ML335

For research use only. Not for therapeutic Use.

  • CAT Number: I013986
  • CAS Number: 825658-06-8
  • Molecular Formula: C15H14Cl2N2O3S
  • Molecular Weight: 373.25
  • Purity: ≥95%
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ML335 is a selective activator of both TREK-1 and TREK-2.
Xenopus oocyte two-electrode voltage-clamp measurements show that ML335 and ML402 activate K2P2.1 and K2P10.1 but not K2P4.1 (14.3±2.7 μM, K2P2.1-ML335; 13.7±7.0 μM, K2P2.1-ML402; 5.2±0.5 μM, K2P10.1-ML335; and 5.9±1.6 μM, K2P10.1-ML402). Swapping the Lys271 equivalent between K2P2.1 and K2P4.1 results in a clear phenotype reversal for ML335 and M402 activation. ML335 and ML402 activate K2P2.1 in HEK293 cells similar to their effects in Xenopus oocytes (5.2±0.8 μM and 5.9±1.6 μM for ML335 and ML402, respectively (n≥3))[1].


Catalog Number I013986
CAS Number 825658-06-8
Synonyms

N-[(2,4-dichlorophenyl)methyl]-4-(methanesulfonamido)benzamide

Molecular Formula C15H14Cl2N2O3S
Purity ≥95%
InChI InChI=1S/C15H14Cl2N2O3S/c1-23(21,22)19-13-6-3-10(4-7-13)15(20)18-9-11-2-5-12(16)8-14(11)17/h2-8,19H,9H2,1H3,(H,18,20)
InChIKey RDFIQTZRJRVFHK-UHFFFAOYSA-N
SMILES CS(=O)(=O)NC1=CC=C(C=C1)C(=O)NCC2=C(C=C(C=C2)Cl)Cl
Reference

[1]. Lolicato M, et al. K2P2.1 (TREK-1)-activator complexes reveal a cryptic selectivity filter binding site. Nature. 2017 Jul 20;547(7663):364-368.
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