Detalhe da pesquisa
1.
Synthesis and biological evaluation of 2,5-disubstituted furan derivatives containing 1,3-thiazole moiety as potential α-glucosidase inhibitors.
Bioorg Med Chem Lett
; 83: 129173, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36764471
2.
2,5-Disubstituted furan derivatives containing imidazole, triazole or tetrazole moiety as potent α-glucosidase inhibitors.
Bioorg Chem
; 131: 106298, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36455481
3.
Derivative of cinnamic acid inhibits T3SS of Xanthomonas oryzae pv. oryzae through the HrpG-HrpX regulatory cascade.
Bioorg Chem
; 141: 106871, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37734193
4.
A novel strategy to control Pseudomonas syringae through inhibition of type III secretion system.
Pestic Biochem Physiol
; 194: 105471, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37532345
5.
Discovery of a series of 5-phenyl-2-furan derivatives containing 1,3-thiazole moiety as potent Escherichia coli ß-glucuronidase inhibitors.
Bioorg Chem
; 116: 105306, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34521047
6.
Thiazolidin-2-cyanamides derivatives as novel potent Escherichia coli ß-glucuronidase inhibitors and their structure-inhibitory activity relationships.
J Enzyme Inhib Med Chem
; 35(1): 1736-1742, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32928007
7.
Discovery of novel inhibitors of phosphodiesterase 4 with 1-phenyl-3,4-dihydroisoquinoline scaffold: Structure-based drug design and fragment identification.
Bioorg Med Chem Lett
; 29(22): 126720, 2019 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31610942
8.
Direct thiocarbamation of imidazoheterocycles via dual C-H sulfurization.
Org Biomol Chem
; 17(34): 7854-7857, 2019 08 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-31408075
9.
Synthesis and fungicidal activity of novel pyrazole derivatives containing 5-Phenyl-2-Furan.
Bioorg Med Chem
; 27(19): 115048, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31439387
10.
Synthesis and bioactivity of 1,3-thiazolidine-2-thione derivatives against type III secretion system of Xanthomonas oryzae.
Bioorg Med Chem
; 27(15): 3364-3371, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31204227
11.
Structure-aided optimization of 3-O-ß-chacotriosyl ursolic acid as novel H5N1 entry inhibitors with high selective index.
Bioorg Med Chem
; 27(18): 4048-4058, 2019 09 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31350154
12.
Synthesis and biological evaluation of 1,3,4-thiadiazole derivatives as type III secretion system inhibitors against Xanthomonas oryzae.
Pestic Biochem Physiol
; 160: 87-94, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31519261
13.
Small Molecule Inhibitors Specifically Targeting the Type III Secretion System of Xanthomonas oryzae on Rice.
Int J Mol Sci
; 20(4)2019 Feb 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-30813400
14.
Synthesis and bioactivity of 3,5-dimethylpyrazole derivatives as potential PDE4 inhibitors.
Bioorg Med Chem Lett
; 28(19): 3276-3280, 2018 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30131240
15.
Tetrahydroquinoline and tetrahydroisoquinoline derivatives as potential selective PDE4B inhibitors.
Bioorg Med Chem Lett
; 28(19): 3271-3275, 2018 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30131242
16.
Synthesis and bioactivity of thiazolidin-2-cyanamide derivatives against type III secretion system of Xanthomonas oryzae on rice.
Pestic Biochem Physiol
; 149: 89-97, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-30033022
17.
Design, synthesis and fungicidal activity of novel 2-substituted aminocycloalkylsulfonamides.
Bioorg Med Chem Lett
; 27(2): 271-276, 2017 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27914797
18.
Rational design of conformationally constrained oxazolidinone-fused 1,2,3,4-tetrahydroisoquinoline derivatives as potential PDE4 inhibitors.
Bioorg Med Chem
; 25(20): 5709-5717, 2017 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28888661
19.
Design, synthesis and biological evaluation of 2,4-disubstituted oxazole derivatives as potential PDE4 inhibitors.
Bioorg Med Chem
; 25(6): 1852-1859, 2017 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28196708
20.
Synthesis and bioactivity of pyrazole and triazole derivatives as potential PDE4 inhibitors.
Bioorg Med Chem Lett
; 26(15): 3632-5, 2016 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27289320