What is the catalog number for Procainamide?

The catalog number for Procainamide is HY-A0084A.

What sizes are available for Procainamide?

Procainamide is available in the following size(s): 100 mg, 10 mM - 1 mL.

How many pack sizes does Procainamide come in?

Procainamide is available in 2 different pack sizes.

Is Procainamide in stock?

Procainamide is currently made to order / not held in immediate stock. Contact us for lead time.

Who manufactures Procainamide?

Procainamide is manufactured by QuantiMol.

What is the estimated delivery time for Procainamide?

Estimated delivery time for Procainamide is approximately 15 business day(s), depending on your location.

Where can I find the safety data sheet (SDS/MSDS) for Procainamide?

The safety data sheet for Procainamide is available here: http://file.medchemexpress.com/batch_PDF/HY-A0084A/Procainamide-SDS-MedChemExpress.pdf.

Procainamide

Procainamide (Procaine amide) is a specific and potent inhibitor of DNA methyltransferase 1 (DNMT1), which reactivates the expression of tumor suppressor factors by demethylating tumor suppressor genes. Procainamide induces vacuolization in various cell types and reduces cell proliferation and migration. Procainamide relaxes airway smooth muscle by activating potassium channels. Procainamide can be used in cancer and arrhythmia research[1][2][3][4][5][6].

Product Specifications

CAS Number

51-06-9

Product Name Alternative

Procaine amide; SP 100

UNSPSC

12352005

Hazard Statement

H301, H315, H319, H335

Target

DNA Methyltransferase; Potassium Channel

Type

Reference compound

Related Pathways

Epigenetics; Membrane Transporter/Ion Channel

Applications

Cancer-programmed cell death

Field of Research

Cancer; Cardiovascular Disease

Assay Protocol

https://www.medchemexpress.com/procainamide.html

Purity

99.80

Solubility

DMSO : 50 mg/mL (ultrasonic)

Smiles

O=C(NCCN(CC)CC)C1=CC=C(N)C=C1

Molecular Formula

C13H21N3O

Molecular Weight

235.33

Precautions

H301, H315, H319, H335

References & Citations

[1]Lee BH, et al. Procainamide is a specific inhibitor of DNA methyltransferase 1. J Biol Chem. 2005;280 (49) :40749-40756.|[2]Pritchard B, et al. Procainamide. [Updated 2021 Aug 8]. In: StatPearls [Internet]. Treasure Island (FL) : StatPearls Publishing; 2022 Jan-.|[3]Gardner I, et al. A comparison of the covalent binding of clozapine, procainamide, and vesnarinone to human neutrophils in vitro and rat tissues in vitro and in vivo[J]. Chemical research in toxicology, 2005, 18 (9) : 1384-1394.|[4]Nakahara T, et al. Involvement of K+ channel in procainamide-induced relaxation of bovine tracheal smooth muscle[J]. European journal of pharmacology, 2000, 402 (1-2) : 143-149.|[5]Morissette G, et al. Massive cell vacuolization induced by organic amines such as procainamide[J]. Journal of Pharmacology and Experimental Therapeutics, 2004, 310 (1) : 395-406.|[6]Segura-Pacheco B, et al. Reactivation of tumor suppressor genes by the cardiovascular drugs hydralazine and procainamide and their potential use in cancer therapy[J]. Clinical Cancer Research, 2003, 9 (5) : 1596-1603.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, protect from light)

Scientific Category

Reference compound1

Clinical Information

Launched

Citation 01

Adv Sci (Weinh) . 2024 Dec 5:e2410360.|Environ Pollut. 2023 Sep 1:332:121931.|Free Radic Biol Med. 2024 Jun 1:S0891-5849 (24) 00506-9.|Clin Chem. 2019 Dec;65 (12) :1522-1531. |Patent. US20180263995A1.