Table 1.
Class | Phenolic Compounds | Chemical Structures (Main Compound) | |
---|---|---|---|
Leaves | Stems | ||
Catechins | (+)-catechin—R1 = H (–)-epicatechin—R1 = H+ gallocatechin—R1 = OH epigallocatechin—R1 = OH |
||
Cinchonains | cinchonains I cinchonains II |
||
Phenolic acids | 3,4–dihydroxybenzoic p–coumaroyl quinic acid isomers p–coumaroyl malonic acid p–coumaroyl derivatives p–coumaroyl glucose coumaroyl iridoid |
||
p–coumaric acid | - | ||
feruloyl quinic acid isomer | - | ||
caffeoyl quinic acid isomers | - | ||
caffeic acid ethyl ester | - | ||
caffeic acid hexoside | - | ||
Proantho- cyanidins |
B–type dimer B–type trimer B–type tetramer B–type pentamer A–type dimer A–type trimer procyanidin A2 procyanidin B1 procyanidin B2 |
||
Flavonols | quercetin–3–O–(4”–HMG)–α–rhamnoside quercetin–3–O–galactoside quercetin–3–O–glucoside quercetin–3–O–rutinoside quercetin–3–O-α–rhamnoside quercetin–3–O–arabinoside quercetin–3–O–glucuronide |
||
kaempferol | - | ||
kaempferol–3–glucuronide | - | ||
kaempferol–hexoside | - | ||
kaempferol–O–pentoside | - | ||
kaempferol–(HMG)–rhamnoside | - | ||
Lignans | - | Lyoniside (9–O–β–D–xylopyranosyl(+)lyoniresinol) |