CAS 4781-58-2
:7-Isoquinolinol,1,2,3,4-tetrahydro-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-,(1S)-
Description:
7-Isoquinolinol, 1,2,3,4-tetrahydro-1-[(3-hydroxy-4-methoxyphenyl)methyl]-6-methoxy-, (1S)-, is a chemical compound characterized by its complex structure, which includes an isoquinoline core and multiple functional groups. This substance features a tetrahydroisoquinoline framework, indicating it has undergone hydrogenation, resulting in a saturated ring system. The presence of methoxy and hydroxy groups suggests it may exhibit interesting solubility and reactivity properties, potentially influencing its biological activity. The stereochemistry indicated by (1S)- denotes a specific three-dimensional arrangement of atoms, which can significantly affect the compound's interactions with biological targets. This compound may be of interest in medicinal chemistry due to its structural features, which could contribute to pharmacological effects. Its CAS number, 4781-58-2, allows for easy identification in chemical databases and literature. Overall, the characteristics of this compound suggest potential applications in drug development and research, particularly in areas related to neurochemistry or as a precursor for synthesizing other bioactive molecules.
Formula:C18H21NO4
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Found 4 products.
Norreticuline
CAS:<p>Norreticuline is a potential adrenoceptor-α/β agonist and CYP2D6 and D2 receptor inhibitor for the study of neurodegenerative diseases.</p>Formula:C18H21NO4Color and Shape:SolidMolecular weight:315.36Nor reticuline
CAS:<p>Norreticuline is a virus-induced gene that is primarily found in the opium poppy, Papaver somniferum. Norreticuline has been shown to be biosynthesized from reticuline by a series of enzymatic reactions. It is also involved in the metabolic pathway of papaverine, which is an alkaloid that has been used as a vasodilator and anti-hypertensive drug. The optimum pH for norreticuline production is between 6 and 7. Norreticuline has demonstrated anticancer activity against various tumor cells, such as breast cancer cells and colon cancer cells. Norreticuline may also have antiviral properties due to its ability to inhibit viral DNA replication and synthesis of viral proteins.</p>Formula:C18H21NO4Purity:Min. 95%Molecular weight:315.36 g/mol




