For research use only. Not for therapeutic Use.
Neotheaflavin（Cat No.:I044886）is a polyphenolic compound formed during the oxidative fermentation of tea leaves, particularly in black and oolong teas. It is a derivative of theaflavins, generated through the enzymatic oxidation of catechins such as epicatechin and epigallocatechin. Neotheaflavin exhibits potent antioxidant, anti-inflammatory, and anticancer properties. It helps neutralize reactive oxygen species, supports cardiovascular health, and may inhibit tumor growth by modulating cellular signaling pathways. Due to its strong bioactivity and natural origin, neotheaflavin is widely studied for its potential applications in nutraceuticals, functional foods, and preventive healthcare.
| CAS Number | 36451-14-6 |
| Synonyms | 3,4,6-trihydroxy-8-[(2R,3R)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]-1-[(2R,3S)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]benzo[7]annulen-5-one |
| Molecular Formula | C29H24O12 |
| Purity | ≥95% |
| IUPAC Name | 3,4,6-trihydroxy-8-[(2R,3R)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]-1-[(2R,3S)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-2-yl]benzo[7]annulen-5-one |
| InChI | InChI=1S/C29H24O12/c30-11-3-17(32)15-8-21(36)28(40-23(15)5-11)10-1-13-14(7-20(35)27(39)25(13)26(38)19(34)2-10)29-22(37)9-16-18(33)4-12(31)6-24(16)41-29/h1-7,21-22,28-33,35-37,39H,8-9H2,(H,34,38)/t21-,22+,28-,29-/m1/s1 |
| InChIKey | IPMYMEWFZKHGAX-WCQFOESSSA-N |
| SMILES | C1[C@H]([C@H](OC2=CC(=CC(=C21)O)O)C3=CC4=C(C(=C(C=C4[C@@H]5[C@H](CC6=C(C=C(C=C6O5)O)O)O)O)O)C(=O)C(=C3)O)O |
| Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |
