Strategy for designing selective α-L-rhamnosidase inhibitors: Synthesis and biological evaluation of DMDP cyclic isothioureas by Miyawaki, S, Hirokami, Y, Kinami, K, Hoshino, M, Minehira, D, Miyamoto, D, Nash, R, Fleet, G, Adachi, I, Toyooka, N, Kato, A

Isolation and SAR studies of bicyclic iminosugars from Castanospermum australe as glycosidase inhibitors by Kato, A, Hirokami, Y, Kinami, K, Tsuji, Y, Miyawaki, S, Adachi, I, Hollinshead, J, Nash, R, Kiappes, J, Zitzmann, N, Cha, J, Molyneux, R, Fleet, G, Asano, N

Isolation and SAR studies of bicyclic iminosugars from Castanospermum australe as glycosidase inhibitors. by Kato, A, Hirokami, Y, Kinami, K, Tsuji, Y, Miyawaki, S, Adachi, I, Hollinshead, J, Nash, R, Kiappes, J, Zitzmann, N, Cha, J, Molyneux, R, Fleet, G, Asano, N

N- and C-alkylation of seven-membered iminosugars generates potent glucocerebrosidase inhibitors and F508del-CFTR correctors. by Désiré, J, Mondon, M, Fontelle, N, Nakagawa, S, Hirokami, Y, Adachi, I, Iwaki, R, Fleet, G, Alonzi, D, Twigg, G, Butters, T, Bertrand, J, Cendret, V, Becq, F, Norez, C, Marrot, J, Kato, A, Blériot, Y