N-Methyllidocaine iodide

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Cat.No. 1042 - N-Methyllidocaine iodide | C15H25IN2O | CAS No. 1462-71-1
Description: Enhances biosynthesis of phosphatidylinositol
Alternative Names: QX 372, N-Methyllignocaine iodide
Chemical Name: 2-[(2,6-Dimethylphenyl)amino]-N,N-diethyl-N-methyl-2-oxoethanaminium iodide
Datasheet
Citations
Literature

Biological Activity

Antiarrhythmic. Enhances the biosynthesis of phosphatidylinositol in hamster heart.

Technical Data

M. Wt 376.28
Formula C15H25IN2O
Storage Desiccate at +4°C
CAS Number 1462-71-1
PubChem ID 2829131
InChI Key QLXGAILYZFJDSH-UHFFFAOYSA-N
Smiles [I-].CC[N+](C)(CC)CC(=O)NC1=C(C)C=CC=C1C

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

All Tocris products are intended for laboratory research use only.

Solubility Data

SolubilitySoluble to 50 mM in water

Preparing Stock Solutions

The following data is based on the product molecular weight 376.28. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 2.66 mL 13.29 mL 26.58 mL
5 mM 0.53 mL 2.66 mL 5.32 mL
10 mM 0.27 mL 1.33 mL 2.66 mL
50 mM 0.05 mL 0.27 mL 0.53 mL

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Product Datasheets

Safety Datasheet

References

References are publications that support the products' biological activity.

Lee et al (1995) The modulation of phosphatidylinositol in hamster hearts by methyl lidocaine. Biochem.J. 309 871 PMID: 7639704

Tardi et al (1992) The effect of methyl-lidocaine on the biosynthesis of phospholipids de novo in the isolated hamster heart. Biochem.J. 285 161 PMID: 1322123


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Citations for N-Methyllidocaine iodide

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