Discovery of 2-aminoquinolone acid derivatives as potent inhibitors of SARS-CoV-2 DOI Creative Commons

Young Sup Shin,

Jun Young Lee, Sangeun Jeon

и другие.

Bioorganic & Medicinal Chemistry Letters, Год журнала: 2023, Номер 85, С. 129214 - 129214

Опубликована: Март 2, 2023

The COVID-19 pandemic caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) continues to threaten human health and create socioeconomic problems worldwide. A library of 200,000 small molecules from Korea Chemical Bank (KCB) were evaluated for their inhibitory activities against SARS-CoV-2 in a phenotypic-based screening assay discover new therapeutics combat COVID-19. primary hit this screen was quinolone structure-containing compound 1. Based on structure 1 enoxacin, which is quinolone-based antibiotic previously reported have weak activity SARS-CoV-2, we designed synthesized 2-aminoquinolone acid derivatives. Among them, 9b exhibited potent antiviral (EC

Язык: Английский

Structure-Based Discovery of Thiosemicarbazones As SARS-CoV-2 Main Protease Inhibitors DOI
Vinícius Gonçalves Maltarollo, Elany Barbosa da Silva, Thales Kronenberger

и другие.

Future Medicinal Chemistry, Год журнала: 2023, Номер 15(11), С. 959 - 985

Опубликована: Июнь 1, 2023

Aim: Discovery of novel SARS-CoV-2 main protease (Mpro) inhibitors using a structure-based drug discovery strategy. Materials & methods: Virtual screening employing covalent and noncovalent docking was performed to discover Mpro inhibitors, which were subsequently evaluated in biochemical cellular assays. Results: 91 virtual hits selected for assays, four confirmed as reversible SARS CoV-2 with IC50 values 0.4–3 μM. They also shown inhibit SARS-CoV-1 human cathepsin L. Molecular dynamics simulations indicated the stability inhibitor complexes interaction ligands at subsites. Conclusion: This approach led thiosemicarbazones potent inhibitors.

Язык: Английский

Процитировано

7

Case report: Successful combination therapy with isavuconazole and amphotericin B in treatment of disseminated Candida tropicalis infection DOI Creative Commons

Qibei Teng,

Xueshi Ye,

Ji‐Yu Wang

и другие.

Frontiers in Medicine, Год журнала: 2024, Номер 11

Опубликована: Июнь 24, 2024

Disseminated candidiasis is a severe complication in patients with hematological malignancies who have undergone chemotherapy or hematopoietic stem cell transplantation. It has high mortality rate. When disseminated caused by Candida tropicalis involves either the brain heart, prognosis extremely poor. Traditional methods such as cultures are limited diagnosing candidiasis. We describe case report of 55-year-old man acute myeloid leukemia developed candidemia after chemotherapy, which extensively to brain, skin, liver, spleen and kidneys. In this instance, patient was rapidly diagnosed candida infection metagenomic next generation sequencing, successfully treated combination therapy isavuconazole amphotericin B. The continued treatment while simultaneously receiving antifungal therapy, both were effectively controlled. This provides real-world experience for complicated

Язык: Английский

Процитировано

2

Overview of Antiviral Drug Therapy for COVID-19: Where Do We Stand? DOI Creative Commons
Renata Esposito, Davida Mirra, Liberata Sportiello

и другие.

Biomedicines, Год журнала: 2022, Номер 10(11), С. 2815 - 2815

Опубликована: Ноя. 4, 2022

The vaccine weapon has resulted in being essential fighting the COVID-19 outbreak, but it is not fully preventing infection due to an alarming spreading of several identified variants concern. In fact, recent emergence pointed out how SARS-CoV-2 pandemic still represents a global health threat. Moreover, oral antivirals also develop resistance, supporting need find new targets as therapeutic tools. However, cocktail therapy useful reduce drug resistance and maximize vaccination efficacy. Natural products metal-drug-based treatments have shown interesting antiviral activity, representing valid contribution counter outbreak. This report summarizes available evidence which supports use approved drugs further focuses on significant clinical trials that investigated safety efficacy repurposing molecules different phenotypes. To date, there are many individuals vulnerable exhibiting severe symptoms, thus characterizing strategies for better management disease challenge.

Язык: Английский

Процитировано

9

COVID-19 Treatment—Current Status, Advances, and Gap DOI Creative Commons
C. M. Ho, Lee C

Pathogens, Год журнала: 2022, Номер 11(10), С. 1201 - 1201

Опубликована: Окт. 18, 2022

COVID-19, which emerged in December 2019, was declared a global pandemic by the World Health Organization (WHO) March 2020. The disease caused severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It has millions of deaths worldwide and social economic disruption. While clinical trials on therapeutic drugs are going an Accelerating COVID-19 Therapeutic Interventions Vaccines (ACTIV) public–private partnership collaboration, current approaches options to counter remain few. include FDA-approved antiviral drugs, Remdesivir, immune modulator, Baricitinib. Hence, alternatives for treatment need be broadened. This paper discusses efforts find such as inhibiting viral entry disrupting virus life cycle, highlights gap that needs filled these approaches.

Язык: Английский

Процитировано

8

Discovery of 2-aminoquinolone acid derivatives as potent inhibitors of SARS-CoV-2 DOI Creative Commons

Young Sup Shin,

Jun Young Lee, Sangeun Jeon

и другие.

Bioorganic & Medicinal Chemistry Letters, Год журнала: 2023, Номер 85, С. 129214 - 129214

Опубликована: Март 2, 2023

The COVID-19 pandemic caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) continues to threaten human health and create socioeconomic problems worldwide. A library of 200,000 small molecules from Korea Chemical Bank (KCB) were evaluated for their inhibitory activities against SARS-CoV-2 in a phenotypic-based screening assay discover new therapeutics combat COVID-19. primary hit this screen was quinolone structure-containing compound 1. Based on structure 1 enoxacin, which is quinolone-based antibiotic previously reported have weak activity SARS-CoV-2, we designed synthesized 2-aminoquinolone acid derivatives. Among them, 9b exhibited potent antiviral (EC

Язык: Английский

Процитировано

4