CAS 60660-72-2

5,12-Naphthacenedione, 9-acetyl-7-[(3-amino-2,3,6-trideoxy-β-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-, hydrochloride, (7S-cis)-

Description:

5,12-Naphthacenedione, 9-acetyl-7-[(3-amino-2,3,6-trideoxy-β-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-, hydrochloride, (7S-cis)-, is a complex organic compound characterized by its multi-ring structure and various functional groups. This substance features a naphthacenedione core, which contributes to its potential biological activity, particularly in medicinal chemistry. The presence of hydroxyl groups indicates that it may exhibit hydrogen bonding capabilities, influencing its solubility and reactivity. The acetyl and amino groups suggest that it may participate in various biochemical interactions, potentially acting as a substrate or inhibitor in enzymatic processes. The trideoxy-β-L-lyxo-hexopyranosyl moiety indicates that it has glycosidic characteristics, which could enhance its biological activity and interaction with biological macromolecules. As a hydrochloride salt, it is likely to be more soluble in water, facilitating its use in pharmaceutical formulations. Overall, this compound's structural complexity and functional diversity suggest potential applications in drug development and therapeutic research.

Formula: C₂₆H₂₇NO₉·ClH

InChI: InChI=1S/C26H27NO9.ClH/c1-10-21(29)15(27)7-17(35-10)36-16-9-26(34,11(2)28)8-14-18(16)25(33)20-19(24(14)32)22(30)12-5-3-4-6-13(12)23(20)31;/h3-6,10,15-17,21,29,32-34H,7-9,27H2,1-2H3;1H/t10-,15-,16-,17+,21+,26-;/m0./s1

InChI key: InChIKey=JVHPTYWUBOQMBP-XAFFRJQSSA-N

SMILES: O([C@@H]1C2=C(C(O)=C3C(=C2O)C(=O)C=4C(C3=O)=CC=CC4)C[C@](C(C)=O)(O)C1)[C@@H]5C[C@H](N)[C@H](O)[C@H](C)O5.Cl

Synonyms:

• 5,12-Naphthacenedione, 9-acetyl-7-[(3-amino-2,3,6-trideoxy-β-L-lyxo-hexopyranosyl)oxy]-7,8,9,10-tetrahydro-6,9,11-trihydroxy-, hydrochloride, (7S-cis)-

Idarubicin Impurity 6

CAS: 60660-72-2

Formula: C₂₆H₂₇NO₉HCl

Molecular weight: 497.5 : 36.5

Ref: ST-EA-CP-I51007