5-(N-(8-Methoxy-4-quinolyl)amino)pentyl nitrate, with the CAS number 47208-82-2, is a chemical compound that features a quinoline moiety, which is known for its biological activity and potential pharmacological applications. The structure includes a pentyl chain linked to a nitrate group, which may influence its solubility and reactivity. The presence of the methoxy group on the quinoline ring can enhance lipophilicity, potentially affecting the compound's ability to penetrate biological membranes. This compound may exhibit properties such as antimicrobial or antitumor activity, typical of quinoline derivatives, although specific biological activities would depend on further empirical studies. Additionally, the nitrate functional group may impart vasodilatory effects, which are characteristic of many nitrate compounds. Overall, the unique combination of functional groups in this compound suggests it could be of interest in medicinal chemistry, particularly in the development of new therapeutic agents. However, detailed studies would be necessary to fully elucidate its properties and potential applications.

5-(N-(8-METHOXY-4-QUINOLYL)AMINO)PENTYL NITRATE

47208-82-2: 5-(N-(8-Methoxy-4-quinolyl)amino)pentyl nitrate, with the CAS number 47208-82-2, is a chemical compound that features a quinoline moiety, which is known for its biological activity and potential pharmacological applications. The structure includes a pentyl chain linked to a nitrate group, which may influence its solubility and reactivity. The presence of the methoxy group on the quinoline ring can enhance lipophilicity, potentially affecting the compound's ability to penetrate biological membranes. This compound may exhibit properties such as antimicrobial or antitumor activity, typical of quinoline derivatives, although specific biological activities would depend on further empirical studies. Additionally, the nitrate functional group may impart vasodilatory effects, which are characteristic of many nitrate compounds. Overall, the unique combination of functional groups in this compound suggests it could be of interest in medicinal chemistry, particularly in the development of new therapeutic agents. However, detailed studies would be necessary to fully elucidate its properties and potential applications.

<p>5MPN is a PFKFB4 inhibitor that inhibits the F6P binding site and suppresses the proliferation of myeloma cells.</p>

CAS 47208-82-2

5-(N-(8-METHOXY-4-QUINOLYL)AMINO)PENTYL NITRATE

5MPN

Ref: TM-T40565