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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)
| Member | Definition | Role |
|---|---|---|
| (-)-catechin-3-O-gallate | A 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 gallate | A 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-glucose | A 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-tetragalloylglucose | A 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-glucopyranose | A 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 gallate | A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3S)-hydroxy group of (+)-catechin. | (+)-catechin-3-O-gallate |
| corilagin | An ellagitannin with a hexahydroxydiphenoyl group bridging over the 3-O and 6-O of the glucose core. | corilagin |
| digallic acid | digallic acid | |
| epicatechin gallate | A 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 gallate | A gallate ester obtained by the formal condensation of gallic acid with the (3R)-hydroxy group of (-)-epigallocatechin. | (-)-epigallocatechin 3-gallate |
| ethyl gallate | A gallate ester obtained by the formal condensation of gallic acid with ethanol. | ethyl gallate |
| eugeniin | An 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-gallate | A gallate ester obtained by formal condensation of the carboxy group of gallic acid with the (3S)-hydroxy group of (+)-gallocatechin. | (+)-gallocatechin gallate |
| hamamelitannin | Hamamelitannin | |
| lauryl gallate | Dodecyl gallate | |
| methyl gallate | A 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 gallate | A gallate ester obtained by condensation of the carboxy group of gallic acid with the hydroxy group of octanol. | octyl gallate |
| theasinensin a | A 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 |
| theogallin | A 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)
| Timeframe | Studies, Drugs in This Class (%) | All Drugs % |
|---|---|---|
| pre-1990 | 24 (0.38) | 18.7374 |
| 1990's | 223 (3.54) | 18.2507 |
| 2000's | 1,726 (27.39) | 29.6817 |
| 2010's | 3,226 (51.20) | 24.3611 |
| 2020's | 1,102 (17.49) | 2.80 |
Study Types
| Publication Type | Studies, Drugs in This Class (%) | All Drugs (%) |
|---|---|---|
| Trials | 178 (2.52%) | 5.53% |
| Reviews | 513 (7.26%) | 6.00% |
| Case Studies | 17 (0.24%) | 4.05% |
| Observational | 1 (0.01%) | 0.25% |
| Other | 6,355 (89.96%) | 84.16% |