Pinostrobin chalcone

CAS: 18956-15-5

Ref. 3D-FP158556

Product Information

• Name: Pinostrobin chalcone
• Synonyms: 2',6'-Dihydroxy-4'-methoxychalcone, (2E)-1-(2,6-Dihydroxy-4-methoxyphenyl)-3-phenyl-2-propen-1-one, (2E)-1-(2,6-dihydroxy-4-methoxyphenyl)-3-phenylprop-2-en-1-one, (E)-1-(2,6-Dihydroxy-4-Methoxy-Phenyl)-3-Phenyl-Propenone, (E)-1-(2,6-Dihydroxy-4-methoxy-phenyl)-3-phenyl-, (E)-1-(2,6-Dihydroxy-4-methoxyphenyl)-3-phenyl-2-propen-1-one, 2-Propen-1-one, 1-(2,6-dihydroxy-4-methoxyphenyl)-3-phenyl-, (2E)-, 2-Propen-1-one, 1-(2,6-dihydroxy-4-methoxyphenyl)-3-phenyl-, (E)-, 2-Propen-1-one,1-(2,6-dihy, 2′,6′-Dihydroxy-4′-methoxychalcone, Chalcone, 2′,6′-dihydroxy-4′-methoxy-, Dihydroxy-4'-Methoxychalcone, 2',6'-

Description

Pinostrobin chalcone is a natural compound with hypoglycemic effects. It has been shown to have significant cytotoxicity against oral pathogens and may be useful as an antibacterial agent. Pinostrobin chalcone has also been shown to inhibit the growth of some fungi, such as Candida albicans, and exhibits strong antioxidant activity. Pinostrobin chalcone inhibits glucose uptake in mammalian cells by inhibiting mitochondrial functions and decreasing the release of growth factor-β1. This compound also suppresses the expression of ribosomal protein S6 kinase 1 (S6K1), which is a signaling molecule that regulates cellular metabolism and growth. Pinostrobin chalcone decreases the amount of glucose-6-phosphate dehydrogenase (G6PDH) in cells, which may contribute to its hypoglycemic effect. The molecular docking analysis indicates that pinostrobin binds to ATP synthase beta chain (ATP5B),

• Brand: Biosynth

Chemical properties

• Molecular weight: 270.28 g/mol
• Formula: C₁₆H₁₄O₄
• Purity: Min. 95%
• Color/Form: Yellow To Orange Or Brown Solid
• InChI: InChI=1S/C16H14O4/c1-20-12-9-14(18)16(15(19)10-12)13(17)8-7-11-5-3-2-4-6-11/h2-10,18-19H,1H3/b8-7+
• InChI key: InChIKey=CUGDOWNTXKLQMD-BQYQJAHWSA-N
• SMILES: COc1cc(O)c(C(=O)/C=C/c2ccccc2)c(O)c1