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Verdinexor

Chemical Structure : Verdinexor

CAS No.: 1392136-43-4

Verdinexor (KPT-335, KPT335)

Catalog No.: PC-35933Not For Human Use, Lab Use Only.

Verdinexor (KPT-335, KPT335) is an orally bioavailable, selective inhibitor of nuclear export (SINE), inhibits the function of nuclear export protein Exportin 1 (XPO1/CRM1) and the viability of Jurkat and canine DLBCL cells with IC50 of 8.7 nM and 13.3 nM, respectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Verdinexor (KPT-335, KPT335) is an orally bioavailable, selective inhibitor of nuclear export (SINE), inhibits the function of nuclear export protein Exportin 1 (XPO1/CRM1) and the viability of Jurkat and canine DLBCL cells with IC50 of 8.7 nM and 13.3 nM, respectively.
KPT-335 induces apoptosis in CLBL1 cells and primary canine DLBCL cells.
KPT-335 reduces influenza a virus replication in vitro and in vivo.
KPT-335 also inhibits XPO1-mediated transport and reduces RSV replication in vitro, shows effectivity against RSV A and B strains and reduces viral replication following prophylactic or therapeutic administration.

Physicochemical Properties

M.Wt 441.337
Formula C19H13F6N5O
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(Z)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)-N-(pyridin-2-ylmethyl)acrylamide

References

1. London CA, et al. PLoS One. 2014 Feb 4;9(2):e87585.

2. Perwitasari O, et al. J Virol. 2014 Sep 1;88(17):10228-43.

3. Perwitasari O, et al. PLoS One. 2016 Nov 28;11(11):e0167221.

4. Jorquera PA, et al. J Virol. 2018 Dec 12. pii: JVI.01684-18.

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