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Compound category: Organoheterocyclic compounds
(total 322 related compounds in database, current show from 31 to 40)
 
Compound name 2D structure Target pathogen(s) Related VF/VFcategory Max phase Reference(s)
4,6-dimethyl-N-[(Z)-1-pyridin-2-ylethylideneamino]pyrimidin-2-amine Depiction based on curated SMILES CH 3 N CH 3 CH 3 N HN N N Brucella VirB type IV secretion system Preclinical (in vivo) Paschos A, et al. 2011. Infect Immun
5,7-diiodo-1,2,3,4,4a,5,6,7,8,8a-decahydroquinolin-8-ol Depiction based on curated SMILES OH I I N H Brucella VirB type IV secretion system Preclinical (in vivo) Paschos A, et al. 2011. Infect Immun
5,7-dinitroquinolin-8-ol Depiction based on curated SMILES _ O N OH O O + N _ O + N Brucella VirB type IV secretion system Preclinical (in vivo) Paschos A, et al. 2011. Infect Immun
Diethyl 6-bromo-2,4-quinolinedicarboxylate Depiction based on curated SMILES H 3 C O O Br CH 3 N O O Brucella VirB type IV secretion system Preclinical (in vivo) Paschos A, et al. 2011. Infect Immun
2-(4-tert-Butyl-phenoxymethyl)-4-hydroxy-pyrimidine-5-carboxylic acid ethyl ester Depiction based on curated SMILES CH 3 H 3 C H 3 C O CH 3 O HN N O O Brucella VirB type IV secretion system Preclinical (in vivo) Paschos A, et al. 2011. Infect Immun
(2R,3S,4S,5S,6R)-2-[(R)-hydroxy-(4-isoquinolin-5-yl-2-methylphenyl)methyl]-6-(hydroxymethyl)oxane-3,4,5-triol Depiction based on curated SMILES HO OH OH OH O HO H CH 3 N Escherichia Type 1 fimbriae Preclinical (in vivo) Mydock-McGrane L, et al. 2016. J Med Chem
(2R,3S,4S,5S,6R)-2-[(R)-[4-(1-aminoisoquinolin-7-yl)-2-methylphenyl]-hydroxymethyl]-6-(hydroxymethyl)oxane-3,4,5-triol Depiction based on curated SMILES HO OH OH OH O HO H CH 3 NH 2 N Escherichia Type 1 fimbriae Preclinical (in vivo) Mydock-McGrane L, et al. 2016. J Med Chem
7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinolin-1-amine Depiction based on curated SMILES NH 2 N B CH 3 CH 3 CH 3 H 3 C O O Escherichia Type 1 fimbriae Preclinical (in vivo) Mydock-McGrane L, et al. 2016. J Med Chem
7-[4-[(R)-hydroxy-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methyl]-3-methylphenyl]-2H-isoquinolin-1-one Depiction based on curated SMILES HO OH OH OH O HO H CH 3 O N H Escherichia Type 1 fimbriae Preclinical (in vivo) Mydock-McGrane L, et al. 2016. J Med Chem
7-[4-[(R)-hydroxy-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methyl]-3-methylphenyl]-3,4-dihydro-2H-isoquinolin-1-one Depiction based on curated SMILES HO OH OH OH O HO H CH 3 O N H Escherichia Type 1 fimbriae Preclinical (in vivo) Mydock-McGrane L, et al. 2016. J Med Chem
   


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