CAS 97457-31-3
:(6E)-6-(3-oxo-1,3-dihydro-2H-indol-2-ylidene)indolo[2,1-b]quinazolin-12(6H)-one
Description:
The chemical substance known as (6E)-6-(3-oxo-1,3-dihydro-2H-indol-2-ylidene)indolo[2,1-b]quinazolin-12(6H)-one, with the CAS number 97457-31-3, is a complex organic compound characterized by its unique indole and quinazoline structural motifs. This compound features a conjugated system that contributes to its potential biological activity, particularly in medicinal chemistry. The presence of the indole moiety suggests possible interactions with biological targets, making it of interest in drug discovery. Its structure includes a ketone functional group, which may influence its reactivity and solubility properties. The compound's stereochemistry, indicated by the (6E) configuration, suggests specific spatial arrangements that can affect its pharmacological properties. Overall, this substance may exhibit various chemical behaviors, including potential antioxidant, anti-inflammatory, or anticancer activities, warranting further investigation into its applications in therapeutic contexts. As with many complex organic compounds, its synthesis, stability, and reactivity are critical factors for practical use in research and development.
Formula:C23H13N3O2
InChI:InChI=1/C23H13N3O2/c27-21-13-7-1-4-10-16(13)24-20(21)19-15-9-3-6-12-18(15)26-22(19)25-17-11-5-2-8-14(17)23(26)28/h1-12,24H/b20-19+
Synonyms:- indolo[2,1-b]quinazolin-12(6H)-one, 6-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-, (6E)-
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Found 3 products.
Qingdainone
CAS:<p>Qingdainone is a natural product that can be used as a reference standard.</p>Formula:C23H13N3O2Color and Shape:SolidMolecular weight:363.376Qingdainone
CAS:Natural alkaloidFormula:C23H13N3O2Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:363.37Qingdainone
CAS:Qingdainone is a potent antibiotic compound, which is derived from microbial fermentation processes, specifically from the Streptomyces genus. This compound operates primarily by inhibiting the DNA gyrase enzyme, a crucial component in bacterial DNA replication and transcription. The unique mechanism of action targets the bacterial topoisomerase II, preventing the supercoiling essential for DNA synthesis and thus inhibiting bacterial growth.Formula:C23H13N3O2Purity:90%Color and Shape:PowderMolecular weight:363.37 g/mol


