trans-Cinnamic acid (BioDeep_00001867464)

Main id: BioDeep_00000000105

Secondary id: BioDeep_00000014351, BioDeep_00000017235, BioDeep_00000270977, BioDeep_00000861309

human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite BioNovoGene_Lab2019


代谢物信息卡片


(2E)-3-Phenyl-2-propenoic acid

化学式: C9H8O2 (148.0524)
中文名称: 反式肉桂酸, 肉桂酸
谱图信息: 最多检出来源 Macaca mulatta(otcml) 21.42%

Reviewed

Last reviewed on 2024-07-29.

Cite this Page

trans-Cinnamic acid. BioDeep Database v3. PANOMIX ltd, a top metabolomics service provider from China. https://query.biodeep.cn/s/trans-cinnamic_acid (retrieved 2024-12-22) (BioDeep RN: BioDeep_00001867464). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

分子结构信息

SMILES: c1(/C=C/C(=O)O)ccccc1
InChI: InChI=1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)

描述信息

trans-Cinnamic acid, also known as (e)-cinnamic acid or phenylacrylic acid, belongs to the class of organic compounds known as cinnamic acids. These are organic aromatic compounds containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. trans-Cinnamic acid exists in all living species, ranging from bacteria to humans. trans-Cinnamic acid is a sweet, balsam, and cinnamon tasting compound. Outside of the human body, trans-Cinnamic acid is found, on average, in the highest concentration within a few different foods, such as chinese cinnamons, olives, and lingonberries and in a lower concentration in redcurrants, red raspberries, and corianders. trans-Cinnamic acid has also been detected, but not quantified in several different foods, such as common oregano, pepper (spice), fennels, pomegranates, and european cranberries. This could make trans-cinnamic acid a potential biomarker for the consumption of these foods. Cinnamic acid has been shown to be a microbial metabolite; it can be found in Alcaligenes, Brevibacterium, Cellulomonas, and Pseudomonas (PMID:16349793). trans-Cinnamic acid is a potentially toxic compound.
Cinnamic acid is a monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. It is found in Cinnamomum cassia. It has a role as a plant metabolite. It is a member of styrenes and a member of cinnamic acids. It is a conjugate acid of a cinnamate.
Cinnamic acid is a metabolite found in or produced by Escherichia coli (strain K12, MG1655).
Cinnamic acid is a natural product found in Marsypopetalum crassum, Aiouea brenesii, and other organisms with data available.
Cinnamic acid has the formula C6H5CHCHCOOH and is an odorless white crystalline acid, which is slightly soluble in water. It has a melting point of 133 degree centigrade and a boiling point of 300 degree centigrade.
Cinnamic acid is a metabolite found in or produced by Saccharomyces cerevisiae.
See also: Cinnamon (part of); Chinese Cinnamon (part of); Stevia rebaudiuna Leaf (part of) ... View More ...
Cinnamic acid is a white crystalline hydroxycinnamic acid, which is slightly soluble in water. It is obtained from oil of cinnamon, or from balsams such as storax. Cinnamic acid is found in many foods, some of which are green bell pepper, olive, pepper (spice), and pear.
A monocarboxylic acid that consists of acrylic acid bearing a phenyl substituent at the 3-position. It is found in Cinnamomum cassia.
trans-Cinnamic acid is a natural antimicrobial, with minimal inhibitory concentration (MIC) of 250 μg/mL against fish pathogen A. sobria, SY-AS1[1].
trans-Cinnamic acid is a natural antimicrobial, with minimal inhibitory concentration (MIC) of 250 μg/mL against fish pathogen A. sobria, SY-AS1[1].

同义名列表

138 个代谢物同义名

Cinnamic acid, United States Pharmacopeia (USP) Reference Standard; TRANS-CINNAMIC ACID (CONSTITUENT OF CINNAMOMUM CASSIA BARK) [DSC]; InChI=1/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6; CINNAMIC ACID (CONSTITUENT OF CINNAMOMUM VERUM BARK) [DSC]; trans-Cinnamic acid; Phenylacrylic acid;Cinnamylic acid; trans-Cinnamic Acid Zone Refined (number of passes:40); trans-cinnamic acid (trans-3-phenylacrylic acid); trans-Cinnamic acid, natural, >=99\\%, FCC, FG; trans-Cinnamic Acid [Matrix for MALDI-TOF/MS]; 4-09-00-02002 (Beilstein Handbook Reference); cinnamic acid, 14C-labeled cpd (E)-isomer; 3-Phenylacrylic acid; -Phenylacrylic acid; trans-Cinnamic acid, analytical standard; trans-Cinnamic acid, purum, >=99.0\\% (T); cinnamic acid, 3H-labeled cpd (Z)-isomer; cinnamic acid, 3H-labeled cpd (E)-isomer; (E)-cinnamic acid, 2-(14)C-labeled cpd; cinnamic acid, sodium salt(Z)-isomer; cinnamic acid, sodium salt(E)-isomer; 1BE36587-A165-4142-9340-18FFE3E03426; cinnamic acid, zinc salt(E)-isomer; 2-Propenoic acid, 3-phenyl-, (2E)-; cinnamic acid, 2-(13)C-labeled cpd; cinnamic acid, 2-(14)C-labeled cpd; cinnamic acid, 1-(13)C-labeled cpd; cinnamic acid, 3-(14)C-labeled cpd; tritium labeled (Z)-cinnamic acid; cinnamic acid, ion(1-)-(E)-isomer; cinnamic acid, (trans)-(E)-isomer; 2-Propenoic acid, 3-phenyl-, (E)-; tritium labeled (E)-cinnamic acid; cinnamic acid, 1-14C-labeled cpd; trans-Cinnamic acid, >=99\\%, FG; trans-3-Phenyl-2-propenoic acid; cinnamic acid, nickel (+2) salt; tert-.beta.-Phenylacrylic acid; cinnamic acid, 13C-labeled cpd; (2E)-3-phenylprop-2-enoic acid; (2E)-3-Phenyl-2-propenoic acid; cinnamic acid, radical ion(1-); cinnamic acid, 14C-labeled cpd; (2E)-2-Phenyl-2-propenoic acid; cinnamic acid, potassium salt; PHENYLETHYLENECARBOXYLIC ACID; (E)-3-Phenyl-2-propenoic acid; 3-Phenyl-(e)-2-propenoic acid; (E)-3-phenylprop-2-enoic acid; Zimtsaeure | trans-Cinnamate; trans-Cinnamic acid, >=99\\%; trans-.beta.-Carboxystyrene; trans-3-Phenyl-2-propenoate; trans-3-Phenylacrylic acid; cinnamic acid, sodium salt; (2E)-3-phenylprop-2-enoate; (2E)-3-Phenyl-2-propenoate; (2E)-2-Phenyl-2-propenoate; 3-phenyl-2E-propenoic acid; 3-Phenyl-2-propenoic acid; (2E)-3-phenylacrylic acid; trans-Cinnamic acid, 97\\%; (E)-3-phenyl-acrylic acid; (E)-3-phenylprop-2-enoate; (e)-3-Phenyl-2-propenoate; trans-beta-Carboxystyrene; trans-Cinnamic acid, 99\\%; cinnamic acid, (Z)-isomer; Cinnamic acid(only trans); 3-phenylprop-2-enoic acid; .beta.-Phenylacrylic acid; PHENYLETHYLENECARBOXYLate; .beta-Phenylacrylic acid; E-3-phenylpropenoic acid; (E)-3-Phenylacrylic acid; beta-Phenylacrylic acid; Cinnamic acid (natural); Cinnamicacid(onlytrans); Trans-Cinnamic Acid,(S); trans-3-Phenylacrylate; CINNAMIC ACID [USP-RS]; cinnamic acid, ion(1-); Benzylideneacetic acid; 3-Phenylpropenoic acid; trans-Β-carboxystyrene; TRANS-CINNAMIC-D5 ACID; CINNAMIC ACID [WHO-DD]; trans-b-Carboxystyrene; CINNAMIC ACID (USP-RS); Cinnamic acid, trans-; (2E)-3-Phenylacrylate; CINNAMIC ACID (MART.); CINNAMIC ACID [MART.]; Cinnamic Acid Natural; Benzenepropenoic acid; Heparin, lithium salt; CINNAMIC ACID [INCI]; CINNAMIC ACID [FHFI]; (E)-3-Phenylacrylate; 3-Phenylacrylic acid; b-Phenylacrylic acid; Β-phenylacrylic acid; Acidum cinnamylicum; CINNAMIC ACID [FCC]; trans cinnamic acid; Cinnamic acid, (E)-; Benzeneacrylic acid; trans-cinnamic acid; Phenylacrylic acid; CINNAMIC ACID [MI]; Kyselina skoricove; 5-Thiazolamine?HCl; (2E)-Cinnamic acid; cis-cinnamic acid; Cinnamic acid, E-; (E)-Cinnamic acid; E-Z cinnamic acid; trans-Zimtsaeure; sodium cinnamate; UNII-U14A832J8D; CINNAMIC ACIDUM; Cinnamylic acid; trans-Cinnamate; E-cinnamic acid; t-Cinnamic acid; Benzeneacrylate; (E)-cinnamate; Cinnamic Acid; Tox21_302137; Tox21_112279; PhCH=CHCO2H; WLN: QV1U1R; U14A832J8D; Zimtsaeure; AI3-23709; cinnamate; AI3-00891; Cinnamic; trans-Cinnamate; trans-Cinnamic acid



数据库引用编号

32 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

208 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 10 AKT1, BCL2, CASP3, CAT, HPGDS, NLRP3, PPARG, PTGS2, TLR4, TYR
Peripheral membrane protein 3 ACHE, CYP1B1, PTGS2
Endosome membrane 1 TLR4
Endoplasmic reticulum membrane 3 BCL2, CYP1B1, PTGS2
Nucleus 7 ACHE, AKT1, BCL2, CASP3, FOS, NLRP3, PPARG
cytosol 9 AKT1, BCL2, CASP3, CAT, FOS, HPGDS, LIPE, NLRP3, PPARG
nucleoplasm 5 AKT1, CASP3, FOS, HPGDS, PPARG
RNA polymerase II transcription regulator complex 2 FOS, PPARG
Cell membrane 5 ACHE, AKT1, LIPE, TLR4, TNF
lamellipodium 1 AKT1
Golgi apparatus membrane 1 NLRP3
Synapse 1 ACHE
cell cortex 1 AKT1
cell surface 3 ACHE, TLR4, TNF
glutamatergic synapse 2 AKT1, CASP3
Golgi apparatus 1 ACHE
Golgi membrane 2 INS, NLRP3
lysosomal membrane 1 GAA
neuromuscular junction 1 ACHE
neuronal cell body 2 CASP3, TNF
postsynapse 1 AKT1
Cytoplasm, cytosol 2 LIPE, NLRP3
Lysosome 2 GAA, TYR
plasma membrane 6 ACHE, AKT1, BCHE, GAA, TLR4, TNF
Membrane 9 ACHE, AKT1, BCL2, CAT, CYP1B1, GAA, LIPE, NLRP3, TLR4
caveola 2 LIPE, PTGS2
extracellular exosome 2 CAT, GAA
Lysosome membrane 1 GAA
endoplasmic reticulum 4 BCL2, FOS, NLRP3, PTGS2
extracellular space 6 ACHE, BCHE, IL10, IL6, INS, TNF
lysosomal lumen 1 GAA
perinuclear region of cytoplasm 4 ACHE, PPARG, TLR4, TYR
mitochondrion 4 BCL2, CAT, CYP1B1, NLRP3
protein-containing complex 4 AKT1, BCL2, CAT, PTGS2
intracellular membrane-bounded organelle 6 CAT, CYP1B1, GAA, HPGDS, PPARG, TYR
Microsome membrane 2 CYP1B1, PTGS2
postsynaptic density 1 CASP3
Single-pass type I membrane protein 2 TLR4, TYR
Secreted 7 ACHE, BCHE, GAA, IL10, IL6, INS, NLRP3
extracellular region 9 ACHE, BCHE, CAT, GAA, IL10, IL6, INS, NLRP3, TNF
Mitochondrion outer membrane 1 BCL2
Single-pass membrane protein 1 BCL2
mitochondrial outer membrane 1 BCL2
mitochondrial matrix 1 CAT
Extracellular side 1 ACHE
Nucleus membrane 1 BCL2
Bcl-2 family protein complex 1 BCL2
nuclear membrane 1 BCL2
external side of plasma membrane 2 TLR4, TNF
microtubule cytoskeleton 1 AKT1
Melanosome membrane 1 TYR
Early endosome 1 TLR4
cell-cell junction 1 AKT1
Golgi-associated vesicle 1 TYR
recycling endosome 1 TNF
Single-pass type II membrane protein 1 TNF
vesicle 1 AKT1
Membrane raft 1 TNF
pore complex 1 BCL2
focal adhesion 1 CAT
spindle 1 AKT1
Peroxisome 1 CAT
basement membrane 1 ACHE
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
Cytoplasm, cytoskeleton, microtubule organizing center 1 NLRP3
Inflammasome 1 NLRP3
interphase microtubule organizing center 1 NLRP3
NLRP3 inflammasome complex 1 NLRP3
Nucleus inner membrane 1 PTGS2
Nucleus outer membrane 1 PTGS2
nuclear inner membrane 1 PTGS2
nuclear outer membrane 1 PTGS2
Cell projection, ruffle 1 TLR4
ruffle 1 TLR4
receptor complex 2 PPARG, TLR4
neuron projection 1 PTGS2
ciliary basal body 1 AKT1
chromatin 2 FOS, PPARG
phagocytic cup 2 TLR4, TNF
blood microparticle 1 BCHE
Lipid-anchor, GPI-anchor 1 ACHE
Endomembrane system 1 NLRP3
endosome lumen 1 INS
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
microtubule organizing center 1 NLRP3
tertiary granule membrane 1 GAA
Melanosome 1 TYR
side of membrane 1 ACHE
myelin sheath 1 BCL2
lipopolysaccharide receptor complex 1 TLR4
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 2 CAT, INS
Golgi lumen 1 INS
endoplasmic reticulum lumen 4 BCHE, IL6, INS, PTGS2
nuclear matrix 1 FOS
transport vesicle 1 INS
azurophil granule membrane 1 GAA
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
nuclear envelope lumen 1 BCHE
synaptic cleft 1 ACHE
protein-DNA complex 1 FOS
ficolin-1-rich granule membrane 1 GAA
death-inducing signaling complex 1 CASP3
transcription factor AP-1 complex 1 FOS
[Tumor necrosis factor, soluble form]: Secreted 1 TNF
catalase complex 1 CAT
interleukin-6 receptor complex 1 IL6
autolysosome lumen 1 GAA
BAD-BCL-2 complex 1 BCL2
[Isoform H]: Cell membrane 1 ACHE
[C-domain 2]: Secreted 1 TNF
[Tumor necrosis factor, membrane form]: Membrane 1 TNF
[C-domain 1]: Secreted 1 TNF


文献列表

  • Menglu Wu, Zi-An Deng, Chaoyi Shen, Zhichao Yang, Zihan Cai, Di Wu, Kunsong Chen. Fabrication of antimicrobial PCL/EC nanofibrous films containing natamycin and trans-cinnamic acid by microfluidic blow spinning for fruit preservation. Food chemistry. 2024 Jun; 442(?):138436. doi: 10.1016/j.foodchem.2024.138436. [PMID: 38244441]
  • Micheli Negri Brusamarello, Antonio Pedro Brusamarello, Mário Antônio Alves da Cunha, Cleverson Busso. Biological and phytochemical potential of Baccharis trimera (Less.) DC leaf extract on swine clinical isolates. Natural product research. 2024 May; 38(10):1799-1805. doi: 10.1080/14786419.2023.2222217. [PMID: 37292020]
  • Rong Fan, Zining Liang, Qing Wang, Sizhe Chen, Shiting Huang, Jiansu Liu, Rui Huang, Jie Chen, Feilan Zhao, Wei Huang. Beneficial action of cinnamic acid against ovarian cancer via network pharmacology analysis and the pharmacological activity assessment. Naunyn-Schmiedeberg's archives of pharmacology. 2024 05; 397(5):2987-2994. doi: 10.1007/s00210-023-02766-1. [PMID: 37870582]
  • Yanan Lu, Xue Han. Therapeutic Implications of Phenolic Acids for Ameliorating Inflammatory Bowel Disease. Nutrients. 2024 Apr; 16(9):. doi: 10.3390/nu16091347. [PMID: 38732594]
  • Tarun Kumar Kar, Sananda Sil, Angshita Ghosh, Ananya Barman, Sandip Chattopadhyay. Mitigation of letrozole induced polycystic ovarian syndrome associated inflammatory response and endocrinal dysfunction by Vitex negundo seeds. Journal of ovarian research. 2024 Apr; 17(1):76. doi: 10.1186/s13048-024-01378-4. [PMID: 38589892]
  • O V Ravikumar, Vanitha Marunganathan, Meenakshi Sundaram Kishore Kumar, Magesh Mohan, Mohammed Rafi Shaik, Baji Shaik, Ajay Guru, Khairiyah Mat. Zinc oxide nanoparticles functionalized with cinnamic acid for targeting dental pathogens receptor and modulating apoptotic genes in human oral epidermal carcinoma KB cells. Molecular biology reports. 2024 Feb; 51(1):352. doi: 10.1007/s11033-024-09289-9. [PMID: 38400866]
  • Hanru Liu, Chonglin Cai, Xingjia Zhang, Wenkui Li, Zhiqing Ma, Juntao Feng, Xili Liu, Peng Lei. Discovery of Novel Cinnamic Acid Derivatives as Fungicide Candidates. Journal of agricultural and food chemistry. 2024 Feb; 72(5):2492-2500. doi: 10.1021/acs.jafc.3c05655. [PMID: 38271672]
  • Fábio Florença Cardoso, Guilherme Henrique Marchi Salvador, Walter Luís Garrido Cavalcante, Maeli Dal-Pai, Marcos Roberto de Mattos Fontes. BthTX-I, a phospholipase A2-like toxin, is inhibited by the plant cinnamic acid derivative: chlorogenic acid. Biochimica et biophysica acta. Proteins and proteomics. 2024 02; 1872(2):140988. doi: 10.1016/j.bbapap.2023.140988. [PMID: 38142025]
  • Baoyun Shan, Jian Mo, Jiayi Yang, Xiaochun Qin, Haina Yu. Cloning and functional characterization of a cinnamate 4-hydroxylase gene from the hornwort Anthoceros angustus. Plant science : an international journal of experimental plant biology. 2024 Jan; 341(?):111989. doi: 10.1016/j.plantsci.2024.111989. [PMID: 38232819]
  • Runqin Wang, Xueling Zhang, Xiangyu Meng, Li Yang, Rongrong Xing, Xuan Chen, Shuang Hu. Hydroxyl-rich ferrofluid for efficient liquid phase microextraction of cinnamic acid derivatives in traditional Chinese medicine. Journal of separation science. 2024 Jan; 47(1):e2300796. doi: 10.1002/jssc.202300796. [PMID: 38234030]
  • Mariza Severina de Lima Silva, Marcilene Souza da Silva, Rômulo Carlos Dantas da Cruz, Bruno de Oliveira Veras, Ivone Antonia de Souza, Rafael Matos Ximenes, Thiago Mendonça de Aquino, Alexandre José da Silva Góes. Biological evaluation of 1,3-benzodioxole acids points to 3,4-(methylenedioxy) cinnamic acid as a potential larvicide against Aedes aegypti (Diptera: Culicidae). Experimental parasitology. 2024 Jan; 256(?):108657. doi: 10.1016/j.exppara.2023.108657. [PMID: 38043764]
  • Yao Zhao, Jitao Hu, Yilin Zhang, Han Tao, Linying Li, Yuqing He, Xueying Zhang, Chi Zhang, Gaojie Hong. Unveiling targeted spatial metabolome of rice seed at the dough stage using Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry imaging. Food research international (Ottawa, Ont.). 2023 Dec; 174(Pt 1):113578. doi: 10.1016/j.foodres.2023.113578. [PMID: 37986446]
  • Agata Wilczańska, Barbara Sparzak-Stefanowska, Adam Kokotkiewicz, Anna Jesionek, Aleksandra Królicka, Maria Łuczkiewicz, Mirosława Krauze-Baranowska. Biotechnological strategies for controlled accumulation of flavones in hairy root culture of Scutellaria lateriflora L. Scientific reports. 2023 11; 13(1):20422. doi: 10.1038/s41598-023-47757-7. [PMID: 37990031]
  • Xiaoxue Li, Yue Hu, Bingxin He, Lingyu Li, Yu Tian, Yingjie Xiao, Hai Shang, Zhongmei Zou. Design, synthesis and evaluation of ursodeoxycholic acid-cinnamic acid hybrids as potential anti-inflammatory agents by inhibiting Akt/NF-κB and MAPK signaling pathways. European journal of medicinal chemistry. 2023 Nov; 260(?):115785. doi: 10.1016/j.ejmech.2023.115785. [PMID: 37678142]
  • Fangping Zhong, Qi Zhang, Kejia Chen, Shichao Lan, Wenchao Yang, Xiuhai Gan. Eco-Friendly Cinnamic Acid Derivatives Containing Glycoside Scaffolds as Potential Antiviral Agents. Journal of agricultural and food chemistry. 2023 Nov; ?(?):. doi: 10.1021/acs.jafc.3c06318. [PMID: 37943715]
  • Yu Shi, Lan-Tu Xiong, Hui Li, Wen-Long Li, Dylan O'Neill Rothenberg, Li-Sheng Liao, Xin Deng, Gao-Peng Song, Zi-Ning Cui. Derivative of cinnamic acid inhibits T3SS of Xanthomonas oryzae pv. oryzae through the HrpG-HrpX regulatory cascade. Bioorganic chemistry. 2023 Sep; 141(?):106871. doi: 10.1016/j.bioorg.2023.106871. [PMID: 37734193]
  • Farkhondeh Safari, Hamid Hassanpour, Ahmad Alijanpour. Evaluation of hackberry (Celtis australis L.) fruits as sources of bioactive compounds. Scientific reports. 2023 07; 13(1):12233. doi: 10.1038/s41598-023-39421-x. [PMID: 37507445]
  • Yimeng Cui, Peiwei Wang, Mengli Li, Yujue Wang, Xinmiao Tang, Jingang Cui, Yu Chen, Teng Zhang. Cinnamic acid mitigates left ventricular hypertrophy and heart failure in part through modulating FTO-dependent N6-methyladenosine RNA modification in cardiomyocytes. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2023 Jul; 165(?):115168. doi: 10.1016/j.biopha.2023.115168. [PMID: 37453198]
  • Giuseppe Di Pede, Pedro Mena, Letizia Bresciani, Mariem Achour, Rosa Mª Lamuela, Ramón Estruch, Rikard Landberg, Sabine E Kulling, David Wishart, Ana Rodriguez-Mateos, Michael N Clifford, Alan Crozier, Claudine Manach, Daniele Del Rio. A systematic review and comprehensive evaluation of human intervention studies to unravel the bioavailability of hydroxycinnamic acids. Antioxidants & redox signaling. 2023 Jun; ?(?):. doi: 10.1089/ars.2023.0254. [PMID: 37382416]
  • Kateryna Kukil, Elias Englund, Nick Crang, Elton P Hudson, Pia Lindberg. Laboratory evolution of Synechocystis PCC6803 for phenylpropanoid production. Metabolic engineering. 2023 Jun; ?(?):. doi: 10.1016/j.ymben.2023.06.014. [PMID: 37392984]
  • Zühal Bayrakçeken Güven, Iclal Saracoglu, Akito Nagatsu, Mustafa Abdullah Yilmaz, A Ahmet Basaran. Anti-tyrosinase and antimelanogenic effect of cinnamic acid derivatives from Prunus mahaleb L.: Phenolic composition, isolation, identification and inhibitory activity. Journal of ethnopharmacology. 2023 Jun; 310(?):116378. doi: 10.1016/j.jep.2023.116378. [PMID: 36924865]
  • Aline Costa Santos, Felipe Akihiro Melo Otsuka, Rodrigo Brito Santos, Danielle de Jesus Trindade, Humberto Reis Matos. Antiglycation potential and antioxidant activity of genipap (Genipa americana L.) in oxidative stress mediated by hydrogen peroxide on cell culture. Natural product research. 2023 Jun; 37(12):2065-2069. doi: 10.1080/14786419.2022.2116700. [PMID: 36093565]
  • Nariman E Mahdy, Passent M Abdel-Baki, Ahmed A El-Rashedy, Rana M Ibrahim. Modulatory Effect of Pyrus pyrifolia Fruit and its Phenolics on Key Enzymes against Metabolic Syndrome: Bioassay-Guided Approach, HPLC Analysis, and In Silico Study. Plant foods for human nutrition (Dordrecht, Netherlands). 2023 May; ?(?):. doi: 10.1007/s11130-023-01069-3. [PMID: 37219720]
  • Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
  • Abdullah Mashraqi, Yosra Modafer, Mohamed A Al Abboud, Hanaa M Salama, Emad Abada. HPLC Analysis and Molecular Docking Study of Myoporum serratum Seeds Extract with Its Bioactivity against Pathogenic Microorganisms and Cancer Cell Lines. Molecules (Basel, Switzerland). 2023 May; 28(10):. doi: 10.3390/molecules28104041. [PMID: 37241781]
  • M Amundsen, L Jaakola, K Aaby, I Martinussen, N Kelanne, S Tuominen, O Laaksonen, B Yang, A L Hykkerud. Effect of ripening temperature on the chemical composition of lingonberries (Vaccinium vitis-idaea L.) of northern and southern origin. Food research international (Ottawa, Ont.). 2023 05; 167(?):112738. doi: 10.1016/j.foodres.2023.112738. [PMID: 37087220]
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