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dc.contributor.author
Testero, Sebastian Andres
dc.contributor.author
Lee, Mijoon
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Staran, Rachel T.
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Espahbodi, Mana
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Llarrull, Leticia Irene
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Toth, Marta
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Mobashery, Shahriar
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Chang, Mayland
dc.date.available
2021-03-08T13:47:53Z
dc.date.issued
2011-02
dc.identifier.citation
Testero, Sebastian Andres; Lee, Mijoon; Staran, Rachel T.; Espahbodi, Mana; Llarrull, Leticia Irene; et al.; Sulfonate-Containing Thiiranes as Selective Gelatinase Inhibitors; American Chemical Society; ACS Medicinal Chemistry Letters; 2; 2; 2-2011; 177-181
dc.identifier.issn
1948-5875
dc.identifier.uri
http://hdl.handle.net/11336/127718
dc.description.abstract
Matrix metalloproteinases (MMPs) are important zinc-dependent endopeptidases. Two members of this family of enzymes called gelatinases (MMP-2 and MMP-9) have been implicated in a number of human diseases, including cancer, neurological and cardiovascular diseases, and inflammation, to name a few. We describe in this report the preparation and evaluation of two structural types of thiirane inhibitors that show selectivity toward gelatinases. The biphenyl series targets both gelatinases, whereas the monophenyl analogues exhibit potent inhibition of only MMP-2. The latter structural type also exhibits improved water solubility and metabolic stability, both traits desirable for progress of these molecules forward in gelatinase-dependent animal models of disease.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
American Chemical Society
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
MATRIX METALLOPROTEINASES
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SLOW-BINDING GELATINASE INHIBITORS
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THIIRANES
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Química Orgánica
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Sulfonate-Containing Thiiranes as Selective Gelatinase Inhibitors
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2021-02-18T15:20:52Z
dc.journal.volume
2
dc.journal.number
2
dc.journal.pagination
177-181
dc.journal.pais
Estados Unidos
dc.journal.ciudad
Washington DC
dc.description.fil
Fil: Testero, Sebastian Andres. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina. University of Notre Dame; Estados Unidos
dc.description.fil
Fil: Lee, Mijoon. University of Notre Dame; Estados Unidos
dc.description.fil
Fil: Staran, Rachel T.. University of Notre Dame; Estados Unidos
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Fil: Espahbodi, Mana. University of Notre Dame; Estados Unidos
dc.description.fil
Fil: Llarrull, Leticia Irene. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. University of Notre Dame; Estados Unidos
dc.description.fil
Fil: Toth, Marta. University of Notre Dame; Estados Unidos
dc.description.fil
Fil: Mobashery, Shahriar. University of Notre Dame; Estados Unidos
dc.description.fil
Fil: Chang, Mayland. University of Notre Dame; Estados Unidos
dc.journal.title
ACS Medicinal Chemistry Letters
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/ml100254e
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1021/ml100254e
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018095/
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