Evaluation of |
Lee, Yoo-Jin
(College of Pharmacy, Ewha Womans University)
Lee, Eun-Young (College of Pharmacy, Ewha Womans University) Han, Ah-Reum (College of Pharmacy, Ewha Womans University) Song, Jun-Im (Department of Biological Science, Ewha Womans University) Kwon, Young-Joo (College of Pharmacy, Ewha Womans University) Seo, Eun-Kyoung (College of Pharmacy, Ewha Womans University) |
1 | Abell, A.D., Jones, M.A., Neffe, A.T., Aitken, S.G., Cain, T.P., Payne, R.J., McNabb, S.B., Coxon, J.M., Stuart, B.G., Pearson, D., Lee, H.Y.Y., and Morton, J.D., Investigation into the P3 binding domain of m-Calpain using photoswitchable diazo- and triazene-dipeptide aldehydes: new anticataract agents. J. Med. Chem. 50, 2916-2920 (2007). DOI |
2 |
Boland, B. and Campbell, V., A |
3 | Carragher, N.O., Calpain inhibition: a therapeutic strategy targeting multiple disease states. Curr. Pharm. Des. 12, 615-638 (2006). DOI |
4 | Cuerrier, D., Moldoveanu, T., Campbell, R.L., Kelly, J., Yoruk, B., Verhelst, S.H., Greenbaum, D., Bogyo, M., and Davies, P. L., Development of calpain-specific inactivators by screening of positional scanning epoxide libraries. J. Biol. Chem. 282, 9600-9611 (2007). DOI |
5 |
Donkor, I.O., Assefa, H., and Liu, J., Structural basis for the potent calpain inhibitory activity of peptidyl |
6 | Han, A.-R., Song, J.-I., Jang, D.S., Min, H.-Y., Lee, S.K., and Seo, E.-K., Cytotoxic constituents of the octocoral Dendronephthya gigantean. Arch. Pharm. Res. 28, 290-293 (2005). DOI |
7 | Ieda, N., Mantri, K., Miyata, Y., Ozaki, A., Komura, K., and Sugi, Y., Esterification of long-chain acids and alcohols catalyzed by ferric chloride hexahydrate. Ind. Eng. Chem. Res. 47, 8631-8638 (2008). DOI |
8 | Kang, D.-H, Jun, K.-Y., Lee, J.P., Pak, C.S., Na, Y.h., and Kwon, Y., Identification of 3-acetyl-2-aminoquinolin-4-one as a novel, nonpeptidic scaffold for specific calpain inhibitory activity. J. Med. Chem. 52, 3093-3097 (2009). DOI |
9 | Kim, I.K., Park, S.K., Park, S.H., and Jhang, S.K., Lipids Constituents of the Korean marine sponges. J. Korean Chem. Soc. 35, 85-89 (1991). |
10 |
Lee, E.Y., Jang, I.H., Shin, M.J., Cho, H.J., Kim, J.S., Eom, J.E., Kwon, Y., and Na, Y.H., Chalcones as novel non-peptidic |
11 | Mueller-Steiner, S., Zhou, Y., Arai, H., Roberson, E.D., Sun, B., Chen, J., Wang, X., Yu, G., Esposito, L., Mucke, L., and Gan, L., Antiamyloidogenic and neuroprotective functions of cathepsin B: implications for Alzheimer's disease. Neuron 51, 703-714 (2006). DOI ScienceOn |
12 | Perrin, B.J. and Huttenlocher, A., Calpain. Int. J. Biochem. Cell. Biol. 34, 722-725 (2002). DOI ScienceOn |
13 | Pietsch, M., Chua, K.C.H., and Abell, A.D., Attractive targets for the development of synthetic inhibitors. Curr. Top. Med. Chem. 10, 270-293 (2010). DOI ScienceOn |
14 | Reverter, D., Sorimachi, H., and Bode, W., The structure of calcium-free human m-calpain. implications for calcium activation and function. Trends Cardiovasc. Med. 11, 222-229 (2001). DOI ScienceOn |
15 | Youn, U.J., Lee, Y.J., Jeon, H.R., Shin, H.J., Son, Y.M., Nam, J.-W., Han, A.-R., Song, J.-I., Won, Y.-J., and Seo, E.-K., Chemical constituents from the stony coral alveopora japonica. Nat. Prod. Sci. 17, 1-4 (2011). |
16 | Zhang, Y., Jung, S.Y., Jin, C.B., Kim, N.D., Gong, P., and Lee, Y.S., Design and synthesis of 4-aryl-4-oxobutanoic acid amides as calpain inhibitors. Bioorg. Med. Chem. Lett. 19, 502-507 (2009). DOI ScienceOn |
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