| Literature DB >> 11551767 |
P Wipf1, T D Hopkins, J K Jung, S Rodriguez, A Birmingham, E C Southwick, J S Lazo, G Powis.
Abstract
Natural products of the naphthoquinone spiroketal structural type served as lead structures for the development of novel inhibitors of the thioredoxin-thioredoxin reductase redox system. The most potent compound in this series inhibited thioredoxin with an IC(50) of 350 nM, and many derivatives showed low micromolar activities for growth inhibition against two breast cancer cell lines.Entities:
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Year: 2001 PMID： 11551767 DOI： 10.1016/s0960-894x(01)00525-x
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN： 0960-894X Impact factor: 2.823