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R-10015

Catalog No.GC65207

R-10015, un composé antiviral À large spectre pour l'infection par le VIH, agit comme un inhibiteur puissant et sélectif de la kinase du domaine LIM (LIMK) et se lie À la poche de liaison À l'ATP, avec une IC50 de 38 nM pour LIMK1 humain .

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R-10015 Chemical Structure

Cas No.: 2097938-51-5

Taille Prix Stock Qté
10mM (in 1mL DMSO)
297,00 $US
En stock
5mg
270,00 $US
En stock
10mg
423,00 $US
En stock
50mg
1 260,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

R-10015, a broad-spectrum antiviral compound for HIV infection, acts as a potent and selective inhibitor of LIM domain kinase (LIMK) and binds to the ATP-binding pocket, with an IC50 of 38 nM for human LIMK1[1].

R-10015 (100 μM; 0-4 hours) inhibits cofilin phosphorylation directly through blocking LIM kinase in CEM-SS T cells[1].R-10015 inhibits HIV-1 DNA synthesis, nuclear migration, and virion release[1].R-10015 inhibits multiple viruses, including Zaire ebolavirus (EBOV), Rift Valley fever virus (RVFV), Venezuelan equine encephalitis virus (VEEV), and herpes simplex virus 1 (HSV-1) [1].

R-10015 (10 mg/kg; i.p.) displays none indication of toxicity. The result suggests the possibility of short-term use of LIMK inhibitors to block viral infections[1].

[1]. Yi F, et al. Discovery of Novel Small-Molecule Inhibitors of LIM Domain Kinase for Inhibiting HIV-1. J Virol. 2017 Jun 9;91(13). pii: e02418-16.

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