1. Membrane Transporter/Ion Channel
  2. Sodium Channel
  3. Zorevunersen

Zorevunersen is an antisense oligonucleotide targeting the Scn1a gene based on TANGO technology. Zorevunersen increases Scn1a mRNA transcripts and elevates the expression level of NaV1.1 protein. Zorevunersen restores the excitability of PV interneurons, thereby reducing seizures and prolonging survival in mice. Zorevunersen can be used for research on Dravet syndrome.

The free form of the compound is prone to instability, it is advisable to consider the stable salt form (Zorevunersen sodium) that retains the same biological activity.

For research use only. We do not sell to patients.

RNA, (P-thio)[2′-O-(2-methoxyethyl)](A-G-m5U-m5U-G-G-A-G-m5C-A-A-G-A-m5U-m5U-A-m5U-m5C)

Zorevunersen Chemical Structure

CAS No. : 2415330-04-8

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Description

Zorevunersen is an antisense oligonucleotide targeting the Scn1a gene based on TANGO technology. Zorevunersen increases Scn1a mRNA transcripts and elevates the expression level of NaV1.1 protein. Zorevunersen restores the excitability of PV interneurons, thereby reducing seizures and prolonging survival in mice. Zorevunersen can be used for research on Dravet syndrome[1].

IC50 & Target

Nav1.1

 

In Vivo

Zorevunersen (20 μg; intracerebroventricular injection; unilateral single injection; postnatal day 2) prevents seizures in pre-weaning Scn1a+/- mice[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 75% C57BL/6:25% 129S6/SvEvTac (Scn1a+/− Dravet Syndrome model)[1]
Dosage: 20 μg
Administration: i.c.v.; single unilateral injection; postnatal day 2 (P2)
Result: Completely prevented seizures in pre-weaning cohort.
Significantly reduced seizure frequency in post-weaning cohort.
Prolonged survival in post-weaning cohort.
Restored PV interneuron intrinsic excitability to vehicle-treated wild-type levels.
Significantly elevated action potential firing frequencies compared to vehicle-treated Scn1a+/− mice .
Failed to rescue reduced AP upstroke velocity of vehicle-treated Scn1a+/− PV interneurons.
Caused no significant difference in seizure frequency compared to vehicle-treated WT mice in wild-type cohort.
Significantly reduced PV interneuron excitability relative to vehicle-treated WT mice in wild-type cohort.
Molecular Weight

7197.20

Formula

C204H263N63O114P20S20

CAS No.
SMILES

[Zorevunersen]

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Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Zorevunersen
Cat. No.:
HY-148410
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