CAS 116064-76-7
:1,2,3-Trimethoxydibenz[cd,f]indol-4(5H)-one
Description:
1,2,3-Trimethoxydibenz[cd,f]indol-4(5H)-one is a complex organic compound characterized by its unique structure, which includes a dibenzindole framework and three methoxy groups. This compound is notable for its potential biological activity, particularly in the field of medicinal chemistry, where it may exhibit properties such as anti-cancer or anti-inflammatory effects. The presence of the methoxy groups enhances its solubility and may influence its interaction with biological targets. The compound's molecular structure contributes to its stability and reactivity, making it of interest for further research and development. Additionally, its CAS number, 116064-76-7, serves as a unique identifier for regulatory and safety information. As with many organic compounds, its synthesis and characterization involve various analytical techniques, including NMR and mass spectrometry, to confirm its identity and purity. Overall, 1,2,3-Trimethoxydibenz[cd,f]indol-4(5H)-one represents a fascinating subject for ongoing studies in organic and medicinal chemistry.
Formula:C18H15NO4
InChI:InChI=1S/C18H15NO4/c1-21-15-12-10-7-5-4-6-9(10)8-11-13(12)14(18(20)19-11)16(22-2)17(15)23-3/h4-8H,1-3H3,(H,19,20)
InChI key:InChIKey=GYYIMUXZCUHECT-UHFFFAOYSA-N
SMILES:O(C)C=1C2=C3C(=C(OC)C1OC)C(=O)NC3=CC=4C2=CC=CC4
Synonyms:- 1,2,3-Trimethoxydibenz[cd,f]indol-4(5H)-one
- 2-O-Methylaristolactam FII
- 3-Methoxyaristolactam BII
- O-Methylpiperolactam B
- O-MethylpiperolactamB
- Piperolactam B methyl ether
- Piperolactam C
- Dibenz[cd,f]indol-4(5H)-one, 1,2,3-trimethoxy-
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Found 3 products.
Piperolactam C
CAS:Piperolactam C possesses anti-platelet aggregation activity in vitro. It can inhibit the growth of the fungi Cladosporium sphaerospermum and C. cladosporioides.Formula:C18H15NO4Purity:98%Color and Shape:SolidMolecular weight:309.32Piperolactam C
CAS:Formula:C18H15NO4Purity:95%~99%Color and Shape:Yellow powderMolecular weight:309.321Piperolactam C
CAS:<p>Piperolactam C is a naturally occurring alkaloid, which is derived from various plant sources, particularly those in the Piper species. It exhibits a complex structure typical of compounds isolated from plants known for their pharmacological potential. The mode of action of Piperolactam C is linked to its interaction with specific cellular pathways, although the precise biochemical mechanisms are still under investigation. Early studies suggest it may influence enzyme activity or receptor binding, contributing to its observed bioactive effects. Piperolactam C is primarily explored in scientific research for its potential therapeutic applications. It has shown promise in preliminary studies as an anti-inflammatory and anticancer agent. Researchers continue to investigate its efficacy and safety in vitro and in vivo, aiming to understand its full range of biological activities and potential for drug development. Its study aids in uncovering new possibilities for treatment strategies against various diseases, contributing to the expanding field of natural product research.</p>Formula:C18H15NO4Purity:Min. 95%Molecular weight:309.3 g/mol


