ATR-IN-21

SKU:BHB20443408
Overview
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ATR-IN-21 (CAS 2905312-17-4) is a kinase inhibitor supplied as a solid powder by TargetMol. For biochemical profiling and cell-based assay applications.
Activity Kinase Inhibitor
CAS No. 2905312-17-4
Molecular Weight 417.51 g/mol
Form Solid
Shipping Room Temperature
Options selector
Catalog no. Size
T79031-5MG 5 mg
T79031-50MG 50 mg
Available Options

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

  • Options: Size: 5 mg, 50 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 T79031
Activity
  • Kinase Inhibitor
Cas No. 2905312-17-4
Molecular Weight 417.51
Product Type
  • Small Molecule Inhibitor
Signaling Pathway PI3K/Akt/mTOR signaling///DNA Damage/DNA Repair
Target ATM/ATR

Compound Overview

ATR-IN-21 (CAS 2905312-17-4) is a research-grade small molecule supplied by TargetMol.

Physical Properties

CAS Number 2905312-17-4
Molecular Formula C23H27N7O
Molecular Weight 417.51 g/mol
Form Solid
Shipping Room Temperature (RT)

Biological Activity

ATR-IN-21, also known as compound 60, is a potent inhibitor of ATR, exhibiting an IC50 of less than 1000 nM (1).

Target(s): ATM/ATR

Signaling pathway(s): PI3K/Akt/mTOR signaling, DNA Damage/DNA Repair

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's the meaning of "< 1 mg/mL refers to the slightly soluble or insoluble"?

When solubility is listed as < 1 mg/mL, the compound dissolves to less than 1 mg per milliliter in water at 25 °C, pH 7.4. Such compounds require an organic co-solvent such as DMSO to prepare a concentrated stock, which is then diluted into aqueous assay buffer. For cell-based assays, keep the final DMSO concentration below 0.1% (v/v) to avoid solvent-induced cytotoxicity.

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.

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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