Free shipping on all orders over $ 500

Probenecid sodium

Cat. No. M10535

All AbMole products are for research use only, cannot be used for human consumption.

Probenecid sodium Structure
Size Price Availability Quantity
500mg USD 32 In stock
1g USD 48 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

Probenecid sodium is a sodium salt of Probenecid that is soluble in water. Probenecid (Benemid) is an organic anionic transport competitive inhibitor, as well as an agonist of transient receptor potential vanillin receptor subfamily 2(TRPV2) and an inhibitor of human bitter taste receptor TAS2R16. Probenecid effectively inhibits the MRP1- and MRP2-mediated uptake of the ATP-dependent active vesicle N-ethylmaleimide-glutathione (NEM-GS). Probenecid can competitively or non-competitively inhibit the transport function of MRP2 for organic anions. In vitro studies have shown that probenecid significantly inhibits MRP2-dependent ATPase activity and blocks the efflux of substrates (such as glutathione conjugates, certain antibiotics and chemotherapeutic agents) by MRP2. In addition to MRP2, probenecid is also an effective inhibitor of MRP1.

Chemical Information
Molecular Weight 307.34
Formula C13H18NNaO4S
CAS Number 23795-03-1
Solubility (25°C) Water
Storage 2-8°C, sealed
References

[1] Tetsuya Taniguchi, et al. Sci Rep. Hypouricemic agents reduce indoxyl sulfate excretion by inhibiting the renal transporters OAT1/3 and ABCG2

[2] Masato Kobayashi, et al. Nucl Med Biol. Assessment of drug transporters involved in the urinary secretion of [ 99m Tc]dimercaptosuccinic acid

[3] Stephanie N Liu, et al. CPT Pharmacometrics Syst Pharmacol. Probenecid-Boosted Tenofovir: A Physiologically-Based Pharmacokinetic Model-Informed Strategy for On-Demand HIV Preexposure Prophylaxis

[4] D Jimnez-Gallo, et al. Actas Dermosifiliogr. Calcinosis Cutis and Calciphylaxis

[5] F G MARSON. Ann Rheum Dis. Sodium salicylate and probenecid in the treatment of chronic gout; assessment of their relative effects in lowering serum uric acid levels

Related TRP Channel Products
SB-705498

SB-705498 is a potent, selective and orally bioavailable transient receptor potential vanilloid 1 (TRPV1) receptor antagonist with a pIC50 of 7.1.

HC-030031

HC-030031 is a selective TRPA1 blocker, antagonizing TRPA1-mediated calcium influx induced by AITC and formalin (IC50 = 6.2 and 5.3 μM, respectively).

AMG-517

AMG 517 is a potent and selective TRPV1 antagonist, antagonizes capsaicin, proton, and heat activation of TRPV1 with IC50 of 0.76 nM, 0.62 nM and 1.3 nM.

Icilin

Icilin is a synthetic super-agonist of the transient receptor potential M8 (TRPM8) ion channel.

Phenazopyridine hydrochloride

Phenazopyridine HCl is a competitive SARM1 inhibitor as well as a TRPM8 antagonist with an IC50 for SARM1 inhibition of 145 μM. It has local anesthetic/analgesic activity and can be used in studies related to traumatic brain injury, peripheral neuropathy, and neurodegenerative diseases.

  Catalog
Abmole Inhibitor Catalog




Keywords: Probenecid sodium supplier, TRP Channel, inhibitors, activators

All AbMole products are for research use only, cannot be used for human consumption or veterinary use. We do not provide products or services to individuals. Please comply with the intended use and do not use AbMole products for any other purpose.



Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.