LUCIGENIN CAS 2315-97-1
Introduction：Basic information about LUCIGENIN CAS 2315-97-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
LUCIGENIN Basic information
| Product Name: | LUCIGENIN |
| Synonyms: | lucigenin or N,N′-dimethyl-9,9′-biacridinium dinitrate;L-6868;NSC-151912;9,9'-BIS(N-METHYLACRIDINIUM NITRATE);LUCIGENIN;10,10'-Dimethyl-9,9'-biacridinium Dinitrate [for Chemiluminescence Research];BIS(N-METHYLACRIDINIUM) DINITRATE;BIS(N-METHYLACRIDINIUM) NITRATE |
| CAS: | 2315-97-1 |
| MF: | C28H22N4O6 |
| MW: | 510.5 |
| EINECS: | 219-023-4 |
| Product Categories: | Miscellaneous Natural Products;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Acridinium (Chemiluminescence);Acridine;Analytical Chemistry;Chemiluminescence |
| Mol File: | 2315-97-1.mol |
LUCIGENIN Chemical Properties
| Melting point | 250°C |
| storage temp. | room temp |
| solubility | acetic acid: soluble10mg/mL |
| form | powder |
| color | Yellow powder with orange to brown cast |
| λmax | 455nm |
| BRN | 3901768 |
| Biological Applications | Chloride indicator; diagnosis of hemostatic disorders; detecting bacteria,nucleicacids,proteins,pathogens; identifying respiratory infections; generating and detecting reactive oxygen species; chemiluminescent indicator |
| Major Application | diagnostic assay manufacturing hematology histology |
| InChI | InChI=1S/C28H22N2.2NO3/c1-29-23-15-7-3-11-19(23)27(20-12-4-8-16-24(20)29)28-21-13-5-9-17-25(21)30(2)26-18-10-6-14-22(26)28;2*2-1(3)4/h3-18H,1-2H3;;/q+2;2*-1 |
| InChIKey | KNJDBYZZKAZQNG-UHFFFAOYSA-N |
| SMILES | C1(=C2C=CC=CC2=[N+](C)C2=CC=CC=C12)C1=C2C=CC=CC2=[N+](C)C2=CC=CC=C12.[N+]([O-])([O-])=O.[N+]([O-])([O-])=O |
Safety Information
| Safety Statements | 24/25 |
| RIDADR | 1479 |
| WGK Germany | 3 |
| HazardClass | 5.1 |
| PackingGroup | III |
| HS Code | 29339900 |
| Storage Class | 11 - Combustible Solids |
| Description | Lucigenin is a chemiluminescent probe used to detect superoxide production and the presence of chloride. It can be used to detect superoxide production by enzymatic and cellular sources. It is a sensitive method that has been applied to the monitoring of superoxide production from xanthine oxidase, microsomal NADPH cytochrome reductase, and NADPH oxidases of phagocytes, endothelial cells, fibroblasts, and smooth muscle cells of blood vessel walls. However, it produces similar chemiluminescence signals in isolated aortic and cardiac tissues from wild-type and Nox1-Nox2-Nox4 triple knockout mice, suggesting that it is not selective for NADPH-based ROS production. It also reacts with hydrogen peroxide without generating free radical intermediates and has been used to detect lipid hydroperoxide in oils. Lucigenin is also used as a fluorescent chloride-sensitive indicator, with its fluorescence being quenched by chloride (ex/em = 455/505 nm, respectively). Lucigenin fluorescence is insensitive to phosphate, sulfate, and nitrate. |
| Chemical Properties | Dark yellow powder |
| Uses | Lucigenine, is used as chemiluminescence. It exhibits a bluish-green fluorescence. Dyes and metabolites. |
| Uses | Chemiluminescent probe for the detection of peroxides in biological systems. |
| Mechanism of action | In the case of lucigenin it is first reduced to a cation radical. Then it reacts in its univalently reduced form with ROS to produce dioxetane, which breaks down to generate photons. These probes cannot measure the individual free radicals but measure global ROS levels in the sample. Luminescence signals are expressed in relative light units (RLU), a direct measure of free radicals produced. |
| References | [1] Y LI. Validation of lucigenin (bis-N-methylacridinium) as a chemilumigenic probe for detecting superoxide anion radical production by enzymatic and cellular systems.[J]. The Journal of Biological Chemistry, 1998, 273 4: 2015-2023. DOI: 10.1074/jbc.273.4.2015 [2] BIWERSI J. Verkman A S Tulk B. Long-Wavelength Chloride-Sensitive Fluorescent Indicators[J]. Analytical biochemistry, 1994, 219 1: Pages 139-143. DOI: 10.1006/abio.1994.1242 [3] YU. A. VLADIMIROV E. V P. Free radicals and cell chemiluminescence[J]. Biochemistry (Moscow), 2010, 74 13: 1545-1566. DOI: 10.1134/s0006297909130082 [4] MIKHAIL P. SKATCHKOV . Validation of Lucigenin as a Chemiluminescent Probe to Monitor Vascular Superoxide as Well as Basal Vascular Nitric Oxide Production[J]. Biochemical and biophysical research communications, 1999, 254 2: Pages 319-324. DOI: 10.1006/bbrc.1998.9942 [5] HUA CAI. Detection of reactive oxygen species and nitric oxide in vascular cells and tissues: comparison of sensitivity and specificity.[J]. Methods in molecular medicine, 2007, 139: 293-311. DOI: 10.1007/978-1-59745-571-8_20 [6] FLáVIA REZENDE. Unchanged NADPH Oxidase Activity in Nox1-Nox2-Nox4 Triple Knockout Mice: What Do NADPH-Stimulated Chemiluminescence Assays Really Detect?[J]. Antioxidants & redox signaling, 2016, 24 7: 392-399. DOI: 10.1089/ars.2015.6314 [7] JOHN P. BUNTING David A G. Development of a flow injection chemiluminescent assay for the quantification of lipid hydroperoxides[J]. Journal of the American Oil Chemists Society, 2003, 80 10: 951-955. DOI: 10.1007/s11746-003-0802-1 [8] FERDANI R, LI R, PAJEWSKI R, et al. Transport of chloride and carboxyfluorescein through phospholipid vesicle membranes by heptapeptide amphiphiles[J]. Organic & Biomolecular Chemistry, 2007, 15: 2423-2432. DOI: 10.1039/b705544g [9] RUEDAS-RAMA M J, ORTE A, HALL E A H, et al. A chloride ion nanosensor for time-resolved fluorimetry and fluorescence lifetime imaging?[J]. Analyst, 2012, 6: 1500-1508. DOI: 10.1039/c2an15851e |
LUCIGENIN Preparation Products And Raw materials
