| Assay ID | Title | Year | Journal | Article |
|---|
| AID1684764 | Inhibition of rat intestinal isomaltase using isomaltose as substrate incubated for 30 mins and immediately heated for 2 mins by glucose oxidase method | 2021 | Bioorganic & medicinal chemistry letters, 02-01, Volume: 33 | Elongation of the side chain by linear alkyl groups increases the potency of salacinol, a potent α-glucosidase inhibitor from the Ayurvedic traditional medicine "Salacia," against human intestinal maltase. |
| AID1684766 | Inhibition of rat intestinal maltase using maltose as substrate incubated for 30 mins and immediately heated for 2 mins by glucose oxidase method | 2021 | Bioorganic & medicinal chemistry letters, 02-01, Volume: 33 | Elongation of the side chain by linear alkyl groups increases the potency of salacinol, a potent α-glucosidase inhibitor from the Ayurvedic traditional medicine "Salacia," against human intestinal maltase. |
| AID578320 | Inhibition of rat intestinal sucrase | 2011 | Bioorganic & medicinal chemistry, Mar-15, Volume: 19, Issue:6
| Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors. |
| AID594101 | Inhibition of rat small intestinal isomaltase after 30 mins by glucose-oxidase method | 2011 | Bioorganic & medicinal chemistry letters, May-15, Volume: 21, Issue:10
| Biological evaluation of 3'-O-alkylated analogs of salacinol, the role of hydrophobic alkyl group at 3' position in the side chain on the α-glucosidase inhibitory activity. |
| AID493815 | Inhibition of alpha glucosidase | 2010 | Bioorganic & medicinal chemistry letters, Aug-01, Volume: 20, Issue:15
| Docking and SAR studies of salacinol derivatives as alpha-glucosidase inhibitors. |
| AID594100 | Inhibition of rat small intestinal sucrase after 30 mins by glucose-oxidase method | 2011 | Bioorganic & medicinal chemistry letters, May-15, Volume: 21, Issue:10
| Biological evaluation of 3'-O-alkylated analogs of salacinol, the role of hydrophobic alkyl group at 3' position in the side chain on the α-glucosidase inhibitory activity. |
| AID578321 | Inhibition of rat intestinal isomaltase | 2011 | Bioorganic & medicinal chemistry, Mar-15, Volume: 19, Issue:6
| Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors. |
| AID1684765 | Inhibition of rat intestinal sucrase using sucrose as substrate incubated for 30 mins and immediately heated for 2 mins by glucose oxidase method | 2021 | Bioorganic & medicinal chemistry letters, 02-01, Volume: 33 | Elongation of the side chain by linear alkyl groups increases the potency of salacinol, a potent α-glucosidase inhibitor from the Ayurvedic traditional medicine "Salacia," against human intestinal maltase. |
| AID594099 | Inhibition of rat small intestinal maltase after 30 mins by glucose-oxidase method | 2011 | Bioorganic & medicinal chemistry letters, May-15, Volume: 21, Issue:10
| Biological evaluation of 3'-O-alkylated analogs of salacinol, the role of hydrophobic alkyl group at 3' position in the side chain on the α-glucosidase inhibitory activity. |
| AID578319 | Inhibition of rat intestinal maltase | 2011 | Bioorganic & medicinal chemistry, Mar-15, Volume: 19, Issue:6
| Isolation, structure identification and SAR studies on thiosugar sulfonium salts, neosalaprinol and neoponkoranol, as potent α-glucosidase inhibitors. |
| AID1684763 | Inhibition of human intestinal maltase using maltose as substrate incubated for 30 mins and immediately heated for 2 mins by glucose oxidase method | 2021 | Bioorganic & medicinal chemistry letters, 02-01, Volume: 33 | Elongation of the side chain by linear alkyl groups increases the potency of salacinol, a potent α-glucosidase inhibitor from the Ayurvedic traditional medicine "Salacia," against human intestinal maltase. |
| AID324681 | Inhibition of human lysosomal alpha glucosidase | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| AID324673 | Inhibition of amylo-1,6-glucosidase | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| AID324677 | Inhibition of yeast alpha-glucosidase | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| AID324672 | Inhibition of rabbit muscle glycogen phosphorylase b at 400 uM | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| AID324679 | Inhibition of rat isomaltase | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| AID324680 | Inhibition of rat sucrase | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| AID324676 | Inhibition of rice alpha-glucosidase | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| AID324683 | Inhibition of maltase in human Caco-2 cell membrane at 1 uM | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| AID324678 | Inhibition of rat intestinal maltase | 2008 | Bioorganic & medicinal chemistry, Mar-15, Volume: 16, Issue:6
| Effect of five-membered sugar mimics on mammalian glycogen-degrading enzymes and various glucosidases. |
| [information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |