Ontology highlight
ABSTRACT:
SUBMITTER: Ishikawa F
PROVIDER: S-EPMC8694024 | biostudies-literature | 2021 Jan
REPOSITORIES: biostudies-literature
Ishikawa Fumihiro F Hirano Aiko A Yoshimori Yuuto Y Nishida Kana K Nakamura Shinya S Takashima Katsuki K Marumoto Shinsuke S Ninomiya Kiyofumi K Nakanishi Isao I Xie Weijia W Morikawa Toshio T Muraoka Osamu O Tanabe Genzoh G
RSC advances 20210115 6
We show that salacinol-type α-glucosidase inhibitors are ligand-compatible with the GH 31 family. Salacinol and its 3'-<i>O</i>-benzylated analogs inhibit human lysosomal α-glucosidase at submicromolar levels. Simple structure-activity relationship studies reveal that the salacinol side-chain stereochemistry significantly influences binding to GH31 α-glucosidases. ...[more]