CAS No. 422513-13-1

Batch: Purity:99.09
Hesperadin Chemical Structure
Chemical Structure
Check the Hesperadin product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name N-[2-hydroxy-3-[C-phenyl-N-[4-(piperidin-1-ylmethyl)phenyl]carbonimidoyl]-1H-indol-5-yl]ethanesulfonamide
CAS Number 422513-13-1
Molecular Formula

C29H32N4O3S

Molecular Weight (MW) 516.65
SMILES CCS(=O)(=O)NC1=CC2=C(C=C1)NC(=C2C(=NC3=CC=C(C=C3)CN4CCCCC4)C5=CC=CC=C5)O
InChIKey HYHIYZMIFPJROG-UHFFFAOYSA-N

Biological Activity

Hesperadin is a potent ATP-competitive Aurora B kinase inhibitor that inhibits human Aurora B with an IC50 ofin cell-free assays. Target inhibition disrupts histone H3 phosphorylation, chromosome alignment, and spindle assembly checkpoint function during mitosis. Consequently, Hesperadin treatment leads to abnormal nuclear division, syntelic chromosome attachment, and cytokinesis failure, ultimately suppressing cell proliferation. [1]

How to Prepare Stock Solution?

Concentration Volume Mass
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Solubility

Batch:
All in vitro solubility values are batch-tested experimental data (non-literature values).
Solvent Solubility & Note
DMSO 100 mg/mL (193.55 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Water Insoluble
Ethanol Insoluble
FAQ
Q: Why does a DMSO stock precipitate in media/saline?
A: It is caused by unheated aqueous media (supersaturation), local solvent shock, or incorrect mixing sequence.
How to fix it?
  • Preheat media/saline to 37°C.
  • Mix rapidly (pipette/vortex) upon addition.
  • For complex mixes, always add the aqueous phase last.
  • Re-dissolve minor precipitates with a 37°C water bath and sonication (≤30 min).
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Reference

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Note: Technical data last updated: Sep 1, 2026.