3,4-Dihydroxybenzoic Acid 97.0% (T) - 100 Gr - Sigma
Código: 25285
3,4-Dihydroxybenzoic acid
≥97.0% (T)
Sinônimo(s):
Protocatechuic acid
Sobre este item
Fórmula linear:
(HO)2C6H3CO2H
Número CAS:
Peso molecular:
154.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-760-0
Beilstein/REAXYS Number:
1448841
MDL number:
Assay:
≥97.0% (T)
InChI key
YQUVCSBJEUQKSH-UHFFFAOYSA-N
InChI
1S/C7H6O4/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3,8-9H,(H,10,11)
SMILES string
OC(=O)c1ccc(O)c(O)c1
assay
≥97.0% (T)
Quality Level
functional group
carboxylic acid
General description
3,4-Dihydroxybenzoic acid is reported as dietery polyphenol.[1] Antiviral activity of 3,4-dihydroxybenzoic acid (protocatechuic acid, PCA) against a virulent H9N2 strain in a mouse model is reported.[2] Cytotoxic effects of PCA on 3 non-small cell lung cancer (NSCLC) cell lines, A549, H3255, and Calu-6 cell lines is reported.[3] PCA is reported to prevent the carcinogenesis or antitumor growth in vivo. Signaling pathway involved in PCA-induced apoptosis in human gastric adenocarcinoma (AGS) cells is reported.[4] The oxidation of 3,4-dihydroxybenzoic acid by H2O2 in aqueous/goethite slurry at varying operating conditions (catalyst load, temperature, pH, substrate and hydrogen peroxide starting concentration) is investigated.[5]
Application
3,4-Dihydroxybenzoic acid is suitable for use in a study to investigate the effect of 4-coumaric and 3,4-dihydroxybenzoic acid on the basal oxidative DNA damage of rat colonic mucosa in vivo.[1] It may be used in the derivatization of chitosan resin.[6]
Biochem/physiol Actions
Chemopreventive in several animal models of carcinogenesis. Blocks cell proliferation in the post-initiation phase.

