Date published: 2026-4-24

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Bumadizon (CAS 3583-64-0)

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Alternate Names:
N-(2-Carboxycaproyl)hydrazobenzene
CAS Number:
3583-64-0
Molecular Weight:
326.39
Molecular Formula:
C19H22N2O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Bumadizon represents a synthetic compound with intriguing biochemical properties that have garnered attention in various fields of chemical and biological research. Its molecular structure, characterized by a diazinane ring fused with a butyl side chain, imparts unique physicochemical characteristics that facilitate its interaction with a diverse array of molecular targets. The compound operates primarily through its capacity to modulate enzymatic activities, where it acts as a regulator of protein function by binding to enzyme active sites. This modulation is critical for elucidating the roles of specific enzymes in cellular processes, making Bumadizon useful in the study of enzyme kinetics and mechanism of action. Additionally, its interaction with proteins can serve as a model for the development of new molecules with improved specificity and efficacy in modulating biochemical pathways. Through these mechanisms, Bumadizon contributes significantly to the advancement of biochemical research, offering insights into enzyme function and aiding in the exploration of novel therapeutic targets.


Bumadizon (CAS 3583-64-0) References

  1. Indices of differences of path lengths: novel topological descriptors derived from electronic interferences in graphs.  |  Gálvez, J., et al. 2000. J Comput Aided Mol Des. 14: 679-87. PMID: 11008889
  2. Structure-based classification of antibacterial activity.  |  Cronin, MT., et al. 2002. J Chem Inf Comput Sci. 42: 869-78. PMID: 12132888
  3. Discrimination and selection of new potential antibacterial compounds using simple topological descriptors.  |  Murcia-Soler, M., et al. 2003. J Mol Graph Model. 21: 375-90. PMID: 12543136
  4. Drugs and nondrugs: an effective discrimination with topological methods and artificial neural networks.  |  Murcia-Soler, M., et al. 2003. J Chem Inf Comput Sci. 43: 1688-702. PMID: 14502504
  5. Untersuchungen zur Eiweißbindung von Arzneistoffen durch kontinuierliche Ultrafiltration, 9. Mitt. Vergleichende Untersuchungen zur Bindung nichtsteroidaler Antirheumatika an Humanserumalbumin und deren Interaktion mit Phenprocoumon  |   and Klaus Rehse, Bettina Fiedler. 1989. Archiv der Pharmazie. 322, 4: 241-243.
  6. Inductive QSAR Descriptors. Distinguishing Compounds with Antibacterial Activity by Artificial Neural Networks  |  Artem Cherkasov. 2005. Int. J. Mol. Sci. 6(1): 63-86.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Bumadizon, 100 mg

sc-504339
100 mg
$393.00