CAS 64291-45-8

Acetic acid, diethoxy-, 2-[4-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-1,2,3,4,6,11-hexahydro-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-2-naphthacenyl]-2-oxoethyl ester, hydrochloride, (2S-cis)-

Description:

Acetic acid, diethoxy-, 2-[4-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-1,2,3,4,6,11-hexahydro-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-2-naphthacenyl]-2-oxoethyl ester, hydrochloride, (2S-cis)-, is a complex organic compound characterized by its intricate structure that includes multiple functional groups such as esters, amines, and hydroxyl groups. This compound features a naphthacene backbone, which contributes to its potential biological activity. The presence of the trideoxy sugar moiety suggests possible interactions with biological systems, particularly in the context of glycosylation. The hydrochloride form indicates that it is a salt, which may enhance its solubility in aqueous solutions. This compound is likely to exhibit properties typical of both naphthalene derivatives and carbohydrate-based molecules, potentially leading to applications in pharmaceuticals or biochemistry. Its specific stereochemistry, denoted by the (2S-cis) configuration, may influence its reactivity and interaction with biological targets. Overall, this compound represents a unique combination of structural features that could be of interest in medicinal chemistry and drug development.

Formula: C₃₃H₃₉NO₁₄·ClH

InChI: InChI=1S/C33H39NO14.ClH/c1-5-44-32(45-6-2)31(41)46-13-20(35)33(42)11-16-23(19(12-33)48-21-10-17(34)26(36)14(3)47-21)30(40)25-24(28(16)38)27(37)15-8-7-9-18(43-4)22(15)29(25)39;/h7-9,14,17,19,21,26,32,36,38,40,42H,5-6,10-13,34H2,1-4H3;1H/t14-,17-,19-,21-,26+,33-;/m0./s1

InChI key: InChIKey=PJODMULXZJQLDJ-NMELVCTCSA-N

SMILES: OC=1C2=C([C@@H](O[C@H]3C[C@H](N)[C@H](O)[C@H](C)O3)C[C@@](C(COC(C(OCC)OCC)=O)=O)(O)C2)C(O)=C4C1C(=O)C=5C(C4=O)=C(OC)C=CC5.Cl

Synonyms:

• Acetic acid, diethoxy-, 2-[4-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-1,2,3,4,6,11-hexahydro-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-2-naphthacenyl]-2-oxoethyl ester, hydrochloride, (2S-cis)-
• Detorubicin hydrochloride

Detorubicin HCl

CAS: 64291-45-8

Detorubicin, a less toxic daunorubicin derivative, inhibits DNA replication and repair by intercalating DNA and targeting topoisomerase II.

Formula: C₃₃H₄₀ClNO₁₄

Color and Shape: Solid

Molecular weight: 710.126

Ref: TM-T68948