The chemical substance known as "(+)-(7S,9S)-9-Acetyl-9-amino-7-[(2-deoxy-beta-D-erythro-pentopyranosyl)oxy]-7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenedione hydrochloride" with CAS number 92395-36-3 is a complex organic compound characterized by its unique structural features. It contains a naphthacenedione core, which is a polycyclic aromatic structure known for its potential biological activity. The presence of hydroxyl groups contributes to its solubility and reactivity, while the acetyl and amino functional groups suggest potential interactions with biological systems, possibly influencing its pharmacological properties. The compound also includes a sugar moiety, specifically a 2-deoxy-beta-D-erythro-pentopyranosyl group, which may enhance its bioavailability and cellular uptake. As a hydrochloride salt, it is likely to be more stable and soluble in aqueous environments, making it suitable for various applications in medicinal chemistry and drug development. Overall, this compound's intricate structure and functional groups indicate potential for significant biological activity, warranting further investigation.

(+)-(7S,9S)-9-Acetyl-9-amino-7-[(2-deoxy-beta-D-erythro-pentopyranosyl)oxy]-7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenedione hydrochloride

92395-36-3: The chemical substance known as "(+)-(7S,9S)-9-Acetyl-9-amino-7-[(2-deoxy-beta-D-erythro-pentopyranosyl)oxy]-7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenedione hydrochloride" with CAS number 92395-36-3 is a complex organic compound characterized by its unique structural features. It contains a naphthacenedione core, which is a polycyclic aromatic structure known for its potential biological activity. The presence of hydroxyl groups contributes to its solubility and reactivity, while the acetyl and amino functional groups suggest potential interactions with biological systems, possibly influencing its pharmacological properties. The compound also includes a sugar moiety, specifically a 2-deoxy-beta-D-erythro-pentopyranosyl group, which may enhance its bioavailability and cellular uptake. As a hydrochloride salt, it is likely to be more stable and soluble in aqueous environments, making it suitable for various applications in medicinal chemistry and drug development. Overall, this compound's intricate structure and functional groups indicate potential for significant biological activity, warranting further investigation.

Amrubicin (SM-5887), an anthracycline, treats lung cancer by inhibiting DNA replication and topoisomerase II, with less cardiac toxicity.

CAS 92395-36-3

(+)-(7S,9S)-9-Acetyl-9-amino-7-[(2-deoxy-beta-D-erythro-pentopyranosyl)oxy]-7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenedione hydrochloride

Amrubicin HCl

Ref: TM-T68336