CAS 138544-91-9

9-Hydroxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one

Description:

9-Hydroxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one, with the CAS number 138544-91-9, is a heterocyclic compound characterized by its complex fused ring structure, which incorporates both indole and naphthyridine moieties. This compound typically exhibits a range of biological activities, making it of interest in medicinal chemistry and pharmacology. Its structure includes a hydroxyl group, which can influence its solubility and reactivity, as well as its potential interactions with biological targets. The presence of nitrogen atoms in the ring system contributes to its basicity and can affect its binding properties in biological systems. Additionally, compounds of this type may exhibit fluorescence, which can be useful in various analytical applications. The specific properties, such as melting point, solubility, and spectral characteristics, would depend on the compound's purity and the conditions under which it is studied. Overall, 9-Hydroxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one represents a fascinating area of study due to its structural complexity and potential applications in drug development.

Formula: C₁₄H₈N₂O₂

InChI: InChI=1S/C14H8N2O2/c17-8-1-2-9-10-5-6-15-11-3-4-13(18)16(14(10)11)12(9)7-8/h1-7,17H

InChI key: InChIKey=JHPIJMUNSMWWAA-UHFFFAOYSA-N

SMILES: O=C1N2C=3C(C=4C2=CC(O)=CC4)=CC=NC3C=C1

Synonyms:

• 9-Hydroxycanthin-6-one
• 9-Hydroxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one
• 6H-Indolo[3,2,1-de][1,5]naphthyridin-6-one, 9-hydroxy-

9-Hydroxycanthin-6-one

CAS: 138544-91-9

9-Hydroxycanthin-6-one might be the active component that contributed to the aphrodisiac effect of E.

Formula: C₁₄H₈N₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 236.23

Ref: TM-TN3319

9-Hydroxycanthin-6-one

CAS: 138544-91-9

9-Hydroxycanthin-6-one is a naturally derived alkaloid compound, which is isolated from several species of the Zanthoxylum plant, also known as prickly ash. This compound exhibits a unique mode of action by intercalating into DNA strands and inhibiting topoisomerase activities, which disrupts DNA replication and transcription processes. As a result, it exerts cytotoxic effects, which are particularly potent in cancer cells.

Formula: C₁₄H₈N₂O₂

Purity: Min. 95%

Molecular weight: 236.22 g/mol

Ref: 3D-NFA54491