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3,4-Dihydroxymandelic acid is an active metabolite of the endogenous catecholamine (-)-norepinephrine (Cay-16673). It is formed from (-)-norepinephrine via the intermediate norepinephrine aldehyde by aldehyde dehydrogenase. 3,4-Dihydroxymandelic acid scavenges superoxide radicals (IC50 = 130 nM) and reduces lipid peroxidation in cell-free assays. 3,4-Dihydroxymandelic acid is also formed from norepinephrine by gut microbiota, such as E. coli. It is a chemoattractant for enterohemorrhagic E. coli that induces the expression of virulence genes when used at a concentration of 50 µM and increases the attachment of enterohemorrhagic E. coli to HeLa cells in vitro.Formal Name: alpha,3,4-trihydroxy-benzeneacetic acid. CAS Number: 775-01-9. Synonyms: DHMA, DOMA. Molecular Formula: C8H8O5. Formula Weight: 184.1. Purity: >95%. Formulation: (Request formulation change), A solid. Solubility: DMF: 30 mg/ml, DMSO: 10 mg/ml, Ethanol: 30 mg/ml, PBS (pH 7.2): 10 mg/ml. SMILES: O=C(C(C1=CC=C(C(O)=C1)O)O)O. InChi Code: InChI=1S/C8H8O5/c9-5-2-1-4(3-6(5)10)7(11)8(12)13/h1-3,7,9-11H,(H,12,13). InChi Key: RGHMISIYKIHAJW-UHFFFAOYSA-N.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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