ZM 336372

SKU:BHB11900271
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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ZM 336372 is a research-grade small-molecule inhibitor of c-Raf kinase supporting Cell Signaling and Cancer research. Supplied as a white to off-white solid with 95% purity (CAS 208260-29-1, MW 389.4) soluble in DMSO; store at -20°C. For research use only.
Cas No. 208260-29-1
Molecular Formula C23H23N3O3
Purity ≥95% (HPLC)
Application Notes c-Raf kinase inhibitor
Options selector
Catalog no. Size
SIH-488-5MG 5 mg
SIH-488-25MG 25 mg
Available Options

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

  • Options: Size (2) — 25 mg, 5 mg.
  • Lead time: options listed as “in stock at manufacturer” typically ship in 2-3 business days; other statuses may take longer.
  • Storage: -20ºC
  • Shipping: ships at ambient temperature.
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Alternative names N-[5-(3-Dimethylaminobenzamido)-2-methylphenyl]-4-hydroxybenzamide
CAS no. 208260-29-1
Applications
  • Functional Assay (In Vitro)
Source Synthetic
Molecular weight 389.4
Molecular formula C23H23N3O3
Purity ≥95% (HPLC)
Bioactivity Inhibitor
Activity
  • Inhibitor
Solubility Soluble in DMSO (200 mg/ml)
SMILES CC1=C(C=C(C=C1)NC(=O)C2=CC(=CC=C2)N(C)C)NC(=O)C3=CC=C(C=C3)O
InChIKey PYEFPDQFAZNXLI-UHFFFAOYSA-N
Form White to off-white solid
Storage -20ºC
Shipping Shipped Ambient
Catalog no. (Mfr.) SIH-488
Main SKU BHB11900271

ZM 336372 is a potent, specific, and reversible inhibitor of the c-Raf protein kinase. It also inhibits SAPK2/p38 and is cell-permeable. In neurodegenerative disease research, ZM 336372 is used to investigate the role of Raf signaling in neuronal survival, apoptosis, and stress responses. Its ability to modulate MAPK pathways makes it a valuable compound for studying neuroprotective mechanisms and therapeutic targets in conditions such as stroke and neuroinflammation.

Classification: Acute toxicity, Oral (Category 5)

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.

Hazard statements:

H303 May be harmful if swallowed.

ZM 336372 (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-488)

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).

1. Hall-Jackson C.A., et al. (1999) Chem. Biol. 6(8): 559–568.
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