CAS No. 2182-14-1

Batch: Purity:99.86
Vindoline Chemical Structure
Chemical Structure
Check the Vindoline product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name methyl (1R,9R,10S,11R,12R,19R)-11-acetyloxy-12-ethyl-10-hydroxy-5-methoxy-8-methyl-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5,13-tetraene-10-carboxylate
CAS Number 2182-14-1
Molecular Formula

C25H32N2O6

Molecular Weight (MW) 456.53
SMILES CCC12C=CCN3C1C4(CC3)C(C(C2OC(=O)C)(C(=O)OC)O)N(C5=C4C=CC(=C5)OC)C
InChIKey CXBGOBGJHGGWIE-ACSXSLCXSA-N

Ordering Information

Biological Activity

Vindoline is a monomeric indole alkaloid and chemical precursor to vinblastine that acts as an antimitotic agent through the inhibition of microtubule assembly. By interfering with tubulin dynamics and spindle formation during mitosis, vindoline disrupts cell division pathways, leading to cell cycle arrest at the G2/M phase and subsequent inhibition of cellular 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 91 mg/mL (199.32 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
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).
Note: Technical data last updated: Sep 1, 2026.