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CAS 2555-23-9

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7-Hydroxy-4-methyl-3-phenyl-2H-1-benzopyran-2-one

Description:
7-Hydroxy-4-methyl-3-phenyl-2H-1-benzopyran-2-one, commonly known as a flavonoid compound, exhibits several notable characteristics. This substance features a benzopyran core structure, which is typical of flavonoids, contributing to its potential biological activities. The presence of hydroxyl (-OH) and methyl (-CH3) groups enhances its solubility and reactivity, while the phenyl group can influence its interaction with biological targets. This compound is often studied for its antioxidant properties, which may provide protective effects against oxidative stress. Additionally, it may exhibit anti-inflammatory and anticancer activities, making it of interest in pharmacological research. The molecular structure allows for various interactions with enzymes and receptors, potentially leading to diverse therapeutic applications. Its CAS number, 2555-23-9, facilitates its identification in chemical databases and literature. Overall, this compound represents a significant area of interest in natural product chemistry and medicinal research due to its diverse biological activities and potential health benefits.
Formula:C16H12O3
InChI:InChI=1/C16H12O3/c1-10-13-8-7-12(17)9-14(13)19-16(18)15(10)11-5-3-2-4-6-11/h2-9,17H,1H3
InChI key:InChIKey=DTDWZXAWHROHIO-UHFFFAOYSA-N
SMILES:CC1=C(C(=O)OC=2C1=CC=C(O)C2)C3=CC=CC=C3
Synonyms:
  • Umbelliferone, 4-methyl-3-phenyl-
  • 7-Hydroxy-4-methyl-3-phenyl-2H-1-benzopyran-2-one
  • 7-Hydroxy-4-methyl-3-phenylcoumarin
  • 2H-1-Benzopyran-2-one, 7-hydroxy-4-methyl-3-phenyl-
  • Coumarin, 7-hydroxy-4-methyl-3-phenyl-
  • 2555-23-9
  • 7-Hydroxy-4-methyl-3-phenyl-2H-chromen-2-one
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Found 1 products.
  • 7-Hydroxy-4-methyl-3-phenyl-2H-chromen-2-one
    Biosynth
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    7-Hydroxy-4-methyl-3-phenyl-2H-chromen-2-one

    CAS:
    7-Hydroxy-4-methyl-3-phenyl-2H-chromen-2-one is a disubstituted coumarin nucleus and a potent anti-HIV agent. It has been synthesised as a lead compound to inhibit HIV reverse transcriptase by binding to its active site, which is the enzyme responsible for DNA synthesis. The probe exhibits dose dependent inhibition of HIV replication, with an IC50 of 0.5 μM. This compound also inhibits cysteine proteases, such as cathepsin B, and reverses the effects of certain chemotherapeutic agents on cancer cells. 7-Hydroxy-4-methyl-3-phenyl-2H-chromen-2-one is fluorescent in solution and this property can be used for detection purposes.
    Formula:C16H12O3
    Purity:Min. 95%
    Molecular weight:252.26 g/mol

    Ref: 3D-CAA55523

    250mg
    390.00€
    2500mg
    1,393.00€