A83-01

SKU:BHB11900209
Suppliers
StressMarq Biosciences Inc.
StressMarq Biosciences Inc.
Details Products
Overview
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A83-01 is a research-grade small-molecule inhibitor of ALK kinase supporting Cell Signaling and Cancer research. Supplied as a white to beige powder with 98% purity (CAS 909910-43-6, MW 421.5) Soluble to 50 mM in DMSO; store at -20°C. For research use only.
Cas No. 909910-43-6
Molecular Formula C25H19N5S
Purity ≥98% (HPLC)
Application Notes ALK kinase inhibitor
Options selector
Catalog no. Size
SIH-423-5MG 5 mg
SIH-423-25MG 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 3-(6-Methyl-2-pyridinyl)-N-phenyl-4-(4-quinolinyl)-1H-pyrazole-1-carbothioamide, A-83-01, A83-01
CAS no. 909910-43-6
Applications
  • Functional Assay (In Vitro)
Source Synthetic
Molecular weight 421.5
Molecular formula C25H19N5S
Purity ≥98% (HPLC)
Bioactivity Inhibitor
Activity
  • Inhibitor
Solubility Soluble to 50 mM in DMSO
SMILES CC1=NC(=CC=C1)C2=NN(C=C2C3=CC=NC4=CC=CC=C34)C(=S)NC5=CC=CC=C5
InChIKey HIJMSZGHKQPPJS-UHFFFAOYSA-N
Form White to beige powder
Storage -20ºC
Shipping Shipped Ambient
Catalog no. (Mfr.) SIH-423
Main SKU BHB11900209

A83-01 is a selective inhibitor of TGF-β type I receptor ALK5 kinase. It blocks phosphorylation of Smad2 and inhibits TGF-β-induced epithelial-to-mesenchymal transition. A83-01 also inhibits the transcriptional activity induced by TGFβ type I receptor ALK-5, activin type IB receptor ALK-4 and nodal type I receptor ALK-7.

Classification: Acute toxicity, Oral (Category 4) Skin irritation (Category 2) Eye irritation (Category 2A) Specific target organ toxicity-single exposure (Category 3), Respiratory system

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:

  • H302 Harmful if swallowed.
  • H315 Causes skin irritation.
  • H319 Causes serious eye irritation.
  • H335 May cause respiratory irritation..

Precautionary statements:

  • P261 Avoid breathing dust/ fume/ gas/ mist/ vapours/ spray.
  • P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

A83-01 (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-423)

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. Li W., et al. (2009) Stem Cell 4(1): 16–19.
2. Cherukuri P., et al. (2012). PloS One. 7(11): e50066.
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