ATE364615T1 - Ribofuranosyluronamid derivate als kristall; ein menschlicher adenosin a2a rezeptor agonsit - Google Patents

Ribofuranosyluronamid derivate als kristall; ein menschlicher adenosin a2a rezeptor agonsit

Info

Publication number
ATE364615T1
ATE364615T1 AT02783443T AT02783443T ATE364615T1 AT E364615 T1 ATE364615 T1 AT E364615T1 AT 02783443 T AT02783443 T AT 02783443T AT 02783443 T AT02783443 T AT 02783443T AT E364615 T1 ATE364615 T1 AT E364615T1
Authority
AT
Austria
Prior art keywords
agonsite
ribofuranosyluronamide
receptor
derivatives
crystal
Prior art date
Application number
AT02783443T
Other languages
English (en)
Inventor
Terence Vernon Silk
Julian Duncan Smith
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Application granted granted Critical
Publication of ATE364615T1 publication Critical patent/ATE364615T1/de

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16—Purine radicals
    • 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
    • A61K31/435—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
    • A61K31/439—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 the ring forming part of a bridged ring system, e.g. quinuclidine
    • A—HUMAN NECESSITIES
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    • 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
    • A61K31/435—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
    • A61K31/46—8-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
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    • A61K31/33—Heterocyclic compounds
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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
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
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    • A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
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    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
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    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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    • A61P9/12—Antihypertensives

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Pulmonology (AREA)
  • Diabetes (AREA)
  • Nanotechnology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Dermatology (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Biochemistry (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Hematology (AREA)
  • Neurosurgery (AREA)
  • Immunology (AREA)
  • Reproductive Health (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • General Engineering & Computer Science (AREA)
  • Medical Informatics (AREA)
AT02783443T 2001-12-06 2002-11-27 Ribofuranosyluronamid derivate als kristall; ein menschlicher adenosin a2a rezeptor agonsit ATE364615T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0129273.9A GB0129273D0 (en) 2001-12-06 2001-12-06 Crystalline drug form

Publications (1)

Publication Number Publication Date
ATE364615T1 true ATE364615T1 (de) 2007-07-15

Family

ID=9927165

Family Applications (1)

Application Number Title Priority Date Filing Date
AT02783443T ATE364615T1 (de) 2001-12-06 2002-11-27 Ribofuranosyluronamid derivate als kristall; ein menschlicher adenosin a2a rezeptor agonsit

Country Status (41)

Country Link
US (3) US20030144243A1 (de)
EP (1) EP1456219B1 (de)
JP (1) JP4184279B2 (de)
KR (1) KR100554333B1 (de)
CN (1) CN100381454C (de)
AP (1) AP2004003056A0 (de)
AR (2) AR037633A1 (de)
AT (1) ATE364615T1 (de)
AU (2) AU2002347509B2 (de)
BR (1) BR0214747A (de)
CA (1) CA2468847C (de)
CY (1) CY1106822T1 (de)
DE (1) DE60220713T2 (de)
DK (1) DK1456219T3 (de)
EA (1) EA006857B1 (de)
EC (1) ECSP045141A (de)
ES (1) ES2286303T3 (de)
GB (1) GB0129273D0 (de)
GT (2) GT200200256A (de)
HK (1) HK1071143A1 (de)
HN (1) HN2002000352A (de)
HR (1) HRP20040516A2 (de)
HU (1) HUP0700046A2 (de)
IL (2) IL162101A0 (de)
IS (1) IS7279A (de)
MA (1) MA27151A1 (de)
MX (1) MXPA04005505A (de)
NO (1) NO20042837L (de)
NZ (1) NZ533053A (de)
OA (1) OA12737A (de)
PA (2) PA8560301A1 (de)
PE (2) PE20030722A1 (de)
PL (1) PL370971A1 (de)
PT (1) PT1456219E (de)
RS (1) RS49504A (de)
SV (1) SV2004001425A (de)
TN (1) TNSN04103A1 (de)
TW (2) TW200301130A (de)
UY (1) UY27568A1 (de)
WO (2) WO2003048180A1 (de)
ZA (1) ZA200403967B (de)

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Publication number Priority date Publication date Assignee Title
US20030225089A1 (en) * 2002-04-10 2003-12-04 Boehringer Ingelheim Pharma Gmbh & Co. Kg Pharmaceutical compositions based on anticholinergics and p38 kinase inhibitors
DE10345065A1 (de) * 2003-09-26 2005-04-14 Boehringer Ingelheim Pharma Gmbh & Co. Kg Aerosolformulierung für die Inhalation enthaltend ein Anticholinergikum
AR049384A1 (es) 2004-05-24 2006-07-26 Glaxo Group Ltd Derivados de purina
GB0514809D0 (en) 2005-07-19 2005-08-24 Glaxo Group Ltd Compounds
JPWO2021084791A1 (de) * 2019-10-28 2021-05-06
CN115400140B (zh) * 2022-01-27 2024-02-20 宁波熙健医药科技有限公司 呋喃核糖基吡啶衍生物用于预防或治疗癫痫或惊厥的用途

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US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
IT1254915B (it) * 1992-04-24 1995-10-11 Gloria Cristalli Derivati di adenosina ad attivita' a2 agonista
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
GB9913932D0 (en) * 1999-06-15 1999-08-18 Pfizer Ltd Purine derivatives
WO2001020089A1 (fr) 1999-09-10 2001-03-22 Maeda Corporation Structure de beton et procede de construction
GB0003960D0 (en) * 2000-02-18 2000-04-12 Pfizer Ltd Purine derivatives
GB0009592D0 (en) * 2000-04-18 2000-06-07 Glaxo Group Ltd Respiratory combinations
GB0009606D0 (en) * 2000-04-18 2000-06-07 Glaxo Group Ltd Therapeutic combinations
GB0009583D0 (en) * 2000-04-18 2000-06-07 Glaxo Group Ltd Respiratory formulations
GB0009605D0 (en) * 2000-04-18 2000-06-07 Glaxo Group Ltd Medicaments
TWI227240B (en) * 2000-06-06 2005-02-01 Pfizer 2-aminocarbonyl-9H-purine derivatives
JP2004505526A (ja) 2000-07-26 2004-02-19 スイスコム　モービル　アーゲー 移動体通信網の基地局を設置し、基地局と移動体通信網とを接続する方法
WO2002096462A1 (en) * 2001-05-25 2002-12-05 Pfizer Inc. An adenosine a2a receptor agonist and an anticholinergic agent in combination for treating obstructive airways diseases

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ZA200403967B (en) 2006-05-31
US20050085437A1 (en) 2005-04-21
CA2468847C (en) 2008-10-21
JP2005513043A (ja) 2005-05-12
DE60220713D1 (de) 2007-07-26
CA2468847A1 (en) 2003-06-12
GT200200256A (es) 2003-07-03
EA200400638A1 (ru) 2004-10-28
IS7279A (is) 2004-05-21
IL162101A0 (en) 2005-11-20
KR20050058272A (ko) 2005-06-16
KR100554333B1 (ko) 2006-02-22
ECSP045141A (es) 2004-07-23
MXPA04005505A (es) 2005-06-03
US20030158145A1 (en) 2003-08-21
RS49504A (en) 2006-10-27
JP4184279B2 (ja) 2008-11-19
DE60220713T2 (de) 2008-03-06
PE20030722A1 (es) 2003-08-29
US20030144243A1 (en) 2003-07-31
UY27568A1 (es) 2003-07-31
AU2002347509A1 (en) 2003-06-17
BR0214747A (pt) 2004-09-14
EA006857B1 (ru) 2006-04-28
TW200301130A (en) 2003-07-01
EP1456219B1 (de) 2007-06-13
PE20030822A1 (es) 2003-10-04
AR038547A1 (es) 2005-01-19
PL370971A1 (en) 2005-06-13
GT200200257A (es) 2003-07-11
PT1456219E (pt) 2007-08-03
WO2003047597A1 (en) 2003-06-12
HK1071143A1 (en) 2005-07-08
US7022727B2 (en) 2006-04-04
MA27151A1 (fr) 2005-01-03
AU2002347509B2 (en) 2008-09-18
TNSN04103A1 (fr) 2006-06-01
GB0129273D0 (en) 2002-01-23
SV2004001425A (es) 2004-05-07
AP2004003056A0 (en) 2004-06-30
PA8560301A1 (es) 2003-11-12
HRP20040516A2 (en) 2004-10-31
DK1456219T3 (da) 2007-09-24
IL162101A (en) 2010-04-29
HN2002000352A (es) 2003-07-23
ES2286303T3 (es) 2007-12-01
PA8560501A1 (es) 2003-09-17
US6852746B2 (en) 2005-02-08
CY1106822T1 (el) 2012-05-23
HUP0700046A2 (en) 2007-03-28
TW200301129A (en) 2003-07-01
OA12737A (en) 2006-06-29
CN1599745A (zh) 2005-03-23
NZ533053A (en) 2006-09-29
EP1456219A1 (de) 2004-09-15
CN100381454C (zh) 2008-04-16
NO20042837L (no) 2004-08-24
AR037633A1 (es) 2004-11-17
AU2002351056A1 (en) 2003-06-17
WO2003048180A1 (en) 2003-06-12

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