NCBI Taxonomy: 714486

Archidendron clypearia (ncbi_taxid: 714486)

found 37 associated metabolites at species taxonomy rank level.

Ancestor: Archidendron

Child Taxonomies: none taxonomy data.

Gallic acid

3,4,5-trihydroxybenzoic acid

C7H6O5 (170.0215226)


Gallic acid is an odorless white solid. Sinks in water. (USCG, 1999) Gallic acid is a trihydroxybenzoic acid in which the hydroxy groups are at positions 3, 4, and 5. It has a role as an astringent, a cyclooxygenase 2 inhibitor, a plant metabolite, an antioxidant, an antineoplastic agent, a human xenobiotic metabolite, an EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor, an apoptosis inducer and a geroprotector. It is a conjugate acid of a gallate. Gallic acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655). Gallic Acid is a natural product found in Visnea mocanera, Ardisia paniculata, and other organisms with data available. Gallic acid is a metabolite found in or produced by Saccharomyces cerevisiae. A colorless or slightly yellow crystalline compound obtained from nutgalls. It is used in photography, pharmaceuticals, and as an analytical reagent. See also: Gallic acid monohydrate (active moiety of); Paeonia lactiflora root (part of); Galium aparine whole (part of) ... View More ... Gallic acid is an organic acid, also known as 3,4,5-trihydroxybenzoic acid, found in gallnuts, sumac, witch hazel, tea leaves, oak bark, and other plants. The chemical formula is C6H2(OH)3CO2H. Gallic acid is widely distributed in plants and is found both free and as part of tannins. It is commonly used in the pharmaceutical industry. Gallic acid can also be used to synthesize the hallucinogenic alkaloid mescaline, also known as 3,4,5-trimethoxyphenethylamine. Salts and esters of gallic acid are termed gallates. Gallic acid has been found to be s metabolite of Aspergillus (PMID:24031294). A trihydroxybenzoic acid in which the hydroxy groups are at positions 3, 4, and 5. Present in red wine. Japan approved food antioxidant additive Gallic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=149-91-7 (retrieved 2024-07-01) (CAS RN: 149-91-7). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Gallic acid (3,4,5-Trihydroxybenzoic acid) is a natural polyhydroxyphenolic compound and an free radical scavenger to inhibit cyclooxygenase-2 (COX-2)[1]. Gallic acid has various activities, such as antimicrobial, antioxidant, antimicrobial, anti-inflammatory, and anticance activities[2]. Gallic acid (3,4,5-Trihydroxybenzoic acid) is a natural polyhydroxyphenolic compound and an free radical scavenger to inhibit cyclooxygenase-2 (COX-2)[1]. Gallic acid has various activities, such as antimicrobial, antioxidant, antimicrobial, anti-inflammatory, and anticance activities[2].

   

Ethyl gallate

2-([(4-CHLOROPHENYL)SULFONYL]AMINO)PROPANOICACID

C9H10O5 (198.052821)


Ethyl gallate is a gallate ester obtained by the formal condensation of gallic acid with ethanol. It has a role as a plant metabolite. Ethyl gallate is a natural product found in Limonium axillare, Dimocarpus longan, and other organisms with data available. Ethyl gallate occurs, inter alia, in Indian gooseberry (Phyllanthus emblica). Ethyl gallate is found in many foods, some of which include grape wine, fruits, guava, and vinegar. Occurs, inter alia, in Indian gooseberry (Phyllanthus emblica). Ethyl gallate is found in many foods, some of which are grape wine, fruits, guava, and vinegar. A gallate ester obtained by the formal condensation of gallic acid with ethanol. Ethyl gallate is a nonflavonoid phenolic compound and also a scavenger of hydrogen peroxide. Ethyl gallate is a nonflavonoid phenolic compound and also a scavenger of hydrogen peroxide.

   

Epigallocatechin 7-O-gallate

(2R,3R) -3,5,7,3,4,5-Hexahydroxyflavan 7-O-gallate

C22H18O11 (458.0849078)


   

7-O-Galloyltricetiflavan

7-O-Galloyltricetiflavan

C22H18O10 (442.0899928)


A gallate ester obtained by the formal condensation of gallic acid with the hydroxy group at position 7 of 3,4,5,5,7-pentahydroxyflavan. Isolated from the leaves of Pithecellobium clypearia, it exhibits antiviral activity.

   

Progallin A

Benzoic acid, 3,4,5-trihydroxy-, ethyl ester

C9H10O5 (198.052821)


Ethyl gallate is a nonflavonoid phenolic compound and also a scavenger of hydrogen peroxide. Ethyl gallate is a nonflavonoid phenolic compound and also a scavenger of hydrogen peroxide.

   

GALOP

InChI=1\C7H6O5\c8-4-1-3(7(11)12)2-5(9)6(4)10\h1-2,8-10H,(H,11,12

C7H6O5 (170.0215226)


C26170 - Protective Agent > C275 - Antioxidant Gallic acid (3,4,5-Trihydroxybenzoic acid) is a natural polyhydroxyphenolic compound and an free radical scavenger to inhibit cyclooxygenase-2 (COX-2)[1]. Gallic acid has various activities, such as antimicrobial, antioxidant, antimicrobial, anti-inflammatory, and anticance activities[2]. Gallic acid (3,4,5-Trihydroxybenzoic acid) is a natural polyhydroxyphenolic compound and an free radical scavenger to inhibit cyclooxygenase-2 (COX-2)[1]. Gallic acid has various activities, such as antimicrobial, antioxidant, antimicrobial, anti-inflammatory, and anticance activities[2].

   

(2s,3r,4r,5r,6s)-2-{[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4h-chromen-3-yl]oxy}-6-methyloxane-3,4,5-triol

(2s,3r,4r,5r,6s)-2-{[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4h-chromen-3-yl]oxy}-6-methyloxane-3,4,5-triol

C21H22O10 (434.1212912)


   

3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-7-yl 3,4,5-trihydroxybenzoate

3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-7-yl 3,4,5-trihydroxybenzoate

C22H18O11 (458.0849078)


   

2-{3,5-dihydroxy-4-[(phenoxycarbonyl)oxy]phenyl}-5-hydroxy-3,4-dihydro-2h-1-benzopyran-7-yl 3,4,5-trihydroxybenzoate

2-{3,5-dihydroxy-4-[(phenoxycarbonyl)oxy]phenyl}-5-hydroxy-3,4-dihydro-2h-1-benzopyran-7-yl 3,4,5-trihydroxybenzoate

C29H22O12 (562.1111212000001)


   

2,6-dihydroxy-4-[(2r)-5-hydroxy-7-(3,4,5-trihydroxybenzoyloxy)-3,4-dihydro-2h-1-benzopyran-2-yl]phenyl 3,4,5-trihydroxybenzoate

2,6-dihydroxy-4-[(2r)-5-hydroxy-7-(3,4,5-trihydroxybenzoyloxy)-3,4-dihydro-2h-1-benzopyran-2-yl]phenyl 3,4,5-trihydroxybenzoate

C29H22O14 (594.1009512)


   

(2s,3r,4r,5r,6s)-2-{[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4h-chromen-3-yl]oxy}-6-methyloxane-3,4,5-triol

(2s,3r,4r,5r,6s)-2-{[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4h-chromen-3-yl]oxy}-6-methyloxane-3,4,5-triol

C21H22O11 (450.11620619999997)


   

(2r)-5-hydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-7-yl 3,4,5-trihydroxybenzoate

(2r)-5-hydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-7-yl 3,4,5-trihydroxybenzoate

C22H18O10 (442.0899928)


   

(2s)-5-hydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-7-yl 3,4,5-trihydroxybenzoate

(2s)-5-hydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-7-yl 3,4,5-trihydroxybenzoate

C22H18O10 (442.0899928)


   

2,6-dihydroxy-4-[5-hydroxy-7-(3,4,5-trihydroxybenzoyloxy)-3,4-dihydro-2h-1-benzopyran-2-yl]phenyl 3,4,5-trihydroxybenzoate

2,6-dihydroxy-4-[5-hydroxy-7-(3,4,5-trihydroxybenzoyloxy)-3,4-dihydro-2h-1-benzopyran-2-yl]phenyl 3,4,5-trihydroxybenzoate

C29H22O14 (594.1009512)


   

5-[(2s)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-2-yl]benzene-1,2,3-triol

5-[(2s)-5,7-dihydroxy-3,4-dihydro-2h-1-benzopyran-2-yl]benzene-1,2,3-triol

C15H14O6 (290.0790344)