A Sweet Origin for the Key Congocidine Precursor 4??Acetamidopyrrole??2??carboxylate
S Lautru, L Song, L Demange, T Lombès…
Index: Lautru, Sylvie; Song, Lijiang; Demange, Luc; Lombes, Thomas; Galons, Herve; Challis, Gregory L.; Pernodet, Jean-Luc Angewandte Chemie - International Edition, 2012 , vol. 51, # 30 p. 7454 - 7458
Full Text: HTML
Citation Number: 12
Abstract
Pyrrole groups are found in nature in two primary metabolites (heme and tryptophan) and in a large variety of secondary metabolites (eg pyoluteorin, clorobiocin, congocidine, and prodigiosins). The diversity of these metabolites is mirrored in the multiple biosynthetic pathways leading to pyrrole groups. Six different biosynthetic pathways have been characterized to date,[1, 2] involving various primary metabolite precursors, such as amino ...
Related Articles:
Design, synthesis, DNA-binding and cytotoxicity evaluation of new potential combilexines
[Hotzel, Christian; Marotto, Annalisa; Pindur, Ulf European Journal of Medicinal Chemistry, 2002 , vol. 37, # 5 p. 367 - 378]
[Dudouit, Fabienne; Goossens, Jean-Francois; Houssin, Raymond; Henichart, Jean-Pierre; Colson, Pierre; Houssier, Claude; Gelus, Nathalie; Bailly, Christian Bioorganic and Medicinal Chemistry Letters, 2000 , vol. 10, # 6 p. 553 - 557]
[Tetrahedron Letters, , vol. 46, # 42 p. 7101 - 7105]
[Organic and Biomolecular Chemistry, , vol. 1, # 19 p. 3327 - 3342]