CAS 86293-41-6

10-Hydroxycanthin-6-one

Description:

10-Hydroxycanthin-6-one is an organic compound belonging to the class of canthin alkaloids, which are known for their diverse biological activities. This compound features a fused ring structure characteristic of the canthin family, with a hydroxyl group at the 10-position and a ketone at the 6-position. It is typically characterized by its molecular formula, which reflects its complex structure, and it exhibits properties such as solubility in organic solvents. The compound has garnered interest in medicinal chemistry due to its potential pharmacological effects, including antimicrobial, anticancer, and anti-inflammatory activities. Its unique structural features contribute to its reactivity and interaction with biological targets. As with many alkaloids, the study of 10-Hydroxycanthin-6-one may provide insights into the development of new therapeutic agents. However, detailed studies on its mechanism of action and safety profile are essential for understanding its full potential in medicinal applications.

Formula: C₁₄H₈N₂O₂

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

InChI key: InChIKey=FZLISVGXWLVEPB-UHFFFAOYSA-N

SMILES: O=C1N2C=3C(C=4C2=CC=C(O)C4)=CC=NC3C=C1

Synonyms:

• Aervine
• Ervine
• 6H-Indolo[3,2,1-de][1,5]naphthyridin-6-one, 10-hydroxy-
• 10-Hydroxycanthin-6-one
• 10-Hydroxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one

10-Hydroxycanthin-6-one

CAS: 86293-41-6

10-Hydroxycanthin-6-one shows antimicrobial, antimalarial, and potential plant-derived anticancer properties.

Formula: C₁₄H₈N₂O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 236.23

Ref: TM-TN2567

10-Hydroxycanthin-6-one

CAS: 86293-41-6

10-Hydroxycanthin-6-one is a natural alkaloid compound, which is derived from several plant sources, particularly those belonging to the Simaroubaceae family. It exerts its effects primarily through the inhibition of topoisomerase I and II, enzymes critical for DNA replication and transcription processes. This mode of action interrupts the DNA replication cycle, leading to potential antiproliferative and anticancer effects.

Formula: C₁₄H₈N₂O₂

Purity: Min. 95%

Molecular weight: 236.22 g/mol

Ref: 3D-LDA29341