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Compound category: Organic acids and derivatives
(total 132 related compounds in database, current show from 61 to 70)
 
Compound name 2D structure Target pathogen(s) Related VF/VFcategory Max phase Reference(s)
(2S,3S)-N-hydroxy-3-methyl-2-[[3-(4-nitrophenyl)phenyl]sulfonylamino]pentanamide Depiction based on curated SMILES OH N H O _ O O + N H 3 C O O S HN CH 3 Clostridium BoNT (Botulinum neurotoxin) Preclinical (in vitro) Thompson JC, et al. 2020. Bioorg Med Chem
3-(2,5-dichlorophenyl)-N-[(2S,3S)-1-(hydroxyamino)-3-methyl-1-oxopentan-2-yl]benzamide Depiction based on curated SMILES HO NH O Cl Cl H 3 C O NH CH 3 Clostridium BoNT (Botulinum neurotoxin) Preclinical (in vitro) Thompson JC, et al. 2020. Bioorg Med Chem
3-(2-chlorophenyl)-N-[(2S,3S)-1-(hydroxyamino)-3-methyl-1-oxopentan-2-yl]benzamide Depiction based on curated SMILES OH HN O Cl CH 3 O HN H 3 C Clostridium BoNT (Botulinum neurotoxin) Preclinical (in vitro) Thompson JC, et al. 2020. Bioorg Med Chem
3-(3-chlorophenyl)-N-[(2S,3S)-1-(hydroxyamino)-3-methyl-1-oxopentan-2-yl]benzamide Depiction based on curated SMILES OH NH O Cl CH 3 O N H CH 3 Clostridium BoNT (Botulinum neurotoxin) Preclinical (in vitro) Thompson JC, et al. 2020. Bioorg Med Chem
3-(furan-2-yl)-N-[(2S,3S)-1-(hydroxyamino)-3-methyl-1-oxopentan-2-yl]benzamide Depiction based on curated SMILES HO N H O O CH 3 O NH CH 3 Clostridium BoNT (Botulinum neurotoxin) Preclinical (in vitro) Thompson JC, et al. 2020. Bioorg Med Chem
Potassium acetate Depiction based on curated SMILES CH 3 O _ O + K Clostridium TcdA (Toxin A) Preclinical (in vitro) Lu LF, et al. 2016. J Microbiol Biotechnol
Guadinomine C1 Depiction based on curated SMILES H 3 C O OH H H H 3 C H N N NH 2 O H 2 N OH HO O H O N H H H N H H 3 C NH H CH 3 O N H H Escherichia TTSS (Type III secretion system) Preclinical (in vitro) Iwatsuki M, et al. 2008. J Antibiot (Tokyo)
Guadinomine C2 Depiction based on curated SMILES H 3 C O OH H H H 3 C H N N NH 2 O H 2 N OH HO O H O N H H H N H H 3 C NH H CH 3 O N H H Escherichia TTSS (Type III secretion system) Preclinical (in vitro) Iwatsuki M, et al. 2008. J Antibiot (Tokyo)
Guadinomine A Depiction based on curated SMILES H 2 N N N O NH 2 OH OH OH NH 2 NH 2 H 3 C H O N H H CH 3 CH 3 O HO N H O Escherichia TTSS (Type III secretion system) Preclinical (in vitro) Iwatsuki M, et al. 2008. J Antibiot (Tokyo)
Guadinomine D Depiction based on curated SMILES N N H 2 N O NH 2 OH OH NH 2 N H O H 3 C H 3 C H O N H H CH 3 CH 3 O OH N H O Escherichia TTSS (Type III secretion system) Preclinical (in vitro) Iwatsuki M, et al. 2008. J Antibiot (Tokyo)
   


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