HK1152708A1 - Arylsulfonyl pyrazoline carboxamidine derivatives as 5-ht6 antagonists 5-ht6 - Google Patents

Arylsulfonyl pyrazoline carboxamidine derivatives as 5-ht6 antagonists 5-ht6

Info

Publication number
HK1152708A1
HK1152708A1 HK11106876.3A HK11106876A HK1152708A1 HK 1152708 A1 HK1152708 A1 HK 1152708A1 HK 11106876 A HK11106876 A HK 11106876A HK 1152708 A1 HK1152708 A1 HK 1152708A1
Authority
HK
Hong Kong
Prior art keywords
antagonists
carboxamidine derivatives
arylsulfonyl
pyrazoline carboxamidine
arylsulfonyl pyrazoline
Prior art date
Application number
HK11106876.3A
Other languages
English (en)
Chinese (zh)
Inventor
‧梵洛維金
‧伊維瑪巴克
‧斯托伊特
‧仁辛克
‧雯霍斯特
‧范德紐特
‧德漢
‧克魯斯
Original Assignee
雅培衛生保健產品有限責任公司
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
Application filed by 雅培衛生保健產品有限責任公司 filed Critical 雅培衛生保健產品有限責任公司
Publication of HK1152708A1 publication Critical patent/HK1152708A1/xx

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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/06—Heterocyclic 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic 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
    • A61K31/415—1,2-Diazoles
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic 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
    • A61K31/415—1,2-Diazoles
    • A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic 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
    • A61K31/415—1,2-Diazoles
    • A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
    • A—HUMAN NECESSITIES
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    • A61K31/435—Heterocyclic 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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    • A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
    • A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
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    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/10—Spiro-condensed systems
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    • 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
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    • 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
    • C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Epidemiology (AREA)
  • Addiction (AREA)
  • Psychiatry (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Psychology (AREA)
  • Endocrinology (AREA)
  • Hospice & Palliative Care (AREA)
  • Child & Adolescent Psychology (AREA)
  • Anesthesiology (AREA)
  • Rheumatology (AREA)
  • Nutrition Science (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
HK11106876.3A 2008-03-18 2011-07-05 Arylsulfonyl pyrazoline carboxamidine derivatives as 5-ht6 antagonists 5-ht6 HK1152708A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08152873 2008-03-18
PCT/EP2009/053133 WO2009115515A1 (en) 2008-03-18 2009-03-17 Arylsulfonyl pyrazoline carboxamidine derivatives as 5-ht6 antagonists

Publications (1)

Publication Number Publication Date
HK1152708A1 true HK1152708A1 (en) 2012-03-09

Family

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Family Applications (2)

Application Number Title Priority Date Filing Date
HK11106876.3A HK1152708A1 (en) 2008-03-18 2011-07-05 Arylsulfonyl pyrazoline carboxamidine derivatives as 5-ht6 antagonists 5-ht6
HK15101929.7A HK1201823A1 (en) 2008-03-18 2011-07-05 Arylsulfonyl pyrazoline carboxamidine derivatives as 5-ht6 antagonists 5-ht6

Family Applications After (1)

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HK15101929.7A HK1201823A1 (en) 2008-03-18 2011-07-05 Arylsulfonyl pyrazoline carboxamidine derivatives as 5-ht6 antagonists 5-ht6

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US (3) US8563723B2 (xx)
EP (2) EP2610247B1 (xx)
JP (1) JP5504252B2 (xx)
KR (1) KR101623357B1 (xx)
CN (2) CN102036967B (xx)
AR (1) AR070898A1 (xx)
AU (1) AU2009226956C1 (xx)
BR (1) BRPI0908738A8 (xx)
CA (1) CA2717922A1 (xx)
CO (1) CO6290679A2 (xx)
CR (1) CR11742A (xx)
DK (2) DK2610247T3 (xx)
DO (2) DOP2010000276A (xx)
EA (1) EA023176B1 (xx)
EC (1) ECSP10010476A (xx)
ES (2) ES2565184T3 (xx)
HK (2) HK1152708A1 (xx)
IL (1) IL207846A0 (xx)
MX (1) MX2010010299A (xx)
MY (1) MY155318A (xx)
NZ (1) NZ587743A (xx)
PH (1) PH12013502376B1 (xx)
PL (2) PL2610247T3 (xx)
PT (1) PT2610247T (xx)
SG (1) SG183688A1 (xx)
TW (1) TWI557110B (xx)
UA (1) UA105629C2 (xx)
WO (1) WO2009115515A1 (xx)
ZA (1) ZA201006272B (xx)

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AR079935A1 (es) 2010-01-29 2012-02-29 Abbott Healthcare Products Bv Sintesis de derivados de pirazolin carboxamidina sustituida
MX356486B (es) * 2011-08-15 2018-05-30 Univ Utah Res Found Análogos sustituidos de la (e)-n' -(1-feniletiliden)benzohidrazida como inhibidores de la histona desmetilasa.
SG11201503562PA (en) 2012-11-16 2015-06-29 Bristol Myers Squibb Co Dihydropyrazole gpr40 modulators
DK2920165T3 (en) * 2012-11-16 2017-01-16 Bristol Myers Squibb Co Dihydropyrazol-GPR40-MODULATORS
CN104918935B (zh) * 2012-11-16 2017-07-28 百时美施贵宝公司 二氢吡唑gpr40调节剂
CN106660968B (zh) * 2014-05-09 2020-02-07 美国政府(由卫生和人类服务部的部长所代表) 吡唑衍生物及其作为大麻素受体介体的用途
US10385040B2 (en) 2014-08-12 2019-08-20 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
MX2022004367A (es) 2019-10-09 2022-05-06 Bayer Ag Nuevos compuestos de heteroarilo-triazol como pesticidas.
CA3185968A1 (en) 2020-07-13 2022-01-20 Tony Lahoutte 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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EP1429762A1 (en) * 2001-09-21 2004-06-23 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
AR062907A1 (es) * 2006-09-22 2008-12-17 Solvay Pharm Bv Derivados de sulfonilpirazol y sulfonilpirazolincarboxamidina como antagonistas de 5-ht6

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ES2577867T3 (es) 2016-07-19
US8563723B2 (en) 2013-10-22
CN102036967A (zh) 2011-04-27
DOP2010000276A (es) 2010-11-15
CO6290679A2 (es) 2011-06-20
CN104003937A (zh) 2014-08-27
US20150051239A1 (en) 2015-02-19
PH12013502376A1 (en) 2015-01-12
EA023176B1 (ru) 2016-05-31
US8901108B2 (en) 2014-12-02
KR20100136504A (ko) 2010-12-28
IL207846A0 (en) 2010-12-30
DK2610247T3 (en) 2016-06-13
NZ587743A (en) 2012-06-29
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