In silico design, synthesis and evaluation of 3′-O-benzylated analogs of salacinol, a potent α-glucosidase inhibitor isolated from an Ayurvedic traditional medicine “Salacia”†
Abstract
With the aid of an in silico method, α-glucosidase
* Corresponding authors
a
School of Pharmacy, Kinki University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, Japan
E-mail:
muraoka@phar.kindai.ac.jp
b
Department of Medicinal Chemistry, China Pharmaceutical University, 24 Tongjia Xiang, Nanjing, Jiang su 210009, PR China
Fax: +86-25-83242366
Tel: +86-25-83271445
c
Pharmaceutical Research and Technology Institute, Kinki University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, Japan
Fax: +81-6-6721-2505
Tel: +81-6-6721-2332
d
Kyoto Pharmaceutical University, 1 Shichono-cho, Misasagi, Yamashina-ku, Kyoto 607-8412, Japan
Fax: +81-75-595-4768
Tel: +81-75-595-4633
With the aid of an in silico method, α-glucosidase
G. Tanabe, S. Nakamura, N. Tsutsui, G. Balakishan, W. Xie, S. Tsuchiya, J. Akaki, T. Morikawa, K. Ninomiya, I. Nakanishi, M. Yoshikawa and O. Muraoka, Chem. Commun., 2012, 48, 8646 DOI: 10.1039/C2CC34144A
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