Detalhe da pesquisa
1.
Exploration of 1,2,3-triazolo fused triterpenoids as inhibitors of human coronavirus 229E targeting the viral nsp15 protein.
Arch Pharm (Weinheim)
; 357(1): e2300442, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37840345
2.
The SARS-CoV-2 and other human coronavirus spike proteins are fine-tuned towards temperature and proteases of the human airways.
PLoS Pathog
; 17(4): e1009500, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33886690
3.
Novel Polymyxin-Inspired Peptidomimetics Targeting the SARS-CoV-2 Spike:hACE2 Interface.
Int J Mol Sci
; 24(10)2023 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37240111
4.
Amphiphilic Sialic Acid Derivatives as Potential Dual-Specific Inhibitors of Influenza Hemagglutinin and Neuraminidase.
Int J Mol Sci
; 24(24)2023 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38139095
5.
Synthesis of new N-(3-oxo-1-thia-4-azaspiro[4.5]decan-4-yl)pyridine-3-carboxamide derivatives and evaluation of their anti-influenza virus and antitubercular activities.
Arch Pharm (Weinheim)
; 355(10): e2200224, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35849096
6.
Synthesis and Anticancer and Antiviral Activities of C-2'-Branched Arabinonucleosides.
Int J Mol Sci
; 23(20)2022 Oct 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36293420
7.
In Vitro Characterization of the Carbohydrate-Binding Agents HHA, GNA, and UDA as Inhibitors of Influenza A and B Virus Replication.
Antimicrob Agents Chemother
; 65(3)2021 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33288640
8.
Design, synthesis and anti-influenza virus activity of furan-substituted spirothiazolidinones.
Bioorg Chem
; 112: 104958, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33979734
9.
Facile synthesis, antimicrobial and antiviral evaluation of novel substituted phenyl 1,3-thiazolidin-4-one sulfonyl derivatives.
Bioorg Chem
; 114: 105153, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34328851
10.
Exploration of the 2,3-dihydroisoindole pharmacophore for inhibition of the influenza virus PA endonuclease.
Bioorg Chem
; 116: 105388, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34670331
11.
Hemagglutinin Cleavability, Acid Stability, and Temperature Dependence Optimize Influenza B Virus for Replication in Human Airways.
J Virol
; 94(1)2019 12 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31597759
12.
Superior inhibition of influenza virus hemagglutinin-mediated fusion by indole-substituted spirothiazolidinones.
Bioorg Med Chem
; 28(1): 115130, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31753804
13.
Design and synthesis of novel Imidazo[2,1-b]thiazole derivatives as potent antiviral and antimycobacterial agents.
Bioorg Chem
; 95: 103496, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31862455
14.
Synthesis and biological evaluation of substituted phenyl azetidine-2-one sulphonyl derivatives as potential antimicrobial and antiviral agents.
Bioorg Chem
; 104: 104320, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33142428
15.
Anti-influenza virus activity of benzo[d]thiazoles that target heat shock protein 90.
Bioorg Chem
; 98: 103733, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32171985
16.
Synthesis and Biological Evaluation of Novel (thio)semicarbazone-Based Benzimidazoles as Antiviral Agents against Human Respiratory Viruses.
Molecules
; 25(7)2020 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-32218301
17.
Influenza virus entry via the GM3 ganglioside-mediated platelet-derived growth factor receptor ß signalling pathway.
J Gen Virol
; 100(4): 583-601, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30762518
18.
Synthesis and anti-coronavirus activity of a series of 1-thia-4-azaspiro[4.5]decan-3-one derivatives.
Arch Pharm (Weinheim)
; 352(6): e1800330, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31073993
19.
Novel N-(1-thia-4-azaspiro[4.5]decan-4-yl)carboxamide derivatives as potent and selective influenza virus fusion inhibitors.
Arch Pharm (Weinheim)
; 352(11): e1900028, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31531897
20.
Identification of influenza PA-Nter endonuclease inhibitors using pharmacophore- and docking-based virtual screening.
Bioorg Med Chem
; 26(15): 4544-4550, 2018 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30082105