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gallate ester

A benzoate ester that is any ester resulting from the formal condensation of the carboxy group of gallic acid (3,4,5-trihydroxybenzoic acid) with an alcoholic or phenolic hydroxy group.

ChEBI ID: 37576

Members (19)

MemberDefinitionRole
(-)-catechin-3-O-gallateA gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of (-)-catechin.(-)-catechin-3-O-gallate
(-)-gallocatechin gallateA gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of (-)-gallocatechin. A natural product found in found in green tea.(-)-gallocatechin gallate
1,2,3,4,6-pentakis-O-galloyl-beta-D-glucoseA galloyl-beta-D-glucose compound having five galloyl groups in the 1-, 2-, 3-, 4- and 6-positions.1,2,3,4,6-pentakis-O-galloyl-beta-D-glucose
1,2,3,6-tetragalloylglucoseA galloyl-beta-D-glucose compound having four galloyl groups in the 1-, 2-, 3- and 6-positions.1,2,3,6-tetrakis-O-galloyl-beta-D-glucose
1,2,6-tri-o-galloyl-beta-d-glucopyranoseA galloyl-beta-D-glucose compound having the galloyl groups in the 1-, 2- and 6-positions.1,2,6-tris-O-galloyl-beta-D-glucose
catechin gallateA gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3S)-hydroxy group of (+)-catechin.(+)-catechin-3-O-gallate
corilaginAn ellagitannin with a hexahydroxydiphenoyl group bridging over the 3-O and 6-O of the glucose core.corilagin
digallic aciddigallic acid
epicatechin gallateA gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3R)-hydroxy group of epicatechin. A natural product found in Parapiptadenia rigida.(-)-epicatechin-3-O-gallate
epigallocatechin gallateA gallate ester obtained by the formal condensation of gallic acid with the (3R)-hydroxy group of (-)-epigallocatechin.(-)-epigallocatechin 3-gallate
ethyl gallateA gallate ester obtained by the formal condensation of gallic acid with ethanol.ethyl gallate
eugeniinAn ellagitannin isolated from the dried flower buds of Eugenia caryophyllata. It exhibits alpha-glucosidase inhibitory activity and antiviral activity against acyclovir and phosphonoacetic acid (PAA)-resistant herpes simplex virus type 1 (HSV-1) as well as the wild-type HSV-1.eugeniin
gallocatechin-3-gallateA gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3S)-hydroxy group of (+)-gallocatechin.(+)-gallocatechin gallate
hamamelitanninHamamelitannin
lauryl gallateDodecyl gallate
methyl gallateA gallate ester obtained by the formal condensation of gallic acid with methanol. It exhibits anti-oxidant, anti-tumor, anti-microbial and anti-inflammatory properties.methyl 3,4,5-trihydroxybenzoate
octyl gallateA gallate ester obtained by condensation of the carboxy group of gallic acid with the hydroxy group of octanol.octyl gallate
theasinensin aA biflavonoid that is obtained by coupling of two molecules of (-)-epigallocatechin 3-gallate resulting in a bond between positions C-2 of the hydroxyphenyl ring. It is a natural product found in oolong tea.theasinensin A
theogallinA gallate ester resulting from the formal condensation of gallic acid with the (5R)-hydroxy group of (-)-quinic acid (i.e. the hydroxy group on the same side of the cyclohexane ring as the carboxy group).theogallin

Research

Studies (6,301)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-199024 (0.38)18.7374
1990's223 (3.54)18.2507
2000's1,726 (27.39)29.6817
2010's3,226 (51.20)24.3611
2020's1,102 (17.49)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials178 (2.52%)5.53%
Reviews513 (7.26%)6.00%
Case Studies17 (0.24%)4.05%
Observational1 (0.01%)0.25%
Other6,355 (89.96%)84.16%