ML 335
Chemical Name: N-[(2,4-Dichlorophenyl)methyl]-4-[(methylsulfonyl)amino]benzamide
Purity: ≥98%
Biological Activity
ML 335 is a selective K2P2.1 (TREK-1; KCNK2) and K2P10.1 (TREK-2; KCNK10) activator (EC50 values of 14.3 μM and 5.2 μM, respectively); directly stimulates the C-type gate via the K2P modulator pocket. Does not activate K2P4.1 (TRAAK).Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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A pharmacological master key mechanism that unlocks the selectivity filter gate in K+ channels.
Schewe et al.
Science, 2019;363:875 -
Protein and chemical determinants of BL-1249 action and selectivity for K2P channels.
Pope et al.
ACS Chem.Neurosci., 2018;9:3153 -
Two-pore domain potassium channels: emerging targets for novel analgesic drugs: IUPHAR Review 26.
Gada et al.
Br.J.Pharmacol., 2019;176:256 -
K2P2.1 (TREK-1)-activator complexes reveal a cryptic selectivity filter binding site.
Lolicato et al.
Nature, 2017;547:364
Product Datasheets
Citations for ML 335
The citations listed below are publications that use Tocris products. Selected citations for ML 335 include:
2 Citations: Showing 1 - 2
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Albumin Reduces Oxidative Stress and Neuronal Apoptosis via the ERK/Nrf2/HO-1 Pathway after Intracerebral Hemorrhage in Rats.
Authors: Peng Et al.
Oxid Med Cell Longev 2021;2021:8891373
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Recombinant CCL17 Enhances Hematoma Resolution and Activation of CCR4/ERK/Nrf2/CD163 Signaling Pathway After Intracerebral Hemorrhage in Mice.
Authors: Lei Et al.
Neurotherapeutics 2020;17:1940-1953
FAQs
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