ácido trans-quinámico - AR, ≥99% , CAS No.140-10-3

CAS: 140-10-3 Cat. No.: C108496 Peso molecular: 148.16 Beilstein Registry Number: 1905952 Número EC: 205-398-1
Disponible para pedir
GRADE & PURITY AR ? Analytical Reagent grade — high-purity chemicals meeting strict assay limits for lab analysis. Use when accuracy matters and trace impurities could skew results. ≥99%
Synonyms
Cinnamic acid, E- | tert-.beta.-Phenylacrylic acid | 3-Phenylpropenoic acid | (E)-3-Phenylacrylate | (E)-3-phenylprop-2-enoic acid | NSC44010 | NSC-44010 | Trans-Cinnamic Acid,(S) | trans-Zimtsaeure | CINNAMIC ACID | (E)-Cinnamic acid | 5-Thiazolamine?HCl
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25g
C108496-25g
10
9,90US$
100g
C108496-100g
3
18,90US$
500g
C108496-500g
1
55,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

AR, ≥99% AR for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 29 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Un elemento básico para la investigación proteómica.

Specifications

Sinónimos
Cinnamic acid, E- | tert-.beta.-Phenylacrylic acid | 3-Phenylpropenoic acid | (E)-3-Phenylacrylate | (E)-3-phenylprop-2-enoic acid | NSC44010 | NSC-44010 | Trans-Cinnamic Acid, (S) | trans-Zimtsaeure | CINNAMIC ACID | (E)-Cinnamic acid | 5-Thiazolamine?HCl
Especificaciones y pureza
AR, ≥99%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
AR
Pureza
≥99%
Nombres e identificadores
Sonrisas canónicasC1=CC=C(C=C1)C=CC(=O)O
IUPAC Name(E)-3-phenylprop-2-enoic acid
InChIKeyWBYWAXJHAXSJNI-VOTSOKGWSA-N
INCHI1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+
Isómeros SMILES C1=CC=C(C=C1)/C=C/C(=O)O
WGK Alemania 1
RTECS GD7850000
CAS alternativo 621-82-9
Peso molecular 148.16
Beilstein 1905952
Reaxy-Rn 507757
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=507757&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
ClaseCinnamic acids and derivatives
SubclassCinnamic acids
Intermediate Tree Nodes Not available
Direct ParentCinnamic acids
Alternative Parents Styrenes  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Cinnamic acid - Styrene - Benzenoid - Monocyclic benzene moiety - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound
DescripciónThis compound 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.
External Descriptors Monolignols
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
HCAR2 Tclin Hydroxycarboxylic acid receptor 2 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PMVK Tchem Phosphomevalonate kinase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
XDH Tclin Xanthine dehydrogenase (1038 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKR1B1 Tclin Aldose reductase (1404 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Butyrylcholinesterase (7174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APP Tclin Amyloid-beta A4 protein (8510 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SYK Tclin Tyrosine-protein kinase SYK (7372 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAMK2A Tchem CaM kinase II alpha (1938 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A-375 (9258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHN (49357 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PANC-1 (6144 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
WISH (126 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MIA PaCa-2 (5949 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A2780 (11979 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-144 (176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TNKS2 Tchem Tankyrase 1/2 (384 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Papain (844 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryz Quinone oxidoreductase (288 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HD1 Histone deacetylase (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hcar2 Hydroxycarboxylic acid receptor 2 (55 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAL62 Alpha-glucosidase MAL62 (106 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Echinochloa crus-galli (3685 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Burkholderia cepacia (649 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ralstonia solanacearum (520 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterobacter cloacae (7976 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Micrococcus luteus (7463 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus epidermidis (22802 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptococcus pyogenes (16140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus niger (16508 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecalis (29875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycolicibacterium smegmatis (8003 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pichia kudriavzevii (7448 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trichophyton rubrum (3646 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leishmania amazonensis (3813 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leishmania donovani (89745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trypanosoma cruzi (99888 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meloidogyne incognita (862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tenebrio molitor (178 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Musca domestica (713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human immunodeficiency virus 1 (70413 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trypanosoma brucei rhodesiense (7991 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-12 (7051 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RBL-2H3 (1162 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BV-2 (3710 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-22 (3261 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fabH 3-oxoacyl-[acyl-carrier-protein] synthase 3 (47 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rdl GABA receptor subunit (76 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BALB/3T3 (534 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Abutilon theophrasti (831 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus parasiticus (296 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Athelia rolfsii (768 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Neurospora crassa (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycobacterium tuberculosis variant bovis BCG (1626 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Fusarium oxysporum f. sp. niveum (47 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus sydowii (55 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

29 results found

Lot NumberCertificate TypeFechaArticulo
A2613026Certificate of AnalysisJan 15, 2026 C108496
A2627251Certificate of AnalysisJan 10, 2026 C108496
A2627253Certificate of AnalysisJan 10, 2026 C108496
A2627327Certificate of AnalysisJan 10, 2026 C108496
D2608237Certificate of AnalysisJan 10, 2026 C108496
D2608234Certificate of AnalysisJan 10, 2026 C108496
D2608204Certificate of AnalysisJan 10, 2026 C108496
D2608203Certificate of AnalysisJan 10, 2026 C108496
B2609043Certificate of AnalysisJan 10, 2026 C108496
A2607070Certificate of AnalysisAug 15, 2025 C108496
I2501419Certificate of AnalysisAug 15, 2025 C108496
H2528241Certificate of AnalysisAug 15, 2025 C108496
H2528239Certificate of AnalysisAug 15, 2025 C108496
G2529034Certificate of AnalysisAug 05, 2025 C108496
B2506056Certificate of AnalysisFeb 10, 2025 C108496
C2125204Certificate of AnalysisJan 10, 2025 C108496
G2415493Certificate of AnalysisApr 29, 2024 C108496
G2415494Certificate of AnalysisApr 29, 2024 C108496
C23101313Certificate of AnalysisOct 10, 2022 C108496
C2414042Certificate of AnalysisOct 10, 2022 C108496
B2324221Certificate of AnalysisOct 10, 2022 C108496
B2324192Certificate of AnalysisOct 10, 2022 C108496
B2324190Certificate of AnalysisOct 10, 2022 C108496
B2324187Certificate of AnalysisOct 10, 2022 C108496
B2324166Certificate of AnalysisOct 10, 2022 C108496
A2412063Certificate of AnalysisOct 10, 2022 C108496
F2210396Certificate of AnalysisMar 24, 2022 C108496
F2210397Certificate of AnalysisMar 24, 2022 C108496
F2210402Certificate of AnalysisMar 24, 2022 C108496

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Propiedades químicas y físicas
SolubilidadSoluble in many organic solvents. Slightly soluble in water. ,
SensibilidadMoisture sensitive.
Punto de inflamación (°F)212 °F
Punto de inflamación (°C)166℃
Punto de ebullición (°C)300°C
Punto de fusión (°C)133-136℃
Peso molecular148.160 g/mol
XLogP32.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Exact Mass148.052 Da
Monoisotopic Mass148.052 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count11
Formal Charge0
Complexity155.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Shuai-Nan Zhang, Qi Liu, Xu-Zhao Li, Wu-De Yang, Ying Zhou.  (2023)  Sophora tonkinensis and active compounds inhibit mitochondrial impairments, inflammation, and LDLR deficiency in myocardial ischemia mice through regulating the vesicle-mediated transport pathway.  FITOTERAPIA,      [PMID:38007052] [10.1016/j.fitote.2023.105756]
2. Rongkun Zhu, Zengcheng Du, Mingfang Zhu, Huanru Liang, Shumei Wang, Qing Zhou, Rui Li, Yulan Li, Chaoying Zeng, Wenhao Liu, Qiqing Chen.  (2023)  Molecularly imprinted polymers embedded with double perovskite quantum dots: A ratiometric fluorescence sensor for visible and fluorescent determination of Rhein.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.143618]
3. Jiao Wu, Bingjun Han, Xiaoyu Chen, Jinglin Gao, Shan Zhao, Liping Sun, Shijie Wang.  (2023)  Quantification of bioactive components and evaluation of microbial community and antibacterial activity from Heterotrigona itama and Tetrigona binghami honeys.  INTERNATIONAL JOURNAL OF FOOD SCIENCE AND TECHNOLOGY,  58  (5): (2247-2257).  [PMID:] [10.1111/ijfs.16325]
4. Xiang Zhou, Yi-Hong Fu, Ya-Yu Zou, Jiao Meng, Gui-Ping Ou-Yang, Qiang-Sheng Ge, Zhen-Chao Wang.  (2022)  Discovery of Simple Diacylhydrazine-Functionalized Cinnamic Acid Derivatives as Potential Microtubule Stabilizers.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  23  (20): (12365).  [PMID:36293224] [10.3390/ijms232012365]
5. Yaping Li, Ningning Sun, Songxin Ma, Xin Zhang, Yingfeng Wang, Xingru Li.  (2022)  Magnetic thermo-responsive branched polymer for fast extraction and enrichment of phenolic acids in olive oil with tunable and enhanced performance.  ANALYTICA CHIMICA ACTA,      [PMID:36156232] [10.1016/j.aca.2022.340359]
6. Jing Wang, Mengru Li, Hui Wang, Wenjing Huang, Fang Li, Lili Wang, Chi-Tang Ho, Yanyan Zhang, Liang Zhang, Xiaoting Zhai, Xiaochun Wan.  (2022)  Decoding the Specific Roasty Aroma Wuyi Rock Tea (Camellia sinensis: Dahongpao) by the Sensomics Approach.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:35973132] [10.1021/acs.jafc.2c02249]
7. Xuehui Cao, Ge Bai, Jianrong Zheng, Danshi Zhu, Jianrong Li.  (2022)  Effects of freeze–thaw cycles on the texture of Nanguo pear.  JOURNAL OF TEXTURE STUDIES,  53  (5): (662-671).  [PMID:35661160] [10.1111/jtxs.12701]
8. Ya zhu Wang, Jin Zheng, Muhammad Nawaz, Fan Yang, Jiajun Hu, Min-Tian Gao.  (2022)  Oligosaccharide-phenolic compound conjugates in soluble polysaccharides from rice straw alleviate ethanol fermentation stresses in Saccharomyces cerevisiae.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2022.114782]
9. Yuan Deng, Kai Li, Qingqing Guan, Tianding Hu, Liang He.  (2022)  Novel CNFs-based organic UV-adsorber intercalated ZnAl-LDHs composited films with superior photothermal stability and mechanical properties.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2022.114555]
10. Yuandong Yu, Guizhao Liang.  (2021)  Interaction mechanism of phenolic acids and zein: A spectrofluorometric and molecular dynamics investigation.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2021.118032]
11. Rongkun Zhu, Mushen Lai, Mingfang Zhu, Huanru Liang, Qing Zhou, Rui Li, Wenhao Zhang, Hongqing Ye.  (2020)  A functional ratio fluorescence sensor platform based on the graphene/Mn-ZnS quantum dots loaded with molecularly imprinted polymer for selective and visual detection sinapic acid.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:32882656] [10.1016/j.saa.2020.118845]
12. Xiang Zhou, Yu-Mei Feng, Pu-Ying Qi, Wu-Bin Shao, Zhi-Bing Wu, Li-Wei Liu, Yi Wang, Hao-Dong Ma, Pei-Yi Wang, Zhong Li, Song Yang.  (2020)  Synthesis and Docking Study of N-(Cinnamoyl)-N′-(substituted)acryloyl Hydrazide Derivatives Containing Pyridinium Moieties as a Novel Class of Filamentous Temperature-Sensitive Protein Z Inhibitors against the Intractable Xanthomonas oryzae pv. oryzae Infections in Rice.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:32649185] [10.1021/acs.jafc.0c01565]
13. Huihui Shen, Xin Tong, Jiehong Yang, Li Yu, Huifen Zhou, Yu Wang, Yu He, Haitong Wan, Chang Li.  (2020)  Biotransformation of natural hydroxycinnamic acids by gut microbiota from normal and cerebral ischemia-reperfusion injured rats: a comparative study.  Food & Function,  11  (6): (5389-5395).  [PMID:32469016] [10.1039/D0FO00775G]
14. Zhenhao Li, Yi Wang, Yiyu Cheng.  (2019)  Mass Spectrometry-Sensitive Probes Coupled with Direct Analysis in Real Time for Simultaneous Sensing of Chemical and Biological Properties of Botanical Drugs.  ANALYTICAL CHEMISTRY,      [PMID:31246426] [10.1021/acs.analchem.9b01251]
15. Li-Xian Zhu, Qin-Bao Lin, Jia-Yi Li, Hong-Mei Zhu, Hong-Sheng Ma, Huai-Ning Zhong, Jing-Jing Pan.  (2019)  Sources of potassium permanganate consumption for food contact paper.  Food Packaging and Shelf Life,      [PMID:] [10.1016/j.fpsl.2019.100319]
16. Zhao Kai-jing, Chen Yang, Hong Shi-jin, Yang Yi-ting, Xu Jiong, Yang Han-yu, Zhu Liang, Liu Ming, Xie Qiu-shi, Tang Xian-ge, Yang Ting-ting, Zhou Ya-qian, Liu Li, Liu Xiao-dong.  (2019)  Characteristics of β-oxidative and reductive metabolism on the acyl side chain of cinnamic acid and its analogues in rats.  ACTA PHARMACOLOGICA SINICA,  40  (8): (1106-1118).  [PMID:30792487] [10.1038/s41401-019-0218-8]
17. Lintao Guo, Mingjie Qu, Junsu Jin, Hong Meng.  (2018)  Solubility of cinnamic acid in supercritical carbon dioxide and subcritical 1,1,1,2-tetrafluoroethane: Experimental data and modelling.  FLUID PHASE EQUILIBRIA,      [PMID:] [10.1016/j.fluid.2018.10.009]
18. Meirong Bai, Jing He, Liangfa Kang, Jun Nie, Ruixue Yin.  (2018)  Regulated basal and bolus insulin release from glucose-responsive core-shell microspheres based on concanavalin A-sugar affinity.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:29524488] [10.1016/j.ijbiomac.2018.03.030]
19. Mingwei Zhao, Mingwei Gao, Caili Dai, Chenwei Zou, Zhe Yang, Xuepeng Wu, Yifei Liu, Yining Wu, Sisi Fang, Wenjiao Lv.  (2017)  Investigation of Novel Triple-Responsive Wormlike Micelles.  LANGMUIR,      [PMID:28391678] [10.1021/acs.langmuir.7b01011]
20. Rui Xiao, Xiaoting Zhang, Xiaona Zhang, Jiahua Niu, Minghua Lu, Xiuhua Liu, Zongwei Cai.  (2017)  Analysis of flavors and fragrances by HPLC with Fe3O4@GO magnetic nanocomposite as the adsorbent.  TALANTA,      [PMID:28213232] [10.1016/j.talanta.2017.01.065]
21. Juan Li, Zuo-Xiang Zeng, Li Sun, Wei-Lan Xue, Hui-Hui Wang.  (2016)  Solid–Liquid Phase Equilibrium of trans-Cinnamic Acid in Several Alcohols: Measurements and Thermodynamic Modeling.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/acs.jced.5b00814]
22. Yukang Wang, Gaochen Jin, Shuyan Song, Yijun Jin, Xiaowen Wang, Shuaiqi Yang, Xingxing Shen, Yinbo Gan, Yuexing Wang, Ran Li, Jian-Xiang Liu, Jianping Hu, Ronghui Pan.  (2024)  A peroxisomal cinnamate:CoA ligase-dependent phytohormone metabolic cascade in submerged rice germination.  DEVELOPMENTAL CELL,      [PMID:38579719] [10.1016/j.devcel.2024.03.023]
23. Jiangmei Zheng, Ruobin Sun, Dan Wu, Pengcheng Chen, Pu Zheng.  (2024)  Engineered Zea mays phenylalanine ammonia-lyase for improve the catalytic efficiency of biosynthesis trans-cinnamic acid and p-coumaric acid.  ENZYME AND MICROBIAL TECHNOLOGY,      [PMID:38442476] [10.1016/j.enzmictec.2024.110423]
24. Yang Ting, Deng Haoyun, Zhang Zhengli, Hu Mi, Cheng Kaiqiang, Chen Yuanjian, Li Junli.  (2024)  Enhanced efficiency of organic solar cells through trans-cinnamic acid doped cathode interface layer.  JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS,  35  (9): (1-11).  [PMID:] [10.1007/s10854-024-12380-3]
25. Boyu Pan, Han Zhu, Jiaqi Yang, Liangjiao Wang, Zizhen Chen, Jian Ma, Bo Zhang, Zhanyu Pan, Guoguang Ying, Shao Li, Liren Liu.  (2024)  From complexity to clarity: development of CHM-FIEFP for predicting effective components in Chinese herbal formulas by using big data.  Cancer Biology & Medicine,  21  (11): (1067).  [PMID:39468922] [10.20892/j.issn.2095-3941.2023.0442]
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