Synonym: FR 900494; Hexahydro-6R,7S,8aS-trihydroxy-5R-(hydroxymethyl)-imidazo[1,2-a] pyridine-2,3-dione
CAS Number: 109944-15-2
Empirical Formula (Hill Notation): C8H12N2O6
Molecular Weight: 232.19
Linear Formula: C8H12N2O6
Product Type: Chemical
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| assay |
≥98% |
| biological source |
synthetic (organic) |
| form |
film or powder |
| |
solid |
| InChI |
1S/C8H12N2O6/c11-1-2-3(12)4(13)5(14)6-9-7(15)8(16)10(2)6/h2-6,11-14H,1H2,(H,9,15)/t2-,3-,4+,5+,6+/m1/s1 |
| InChI key |
OIURYJWYVIAOCW-PQMKYFCFSA-N |
| Quality Level |
100  |
| SMILES string |
N21[C@H](NC(=O)C2=O)[C@H]([C@H]([C@@H]([C@H]1CO)O)O)O |
| solubility |
water, double-distilled: 50 mM |
| storage temp. |
−20°C |
| Application: |
Kifunensine has been used as an inhibitor of mannosidase I in Jurkat T-cells, human embryonic kidney (HEK293T/17) cells and in mouse embryonic fibroblast cells. |
| Biochem/physiol Actions: |
Kifunensine is a selective inhibitor of class I glycoprotein-processing α-mannosidases. |
| Biochem/physiol Actions: |
Kifunensine suppresses endoplasmic reticulum-associated degradation (ERAD) via the inhibition of endoplasmic reticulum-associated mannosidase activity. It is also a glycosidase inhibitor for Class I CAZy glycosylhydrolase family 47. |
| General description: |
Kifunensine is an alkaloid compound, isolated from the actinomycete Kitasporia kifunensis. |
| Purity |
≥98% |
| Storage Temp. |
−20°C |
| UNSPSC |
12352204 |