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dc.contributor.author
Testero, Sebastian Andres  
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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  
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Fil: Lee, Mijoon. University of Notre Dame; Estados Unidos  
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Fil: Staran, Rachel T.. University of Notre Dame; Estados Unidos  
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Fil: Espahbodi, Mana. University of Notre Dame; Estados Unidos  
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Fil: Llarrull, Leticia Irene. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario; Argentina. University of Notre Dame; Estados Unidos  
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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  
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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/