|
3-hydroxy-3-[2-oxo-2-(pyridin-4-yl)ethyl]-1,3-dihydro-2H-indol-2-one |
|
Pseudomonas |
Biofilm |
Preclinical (in vitro) |
von Ambüren J, et al. 2020. Microorganisms |
|
1H-Indole, 3-(2-pyridin-4-yl-thiazol-4-yl)- |
Depiction based on curated SMILES
N
N
S
HN
|
Pseudomonas Yersinia |
TTSS (Type III secretion system) TTSS (Type III secretion system) |
Preclinical (in vitro) Preclinical (in vitro) |
Harmon DE, et al. 2010. Antimicrob Agents Chemother
|
|
5-Hydroxyindole |
Depiction based on curated SMILES
OH
N
H
|
Salmonella Shigella |
TTSS (SPI-1 encode) TTSS (Type III secretion system) |
Preclinical (in vitro) Preclinical (in vitro) |
McShan AC, et al. 2016. ChemMedChem Dey S, et al. 2017. ChemMedChem |
|
Indole-3-acetic acid |
Depiction based on curated SMILES
O
OH
N
H
|
Salmonella |
TTSS (SPI-1 encode) |
Preclinical (in vitro) |
McShan AC, et al. 2016. ChemMedChem |
|
Pirlindole mesylate |
Depiction based on curated SMILES
HO
O
O
S
CH
3
CH
3
HN
N
|
Salmonella |
Invasion |
Preclinical (in vitro) |
Ridge Y, et al. 2018. J Appl Microbiol |
|
4-(5-bromo-1-butylindol-3-yl)pyrimidin-2-amine |
Depiction based on curated SMILES
N
Br
N
NH
2
CH
3
N
|
Staphylococcus |
Biofilm |
Preclinical (in vitro) |
Huggins WM, et al. 2018. ACS Med Chem Lett |
|
4-(5-bromo-1-ethylindol-3-yl)pyrimidin-2-amine |
Depiction based on curated SMILES
Br
N
NH
2
H
3
C
N
N
|
Staphylococcus |
Biofilm |
Preclinical (in vitro) |
Huggins WM, et al. 2018. ACS Med Chem Lett |
|
4-(5-bromo-1-propylindol-3-yl)pyrimidin-2-amine |
Depiction based on curated SMILES
Br
N
NH
2
H
3
C
N
N
|
Staphylococcus |
Biofilm |
Preclinical (in vitro) |
Huggins WM, et al. 2018. ACS Med Chem Lett |
|
4-(5-Bromo-1H-indol-3-yl)-N,N-dimethylpyrimidin-2-amine |
Depiction based on curated SMILES
N
Br
CH
3
N
H
N
H
3
C
N
|
Staphylococcus |
Biofilm |
Preclinical (in vitro) |
Huggins WM, et al. 2018. ACS Med Chem Lett |
|
4-(5-bromo-1H-indol-3-yl)-N-ethylpyrimidin-2-amine |
Depiction based on curated SMILES
N
Br
H
3
C
N
H
N
NH
|
Staphylococcus |
Biofilm |
Preclinical (in vitro) |
Huggins WM, et al. 2018. ACS Med Chem Lett |
|
| | |