Mefuparib hydrochloride

A PARP inhibitor.

Phase of research

Potential treatment - pre-clinical evidence

How it helps

Antiviral

Drug status

Experimental

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Contradictory references
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Clinical trials

General information

Mefuparib (hydrochloride) is a poly-ADP-ribose polymerase inhibitor. It was shown to bind SARS-CoV-2 Nucleocapsid protein in vitro. It inhibited SARS-CoV-2 in cell culture. The EC50 of either mefuparib or remdesivir in their mixture was observed to be decreased, which was suggested to be linked to mefuparib’s capability to decrease the local density of SARS-CoV-2 Nucleocapside-RNA-nsp12 condensates (as a phase separation modulator), and thus make it more accessible to other antivirals (Zhao et al., 2021).

Mefuparib hydrochloride on PubChem


Synonyms

CVL218; CVL-218

 

Structure image - Mefuparib hydrochloride

CNCC1=CC=C(C=C1)C2=CC3=CC(=CC(=C3O2)C(=O)N)F.Cl


Supporting references

Link Tested on Impact factor Notes Publication date
Understanding the phase separation characteristics of nucleocapsid protein provides a new therapeutic opportunity against SARS-CoV-2
Nucleocapsid protein nsp12 Biophysical assay Small molecule In vitro Mechanism
in vitro biophysical assay; Vero E6 cells; SARS-CoV-2 strain BetaCoV/JS03/human/2020 10.16

The compound inhibited SARS-CoV-2 in Vero E6 cells with an EC50 of 3.46 μM. The EC50 of either mefuparib or remdesivir in their mixture was observed to be decreased.

Mar/26/2021

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