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CAS 210357-38-3

:

2H-1-Benzopyran-2-one, 7-[[2-(acetylamino)-2-deoxy-6-O-sulfo-β-D-glucopyranosyl]oxy]-4-methyl-, monopotassium salt

Description:
2H-1-Benzopyran-2-one, 7-[[2-(acetylamino)-2-deoxy-6-O-sulfo-β-D-glucopyranosyl]oxy]-4-methyl-, monopotassium salt, commonly referred to as a flavonoid derivative, exhibits several notable characteristics. This compound features a benzopyran core, which is characteristic of many flavonoids, contributing to its potential biological activities, including antioxidant and anti-inflammatory properties. The presence of the acetylamino and sulfonate groups enhances its solubility in water and may influence its interaction with biological systems. The monopotassium salt form indicates that it can dissociate in solution, potentially affecting its bioavailability and pharmacokinetics. This compound may be of interest in pharmaceutical research due to its structural complexity and potential therapeutic applications, particularly in the fields of glycoscience and medicinal chemistry. Its unique functional groups suggest that it could interact with various biological targets, making it a candidate for further investigation in drug development and biochemistry. Overall, the compound's characteristics highlight its potential utility in both research and therapeutic contexts.
Formula:C18H21NO11S·K
InChI:InChI=1S/C18H21NO11S.K/c1-8-5-14(21)29-12-6-10(3-4-11(8)12)28-18-15(19-9(2)20)17(23)16(22)13(30-18)7-27-31(24,25)26;/h3-6,13,15-18,22-23H,7H2,1-2H3,(H,19,20)(H,24,25,26);/t13-,15-,16-,17-,18-;/m1./s1
InChI key:InChIKey=XYARVLIQLAIXKI-SZSLDHOESA-N
SMILES:O([C@H]1[C@H](NC(C)=O)[C@@H](O)[C@H](O)[C@@H](COS(=O)(=O)O)O1)C=2C=C3C(=CC2)C(C)=CC(=O)O3.[K]
Synonyms:
  • 2H-1-Benzopyran-2-one, 7-[[2-(acetylamino)-2-deoxy-6-O-sulfo-β-D-glucopyranosyl]oxy]-4-methyl-, monopotassium salt
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