AU2001284466A1 - Tetraphenylbacteriochlorin derivatives and compositions containing the same - Google Patents
Tetraphenylbacteriochlorin derivatives and compositions containing the sameInfo
- Publication number
- AU2001284466A1 AU2001284466A1 AU2001284466A AU8446601A AU2001284466A1 AU 2001284466 A1 AU2001284466 A1 AU 2001284466A1 AU 2001284466 A AU2001284466 A AU 2001284466A AU 8446601 A AU8446601 A AU 8446601A AU 2001284466 A1 AU2001284466 A1 AU 2001284466A1
- Authority
- AU
- Australia
- Prior art keywords
- same
- compositions containing
- tetraphenylbacteriochlorin
- chem
- salt
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/20—Carbocyclic rings
- C07H15/203—Monocyclic carbocyclic rings other than cyclohexane rings; Bicyclic carbocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/26—Acyclic or carbocyclic radicals, substituted by hetero rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Provided is a tetraphenylbacteriochlorin derivative represented by the formula (I): <CHEM> Äwherein R<1>, R<2>, R<3> and R<4>, independently from each other, are a residue of a monosaccharide represented by the formulae: <CHEM> (wherein, R is a hydrogen or a protecting group)Ü, or its salt. The tetraphenylbacteriochlorin derivative or its salt has a large molar extinction coefficient at long wavelengths which are expected to have a high tissue-penetrating property, and exhibits high selectivity to tumor cells and hydrophilicity. <IMAGE>
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000273649 | 2000-09-08 | ||
JP2000-273649 | 2000-09-08 | ||
PCT/JP2001/007758 WO2002020536A1 (en) | 2000-09-08 | 2001-09-06 | Tetraphenylbacteriochlorin derivatives and compositions containing the same |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001284466A1 true AU2001284466A1 (en) | 2002-03-22 |
Family
ID=18759554
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001284466A Abandoned AU2001284466A1 (en) | 2000-09-08 | 2001-09-06 | Tetraphenylbacteriochlorin derivatives and compositions containing the same |
Country Status (7)
Country | Link |
---|---|
US (2) | US6958389B2 (en) |
EP (1) | EP1316558B9 (en) |
JP (1) | JP4944348B2 (en) |
AT (1) | ATE302209T1 (en) |
AU (1) | AU2001284466A1 (en) |
DE (1) | DE60112769T2 (en) |
WO (1) | WO2002020536A1 (en) |
Families Citing this family (8)
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US8287839B2 (en) * | 2006-12-04 | 2012-10-16 | Brookhaven Science Associates, Llc | Carboranylporphyrins and uses thereof |
US20090318370A1 (en) * | 2007-02-19 | 2009-12-24 | Rei Medical Co., Ltd. | Novel glycoconjugated chlorin derivatives and method of producing the same |
US8444953B2 (en) * | 2007-03-22 | 2013-05-21 | Brookhaven Science Associates, Llc | Symmetric and asymmetric halogen-containing metallocarboranylporphyrins and uses thereof |
US20080279781A1 (en) * | 2007-05-10 | 2008-11-13 | Brookhaven Science Associates, Llc | Glycosylated Carboranylporphyrins and Uses Thereof |
JP6041360B2 (en) * | 2011-07-22 | 2016-12-07 | バイオリテック ウンターネーメンスベタイリグンクス ツヴァイ アクツィエンゲゼルシャフト | Sugar-substituted dihydroxy-chlorins and β-functionalized chlorins for antibacterial photodynamic therapy |
CN102558187B (en) * | 2011-12-29 | 2014-02-26 | 东华大学 | Tetrahydroporphin compound and preparation method and application thereof |
CN108715591B (en) * | 2018-06-01 | 2021-04-13 | 华东理工大学 | Near infrared absorbing porphyrin compounds as photosensitizers and uses thereof |
CN109481696B (en) * | 2018-12-22 | 2020-10-02 | 吉林大学 | Medicine for cancer photodynamic therapy and chemotherapy and preparation method thereof |
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US5648485A (en) * | 1994-10-26 | 1997-07-15 | University Of British Columbia | β, β-dihydroxy meso-substituted chlorins, isobacteriochlorins, and bacteriochlorins |
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-
2001
- 2001-09-06 DE DE60112769T patent/DE60112769T2/en not_active Expired - Lifetime
- 2001-09-06 EP EP01963492A patent/EP1316558B9/en not_active Expired - Lifetime
- 2001-09-06 AU AU2001284466A patent/AU2001284466A1/en not_active Abandoned
- 2001-09-06 WO PCT/JP2001/007758 patent/WO2002020536A1/en active IP Right Grant
- 2001-09-06 US US10/363,824 patent/US6958389B2/en not_active Expired - Fee Related
- 2001-09-06 AT AT01963492T patent/ATE302209T1/en not_active IP Right Cessation
- 2001-09-06 JP JP2002525157A patent/JP4944348B2/en not_active Expired - Fee Related
-
2005
- 2005-09-07 US US11/219,853 patent/US7157432B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
DE60112769D1 (en) | 2005-09-22 |
DE60112769T2 (en) | 2006-06-08 |
EP1316558B9 (en) | 2005-12-07 |
EP1316558B1 (en) | 2005-08-17 |
EP1316558A4 (en) | 2004-04-07 |
US20030171305A1 (en) | 2003-09-11 |
ATE302209T1 (en) | 2005-09-15 |
US7157432B2 (en) | 2007-01-02 |
JPWO2002020536A1 (en) | 2004-01-15 |
US6958389B2 (en) | 2005-10-25 |
US20060003946A1 (en) | 2006-01-05 |
WO2002020536A1 (en) | 2002-03-14 |
JP4944348B2 (en) | 2012-05-30 |
EP1316558A1 (en) | 2003-06-04 |
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