The chemical substance known as Propanoic acid, 2-[[(2,4,5,7-tetranitro-9H-fluoren-9-ylidene)amino]oxy]-, (4S)-10-[(dimethylamino)methyl]-4-ethyl-3,4,12,14-tetrahydro-9-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl ester, with the CAS number 1432468-79-5, is a complex organic compound characterized by its intricate molecular structure. It features a propanoic acid moiety, which contributes to its acidic properties, and a variety of functional groups including nitro, amino, and ester functionalities. The presence of the tetranitro group suggests significant electron-withdrawing characteristics, which may influence its reactivity and stability. The compound's stereochemistry is indicated by the (4S) designation, suggesting specific spatial arrangements that could affect its biological activity. Additionally, the presence of a dimethylamino group may enhance its solubility and interaction with biological systems. Overall, this compound's unique structure likely imparts specific pharmacological properties, making it of interest in medicinal chemistry and drug development.

Propanoic acid, 2-[[(2,4,5,7-tetranitro-9H-fluoren-9-ylidene)amino]oxy]-, (4S)-10-[(dimethylamino)methyl]-4-ethyl-3,4,12,14-tetrahydro-9-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl ester

1432468-79-5: The chemical substance known as Propanoic acid, 2-[[(2,4,5,7-tetranitro-9H-fluoren-9-ylidene)amino]oxy]-, (4S)-10-[(dimethylamino)methyl]-4-ethyl-3,4,12,14-tetrahydro-9-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl ester, with the CAS number 1432468-79-5, is a complex organic compound characterized by its intricate molecular structure. It features a propanoic acid moiety, which contributes to its acidic properties, and a variety of functional groups including nitro, amino, and ester functionalities. The presence of the tetranitro group suggests significant electron-withdrawing characteristics, which may influence its reactivity and stability. The compound's stereochemistry is indicated by the (4S) designation, suggesting specific spatial arrangements that could affect its biological activity. Additionally, the presence of a dimethylamino group may enhance its solubility and interaction with biological systems. Overall, this compound's unique structure likely imparts specific pharmacological properties, making it of interest in medicinal chemistry and drug development.

<p>TLC 388, a DNA topoisomerase I inhibitor, is used potentially for the treatment of Renal carcinoma and Hepatocellular carcinoma</p>

CAS 1432468-79-5

Propanoic acid, 2-[[(2,4,5,7-tetranitro-9H-fluoren-9-ylidene)amino]oxy]-, (4S)-10-[(dimethylamino)methyl]-4-ethyl-3,4,12,14-tetrahydro-9-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-4-yl ester

TLC 388

Ref: TM-T28982