Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent
- Autores
- Escudero, Graciela Estela; Laino, Carlos Horacio; Martini, Nancy; Echeverría, Gustavo Alberto; Piro, Oscar Enrique; Williams, Patricia Ana María; Ferrer, Evelina Gloria
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- A novel compound for depression treatment and other psychiatric disorders has been obtained being capable of displaying the combined benefits of sertraline and an essential element such as zinc in order to get better antidepressant and negative side effects. Our working group has synthesized a salt formulation (SerH2 ) 2 +[ZnCl4 ] 2- (C34H36N2 Cl8 Zn, sertralonium tetrachlorozincate(II)). The crystal structure was determined by X-ray diffraction methods. It crystallizes in the monoclinic P21 space group with a=7.3869(2) Å, b=13.2888(4) Å, c=19.3541(6) Å, β=96.596(3)° Å, β=91.792(4)°, and Z=2 molecules per unit cell. Their antidepressant activity in the forced swimming test (FST) proved to be stronger than the one shown by the commercial drug sertraline hydrochloride per se. Furthermore, this compound suppressed the anorexigenic effect caused by the antidepressant and showed an improvement in the assimilation time during in vitro fluorescence studies with bovine serum albumin. The results of this work have led to a patent application which was filed (Nº 20150103320) in Argentine country.
Centro de Química Inorgánica
Facultad de Ciencias Exactas
Instituto de Física La Plata - Materia
-
Química
Antidepressant
Drug design
Sertraline derivative
Selective serotonin reuptake inhibitors
Bioavailability - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/95118
Ver los metadatos del registro completo
id |
SEDICI_749d1435b68ccde31a9102ea089cb45d |
---|---|
oai_identifier_str |
oai:sedici.unlp.edu.ar:10915/95118 |
network_acronym_str |
SEDICI |
repository_id_str |
1329 |
network_name_str |
SEDICI (UNLP) |
spelling |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant AgentEscudero, Graciela EstelaLaino, Carlos HoracioMartini, NancyEcheverría, Gustavo AlbertoPiro, Oscar EnriqueWilliams, Patricia Ana MaríaFerrer, Evelina GloriaQuímicaAntidepressantDrug designSertraline derivativeSelective serotonin reuptake inhibitorsBioavailabilityA novel compound for depression treatment and other psychiatric disorders has been obtained being capable of displaying the combined benefits of sertraline and an essential element such as zinc in order to get better antidepressant and negative side effects. Our working group has synthesized a salt formulation (SerH2 ) 2 +[ZnCl4 ] 2- (C34H36N2 Cl8 Zn, sertralonium tetrachlorozincate(II)). The crystal structure was determined by X-ray diffraction methods. It crystallizes in the monoclinic P21 space group with a=7.3869(2) Å, b=13.2888(4) Å, c=19.3541(6) Å, β=96.596(3)° Å, β=91.792(4)°, and Z=2 molecules per unit cell. Their antidepressant activity in the forced swimming test (FST) proved to be stronger than the one shown by the commercial drug sertraline hydrochloride per se. Furthermore, this compound suppressed the anorexigenic effect caused by the antidepressant and showed an improvement in the assimilation time during in vitro fluorescence studies with bovine serum albumin. The results of this work have led to a patent application which was filed (Nº 20150103320) in Argentine country.Centro de Química InorgánicaFacultad de Ciencias ExactasInstituto de Física La Plata2017-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1-11http://sedici.unlp.edu.ar/handle/10915/95118enginfo:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/66990info:eu-repo/semantics/altIdentifier/url/https://www.jscimedcentral.com/MedicinalChemistry/medicinalchemistry-3-1017.pdfinfo:eu-repo/semantics/altIdentifier/issn/2378-9336info:eu-repo/semantics/altIdentifier/hdl/11336/66990info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T10:52:32Zoai:sedici.unlp.edu.ar:10915/95118Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 10:52:32.673SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent |
title |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent |
spellingShingle |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent Escudero, Graciela Estela Química Antidepressant Drug design Sertraline derivative Selective serotonin reuptake inhibitors Bioavailability |
title_short |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent |
title_full |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent |
title_fullStr |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent |
title_full_unstemmed |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent |
title_sort |
Zn(II) Based Potential Drug Containing Sertraline as a Strong Antidepressant Agent |
dc.creator.none.fl_str_mv |
Escudero, Graciela Estela Laino, Carlos Horacio Martini, Nancy Echeverría, Gustavo Alberto Piro, Oscar Enrique Williams, Patricia Ana María Ferrer, Evelina Gloria |
author |
Escudero, Graciela Estela |
author_facet |
Escudero, Graciela Estela Laino, Carlos Horacio Martini, Nancy Echeverría, Gustavo Alberto Piro, Oscar Enrique Williams, Patricia Ana María Ferrer, Evelina Gloria |
author_role |
author |
author2 |
Laino, Carlos Horacio Martini, Nancy Echeverría, Gustavo Alberto Piro, Oscar Enrique Williams, Patricia Ana María Ferrer, Evelina Gloria |
author2_role |
author author author author author author |
dc.subject.none.fl_str_mv |
Química Antidepressant Drug design Sertraline derivative Selective serotonin reuptake inhibitors Bioavailability |
topic |
Química Antidepressant Drug design Sertraline derivative Selective serotonin reuptake inhibitors Bioavailability |
dc.description.none.fl_txt_mv |
A novel compound for depression treatment and other psychiatric disorders has been obtained being capable of displaying the combined benefits of sertraline and an essential element such as zinc in order to get better antidepressant and negative side effects. Our working group has synthesized a salt formulation (SerH2 ) 2 +[ZnCl4 ] 2- (C34H36N2 Cl8 Zn, sertralonium tetrachlorozincate(II)). The crystal structure was determined by X-ray diffraction methods. It crystallizes in the monoclinic P21 space group with a=7.3869(2) Å, b=13.2888(4) Å, c=19.3541(6) Å, β=96.596(3)° Å, β=91.792(4)°, and Z=2 molecules per unit cell. Their antidepressant activity in the forced swimming test (FST) proved to be stronger than the one shown by the commercial drug sertraline hydrochloride per se. Furthermore, this compound suppressed the anorexigenic effect caused by the antidepressant and showed an improvement in the assimilation time during in vitro fluorescence studies with bovine serum albumin. The results of this work have led to a patent application which was filed (Nº 20150103320) in Argentine country. Centro de Química Inorgánica Facultad de Ciencias Exactas Instituto de Física La Plata |
description |
A novel compound for depression treatment and other psychiatric disorders has been obtained being capable of displaying the combined benefits of sertraline and an essential element such as zinc in order to get better antidepressant and negative side effects. Our working group has synthesized a salt formulation (SerH2 ) 2 +[ZnCl4 ] 2- (C34H36N2 Cl8 Zn, sertralonium tetrachlorozincate(II)). The crystal structure was determined by X-ray diffraction methods. It crystallizes in the monoclinic P21 space group with a=7.3869(2) Å, b=13.2888(4) Å, c=19.3541(6) Å, β=96.596(3)° Å, β=91.792(4)°, and Z=2 molecules per unit cell. Their antidepressant activity in the forced swimming test (FST) proved to be stronger than the one shown by the commercial drug sertraline hydrochloride per se. Furthermore, this compound suppressed the anorexigenic effect caused by the antidepressant and showed an improvement in the assimilation time during in vitro fluorescence studies with bovine serum albumin. The results of this work have led to a patent application which was filed (Nº 20150103320) in Argentine country. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-05 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/95118 |
url |
http://sedici.unlp.edu.ar/handle/10915/95118 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://ri.conicet.gov.ar/11336/66990 info:eu-repo/semantics/altIdentifier/url/https://www.jscimedcentral.com/MedicinalChemistry/medicinalchemistry-3-1017.pdf info:eu-repo/semantics/altIdentifier/issn/2378-9336 info:eu-repo/semantics/altIdentifier/hdl/11336/66990 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
dc.format.none.fl_str_mv |
application/pdf 1-11 |
dc.source.none.fl_str_mv |
reponame:SEDICI (UNLP) instname:Universidad Nacional de La Plata instacron:UNLP |
reponame_str |
SEDICI (UNLP) |
collection |
SEDICI (UNLP) |
instname_str |
Universidad Nacional de La Plata |
instacron_str |
UNLP |
institution |
UNLP |
repository.name.fl_str_mv |
SEDICI (UNLP) - Universidad Nacional de La Plata |
repository.mail.fl_str_mv |
alira@sedici.unlp.edu.ar |
_version_ |
1842260407573544960 |
score |
13.13397 |