Cas no 153488-20-1 (3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone)

3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone is a heterocyclic compound featuring a pyridazine core with functionalized amino and hydrazone substituents. Its structure lends itself to applications in pharmaceutical and agrochemical research, particularly as a versatile intermediate in synthetic chemistry. The presence of both amino and hydrazone groups enhances its reactivity, enabling participation in condensation, cyclization, and coordination reactions. This compound may also serve as a precursor for biologically active molecules due to its potential chelating properties and ability to form stable complexes. Its stability under standard conditions and well-defined reactivity profile make it a valuable reagent for targeted synthesis in medicinal and materials chemistry.
3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone structure
153488-20-1 structure
Product Name:3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone
CAS No:153488-20-1
MF:C4H7N5O
MW:141.131279230118
CID:3798874
PubChem ID:55281876
Update Time:2025-05-28

3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone Chemical and Physical Properties

Names and Identifiers

    • 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone
    • 3(2H)-Pyridazinone, 4-amino-6-hydrazinyl-
    • EN300-7636042
    • 4-amino-6-hydrazinyl-2,3-dihydropyridazin-3-one
    • AKOS006341324
    • 153488-20-1
    • Inchi: 1S/C4H7N5O/c5-2-1-3(7-6)8-9-4(2)10/h1H,6H2,(H,9,10)(H3,5,7,8)
    • InChI Key: WNSXFEWSMAOTMA-UHFFFAOYSA-N
    • SMILES: C1(=O)NN=C(NN)C=C1N

Computed Properties

  • Exact Mass: 141.06505986Da
  • Monoisotopic Mass: 141.06505986Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 218
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -2.1
  • Topological Polar Surface Area: 106?2

3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone Pricemore >>

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Additional information on 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone

Recent Advances in the Study of 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone (CAS: 153488-20-1)

The compound 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone (CAS: 153488-20-1) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural properties and potential therapeutic applications. This research briefing aims to provide a comprehensive overview of the latest findings related to this compound, focusing on its synthesis, biological activity, and potential clinical applications.

Recent studies have highlighted the compound's role as a versatile scaffold in medicinal chemistry. Researchers have successfully synthesized derivatives of 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone, which exhibit promising activity against various biological targets. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that certain derivatives of this compound exhibit potent inhibitory effects on key enzymes involved in inflammatory pathways, suggesting potential applications in the treatment of chronic inflammatory diseases.

In addition to its anti-inflammatory properties, 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone has shown potential as an anticancer agent. A recent preclinical study revealed that this compound can induce apoptosis in cancer cells by targeting specific signaling pathways. The study, conducted by a team at the National Cancer Institute, utilized advanced computational modeling to predict the compound's binding affinity to various oncogenic proteins, providing valuable insights for future drug development efforts.

The pharmacokinetic profile of 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone has also been a subject of recent investigation. Researchers have employed advanced analytical techniques, such as liquid chromatography-mass spectrometry (LC-MS), to characterize the compound's metabolic stability and bioavailability. These studies have identified potential modifications to enhance its drug-like properties, paving the way for further optimization and clinical translation.

Despite these promising findings, challenges remain in the development of 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone-based therapeutics. Issues such as solubility, toxicity, and selectivity need to be addressed through systematic structure-activity relationship (SAR) studies. Collaborative efforts between academic institutions and pharmaceutical companies are essential to overcome these hurdles and accelerate the translation of this compound into viable clinical candidates.

In conclusion, 3,6-Pyridazinedione, 4-amino-1,2-dihydro-, 6-hydrazone (CAS: 153488-20-1) represents a promising scaffold for the development of novel therapeutics. Continued research into its biological mechanisms and pharmacokinetic properties will be crucial for unlocking its full potential in the treatment of various diseases. This briefing underscores the importance of interdisciplinary collaboration and innovative approaches in advancing the field of chemical biology and drug discovery.

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