| Field | Specification |
|---|---|
| Mfr No | |
| Activity | |
| Alternative Names | ZM-306416 |
| Cas No. | |
| Form | Off-white solid |
| Molecular Weight | |
| Product Type | |
| Purity | |
| Shipping | |
| SMILES | |
| Solubility | Soluble in DMSO (3 mg/ml) or ethanol (1 mg/ml) |
| Source | Synthetic |
| Storage |
ZM 306416 is a potent and selective inhibitor of vascular endothelial growth factor (VEGF) receptor tyrosine kinases, particularly Flk-1 (KDR) and Flt. In neuroscience, ZM 306416 is used to explore the role of VEGF signaling in neurovascular function, blood-brain barrier integrity, and neuroinflammation. Its ability to modulate angiogenic pathways makes it a useful tool in studying neurovascular contributions to neurodegenerative diseases such as Alzheimer’s and multiple sclerosis.
Classification: Not a hazardous substance or mixture.
Safety Phrases:
- S22 - Do not breathe dust.
- S24/25 - Avoid contact with skin and eyes.
- S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
ZM 306416 (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-487)
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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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).
2. Kawai, T., et al. (2006) Neurosci. 141(3): 1209–1216.
