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4-Carboxymethyl-6,7-methylenedioxycoumarin | CAS 97744-77-9
| Catalog Number | F05-0018 |
| Category | Coumarin |
| Molecular Formula | C12H8O6 |
| Molecular Weight | 248.19 |
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Product Introduction
4-Carboxymethyl-6,7-methylenedioxycoumarin is a biomedical chemical that embodies an extensive application in the realm of scientific research and diagnostics. This fluorescent probe, revered for its exceptional photophysical traits, serves as an indispensable tool in the world of protein and peptide labeling, promoting their insightful visualization and meticulous analysis. By virtue of its prowess, 4-Carboxymethyl-6,7-methylenedioxycoumarin unravels novel avenues in drug discovery, protein mapping, and the comprehension of pernicious ailments, including cancer and neurodegenerative disorders.
Chemical Information
Product Specification
Application
Computed Properties
Patents
| Synonyms | 2-(6-oxo-[1,3]dioxolo[4,5-g]chromen-8-yl)acetic acid; 2-(6-Oxo-6H-[1,3]dioxolo[4,5-g]chromen-8-yl)acetic acid; 2-(6-Oxo-6H-[1,3]dioxolo[4,5-g]chromen-8-yl)aceticacid; (6-Oxo-2H,6H-[1,3]dioxolo[4,5-g][1]benzopyran-8-yl)acetic acid |
| Purity | >95.0%(T) |
| IUPAC Name | 2-(6-oxo-[1,3]dioxolo[4,5-g]chromen-8-yl)acetic acid |
| Canonical SMILES | C1OC2=C(O1)C=C3C(=C2)C(=CC(=O)O3)CC(=O)O |
| InChI | InChI=1S/C12H8O6/c13-11(14)1-6-2-12(15)18-8-4-10-9(3-7(6)8)16-5-17-10/h2-4H,1,5H2,(H,13,14) |
| InChIKey | PIHRLFGNZWHKIO-UHFFFAOYSA-N |
| Appearance | Solid |
| MDL Number | MFCD00143278 |
| Condition To Avoid | Light Sensitive |
4-Carboxymethyl-6,7-methylenedioxycoumarin is a specialized compound with various applications in biochemistry and pharmacology. Here are some key applications of 4-Carboxymethyl-6,7-methylenedioxycoumarin:
Fluorescent Probes: 4-Carboxymethyl-6,7-methylenedioxycoumarin is used as a fluorescent probe in biochemical assays. Due to its unique fluorescent properties, it can be employed to detect the presence of specific biomolecules in complex mixtures. This makes it a valuable tool in molecular biology for tracking reactions and visualizing cellular components.
Enzyme Inhibitor Studies: This compound serves as a critical tool in studying enzyme inhibition. Researchers can use 4-Carboxymethyl-6,7-methylenedioxycoumarin to investigate the inhibitory effects on various enzymes, providing insights into enzyme function and regulation. Such studies are essential for drug development and understanding metabolic control mechanisms.
Antioxidant Activity Research: 4-Carboxymethyl-6,7-methylenedioxycoumarin is employed in the study of antioxidant mechanisms. By incorporating this compound into assays, scientists can evaluate its effectiveness in neutralizing free radicals and reducing oxidative stress. This research is important for developing therapies aimed at mitigating oxidative damage associated with various diseases.
Chemical Synthesis: This compound acts as a versatile intermediate in organic synthesis. By utilizing 4-Carboxymethyl-6,7-methylenedioxycoumarin, chemists can develop novel derivatives with potential pharmacological activities. Its structural framework allows for modifications that can lead to the discovery of new bioactive molecules, contributing to medicinal chemistry and drug discovery efforts.
| XLogP3 | 0.7 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 2 |
| Exact Mass | 248.03208797 g/mol |
| Monoisotopic Mass | 248.03208797 g/mol |
| Topological Polar Surface Area | 82.1Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 415 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
| Publication Number | Title | Priority Date |
|---|---|---|
| EP-2694707-A1 | Monomers capable of dimerizing in an aqueous solution, and methods of using same | 2011-04-07 |
| EP-2694707-B1 | Monomers capable of dimerizing in an aqueous solution, and methods of using same | 2011-04-07 |
| JP-2014512364-A | Monomers that can dimerize in aqueous solution and methods of use thereof | 2011-04-07 |
| US-2014161729-A1 | Cofluorons and methods of making and using them | 2011-04-07 |
| US-2014194383-A1 | Monomers capable of dimerizing in an aqueous solution, and methods of using same | 2011-04-07 |
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