CAS No. 518-34-3

Batch: Purity:99.95
Tetrandrine Chemical Structure
Chemical Structure
Check the Tetrandrine product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

IUPAC Name (1S,14S)-9,20,21,25-tetramethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaene
CAS Number 518-34-3
Molecular Formula

C38H42N2O6

Molecular Weight (MW) 622.75
InChIKey WVTKBKWTSCPRNU-KYJUHHDHSA-N

Ordering Information

Biological Activity

Tetrandrine is a bis-benzylisoquinoline alkaloid and calcium channel blocker with anti-inflammatory and antineoplastic activities. It induces G1 phase cell cycle arrest and apoptosis through the upregulation of p21, downregulation of cyclin D1, and activation of caspase-3. Furthermore, tetrandrine alters cytoskeletal architecture by reorganizing F-actin distribution and inhibiting endosomal two-pore calcium channels. [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 12 mg/mL (19.26 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Ethanol 3 mg/mL
Water 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).
Note: Technical data last updated: Sep 1, 2026.