trans-Cinnamic acid (BioDeep_00001867464)

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 (148.0524268)
中文名称: 反式肉桂酸, 肉桂酸, 反式肉桂酸, 反式肉桂酸, 肉桂酸, 肉桂酸, 肉桂酸, 肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸, 反式肉桂酸
谱图信息: 最多检出来源 Macaca mulatta(otcml) 0.11%

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 2024-11-05) (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

136 个代谢物同义名

数据库引用编号

28 个数据库交叉引用编号

ChEBI: CHEBI:35697
ChEBI: CHEBI:27386
KEGG: C00423
KEGGdrug: D70605
PubChem: 444539
HMDB: HMDB0000930
ChEMBL: CHEMBL27246
Wikipedia: Cinnamic_acid
Wikipedia: Cinnamic acid
MeSH: cinnamic acid
ChemIDplus: 0000140103
MetaCyc: CPD-674
KNApSAcK: C00029961
KNApSAcK: C00000170
foodb: FDB012052
chemspider: 392447
CAS: 140-10-3
medchemexpress: HY-N0610
MetaboLights: MTBLC27386
ChEBI: CHEBI:15669
PDB-CCD: TCA
3DMET: B00108
NIKKAJI: J2.024I
3DMET: B03846
NIKKAJI: J2.087G
RefMet: trans-Cinnamic acid
BioNovoGene_Lab2019: BioNovoGene_Lab2019-782
BioNovoGene_Lab2019: BioNovoGene_Lab2019-619

分类词条

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

32216 - Adenostoma sparsifolium:
68527 - Aegle marmelos: 10.1080/14786410310001608037
175969 - Aeschynanthus bracteatus: 10.1016/J.PHYTOCHEM.2008.05.012
1125367 - Aiouea brenesii: 10.1021/NP50040A021
25641 - Aloe: -
1389495 - Aloe castellorum: 10.1080/14786410802242851
125257 - Alpinia formosana: 10.1016/0031-9422(88)83115-7
94327 - Alpinia galanga: 10.1021/JF00026A001
125268 - Alpinia tonkinensis: 10.1080/10286020310001653291
2508388 - Alsidium triquetrum: 10.1016/J.PHYMED.2003.10.009
148671 - Anadenanthera colubrina: 10.1055/S-2004-818920
4615 - Ananas comosus:
663965 - Anastatica hierochuntica:
175694 - Andrographis paniculata: 10.1016/J.PHYTOCHEM.2004.05.008
268004 - Andryala pinnatifida: 10.1016/S0031-9422(82)85069-3
95948 - Anigozanthos preissii: 10.1002/1099-1565(200101/02)12:1<43::AID-PCA546>3.0.CO;2-Z
3702 - Arabidopsis thaliana: 10.2307/3869512
2675989 - Aragoa lucidula: 10.1055/S-0028-1097783
143780 - Aristolochia elegans: 10.1016/J.BMC.2003.10.031
325095 - Aristolochia littoralis: 10.1016/J.BMC.2003.10.031
205369 - Artemisia judaica: 10.1080/10412905.1990.9697881
2867270 - Artemisia pallens: 10.1002/PCA.564
4686 - Asparagus officinalis:
2781882 - Astianthus viminalis: 10.1055/S-2006-959424
29813 - Balanophora fungosa: 10.1248/CPB.57.1352
1128104 - Balanophora tobiracola: 10.1016/0031-9422(80)83209-2
230209 - Balsamorhiza sagittata: 10.1016/S0031-9422(00)83116-7
3505 - Betula pendula: 10.1007/BF00575727
38787 - Betula pubescens: 10.1016/0305-1978(94)00092-U
78707 - Bletilla striata: 10.1016/0031-9422(83)85044-4
78707 - Bletilla striata (Thunb. ) Reichb.f.: -
78707 - Bletilla Striata (Thunb.Ex A.Murray)Rchb.F.: -
48555 - Boschniakia Rossica Herba: -
3708 - Brassica napus:
3711 - Brassica rapa: 10.1007/BF02671339
4442 - Camellia sinensis: 10.1248/CPB.55.598
13393 - Cananga odorata: 10.1002/JCCS.199900084
3483 - Cannabis sativa: 10.1021/NP50008A001
4072 - Capsicum annuum: 10.1271/BBB.58.1141
40321 - Capsicum annuum var. annuum: 10.1021/JF00024A024
54785 - Ceanothus velutinus: 10.1016/S0031-9422(00)97178-4
36622 - Chaenomeles Sinensis (Thouin) Koehne: -
228520 - Cheniella glauca: 10.1016/J.BMCL.2015.05.089
3559 - Chenopodium album: 10.1007/BF01984952
119260 - Cinnamomum aromaticum:
1155220 - Cinnamomum iners:
128608 - Cinnamomum verum:
13442 - Coffea:
199218 - Colocasia antiquorum: 10.1021/JF100323Q
4460 - Colocasia esculenta: 10.1021/JF100323Q
41839 - Conocephalum conicum: 10.1016/0031-9422(96)83287-0
246543 - Cordia curassavica: 10.1080/10412905.1990.9697864
87660 - Corymbia maculata: 10.1002/CHIN.200047190
2580221 - Cryptocarya amygdalina: 10.1002/JCCS.200200041
3659 - Cucumis sativus: 10.1007/BF02065988
6669 - Daphnia pulex: 10.1038/SREP25125
4039 - Daucus carota:
361549 - Dicksonia gigantea: 10.1248/CPB.32.4620
2071583 - Dicksonia karsteniana: 10.1248/CPB.32.4620
461339 - Dicksonia sellowiana: 10.1248/CPB.32.4620
167917 - Duranta erecta: 10.1248/CPB.44.429
139932 - Engelhardia roxburghiana: 10.1016/J.PHYTOCHEM.2007.01.018
3389 - Ephedra distachya:
173280 - Ephedra equisetina: 10.1007/BF00563959
33136 - Epilobium dodonaei: 10.1016/S0021-9673(97)01259-4
1333928 - Euphorbia micractina: 10.1021/NP900305J
212310 - Euphorbia tithymaloides: 10.1016/J.FITOTE.2005.08.020
4414 - Euryale ferox Salisb.: -
3746 - Fragaria:
64940 - Fragaria moschata: 10.1002/RECL.19390580805
157505 - Gaultheria borneensis: 10.1002/CBDV.200800270
174247 - Gaultheria itoana: 10.1002/CBDV.200800270
38851 - Gentiana lutea: 10.1371/JOURNAL.PONE.0212062
1533088 - Globularia alypum:
1602035 - Goniothalamus amuyon:
270108 - Goniothalamus tenuifolius: 10.1007/BF02969393
39314 - Goupia glabra: 10.1002/EJOC.200300284
665695 - Gymnophyton isatidicarpum: 10.1021/NP50005A016
42053 - Gynerium sagittatum: 10.1016/J.PHYTOCHEM.2007.03.007
147773 - Haplopappus foliosus: 10.1016/S0305-1978(99)00080-0
222879 - Harpagophytum procumbens: 10.1021/NP0601612
1503107 - Harpagophytum zeyheri: 10.1055/S-2003-43225
9606 - Homo sapiens: -
9606 - Homo sapiens: 10.1007/S11306-012-0464-Y
141487 - Hoya australis: 10.1016/S0031-9422(00)82606-0
52832 - Hoya bella: 10.1016/S0031-9422(00)82606-0
206228 - Hoya cinnamomifolia: 10.1016/S0031-9422(00)82606-0
1167121 - Hoya coronaria: 10.1016/S0031-9422(00)82606-0
206229 - Hoya crassipes: 10.1016/S0031-9422(00)82606-0
206232 - Hoya diversifolia: 10.1016/S0031-9422(00)82606-0
2058639 - Hoya fraterna: 10.1016/S0031-9422(00)82606-0
2058643 - Hoya imperialis: 10.1016/S0031-9422(00)82606-0
365762 - Hoya lacunosa: 10.1016/S0031-9422(00)82606-0
2058646 - Hoya latifolia: 10.1016/S0031-9422(00)82606-0
945165 - Hoya longifolia: 10.1016/S0031-9422(00)82606-0
1167151 - Hoya macrophylla: 10.1016/S0031-9422(00)82606-0
206240 - Hoya multiflora: 10.1016/S0031-9422(00)82606-0
206243 - Hoya obovata: 10.1016/S0031-9422(00)82606-0
1167174 - Hoya pseudolanceolata: 10.1016/S0031-9422(00)82606-0
2058661 - Hoya shepherdii: 10.1016/S0031-9422(00)82606-0
365776 - Hoya tsangii: 10.1016/S0031-9422(00)82606-0
3486 - Humulus lupulus: 10.3390/NU11061377
124774 - Illicium fargesii: 10.1248/CPB.56.1201
1202800 - Illicium simonsii: 10.1248/CPB.56.1201
124778 - Illicium verum: 10.1021/NP50043A024
1548589 - Inula grandis: 10.1007/BF00564453
89648 - Ipomoea leptophylla: 10.1021/NP030197J
425908 - Isodon japonicus: 10.1271/BBB.59.1780
588648 - Isotachis japonica: 10.1016/S0031-9422(00)81055-9
97750 - Kaempferia galanga: 10.1016/0031-9422(93)80020-S
2338863 - Kalanchoe deficiens: 10.1016/J.TET.2008.01.090
1310066 - Lagotis yunnanensis:
1382326 - Leucophyllum ambiguum:
641172 - Lindsaea javanensis: 10.1248/CPB.31.3865
63360 - Liquidambar orientalis: 10.1016/0027-5107(92)90067-C
63360 - Liquidambar orientalis Mill.: -
594549 - Lychnophora ericoides: 10.1007/S10600-005-0179-7
437899 - Lychnophora pinaster: 10.1007/S10600-005-0179-7
112863 - Lycium barbarum L.: -
112883 - Lycium chinense Mill.: -
85856 - Magnolia denudata: 10.3390/MOLECULES23071558
3403 - Magnolia liliiflora: 10.3390/MOLECULES23071558
3750 - Malus domestica: 10.1021/JF020028P
283210 - Malus pumila: 10.1021/JF020028P
389206 - Mandragora autumnalis: 10.1016/J.PHYTOCHEM.2005.07.016
33117 - Mandragora officinarum: 10.1016/J.PHYTOCHEM.2005.07.016
1052074 - Marsypopetalum crassum: 10.1021/NP060323U
1462929 - Marsypopetalum modestum: 10.1021/NP060323U
3879 - Medicago sativa:
155640 - Melia azedarach: 10.1055/S-0028-1097188
39338 - Melissa officinalis: 10.1007/S00425-010-1206-X
121078 - Mespilodaphne quixos: 10.1016/0378-8741(81)90038-6
3673 - Momordica charantia: 10.3390/MOLECULES23020469
262757 - Morella rubra: 10.1271/BBB.90697
3498 - Morus alba: 10.1002/PTR.4803
66392 - Morus australis: 10.1002/PTR.4803
66393 - Morus bombycis: 10.1002/PTR.4803
248361 - Morus indica: 10.1002/PTR.4803
204141 - Ocimum americanum: 10.1007/BF02907824
39350 - Ocimum basilicum:
4146 - Olea europaea:
238830 - Onychium contiguum: 10.1016/0031-9422(74)85048-X
164276 - Onychium lucidum: 10.1016/0031-9422(74)85048-X
39352 - Origanum vulgare:
53809 - Oxalis pes-caprae: 10.1002/CBDV.200800179
125742 - Ozothamnus diosmifolius: 10.1016/S0031-9422(00)84791-3
35935 - Parthenium argentatum: 10.1002/CBER.19110440350
163034 - Pelargonium incrassatum: 10.1007/BF00579446
48386 - Perilla Frutescens: -
33119 - Petunia axillaris: 10.1271/BBB.60507
68554 - Phellodendron amurense: 10.1021/NP030034V
697203 - Phellodendron amurense var. wilsonii: 10.1021/NP030034V
354509 - Phellodendron chinense var. glabriusculum: 10.1021/NP030034V
296036 - Phyllanthus emblica: 10.1002/JCCS.200700228
126903 - Physalis peruviana: 10.1016/0031-9422(96)00303-2
260139 - Pimenta racemosa: 10.1080/10412905.1991.9697952
3343 - Pinus lambertiana: 10.1021/JA01143A502
101996 - Plantago coronopus: 10.1016/S0031-9422(98)00210-6
39414 - Plantago lanceolata: 10.1016/S0031-9422(98)00210-6
29818 - Plantago major:
33090 - Plants: -
204156 - Platostoma africanum: 10.1055/S-2006-962093
71910 - Pleurocybella porrigens: 10.1248/CPB.54.1213
375264 - Plinia cauliflora: 10.1021/NP0600999
73824 - Populus balsamifera: 10.1016/S0021-9673(00)94139-6
1616482 - Populus candicans: 10.1016/S0021-9673(00)94139-6
3696 - Populus deltoides: 10.1515/ZNC-1990-0604
3691 - Populus nigra: 10.1002/JPS.3080110306
3694 - Populus trichocarpa: 10.1515/ZNC-1987-9-1004
46147 - Portulaca oleracea: 10.1016/0378-8741(93)90067-F
55489 - Posidonia oceanica:
42229 - Prunus avium: 10.1371/JOURNAL.PONE.0121164
120290 - Psidium guajava: 10.1016/0031-9422(96)00303-2
22663 - Punica granatum: 10.3390/MOLECULES22101606
203015 - Rhodiola rosea:
32247 - Rubus idaeus: 10.1021/JF020028P
227256 - Sauromatum giganteum: 10.1007/S10600-014-1163-X
50507 - Schisandra chinensis: 10.1016/S0731-7085(00)00539-2
508984 - Schnella guianensis: 10.1016/0031-9422(88)80455-2
476207 - Scrophularia buergeriana: 10.1016/S0031-9422(00)00110-2
291326 - Scrophularia ningpoensis:
291326 - Scrophularia ningpoensis Hemsl.: -
2858926 - Scutellaria grossa:
186426 - Selaginella Doederleinii Hieron: -
3728 - Sinapis alba: 10.1007/BF02671339
4081 - Solanum lycopersicum: 10.1021/JF020028P
53737 - Sphagneticola trilobata: 10.1002/HLCA.201000301
409519 - Spiraea salicifolia: 10.1007/S10600-018-2530-9
409520 - Spiraea thunbergii: 10.1271/BBB.62.1546
1889 - Streptomyces ambofaciens: 10.3390/MD15120389
68174 - Streptomyces anthocyanicus: 10.1016/J.BIORTECH.2011.10.045
1916 - Streptomyces lividans: 10.1016/J.BIORTECH.2011.10.045
2054576 - Strobilanthes yunnanensis: 10.1248/CPB.55.1744
13699 - Styrax: -
153559 - Styrax tonkinensis (Pierre) Craib ex Hart.: -
1547788 - Tarenna attenuata: 10.1021/NP0603931
25629 - Taxus baccata: 10.1016/S0031-9422(00)80522-1
46417 - Tetrapanax papyrifer: 10.1021/NP050185T
3641 - Theobroma cacao: 10.1021/JF0615247
40145 - Tricholoma matsutake: 10.1080/00021369.1981.10864530
13750 - Vaccinium macrocarpon: 10.1021/JF020055F
180772 - Vaccinium vitis-idaea: 10.1016/0031-9422(96)00303-2
159976 - Viscum coloratum: 10.1248/CPB.54.1063
29760 - Vitis vinifera: 10.1021/JF020028P
67938 - Zanthoxylum armatum: 10.1007/978-3-642-71425-2_1
33090 - 安息香: -
33090 - 肉桂: -
569774 - 金线莲: -

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。

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]
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Angelica E Graminha, João Honorato, Liany Luna Dulcey, Luani Rezende Godoy, Marília F Barbosa, Marcia R Cominetti, Antonio C Menezes, Alzir A Batista. Evaluation of the biological potential of ruthenium(II) complexes with cinnamic acid. Journal of inorganic biochemistry. 2020 05; 206(?):111021. doi: 10.1016/j.jinorgbio.2020.111021. [PMID: 32163810]
Shahla Amani, Mehdi Mohebodini, Shahram Khademvatan, Morad Jafari. Agrobacterium rhizogenes mediated transformation of Ficus carica L. for the efficient production of secondary metabolites. Journal of the science of food and agriculture. 2020 Mar; 100(5):2185-2197. doi: 10.1002/jsfa.10243. [PMID: 31901132]
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Maria Medvedeva, Kseniya Barinova, Aleksandra Melnikova, Pavel Semenyuk, Vasillii Kolmogorov, Petr Gorelkin, Alexander Erofeev, Vladimir Muronetz. Naturally occurring cinnamic acid derivatives prevent amyloid transformation of alpha-synuclein. Biochimie. 2020 Mar; 170(?):128-139. doi: 10.1016/j.biochi.2020.01.004. [PMID: 31945397]
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Zhenyu Wang, Shenghan Ge, Shiyang Li, Huiting Lin, Shaoling Lin. Anti-obesity effect of trans-cinnamic acid on HepG2 cells and HFD-fed mice. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association. 2020 Mar; 137(?):111148. doi: 10.1016/j.fct.2020.111148. [PMID: 31982449]
Mariam Abotaleb, Alena Liskova, Peter Kubatka, Dietrich Büsselberg. Therapeutic Potential of Plant Phenolic Acids in the Treatment of Cancer. Biomolecules. 2020 02; 10(2):. doi: 10.3390/biom10020221. [PMID: 32028623]
Shashank Sagar Saini, Mariam Gaid, Debabrata Sircar. Benzoate-CoA ligase contributes to the biosynthesis of biphenyl phytoalexins in elicitor-treated pear cell cultures. Plant cell reports. 2020 Feb; 39(2):207-215. doi: 10.1007/s00299-019-02484-0. [PMID: 31713663]
Xuemei Huang, Penglong Wang, Tong Li, Xuehao Tian, Wenbo Guo, Bing Xu, Guangrui Huang, Desheng Cai, Fei Zhou, Hao Zhang, Haimin Lei. Self-Assemblies Based on Traditional Medicine Berberine and Cinnamic Acid for Adhesion-Induced Inhibition Multidrug-Resistant Staphylococcus aureus. ACS applied materials & interfaces. 2020 Jan; 12(1):227-237. doi: 10.1021/acsami.9b17722. [PMID: 31829617]
Wenqi Qian, Weilin Wu, Yun Kang, Yaqin Wang, Ping Yang, Yuanrong Deng, Chengjie Ni, Jianming Huang. Comprehensive identification of minor components and bioassay-guided isolation of an unusual antioxidant from Azolla imbricata using ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry combined with multicomponent knockout and bioactivity evaluation. Journal of chromatography. A. 2020 Jan; 1609(?):460435. doi: 10.1016/j.chroma.2019.460435. [PMID: 31515075]
Thomas Buxton, Shiori Takahashi, Akpe-Mary Eddy Doh, Joshua Baffoe-Ansah, Ebenezer Oduro Owusu, Chul-Sa Kim. Insecticidal activities of cinnamic acid esters isolated from Ocimum gratissimum L. and Vitellaria paradoxa Gaertn leaves against Tribolium castaneum Hebst (Coleoptera: Tenebrionidae). Pest management science. 2020 Jan; 76(1):257-267. doi: 10.1002/ps.5509. [PMID: 31180169]
Panagiotis Theodosis-Nobelos, Georgios Papagiouvanis, Maria Pantelidou, Panos N Kourounakis, Chrysoula Athanasekou, Eleni A Rekka. Design, Synthesis and Study of Nitrogen Monoxide Donors as Potent Hypolipidaemic and Anti-Inflammatory Agents. Molecules (Basel, Switzerland). 2019 Dec; 25(1):. doi: 10.3390/molecules25010019. [PMID: 31861583]
Daniel Chavarria, Carlos Fernandes, Brandon Aguiar, Tiago Silva, Jorge Garrido, Fernando Remião, Paulo J Oliveira, Eugenio Uriarte, Fernanda Borges. Insights into the Discovery of Novel Neuroprotective Agents: A Comparative Study between Sulfanylcinnamic Acid Derivatives and Related Phenolic Analogues. Molecules (Basel, Switzerland). 2019 Dec; 24(23):. doi: 10.3390/molecules24234405. [PMID: 31810314]