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ML 365

Cat. No. 5337 4 Citations 1 Review Submit a Review Datasheet / COA / SDS
Pricing Availability   Qty
Description: Potent and selective K2P3.1 (TASK-1) channel blocker
Chemical Name: 2-Methoxy-N-[3-[(3-methylbenzoyl)amino]phenyl]benzamide
Purity: ≥99% (HPLC)
Datasheet
Citations (4)
Reviews (1)
Biological Activity Technical Data Solubility Calculators Datasheets References

Biological Activity for ML 365

ML 365 is a potent and selective TASK-1 (K2P3.1/KCNK3) channel blocker (IC50 values are 4 and 390 nM at TASK-1 and TASK-3, respectively). Displays little or no inhibition at Kir2.1, voltage-gated potassium channels, KCNQ2 and KV11.1 (hERG).

Compound Libraries for ML 365

ML 365 is also offered as part of the Tocriscreen 2.0 Max. Find out more about compound libraries available from Tocris.

Technical Data for ML 365

M. Wt 360.41
Formula C22H20N2O3
Storage Store at +4°C
Purity ≥99% (HPLC)
CAS Number 947914-18-3
PubChem ID 46785920
InChI Key UTAJHKSGYJSZBR-UHFFFAOYSA-N
Smiles CC1=CC=CC(C(NC2=CC(NC(C3=CC=CC=C3OC)=O)=CC=C2)=O)=C1

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.

Solubility Data for ML 365

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 36.04 100
ethanol 18.02 50

Preparing Stock Solutions for ML 365

The following data is based on the product molecular weight 360.41. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 2.77 mL 13.87 mL 27.75 mL
5 mM 0.55 mL 2.77 mL 5.55 mL
10 mM 0.28 mL 1.39 mL 2.77 mL
50 mM 0.06 mL 0.28 mL 0.55 mL

Molarity Calculator

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Reconstitution Calculator

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Dilution Calculator

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References for ML 365

References are publications that support the biological activity of the product.

Flaherty et al (2014) Potent and selective inhibitors of the TASK-1 potassium channel through chemical optimization of a bis-amide scaffold. Bioorg.Med.Chem.Lett. 24 3968 PMID: 25017033

Zou et al (2013) ML365: Development of bis-amides as selective inhibitors of the KCNK3/TASK1 two pore potassium channel. Probe Reports from the NIH Molecular Libraries Program PMID: 24479195

If you know of a relevant reference for ML 365, please let us know.

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Keywords: ML 365, ML 365 supplier, ML365, Potassium, channels, subfamily, K, member, 3, k2p3.1, KCNK3, potent, selective, TASK1, inhibitors, inhibits, TASK3, TWIK, related, acid, sensitive, K+, two, pore, potassium, channel, Two-P, Channels, 5337, Tocris Bioscience

4 Citations for ML 365

Citations are publications that use Tocris products. Selected citations for ML 365 include:

Veldkamp et al (2018) Neurokinin-3 receptor activation selectively prolongs atrial refractoriness by inhibition of a background K+ channel. Nat. Commun. 9 4357 PMID: 30341287

Vierra et al (2017) TALK-1 channels control β cell endoplasmic reticulum Ca2+ homeostasis. Sci Signal 10 PMID: 28928238

Richard L et al (2021) Modulation of TASK-1/3 channels at the hypoglossal motoneuron pool and effects on tongue motor output and responses to excitatory inputs in vivo: implications for strategies for obstructive sleep apnea pharmacotherapy. Sleep 44 PMID: 32745213

Pagani et al (2019) How Gastrin-Releasing Peptide Opens the Spinal Gate for Itch. Neuron PMID: 31103358

Do you know of a great paper that uses ML 365 from Tocris? Please let us know.

Reviews for ML 365

Average Rating: 5 (Based on 1 Review.)

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Ml 365 used to study the channel blocking activity on K2p1.1 channels.
By Anonymous on 11/27/2018
Assay Type: In Vitro
Species: Human

This product was used to study the channel blocking activity on K2p1.1 channels. It was identified that it shows certain degree of channel blocking although that is not concentration dependent. Would buy again as the results obtained were reproducible at every trial study.

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