2-O-Ethyl PAF C-16

SKU:BHB20445885
Overview
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2-O-Ethyl PAF C-16 (CAS 78858-42-1) is a receptor agonist supplied as a solid powder by TargetMol. For biochemical profiling and cell-based assay applications.
Activity Receptor Agonist
CAS No. 78858-42-1
Molecular Weight 509.71 g/mol
Form Solid
Shipping Room Temperature
Options selector
Catalog no. Size
T84613-1MG 1 mg
T84613-5MG 5 mg
T84613-25MG 25 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options: Size: 1 mg, 5 mg, 25 mg
  • Lead time: In Stock at Manufacturer — options listed in "Availability Content"; other statuses may take longer.
  • Storage: −20 °C
  • Shipping: Room temperature (RT) shipment.
  • Upon receipt: Store at −20 °C as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No T84613
Activity
  • Receptor Agonist
Cas No. 78858-42-1
Molecular Weight 509.709
Product Type
  • Small Molecule Inhibitor
Signaling Pathway Others
SMILES CCCCCCCCCCCCCCCCOC(CH)(COP((O-))(=O)OCC(N+)(C)(C)C)OCC
Target Others

Compound Overview

2-O-Ethyl PAF C-16 (CAS 78858-42-1) is a research-grade small molecule supplied by TargetMol.

Physical Properties

CAS Number 78858-42-1
Molecular Formula C26H56NO6P
Molecular Weight 509.71 g/mol
SMILES CCCCCCCCCCCCCCCCOC(CH)(COP((O-))(=O)OCC(N+)(C)(C)C)OCC
Form Solid
Shipping Room Temperature (RT)

Biological Activity

2-O-Ethyl PAF C-16, a homolog of Platelet-activating Factor (PAF) and competitive ligand for the Platelet-activating Factor Receptor (PAFR), inhibits the binding of PAF antagonist WEB 2086 to PAFR with an IC50 of 21 nM (1).

Safety & Regulatory

For Research Use Only (RUO). Not for therapeutic, diagnostic, or clinical use. Wear appropriate PPE and consult the Safety Data Sheet (SDS) prior to handling.

What equipment should be used for ultrasound?

Use a bath-type ultrasonic cleaner rather than a high-intensity ultrasonic disruptor. Bath sonicators provide gentle, uniform agitation appropriate for dissolving solid compounds without generating cavitation damage or excessive heat. Ensure the solvent tube is fully submerged and use short sonication pulses of 5–10 seconds.

Animals cannot tolerate DMSO well. How should the dosage of DMSO be controlled during administration?

For normal mice, the concentration of DMSO should be kept below 10%. For nude mice, transgenic mice, or mice with weak tolerance, the concentration of DMSO should be kept below 2%. For inhibitors being used for the first time, it is recommended to perform a solvent-negative control experiment to confirm that the solvent has no nonspecific effects on the animals.

Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

  • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
  • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
  • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
  • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
  • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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