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Sökning: WFRF:(Durrant J. R.) > Novel Cruzain Inhib...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002542naa a2200421 4500
001oai:DiVA.org:uu-179897
003SwePub
008120827s2012 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1798972 URI
024a https://doi.org/10.1111/j.1747-0285.2012.01416.x2 DOI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Rogers, Kathleen E.4 aut
2451 0a Novel Cruzain Inhibitors for the Treatment of Chagas' Disease
264 c 2012-06-27
264 1b Wiley,c 2012
338 a print2 rdacarrier
520 a The protozoan parasite Trypanosoma cruzi, the etiological agent of Chagas disease, affects millions of individuals and continues to be an important global health concern. The poor efficacy and unfavorable side effects of current treatments necessitate novel therapeutics. Cruzain, the major cysteine protease of T.similar to cruzi, is one potential novel target. Recent advances in a class of vinyl sulfone inhibitors are encouraging; however, as most potential therapeutics fail in clinical trials and both disease progression and resistance call for combination therapy with several drugs, the identification of additional classes of inhibitory molecules is essential. Using an exhaustive virtual-screening and experimental validation approach, we identify several additional small-molecule cruzain inhibitors. Further optimization of these chemical scaffolds could lead to the development of novel drugs useful in the treatment of Chagas disease.
653 a Chagas' disease
653 a computer-aided drug discovery
653 a cruzain
653 a cruzipain
653 a cysteine protease inhibitor
653 a Trypanosoma cruzi
700a Keränen, Henriku Uppsala universitet,Beräknings- och systembiologi4 aut0 (Swepub:uu)henke383
700a Durrant, Jacob D.4 aut
700a Ratnam, Joseline4 aut
700a Doak, Allison4 aut
700a Arkin, Michelle R.4 aut
700a McCammon, J. Andrew4 aut
710a Uppsala universitetb Beräknings- och systembiologi4 org
773t Chemical Biology and Drug Designd : Wileyg 80:3, s. 398-405q 80:3<398-405x 1747-0277x 1747-0285
856u https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/j.1747-0285.2012.01416.x
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-179897
8564 8u https://doi.org/10.1111/j.1747-0285.2012.01416.x

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