Literature DB >> 10937728

One-pot synthesis and biological evaluation of aspergillamides and analogues.

B Beck1, S Hess, A Dömling.   

Abstract

A one-pot total synthesis of aspergillamide and analogues by a solution phase Ugi multi component reaction (MCR) is described. The reaction is easily performed in 96-well plates and offers a facile access to diverse aspergillamide analogue compound libraries. The antibiotic and cytotoxic activity of these compounds is measured. Several of them are more potent than the natural product.

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Year:  2000        PMID: 10937728     DOI: 10.1016/s0960-894x(00)00305-x

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

Review 1.  Marine-derived Aspergillus species as a source of bioactive secondary metabolites.

Authors:  Yoon Mi Lee; Min Jeong Kim; Huayue Li; Ping Zhang; Baoquan Bao; Ka Jeong Lee; Jee H Jung
Journal:  Mar Biotechnol (NY)       Date:  2013-05-25       Impact factor: 3.619

2.  Applications of the Ugi reaction with ketones.

Authors:  Suvi T M Simila; Stephen F Martin
Journal:  Tetrahedron Lett       Date:  2008       Impact factor: 2.415

3.  New MCRs: the first 4-component reaction leading to 2,4-disubstituted thiazoles.

Authors:  Jürgen Kolb; Barbara Beck; Michael Almstetter; Stefan Heck; Eberhardt Herdtweck; Alexander Dömling
Journal:  Mol Divers       Date:  2003       Impact factor: 2.943

  3 in total

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