FGF/PDGF/VEGF RTK Inhibitor

SKU:BHB20439220
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Overview
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FGF/PDGF/VEGF RTK Inhibitor (CAS 144335-37-5) is a small molecule inhibitor supplied as a solid powder by TargetMol. For biochemical profiling and cell-based assay applications.
Activity Small Molecule Inhibitor
CAS No. 144335-37-5
Molecular Weight 277.28
Form Solid
Shipping Room Temperature
Available Options

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

  • Options: Size: 25 mg, 50 mg, 100 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.
Options selector
Catalog no. Size
T71944-25MG 25 mg
T71944-50MG 50 mg
T71944-100MG 100 mg
Field Specification
Activity
  • Small Molecule Inhibitor
Cas No. 144335-37-5
Molecular Weight 277.28
Product Type
  • Small Molecule Inhibitor
Signaling Pathway Others
SMILES OC1=C(C(=O)NC=2C1=CC=CC2)C=3NC=4C(N3)=CC=CC4
Target Others

Compound Overview

FGF/PDGF/VEGF RTK Inhibitor (CAS 144335-37-5) is a research-grade small molecule supplied by TargetMol.

Physical Properties

CAS Number 144335-37-5
Molecular Formula C16H11N3O2
Molecular Weight 277.28 g/mol
SMILES OC1=C(C(=O)NC=2C1=CC=CC2)C=3NC=4C(N3)=CC=CC4
Form Solid
Shipping Room Temperature (RT)

Biological Activity

FGF/PDGF/VEGF RTK Inhibitor is a potent, reversible, atp-competitive inhibitor against pdgfrbeta, fgfr-1, and vegfr-2 (ic50 = 20, 90, and 240 nm, respectively) and effectively suppresses vegf-stimulated proliferation of hmvecs (ec50 = 420 nm).

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.

Why can't I see anything in the vial when I receive small-sized products?

Due to the small pack, the powder may be highly dispersed during shipping due to static electricity and may adhere to the vial. Please centrifuge and add an appropriate solvent to fully dissolve the product and prepare the stock solution.

How to set the concentration of stock solution?

The concentration of stock solution should be lower than the solubility provided on the official website. Within this range, the concentration of stock solution should be set based on that of working solution. For cell experiments, it is recommended to set the stock solution concentration at least 1000 times higher than that of working solution.

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).

Can’t find the compound you’re looking for?
Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

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