Natural macrocyclic molecules have a possible limited structural diversity

Author:

Frank Aaron T.,Farina Nicola S.,Sawwan Nahed,Wauchope Orrette R.,Qi Mo,Brzostowska Edyta M.,Chan Wang,Grasso Frank W.,Haberfield Paul,Greer Alexander

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Reference26 articles.

1. Wessjohann LA, Ruijter E, Garcia-Rivera D and Brandt W (2005). What can a chemist learn from nature’s macrocycles—A brief, conceptual view. Mol Divers 9: 171–186

2. Databases, such as Chemical Combined Dictionary may be used. The primary literature, such as the Journal of Natural Products also provides a ready source of structural information on natural macrocycles

3. Pettit GR (1977–1989). Biosynthetic products for cancer chemotherapy. Plenum Press, New York

4. Pettit GR (1994). Anticancer drugs from animals, plants and microorganisms. Wiley-Interscience, New York

5. Guggisberg A, Badawi MM, Hesse M and Schmid H (1974). Alkaloids. 151. Structure of the macrocyclic spermidine alkaloids, oncinotine, neooncinotine, and isooncinotine. Helv Chim Acta 57: 414–434

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