For research use only. Not for therapeutic Use.
Benzylurea（Cat No.:I023283）, derived from the stems of Salvadora persica, is notable for its antimicrobial properties as a benzylamine compound. This natural substance serves as a valuable asset in various biochemical research endeavors. Its antimicrobial activity makes it a potent tool for investigating and understanding microbial interactions, offering insights into potential therapeutic applications for combating infections. Additionally, its role in diverse research areas underscores its versatility and significance, allowing scientists to explore a wide range of biochemical processes and applications, from drug development to the study of microbial ecology, further advancing our knowledge and capabilities in the field.
| Catalog Number | I023283 |
| CAS Number | 538-32-9 |
| Synonyms | 1-Benzylurea, AI3-61350, Benzylcarbamide, Benzylurea, N-Benzylurea, Phenylmethylurea |
| Molecular Formula | C8H10N2O |
| Purity | 98% |
| Target | Bacterial |
| Solubility | Soluble in DMSO |
| Appearance | Solid powder |
| Storage | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
| IUPAC Name | Urea, (phenylmethyl)- (9CI) |
| InChI | 1S/C8H10N2O/c9-8(11)10-6-7-4-2-1-3-5-7/h1-5H,6H2,(H3,9,10,11) |
| InChIKey | RJNJWHFSKNJCTB-UHFFFAOYSA-N |
| SMILES | c1(CNC(N)=O)ccccc1 |
| Reference | 1: Kopecný D, Briozzo P, Popelková H, Sebela M, Koncitíková R, Spíchal L, Nisler J, Madzak C, Frébort I, Laloue M, Houba-Hérin N. Phenyl- and benzylurea cytokinins as competitive inhibitors of cytokinin oxidase/dehydrogenase: a structural study. Biochimie. 2010 Aug;92(8):1052-62. doi: 10.1016/j.biochi.2010.05.006. Epub 2010 May 15. PubMed PMID: 20478354. |
