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Compound category: Organic acids and derivatives
(total 132 related compounds in database, current show from 11 to 20)
 
Compound name 2D structure Target pathogen(s) Related VF/VFcategory Max phase Reference(s)
Carfilzomib Depiction based on curated SMILES CH 3 H 3 C N H O HN O N O O CH 3 O O CH 3 NH CH 3 N H O Streptococcus Adherence Preclinical (in vivo) Manzer HS, et al. 2022. PLoS Pathog
Trans-4-Methylcyclohexanecarboxylic acid Depiction based on curated SMILES CH 3 O HO Yersinia TTSS secreted effectors Preclinical (in vivo) Liang F, et al. 2003. J Biol Chem
Bis(carboxycyclopentadienyl) Iron Depiction based on curated SMILES _ 2+ Fe HO O H _ HO O H Yersinia TTSS secreted effectors Preclinical (in vivo) Liang F, et al. 2003. J Biol Chem
3-Noradamantanecarboxylic acid Depiction based on curated SMILES O OH Yersinia TTSS secreted effectors Preclinical (in vivo) Liang F, et al. 2003. J Biol Chem
(3-(Acetylhydroxyamino)propyl)phosphonic acid Depiction based on curated SMILES H 3 C O N P O OH OH OH Burkholderia Motility Preclinical (in vivo) Bove M, et al. 2022. Microbiology (Reading)
Compound 6a
(internal name in literature)		 Depiction based on curated SMILES HN O O O O NH Burkholderia Quorum-sensing Preclinical (in vivo) Scoffone VC, et al. 2016. Sci Rep
Compound 8a
(internal name in literature)		 Depiction based on curated SMILES O O N H O N H O Burkholderia Quorum-sensing Preclinical (in vivo) Scoffone VC, et al. 2016. Sci Rep
Compound 8b
(internal name in literature)		 Depiction based on curated SMILES O NH O O HN O Burkholderia Quorum-sensing Preclinical (in vivo) Scoffone VC, et al. 2016. Sci Rep
Compound 8c
(internal name in literature)		 Depiction based on curated SMILES O HN O O CH 3 O NH CH 3 Burkholderia Quorum-sensing Preclinical (in vivo) Scoffone VC, et al. 2016. Sci Rep
[3,4,5-triacetyloxy-6-[(R)-acetyloxy-(4-bromo-2-methylphenyl)methyl]oxan-2-yl]methyl acetate Depiction based on curated SMILES O Br O CH 3 O CH 3 O O CH 3 O H O O O H 3 C O CH 3 O H 3 C Escherichia Type 1 fimbriae Preclinical (in vivo) Mydock-McGrane L, et al. 2016. J Med Chem
   


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