General description
Kifunensine is an alkaloid compound, isolated from the actinomycete Kitasporia kifunensis.
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.
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.
Molecular Weight: 232.19. Empirical Formula: C8H12N2O6. biological source: synthetic (organic). Quality Level: 100. Assay: ≥. 98%. form: film or powder, solid. solubility: water, double-distilled: 50 . mM. storage temp.: −. 20°C. 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. Gene Information: human ... MAN1A1(4121), MAN1A2(10905), MAN1B1(11253), MAN1C1(57134)mouse ... MAN1A1(17155), MAN1A2(17156), MAN1B1(227619), MAN1C1(230815)
rat ... MAN1A1(294410), MAN1A2(295319), MAN1B1(499751), MAN1C1(362625). Pictograms: GHS07. Signal Word: Warning. Hazard Statements: H319. Precautionary Statements: P264 - P280 - P305 + P351 + P338 - P337 + P313. Hazard Classifications: Eye Irrit. 2. Storage Class Code: 11 - Combustible Solids. WGK: WGK 3. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: Eyeshields, Gloves, type N95 (US).
- UPC:
- 51141704
- Condition:
- New
- HazmatClass:
- No
- MPN:
- K1140-1MG
- CAS:
- 109944-15-2
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