Libraries from natural product-like scaffolds.

Natural products are an attractive source of varied structures that exhibit potent biological activities, and desirable pharmacological profiles. Since the relatively recent advent of high-throughput organic synthesis in the drug discovery process, several design approaches have been applied to the construction of screening libraries. Libraries of natural-product derivatives, natural-product-like compounds prepared by total synthesis, and libraries derived from natural-products are several types that have been reported.

[1]  Jürgen Bajorath Chemoinformatics methods for systematic comparison of molecules from natural and synthetic sources and design of hybrid libraries , 2002, J. Comput. Aided Mol. Des..

[2]  C. Khosla,et al.  Natural product biosynthesis: a new interface between enzymology and medicine. , 2000, The Journal of organic chemistry.

[3]  A. Stevens,et al.  Computational design strategies for combinatorial libraries. , 2003, Current opinion in chemical biology.

[4]  G. Roth,et al.  Combinatorial synthesis of natural product-like molecules using a first-generation spiroketal scaffold. , 2002, Journal of combinatorial chemistry.

[5]  M. Player,et al.  Solid-phase synthesis of a library of hydroxyproline derivatives. , 2004, Journal of combinatorial chemistry.

[6]  M. Pirrung,et al.  Synthesis of 2,5-dihydroxy-3-(indol-3-yl)benzoquinones by acid-catalyzed condensation of indoles with 2,5-dichlorobenzoquinone. , 2002, The Journal of organic chemistry.

[7]  Thomas Henkel,et al.  Statistical Investigation into the Structural Complementarity of Natural Products and Synthetic Compounds. , 1999, Angewandte Chemie.

[8]  R. Hilgenfeld,et al.  Modern Methods of Drug Discovery , 2003, EXS.

[9]  A. Ganesan Integrating natural product synthesis and combinatorial chemistry , 2001 .

[10]  H. Waldmann,et al.  Solid-phase synthesis of dysidiolide-derived protein phosphatase inhibitors. , 2002, Journal of the American Chemical Society.

[11]  P. Arya,et al.  Stereoselective diversity-oriented solution and solid-phase synthesis of tetrahydroquinoline-based polycyclic derivatives. , 2004, Journal of combinatorial chemistry.

[12]  P. Arya,et al.  A solid phase library synthesis of hydroxyindoline-derived tricyclic derivatives by Mitsunobu approach. , 2004, Journal of combinatorial chemistry.

[13]  Zhen Yang,et al.  Palladium(II)-mediated cascade carbonylative annulation of o-alkynyl-phenols on silyl linker-based macrobeads: a combinatorial synthesis of a 2,3-disubstituted benzo[b]furan library. , 2002, Organic letters.

[14]  Reza Fathi,et al.  Diversity oriented synthesis and branching reaction pathway to generate natural product-like compounds. , 2003, Current medicinal chemistry.

[15]  Miklos Feher,et al.  Property Distributions: Differences between Drugs, Natural Products, and Molecules from Combinatorial Chemistry , 2003, J. Chem. Inf. Comput. Sci..

[16]  David J Newman,et al.  Natural products as sources of new drugs over the period 1981-2002. , 2003, Journal of natural products.

[17]  P. Seeberger,et al.  Solid-phase oligosaccharide synthesis and combinatorial carbohydrate libraries. , 2000, Chemical reviews.

[18]  Wei Zhang,et al.  Solution-phase preparation of a 560-compound library of individual pure mappicine analogues by fluorous mixture synthesis. , 2002, Journal of the American Chemical Society.

[19]  A solid-phase, library synthesis of natural-product-like derivatives from an enantiomerically pure tetrahydroquinoline scaffold. , 2004, Journal of combinatorial chemistry.

[20]  S. Schreiber,et al.  Target-oriented and diversity-oriented organic synthesis in drug discovery. , 2000, Science.

[21]  P. Arya,et al.  Diversity-Based Organic Synthesis in the Era of Genomics and Proteomics. , 2001, Angewandte Chemie.

[22]  B. Jiang,et al.  Solution-phase synthesis of a thiazoyl-substituted indolyl library via Suzuki cross-coupling. , 2003, Journal of combinatorial chemistry.

[23]  M. Walters,et al.  Templates for exploratory library preparation. Derivatization of a functionalized spirocyclic 3,6-dihydro-2H-pyran formed by ring-closing metathesis reaction. , 2002, Journal of combinatorial chemistry.

[24]  U. Abel,et al.  Modern methods to produce natural-product libraries. , 2002, Current opinion in chemical biology.

[25]  A. M. Boldi,et al.  Solid-phase library synthesis of alkoxyprolines. , 2001, Journal of combinatorial chemistry.

[26]  M. Pirrung,et al.  Modular, parallel synthesis of an illudinoid combinatorial library. , 2003, Organic letters.

[27]  G. Schneider,et al.  Scaffold architecture and pharmacophoric properties of natural products and trade drugs: application in the design of natural product-based combinatorial libraries. , 2001, Journal of combinatorial chemistry.

[28]  J. Nielsen,et al.  Combinatorial synthesis of natural products. , 2002, Current opinion in chemical biology.

[29]  H. Waldmann,et al.  Natural products are biologically validated starting points in structural space for compound library development: solid-phase synthesis of dysidiolide-derived phosphatase inhibitors. , 2002, Angewandte Chemie.

[30]  Stuart L Schreiber,et al.  Diversity-oriented synthesis of biaryl-containing medium rings using a one bead/one stock solution platform. , 2002, Journal of the American Chemical Society.

[31]  A. Myers,et al.  A solid-supported, enantioselective synthesis suitable for the rapid preparation of large numbers of diverse structural analogues of (-)-saframycin A. , 2002, Journal of the American Chemical Society.

[32]  Stuart L Schreiber,et al.  Generating Diverse Skeletons of Small Molecules Combinatorially , 2003, Science.

[33]  D G Hall,et al.  Solution- and solid-phase strategies for the design, synthesis, and screening of libraries based on natural product templates: a comprehensive survey. , 2001, Journal of combinatorial chemistry.

[34]  L. Wessjohann Synthesis of natural-product-based compound libraries. , 2000, Current opinion in chemical biology.

[35]  Herbert Waldmann,et al.  Natural product guided compound library development. , 2002, Current medicinal chemistry.

[36]  Pedro M. Abreu,et al.  Natural product-like combinatorial libraries , 2003 .

[37]  H. Waldmann,et al.  Development of natural product-derived receptor tyrosine kinase inhibitors based on conservation of protein domain fold. , 2003, Journal of medicinal chemistry.