17437-24-0

Basic information

• Product Name: Octadecanoic acid, 18-amino-
• CAS NO: 17437-24-0
• Molecular Formula: C18H37NO2
• Molecular Weight: 0.00000
• Mol File: 17437-24-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 434.1±18.0 °C(Predicted)
• Density: 0.924±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Octadecanoic acid, 18-amino-(CAS DataBase Reference)
• NIST Chemistry Reference: Octadecanoic acid, 18-amino-(17437-24-0)
• EPA Substance Registry System: Octadecanoic acid, 18-amino-(17437-24-0)

Safety Data

• Hazardous Substances Data: 17437-24-0(Hazardous Substances Data)

Upstream product

• 247063-08-7 18-(dibenzylamino)-12-octadecenoic acid 
• 72849-35-5 1,18-octadecanedioic acid monomethyl ester 
• 1472-93-1 dimethyl 1,18-octadecanedioate 
• 871-70-5 octadecanedioic acid 
• 2380-16-7 methyl 18-hydroxyoctadecanoate 
• 16595-66-7 2-(syn-2-Oxo-cyclohexyliden)-1-aza-cyclotridecan 
• 820-41-7 ω-Amino-7-oxo-stearinsaeure 

Relevant articles and documents

Direct interaction, instrumental for signaling processes, between LacCer and Lyn in the lipid rafts of neutrophil-like cells

Lactosylceramide [LacCer; β-Gal-(1-4)-β-Glc-(1-1)-Cer] has been shown to contain very long fatty acids that specifically modulate neutrophil properties. The interactions between LacCer and proteins and their role in cell signaling processes were assessed

ALBUMIN-BINDING COMPOUNDS

The present invention provides an albumin-binding compound essentially of the following elements: a spacer group, a water-soluble bridging group, a fatty acid chain and an acidic group characterised in that the acidic group is attached to the distal end of the fatty acid chain. The invention also provides an albumin-binding compound to which one or more biologically active moieties are attached.

Superoxide dismutase derivatives

Provided are novel superoxide dismutase derivatives represented by the following general formula (I) wherein [SOD] is a superoxide dismutase residue derived by removal of two mercapto groups, and W is a divalent long chain hydrocarbon residue which may optionally be interrupted by one or more groups each independently selected from the group consisting of an oxygen atom, a sulfur atom and a group of -N(R)- (R being a lower alkyl group). The SOD derivatives retain most of the enzymatic activities of unmodified SOD and have much longer plasma half-life than unmodified SOD. They are effective for treating various diseases caused by active oxygen species. Also provided are chemical modifiers to prepare the above SOD derivatives.