Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation
ABSTRACT: Malaria is the most important parasitic diseases, affecting almost half of the world. This disease increases in the population of Colombia each year. 5 aromatic compounds were sinthetized, they were evaluated as inhibitor of β-hematin formation and we reported the theoretical study of the...
- Autores:
-
Arango Acosta, Gabriel Jaime
Jaramillo Flórez, María Consuelo
Mora Arango, Cristina Lucía
Bravo Muñoz, Karen Elizabeth
Muñoz Durango, Katalina
Quijano Tobón, Jairo
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2006
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/38201
- Acceso en línea:
- https://hdl.handle.net/10495/38201
- Palabra clave:
- Plasmodium falciparum
Modelos Teóricos
Models, Theoretical
β-hematin
https://id.nlm.nih.gov/mesh/D010963
https://id.nlm.nih.gov/mesh/D008962
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc-nd/2.5/co/
| id |
UDEA2_424872d497aceef858028d11f758324b |
|---|---|
| oai_identifier_str |
oai:bibliotecadigital.udea.edu.co:10495/38201 |
| network_acronym_str |
UDEA2 |
| network_name_str |
Repositorio UdeA |
| repository_id_str |
|
| dc.title.spa.fl_str_mv |
Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation |
| title |
Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation |
| spellingShingle |
Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation Plasmodium falciparum Modelos Teóricos Models, Theoretical β-hematin https://id.nlm.nih.gov/mesh/D010963 https://id.nlm.nih.gov/mesh/D008962 |
| title_short |
Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation |
| title_full |
Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation |
| title_fullStr |
Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation |
| title_full_unstemmed |
Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation |
| title_sort |
Theoretical study of aromatic compounds with inhibitory activity of β-hematin formation |
| dc.creator.fl_str_mv |
Arango Acosta, Gabriel Jaime Jaramillo Flórez, María Consuelo Mora Arango, Cristina Lucía Bravo Muñoz, Karen Elizabeth Muñoz Durango, Katalina Quijano Tobón, Jairo |
| dc.contributor.author.none.fl_str_mv |
Arango Acosta, Gabriel Jaime Jaramillo Flórez, María Consuelo Mora Arango, Cristina Lucía Bravo Muñoz, Karen Elizabeth Muñoz Durango, Katalina Quijano Tobón, Jairo |
| dc.contributor.researchgroup.spa.fl_str_mv |
Grupo de Investigación en Sustancias Bioactivas (GISB) |
| dc.subject.decs.none.fl_str_mv |
Plasmodium falciparum Modelos Teóricos Models, Theoretical |
| topic |
Plasmodium falciparum Modelos Teóricos Models, Theoretical β-hematin https://id.nlm.nih.gov/mesh/D010963 https://id.nlm.nih.gov/mesh/D008962 |
| dc.subject.proposal.spa.fl_str_mv |
β-hematin |
| dc.subject.meshuri.none.fl_str_mv |
https://id.nlm.nih.gov/mesh/D010963 https://id.nlm.nih.gov/mesh/D008962 |
| description |
ABSTRACT: Malaria is the most important parasitic diseases, affecting almost half of the world. This disease increases in the population of Colombia each year. 5 aromatic compounds were sinthetized, they were evaluated as inhibitor of β-hematin formation and we reported the theoretical study of the compounds-hematin aggregated in order to determine how the interaction drug-receptor could be established. Theoretical study using Gaussian 03 shows the interaction between carbonyl oxygen and Fe in the porphyrin ring of hemin. The modification of funtional groups in the compounds changes the inhibition of compounds-hemin aggregated. The geometrical parameters of the complexes are relationed with the inhibitory activity. |
| publishDate |
2006 |
| dc.date.issued.none.fl_str_mv |
2006 |
| dc.date.accessioned.none.fl_str_mv |
2024-02-18T18:59:38Z |
| dc.date.available.none.fl_str_mv |
2024-02-18T18:59:38Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
| dc.type.coar.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
| dc.type.redcol.spa.fl_str_mv |
https://purl.org/redcol/resource_type/ART |
| dc.type.coarversion.spa.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
| dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
| format |
http://purl.org/coar/resource_type/c_2df8fbb1 |
| status_str |
publishedVersion |
| dc.identifier.issn.none.fl_str_mv |
1827-8620 |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/38201 |
| identifier_str_mv |
1827-8620 |
| url |
https://hdl.handle.net/10495/38201 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Pharmacologyonline |
| dc.relation.citationendpage.spa.fl_str_mv |
568 |
| dc.relation.citationstartpage.spa.fl_str_mv |
563 |
| dc.relation.citationvolume.spa.fl_str_mv |
3 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Pharmacologyonline |
| dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/2.5/co/ |
| dc.rights.uri.spa.fl_str_mv |
https://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.rights.accessrights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
| dc.rights.coar.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
| rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/2.5/co/ https://creativecommons.org/licenses/by-nc-nd/4.0/ http://purl.org/coar/access_right/c_abf2 |
| eu_rights_str_mv |
openAccess |
| dc.format.extent.spa.fl_str_mv |
6 páginas |
| dc.format.mimetype.spa.fl_str_mv |
application/pdf |
| dc.publisher.spa.fl_str_mv |
University of Salerno |
| dc.publisher.place.spa.fl_str_mv |
Salerno, Italia |
| institution |
Universidad de Antioquia |
| bitstream.url.fl_str_mv |
https://bibliotecadigital.udea.edu.co/bitstreams/1c0a16ec-33f0-4503-8182-e710cbf15596/download https://bibliotecadigital.udea.edu.co/bitstreams/14ad9435-0a14-491d-aeaa-f3479b7c2c0a/download https://bibliotecadigital.udea.edu.co/bitstreams/38bc8234-123f-4995-a5b8-6d88f0e64981/download https://bibliotecadigital.udea.edu.co/bitstreams/67891d35-56f2-4b9e-ab4f-d85f8f9055f0/download https://bibliotecadigital.udea.edu.co/bitstreams/eba1f947-9353-49ce-9d5a-bf0fc959a690/download |
| bitstream.checksum.fl_str_mv |
b88b088d9957e670ce3b3fbe2eedbc13 8a4605be74aa9ea9d79846c1fba20a33 d3de8538e5149dafd9dce79aaccdc393 d4d9751fca30a511bfadf2642f0387b7 cc28672388da938d1405edf28833b642 |
| bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
| repository.name.fl_str_mv |
Repositorio Institucional de la Universidad de Antioquia |
| repository.mail.fl_str_mv |
aplicacionbibliotecadigitalbiblioteca@udea.edu.co |
| _version_ |
1851052251373633536 |
| spelling |
Arango Acosta, Gabriel JaimeJaramillo Flórez, María ConsueloMora Arango, Cristina LucíaBravo Muñoz, Karen ElizabethMuñoz Durango, KatalinaQuijano Tobón, JairoGrupo de Investigación en Sustancias Bioactivas (GISB)2024-02-18T18:59:38Z2024-02-18T18:59:38Z20061827-8620https://hdl.handle.net/10495/38201ABSTRACT: Malaria is the most important parasitic diseases, affecting almost half of the world. This disease increases in the population of Colombia each year. 5 aromatic compounds were sinthetized, they were evaluated as inhibitor of β-hematin formation and we reported the theoretical study of the compounds-hematin aggregated in order to determine how the interaction drug-receptor could be established. Theoretical study using Gaussian 03 shows the interaction between carbonyl oxygen and Fe in the porphyrin ring of hemin. The modification of funtional groups in the compounds changes the inhibition of compounds-hemin aggregated. The geometrical parameters of the complexes are relationed with the inhibitory activity.COL00103596 páginasapplication/pdfengUniversity of SalernoSalerno, Italiahttp://creativecommons.org/licenses/by-nc-nd/2.5/co/https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Theoretical study of aromatic compounds with inhibitory activity of β-hematin formationArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPlasmodium falciparumModelos TeóricosModels, Theoreticalβ-hematinhttps://id.nlm.nih.gov/mesh/D010963https://id.nlm.nih.gov/mesh/D008962Pharmacologyonline5685633PharmacologyonlinePublicationCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8823https://bibliotecadigital.udea.edu.co/bitstreams/1c0a16ec-33f0-4503-8182-e710cbf15596/downloadb88b088d9957e670ce3b3fbe2eedbc13MD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/14ad9435-0a14-491d-aeaa-f3479b7c2c0a/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADORIGINALJaramilloConsuelo_2006_Theoretical_Study_Aromatic.pdfJaramilloConsuelo_2006_Theoretical_Study_Aromatic.pdfArtículo de investigaciónapplication/pdf177572https://bibliotecadigital.udea.edu.co/bitstreams/38bc8234-123f-4995-a5b8-6d88f0e64981/downloadd3de8538e5149dafd9dce79aaccdc393MD51trueAnonymousREADTEXTJaramilloConsuelo_2006_Theoretical_Study_Aromatic.pdf.txtJaramilloConsuelo_2006_Theoretical_Study_Aromatic.pdf.txtExtracted texttext/plain12321https://bibliotecadigital.udea.edu.co/bitstreams/67891d35-56f2-4b9e-ab4f-d85f8f9055f0/downloadd4d9751fca30a511bfadf2642f0387b7MD54falseAnonymousREADTHUMBNAILJaramilloConsuelo_2006_Theoretical_Study_Aromatic.pdf.jpgJaramilloConsuelo_2006_Theoretical_Study_Aromatic.pdf.jpgGenerated Thumbnailimage/jpeg10671https://bibliotecadigital.udea.edu.co/bitstreams/eba1f947-9353-49ce-9d5a-bf0fc959a690/downloadcc28672388da938d1405edf28833b642MD55falseAnonymousREAD10495/38201oai:bibliotecadigital.udea.edu.co:10495/382012025-03-26 19:22:02.465http://creativecommons.org/licenses/by-nc-nd/2.5/co/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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 |
