Target Validation Information | |||||
---|---|---|---|---|---|
TTD ID | T84173 | ||||
Target Name | Glucosylceramidase (GBA) | ||||
Type of Target |
Successful |
||||
Drug Potency against Target | (2R,3S,4S,5R)-2-hexylpiperidine-3,4,5-triol | Drug Info | IC50 = 19 nM | [3] | |
(2R,3S,4S,5R)-2-nonylpiperidine-3,4,5-triol | Drug Info | Ki = 2.2 nM | [3] | ||
(2R,3S,4S,5R)-2-propylpiperidine-3,4,5-triol | Drug Info | IC50 = 560 nM | [3] | ||
1,5-Dideoxy-1,5-imino-D-xylitol | Drug Info | IC50 = 2300 nM | [1] | ||
L-Isofagomine | Drug Info | IC50 = 9000 nM | [1] | ||
N-(Propylamide-acetophenone)-1-deoxynojirimycin | Drug Info | IC50 = 1650 nM | [2] | ||
N-(Propylamide-benzophenone)-1-deoxynojirimycin | Drug Info | IC50 = 350 nM | [2] | ||
Action against Disease Model | Isofagomine tartrate | Drug Info | Isofagomine tartrate increases L444P GCase activity in Gaucher patient-derived cells | [4] | |
References | |||||
REF 1 | In vitro inhibition of glycogen-degrading enzymes and glycosidases by six-membered sugar mimics and their evaluation in cell cultures. Bioorg Med Chem. 2008 Aug 1;16(15):7330-6. | ||||
REF 2 | Nanomolar affinity, iminosugar-based chemical probes for specific labeling of lysosomal glucocerebrosidase. Bioorg Med Chem. 2010 Jan 1;18(1):267-73. | ||||
REF 3 | Synthesis of new beta-1-C-alkylated imino-L-iditols: A comparative study of their activity as beta-glucocerebrosidase inhibitors. Bioorg Med Chem. 2010 Apr 1;18(7):2645-50. | ||||
REF 4 | The pharmacological chaperone isofagomine increases the activity of the Gaucher disease L444P mutant form of beta-glucosidase. FEBS J. 2010 Apr;277(7):1618-38. | ||||
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