Literature DB >> 19497297

Demonstration of microtubule-like structures formed with (-)-rhazinilam from purified tubulin outside of cells and a simple tubulin-based assay for evaluation of analog activity.

Michael C Edler1, Guangli Yang, M Katherine Jung, Ruoli Bai, William G Bornmann, Ernest Hamel.   

Abstract

(-)-Rhazinilam was spontaneously generated from a natural product during isolation. In cultured cells, it causes microtubule bundle formation, like those caused by paclitaxel. With tubulin, (-)-rhazinilam causes formation of an aberrant spiral polymer. Using glutamate and GTP, we developed an assay for spiral formation and applied it to 17 new (+/-)-rhazinilam analogs with either a modified side chain or a different size D ring. There was reasonable correlation between spiral formation and inhibition of human MCF-7 breast carcinoma cell growth. Only one side chain analog was as active as (+/-)-rhazinilam. During these studies, we observed that omitting GTP from the reaction mixture caused a major change in the morphology of the (-)-rhazinilam-induced polymer, with half the observed polymer being microtubule-like and half being spirals. This mixed polymer slowly disassembled at 0 degrees C, but there was no apparent difference in the lability of the microtubules versus the spirals.

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Year:  2009        PMID: 19497297      PMCID: PMC2726660          DOI: 10.1016/j.abb.2009.05.014

Source DB:  PubMed          Journal:  Arch Biochem Biophys        ISSN: 0003-9861            Impact factor:   4.013


  24 in total

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Journal:  Biochemistry       Date:  1993-09-28       Impact factor: 3.162

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  7 in total

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4.  (-)-Rhazinilam and the diphenylpyridazinone NSC 613241: Two compounds inducing the formation of morphologically similar tubulin spirals but binding apparently to two distinct sites on tubulin.

Authors:  Ruoli Bai; Ernest Hamel
Journal:  Arch Biochem Biophys       Date:  2016-06-13       Impact factor: 4.013

5.  Enantioselective construction of quaternary N-heterocycles by palladium-catalysed decarboxylative allylic alkylation of lactams.

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6.  Formal total syntheses of classic natural product target molecules via palladium-catalyzed enantioselective alkylation.

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Journal:  Beilstein J Org Chem       Date:  2014-10-28       Impact factor: 2.883

7.  Biosynthetically inspired divergent approach to monoterpene indole alkaloids: total synthesis of mersicarpine, leuconodines B and D, leuconoxine, melodinine E, leuconolam, and rhazinilam.

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Journal:  Org Lett       Date:  2014-11-20       Impact factor: 6.005

  7 in total

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