IS6821A - Samrunnar afleiður púríns sem mótlyf A1-adenósínviðtakans - Google Patents

Samrunnar afleiður púríns sem mótlyf A1-adenósínviðtakans

Info

Publication number
IS6821A
IS6821A IS6821A IS6821A IS6821A IS 6821 A IS6821 A IS 6821A IS 6821 A IS6821 A IS 6821A IS 6821 A IS6821 A IS 6821A IS 6821 A IS6821 A IS 6821A
Authority
IS
Iceland
Prior art keywords
antagonists
convergence
adenosine receptor
purine derivatives
purine
Prior art date
Application number
IS6821A
Other languages
English (en)
Inventor
Lin Ko-Chung
Vu Chi
Original Assignee
Biogen Idec Ma 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 Biogen Idec Ma Inc. filed Critical Biogen Idec Ma Inc.
Publication of IS6821A publication Critical patent/IS6821A/is

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52—Purines, e.g. adenine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52—Purines, e.g. adenine
    • A61K31/522—Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10—Antimycotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10—Antioedematous agents; Diuretics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/02—Non-specific cardiovascular stimulants, e.g. drugs for syncope, antihypotensives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
    • C07D487/14—Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Epidemiology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pulmonology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Saccharide Compounds (AREA)
IS6821A 2000-12-01 2003-05-20 Samrunnar afleiður púríns sem mótlyf A1-adenósínviðtakans IS6821A (is)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US25065800P 2000-12-01 2000-12-01
PCT/US2001/044991 WO2002044182A1 (en) 2000-12-01 2001-11-30 Condensed purine derivatives as a1 adenosine receptor antagonists

Publications (1)

Publication Number Publication Date
IS6821A true IS6821A (is) 2003-05-20

Family

ID=22948640

Family Applications (1)

Application Number Title Priority Date Filing Date
IS6821A IS6821A (is) 2000-12-01 2003-05-20 Samrunnar afleiður púríns sem mótlyf A1-adenósínviðtakans

Country Status (32)

Country Link
US (2) US6605601B2 (is)
EP (1) EP1347981B1 (is)
JP (2) JP2004514723A (is)
KR (1) KR20040011439A (is)
CN (1) CN100497340C (is)
AR (1) AR035400A1 (is)
AT (1) ATE394402T1 (is)
AU (2) AU1997702A (is)
BG (1) BG107849A (is)
BR (1) BR0115833A (is)
CA (1) CA2430508C (is)
CZ (1) CZ20031513A3 (is)
DE (1) DE60133931D1 (is)
EA (1) EA009814B1 (is)
EE (1) EE200300260A (is)
ES (1) ES2305139T3 (is)
GE (1) GEP20094697B (is)
HU (1) HUP0400530A3 (is)
IL (1) IL156046A0 (is)
IS (1) IS6821A (is)
MX (1) MXPA03004857A (is)
MY (1) MY127120A (is)
NO (1) NO20032483L (is)
NZ (1) NZ526511A (is)
PL (1) PL362642A1 (is)
SK (1) SK6552003A3 (is)
TR (1) TR200300766T2 (is)
TW (1) TWI293301B (is)
UA (1) UA75625C2 (is)
WO (1) WO2002044182A1 (is)
YU (1) YU42903A (is)
ZA (2) ZA200304067B (is)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2238335T3 (es) * 1999-12-24 2005-09-01 Kyowa Hakko Kogyo Co., Ltd. Derivados de purina condensados.
UA75625C2 (en) * 2000-12-01 2006-05-15 Biogen Inc Condensed purine derivatives as a1 adenosine receptor antagonists
JP2006518390A (ja) * 2003-02-19 2006-08-10 エンダシア，インコーポレイテッド Ａ１アデノシンレセプターアンタゴニスト
US20040229901A1 (en) * 2003-02-24 2004-11-18 Lauren Otsuki Method of treatment of disease using an adenosine A1 receptor antagonist
EP1637532A1 (en) * 2003-04-25 2006-03-22 Kyowa Hakko Kogyo Co., Ltd. Fused pyrimidine derivative
AU2004233852A1 (en) 2003-04-25 2004-11-11 Novacardia, Inc. Method of improved diuresis in individuals with impaired renal function
US7247639B2 (en) * 2003-06-06 2007-07-24 Endacea, Inc. A1 adenosine receptor antagonists
JP2008534445A (ja) * 2005-03-11 2008-08-28 アデリス ファーマシューティカルズ， インコーポレイテッド 置換９−アルキルアデニンおよびその使用
WO2007095161A2 (en) * 2006-02-14 2007-08-23 New York University Methods and compositions for treating disorders associated with increased bone turnover and osteopenia
CA2648281A1 (en) * 2006-04-06 2007-10-18 Novacardia, Inc. Co-administration of adenosine a1 receptor antagonists and anticonvulsants
RS52062B (sr) 2006-05-19 2012-06-30 Abbott Laboratories Cns aktivni azabiciklični alkanski derivati koji su supstituisani spojenim bicikloheterociklom
EP2035009A1 (en) * 2006-06-16 2009-03-18 Novacardia, Inc. Prolonged improvement of renal function comprising infrequent administration of an aa1ra
ATE486874T1 (de) 2006-06-23 2010-11-15 Incyte Corp Purinonderivate als hm74a-agonisten
AR061625A1 (es) 2006-06-23 2008-09-10 Incyte Corp Derivados de purinona como agonistas de hm74a
WO2008121882A1 (en) * 2007-03-29 2008-10-09 Novacardia, Inc. Improved methods of administration of adenosine a1 receptor antagonists
WO2008121893A1 (en) * 2007-03-29 2008-10-09 Novacardia, Inc. Methods of treating heart failure and renal dysfunction in individuals with an adenosine a1 receptor antagonist
WO2011063268A2 (en) * 2009-11-19 2011-05-26 Biogen Idec Ma Inc Novel synthetic methods
US20130109645A1 (en) 2010-03-31 2013-05-02 The united States of America,as represented by Secretary,Dept.,of Health and Human Services Adenosine receptor agonists for the treatment and prevention of vascular or joint capsule calcification disorders
IL275817B2 (en) 2018-01-04 2024-04-01 Impetis Biosciences Ltd Tricyclic compounds, compositions and medicinal applications thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06102662B2 (ja) 1989-09-01 1994-12-14 協和醗酵工業株式会社 キサンチン誘導体
JP2988711B2 (ja) * 1989-10-20 1999-12-13 協和醗酵工業株式会社 縮合プリン誘導体
CA2254273C (en) 1991-09-23 2003-03-25 Florida State University Preparation of substituted isoserine esters using metal alkoxides and .beta.-lactams
EP0884318A4 (en) * 1996-10-07 2002-10-23 Kyowa Hakko Kogyo Kk CONDENSED PURINE DERIVATIVES
AU740770B2 (en) 1997-06-18 2001-11-15 Aderis Pharmaceuticals, Inc. Compositions and methods for preventing restenosis following revascularization procedures
WO2000001388A1 (en) * 1998-07-02 2000-01-13 Kyowa Hakko Kogyo Co., Ltd. Remedies for diabetes
ES2238335T3 (es) * 1999-12-24 2005-09-01 Kyowa Hakko Kogyo Co., Ltd. Derivados de purina condensados.
UA75625C2 (en) * 2000-12-01 2006-05-15 Biogen Inc Condensed purine derivatives as a1 adenosine receptor antagonists

Also Published As

Publication number Publication date
SK6552003A3 (en) 2003-12-02
US7022686B2 (en) 2006-04-04
MXPA03004857A (es) 2003-08-19
AU1997702A (en) 2002-06-11
ES2305139T3 (es) 2008-11-01
HK1059927A1 (en) 2004-07-23
AU2002219977B2 (en) 2008-01-24
CZ20031513A3 (cs) 2003-09-17
JP2004514723A (ja) 2004-05-20
EE200300260A (et) 2003-08-15
CA2430508A1 (en) 2002-06-06
UA75625C2 (en) 2006-05-15
NZ526511A (en) 2005-04-29
MY127120A (en) 2006-11-30
DE60133931D1 (de) 2008-06-19
IL156046A0 (en) 2003-12-23
TWI293301B (en) 2008-02-11
KR20040011439A (ko) 2004-02-05
US20030220358A1 (en) 2003-11-27
US20020111333A1 (en) 2002-08-15
ZA200304067B (en) 2005-05-30
PL362642A1 (en) 2004-11-02
HUP0400530A3 (en) 2007-05-29
US6605601B2 (en) 2003-08-12
GEP20094697B (en) 2009-06-10
AR035400A1 (es) 2004-05-26
BG107849A (bg) 2004-01-30
ATE394402T1 (de) 2008-05-15
NO20032483L (no) 2003-07-30
BR0115833A (pt) 2003-10-28
EP1347981A1 (en) 2003-10-01
EA009814B1 (ru) 2008-04-28
HUP0400530A2 (hu) 2004-06-28
NO20032483D0 (no) 2003-06-02
ZA200408755B (en) 2005-07-27
EA200300629A1 (ru) 2003-12-25
JP2010053148A (ja) 2010-03-11
WO2002044182A1 (en) 2002-06-06
CA2430508C (en) 2010-05-18
CN1481387A (zh) 2004-03-10
YU42903A (sh) 2006-05-25
TR200300766T2 (tr) 2004-09-21
EP1347981B1 (en) 2008-05-07
CN100497340C (zh) 2009-06-10

Similar Documents

Publication Publication Date Title
PT1349839E (pt) Derivados de feniletenilo ou feniletinilo como antagonistas do receptor de glutamato
AU1211802A (en) 4-phenyl-pyridine derivatives as neurokinin-1 receptor antagonists
IS6298A (is) Teridínón sem tálmar kínasa
IS7314A (is) 5,6-díarýl-pýrasín-2-amíðafleiður sem cb1 mótlyf
AU5316000A (en) Substituted 8-phenylxanthines useful as antagonists of a2b adenosine receptors
PT1224174E (pt) Derivados de benzodiazepina como antagonistas do receptor metabotropico do glutamato
AU6808901A (en) Adenosine a2a receptor antagonists
IS2758B (is) Setnar kínasólínafleiður sem hemlar gegn Áróra kínösum
DK1416935T3 (da) 4-Amino-6-phenyl-pyrrolo[2,3-d]pyrimidinderivater
PT1131291E (pt) Antagonistas iii do receptor 4-aroil-piperidin-ccr-3
IL161716A0 (en) ADENOSINE A2a RECEPTOR ANTAGONISTS
IL161572A0 (en) Adenosine a2a receptor antagonists
DK1221952T3 (da) Anvendelse af en antagonist til centrale cannaboidreceptorer med henblik på fremstilling af lægemidler
NO20032773D0 (no) Farmasöytisk preparat som omfatter pyrsazolo [4,3-d] pyrimidiner og antitrombotika, kalsiumantagonister, prostaglandiner ellerprostaglandinderivater
SI1305319T1 (sl) 4-fenil-piridinski derivati kot receptorski antagonisti nevrokinina-1
NO20032142L (no) Substituerte 2-fenylaminoimidazolin-fenylketon-derivater som IP-antagonister
EE200300260A (et) Kondenseeritud puriinderivaadid kui A1 adenosiiniretseptori antagonistid
ID29914A (id) Senyawa benzensulfonamida heterosiklik sebagai antagonis bradikinin
NO20016077D0 (no) Makrofag-oppfanger-reseptorantagonister
IS2456B (is) Ímídasókínólínafleiður sem adenósín A3 viðtakabindlar
IL144299A0 (en) N-triazolymethyl-piperazine derivatives as neurokinin receptor antagonists
PL350536A1 (en) Biphenyl derivatives as antagonists of the neurokinine-1 receptor
IS7615A (is) Bísýklískar píperidín afleiður sem mótlyf af CCR1flakkboða viðtakanum
NO20015662D0 (no) Oralt aktive A1-adenosinreseptorantagonister
DE60214408D1 (de) 5-METHOXY-8-ARYL-i1,2,4öTRIAZOLOi1,5-AöPYRIDINE DERIVATIVE ALS ADENOSIN-REZEPTOR ANTAGONISTEN