任公司 一种cho细胞无血清培养基
US10879709B2 (en) 2018-05-31 2020-12-29 National Taipei University Of Technology Power management system and operating method thereof
WO2021069567A1 (en) 2019-10-09 2021-04-15 Bayer Aktiengesellschaft Novel heteroaryl-triazole compounds as pesticides
EP4178982A1 (en) 2020-07-13 2023-05-17 Precirix N.V. Antibody fragment against folr1
WO2023203135A1 (en) 2022-04-22 2023-10-26 Precirix N.V. Improved radiolabelled antibody
WO2023213801A1 (en) 2022-05-02 2023-11-09 Precirix N.V. Pre-targeting

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PL367814A1 (en) * 2001-09-21 2005-03-07 Solvay Pharmaceuticals B.V. 4,5-dihydro-1h-pyrazole derivatives having potent cb1-antagonistic activity
GB0422263D0 (en) 2004-10-07 2004-11-10 Glaxo Group Ltd Novel compounds
SA07280510B1 (ar) 2006-09-22 2012-02-07 سولفاي فارماسوتيكالز بي . في سلفونيل بيرازول ومشتقات سلفونيل كربوكساميدين كمضادات ht6-5

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JP5504252B2 (ja) 2014-05-28
CN104003937A (zh) 2014-08-27
AR070898A1 (es) 2010-05-12
DK2265589T3 (en) 2016-03-21
BRPI0908738A8 (pt) 2017-10-10
EP2265589B1 (en) 2016-01-27
JP2011517443A (ja) 2011-06-09
CR11742A (es) 2011-03-03
MY155318A (en) 2015-09-30
AU2009226956A8 (en) 2010-09-23
PH12013502376B1 (en) 2015-01-12
MX2010010299A (es) 2010-12-15
PH12013502376A1 (en) 2015-01-12
ES2565184T3 (es) 2016-04-01
EA023176B1 (ru) 2016-05-31
PT2610247T (pt) 2016-07-07
DOP2010000276A (es) 2010-11-15
CO6290679A2 (es) 2011-06-20
ZA201006272B (en) 2011-05-25
AU2009226956A1 (en) 2009-09-24
DK2610247T3 (en) 2016-06-13
TWI557110B (zh) 2016-11-11
NZ587743A (en) 2012-06-29
US8563723B2 (en) 2013-10-22
HK1152708A1 (en) 2012-03-09
AU2009226956C1 (en) 2014-03-06
PL2610247T3 (pl) 2017-02-28
DOP2010000277A (es) 2011-01-31
CA2717922A1 (en) 2009-09-24
EP2265589A1 (en) 2010-12-29
EA201071083A1 (ru) 2011-04-29
CN102036967B (zh) 2014-10-15
AU2009226956B2 (en) 2013-05-23
BRPI0908738A2 (pt) 2017-06-13
US9126942B2 (en) 2015-09-08
KR101623357B1 (ko) 2016-05-23
US8901108B2 (en) 2014-12-02
EP2610247A1 (en) 2013-07-03
EP2610247B1 (en) 2016-05-25
US20140011775A1 (en) 2014-01-09
IL207846A0 (en) 2010-12-30
TW200942519A (en) 2009-10-16
UA105629C2 (uk) 2014-06-10
US20150051239A1 (en) 2015-02-19
HK1201823A1 (en) 2015-09-11
SG183688A1 (en) 2012-09-27
US20110046171A1 (en) 2011-02-24
KR20100136504A (ko) 2010-12-28
CN102036967A (zh) 2011-04-27
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ES2577867T3 (es) 2016-07-19
WO2009115515A1 (en) 2009-09-24

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