DK0686155T3 - Xanthinderivater som adenosin A1-receptor-antagonister - Google Patents

Xanthinderivater som adenosin A1-receptor-antagonister

Info

Publication number
DK0686155T3
DK0686155T3 DK94910661T DK94910661T DK0686155T3 DK 0686155 T3 DK0686155 T3 DK 0686155T3 DK 94910661 T DK94910661 T DK 94910661T DK 94910661 T DK94910661 T DK 94910661T DK 0686155 T3 DK0686155 T3 DK 0686155T3
Authority
DK
Denmark
Prior art keywords
adenosine
pct
receptor antagonists
xanthine derivatives
sec
Prior art date
Application number
DK94910661T
Other languages
Danish (da)
English (en)
Inventor
Janice M Hitchcock
Stephen M Sorenson
Mark W Dudley
Norton P Peet
Original Assignee
Merrell Pharma Inc
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 Pharma Inc filed Critical Merrell Pharma Inc
Application granted granted Critical
Publication of DK0686155T3 publication Critical patent/DK0686155T3/da

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)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
DK94910661T 1993-02-26 1994-01-27 Xanthinderivater som adenosin A1-receptor-antagonister DK0686155T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US2350193A 1993-02-26 1993-02-26
PCT/US1994/001009 WO1994019349A1 (en) 1993-02-26 1994-01-27 Xanthine derivatives as adenosine a1 receptor antagonists

Publications (1)

Publication Number Publication Date
DK0686155T3 true DK0686155T3 (da) 1999-02-01

Family

ID=21815459

Family Applications (1)

Application Number Title Priority Date Filing Date
DK94910661T DK0686155T3 (da) 1993-02-26 1994-01-27 Xanthinderivater som adenosin A1-receptor-antagonister

Country Status (19)

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

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998041237A1 (en) * 1997-03-18 1998-09-24 Fujisawa Pharmaceutical Co., Ltd. Preventives and remedies for hyperphosphatemia
EP2011499A3 (en) 1998-06-02 2010-10-20 OSI Pharmaceuticals, Inc. Pyrrolo[2,3d]Pyrimidine compositions and their use
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
AU2002360436A1 (en) 2001-11-30 2003-06-17 Osi Pharmaceuticals, Inc. 2-aryl pyrrologpyrimidines for a1 and a3 receptors
BR0215202A (pt) 2001-12-20 2004-10-13 Osi Pharm Inc Compostos antagonistas seletivos a2b de pirimidina, sua sìntese e uso
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)
EP1709966A4 (en) * 2003-12-09 2009-04-29 PREVENTIVE AND / OR THERAPEUTIC AGENT FOR SEVERE CEREBRAL DYSFUNCTION
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
DE3843117A1 (de) * 1988-12-22 1990-06-28 Boehringer Ingelheim Kg Neue xanthinderivate mit adenosin-antagonistischer wirkung
US5047534A (en) * 1990-03-26 1991-09-10 Merrell Dow Pharmaceuticals Inc. Selective adenosine receptor agents
DE4019892A1 (de) * 1990-06-22 1992-01-02 Boehringer Ingelheim Kg Neue xanthinderivate
JPH0455150A (ja) * 1990-06-22 1992-02-21 Takata Kk 助手席用エアバッグ装置
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
DE69412073D1 (de) 1998-09-03
ZA941176B (en) 1994-09-20
HU9502495D0 (en) 1995-10-30
NO953353L (no) 1995-08-25
TW261532B (cs) 1995-11-01
HUT72677A (en) 1996-05-28
CA2155130C (en) 1994-09-01
IL108750A0 (en) 1994-05-30
WO1994019349A1 (en) 1994-09-01
JPH08512281A (ja) 1996-12-24
AU680241B2 (en) 1997-07-24
US5840729A (en) 1998-11-24
EP0686155B1 (en) 1998-07-29
NO311920B1 (no) 2002-02-18
ES2120025T3 (es) 1998-10-16
KR100315898B1 (ko) 2002-02-28
NZ262984A (en) 1997-05-26
NO953353D0 (no) 1995-08-25
CN1118599A (zh) 1996-03-13
ATE169019T1 (de) 1998-08-15
EP0686155A1 (en) 1995-12-13
CN1041418C (zh) 1998-12-30
IL108750A (en) 2000-09-28
MX9401406A (es) 1994-08-31
DE69412073T2 (de) 1999-02-18
CA2155130A1 (en) 1994-09-01
AU6296894A (en) 1994-09-14

Similar Documents

Publication Publication Date Title
DE69622031D1 (de) INDOLDERIVATE ALS cGMP-PDE INHIBITOREN
ES2091689T3 (es) Aplicacion de la carbamazepina y de la oxcarbazepina en el tratamiento de la enfermedad de parkinson y de los sindromes parkinsonianos.
DE69611377D1 (de) 1,2,4-triazolo[1,5-c]pyrimidin-heterocyclische analoge mit antagonistischer aktivität auf dem adenosine a2a rezeptor
ES2121193T3 (es) Derivados de bencimidazoles.
NO960630L (no) Heterocykler anvendelige som neurokinin antagonister
DE69327536D1 (de) Fibrinogenrezeptor-antagonisten
DK0686155T3 (da) Xanthinderivater som adenosin A1-receptor-antagonister
TR199900501T2 (xx) Benzamin t�revleri ve bunlar�n ila� olarak kullan�m�.
ES2134929T3 (es) Derivados de pirrolo-piridina como ligandos para receptores de dopamina.
NO943133L (no) Benzodiazepinderivater egnet til bruk som CCK-reseptorantagonister
ES2098510T3 (es) Antagonista de galanina.
ATE113056T1 (de) Künstliche rezeptor-analoge.
GR3024854T3 (en) Drugs for preventing the development of tolerance during treatment with benzodiazepine-receptor-binding substances.
ATE153027T1 (de) Zuckerderivate von makroliden
PT958290E (pt) Derivados de 1,4-di-hidropiridina e seu uso em terapia
ES2093515T3 (es) Aplicacion del riluzol como radio-restaurador.
ATE221068T1 (de) Anellierte beta-carboline
ITMI950956A0 (it) Uso degli enantiomeri (s) di derivati 1,4-diidropiridinici per il trattamento dell'insufficienza cardiaca