[. It has a role as a plant metabolite. Syringic acid is an extremely weak basic (essentially neutral) compound (based on its pKa). principal phenolic constituent of soyabean meal (Glycine max) Syringic acid is a phenol present in some distilled alcohol beverages. Int J Food Sci Nutr. This service is an Elixir Core Data Resource. EMBL-EBI, Wellcome Genome Campus, Hinxton, Cambridgeshire, CB10 Specializing in ready to use metabolomics kits. Gallic acid and derivatives are compounds containing a 3,4,5-trihydroxybenzoic acid moiety. Contents. (PMID 15545043). Some species of insects use syringaldehyde in their chemical communication systems. It is also a product of microbial (gut) metabolism of anthocyanins and other polyphenols that have been consumed (in fruits and alcoholic beverages - PMID: 18767860). InChI=1S/C9H10O5/c1-13-6-3-5(9(11)12)4-7(14-2)8(6)10/h3-4,10H,1-2H3,(H,11,12), {{mainSearchVariables.isShowHelp ? It is a member of benzoic acids, a dimethoxybenzene and a member of phenols. Outside of the human body, Syringic acid is found, on average, in the highest concentration within a few different foods, such as common walnuts, swiss chards, and olives and in a lower concentration in apples, tarragons, and peanuts. Gallic acid and derivatives are compounds containing a 3,4,5-trihydroxybenzoic acid moiety. Epub 2008 Sep 4. InChI=1S/C9H10O5/c1-13-6-3-5(9(11)12)4-7(14-2)8(6)10/h3-4,10H,1-2H3,(H,11,12), Found in The review addresses basic information about molecular mechanisms, therapeutic and industrial potential of SA. Download : Download high-res image (240KB)Download : Download full-size image. Sort by. This observation confirms that LigI is not necessary for syringic acid degradation. (. Syringic acid is correlated with high antioxidant activity and inhibition of LDL oxidation. Create . because the search term doesn't match exactly. This could make syringic acid a potential biomarker for the consumption of these foods. hide show. Syringic acid has also been detected, but not quantified in, several different foods, such as sweet marjorams, silver lindens, bulgurs, annual wild rices, and barley. InChI=1S/C9H10O5/c1-13-6-3-5(9(11)12)4-7(14-2)8(6)10/h3-4,10H,1-2H3,(H,11,12). 1 Structures Expand this section. Biology Laboratory | Terms of use, A molecular entity capable of donating a hydron to an acceptor (Br. J Agric Food Chem. Quantitative metabolomics services for biomarker discovery and validation. InChI=1S/C9H10O5/c1-13-6-3-5(9(11)12)4-7(14-2)8(6)10/h3-4,10H,1-2H3,(H,11,12), The Metabolomics Innovation Centre (TMIC). Food Funct. [, Forester SC, Waterhouse AL: Identification of Cabernet Sauvignon anthocyanin gut microflora metabolites. Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive, splash10-0f8a-0900000000-7b568e18ffde6ab04131, Predicted GC-MS Spectrum - GC-MS (2 TMS) - 70eV, Positive, splash10-00fr-8095000000-575a6ec78ed017731cc6, LC-MS/MS Spectrum - Quattro_QQQ 10V, N/A (Annotated), splash10-052f-0900000000-14ec0ce09465c51ccc37, LC-MS/MS Spectrum - Quattro_QQQ 25V, N/A (Annotated), splash10-004l-9800000000-9765822b3b1e2ec9d9de, LC-MS/MS Spectrum - Quattro_QQQ 40V, N/A (Annotated), splash10-004j-9100000000-8d01bd5b04dae916e4aa, LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 10V, Negative, splash10-0002-0900000000-0a0256c7bc33c2d88a4e, LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 20V, Negative, splash10-0fka-0900000000-254d42fb132329839152, LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 30V, Negative, splash10-00di-1900000000-304c5119148e7f55f4d6, LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 40V, Negative, splash10-00b9-9500000000-49a00cfe65ce9eabeb4c, LC-MS/MS Spectrum - LC-ESI-QQ (API3000, Applied Biosystems) 50V, Negative, splash10-004r-9000000000-80475497b3098dd00777, splash10-00di-1900000000-01d0ea76c3ba0db41782, LC-MS/MS Spectrum - Linear Ion Trap , negative, splash10-0f89-0900000000-87ada1ca48a49d9677dd, LC-MS/MS Spectrum - Linear Ion Trap , positive, splash10-001i-0900000000-019cee52e59a254e3fcf, Predicted LC-MS/MS Spectrum - 10V, Positive, splash10-0002-0900000000-6ce63e339a947f904864, Predicted LC-MS/MS Spectrum - 20V, Positive, splash10-001j-0900000000-a397243a2d8f8f9e501d, Predicted LC-MS/MS Spectrum - 40V, Positive, splash10-001r-2900000000-d3241b91846d43efb768, Predicted LC-MS/MS Spectrum - 10V, Negative, splash10-0002-0900000000-e699dd409e203e12842f, Predicted LC-MS/MS Spectrum - 20V, Negative, splash10-0uds-0900000000-b5bde1ce65999b3cf7de, Predicted LC-MS/MS Spectrum - 40V, Negative, splash10-0fa9-2900000000-87c04717df825474388d, splash10-0002-5900000000-0b6163fb3f78b99ad5dd, Consuming polyphenols described by Phenol-Explorer entry 420, Syringic acid → 6-(4-carboxy-2,6-dimethoxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid, Syringic acid → 3,4,5-trihydroxy-6-(4-hydroxy-3,5-dimethoxybenzoyloxy)oxane-2-carboxylic acid, Syringic acid → 2-{[hydroxy(4-hydroxy-3,5-dimethoxyphenyl)methylidene]amino}acetic acid, Syringic acid → 3,5-dimethoxy-4-(sulfooxy)benzoic acid, Goedert JJ, Sampson JN, Moore SC, Xiao Q, Xiong X, Hayes RB, Ahn J, Shi J, Sinha R: Fecal metabolomics: assay performance and association with colorectal cancer. Gallic acid and derivatives are compounds containing a 3,4,5-trihydroxybenzoic acid moiety. [. Syringic acid: Description: Syringic acid, also known as syringate or cedar acid, belongs to the class of organic compounds known as gallic acid and derivatives. SA has greater industrial applications include bioremediation, photocatalytic ozonation, laccase based detoxification. The therapeutic property of SA is attributed by the presence of methoxy groups onto the aromatic ring at positions 3 and 5. The low molecular weight phenolic compounds (include SA) isolated from Inonotus obliquus ( mushroom) might suppress the growth in HCT116 cells and also exhibited inhibitory effects on DNA topoisomerases and DNA polymerases [ 40 ]. field. Epub 2014 Jul 18. It shows a wide range of therapeutic applications in prevention of diabetes, CVDs, cancer, cerebral ischemia; as well as it possess anti-oxidant, antimicrobial, anti-inflammatory, antiendotoxic, neuro and hepatoprotective activities.
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