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AR039122A1 - Derivados de ftalimido como inhibidores de monoamino oxidasa b - Google Patents

Derivados de ftalimido como inhibidores de monoamino oxidasa b

Info

Publication number
AR039122A1
AR039122A1 ARP030101023A ARP030101023A AR039122A1 AR 039122 A1 AR039122 A1 AR 039122A1 AR P030101023 A ARP030101023 A AR P030101023A AR P030101023 A ARP030101023 A AR P030101023A AR 039122 A1 AR039122 A1 AR 039122A1
Authority
AR
Argentina
Prior art keywords
alkyl
halogen
nr5r6
ftalimide
oxidasa
Prior art date
Application number
ARP030101023A
Other languages
English (en)
Inventor
Andrea Cesura
Sarmiento Rosa Maria Rodriguez
Andrew William Thomas
Rene Wyler
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of AR039122A1 publication Critical patent/AR039122A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Reivindicación 1: Compuestos de fórmula general (1) caracterizados porque X es -N= o -CH=; R1 es -CO-NR5R6; -CHR7-(CH2)n-CO-NR5R6; -(CH2)n-NR5R6, -(CH2)n-COOR8; -(CH2)n-CN, -CHR7-(CH2)n-CF3; -(CH2)n-NH-COR9; -(CH2)n-NH-COOR8; -(CH2)n-piperidinilo, -(CH2)n-morfolinilo, -(CH2)n-tetrahidrofuranilo; -(CH2)n-tiofenilo o -(CH2)n-isoxazolilo, donde el anillo heterocíclico puede ser sustituido por alquilo(C1-6), -(CH2)n-fenil, donde el anillo fenilo puede ser sustituido por halógeno o halógeno(C1-6)alquilo; -(CH2)p-OR8; -(CH2)p-SR8; -(CH2)p-SO-R9; o -(CH2)n-CS-NR5R6; R2 es H, alquilo C1-6, -(CH2)p-OR10, -(CH2)p-SR10; o bencilo, R3 es H o alquilo C1-6, R4 es halógeno, halógeno(C1-6)alquilo, ciano, alcoxi C1-6 o halógeno(C1-6)alcoxi; R5 y R6 son independientemente uno del otro H o alquilo C1-6; R7 es H, hidroxi o alcoxi C1-6; R8 es H o alquilo C1-6; R9 es alquilo C1-6; R10 es H o alquilo C1-6; m es 1, 2 o 3; n es 0 1 o 2; p es 1 o 2; como así también sus sales farmacéuticamente aceptables.
ARP030101023A 2002-03-27 2003-03-25 Derivados de ftalimido como inhibidores de monoamino oxidasa b AR039122A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP02007222 2002-03-27

Publications (1)

Publication Number Publication Date
AR039122A1 true AR039122A1 (es) 2005-02-09

Family

ID=28051746

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP030101023A AR039122A1 (es) 2002-03-27 2003-03-25 Derivados de ftalimido como inhibidores de monoamino oxidasa b

Country Status (13)

Country Link
US (2) US6660736B2 (es)
EP (1) EP1490334A1 (es)
JP (1) JP4202270B2 (es)
KR (1) KR100592630B1 (es)
CN (1) CN1277820C (es)
AR (1) AR039122A1 (es)
AU (1) AU2003226680B2 (es)
BR (1) BR0308786A (es)
CA (1) CA2477771A1 (es)
MX (1) MXPA04009335A (es)
PL (1) PL371439A1 (es)
RU (1) RU2317289C2 (es)
WO (1) WO2003080573A1 (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6846832B2 (en) * 2002-08-07 2005-01-25 Hoffman-La Roche Inc. 2,3-dihydro-isoindol-1-one derivatives
DE602004017206D1 (de) * 2003-10-23 2008-11-27 Hoffmann La Roche Benzazepin-derivate als mao-b-hemmer
JP2008531987A (ja) * 2005-02-22 2008-08-14 マギル ユニバーシティー 酸化ストレス測定デバイスおよび関連の方法
EP2281556A1 (en) 2005-02-25 2011-02-09 F. Hoffmann-La Roche AG Tablets with improved drugs substance dispersibility
TW200804347A (en) * 2006-01-10 2008-01-16 Janssen Pharmaceutica Nv Urotensin II receptor antagonists
EP2049120A4 (en) 2006-07-31 2011-09-07 Janssen Pharmaceutica Nv UROTENSIN II RECEPTOR ANTAGONISTS
CA2696609C (en) 2007-08-27 2017-09-05 Helicon Therapeutics, Inc. Therapeutic isoxazole compounds
ES2379762T3 (es) * 2008-08-02 2012-05-03 Janssen Pharmaceutica N.V. Antagonistas del receptor de la urotensina II
US20160362391A1 (en) * 2013-11-25 2016-12-15 Mylan Laboratories Ltd. Improved Process for the Preparation of Pomalidomide and its Purification
WO2016198691A1 (en) 2015-06-11 2016-12-15 Basilea Pharmaceutica Ag Efflux-pump inhibitors and therapeutic uses thereof
CN106188039B (zh) * 2016-06-30 2019-01-01 广东工业大学 一种二酮衍生物及其制备方法与应用
CN111183130B (zh) * 2017-09-07 2023-10-20 恒翼生物医药(上海)股份有限公司 苯并杂环衍生物及包含其的医药组合物
CN108752300B (zh) * 2018-05-16 2022-03-25 中国科学院昆明植物研究所 苄烯叉苯肽类化合物及其药物组合物和其应用
CN111072604B (zh) * 2018-10-18 2022-11-04 广东东阳光药业有限公司 α-氨基酰胺衍生物及其用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4524206A (en) 1983-09-12 1985-06-18 Mead Johnson & Company 1-Heteroaryl-4-(2,5-pyrrolidinedion-1-yl)alkyl)piperazine derivatives
JPH04295470A (ja) 1991-03-22 1992-10-20 Wakamoto Pharmaceut Co Ltd モノアミンオキシダーゼ−b酵素阻害活性を有する1,2,4−オキサジアゾール誘導体及びその製造法
TW219935B (es) * 1991-12-25 1994-02-01 Mitsubishi Chemicals Co Ltd
US5679715A (en) 1995-06-07 1997-10-21 Harris; Richard Y. Method for treating multiple sclerosis
AU709323B2 (en) 1996-03-15 1999-08-26 Somerset Pharmaceuticals, Inc. Method for preventing and treating peripheral neuropathy by administering selegiline
WO2001034172A2 (en) 1999-11-05 2001-05-17 Vela Pharmaceuticals Inc. Methods and compositions for treating reward deficiency syndrome

Also Published As

Publication number Publication date
JP4202270B2 (ja) 2008-12-24
JP2005526796A (ja) 2005-09-08
MXPA04009335A (es) 2005-01-25
US6660736B2 (en) 2003-12-09
RU2317289C2 (ru) 2008-02-20
BR0308786A (pt) 2005-01-11
KR20040108688A (ko) 2004-12-24
RU2004131651A (ru) 2005-07-10
EP1490334A1 (en) 2004-12-29
CN1642911A (zh) 2005-07-20
KR100592630B1 (ko) 2006-06-26
CA2477771A1 (en) 2003-10-02
CN1277820C (zh) 2006-10-04
AU2003226680B2 (en) 2009-05-07
US20040229871A1 (en) 2004-11-18
AU2003226680A1 (en) 2003-10-08
PL371439A1 (en) 2005-06-13
WO2003080573A1 (en) 2003-10-02
US20030195208A1 (en) 2003-10-16
US6903095B2 (en) 2005-06-07

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