2019
DOI: 10.1134/s1070363219090354
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Chemical Transformations of Chlorophyll a and Possible Areas for Application of Its Derivatives

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Cited by 6 publications
(4 citation statements)
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“…Several boron-containing chlorophyll a derivatives have been investigated [ 49 ], including chlorins 14 and 1 5 , shown in Figure 6 . Similar to porphyrins, this type of compound also binds to LDL [ 50 ], and as a result typically shows preferential accumulation in tumor cells.…”
Section: Porphyrin Derivatives For Bnctmentioning
confidence: 99%
“…Several boron-containing chlorophyll a derivatives have been investigated [ 49 ], including chlorins 14 and 1 5 , shown in Figure 6 . Similar to porphyrins, this type of compound also binds to LDL [ 50 ], and as a result typically shows preferential accumulation in tumor cells.…”
Section: Porphyrin Derivatives For Bnctmentioning
confidence: 99%
“…Nowadays, of particular importance is the use of tetrapyrrole macroheterocycles for biomedical pur­poses. Apart from the well-established efficiency of porphyrin-based photodynamic therapy agents [ 6 – 17 ], the ability of these compounds to inactivate various viruses, including SARS-CoV-2, opens prospects of creating new alternative approaches to the treatment of drug-resistant viral and bacterial infections [ 18 20 ].…”
Section: Introductionmentioning
confidence: 99%
“…Thus, the unique properties of chlorophyll a and bacteriochlorophyll a have opened up wide possibilities for creating photosensitizers for antimicrobial and anti­cancer photodynamic therapy [ 6 , 7 ]. Chemical mod­ifica­tion of the peripheral substituents of the original natural macroheterocycle can significantly increase the stability of its derivatives, increase the affinity for malignant neoplasms, and improve physicochemical properties [ 8 – 17 ].…”
Section: Introductionmentioning
confidence: 99%
“…Just as no review can claim an absolute coverage of available data in the area under consideration, our review did not consider the results for some specific very important results for MPXs/MPcXs as molecular materials. We are here obliged to cite significant works on the study and the application of the porphyrin/phthalocyanine sensitizers for PDT/diagnostics, [180][181][182][183][184][185][186][187] the catalysts based on the porphyrin/phthalocyanine complexes of rhenium [188][189][190][191] and iridium [192,193] for redox reactions that are beyond the scope of our review, and the shift reagents based on REE porphyrin complexes in NMR. [194][195][196] Regarding our review, that is the first review of the fundamental parameters and the properties of axially bonded MPs/phthalocyanines for use in their molecular material chemistry.…”
mentioning
confidence: 99%