
Cabergoline Impurity B CAS No.: 166533-36-4
Chemical Structure : Cabergoline Impurity B
CAS No.: 166533-36-4
Description
Chemical Structure : Cabergoline Impurity B
CAS No.: 166533-36-4

Cabergoline Impurity B
Catalog No.: URK-V2460 Only Used For Lab.
Cabergoline Impurity B is an important compound in pharmaceutical research, with great potential for use in the treatment of neurological disorders. Its potent activity as a D2 receptor agonist makes it a valuable tool for investigating the mechanisms behind these diseases, and future research in this area is warranted.
Biological Activity
Cabergoline Impurity B is a chemical compound commonly used in pharmaceutical research. It is a derivative of Cabergoline, which acts as an agonist at the dopamine D2 receptor, making it useful in treating Parkinson's disease and hyperprolactinemia.
Research has shown that Cabergoline Impurity B has potent activity as a D2 receptor agonist, making it a promising candidate for further study. Its ability to bind to and activate the dopamine receptor makes it a powerful tool for investigating the mechanisms behind Parkinson's disease and other neurological disorders.
One study found that Cabergoline Impurity B exhibited high selectivity for the D2 receptor, with minimal activity at other dopamine receptor subtypes. This selectivity is desirable in drug development because it reduces the likelihood of unwanted side effects.
Physicochemical Properties
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M.Wt |
451.604 |
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Formula |
C26H37N5O2 |
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CAS No. |
166533-36-4 |
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Appearance |
Solid |
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Storage |
Solide Powder -20 °C 3years; 4°C 2years |
In Solvent -80°C 6 Months -20°C 1 Months |
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Solubility |
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Chemical Name |
Cabergoline EP Impurity B |
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References
1. Liu J, Li Q, Wang J, et al. Synthesis and biological evaluation of cabergoline derivatives as dopaminergic agonists[J]. Molecules, 2017, 22(7): 1126.
2. Chen B, Wang J, Liu Y, et al. Synthesis, characterization and dopamine D2 receptor binding studies of novel cabergoline derivatives[J]. European journal of medicinal chemistry, 2018, 156: 774-782.
3. Ronca S, Tagliamonte A, Potenza M A, et al. A new, highly selective, full and potent agonist for the dopamine D2 receptor[J]. European journal of medicinal chemistry, 2019, 167: 628-637.
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