Date published: 2026-3-19

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VHR Inhibitors

VHR inhibitors, short for Vaccinia H1-related phosphatase inhibitors, represent a class of small molecules designed to target and modulate the activity of the Vaccinia H1-related phosphatase (VHR) enzyme. VHR is a member of the dual-specificity protein phosphatase (DUSP) family, which plays a pivotal role in the regulation of cellular signaling pathways. These inhibitors are primarily developed for research tools to probe and better understand the intricacies of cellular signal transduction processes. The VHR enzyme, like other DUSPs, is responsible for dephosphorylating both tyrosine and threonine residues in its substrate proteins. By doing so, VHR can modulate the activity of critical signaling molecules, such as mitogen-activated protein kinases (MAPKs), and thus influence various cellular responses, including proliferation, differentiation, and stress responses. VHR inhibitors are designed to interact with the active site of VHR, either through competitive or allosteric mechanisms, effectively preventing the dephosphorylation of specific substrates. This targeted inhibition allows researchers to dissect the contributions of VHR to signal transduction pathways and gain insights into its role in various cellular processes.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

RK-682

332131-32-5sc-202319
sc-202319A
200 µg
1 mg
$112.00
$460.00
4
(1)

RK-682 is a versatile acid halide known for its reactivity with nucleophiles, particularly amines and alcohols, leading to the formation of stable amides and esters. Its unique electronic structure enhances electrophilicity, promoting rapid acylation reactions. The compound exhibits distinct solvation dynamics, which influence its interaction with solvents, thereby affecting reaction rates. Additionally, RK-682's steric properties allow for selective reactivity, making it a valuable tool in synthetic chemistry.

RK-682, Streptomyces sp.

154639-24-4sc-202791
200 µg
$109.00
(0)

RK-682, derived from Streptomyces sp., is characterized by its exceptional reactivity profile as a vhr. It engages in rapid acyl transfer processes, facilitated by its unique steric and electronic characteristics. The compound's ability to form transient intermediates enhances its reactivity with various nucleophiles, leading to diverse synthetic pathways. Its distinct solubility behavior in different solvents further modulates reaction kinetics, allowing for tailored reactivity in complex chemical environments.