sameAs
Effect of overexpression of Saccharomyces cerevisiae Pad1p on the resistance to phenylacrylic acids and lignocellulose hydrolysates under aerobic and oxygen-limited conditions.Catabolism of coffee chlorogenic acids by human colonic microbiota.In vitro colonic metabolism of coffee and chlorogenic acid results in selective changes in human faecal microbiota growth.Identification of novel circulating coffee metabolites in human plasma by liquid chromatography-mass spectrometry.The degradation of curcuminoids in a human faecal fermentation model.The chemical nature of phenolic compounds determines their toxicity and induces distinct physiological responses in Saccharomyces cerevisiae in lignocellulose hydrolysatesHydroxycinnamic acids used as external acceptors of electrons: an energetic advantage for strictly heterofermentative lactic acid bacteriaBioappearance and pharmacokinetics of bioactives upon coffee consumption.Novel biomarkers of the metabolism of caffeic acid derivatives in vivo.[Studies on chemical constituents of root tuber of cultivated Pseudostellaria heterophylla (Zheshen No. 1)].Fungicidal activities of dihydroferulic acid alkyl ester analogues.Oat avenanthramide-C (2c) is biotransformed by mice and the human microbiota into bioactive metabolites.Phenolic acids inhibit the formation of advanced glycation end products in food simulation systems depending on their reducing powers and structures.Impact of dose on the bioavailability of coffee chlorogenic acids in humansA serum metabolomics-driven approach predicts orange juice consumption and its impact on oxidative stress and inflammation in subjects from the BIONAOS studyThe roasting process does not influence the extent of conjugation of coffee chlorogenic and phenolic acids
P921
Q27939296-B8650429-182A-4D41-B21E-4B03B76D66A5Q34886009-97557886-4AFE-4D89-A922-CAA53A852F93Q35586855-637646BE-8A47-41D4-BD21-C6796B84332BQ39738918-430BB5C4-8B01-49BC-8BCD-0AF58354001EQ40427345-43B2A8CF-0388-4D92-B623-32174BA6590FQ40551434-D3A807EF-646C-4E76-AF27-67398EF4DC67Q42248613-A3D45ADC-A4B2-476F-A2FF-BA7CF7ECE76CQ43412099-8A83A6B0-8197-406F-B123-188D9E299659Q43614722-D016FC00-EF03-46A6-8EA4-B8D01F60F29DQ46154849-47F59921-E588-46E9-B8AD-9BEC3158C0CFQ46244734-F2E18E5F-A941-43E1-B163-32C969DC2879Q46778682-912D93DA-C541-4358-9D64-54A2024E0FF3Q53616402-054BEDDA-504C-45F9-82F2-0C3489113D1EQ54510020-CDC02DE5-6A06-4152-8E8D-2DC46C5F48CAQ61686949-68B33F1D-5C95-4B9E-B74D-8A0C849408DBQ87336499-57C700CF-5D1D-4F53-82DA-92538F28B775
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
dihydroferulic acid
@en
Ácido 3-(4-hidroxi-3-metoxifenil)propiônico
@pt
type
label
dihydroferulic acid
@en
Ácido 3-(4-hidroxi-3-metoxifenil)propiônico
@pt
altLabel
3-(4-hydroxy-3-methoxyphenyl)propionic acid
@en
Ácido di-hidroferúlico
@pt
Ácido diidroferúlico
@pt
prefLabel
dihydroferulic acid
@en
Ácido 3-(4-hidroxi-3-metoxifenil)propiônico
@pt
P592
P661
P662
P683
P2067
P231
P232
P233
COC1=C(C=CC(=C1)CCC(=O)O)O
P234
1S/C10H12O4/c1-14-9-6-7(2-4-8(9)11)3-5-10(12)13/h2,4,6,11H,3,5H2,1H3,(H,12,13)
P235
BOLQJTPHPSDZHR-UHFFFAOYSA-N
P2566
100.013.172
P274
P3117
DTXSID90150427
P592
CHEMBL387842
P652
O01RNC700M