New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity

This work studied the synthesis of 5,10,15-tris(4-aminophenyl)-20-(N,N-dialkyl/diaryl-N-phenylurea) porphyrins (P1-P4 with alkyl or aryl groups of Ph, iPr, Et and Me, respectively) and also the preparation of their manganese (III) and cobalt (II) complexes (MnP and CoP). The P1-P4 ligands were chara...

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Main Authors: Gholamreza Karimipour, Saeed Kowkabi, Asghar Naghiha
Format: Article
Language:English
Published: Instituto de Tecnologia do Paraná (Tecpar) 2015-06-01
Series:Brazilian Archives of Biology and Technology
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132015000300431&lng=en&tlng=en
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spelling doaj-236a766b8cec446c98e04aeafad01a792020-11-24T23:11:13ZengInstituto de Tecnologia do Paraná (Tecpar)Brazilian Archives of Biology and Technology1678-43242015-06-0158343144210.1590/S1516-8913201500024S1516-89132015000300431New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activityGholamreza KarimipourSaeed KowkabiAsghar NaghihaThis work studied the synthesis of 5,10,15-tris(4-aminophenyl)-20-(N,N-dialkyl/diaryl-N-phenylurea) porphyrins (P1-P4 with alkyl or aryl groups of Ph, iPr, Et and Me, respectively) and also the preparation of their manganese (III) and cobalt (II) complexes (MnP and CoP). The P1-P4 ligands were characterized by different spectroscopic techniques (1H NMR, FTIR, UV-Vis) and elemental analysis, and metalated with Mn and Co acetate salts. The antibacterial and antifungal activities of these compounds in vitro were investigated by agar-disc diffusion method against Escherichia coli (-), Pseudomonas aeruginosa (-), Staphylococcus aureus(+), Bacillus subtilis (+) and Aspergillus oryzae and Candida albicans. Results showed that antibacterial and antifungal activity of the test samples increased with increase of their concentrations and the highest activity was obtained when the concentration of porphyrin compounds was 100 µg/mL. The activity for the porphyrin ligands depended on the nature of the urea derivative substituents and increased in the order P1 > P2 > P3 >P4, which was consistent with the order of their liposolubility. MnP and CoP complexes exhibited much higher antibacterial and antifungal activity than P1-P4ligands. Further, the growth inhibitory effects of these compounds was generally in the order CoP complexes > MnP complexes > P1-P4 ligands. Among these porphyrin compounds, CoP1displayed the highest antibacterial and antifungal activity, especially with a concentration of 100 µg/mL, against all the four tested bacteria and two fungi, and therefore it could be potential to be used as drug.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132015000300431&lng=en&tlng=enPorphyrinAminoporphyrinsAntibacterial/Antifungal ActivitySynthesisCarbamoyl Chloride
collection DOAJ
language English
format Article
sources DOAJ
author Gholamreza Karimipour
Saeed Kowkabi
Asghar Naghiha
spellingShingle Gholamreza Karimipour
Saeed Kowkabi
Asghar Naghiha
New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
Brazilian Archives of Biology and Technology
Porphyrin
Aminoporphyrins
Antibacterial/Antifungal Activity
Synthesis
Carbamoyl Chloride
author_facet Gholamreza Karimipour
Saeed Kowkabi
Asghar Naghiha
author_sort Gholamreza Karimipour
title New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
title_short New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
title_full New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
title_fullStr New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
title_full_unstemmed New aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
title_sort new aminoporphyrins bearing urea derivative substituents: synthesis, characterization, antibacterial and antifungal activity
publisher Instituto de Tecnologia do Paraná (Tecpar)
series Brazilian Archives of Biology and Technology
issn 1678-4324
publishDate 2015-06-01
description This work studied the synthesis of 5,10,15-tris(4-aminophenyl)-20-(N,N-dialkyl/diaryl-N-phenylurea) porphyrins (P1-P4 with alkyl or aryl groups of Ph, iPr, Et and Me, respectively) and also the preparation of their manganese (III) and cobalt (II) complexes (MnP and CoP). The P1-P4 ligands were characterized by different spectroscopic techniques (1H NMR, FTIR, UV-Vis) and elemental analysis, and metalated with Mn and Co acetate salts. The antibacterial and antifungal activities of these compounds in vitro were investigated by agar-disc diffusion method against Escherichia coli (-), Pseudomonas aeruginosa (-), Staphylococcus aureus(+), Bacillus subtilis (+) and Aspergillus oryzae and Candida albicans. Results showed that antibacterial and antifungal activity of the test samples increased with increase of their concentrations and the highest activity was obtained when the concentration of porphyrin compounds was 100 µg/mL. The activity for the porphyrin ligands depended on the nature of the urea derivative substituents and increased in the order P1 > P2 > P3 >P4, which was consistent with the order of their liposolubility. MnP and CoP complexes exhibited much higher antibacterial and antifungal activity than P1-P4ligands. Further, the growth inhibitory effects of these compounds was generally in the order CoP complexes > MnP complexes > P1-P4 ligands. Among these porphyrin compounds, CoP1displayed the highest antibacterial and antifungal activity, especially with a concentration of 100 µg/mL, against all the four tested bacteria and two fungi, and therefore it could be potential to be used as drug.
topic Porphyrin
Aminoporphyrins
Antibacterial/Antifungal Activity
Synthesis
Carbamoyl Chloride
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132015000300431&lng=en&tlng=en
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