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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.
Artículo
en Inglés
| MEDLINE | ID: mdl-35609741
2.
In Vitro and In Vivo Characterization of the Novel Oxabicyclooctane-Linked Bacterial Topoisomerase Inhibitor AM-8722, a Selective, Potent Inhibitor of Bacterial DNA Gyrase.
Antimicrob Agents Chemother
; 60(8): 4830-9, 2016 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-27246784
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-26141771
4.
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.
Artículo
en Inglés
| MEDLINE | ID: mdl-25978963
5.
Stereoselective synthesis of cis-2-fluorocyclopropanecarboxylic acid.
J Org Chem
; 79(15): 7226-31, 2014 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-25010939
6.
Synthesis and biological evaluation of tubulysin D analogs related to stereoisomers of tubuvaline.
Bioorg Med Chem Lett
; 21(1): 431-4, 2011 Jan 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-21106374
7.
Total syntheses of tubulysins.
Chemistry
; 16(38): 11678-88, 2010 Oct 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-20734394
8.
Structures, biological activities, and total syntheses of 13-hydroxy- and 13-acetoxy-14-nordehydrocacalohastine, novel modified furanoeremophilane-type sesquiterpenes from Trichilia cuneata.
Org Lett
; 7(9): 1765-8, 2005 Apr 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-15844901
9.
Synthesis and structure-activity relationship studies of highly potent novel oxazolidinone antibacterials.
J Med Chem
; 51(20): 6558-62, 2008 Oct 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-18826297
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