Sobotta et al., 2019 - Google Patents
Optical properties of a series of pyrrolyl-substituted porphyrazines and their photoinactivation potential against Enterococcus faecalis after incorporation into …Sobotta et al., 2019
- Document ID
- 3696716409081610857
- Author
- Sobotta L
- Dlugaszewska J
- Ziental D
- Szczolko W
- Koczorowski T
- Goslinski T
- Mielcarek J
- Publication year
- Publication venue
- Journal of Photochemistry and Photobiology A: Chemistry
External Links
Snippet
A series of porphyrazines substituted in the periphery with various pyrrolyl groups was studied regarding its optical properties and biological potential for antimicrobial photodynamic therapy towards Enterococcus faecalis. There were studied magnesium (II) …
- 241000194032 Enterococcus faecalis 0 title abstract description 23
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET 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, rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/409—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil having four such rings, e.g. phorphine derivatives, bilirubin, biliverdine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET 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, rifamycins
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET 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 TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET 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
- A61K41/0076—PDT with expanded (metallo)porphyrins, i.e. having more than 20 ring atoms, e.g. texaphyrins, sapphyrins, hexaphyrins, pentaphyrins, porphocyanines
-
- 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 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 C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Sobotta et al. | Optical properties of a series of pyrrolyl-substituted porphyrazines and their photoinactivation potential against Enterococcus faecalis after incorporation into liposomes | |
| Costa et al. | Comparative photodynamic inactivation of antibiotic resistant bacteria by first and second generation cationic photosensitizers | |
| Uliana et al. | Photobiological characteristics of chlorophyll a derivatives as microbial PDT agents | |
| Pucelik et al. | Properties of halogenated and sulfonated porphyrins relevant for the selection of photosensitizers in anticancer and antimicrobial therapies | |
| Tavares et al. | Mechanisms of photodynamic inactivation of a Gram-negative recombinant bioluminescent bacterium by cationic porphyrins | |
| Ferreyra et al. | Synthesis and properties of 5, 10, 15, 20-tetrakis [4-(3-N, N-dimethylaminopropoxy) phenyl] chlorin as potential broad-spectrum antimicrobial photosensitizers | |
| Lazzeri et al. | Photodynamic Studies and Photoinactivation of Escherichia coli Using meso‐Substituted Cationic Porphyrin Derivatives with Asymmetric Charge Distribution¶ | |
| Huang et al. | Stable synthetic mono-substituted cationic bacteriochlorins mediate selective broad-spectrum photoinactivation of drug-resistant pathogens at nanomolar concentrations | |
| Piskorz et al. | BODIPY‐Based Photosensitizers as Potential Anticancer and Antibacterial Agents: Role of the Positive Charge and the Heavy Atom Effect | |
| Mesquita et al. | Photodynamic inactivation of bioluminescent Escherichia coli by neutral and cationic pyrrolidine-fused chlorins and isobacteriochlorins | |
| Sobotta et al. | Lipid vesicle-loaded meso-substituted chlorins of high in vitro antimicrobial photodynamic activity | |
| US8940775B2 (en) | Use of derivatives of pentaphyrine as antimicrobial and disinfectant agents | |
| Sobotta et al. | Photodynamic inactivation of Enterococcus faecalis by non-peripherally substituted magnesium phthalocyanines entrapped in lipid vesicles | |
| Zhdanova et al. | Synthesis and photodynamic antimicrobial activity of amphiphilic meso-arylporphyrins with pyridyl moieties | |
| Gsponer et al. | Approaches to unravel pathways of reactive oxygen species in the photoinactivation of bacteria induced by a dicationic fulleropyrrolidinium derivative | |
| Ribeiro et al. | Unsymmetrical cationic porphyrin-cyclodextrin bioconjugates for photoinactivation of Escherichia coli | |
| Calmeiro et al. | Versatile thiopyridyl/pyridinone porphyrins combined with potassium iodide and thiopyridinium/methoxypyridinium porphyrins on E. coli photoinactivation | |
| Santos et al. | Pyrazole-pyridinium porphyrins and chlorins as powerful photosensitizers for photoinactivation of planktonic and biofilm forms of E. coli | |
| Sobotta et al. | In vitro photodynamic activity of lipid vesicles with zinc phthalocyanine derivative against Enterococcus faecalis | |
| Farajzadeh et al. | Photophysicochemical, sonochemical, and biological properties of novel hexadeca-substituted phthalocyanines bearing fluorinated groups | |
| Wieczorek et al. | Photophysical properties and photocytotoxicity of free and liposome-entrapped diazepinoporphyrazines on LNCaP cells under normoxic and hypoxic conditions | |
| Szymczak et al. | Menthol modified zinc (II) phthalocyanine regioisomers and their photoinduced antimicrobial activity against Staphylococcus aureus | |
| Scanone et al. | Porphyrins containing basic aliphatic amino groups as potential broad-spectrum antimicrobial agents | |
| van de Winckel et al. | Octacationic and axially di-substituted silicon (IV) phthalocyanines for photodynamic inactivation of bacteria | |
| Baigorria et al. | Synthesis, spectroscopic properties and photodynamic activity of Zn (II) phthalocyanine-polymer conjugates as antimicrobial agents |