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Tyramine - 98%, high purity , CAS No.51-67-2, Agonist of TA 1 receptor

In stock
Item Number
T105543
Grouped product items
SKU Size
Availability
Price Qty
T105543-1g
1g
3
$9.90
T105543-5g
5g
3
$16.90
T105543-25g
25g
1
$35.90
T105543-100g
100g
2
$119.90
T105543-500g
500g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$399.90

Basic Description

Synonyms p-Tyramine | 4-Hydroxyphenethylamine | Tyrosamine | Systogene | Phenol, 4-(2-aminoethyl)- | p-(2-Aminoethyl)phenol | Uteramine | 4-Hydroxyphenylethylamine | p-Hydroxyphenethylamine | 4-(2-Aminoethyl)phenol | Tocosine | Tyramin | 2-(4-Hydroxyphenyl)ethylam
Specifications & Purity Moligand™, ≥98%
Biochemical and Physiological Mechanisms Can enter catecholaminergic terminals and be released as a false transmitter.
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Action Type AGONIST
Mechanism of action Agonist of TA 1 receptor
Product Description

Tyramine is extensively used in the preparation of a variety of hydrogels for biomedical applications. It is used as a key precursor in the total synthesis of (-)-mesembrine[3] and (-)-galanthamine. It can also be used in the preparation of tyramine-functionalized graphene quantum dots (GQDs) as fluorescence reporters for optical sensing of metabolites. Biochem/physiol Actions.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Phenethylamines
Intermediate Tree Nodes Not available
Direct Parent Phenethylamines
Alternative Parents 2-arylethylamines  Aralkylamines  1-hydroxy-2-unsubstituted benzenoids  Organopnictogen compounds  Organooxygen compounds  Monoalkylamines  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Phenethylamine - 2-arylethylamine - 1-hydroxy-2-unsubstituted benzenoid - Aralkylamine - Phenol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Amine - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as phenethylamines. These are compounds containing a phenethylamine moiety, which consists of a phenyl group substituted at the second position by an ethan-1-amine.
External Descriptors Biogenic amines - Tyramine derivatives

Associated Targets(Human)

TAAR1 Tclin Trace amine-associated receptor 1 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
F2 Tclin Thrombin (11687 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MAOB Tclin Monoamine oxidase B (8835 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PDE4A Tclin Phosphodiesterase 4A (1943 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PNMT Tchem Phenylethanolamine N-methyltransferase (540 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDR Tclin Vascular endothelial growth factor receptor 2 (20924 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
DBH Tchem Dopamine beta-hydroxylase (131 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BACE1 Tchem Beta-secretase 1 (15641 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Homo sapiens (32628 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HEK293 (82097 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLC22A1 Tchem Solute carrier family 22 member 1 (646 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ABCB11 Tchem Bile salt export pump (2311 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Entamoeba histolytica (2676 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Giardia intestinalis (1290 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Cavia porcellus (23802 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Taar1 Trace amine-associated receptor 1 (899 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Impa1 Inositol monophosphatase 1 (16203 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Slc22a3 Solute carrier family 22 member 3 (35 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Slc16a10 Monocarboxylate transporter 10 (73 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Htr3a Serotonin (5-HT) receptor (353 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Oprd1 Opioid receptor (994 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Maob Monoamine oxidase (439 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRK1 Opioid receptor (mu and kappa) (192 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504750919
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504750919
IUPAC Name 4-(2-aminoethyl)phenol
INCHI InChI=1S/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2
InChIKey DZGWFCGJZKJUFP-UHFFFAOYSA-N
Smiles C1=CC(=CC=C1CCN)O
Isomeric SMILES C1=CC(=CC=C1CCN)O
WGK Germany 3
RTECS SJ5950000
Alternate CAS 51-67-2,71495-67-5
PubChem CID 5610
NSC Number 249188
MeSH Entry Terms 4 Hydroxyphenethylamine;4-(2-Aminoethyl)phenol;4-Hydroxyphenethylamine;p-Tyramine;para-Tyramine;Tyramine
Molecular Weight 137.18
Beilstein 1099914
Reaxy-Rn 1099914

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

34 results found

Lot Number Certificate Type Date Item
D2517463 Certificate of Analysis Apr 03, 2025 T105543
D2517516 Certificate of Analysis Apr 03, 2025 T105543
D2517525 Certificate of Analysis Apr 03, 2025 T105543
D2517526 Certificate of Analysis Apr 03, 2025 T105543
D2517527 Certificate of Analysis Apr 03, 2025 T105543
E2306047 Certificate of Analysis Feb 11, 2025 T105543
I2206054 Certificate of Analysis Aug 14, 2024 T105543
H2412306 Certificate of Analysis Aug 01, 2024 T105543
H2412307 Certificate of Analysis Aug 01, 2024 T105543
H2412308 Certificate of Analysis Aug 01, 2024 T105543
H2412309 Certificate of Analysis Aug 01, 2024 T105543
J2211226 Certificate of Analysis Jul 08, 2024 T105543
J2211223 Certificate of Analysis Jul 08, 2024 T105543
D2501559 Certificate of Analysis Jul 02, 2024 T105543
D2501560 Certificate of Analysis Jul 02, 2024 T105543
D2501561 Certificate of Analysis Jul 02, 2024 T105543
C2224033 Certificate of Analysis Jan 22, 2024 T105543
H2419039 Certificate of Analysis Dec 16, 2023 T105543
A2403268 Certificate of Analysis Dec 16, 2023 T105543
A2403269 Certificate of Analysis Dec 16, 2023 T105543
A2403270 Certificate of Analysis Dec 16, 2023 T105543
A2403271 Certificate of Analysis Dec 16, 2023 T105543
A2403272 Certificate of Analysis Dec 16, 2023 T105543
I2321972 Certificate of Analysis Sep 08, 2023 T105543
I2321973 Certificate of Analysis Sep 08, 2023 T105543
I2321974 Certificate of Analysis Sep 08, 2023 T105543
I2108479 Certificate of Analysis Jun 15, 2023 T105543
I2108481 Certificate of Analysis Jun 15, 2023 T105543
I2108480 Certificate of Analysis Jun 15, 2023 T105543
J2211225 Certificate of Analysis Sep 05, 2022 T105543
L2308094 Certificate of Analysis Sep 05, 2022 T105543
J2211224 Certificate of Analysis Sep 05, 2022 T105543
C2224036 Certificate of Analysis May 20, 2022 T105543
H1622034 Certificate of Analysis May 13, 2022 T105543

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Chemical and Physical Properties

Solubility Soluble in water (10 mg/ml at 15°C), methanol, DMSO, boiling alcohol (100 mg/ml), and ethanol.
Sensitivity Air sensitive
Boil Point(°C) 175-181 °C/8 mmHg
Melt Point(°C) 160-165°C
Molecular Weight 137.180 g/mol
XLogP3 1.100
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 2
Exact Mass 137.084 Da
Monoisotopic Mass 137.084 Da
Topological Polar Surface Area 46.300 Ų
Heavy Atom Count 10
Formal Charge 0
Complexity 87.300
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Jian-Jun Zhong,Ningbo Liao,Tian Ding,Xingqian Ye,Dong-Hong Liu.  (2015-07-05)  Liquid chromatographic method for toxic biogenic amines in foods using a chaotropic salt..  Journal of chromatography. A,  1406  (331-336). 
2. Yiting Xu, Xiaobo Yu, Meiling Chen, Yi Sun, Wei Zhang, Yajin Fang, Lanyun Fang, Haining Na, Fei Liu, Jin Zhu.  (2023)  Dual responsive cellulose-based fluorescent material fabricated in a CO2 switchable solvent for multifunctional applications.  CHEMICAL ENGINEERING JOURNAL,  477  (147272). 
3. Qian Chen, Dayong Ren, Weichen Sheng, Kan Zhang.  (2023)  Synthesis, polymerization and thermal properties of bio-based benzoxazine resins containing imide or amide functionality.  JOURNAL OF APPLIED POLYMER SCIENCE,  141  (2): (e54792). 
4. Yin Lu, Nan Li, Yaliang Peng, Mohamed Gamal Mohamed, Shiao-Wei Kuo, Kan Zhang.  (2024)  Facile and eco-friendly synthesis of hydrogen bonding-rich bio-based bisbenzoxazine resins with low surface free energy, strong adhesion strength and high thermal stability.  Molecular Systems Design & Engineering,  (1): (86-98). 
5. Junjun Wang, Yue Tang, Jia Zheng, Zhengmin Xie, Jianli Zhou, Yuangen Wu.  (2024)  DNAzyme-based and smartphone-assisted colorimetric biosensor for ultrasensitive and highly selective detection of histamine in meats.  FOOD CHEMISTRY,  435  (137526). 
6. Zekun Shi, Yongning Wu, Xue Zhang, Yanyan Gao, Luqin Qiao, Qin Hou, Minglin Wang.  (2023)  Highly sensitive and selective colorimetric and fluorescent dual-readout assay for the analysis of spermine, spermidine and cysteine.  DYES AND PIGMENTS,  220  (111659). 
7. Nuo Duan, Kexin Ren, Mingqian Song, Xinyue Zhang, Zhouping Wang, Fei Jia, Shijia Wu.  (2023)  A dual-donor FRET based aptamer sensor for simultaneous determination of histamine and tyramine in fishes.  MICROCHEMICAL JOURNAL,  191  (108801). 
8. Yuqi Liu, Li Yuan, Guozheng Liang, Aijuan Gu.  (2023)  Synthesis of new biobased benzoxazine through green strategy and its polybenzoxazine resin with high thermal resistance and mechanical strength.  JOURNAL OF POLYMER SCIENCE,  61  (13): (1279-1288). 
9. Xu Yanfen, Lu Ying, Yu Jianna, Liu Wen, Jing Guoxing, Li Wenshan, Liu Wenjie.  (2023)  Determination of Seven Biogenic Amines in Tuna with High-Performance Liquid Chromatography Coupled to Electrospray Ionization Ion Mobility Spectrometry.  Food Analytical Methods,  16  (5): (909-917). 
10. Yi Yang, Yin Lu, Kan Zhang.  (2023)  A highly thermally stable benzoxazine resin derived from norbornene and natural renewable tyramine and furfurylamine.  EUROPEAN POLYMER JOURNAL,  187  (111895). 
11. Si Lin, Hou Juying, Lv Wei, Hou Qin, Xu Zhixiang, Ai Shiyun.  (2023)  An intelligent fluorescence platform based on lignocellulose components and fluorescein for food freshness monitoring.  Biomass Conversion and Biorefinery,    (1-11). 
12. Qiuyang Huang, Xiaoling Zang, Zhiwei Zhang, Hang Yu, Baoyan Ding, Zhuangzhuang Li, Simin Cheng, Xin Zhang, Mustafa R.K. Ali, Xue Qiu, Zhihua Lv.  (2023)  Study on endogenous inhibitors against PD-L1: cAMP as a potential candidate.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  230  (123266). 
13. M. R. Ali, M. S. Bacchu, D. D. Ridoy, P. L. Mozumder, M. N. Hasan, S. Das, M. F. H. Palash, S. Akter, N. Sakib, A. Khaleque, D. Chakrobortty, M. Z. H. Khan.  (2022)  Development of a hematite nanotube and tyramine-based drug carrier against drug-resistant bacteria Klebsiella pneumoniae.  RSC Advances,  12  (48): (31497-31505). 
14. Xun Zhou, Yongxiang Wu, Yao Jiang, Chen Li, Longping Xu, Peng Cui, Xinsong She.  (2023)  Integrated one–dimensional CuO–nanowire arrays/Cu–foam nanoarchitecture for ultrahigh sensitive and non–enzymatic electrochemical determination of histamine levels in different–bacteria fermented mandarin fish.  FOOD CHEMISTRY,  405  (134776). 
15. Xiaofu Wang, Yunsong Zhao, Sufang Zhang, Xinping Lin, Huipeng Liang, Yingxi Chen, Chaofan Ji.  (2022)  Heterologous Expression of the Lactobacillus sakei Multiple Copper Oxidase to Degrade Histamine and Tyramine at Different Environmental Conditions.  Foods,  11  (20): (3306). 
16. Zhuangzhuang Li, Baoyan Ding, Mustafa R. K. Ali, Lizhen Zhao, Xiaoling Zang, Zhihua Lv.  (2022)  Dual Effect of Tryptamine on Prostate Cancer Cell Growth Regulation: A Pilot Study.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  23  (19): (11087). 
17. Jing Han, Xinping Lin, Huipeng Liang, Sufang Zhang, Beiwei Zhu, Chaofan Ji.  (2022)  Improving the safety and quality of Roucha using amine-degrading lactic acid bacteria starters.  FOOD RESEARCH INTERNATIONAL,  161  (111918). 
18. Yangwen Luo, Luchen Shan, Lipeng Xu, Srinivas Patnala, Isadore Kanfer, Jiahao Li, Pei Yu, Xu Jun.  (2022)  A network pharmacology-based approach to explore the therapeutic potential of Sceletium tortuosum in the treatment of neurodegenerative disorders.  PLoS One,  17  (8): (e0273583). 
19. Jianfeng Yan, Quanbin Fu, Shikai Zhang, Yu Liu, Xianbao Shi, Juying Hou, Junling Duan, Shiyun Ai.  (2022)  A sensitive ratiometric fluorescent sensor based on carbon dots and CdTe quantum dots for visual detection of biogenic amines in food samples.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,  282  (121706). 
20. Yikun Ren, Shanshan Ma, Dan Zhang, Shen Guo, Rong Chang, Yuanmeng He, Minghao Yao, Fangxia Guan.  (2022)  Functionalized injectable hyaluronic acid hydrogel with antioxidative and photothermal antibacterial activity for infected wound healing.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  210  (218). 
21. Yujuan Qin, Pengcheng Huang, Fang-Ying Wu.  (2022)  Histamine-responsive dye-incorporated carbon dots for visual monitoring of food spoilage.  SENSORS AND ACTUATORS B-CHEMICAL,  365  (131911). 
22. Tianhang Weng, Zejian He, Zhaohua Zhang, Yulong Chen, Mi Zhou, Bianying Wen.  (2022)  A facile method of functional derivatization based on starch acetoacetate.  CARBOHYDRATE POLYMERS,  289  (119468). 
23. Xu Xu, Jiaxin Gao, Di Cao, Xiang Li, Xin Zhao, Shuang Yue, Lei Zhang.  (2022)  Designed 3D N-doped magnetic porous carbon spheres for sensitive monitoring of biogenic amine by simultaneous microwave-assisted derivatization and magnetic-solid phase extraction.  JOURNAL OF CHROMATOGRAPHY A,  1667  (462882). 
24. Yi Wang, Chengpei Du, Ze Liu, Kanglin Pei, Yan Zhang, Wenjing Qi.  (2022)  Chemiluminescence “turn-on” detection of tyrosinase activity via in situ generation of dopamine based on a lucigenin and riboflavin system.  NEW JOURNAL OF CHEMISTRY,  46  (9): (4156-4161). 
25. Fei Li, Yunlu Wei, Jing Zhao, Luyao Zhang, Quanhong Li.  (2022)  In vivo pharmacokinetic study of a Cucurbita moschata polysaccharide after oral administration.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  203  (19). 
26. Huanhuan Bao, Meifang Yuan, Chengui Xiao, Daofeng Liu, Weihua Lai.  (2022)  Development of a signal-enhanced LFIA based on tyramine-induced AuNPs aggregation for sensitive detection of danofloxacin.  FOOD CHEMISTRY,  375  (131875). 
27. Nuo Duan, Changxin Li, Xiaoyin Zhu, Shuo Qi, Zhouping Wang, Shijia Wu.  (2022)  Simultaneous coupled with Separate SELEX for heterocyclic biogenic amine-specific aptamers screening and their application in establishment of an effective aptasensor.  SENSORS AND ACTUATORS B-CHEMICAL,  352  (130985). 
28. Xinxiu Ma, Jingran Bi, Xinyu Li, Gongliang Zhang, Hongshun Hao, Hongman Hou.  (2021)  Contribution of Microorganisms to Biogenic Amine Accumulation during Fish Sauce Fermentation and Screening of Novel Starters.  Foods,  10  (11): (2572). 
29. Fei Li, Solju Pak, Jing Zhao, Yunlu Wei, Yuyu Zhang, Quanhong Li.  (2021)  Structural Characterization of a Neutral Polysaccharide from Cucurbia moschata and Its Uptake Behaviors in Caco-2 Cells.  Foods,  10  (10): (2357). 
30. Yang Liu, Xiaoping Zhang, Tengling Wu, Bo Liu, Jianhai Yang, Wenguang Liu.  (2021)  Chinese herb-crosslinked hydrogel bearing rBMSCs-laden polyzwitterion microgels: Self-adaptive manipulation of micromilieu and stemness maintenance for restoring infarcted myocardium.  Nano Today,  41  (101306). 
31. Yu Jin, Yingting Xu, Zhengwan Huang, Zhongyu Zhou, Xiaoyi Wei.  (2021)  Metabolite pattern in root nodules of the actinorhizal plant Casuarina equisetifolia.  PHYTOCHEMISTRY,  186  (112724). 
32. Ling Jia, Yue Mao, Siqi Zhang, Hong Li, Ming Qian, Dongbo Liu, Bin Qi.  (2021)  Electrochemical switch sensor toward ephedrine hydrochloride determination based on molecularly imprinted polymer/nafion-MWCNTs modified electrode.  MICROCHEMICAL JOURNAL,  164  (105981). 
33. Zongyan Quan, Hui He, Hang Zhou, Yuting Liang, Lei Wang, Songya Tian, Hongxiang Zhu, Shuangfei Wang.  (2021)  Designing an intelligent nanofiber ratiometric fluorescent sensor sensitive to biogenic amines for detecting the freshness of shrimp and pork.  SENSORS AND ACTUATORS B-CHEMICAL,  333  (129535). 
34. Liping Gao, Yong Li, Zhen-Zhong Huang, Hongliang Tan.  (2021)  Visual detection of alkaline phosphatase based on ascorbic acid-triggered gel-sol transition of alginate hydrogel.  ANALYTICA CHIMICA ACTA,  1148  (238193). 
35. Yi-Fang Li, Zheng-Zhong Lin, Cheng-Yi Hong, Zhi-Yong Huang.  (2021)  Histamine detection in fish samples based on indirect competitive ELISA method using iron-cobalt co-doped carbon dots labeled histamine antibody.  FOOD CHEMISTRY,  345  (128812). 
36. Xixia Liu, Yaoyao Hou, Sirui Chen, Juewen Liu.  (2021)  Controlling dopamine binding by the new aptamer for a FRET-based biosensor.  BIOSENSORS & BIOELECTRONICS,  173  (112798). 
37. Qingqing Chen, Rongrong Ren, Qingqing Zhang, Jingjing Wu, Yufeng Zhang, Mingsong Xue, Dengke Yin, Ye Yang.  (2021)  Coptis chinensis Franch polysaccharides provide a dynamically regulation on intestinal microenvironment, based on the intestinal flora and mucosal immunity.  JOURNAL OF ETHNOPHARMACOLOGY,  267  (113542). 
38. Liu Song, Yang Huang, Marie-Jia Gou, Jacques Crommen, Zhengjin Jiang, Yifan Feng.  (2020)  Method development and validation for the determination of biogenic amines in soy sauce using supercritical fluid chromatography coupled with single quadrupole mass spectrometry.  JOURNAL OF SEPARATION SCIENCE,  43  (13): (2728-2736). 
39. Hailong Sun, Shuangping Liu, Jieqi Mao, Ziwei Yu, Zhijie Lin, Jian Mao.  (2020)  New insights into the impacts of huangjiu compontents on intoxication.  FOOD CHEMISTRY,  317  (126420). 
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