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Compound category: N-alkylindoles
(total 9 related compounds in database)
 
Compound name 2D structure Target pathogen(s) Related VF/VFcategory Max phase Reference(s)
Compound 8
(internal name in literature)
Depiction based on curated SMILES HO O CH 3 N Vibrio TCP (Toxin-coregulated pilus) Preclinical (in vivo) Woodbrey AK, et al. 2018. Biochemistry
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-(6-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-(6-bromo-1-methylindol-3-yl)pyrimidin-2-amine Depiction based on curated SMILES NH 2 Br N CH 3 N N Staphylococcus Biofilm Preclinical (in vitro) Huggins WM, et al. 2018. ACS Med Chem Lett
4-(6-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
Compound 7
(internal name in literature)
Depiction based on curated SMILES HO O H 3 C N Vibrio TCP (Toxin-coregulated pilus) Preclinical (in vitro) Woodbrey AK, et al. 2018. Biochemistry
5-({1-[(2-chloro-1,3-thiazol-5-yl)methyl]-1H-indol-3-yl}methylene)-1,3-dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione Depiction based on curated SMILES Cl O CH 3 N O S H 3 C N N O N Yersinia TTSS secreted effectors Preclinical (in vitro) Hu X, et al. 2013. Bioorg Med Chem Lett
   
   
   


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