(Z)-N-((2S,3R,E)-3-Hydroxy-1-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)octadec-4-en-2-yl)tetracos-15-enamide

99%

Reagent Code: #246391
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CAS Number 887907-50-8

science Other reagents with same CAS 887907-50-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 810.24 g/mol
Formula C₄₈H₉₁NO₈
badge Registry Numbers
MDL Number MFCD22416611
thermostat Physical Properties
Boiling Point 902.3±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.03±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used in advanced lipid research and drug delivery systems due to its structural similarity to natural sphingolipids. Its unique stereochemistry and long-chain unsaturated amide group enable integration into lipid bilayers, making it valuable for studying membrane dynamics and cellular signaling pathways. Frequently employed in the development of synthetic liposomes for targeted therapy, especially in cancer and inflammatory diseases. Also serves as a biochemical tool for enzyme assays involving ceramidases and glycosidases. Its hydrophilic head and hydrophobic tail enhance solubility and bioavailability in physiological environments.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿45,680.00
inventory 100mg
10-20 days ฿131,980.00

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(Z)-N-((2S,3R,E)-3-Hydroxy-1-(((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)octadec-4-en-2-yl)tetracos-15-enamide
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Used in advanced lipid research and drug delivery systems due to its structural similarity to natural sphingolipids. Its unique stereochemistry and long-chain unsaturated amide group enable integration into lipid bilayers, making it valuable for studying membrane dynamics and cellular signaling pathways. Frequently employed in the development of synthetic liposomes for targeted therapy, especially in cancer and inflammatory diseases. Also serves as a biochemical tool for enzyme assays involving ceramidases and glycosidases. Its hydrophilic head and hydrophobic tail enhance solubility and bioavailability in physiological environments.
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