Detalhe da pesquisa
1.
Structure-based discovery of glycomimetic FmlH ligands as inhibitors of bacterial adhesion during urinary tract infection.
Proc Natl Acad Sci U S A
; 115(12): E2819-E2828, 2018 03 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29507247
2.
Methyl isocyanide as a convertible functional group for the synthesis of spirocyclic oxindole γ-lactams via post-Ugi-4CR/transamidation/cyclization in a one-pot, three-step sequence.
Beilstein J Org Chem
; 14: 875-883, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29765468
3.
A one-pot multicomponent coupling/cyclization for natural product herbicide (±)-thaxtomin A.
Org Biomol Chem
; 12(41): 8125-7, 2014 Nov 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25058709
4.
Discovery of Orally Bioavailable FmlH Lectin Antagonists as Treatment for Urinary Tract Infections.
J Med Chem
; 67(5): 3668-3678, 2024 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38308631
5.
Novel approaches to glycomimetic design: development of small molecular weight lectin antagonists.
Expert Opin Drug Discov
; 16(5): 513-536, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33337918
6.
Biphenyl Gal and GalNAc FmlH Lectin Antagonists of Uropathogenic E. coli (UPEC): Optimization through Iterative Rational Drug Design.
J Med Chem
; 62(2): 467-479, 2019 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-30540910
7.
Small Molecule Inhibitors of Metabolic Enzymes Repurposed as a New Class of Anthelmintics.
ACS Infect Dis
; 4(7): 1130-1145, 2018 07 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29718656