Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0049969
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dc.titleWhat Does It Take to Synergistically Combine Sub-Potent Natural Products into Drug-Level Potent Combinations?
dc.contributor.authorQin, C.
dc.contributor.authorTan, K.L.
dc.contributor.authorZhang, C.L.
dc.contributor.authorTan, C.Y.
dc.contributor.authorChen, Y.Z.
dc.contributor.authorJiang, Y.Y.
dc.date.accessioned2014-10-29T02:01:05Z
dc.date.available2014-10-29T02:01:05Z
dc.date.issued2012-11-28
dc.identifier.citationQin, C., Tan, K.L., Zhang, C.L., Tan, C.Y., Chen, Y.Z., Jiang, Y.Y. (2012-11-28). What Does It Take to Synergistically Combine Sub-Potent Natural Products into Drug-Level Potent Combinations?. PLoS ONE 7 (11) : -. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0049969
dc.identifier.issn19326203
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/106511
dc.description.abstractThere have been renewed interests in natural products as drug discovery sources. In particular, natural product combinations have been extensively studied, clinically tested, and widely used in traditional, folk and alternative medicines. But opinions about their therapeutic efficacies vary from placebo to synergistic effects. The important questions are whether synergistic effects can sufficiently elevate therapeutic potencies to drug levels, and by what mechanisms and at what odds such combinations can be assembled. We studied these questions by analyzing literature-reported cell-based potencies of 190 approved anticancer and antimicrobial drugs, 1378 anticancer and antimicrobial natural products, 99 natural product extracts, 124 synergistic natural product combinations, and 122 molecular interaction profiles of the 19 natural product combinations with collective potency enhanced to drug level or by >10-fold. Most of the evaluated natural products and combinations are sub-potent to drugs. Sub-potent natural products can be assembled into combinations of drug level potency at low probabilities by distinguished multi-target modes modulating primary targets, their regulators and effectors, and intracellular bioavailability of the active natural products. © 2012 Qin et al.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1371/journal.pone.0049969
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.doi10.1371/journal.pone.0049969
dc.description.sourcetitlePLoS ONE
dc.description.volume7
dc.description.issue11
dc.description.page-
dc.identifier.isiut000312601700030
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