Detalhe da pesquisa
1.
Structure activity relationship of N-1 substituted 1,5-naphthyrid-2-one analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-9).
Bioorg Med Chem Lett
; 75: 128808, 2022 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35609741
2.
Structure activity relationship of C-2 ether substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-5).
Bioorg Med Chem Lett
; 25(17): 3630-5, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26152426
3.
Structure activity relationship of pyridoxazinone substituted RHS analogs of oxabicyclooctane-linked 1,5-naphthyridinyl novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-6).
Bioorg Med Chem Lett
; 25(17): 3636-43, 2015 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26141771
4.
Structure activity relationship of substituted 1,5-naphthyridine analogs of oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents (Part-4).
Bioorg Med Chem Lett
; 25(11): 2409-15, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25911300
5.
Hydroxy tricyclic 1,5-naphthyridinone oxabicyclooctane-linked novel bacterial topoisomerase inhibitors as broad-spectrum antibacterial agents-SAR of RHS moiety (Part-3).
Bioorg Med Chem Lett
; 25(12): 2473-8, 2015 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25978963
6.
Discovery of BMS-986235/LAR-1219: A Potent Formyl Peptide Receptor 2 (FPR2) Selective Agonist for the Prevention of Heart Failure.
J Med Chem
; 63(17): 9003-9019, 2020 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32407089
7.
Synthesis and biological activity of enantiomeric pairs of 5-(Alk-2-enyl)thiolactomycin and 5-[(E)-Cycloalk-2-enylidenemethyl]thiolactomycin congeners.
Chem Pharm Bull (Tokyo)
; 57(9): 920-36, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19721252
8.
Synthesis and biological activity of enantiomeric pairs of 5-[(E)-cycloalk-2-enylidenemethyl]thiolactomycin congeners.
Bioorg Med Chem Lett
; 18(20): 5598-600, 2008 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18805004
9.
Synthesis and biological activity of enantiomeric pairs of 5-vinylthiolactomycin congeners.
Bioorg Med Chem Lett
; 17(14): 4070-4, 2007 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17507223