Abstract
Previously unknown hydrophilized derivatives of blood porphyrins bearing hydroxyethylamide moieties at the macrocycle periphery were synthesized via the reaction of ethanolamine with dimethyl esters of deuteroporphyrin IX, protoporphyrin IX, and mesoporphyrin IX.
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This work was financially supported by the Ministry of Science and Higher Education of the Russian Federation (State Assignment No. 122040600073-3). The synthesized compounds were analyzed using the equipment of the Center for Collective Use (CCU) “Chemistry” at the Institute of Chemistry of the Federal Research Center “Komi Scientific Centre”, Ural Branch of the Russian Academy of Sciences (Syktyvkar).
No human or animal subjects were used in this research.
The authors declare no competing interests.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, Vol. 72, No. 7, pp. 1612–1617, July, 2023.
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Rocheva, T.K., Belykh, D.V. New amide derivatives of blood porphyrins bearing ethanolamine moieties. Russ Chem Bull 72, 1612–1617 (2023). https://doi.org/10.1007/s11172-023-3941-8
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DOI: https://doi.org/10.1007/s11172-023-3941-8