For research use only. Not for therapeutic Use.
Orientin-2”-O-p-trans-coumarate（Cat No.:I018429）is a naturally occurring flavonoid derivative, formed by the esterification of orientin, a luteolin-based C-glycosyl flavone, with p-coumaric acid. This conjugated structure enhances the antioxidant and free radical scavenging activity, contributing to its protective role against oxidative stress. Studies suggest it may exhibit anti-inflammatory, anti-cancer, and neuroprotective effects by modulating cellular signaling pathways. Found in certain medicinal plants, orientin-2”-O-p-trans-coumarate represents a promising bioactive compound for pharmaceutical and nutraceutical development, supporting cardiovascular, metabolic, and neurological health research.
| CAS Number | 1229437-75-5 |
| Synonyms | [(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate |
| Molecular Formula | C30H26O13 |
| Purity | ≥95% |
| IUPAC Name | [(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-8-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate |
| InChI | InChI=1S/C30H26O13/c31-12-22-26(39)27(40)30(43-23(38)8-3-13-1-5-15(32)6-2-13)29(42-22)25-19(36)10-18(35)24-20(37)11-21(41-28(24)25)14-4-7-16(33)17(34)9-14/h1-11,22,26-27,29-36,39-40H,12H2/b8-3+/t22-,26-,27+,29+,30-/m1/s1 |
| InChIKey | XIKYOEXOYRWIOU-HJBGGDBQSA-N |
| SMILES | C1=CC(=CC=C1/C=C/C(=O)O[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |
