Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D06YQR
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| Former ID |
DNC010720
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| Drug Name |
(2R,3S,4S,5R)-2-propylpiperidine-3,4,5-triol
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| Synonyms |
CHEMBL1089185; (2R,3S,4S,5R)-2-propylpiperidine-3,4,5-triol
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C8H17NO3
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| Canonical SMILES |
CCCC1C(C(C(CN1)O)O)O
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| InChI |
1S/C8H17NO3/c1-2-3-5-7(11)8(12)6(10)4-9-5/h5-12H,2-4H2,1H3/t5-,6-,7+,8+/m1/s1
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| InChIKey |
JFOGNLDWQBZRQJ-NGJRWZKOSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Glucosylceramidase (GBA) | Target Info | Inhibitor | [1] |
| KEGG Pathway | Other glycan degradation | |||
| Sphingolipid metabolism | ||||
| Metabolic pathways | ||||
| Lysosome | ||||
| Pathwhiz Pathway | Sphingolipid Metabolism | |||
| Reactome | Glycosphingolipid metabolism | |||
| WikiPathways | Sphingolipid metabolism | |||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | 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. | |||
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