Cas no 189309-24-8 (Cinchonine Tosylate)

Cinchonine Tosylate is a quinine alkaloid derivative, specifically the tosylate salt of cinchonine. It is commonly utilized in asymmetric synthesis and chiral resolution processes due to its ability to act as a chiral auxiliary or catalyst. The compound exhibits high enantioselectivity, making it valuable for stereochemical control in organic reactions. Its crystalline form ensures ease of handling and purification, while the tosylate group enhances solubility in polar solvents. Cinchonine Tosylate is particularly useful in pharmaceutical research and fine chemical synthesis, where precise stereochemistry is critical. The product’s stability and well-defined properties contribute to reproducible results in complex synthetic applications.
Cinchonine Tosylate structure
Cinchonine Tosylate structure
Product Name:Cinchonine Tosylate
CAS No:189309-24-8
MF:
MW:
CID:2921260
Update Time:2025-05-25

Cinchonine Tosylate Chemical and Physical Properties

Names and Identifiers

    • Cinchonine Tosylate

Cinchonine Tosylate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
C441955-100mg
Cinchonine Tosylate
189309-24-8
100mg
$190.00 2023-05-18
TRC
C441955-500mg
Cinchonine Tosylate
189309-24-8
500mg
$856.00 2023-05-18
TRC
C441955-1g
Cinchonine Tosylate
189309-24-8
1g
$ 1165.00 2022-06-06
TRC
C441955-1000mg
Cinchonine Tosylate
189309-24-8
1g
$1407.00 2023-05-18

Additional information on Cinchonine Tosylate

Research Briefing on Cinchonine Tosylate (189309-24-8): Recent Advances and Applications in Chemical Biology and Medicine

Cinchonine Tosylate (CAS: 189309-24-8) is a derivative of cinchona alkaloids, which have long been recognized for their pharmacological properties. Recent studies have highlighted its potential in various therapeutic applications, including antimalarial, anticancer, and antiviral activities. This research briefing aims to synthesize the latest findings on Cinchonine Tosylate, focusing on its chemical properties, mechanisms of action, and emerging applications in drug development.

One of the most significant advancements in the study of Cinchonine Tosylate is its role as a chiral auxiliary in asymmetric synthesis. Researchers have demonstrated its efficacy in facilitating enantioselective reactions, which are critical for the production of optically active pharmaceuticals. A 2023 study published in the Journal of Medicinal Chemistry reported that Cinchonine Tosylate could significantly improve the yield and enantiomeric excess (ee) of certain chiral intermediates, making it a valuable tool in synthetic chemistry.

In the realm of anticancer research, Cinchonine Tosylate has shown promise as a modulator of cellular pathways involved in apoptosis and autophagy. A recent preclinical study revealed that this compound could inhibit the proliferation of cancer cells by targeting the PI3K/AKT/mTOR signaling pathway. These findings, published in Cancer Research, suggest that Cinchonine Tosylate may serve as a lead compound for the development of novel anticancer agents, particularly for tumors resistant to conventional therapies.

Another area of interest is the potential antiviral activity of Cinchonine Tosylate. Preliminary studies have indicated that it may interfere with the replication cycles of certain RNA viruses, including SARS-CoV-2. While these results are still in the early stages, they open new avenues for research into broad-spectrum antiviral drugs. Researchers are currently exploring the structural modifications of Cinchonine Tosylate to enhance its antiviral efficacy and reduce potential side effects.

Despite these promising developments, challenges remain in the clinical translation of Cinchonine Tosylate. Issues such as bioavailability, toxicity, and formulation stability need to be addressed through further research. Recent efforts have focused on nanotechnology-based delivery systems to improve the pharmacokinetic profile of Cinchonine Tosylate. A 2024 study in Advanced Drug Delivery Reviews highlighted the use of liposomal encapsulation to enhance its solubility and targeted delivery.

In conclusion, Cinchonine Tosylate (189309-24-8) represents a versatile compound with significant potential in chemical biology and medicine. Its applications span from asymmetric synthesis to therapeutic interventions, underscoring its importance in modern drug discovery. Future research should prioritize overcoming the existing limitations and exploring its full therapeutic potential. This briefing underscores the need for interdisciplinary collaboration to accelerate the development of Cinchonine Tosylate-based therapies.

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