WO2009113704A3 - Composé contenant du fluor et procédé de détection de biomplécule l'utilisant - Google Patents
Composé contenant du fluor et procédé de détection de biomplécule l'utilisant Download PDFInfo
- Publication number
- WO2009113704A3 WO2009113704A3 PCT/JP2009/054984 JP2009054984W WO2009113704A3 WO 2009113704 A3 WO2009113704 A3 WO 2009113704A3 JP 2009054984 W JP2009054984 W JP 2009054984W WO 2009113704 A3 WO2009113704 A3 WO 2009113704A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fluorine
- group
- containing compound
- substituted
- same
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
- A61K49/08—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
- A61K49/085—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier conjugated systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
- A61K49/08—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
- A61K49/10—Organic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
- A61K49/08—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
- A61K49/10—Organic compounds
- A61K49/14—Peptides, e.g. proteins
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
- C07C311/18—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by nitrogen atoms, not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D259/00—Heterocyclic compounds containing rings having more than four nitrogen atoms as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/536—Immunoassay; Biospecific binding assay; Materials therefor with immune complex formed in liquid phase
- G01N33/542—Immunoassay; Biospecific binding assay; Materials therefor with immune complex formed in liquid phase with steric inhibition or signal modification, e.g. fluorescent quenching
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Immunology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Radiology & Medical Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Biotechnology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Nanotechnology (AREA)
- Biomedical Technology (AREA)
- General Physics & Mathematics (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Analytical Chemistry (AREA)
- Physics & Mathematics (AREA)
- Food Science & Technology (AREA)
- Microbiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Pathology (AREA)
- Medical Informatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Crystallography & Structural Chemistry (AREA)
- Cell Biology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Magnetic Resonance Imaging Apparatus (AREA)
Abstract
L'invention concerne un composé contenant du fluor amphiphile ayant une structure représentée par la formule générale (1) suivante comportant un ligand hydrophile RI, une sonde fluorée Rf, et des lieurs L1 et L2. Dans cette formule, RI représente un ligand hydrophile ayant un groupe polaire; L2 représente un groupe alkylène ayant un ou plusieurs -CH2- qui peuvent être indépendamment substitués par l'un ou l'autre des -NH-, -O-, -CO-, -SO2-, et un groupe arylène; Rf est sélectionné dans un groupe alkyle qui a un ou plusieurs atomes d'hydrogène substitués par un atome de fluor, et dans un groupe aryle ayant au moins un atome d'hydrogène substitué par un atome de F et un groupe perfluoroalkyle; m est sélectionné entre 0 et 1; et n entre 0 et 1. Un agrégat comprenant les composés est destabilisé par le biais de la liaison à un enzyme.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008-061849 | 2008-03-11 | ||
JP2008061849 | 2008-03-11 | ||
JP2008-199912 | 2008-08-01 | ||
JP2008199912 | 2008-08-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2009113704A2 WO2009113704A2 (fr) | 2009-09-17 |
WO2009113704A3 true WO2009113704A3 (fr) | 2010-04-15 |
Family
ID=40952624
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2009/054984 WO2009113704A2 (fr) | 2008-03-11 | 2009-03-10 | Composé contenant du fluor et procédé de détection de biomplécule l'utilisant |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP5676853B2 (fr) |
WO (1) | WO2009113704A2 (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8927732B2 (en) * | 2012-03-30 | 2015-01-06 | General Electric Company | Biotin stannane for HPLC-free radioiodination |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0592306A2 (fr) * | 1992-10-06 | 1994-04-13 | Terumo Kabushiki Kaisha | Milieu de contraste pour 19F-MRI |
US5690909A (en) * | 1993-05-24 | 1997-11-25 | Schering Aktiengesellschaft | Fluorine-containing macrocyclic metal complexes |
JPH1067728A (ja) * | 1996-04-18 | 1998-03-10 | Mitsubishi Chem Corp | 含フッ素糖誘導体 |
WO2003045441A1 (fr) * | 2001-11-28 | 2003-06-05 | Amersham Health As | Agents de contraste dans la detection in vivo de l'activite enzymatique |
US20060047126A1 (en) * | 2004-08-20 | 2006-03-02 | Georg Gunda I | Lonidamine analogues and their use in male contraception and cancer treatment |
EP1916255A2 (fr) * | 2006-09-19 | 2008-04-30 | FUJIFILM Corporation | Composant comportant un groupe alkyl à fluorine de substitution et support de constraste liposomale comportant le composant |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9313268D0 (en) * | 1993-06-28 | 1993-08-11 | Zeneca Ltd | Chemical compounds |
JP5172188B2 (ja) * | 2007-03-28 | 2013-03-27 | 富士フイルム株式会社 | フッ素置換アルキル基を有するグリセリド化合物 |
-
2009
- 2009-03-10 WO PCT/JP2009/054984 patent/WO2009113704A2/fr active Application Filing
- 2009-03-11 JP JP2009058775A patent/JP5676853B2/ja active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0592306A2 (fr) * | 1992-10-06 | 1994-04-13 | Terumo Kabushiki Kaisha | Milieu de contraste pour 19F-MRI |
US5690909A (en) * | 1993-05-24 | 1997-11-25 | Schering Aktiengesellschaft | Fluorine-containing macrocyclic metal complexes |
JPH1067728A (ja) * | 1996-04-18 | 1998-03-10 | Mitsubishi Chem Corp | 含フッ素糖誘導体 |
WO2003045441A1 (fr) * | 2001-11-28 | 2003-06-05 | Amersham Health As | Agents de contraste dans la detection in vivo de l'activite enzymatique |
US20060047126A1 (en) * | 2004-08-20 | 2006-03-02 | Georg Gunda I | Lonidamine analogues and their use in male contraception and cancer treatment |
EP1916255A2 (fr) * | 2006-09-19 | 2008-04-30 | FUJIFILM Corporation | Composant comportant un groupe alkyl à fluorine de substitution et support de constraste liposomale comportant le composant |
Non-Patent Citations (6)
Title |
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CURRAN DENNIS P ET AL: "Synthesis and reactions of fluorous carbobenzyloxy (FCbz) derivatives of alpha-amino acids.", JOURNAL OF ORGANIC CHEMISTRY, vol. 68, no. 12, 13 June 2003 (2003-06-13), pages 4643 - 4647, XP002569627, ISSN: 0022-3263 * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; 12 October 2006 (2006-10-12), FLIPO M. ET AL: "A library of novel hydroxamic acids targeting the mettalo-protease family: Design, parallel synthesis and screening", XP002569646, Database accession no. 10584330 * |
DATABASE BEILSTEIN [online] BEILSTEIN INSTITUTE FOR ORGANIC CHEMISTRY, FRANKFURT-MAIN, DE; 19 November 1996 (1996-11-19), XP002569629, Database accession no. 5788690 * |
DOYON J B ET AL: "The pattern of fluorine substitution affects binding affinity in a small library of fluoroaromatic inhibitors for carbonic anhydrase.", ORGANIC LETTERS 29 JUL 1999, vol. 1, no. 2, 29 July 1999 (1999-07-29), pages 183 - 185, XP002569645, ISSN: 1523-7060 * |
OISHI MOTOI ET AL: "On-off regulation of F-19 magnetic resonance signals based on pH-Sensitive PEGylated nanogels for potential tumor-specific smart F-19 MRI probes", BIOCONJUGATE CHEMISTRY, vol. 18, no. 5, September 2007 (2007-09-01), pages 1379 - 1382, XP002569683, ISSN: 1043-1802 * |
YAMAZAKI K ET AL: "Synthesis of potent and selective inhibitors of Candida albicans N-myristoyltransferase based on the benzothiazole structure", BIOORGANIC AND MEDICINAL CHEMISTRY 20050401 GB, vol. 13, no. 7, 1 April 2005 (2005-04-01), pages 2509 - 2522, XP004777464, ISSN: 0968-0896 * |
Also Published As
Publication number | Publication date |
---|---|
JP2010053116A (ja) | 2010-03-11 |
JP5676853B2 (ja) | 2015-02-25 |
WO2009113704A2 (fr) | 2009-09-17 |
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