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Excavation of Lead Compounds that Inhibit Mast Cell Degranulation by Combinatorial Chemistry and Activity-Guided  

Hahn, Hoh-Gyu (Life Science Division, Korea Institute of Science and Technology)
Oh, Heong-Sub (Life Science Division, Korea Institute of Science and Technolog)
Cheon, Seung-Hoon (College of Pharmacy, Drug Development Research Institute, Chonnam National University)
Oak, Min-Ho (College of Pharmacy, Drug Development Research Institute, Chonnam National University)
Kim, Young-Ran (College of Pharmacy, Drug Development Research Institute, Chonnam National University)
Kim, Kyeong-Man (College of Pharmacy, Drug Development Research Institute, Chonnam National University)
Publication Information
Archives of Pharmacal Research / v.27, no.5, 2004 , pp. 518-523 More about this Journal
Abstract
An allergic reaction ensues after antigen binds to mast cell or basophil high affinity IgE receptor, Fc$\varepsilon$RI, resulting in degranulation of various inflammatory mediators that produce various allergic symptoms. In this study, i) we isolated the active component for the inhibition of mast cell degranulation from the extract of leaves of Castanea crenata and identified it as quercetin; ii) we established the total synthesis procedure of quercetin; iii) using quercetin as positive control, we excavated some lead compounds that possess inhibitory activities for mast cell degranulation by screening the chemical libraries of 1,3-oxazolidine derivatives prepared by solid phase combinatorial chemistry. Some of 1,3-oxazolidine compounds possessing acetyl and 3',4'-dichlorophenyl group displayed strong inhibitory activities on Fc$\varepsilon$RI-mediated mast cell degranulation, suggesting that they can be used as lead compounds for the development of anti-allergic agents.
Keywords
Castanea crenata; Quercetin; Mast cell degranulation; Combinatorial chemistry; 1,3-Oxazolidines; Allergy;
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1 Cambier, J. C., Antigen and Fc receptor signaling. The awesome power of the immunoreceptor tyrosine-based activation motif (ITAM). J. Immunol., 155, 3281-3285 (1995)
2 Cheong, H., Ryu, S. Y., Oak, M. H., Cheon, S. H., Yoo, G. S., and Kim, K. M., Studies of structure activity relationship of flavonoids for the anti- allergic actions. Arch. Pharm. Res., 21, 478-480 (1989)   DOI   ScienceOn
3 Cox, J. S., Disodium cromoglycate (FPL 670) ('Intal'): a specific inhibitor of reaginic antibody-antigen mechanisms. Nature, 216, 1328-1329 (1967)   DOI   PUBMED   ScienceOn
4 Fischer, M. J., Paulussen, J. J., Horbach, D. A., Roelofsen, E. P., van Miltenburg, J. C., de Mol, N. J., and Janssen, L. H., Inhibition of mediator release in RBL-2H3 cells by some H1-antagonist derived anti-allergic drugs: relation to lipophilicity and membrane effects. Inflamm. Res., 44, 92-97 (1995)   DOI   ScienceOn
5 Kinet, J. P., The high-affinity receptor for IgE. Curr. Opin. Immunol., 2, 499-505(1989)   DOI   PUBMED   ScienceOn
6 Rivera, J., Molecular adapters in Fc(epsilon)RI signaling and the allergic response. Curr. Opin. Immunol., 14, 688-693 (2002)   DOI   PUBMED   ScienceOn
7 Schwartz, L. B., Austen, K. F., and Wasserman, S. I., Immunologic release of beta-hexosaminidase and beta-glucuronidase from purified rat serosal mast cells. J. Immunol., 123, 1445-1450 (1979)
8 Thompson, L. A. and Ellman, J. A., Synthesis and applications of small molecule libraries. Chem. Rev, 96, 555-600 (1996)   DOI   ScienceOn
9 Oh, H. S., Hahn, H. G., Cheon, S. H., and Ha, D. C., Solidphase synthesis of 1,3-oxazolidine derivatives. Terahedron Lett., 41, 5069-5072 (2000)   DOI   ScienceOn
10 Cheong, H., Ryu, S. Y., and Kim, K. M., Anti-allergic action of resveratrol and related hydroxystilbenes. Planta Med., 65, 266-268 (1999)   DOI   ScienceOn
11 Lee, E., Choi, E. J., Cheong, H., Kim, Y. R., Ryu, S. Y., and Kim, K. M., Anti-allergic actions of the leaves of Castanea crenata and isolation of an active component responsible for the inhibition of mast cell degranulation. Arch. Pharm. Res., 22, 320-323 (1999)   DOI   ScienceOn
12 Reth, M., Antigen receptor tail clue. Nature, 338, 383-384 (1989)   PUBMED
13 Blank, U., Ra, C., Miller, L., White, K., Metzger, H., and Kinet, J. P., Complete structure and expression in transfected cells of high affinity IgE receptor. Nature, 337, 187-189 (1989)   DOI   ScienceOn