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"

With the aid of an in silico method, α-glucosidase inhibitors with far more potent activities than salacinol (1), a potent natural α-glucosidase inhibitor isolated from an Ayurvedic traditional medicine Salacia reticulata, have been developed.

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2012-09, Vol.48 (69), p.8646-8648
Hauptverfasser: Tanabe, Genzoh, Nakamura, Shinya, Tsutsui, Nozomi, Balakishan, Gorre, Xie, Weijia, Tsuchiya, Satoshi, Akaki, Junji, Morikawa, Toshio, Ninomiya, Kiyofumi, Nakanishi, Isao, Yoshikawa, Masayuki, Muraoka, Osamu
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Sprache:eng
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Zusammenfassung:With the aid of an in silico method, α-glucosidase inhibitors with far more potent activities than salacinol (1), a potent natural α-glucosidase inhibitor isolated from an Ayurvedic traditional medicine Salacia reticulata, have been developed.
ISSN:1359-7345
1364-548X
DOI:10.1039/c2cc34144a