1338782-98-1

Basic information

• Product Name: (E)-1-(2-(3,5-dibromo-2-hydroxybenzylideneamino)phenyl)-3-phenylthiourea
• Synonyms: (E)-1-(2-(3,5-dibromo-2-hydroxybenzylideneamino)phenyl)-3-phenylthiourea
• CAS NO: 1338782-98-1
• Molecular Weight: 505.233
• Mol File: 1338782-98-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-1-(2-(3,5-dibromo-2-hydroxybenzylideneamino)phenyl)-3-phenylthiourea(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(2-(3,5-dibromo-2-hydroxybenzylideneamino)phenyl)-3-phenylthiourea(1338782-98-1)
• EPA Substance Registry System: (E)-1-(2-(3,5-dibromo-2-hydroxybenzylideneamino)phenyl)-3-phenylthiourea(1338782-98-1)

Safety Data

• Hazardous Substances Data: 1338782-98-1(Hazardous Substances Data)

Upstream product

• 95-54-5 1,2-diamino-benzene 
• 103-72-0 phenyl isothiocyanate 
• 90-59-5 3,5-Dibromosalicylaldehyde 
• 21578-46-1 N-(2-aminophenyl)-N'-phenylthiourea 

Relevant articles and documents

Synthesis, antibacterial activities and molecular docking studies of Schiff bases derived from N-(2/4-benzaldehyde-amino) phenyl-N′-phenyl-thiourea

A series of novel Schiff base derivatives have been designed and synthesized, and their biological activities were also evaluated as potential inhibitors of FabH. These compounds were assayed for antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, Bacillus subtilis, and Staphylococcus aureus. Compounds with potent antibacterial activities were tested for their E. coli FabH inhibitory activity. Compound 3v showed the most potent antibacterial activity with MIC of 1.56-6.25 μg/mL against the tested bacterial strains and exhibited the most potent E. coli FabH inhibitory activity with IC50 of 4.3 μM. Docking simulation was performed to position compound 3v into the E. coli FabH active site to determine the probable binding conformation.