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MX9401406A - Agentes receptores de adenosina selectivos para intensificar el conocimiento. - Google Patents

Agentes receptores de adenosina selectivos para intensificar el conocimiento.

Info

Publication number
MX9401406A
MX9401406A MX9401406A MX9401406A MX9401406A MX 9401406 A MX9401406 A MX 9401406A MX 9401406 A MX9401406 A MX 9401406A MX 9401406 A MX9401406 A MX 9401406A MX 9401406 A MX9401406 A MX 9401406A
Authority
MX
Mexico
Prior art keywords
intensify
knowledge
pct
selective adenosine
receiving agents
Prior art date
Application number
MX9401406A
Other languages
English (en)
Inventor
Norton P Peet
Janice M Hitchcock
Stephen M Sorensen
Mark W Dudley
Original Assignee
Merrell Dow Pharma
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 Merrell Dow Pharma filed Critical Merrell Dow Pharma
Publication of MX9401406A publication Critical patent/MX9401406A/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/04Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms
    • C07D473/06Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3
    • C07D473/08Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two oxygen atoms with radicals containing only hydrogen and carbon atoms, attached in position 1 or 3 with methyl radicals in positions 1 and 3, e.g. theophylline

Landscapes

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

Abstract

La presente invención se refiere a un grupo de compuestos que son derivados de xantina y que actúan en forma selectiva en los receptores A1 de adenosina. Los antagonistas de adenosina que actúan en el receptor A1 despolarizan las neuronas potsinápticas e incrementan la liberación de un numero de neurotransmisores desde la presinápsis, incluyendo la acetilcolina, glutamato, serotorina, y norepinefrina. Esta es una acción potencial para el tratamiento de pérdida del conocimiento como aquéllas asociadas con la enfermedad de Alzheimer, así como los transmisores que se han encontrado implicados en el aprendizaje y la memoria, y cada uno de estos transmisores se debilita en la enfermedad de Alzheimer. Algunos de los compuestos antagonistas de la A1 descritos en la presente invención incrementan la actividad de las neuronas en el hipocampo en un modelo de aprendizaje in vitro de potenciación durante períodos largos, y antagonizan una pérdida inducida por escopolamina en un modelo de aprendizaje in vivo en el laberinto con agua. Por lo tanto, estos compuestos tiene posibilidad para los efectos de intensificación del conocimiento.
MX9401406A 1993-02-26 1994-02-24 Agentes receptores de adenosina selectivos para intensificar el conocimiento. MX9401406A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US2350193A 1993-02-26 1993-02-26

Publications (1)

Publication Number Publication Date
MX9401406A true MX9401406A (es) 1994-08-31

Family

ID=21815459

Family Applications (1)

Application Number Title Priority Date Filing Date
MX9401406A MX9401406A (es) 1993-02-26 1994-02-24 Agentes receptores de adenosina selectivos para intensificar el conocimiento.

Country Status (19)

Country Link
US (1) US5840729A (es)
EP (1) EP0686155B1 (es)
JP (1) JPH08512281A (es)
KR (1) KR100315898B1 (es)
CN (1) CN1041418C (es)
AT (1) ATE169019T1 (es)
AU (1) AU680241B2 (es)
CA (1) CA2155130C (es)
DE (1) DE69412073T2 (es)
DK (1) DK0686155T3 (es)
ES (1) ES2120025T3 (es)
HU (1) HUT72677A (es)
IL (1) IL108750A (es)
MX (1) MX9401406A (es)
NO (1) NO311920B1 (es)
NZ (1) NZ262984A (es)
TW (1) TW261532B (es)
WO (1) WO1994019349A1 (es)
ZA (1) ZA941176B (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6303624B1 (en) * 1997-03-18 2001-10-16 Fujisawa Pharmaceutical Co., Ltd. Preventives and remedies for hyperphosphatemia
CN100528874C (zh) 1998-06-02 2009-08-19 Osi药物公司 吡咯并[2,3d]嘧啶组合物及其应用
US6680322B2 (en) 1999-12-02 2004-01-20 Osi Pharmaceuticals, Inc. Compounds specific to adenosine A1 receptors and uses thereof
US6680324B2 (en) 2000-12-01 2004-01-20 Osi Pharmaceuticals, Inc. Compounds specific to adenosine A1 receptors and uses thereof
US20020115635A1 (en) * 2001-02-21 2002-08-22 Pnina Fishman Modulation of GSK-3beta activity and its different uses
US7504407B2 (en) 2001-11-30 2009-03-17 Osi Pharmaceuticals, Inc. Compounds specific to adenosine A1 and A3 receptors and uses thereof
CN1620294A (zh) 2001-12-20 2005-05-25 Osi药物公司 嘧啶a2b选择性拮抗剂化合物,它们的合成及用途
JP2005538950A (ja) * 2002-05-15 2005-12-22 ジェンザイム、コーポレーション 2−アルキルシステイン、2−(ヒドロキシル化フェニル)−4−アルキルチアゾリン−4−カルボン酸およびそれらの誘導体の合成
WO2004086047A2 (en) * 2003-03-28 2004-10-07 Bayer Healthcare Ag Diagnostics and therapeutics for diseases associated with g-protein-coupled receptor adenosine a1 (adora1)
US20070078148A1 (en) * 2003-12-09 2007-04-05 Kyowa Hakko Kogyo Co., Ltd. Agents for preventing and/or treating higher brain dysfunctions
US7592461B2 (en) 2005-12-21 2009-09-22 Bristol-Myers Squibb Company Indane modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
US7795427B2 (en) * 2006-02-14 2010-09-14 New York University Methods for inhibiting osteoclast differentiation, formation, or function and for increasing bone mass

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE8817122U1 (de) * 1988-12-22 1993-02-04 Boehringer Ingelheim Kg, 55218 Ingelheim Neue Xanthinderivate mit Adenosinantogenistischer Wirkung
US5047534A (en) * 1990-03-26 1991-09-10 Merrell Dow Pharmaceuticals Inc. Selective adenosine receptor agents
JPH0455150A (ja) * 1990-06-22 1992-02-21 Takata Kk 助手席用エアバッグ装置
DE4019892A1 (de) * 1990-06-22 1992-01-02 Boehringer Ingelheim Kg Neue xanthinderivate
US5087827A (en) * 1991-02-11 1992-02-11 Tektronix, Inc. Variable voltage transition circuit
US5208240A (en) * 1991-03-12 1993-05-04 Merrell Dow Pharmaceuticals Inc. 8-substituted purines as selective adenosine receptor agents
US5281607B1 (en) * 1992-10-08 1998-05-19 Univ New York Method of using alpha 2-antagonists for the treatment of neurodegenerative diseases

Also Published As

Publication number Publication date
WO1994019349A1 (en) 1994-09-01
US5840729A (en) 1998-11-24
EP0686155B1 (en) 1998-07-29
HU9502495D0 (en) 1995-10-30
DE69412073D1 (de) 1998-09-03
IL108750A (en) 2000-09-28
DK0686155T3 (da) 1999-02-01
KR100315898B1 (ko) 2002-02-28
NZ262984A (en) 1997-05-26
HUT72677A (en) 1996-05-28
NO953353D0 (no) 1995-08-25
ZA941176B (en) 1994-09-20
NO311920B1 (no) 2002-02-18
CN1041418C (zh) 1998-12-30
CA2155130C (en) 1994-09-01
TW261532B (es) 1995-11-01
DE69412073T2 (de) 1999-02-18
ATE169019T1 (de) 1998-08-15
AU680241B2 (en) 1997-07-24
CN1118599A (zh) 1996-03-13
AU6296894A (en) 1994-09-14
IL108750A0 (en) 1994-05-30
NO953353L (no) 1995-08-25
CA2155130A1 (en) 1994-09-01
ES2120025T3 (es) 1998-10-16
JPH08512281A (ja) 1996-12-24
EP0686155A1 (en) 1995-12-13

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Legal Events

Date Code Title Description
FG Grant or registration
MM Annulment or lapse due to non-payment of fees