Description
Troxerutin, a natural bioflavonoid isolated from Sophora japonica., has been reported to have many benefits and medicinal properties. It can inhibit the production of reactive oxygen species (ROS) and depress ER stress-mediated NOD activation.
Synonyms
Trihydroxyethylrutin; Vitamin P4; Rufen-P4; 2-[3,4-bis(2-Hydroxyethoxy)phenyl]-5-hydroxy-7-(2-hydroxyethoxy)-4-oxo-4H-chromen-3-yl 6-O-(6-deoxy-b-D-mannopyranosyl)-b-D-glucopyranoside; Trihydroxyethylrutin; 3',4',7-Tris[O-(2-hydroxyethyl)]rutin
IUPAC Name
2-[3,4-bis(2-hydroxyethoxy)phenyl]-5-hydroxy-7-(2-hydroxyethoxy)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
Molecular Formula
C33H42O19
Canonical SMILES
CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OCCO)C5=CC(=C(C=C5)OCCO)OCCO)O)O)O)O)O)O
InChI
InChI=1S/C33H42O19/c1-14-23(38)26(41)28(43)32(49-14)48-13-21-24(39)27(42)29(44)33(51-21)52-31-25(40)22-17(37)11-16(45-7-4-34)12-20(22)50-30(31)15-2-3-18(46-8-5-35)19(10-15)47-9-6-36/h2-3,10-12,14,21,23-24,26-29,32-39,41-44H,4-9,13H2,1H3/t14-,21+,23-,24+,26+,27-,28+,29+,32+,33-/m0/s1
InChIKey
IYVFNTXFRYQLRP-VVSTWUKXSA-N
Boiling Point
1058.4±65.0 °C at 760 mmHg
Melting Point
>164°C (dec.)
Solubility
Soluble in DMSO (Slightly), Methanol (Slightly, Heated), Pyridine (Sparingly, Sonicated)
Appearance
Light Yellow to Yellow Solid
Application
Anticoagulants
Storage
Keep tightly closed.
Safety Statements
S22-S24/25
Stability
Stable at normal temperatures and pressures.