ES2311147T3 - Ftalocianinas metalicas boradas, procedimiento para su preparacion, composiciones farmaceuticas que las comprenden y uso de las mismas. - Google Patents
Ftalocianinas metalicas boradas, procedimiento para su preparacion, composiciones farmaceuticas que las comprenden y uso de las mismas. Download PDFInfo
- Publication number
- ES2311147T3 ES2311147T3 ES04719429T ES04719429T ES2311147T3 ES 2311147 T3 ES2311147 T3 ES 2311147T3 ES 04719429 T ES04719429 T ES 04719429T ES 04719429 T ES04719429 T ES 04719429T ES 2311147 T3 ES2311147 T3 ES 2311147T3
- Authority
- ES
- Spain
- Prior art keywords
- phenoxy
- carboran
- methyl
- phthalonitrile
- bis
- 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.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims abstract description 30
- 238000002360 preparation method Methods 0.000 title claims abstract description 23
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 title claims description 10
- 239000002184 metal Substances 0.000 title claims description 10
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 16
- 238000011282 treatment Methods 0.000 claims abstract description 14
- 229910052796 boron Inorganic materials 0.000 claims abstract description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 74
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 73
- 150000001875 compounds Chemical class 0.000 claims description 69
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 claims description 41
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 claims description 37
- 229920006391 phthalonitrile polymer Polymers 0.000 claims description 36
- 239000011701 zinc Substances 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 31
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- 239000007983 Tris buffer Substances 0.000 claims description 16
- 238000002428 photodynamic therapy Methods 0.000 claims description 12
- 238000002560 therapeutic procedure Methods 0.000 claims description 8
- -1 NH 2 Inorganic materials 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 229910052725 zinc Inorganic materials 0.000 claims description 6
- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 claims description 5
- CFNUZRMHHJZBOM-UHFFFAOYSA-N [B]1C2[B][B]C1[B][B][B][B][B][B][B]2 Chemical compound [B]1C2[B][B]C1[B][B][B][B][B][B][B]2 CFNUZRMHHJZBOM-UHFFFAOYSA-N 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 230000001575 pathological effect Effects 0.000 claims description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 2
- PCLITYPZCQBLAC-UHFFFAOYSA-N 3-sulfanylpyrrolidine-2,5-dione Chemical compound SC1CC(=O)NC1=O PCLITYPZCQBLAC-UHFFFAOYSA-N 0.000 claims description 2
- 125000006725 C1-C10 alkenyl group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 claims description 2
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
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- SNKAWJBJQDLSFF-NVKMUCNASA-N 1,2-dioleoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/CCCCCCCC SNKAWJBJQDLSFF-NVKMUCNASA-N 0.000 description 7
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N DMSO Substances CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 7
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 7
- 239000007832 Na2SO4 Substances 0.000 description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- 239000002502 liposome Substances 0.000 description 7
- 239000003504 photosensitizing agent Substances 0.000 description 7
- 229910052938 sodium sulfate Inorganic materials 0.000 description 7
- 235000011152 sodium sulphate Nutrition 0.000 description 7
- 125000001424 substituent group Chemical group 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
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- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 6
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- 239000000725 suspension Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- KILNVBDSWZSGLL-KXQOOQHDSA-N 1,2-dihexadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCC KILNVBDSWZSGLL-KXQOOQHDSA-N 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 4
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 4
- 235000011941 Tilia x europaea Nutrition 0.000 description 4
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- AMXOYNBUYSYVKV-UHFFFAOYSA-M lithium bromide Chemical compound [Li+].[Br-] AMXOYNBUYSYVKV-UHFFFAOYSA-M 0.000 description 4
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- UUIMTYIFGOBYKF-UHFFFAOYSA-N 3-[4-(bromomethyl)phenoxy]benzene-1,2-dicarbonitrile Chemical compound C1=CC(CBr)=CC=C1OC1=CC=CC(C#N)=C1C#N UUIMTYIFGOBYKF-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
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- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
- GUYGJCNTCOUHBK-UHFFFAOYSA-N 3-[3,5-bis(bromomethyl)phenoxy]benzene-1,2-dicarbonitrile Chemical compound BrCC1=CC(CBr)=CC(OC=2C(=C(C#N)C=CC=2)C#N)=C1 GUYGJCNTCOUHBK-UHFFFAOYSA-N 0.000 description 2
- AAWGDBBRKJFKMG-UHFFFAOYSA-N 3-[4-(methylsulfonylmethyl)phenoxy]benzene-1,2-dicarbonitrile Chemical compound C1=CC(CS(=O)(=O)C)=CC=C1OC1=CC=CC(C#N)=C1C#N AAWGDBBRKJFKMG-UHFFFAOYSA-N 0.000 description 2
- DHFCZMUHZPTUOW-UHFFFAOYSA-N 4-[3,5-bis(bromomethyl)phenoxy]benzene-1,2-dicarbonitrile Chemical compound BrCC1=CC(CBr)=CC(OC=2C=C(C(C#N)=CC=2)C#N)=C1 DHFCZMUHZPTUOW-UHFFFAOYSA-N 0.000 description 2
- NGTAGGACDPIXKN-UHFFFAOYSA-N 4-[4-(methylsulfonylmethyl)phenoxy]benzene-1,2-dicarbonitrile Chemical compound C1=CC(CS(=O)(=O)C)=CC=C1OC1=CC=C(C#N)C(C#N)=C1 NGTAGGACDPIXKN-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
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- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 2
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- NFESPLUCWRQSFN-UHFFFAOYSA-N 3-(3,5-dimethylphenoxy)benzene-1,2-dicarbonitrile Chemical compound CC1=CC(C)=CC(OC=2C(=C(C#N)C=CC=2)C#N)=C1 NFESPLUCWRQSFN-UHFFFAOYSA-N 0.000 description 1
- OCNLKRIYTJEXPX-UHFFFAOYSA-N 3-[4-(hydroxymethyl)phenoxy]benzene-1,2-dicarbonitrile Chemical compound C1=CC(CO)=CC=C1OC1=CC=CC(C#N)=C1C#N OCNLKRIYTJEXPX-UHFFFAOYSA-N 0.000 description 1
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- 150000001638 boron Chemical class 0.000 description 1
- ZOXJGFHDIHLPTG-IGMARMGPSA-N boron-11 atom Chemical compound [11B] ZOXJGFHDIHLPTG-IGMARMGPSA-N 0.000 description 1
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- LGAILEFNHXWAJP-BMEPFDOTSA-N macrocycle Chemical group N([C@H]1[C@@H](C)CC)C(=O)C(N=2)=CSC=2CNC(=O)C(=C(O2)C)N=C2[C@H]([C@@H](C)CC)NC(=O)C2=CSC1=N2 LGAILEFNHXWAJP-BMEPFDOTSA-N 0.000 description 1
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Classifications
-
- 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
- C07D487/22—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 four or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K41/00—Medicinal preparations obtained by treating materials with wave energy or particle radiation ; Therapies using these preparations
- A61K41/0057—Photodynamic therapy with a photosensitizer, i.e. agent able to produce reactive oxygen species upon exposure to light or radiation, e.g. UV or visible light; photocleavage of nucleic acids with an agent
- A61K41/0071—PDT with porphyrins having exactly 20 ring atoms, i.e. based on the non-expanded tetrapyrrolic ring system, e.g. bacteriochlorin, chlorin-e6, or phthalocyanines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K41/00—Medicinal preparations obtained by treating materials with wave energy or particle radiation ; Therapies using these preparations
- A61K41/009—Neutron capture therapy, e.g. using uranium or non-boron material
- A61K41/0095—Boron neutron capture therapy, i.e. BNCT, e.g. using boronated porphyrins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/54—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/16—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C317/18—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to acyclic carbon atoms of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/022—Boron compounds without C-boron linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/06—Aluminium compounds
- C07F5/069—Aluminium compounds without C-aluminium linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/025—Silicon compounds without C-silicon linkages
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/045—Special non-pigmentary uses, e.g. catalyst, photosensitisers of phthalocyanine dyes or pigments
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/06—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide
- C09B47/067—Preparation from carboxylic acids or derivatives thereof, e.g. anhydrides, amides, mononitriles, phthalimide, o-cyanobenzamide from phthalodinitriles naphthalenedinitriles, aromatic dinitriles prepared in situ, hydrogenated phthalodinitrile
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/05—Isotopically modified compounds, e.g. labelled
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITFI03A0063 | 2003-03-11 | ||
| IT000063A ITFI20030063A1 (it) | 2003-03-11 | 2003-03-11 | Metallo ftalocianine boronate, loro preparazione, composizioni |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2311147T3 true ES2311147T3 (es) | 2009-02-01 |
Family
ID=32983184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES04719429T Expired - Lifetime ES2311147T3 (es) | 2003-03-11 | 2004-03-11 | Ftalocianinas metalicas boradas, procedimiento para su preparacion, composiciones farmaceuticas que las comprenden y uso de las mismas. |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7842682B2 (enExample) |
| EP (1) | EP1603918B1 (enExample) |
| JP (1) | JP4968673B2 (enExample) |
| CN (1) | CN100374442C (enExample) |
| AT (1) | ATE402936T1 (enExample) |
| AU (1) | AU2004220406B2 (enExample) |
| CA (1) | CA2518934C (enExample) |
| DE (1) | DE602004015428D1 (enExample) |
| DK (1) | DK1603918T3 (enExample) |
| ES (1) | ES2311147T3 (enExample) |
| IL (1) | IL170761A (enExample) |
| IT (1) | ITFI20030063A1 (enExample) |
| PL (1) | PL1603918T3 (enExample) |
| WO (1) | WO2004081014A1 (enExample) |
| ZA (1) | ZA200507975B (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7910755B2 (en) * | 2004-09-29 | 2011-03-22 | Harbor Biosciences, Inc. | Stem cell expansion and uses |
| WO2007098968A1 (en) * | 2006-03-03 | 2007-09-07 | Universität Bremen | Triggered release of liposome contents |
| US8287839B2 (en) | 2006-12-04 | 2012-10-16 | Brookhaven Science Associates, Llc | Carboranylporphyrins and uses thereof |
| CN102284059A (zh) * | 2011-08-23 | 2011-12-21 | 福州大学 | 一种光敏剂及其制备方法和应用 |
| US10723694B2 (en) | 2018-10-02 | 2020-07-28 | Kuwait University | Propargyl-functionalized macrocyclic compounds |
| CN113968878B (zh) * | 2021-11-10 | 2023-07-07 | 中国科学院宁波材料技术与工程研究所 | 超支化硼酸改性的酞腈单体及其制备方法与应用 |
| CN116731315B (zh) * | 2022-03-04 | 2024-06-21 | 中国科学院化学研究所 | 一种含硼邻苯二甲腈树脂及其制备方法和应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3730950A (en) * | 1972-02-01 | 1973-05-01 | Singer Co | Polyurethane copolymers derived from the carborane-silicon phthalocyanine monomer |
| JPH08225751A (ja) * | 1994-10-26 | 1996-09-03 | Nippon Shokubai Co Ltd | 新規フタロシアニン化合物、その製造方法およびそれらを用いた光記録媒体 |
| IT1294325B1 (it) * | 1997-08-14 | 1999-03-24 | Molteni L E C Dei Fratelli Ali | Zinco-ftalocianine e relativi coniugati, preparazione e uso nella terapia fotodinamica e come diagnostici |
-
2003
- 2003-03-11 IT IT000063A patent/ITFI20030063A1/it unknown
-
2004
- 2004-03-11 US US10/548,793 patent/US7842682B2/en not_active Expired - Fee Related
- 2004-03-11 WO PCT/EP2004/002505 patent/WO2004081014A1/en not_active Ceased
- 2004-03-11 CA CA2518934A patent/CA2518934C/en not_active Expired - Fee Related
- 2004-03-11 JP JP2006504641A patent/JP4968673B2/ja not_active Expired - Fee Related
- 2004-03-11 ES ES04719429T patent/ES2311147T3/es not_active Expired - Lifetime
- 2004-03-11 AT AT04719429T patent/ATE402936T1/de active
- 2004-03-11 DE DE602004015428T patent/DE602004015428D1/de not_active Expired - Lifetime
- 2004-03-11 DK DK04719429T patent/DK1603918T3/da active
- 2004-03-11 AU AU2004220406A patent/AU2004220406B2/en not_active Ceased
- 2004-03-11 CN CNB2004800065335A patent/CN100374442C/zh not_active Expired - Fee Related
- 2004-03-11 PL PL04719429T patent/PL1603918T3/pl unknown
- 2004-03-11 EP EP04719429A patent/EP1603918B1/en not_active Expired - Lifetime
-
2005
- 2005-09-08 IL IL170761A patent/IL170761A/en not_active IP Right Cessation
- 2005-10-03 ZA ZA200507975A patent/ZA200507975B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1603918B1 (en) | 2008-07-30 |
| JP4968673B2 (ja) | 2012-07-04 |
| ITFI20030063A1 (it) | 2004-09-12 |
| AU2004220406A1 (en) | 2004-09-23 |
| PL1603918T3 (pl) | 2009-01-30 |
| CN1788009A (zh) | 2006-06-14 |
| JP2006519810A (ja) | 2006-08-31 |
| DK1603918T3 (da) | 2008-11-17 |
| US7842682B2 (en) | 2010-11-30 |
| EP1603918A1 (en) | 2005-12-14 |
| CA2518934A1 (en) | 2004-09-23 |
| WO2004081014A1 (en) | 2004-09-23 |
| IL170761A (en) | 2012-03-29 |
| DE602004015428D1 (de) | 2008-09-11 |
| CN100374442C (zh) | 2008-03-12 |
| CA2518934C (en) | 2012-07-03 |
| AU2004220406B2 (en) | 2010-03-04 |
| ZA200507975B (en) | 2006-12-27 |
| US20060135478A1 (en) | 2006-06-22 |
| US20080009464A9 (en) | 2008-01-10 |
| ATE402936T1 (de) | 2008-08-15 |
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