Umbrella Project IV
Diversity-Oriented Synthesis (DOS)
Although rational planning is widely used in the development of new drugs by research groups, both in industry and academia, it is not the only work strategy. Identifying small molecules that have biological and medical applications does not always require knowledge about the macromolecule on which the compound will act. The biological evaluation of compounds in cells and even in microorganisms can also be of great value and enlightening. However, in order to achieve good results in evaluating the potential of these small molecules, it is necessary that they be part of a quite diverse collection regarding their structural variations. Compound libraries designed using combinatorial chemistry (target-oriented synthesis) are rarely effective when the structure of the target protein is unknown, and this is due to the low diversity found in these libraries [1, 2]. Recently, some research groups have explored novel approaches based on modifying a given structure to generate molecular diversity with spectacular results [3-6]. Given the novelty of this strategy, in this project we are interested in discovering new antimicrobial agents (antibacterial, antifungal, antivirus) by screening small molecules with high structural diversity based on the Diels-Alder adduct tricyclo [6.2.1.02,7]-undeca-4,9-diene-3,6-dione (1), obtained from the reaction between cyclopentadiene and para-benzoquinone. In order to obtain a library of these molecules, we are proposing to use diversity-oriented synthesis (DOS) as a strategy [2]. The proposal seeks to synthesize at least nine distinct molecular skeletons from this raw material, which corresponds to the reagent-based approach (i.e., common starting material and different reagents). Therefore, several reagents will be used to promote 1,3-dipolar cycloadditions, additions, reductions and cyclizations, molecular rearrangements, ring expansions, etc. From these different molecular skeletons, it will be possible to attain a hundred new organic compounds with four types of molecular diversity incorporated into their structures: i) diversity of substituents; ii) diversity of functional groups; iii) stereochemical diversity; and iv) diversity of molecular skeletons.
References:
[1] Sangi, D. P. Quim. Nova 2016, 39, 995.
[2] Schreiber, S. L. Science 2000, 287, 1964.
[3] Llabani, E.; Hicklin, R. W.; Lee, H. Y. et al. Nature Chem. 2019, 11, 521.
[4] Kato, N.; Comer, E.; Sakata-Kato, T. et al. Nature 2016, 538,344.
[5] Morrison, K. C.; Hergenrother, P. J. Nat. Prod. Rep. 2014, 31, 6.
[6] Huigens III, R. W.; Morrison, K. C.; Hicklin, R. et al. Nature Chem. 2013, 5, 195.
Selected Publications
- Alisson Richard Novais; Alisson Meza; Dênis Pires de Lima; Adilson Beatriz. Using Diversity Oriented Synthesis (DOS) as a Strategy for the Discovery of New GPCR ligands. In: 44ª REUNIÃO ANUAL VIRTUAL DA SBQ, 2021, Online. Anais eletrônicos… Campinas, Galoá, 2021. Available: https://proceedings.science/rasbq-2021/papers/using-diversity-oriented-synthesis–dos–as-a-strategy-for-the-discovery-of-new-gpcr-ligands.
- Beatriz, A; Gomes, R. S. ; Constantino, M. G. ; da Silva, G. V. J.; de Oliveira, K. T. Synthesis of the Bicyclo[6.2.1]undecane Ring System by a Solvent-free Diels-Alder Reaction. Tetrahedron Lett. 2014, 55, 679.
- Salles, R. C. ; Lacerda Jr, V. et al. GIAO chemical shifts calculations of some polycyclic cage compounds: Unambiguous assignment of NMR signals and stereoisomers. Journal of Molecular Structure 2011, 1007, 191.
- Salles, R. C. ; Lacerda Jr, V. et al. 1H and 13C NMR spectral data of bioactive cage-like polycyclic compounds. Magnetic Resonance in Chemistry 2010, 48, 409.
- Ito, F. M.; Mena, A. E. M. et al. Biotransformation of a cage-like diels-alder adduct and derivatives by Mucor ramosissimus samutsevitsch. Brazilian Journal of Microbiology 2009, 40, 563.
- Ito, F. M.; Petroni, J. M.; Beatriz, A. et al. Synthesis and Biological Evaluation of Rigid Polycyclic Derivatives of the Diels-Alder Adduct Tricyclo[6.2.1.02,7]undeca-4,9-dien-3,6-dione. Molecules 2007, 12, 271.
- Ito, F. M.; Copini, S. et al. Determination of the absolute configuration of 6 -Hydroxitricyclo[ 6.2.1.02,7]undeca-9-ene-3-one by chemical correlation. In: 15th BMOS Brazilian Meeting on Organic Synthesis, 2013, 1, p. 208-208.
- Braga, F. C.; de Lima, D. P.; Beatriz, A.; Ito, F. M. Studies on the Diels-Alder adduct from cyclopentadiene and p-benzoquinone: Biotransformation, enantiomeric excess and absolute configuration. Orbital: Electron. J. Chem. 2012, 4 (suppl. 1), 65.
- Copini, S.; Ito, F. M.; Ungari, C. C.; de Lima, D. P.; Gomes, R. S.; Beatriz, A. Development of new chiral auxiliary from the Diels-Alder adduct endo-tricyclo[6.2.1.02,7] undeca-4 ,9-dien-3 ,6-dione. Orbital: Electron. J. Chem. 2012, 4 (suppl. 1), 25.