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Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0cc01276a
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dc.titleClick-based synthesis and proteomic profiling of lipstatin analogues
dc.contributor.authorNgai, M.H.
dc.contributor.authorYang, P.-Y.
dc.contributor.authorLiu, K.
dc.contributor.authorShen, Y.
dc.contributor.authorWenk, M.R.
dc.contributor.authorYao, S.Q.
dc.contributor.authorLear, M.J.
dc.date.accessioned2014-06-23T05:34:20Z
dc.date.available2014-06-23T05:34:20Z
dc.date.issued2010-11-28
dc.identifier.citationNgai, M.H., Yang, P.-Y., Liu, K., Shen, Y., Wenk, M.R., Yao, S.Q., Lear, M.J. (2010-11-28). Click-based synthesis and proteomic profiling of lipstatin analogues. Chemical Communications 46 (44) : 8335-8337. ScholarBank@NUS Repository. https://doi.org/10.1039/c0cc01276a
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75762
dc.description.abstractUsing click chemistry to enable both structural diversity and proteome profiling within a natural product derived library, two out of nineteen lipstatin analogues showed similar activity to Orlistat against fatty acid synthase (FAS), but with an improved ability to induce tumour cell death. © 2010 The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0cc01276a
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c0cc01276a
dc.description.sourcetitleChemical Communications
dc.description.volume46
dc.description.issue44
dc.description.page8335-8337
dc.description.codenCHCOF
dc.identifier.isiut000283690400003
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