CAS No. 1933528-96-1

Batch: Purity:99.94
MDR-652 Chemical Structure
Chemical Structure
Check the MDR-652 product page for in-depth specifications, including solubility, stock solutions, MOA, and working concentrations.

Chemical Information

CAS Number 1933528-96-1
Molecular Formula

C22H23ClFN3O2S

Molecular Weight (MW) 447.95
SMILES CC(C)(C)C1=NC(=C(S1)CNC(=O)NC2=CC(=C(C=C2)CO)F)C3=CC(=CC=C3)Cl

Ordering Information

Biological Activity

MDR-652 is a potent and specific agonist of transient receptor potential vanilloid 1 (TRPV1). Activation of TRPV1 by MDR-652 modulates cation influx in sensory neurons, leading to desensitization of nociceptive nerve fibers. This pathway modulation results in dose-dependent analgesic effects and attenuation of pain signaling without inducing traditional pungency. Consequently, MDR-652 serves as a valuable tool for investigating TRPV1 channel gating and nociceptive signaling pathways. [1][2]

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 90 mg/mL (200.91 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO. The recommended stock concentration is 10 mM in DMSO.)
Ethanol 90 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.