(S)-Pinocembrin

• CAT Number: R039434
• CAS Number: 480-39-7
• Molecular Formula: C15H12O4
• Molecular Weight: 256.25
• Purity: ≥95%
• Synonyms: (2S)-2,3-Dihydro-5,7-dihydroxy-2-phenyl-4H-1-benzopyran-4-one; (S)-2,3-dihydro-5,7-dihydroxy-2-phenyl-4H-1-benzopyran-4-one; (+)-Pinocembrin; (+)-Pinocoembrin; (2S)-Pinocembrin; 5,7-Dihydroxyflavanone; Dihydrochrysin; Galangin Flavanone; NSC 279005
• Target: NF-κB
• Storage: -20°C
• IUPAC Name: (2S)-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one
• InChI: InChI=1S/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2/t13-/m0/s1
• InChIKey: URFCJEUYXNAHFI-ZDUSSCGKSA-N
• SMILES: C1[C@H](OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3

(S)-Pinocembrin（Cat No.:R039434）is a naturally occurring flavonoid with antioxidant, anti-inflammatory, and neuroprotective properties. It is found in various plants, including Citrus species and honey. The (S)-enantiomer of pinocembrin has been studied for its potential therapeutic effects in neurodegenerative diseases and cardiovascular health. Its mechanisms include modulating oxidative stress, inhibiting pro-inflammatory pathways, and enhancing endothelial function. Due to its neuroprotective and anti-inflammatory actions, (S)-Pinocembrin holds promise in research related to brain health, chronic inflammation, and cardiovascular disorders, offering a valuable tool for drug development and metabolic studies.

Reference

– Batirov et al., Chem. Nat. Comp. (1986). 1:111-112