In silico-driven identification of Pranlukast as a Stabilizer of PD-L1 Homodimers

Our results suggest that pranlukast inhibits the PD-1/PD-L1 axis, meriting its repurposing as an antitumor drug.

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Publication Details

Journal
Anti-Cancer Agents in Medicinal Chemistry
Published
2024-10-16
DOI
https://doi.org/10.2174/0118715206303675241009104647
Primary Topic
Computational Drug Discovery Methods
Type
article
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article

In silico-driven identification of Pranlukast as a Stabilizer of PD-L1 Homodimers

Alexis Paulina Jiménez‐Uribe, Nohemí Salinas-Jazmín, Zhiqiang An, Marco A. Velasco‐Velázquez et al.
Anti-Cancer Agents in Medicinal Chemistry
Computational Drug Discovery Methods
article

In silico-driven identification of Pranlukast as a Stabilizer of PD-L1 Homodimers

Alexis Paulina Jiménez‐Uribe, Nohemí Salinas-Jazmín, Zhiqiang An, Marco A. Velasco‐Velázquez, Luis Córdova-Bahena, Carlos Landero-Marín, Xcaret Flores-Hernández, Leonardo Daniel Alvarez-Coronel
article en

Abstract

Our results suggest that pranlukast inhibits the PD-1/PD-L1 axis, meriting its repurposing as an antitumor drug.

Anti-Cancer Agents in Medicinal ChemistryVol. 25(3)
Brown Foundation (US), Secretaría de Ciencia, Humanidades, Tecnología e Innovación (MX), Universidad Nacional Autónoma de México (MX)
Good health and well-being
Openalex Percentile: Top 78%
Computational Drug Discovery Methods
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