# Correction: Construction of antifungal dual-target (SE, CYP51) pharmacophore models and the discovery of novel antifungal inhibitors

**Authors:** Yue Dong, Min Liu, Jian Wang, Zhuang Ding, Bin Sun

PMC · DOI: 10.1039/d4ra90079k · RSC Advances · 2024-07-26

## TL;DR

This paper corrects a previous study on developing antifungal drug models targeting two enzymes and identifying new inhibitors.

## Contribution

The correction provides updated information or clarifications regarding the pharmacophore models and antifungal inhibitors described in the original paper.

## Key findings

- The original study aimed to construct dual-target pharmacophore models for antifungal agents.
- The correction addresses potential errors or omissions in the initial findings and methodology.
- New insights or revised conclusions may improve the development of antifungal drugs.

## Abstract

Correction for ‘Construction of antifungal dual-target (SE, CYP51) pharmacophore models and the discovery of novel antifungal inhibitors’ by Yue Dong et al., RSC Adv., 2019, 9, 26302–26314, https://doi.org/10.1039/c9ra03713f.

## Linked entities

- **Proteins:** FUT2 (fucosyltransferase 2 (H blood group)), CYP51A1 (cytochrome P450 family 51 subfamily A member 1)

## Full-text entities

- **Genes:** CYP51A1 (cytochrome P450 family 51 subfamily A member 1) [NCBI Gene 1595] {aka CP51, CYP51, CYPL1, LDM, P450-14DM, P450L1}

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11274097/full.md

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Source: https://tomesphere.com/paper/PMC11274097