A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents

A sulfonamide 1-tosyl-1-H-benzo(d)imidazol-2-amine (TBZA) and three new complexes of Co(II), Cu(II), and Zn(II) have been synthesized. The compounds have been characterized by elemental analyses, FTIR, <sup>1</sup>H, and <sup>13</sup>C-NMR spectroscopy. The structure of the T...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Díaz, Jorge R. A., Fernández Baldo, Martín Alejandro, Echeverría, Gustavo Alberto, Baldoni, Héctor Armando, Vullo, Daniela, Soria, Delia Beatriz, Supuran, Claudiu T., Camí, Gerardo Enrique
Formato: Articulo
Lenguaje:Inglés
Publicado: 2016
Materias:
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/103239
https://www.tandfonline.com/doi/full/10.1080/14756366.2016.1187143
Aporte de:
id I19-R120-10915-103239
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Ciencias Exactas
Física
Química
antifungal
carbonic anhydrase
metal complex
sulfonamide
thermal stability
spellingShingle Ciencias Exactas
Física
Química
antifungal
carbonic anhydrase
metal complex
sulfonamide
thermal stability
Díaz, Jorge R. A.
Fernández Baldo, Martín Alejandro
Echeverría, Gustavo Alberto
Baldoni, Héctor Armando
Vullo, Daniela
Soria, Delia Beatriz
Supuran, Claudiu T.
Camí, Gerardo Enrique
A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents
topic_facet Ciencias Exactas
Física
Química
antifungal
carbonic anhydrase
metal complex
sulfonamide
thermal stability
description A sulfonamide 1-tosyl-1-H-benzo(d)imidazol-2-amine (TBZA) and three new complexes of Co(II), Cu(II), and Zn(II) have been synthesized. The compounds have been characterized by elemental analyses, FTIR, <sup>1</sup>H, and <sup>13</sup>C-NMR spectroscopy. The structure of the TBZA, and its Co(II) and Cu(II) complexes, was determined by X-ray diffraction methods. TBZA and its Co(II) complex crystallize in the triclinic P-1 space group, while the Cu(II) complex crystallizes in the monoclinic P2<sub>1</sub>/c space group. Antifungal activity was screened against eight pathogenic yeasts: <i>Candida albicans</i> (DMic 972576), <i>Candida krusei</i> (DMic 951705), <i>Candida glabrata</i> (DMic 982882), <i>Candida tropicalis</i> (DMic 982884), <i>Candida dubliniensis</i> (DMic 93695), <i>Candida guilliermondii</i> (DMic 021150), <i>Cryptococcus neoformans</i> (ATCC 24067), and <i>Cryptococcus gattii</i> (ATCC MYA-4561). Results on the inhibition of various human (h) CAs, hCA I, II, IV, VII, IX, and XII, and pathogenic beta and gamma CAs are also reported.
format Articulo
Articulo
author Díaz, Jorge R. A.
Fernández Baldo, Martín Alejandro
Echeverría, Gustavo Alberto
Baldoni, Héctor Armando
Vullo, Daniela
Soria, Delia Beatriz
Supuran, Claudiu T.
Camí, Gerardo Enrique
author_facet Díaz, Jorge R. A.
Fernández Baldo, Martín Alejandro
Echeverría, Gustavo Alberto
Baldoni, Héctor Armando
Vullo, Daniela
Soria, Delia Beatriz
Supuran, Claudiu T.
Camí, Gerardo Enrique
author_sort Díaz, Jorge R. A.
title A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents
title_short A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents
title_full A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents
title_fullStr A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents
title_full_unstemmed A substituted sulfonamide and its Co (II), Cu (II), and Zn (II) complexes as potential antifungal agents
title_sort substituted sulfonamide and its co (ii), cu (ii), and zn (ii) complexes as potential antifungal agents
publishDate 2016
url http://sedici.unlp.edu.ar/handle/10915/103239
https://www.tandfonline.com/doi/full/10.1080/14756366.2016.1187143
work_keys_str_mv AT diazjorgera asubstitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT fernandezbaldomartinalejandro asubstitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT echeverriagustavoalberto asubstitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT baldonihectorarmando asubstitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT vullodaniela asubstitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT soriadeliabeatriz asubstitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT supuranclaudiut asubstitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT camigerardoenrique asubstitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT diazjorgera substitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT fernandezbaldomartinalejandro substitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT echeverriagustavoalberto substitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT baldonihectorarmando substitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT vullodaniela substitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT soriadeliabeatriz substitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT supuranclaudiut substitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
AT camigerardoenrique substitutedsulfonamideanditscoiicuiiandzniicomplexesaspotentialantifungalagents
bdutipo_str Repositorios
_version_ 1764820441719898113