Cas no 155861-51-1 (9,10-Dimethoxycanthin-6-one)
9,10-Dimethoxycanthin-6-one Chemical and Physical Properties
Names and Identifiers
-
- 9,10-Dimethoxycanthin-6-one
- 9,10-Dimethoxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one
- HY-N7182
- SCHEMBL12067601
- DTXSID701196166
- 155861-51-1
- 12,13-dimethoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one
- CS-0103811
- AKOS040761285
- CHEMBL3139513
- FS-7528
- 12,13-dimethoxy-1,6-diazatetracyclo[7.6.1.0?,(1)?.0(1)?,(1)?]hexadeca-3,5,7,9(16),10(15),11,13-heptaen-2-one
-
- Inchi: 1S/C16H12N2O3/c1-20-13-7-10-9-5-6-17-11-3-4-15(19)18(16(9)11)12(10)8-14(13)21-2/h3-8H,1-2H3
- InChI Key: VKMIBFAQYHUWCU-UHFFFAOYSA-N
- SMILES: O(C)C1C(=CC2C3C=CN=C4C=CC(N(C=2C=1)C=34)=O)OC
Computed Properties
- Exact Mass: 280.08479225g/mol
- Monoisotopic Mass: 280.08479225g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 21
- Rotatable Bond Count: 2
- Complexity: 466
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.4
- Topological Polar Surface Area: 53.4?2
Experimental Properties
- Color/Form: Yellow powder
- Density: 1.40±0.1 g/cm3 (20 oC 760 Torr),
- Solubility: Very slightly soluble (0.31 g/l) (25 o C),
9,10-Dimethoxycanthin-6-one Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| ChemFaces | CFN92127-5mg |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | >=98% | 5mg |
$413 | 2021-07-22 | |
| SHANG HAI TAO SHU Biotechnology Co., Ltd. | TN3307-5 mg |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | 5mg |
¥4336.00 | 2022-04-26 | ||
| ChemFaces | CFN92127-5mg |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | >=98% | 5mg |
$413 | 2023-09-19 | |
| TargetMol Chemicals | TN3307-1 ml * 10 mm |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | 1 ml * 10 mm |
¥ 1650 | 2024-07-20 | ||
| TargetMol Chemicals | TN3307-5mg |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | 5mg |
¥ 2350 | 2024-07-24 | ||
| TargetMol Chemicals | TN3307-1 ml * 10 mm |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | 1 ml * 10 mm |
¥ 1650 | 2024-07-24 | ||
| A2B Chem LLC | AF03533-5mg |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | 95% | 5mg |
$1620.00 | 2024-04-20 | |
| TargetMol Chemicals | TN3307-5 mg |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | 98% | 5mg |
¥ 2,350 | 2023-07-11 | |
| TargetMol Chemicals | TN3307-1 mL * 10 mM (in DMSO) |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | 98% | 1 mL * 10 mM (in DMSO) |
¥ 1650 | 2023-09-15 | |
| TargetMol Chemicals | TN3307-5mg |
9,10-Dimethoxycanthin-6-one |
155861-51-1 | 5mg |
¥ 2350 | 2024-07-20 |
9,10-Dimethoxycanthin-6-one Related Literature
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
-
Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
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A. B. F. da Silva,K. Capelle Phys. Chem. Chem. Phys., 2009,11, 4564-4569
Additional information on 9,10-Dimethoxycanthin-6-one
Exploring the Potential of 9,10-Dimethoxycanthin-6-one (CAS No. 155861-51-1): A Comprehensive Overview
In the realm of bioactive natural products, 9,10-Dimethoxycanthin-6-one (CAS No. 155861-51-1) stands out as a compound of significant scientific interest. This alkaloid, derived from the canthin-6-one family, has garnered attention for its unique structural properties and potential applications in various fields, including pharmacology and biochemistry. Researchers and industry professionals are increasingly exploring its mechanisms of action, particularly in the context of natural product drug discovery and bioactive compound research.
The molecular structure of 9,10-Dimethoxycanthin-6-one features a canthin-6-one backbone with two methoxy groups at positions 9 and 10, which contribute to its distinct chemical behavior. This structural motif is often associated with interactions with biological targets, making it a promising candidate for further study. Recent trends in phytochemical analysis and medicinal chemistry have highlighted the importance of such compounds in developing novel therapeutic agents, especially those targeting oxidative stress and inflammation.
One of the key areas of interest surrounding 9,10-Dimethoxycanthin-6-one is its potential role in antioxidant activity. With growing public awareness of oxidative stress-related diseases, the demand for natural antioxidants has surged. This compound's ability to scavenge free radicals and modulate cellular redox balance aligns with current health and wellness trends, such as the search for plant-derived bioactive molecules and nutraceutical applications. These properties make it a subject of interest for both academic researchers and the nutraceutical industry.
Another hot topic in the scientific community is the exploration of natural products for drug development. 9,10-Dimethoxycanthin-6-one has shown promise in preliminary studies for its potential to interact with enzymes and receptors involved in various metabolic pathways. This has led to increased searches for terms like "canthin-6-one derivatives" and "alkaloid biological activity", reflecting the compound's relevance in modern pharmacology. Its structural versatility also makes it a valuable scaffold for structure-activity relationship (SAR) studies, a critical step in optimizing drug candidates.
From a technical perspective, the synthesis and isolation of 9,10-Dimethoxycanthin-6-one require specialized knowledge in organic chemistry techniques. Researchers often employ methods such as column chromatography and spectroscopic analysis (e.g., NMR and mass spectrometry) to characterize this compound. The growing interest in natural product isolation and analytical chemistry has further propelled the visibility of this alkaloid in scientific literature and online databases.
In the context of sustainability and green chemistry, 9,10-Dimethoxycanthin-6-one represents an example of how plant-based compounds can contribute to eco-friendly research. As consumers and industries shift toward sustainable alternatives, the demand for naturally sourced bioactive molecules has increased. This aligns with broader trends in green pharmaceuticals and biobased materials, making the study of such compounds both timely and impactful.
Looking ahead, the potential applications of 9,10-Dimethoxycanthin-6-one extend beyond traditional medicine. Its unique properties may find use in cosmeceuticals, where natural ingredients are highly sought after for their skin-beneficial effects. Additionally, its role in plant defense mechanisms offers insights into agricultural applications, such as developing natural pesticides or plant growth regulators. These diverse possibilities underscore the compound's versatility and relevance across multiple disciplines.
For researchers and professionals seeking detailed information on 9,10-Dimethoxycanthin-6-one, reliable sources include peer-reviewed journals focusing on phytochemistry and natural product research. Databases like SciFinder and PubChem provide valuable data on its physicochemical properties and biological activities. As interest in this compound grows, so does the need for high-quality research to unlock its full potential in science and industry.
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