2-Naphthaldehyde-13C
2-Naphthaldehyde-13C is the 13C-labeled 2-Naphthaldehyde (HY-Y0075). 2-Naphthaldehyde belongs to naphthalene-based bis-aromatic aldehyde compounds. 2-Naphthaldehyde scavenges DPPH and ABTS+ free radicals, and exerts reductive effects by donating hydrogen atoms to interrupt free radical chain reactions. 2-Naphthaldehyde inhibits the growth and proliferation of colon cancer cells. 2-Naphthaldehyde serves as a substrate for NAD+-dependent salicylaldehyde dehydrogenase from Pseudomonas strain C6 and is catalytically oxidized. 2-Naphthaldehyde acts as a precursor material for the chemical synthesis of antioxidant Schiff bases.
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- No. CAS: 116815-49-7
- Fòrmula: C1013CH8O
- Peso molecular:157.17
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Almacenamiento:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Actividad biológica
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Chemical Information
- Protocolo
- Pureza y Documentación
- Referencias
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Help & FAQs
Actividad biológica
Descripciòn
Aplicación
1. This compound can be used as a tracer
2. This compound can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Chemical Information
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No. CAS 116815-49-7
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Unlabeled CAS 66-99-9
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Peso molecular 157.17
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Fòrmula C1013CH8O
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SMILES
O=[13CH]C1=CC2=C(C=CC=C2)C=C1
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Envío
Room temperature in continental US; may vary elsewhere.
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Almacenamiento
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocolo
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Cell Viability Determination by MTT Colorimetric Assay
The following protocol uses the MTT colorimetric assay as a classic literature-established method for assessing cell viability/metabolic activity in cultured mammalian cells. MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] is reduced by metabolically active cells to a colored formazan product; the amount of formazan is quantified spectrophotometrically and provides an indirect measure of metabolically active viable cells. Importantly, MTT reduction reflects cellular oxidoreductase/metabolic activity rather than an absolute direct count of living cells, so changes in cellular metabolism can alter the signal independently of cell number.
Pureza y Documentación
Referencias
[2]. Singh R, et al. Purification and characterization of NAD+ -dependent salicylaldehyde dehydrogenase from carbaryl-degrading Pseudomonas sp. strain C6. Applied biochemistry and biotechnology. 2014 Jan;172(2):806-19. [Content Brief]
[3]. Oladipo SD, et al. Antidiabetes and antioxidant potential of Schiff bases derived from 2-naphthaldehye and substituted aromatic amines: Synthesis, crystal structure, Hirshfeld surface analysis, computational, and studies. Heliyon. 2024 Jan 15;10(1):e23174. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
2-Naphthaldehyde-13C Related Classifications
HY-Y0075S1 Related Classifications
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Keywords
- 2-Naphthaldehyde-13C
- 116815-49-7
- Isotope-Labeled Compounds
- Biochemical Assay Reagents
- Drug Intermediate
- antioxidant Schiff bases
- NAD+-dependent salicylaldehyde dehydrogenase
- Pseudomonas sp. strain C6
- Diospyros kaki
- colon cancer
- DPPH
- 2-naphthoic acid
- ABTS+ free radicals
- colon cancer cells
- Inhibitor
- inhibitor
- inhibit