ES2301840T5 - Porfirinas mesosustituidas. - Google Patents
Porfirinas mesosustituidas. Download PDFInfo
- Publication number
- ES2301840T5 ES2301840T5 ES03769429T ES03769429T ES2301840T5 ES 2301840 T5 ES2301840 T5 ES 2301840T5 ES 03769429 T ES03769429 T ES 03769429T ES 03769429 T ES03769429 T ES 03769429T ES 2301840 T5 ES2301840 T5 ES 2301840T5
- Authority
- ES
- Spain
- Prior art keywords
- phenyl
- porphyrin
- tris
- bis
- decyloxy
- 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
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 107
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 72
- -1 CH2 Inorganic materials 0.000 claims abstract description 59
- 150000001875 compounds Chemical class 0.000 claims abstract description 47
- 229910052751 metal Inorganic materials 0.000 claims abstract description 15
- 239000002184 metal Substances 0.000 claims abstract description 15
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 14
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 8
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 7
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- 150000003839 salts Chemical class 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 6
- 125000005842 heteroatom Chemical group 0.000 claims abstract 4
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 4
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims abstract 3
- 125000006732 (C1-C15) alkyl group Chemical group 0.000 claims abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract 2
- 150000003973 alkyl amines Chemical group 0.000 claims abstract 2
- 125000005210 alkyl ammonium group Chemical group 0.000 claims abstract 2
- 125000004429 atom Chemical group 0.000 claims abstract 2
- 229910052799 carbon Inorganic materials 0.000 claims abstract 2
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 claims abstract 2
- 229910052763 palladium Inorganic materials 0.000 claims abstract 2
- 150000004032 porphyrins Chemical class 0.000 claims description 76
- 230000015572 biosynthetic process Effects 0.000 claims description 57
- 238000003786 synthesis reaction Methods 0.000 claims description 49
- 239000000203 mixture Substances 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 25
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims description 25
- 239000007983 Tris buffer Substances 0.000 claims description 24
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 15
- 238000007306 functionalization reaction Methods 0.000 claims description 15
- 238000002428 photodynamic therapy Methods 0.000 claims description 14
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 13
- 238000011282 treatment Methods 0.000 claims description 13
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 claims description 12
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 12
- 150000001768 cations Chemical class 0.000 claims description 10
- PBTPREHATAFBEN-UHFFFAOYSA-N dipyrromethane Chemical class C=1C=CNC=1CC1=CC=CN1 PBTPREHATAFBEN-UHFFFAOYSA-N 0.000 claims description 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 10
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 125000003277 amino group Chemical group 0.000 claims description 7
- 229940039227 diagnostic agent Drugs 0.000 claims description 6
- 239000000032 diagnostic agent Substances 0.000 claims description 6
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- 150000001413 amino acids Chemical class 0.000 claims description 5
- 239000010836 blood and blood product Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000001544 thienyl group Chemical group 0.000 claims description 5
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- 229940125691 blood product Drugs 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- DXASQZJWWGZNSF-UHFFFAOYSA-N n,n-dimethylmethanamine;sulfur trioxide Chemical group CN(C)C.O=S(=O)=O DXASQZJWWGZNSF-UHFFFAOYSA-N 0.000 claims description 4
- 102000004169 proteins and genes Human genes 0.000 claims description 4
- 108090000623 proteins and genes Proteins 0.000 claims description 4
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- 125000001424 substituent group Chemical group 0.000 claims description 4
- 201000004681 Psoriasis Diseases 0.000 claims description 3
- 230000001413 cellular effect Effects 0.000 claims description 3
- 150000004696 coordination complex Chemical class 0.000 claims description 3
- 150000004676 glycans Chemical class 0.000 claims description 3
- 230000004048 modification Effects 0.000 claims description 3
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- 229920001184 polypeptide Polymers 0.000 claims description 3
- 229920001282 polysaccharide Polymers 0.000 claims description 3
- 239000005017 polysaccharide Substances 0.000 claims description 3
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 3
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 3
- UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical compound I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 claims description 3
- LMYFRTDDHHISFR-UHFFFAOYSA-N 2-[2-(21,23-dihydro-2h-porphyrin-1-yl)phenyl]sulfanyl-n,n-dimethylethanamine Chemical compound CN(C)CCSC1=CC=CC=C1C1(C=C2N=C(C=C2)C=C2C=CC(N2)=CC=2C=CC(N=2)=C2)NC2=CC1 LMYFRTDDHHISFR-UHFFFAOYSA-N 0.000 claims description 2
- 208000037260 Atherosclerotic Plaque Diseases 0.000 claims description 2
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- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 2
- 206010017533 Fungal infection Diseases 0.000 claims description 2
- GMAAGHGZFAFYPB-UHFFFAOYSA-L I.I[Zn]I Chemical compound I.I[Zn]I GMAAGHGZFAFYPB-UHFFFAOYSA-L 0.000 claims description 2
- 208000031888 Mycoses Diseases 0.000 claims description 2
- 208000004403 Prostatic Hyperplasia Diseases 0.000 claims description 2
- 208000036142 Viral infection Diseases 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 208000022362 bacterial infectious disease Diseases 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 2
- 125000004705 ethylthio group Chemical group C(C)S* 0.000 claims description 2
- 206010020718 hyperplasia Diseases 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
- DSNYFFJTZPIKFZ-UHFFFAOYSA-N propoxybenzene Chemical group CCCOC1=CC=CC=C1 DSNYFFJTZPIKFZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003206 sterilizing agent Substances 0.000 claims description 2
- WRTMQOHKMFDUKX-UHFFFAOYSA-N triiodide Chemical compound I[I-]I WRTMQOHKMFDUKX-UHFFFAOYSA-N 0.000 claims description 2
- 230000003612 virological effect Effects 0.000 claims description 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
- DZFWNZJKBJOGFQ-UHFFFAOYSA-N julolidine Chemical compound C1CCC2=CC=CC3=C2N1CCC3 DZFWNZJKBJOGFQ-UHFFFAOYSA-N 0.000 claims 4
- 239000004480 active ingredient Substances 0.000 claims 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims 3
- RSEBUVRVKCANEP-UHFFFAOYSA-N 2-pyrroline Chemical compound C1CC=CN1 RSEBUVRVKCANEP-UHFFFAOYSA-N 0.000 claims 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 2
- ZVJHJDDKYZXRJI-UHFFFAOYSA-N pyrroline Natural products C1CC=NC1 ZVJHJDDKYZXRJI-UHFFFAOYSA-N 0.000 claims 2
- PPNUDMAOXHXNQE-UHFFFAOYSA-N 1-(3-decoxyphenyl)-21,23-dihydro-2H-porphyrin Chemical compound C(CCCCCCCCC)OC=1C=C(C=CC=1)C12CC=C(N1)C=C1C=CC(C=C3C=CC(=CC=4C=CC(=C2)N=4)N3)=N1 PPNUDMAOXHXNQE-UHFFFAOYSA-N 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 229920002521 macromolecule Polymers 0.000 claims 1
- 229910052727 yttrium Inorganic materials 0.000 abstract 2
- 125000005543 phthalimide group Chemical group 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 54
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 51
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 48
- 239000000243 solution Substances 0.000 description 42
- 239000000047 product Substances 0.000 description 41
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 36
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 35
- 238000005160 1H NMR spectroscopy Methods 0.000 description 25
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 24
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 24
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 24
- 238000001704 evaporation Methods 0.000 description 23
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- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 22
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- 239000007832 Na2SO4 Substances 0.000 description 20
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 20
- 229910052938 sodium sulfate Inorganic materials 0.000 description 20
- 235000011152 sodium sulphate Nutrition 0.000 description 20
- 239000012043 crude product Substances 0.000 description 19
- 238000003760 magnetic stirring Methods 0.000 description 18
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 18
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Classifications
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- 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
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- 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
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- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
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- 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
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
Landscapes
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- Radiation-Therapy Devices (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Applications Claiming Priority (2)
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| ITFI02A0200 | 2002-10-21 | ||
| IT000200A ITFI20020200A1 (it) | 2002-10-21 | 2002-10-21 | Porfirine meso-sostituite. |
Publications (2)
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| ES (1) | ES2301840T5 (enExample) |
| IL (1) | IL168104A0 (enExample) |
| IT (1) | ITFI20020200A1 (enExample) |
| PT (1) | PT1558616E (enExample) |
| SI (1) | SI1558616T2 (enExample) |
| WO (1) | WO2004035590A2 (enExample) |
| ZA (1) | ZA200504102B (enExample) |
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| ES2244694T3 (es) * | 2002-04-25 | 2005-12-16 | L. MOLTENI & C. DEI FRATELLI ALITTI SOCIETA' DI ESERCIZIO SOCIETA' PER AZIONI | Composiciones antibacterianas que comprenden analogos de metal ftalocianina. |
| ITFI20020200A1 (it) * | 2002-10-21 | 2004-04-22 | Molteni & C Dei Flii Alitti S P A Societa L | Porfirine meso-sostituite. |
| GB2397067B (en) * | 2002-12-23 | 2005-05-11 | Destiny Pharma Ltd | Porphin & azaporphin derivatives with at least one cationic-nitrogen-containing meso-substituent for use in photodynamic therapy & in vitro sterilisation |
| EP1631572A2 (en) * | 2003-06-06 | 2006-03-08 | Eukarion, Inc. | Orally bioavailable low molecular weight metalloporphyrins as antioxidants |
| GB2415372A (en) * | 2004-06-23 | 2005-12-28 | Destiny Pharma Ltd | Non photodynamical or sonodynamical antimicrobial use of porphyrins and azaporphyrins containing at least one cationic-nitrogen-containing substituent |
| GB2415373A (en) * | 2004-06-23 | 2005-12-28 | Destiny Pharma Ltd | Porphyrins for sonodynamic therapy |
| GB0526474D0 (en) * | 2005-12-24 | 2006-02-08 | Destiny Pharma Ltd | Novel process |
| US7745618B2 (en) | 2007-03-05 | 2010-06-29 | North Carolina State University | Method of making porphyrins |
| EP3459955B1 (en) * | 2008-09-18 | 2022-11-02 | biolitec Unternehmensberatungs II AG | Novel method and application of unsymmetrically meso-substituted porphyrins and chlorins for pdt |
| CN102180881A (zh) * | 2011-03-25 | 2011-09-14 | 西北农林科技大学 | 3,8,13-三碘-5,10,15-三烷基三聚吲哚的制备方法 |
| JP6182775B2 (ja) * | 2011-09-21 | 2017-08-23 | 国立大学法人 岡山大学 | 金属ポルフィリン錯体、その製造方法及びそれからなる二酸化炭素固定化触媒、並びに、環状炭酸エステルの製造方法 |
| CN102499924B (zh) * | 2011-11-23 | 2013-07-24 | 中国医学科学院生物医学工程研究所 | 二乙撑三胺五乙酸或乙二胺四乙酸或胺三乙酸修饰卟啉的用途 |
| US9364537B2 (en) | 2014-08-22 | 2016-06-14 | University Of Dayton | Transition metal porphyrin complexes and methods of treatment using same |
| CN104725388B (zh) * | 2015-03-25 | 2017-03-15 | 南京林业大学 | 一种meso位芳胺基单取代卟啉衍生物及其制备方法 |
| WO2017122697A1 (ja) * | 2016-01-13 | 2017-07-20 | Jsr株式会社 | 感放射線性樹脂組成物、レジストパターン形成方法、酸拡散制御剤及び化合物 |
| CN106117220A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲十二烷氧基桥连异辛烷氧基苯基卟啉金属Zn配合物的合成方法 |
| CN106046010A (zh) * | 2016-06-27 | 2016-10-26 | 桂林理工大学 | 5‑对苯甲酸基‑10, 15, 20‑三对异辛烷氧基苯基卟啉的合成方法 |
| CN106117224A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲十二烷氧基桥连十二烷氧基苯基卟啉二元化合物盘状液晶材料的合成方法 |
| CN106146522A (zh) * | 2016-06-27 | 2016-11-23 | 桂林理工大学 | 苯并菲癸烷氧基桥连十二烷氧基苯基卟啉金属Ni配合物的合成方法 |
| CN105949208A (zh) * | 2016-06-27 | 2016-09-21 | 桂林理工大学 | 苯并菲己烷氧基桥连十二烷氧基苯基卟啉金属Zn配合物的合成方法 |
| CN106047369A (zh) * | 2016-06-27 | 2016-10-26 | 桂林理工大学 | 苯并菲己烷氧基桥连十二烷氧基苯基卟啉二元化合物盘状液晶材料的合成方法 |
| CN106146523A (zh) * | 2016-06-27 | 2016-11-23 | 桂林理工大学 | 苯并菲十二烷氧基桥连十二烷氧基苯基卟啉金属Ni配合物的合成方法 |
| CN106117221A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲己烷氧基桥连异辛烷氧基苯基卟啉金属Ni配合物的合成方法 |
| CN106117228A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲癸烷氧基桥连异辛烷氧基苯基卟啉金属Ni配合物的合成方法 |
| CN105924448A (zh) * | 2016-06-27 | 2016-09-07 | 桂林理工大学 | 苯并菲己烷氧基桥连十二烷氧基苯基卟啉金属Ni配合物的合成方法 |
| CN106117222A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲十二烷氧基桥连异辛烷氧基苯基卟啉二元化合物盘状液晶材料合成方法 |
| CN106117225A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲癸烷氧基桥连异辛烷氧基苯基卟啉金属Zn配合物的合成方法 |
| CN106118688A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲癸烷氧基桥连异辛烷氧基苯基卟啉二元化合物盘状液晶材料的合成方法 |
| CN106117223A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲十二烷氧基桥连异辛烷氧基苯基卟啉金属Ni配合物的合成方法 |
| CN106117227A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲癸烷氧基桥连十二烷氧基苯基卟啉二元化合物盘状液晶材料的合成方法 |
| CN106118689A (zh) * | 2016-06-27 | 2016-11-16 | 桂林理工大学 | 苯并菲己烷氧基桥连异辛烷氧基苯基卟啉二元化合物盘状液晶材料的合成方法 |
| CN106588940A (zh) * | 2016-12-08 | 2017-04-26 | 桂林理工大学 | 苯并菲癸氧基桥连异辛烷氧基苯基卟啉三元化合物盘状液晶材料的合成方法 |
| CN106749284A (zh) * | 2016-12-08 | 2017-05-31 | 桂林理工大学 | 苯并菲十二烷氧基桥连异辛烷氧基苯基卟啉三元化合物盘状液晶材料的合成方法 |
| CN106588941A (zh) * | 2016-12-08 | 2017-04-26 | 桂林理工大学 | 苯并菲十二烷氧基桥连四苯基卟啉三元化合物盘状液晶材料的合成方法 |
| CN106588942A (zh) * | 2016-12-08 | 2017-04-26 | 桂林理工大学 | 并菲癸氧基桥连四苯基卟啉三元化合物盘状液晶材料的合成方法 |
| CN106749285A (zh) * | 2016-12-08 | 2017-05-31 | 桂林理工大学 | 苯并菲己氧基桥连异辛烷氧基苯基卟啉三元化合物盘状液晶材料的合成方法 |
| CN107089987A (zh) * | 2017-04-22 | 2017-08-25 | 桂林理工大学 | 苯并菲己烷氧基桥连异辛烷氧基苯基卟啉金属Zn配合物的合成方法 |
| CN106967075A (zh) * | 2017-04-22 | 2017-07-21 | 桂林理工大学 | 苯并菲癸烷氧基桥连甲氧羰基苯基卟啉金属Zn配合物的合成方法 |
| CN107043381A (zh) * | 2017-04-22 | 2017-08-15 | 桂林理工大学 | 苯并菲十二烷氧基桥连异辛烷氧基苯基卟啉金属Zn配合物的合成方法 |
| CN106905334A (zh) * | 2017-04-22 | 2017-06-30 | 桂林理工大学 | 苯并菲十二烷氧基桥连甲氧羰基苯基卟啉金属Zn配合物的合成方法 |
| CN107011349A (zh) * | 2017-04-22 | 2017-08-04 | 桂林理工大学 | 苯并菲癸烷氧基桥连异辛烷氧基苯基卟啉金属Zn配合物的合成方法 |
| US10722582B2 (en) * | 2018-04-12 | 2020-07-28 | Purdue Research Foundation | Targeted antimicrobial photodynamic therapy |
| CN110354770B (zh) * | 2019-07-23 | 2022-10-04 | 中国石油大学(华东) | 一种人工光合微反应器及制备方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8805849D0 (en) * | 1988-03-11 | 1988-04-13 | Efamol Holdings | Porphyrins & cancer treatment |
| FR2632187B1 (fr) * | 1988-06-02 | 1990-09-14 | Centre Nat Rech Scient | Derives de metalloporphyrines, leur preparation, leur application en therapeutique et leur utilisation pour la preparation de molecules hybrides |
| EP0831891B1 (en) * | 1995-06-07 | 2005-10-19 | Duke University | Oxidant scavengers |
| AU6650198A (en) * | 1997-02-05 | 1998-08-25 | Board Of Regents, The University Of Texas System | Porphyrin compounds as telomerase inhibitors |
| 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 |
| ES2237146T3 (es) * | 1998-08-28 | 2005-07-16 | Destiny Pharma Limited | Derivados de porfirina, su uso en terapia fotodinamica y dispositivos medicos que los contienen. |
| PT1164135E (pt) * | 2000-06-15 | 2004-06-30 | Molteni & C Frat Alitti Soc Es | Metal-ftalocianinas substituidas sua preparacao e utilizacao |
| FR2812637B1 (fr) * | 2000-08-01 | 2002-10-25 | Anulm Ass Nantaise Pour L Util | Nouveaux composes derives de dihydroporphyrine et leurs applications |
| DE60204767T2 (de) | 2001-03-21 | 2006-05-18 | L. Molteni & C. dei Fratelli Alitti Società di Esercizio S.p.A. | Metallsubstituierte, nicht zentrosymmetrische phthalocyanin-analoga, deren herstellung und verwendung zur photodynamischen therapie, und als in-vivo-diagnostikum |
| ITFI20020200A1 (it) * | 2002-10-21 | 2004-04-22 | Molteni & C Dei Flii Alitti S P A Societa L | Porfirine meso-sostituite. |
| GB2397067B (en) * | 2002-12-23 | 2005-05-11 | Destiny Pharma Ltd | Porphin & azaporphin derivatives with at least one cationic-nitrogen-containing meso-substituent for use in photodynamic therapy & in vitro sterilisation |
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2002
- 2002-10-21 IT IT000200A patent/ITFI20020200A1/it unknown
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- 2003-10-21 CN CNA2003801017372A patent/CN1714091A/zh active Pending
- 2003-10-21 JP JP2004544280A patent/JP4751068B2/ja not_active Expired - Fee Related
- 2003-10-21 DE DE60319406T patent/DE60319406T3/de not_active Expired - Lifetime
- 2003-10-21 WO PCT/EP2003/011642 patent/WO2004035590A2/en not_active Ceased
- 2003-10-21 AU AU2003278118A patent/AU2003278118B8/en not_active Ceased
- 2003-10-21 SI SI200331212T patent/SI1558616T2/sl unknown
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- 2003-10-21 DK DK03769429.6T patent/DK1558616T4/da active
- 2003-10-21 ES ES03769429T patent/ES2301840T5/es not_active Expired - Lifetime
- 2003-10-21 PT PT03769429T patent/PT1558616E/pt unknown
- 2003-10-21 EP EP03769429A patent/EP1558616B2/en not_active Expired - Lifetime
- 2003-10-21 CA CA2503223A patent/CA2503223C/en not_active Expired - Fee Related
- 2003-10-21 US US10/532,278 patent/US7947674B2/en not_active Expired - Fee Related
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- 2005-05-20 ZA ZA200504102A patent/ZA200504102B/en unknown
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| WO2004035590A2 (en) | 2004-04-29 |
| AU2003278118B8 (en) | 2009-09-17 |
| AU2003278118A1 (en) | 2004-05-04 |
| US20060040914A1 (en) | 2006-02-23 |
| US7947674B2 (en) | 2011-05-24 |
| IL168104A0 (en) | 2009-02-11 |
| CY1107963T1 (el) | 2013-09-04 |
| ES2301840T3 (es) | 2008-07-01 |
| ATE387450T1 (de) | 2008-03-15 |
| ITFI20020200A1 (it) | 2004-04-22 |
| DE60319406T2 (de) | 2009-03-19 |
| US8288528B2 (en) | 2012-10-16 |
| SI1558616T1 (sl) | 2008-08-31 |
| JP2006512301A (ja) | 2006-04-13 |
| EP1558616B1 (en) | 2008-02-27 |
| CN1714091A (zh) | 2005-12-28 |
| JP4751068B2 (ja) | 2011-08-17 |
| SI1558616T2 (sl) | 2011-12-30 |
| AU2003278118B2 (en) | 2009-05-21 |
| DK1558616T4 (da) | 2011-12-12 |
| CA2503223C (en) | 2010-11-23 |
| DE60319406T3 (de) | 2012-02-23 |
| DK1558616T3 (da) | 2008-06-23 |
| CA2503223A1 (en) | 2004-04-29 |
| PT1558616E (pt) | 2008-05-12 |
| DE60319406D1 (de) | 2008-04-10 |
| EP1558616A2 (en) | 2005-08-03 |
| IT1333697B (enExample) | 2006-05-09 |
| ZA200504102B (en) | 2006-07-26 |
| US20110112464A1 (en) | 2011-05-12 |
| WO2004035590A3 (en) | 2004-07-29 |
| EP1558616B2 (en) | 2011-08-24 |
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