Caroline S. de Freitas

发表

Agathisflavone, a natural biflavonoid that inhibits SARS-CoV-2 replication by targeting its proteases

Carolina Q. Sacramento, N. Carels, H. Castro-Faria-Neto, 2022, International Journal of Biological Macromolecules.

Agathisflavone, a biflavonoid from Anacardium occidentale L., inhibits influenza virus' neuraminidase.

P. Bozza, S. P. C. Barroso, A. C. de Oliveira, 2019, Current topics in medicinal chemistry.

Macrophages undergo necroptosis during severe influenza A infection and contribute to virus-associated cytokine storm

Carolina Q. Sacramento, F. Bozza, P. Bozza, 2022, bioRxiv.

The clinically approved antiviral drug sofosbuvir impairs brazilian zika virus replication

Carolina Q. Sacramento, F. Thompson, F. Bozza, 2016, bioRxiv.

2,8-bis(trifluoromethyl)quinoline analogs show improved anti-Zika virus activity, compared to mefloquine.

P. Bozza, G. Barbosa-Lima, T. Souza, 2017, European journal of medicinal chemistry.

In vitro antiviral activity of the anti-HCV drugs daclatasvir and sofosbuvir against SARS-CoV-2, the aetiological agent of COVID-19

Carolina Q. Sacramento, T. Tuschl, D. Patel, 2021, The Journal of antimicrobial chemotherapy.

Atazanavir, Alone or in Combination with Ritonavir, Inhibits SARS-CoV-2 Replication and Proinflammatory Cytokine Production

Carolina Q. Sacramento, N. Carels, F. Bozza, 2020, Antimicrobial Agents and Chemotherapy.

Atazanavir inhibits SARS-CoV-2 replication and pro-inflammatory cytokine production

Carolina Q. Sacramento, N. Carels, F. Bozza, 2020, bioRxiv.

Beyond Members of the Flaviviridae Family, Sofosbuvir Also Inhibits Chikungunya Virus Replication

S. Rehen, F. Bozza, P. Bozza, 2018, Antimicrobial Agents and Chemotherapy.

N-(2-(arylmethylimino)ethyl)-7-chloroquinolin-4-amine derivatives, synthesized by thermal and ultrasonic means, are endowed with anti-Zika virus activity.

P. Bozza, C. Kaiser, G. Barbosa-Lima, 2017, European journal of medicinal chemistry.

The clinically approved antiviral drug sofosbuvir inhibits Zika virus replication

Carolina Q. Sacramento, F. Thompson, S. Rehen, 2017, Scientific Reports.

SARS-CoV-2 engages inflammasome and pyroptosis in human primary monocytes

Carolina Q. Sacramento, F. Bozza, P. Bozza, 2021, Cell death discovery.

Correction: Aureonitol, a Fungi-Derived Tetrahydrofuran, Inhibits Influenza Replication by Targeting Its Surface Glycoprotein Hemagglutinin

Carolina Q. Sacramento, O. Santos-Filho, C. Kaiser, 2015, PloS one.

Aureonitol, a Fungi-Derived Tetrahydrofuran, Inhibits Influenza Replication by Targeting Its Surface Glycoprotein Hemagglutinin

Carolina Q. Sacramento, O. Santos-Filho, C. Kaiser, 2015, PloS one.

Yellow fever virus is susceptible to sofosbuvir both in vitro and in vivo

Carolina Q. Sacramento, A. Tanuri, M. Teixeira, 2019, PLoS neglected tropical diseases.

Severe influenza infection is associated with inflammatory programmed cell death in infected macrophages

Carolina Q. Sacramento, F. Bozza, P. Bozza, 2023, Frontiers in Cellular and Infection Microbiology.

VIP plasma levels associate with survival in severe COVID‐19 patients, correlating with protective effects in SARS‐CoV‐2‐infected cells

F. Bozza, P. Bozza, V. C. Soares, 2022, Journal of leukocyte biology.

Protective effects of VIP and PACAP in SARS-CoV-2 infection

Carolina Q. Sacramento, F. Bozza, P. Bozza, 2021 .

Lipid droplets fuel SARS-CoV-2 replication and production of inflammatory mediators

Carolina Q. Sacramento, F. Bozza, P. Bozza, 2020, bioRxiv.

Simvastatin Downregulates the SARS-CoV-2-Induced Inflammatory Response and Impairs Viral Infection Through Disruption of Lipid Rafts

Carolina Q. Sacramento, J. Viola, F. Bozza, 2022, Frontiers in Immunology.

SARS-CoV-2 engages inflammasome and pyroptosis in human primary monocytes

F. Bozza, P. Bozza, V. C. Soares, 2021, Cell Death Discovery.

The in vitro antiviral activity of the anti-hepatitis C virus (HCV) drugs daclatasvir and sofosbuvir against SARS-CoV-2

Carolina Q. Sacramento, S. Rehen, F. Bozza, 2020, bioRxiv.

VIP plasma levels associate with survival in severe COVID‐19 patients, correlating with protective effects in SARS‐CoV‐2‐infected cells

Carolina Q. Sacramento, F. Bozza, P. Bozza, 2020, bioRxiv.

Neuraminidase from Influenza A and B viruses is susceptible to the compound 4-(4-Phenyl-1H-1,2,3-Triazol-1-yl)-2,2,6,6-Tetramethylpiperidine-1-Oxyl.

V. Ferreira, A. Cunha, C. Sacramento, 2019, Current topics in medicinal chemistry.

N-(2-(arylmethylimino)ethyl)-7-chloroquinolin-4-amine derivatives, synthesized by thermal and ultrasonic means, are endowed with anti-Zika virus activity.

P. Bozza, C. Kaiser, G. Barbosa-Lima, 2017, European journal of medicinal chemistry.

Correction: SARS-CoV-2 engages inflammasome and pyroptosis in human primary monocytes

Carolina Q. Sacramento, F. Bozza, P. Bozza, 2021, Cell death discovery.

Beyond Members of the Flaviviridae Family, Sofosbuvir Also Inhibits Chikungunya Virus Replication

Carolina Q. Sacramento, S. Rehen, F. Bozza, 2018, Antimicrobial Agents and Chemotherapy.