Phloridzin - Moligand™, ≥98% , Inhibitor of major facilitator superfamily domain containing 4B;Inhibitor of SGLT6;Inhibitor of SMIT, CAS No.60-81-1, Inhibitor of major facilitator superfamily domain containing 4B;Inhibitor of SGLT6;Inhibitor of SMIT

CAS: 60-81-1 Cat. No.: P139206 Molecular Weight: 436.45 Beilstein Registry Number: 66621 EC Number: 200-487-1 PubChem CID: 6072
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
BRD-K73756878-001-02-9 | BSPBio_002674 | Phlorrhizin | CCG-38341 | DivK1c_006421 | SCHEMBL17290 | SDCCGMLS-0066626.P001 | Phlorizoside | s2343 | 1-Propanone, 1-[2-(beta-D-glucopyranosyloxy)-4,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)- | O-glucoside, 1 | Phlo
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
250mg
P139206-250mg
5

$9.90

$14.90
Save $5.00 (33.56%)
1g
P139206-1g
5

$16.90

$25.90
Save $9.00 (34.75%)
5g
P139206-5g
1

$26.90

$40.90
Save $14.00 (34.23%)
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥98% Moligand™ 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 34 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Phloridzin is a dihydrochalcone found in all parts of the apple tree, except the mature fruit, and acts as an inhibitor of SGLT-1 and SGLT-2.
An SGLT-1 and SGLT-2 inhibitor found in apple trees

Specifications

Synonyms
BRD-K73756878-001-02-9 | BSPBio_002674 | Phlorrhizin | CCG-38341 | DivK1c_006421 | SCHEMBL17290 | SDCCGMLS-0066626.P001 | Phlorizoside | s2343 | 1-Propanone, 1-[2-(beta-D-glucopyranosyloxy)-4, 6-dihydroxyphenyl]-3-(4-hydroxyphenyl)- | O-glucoside, 1 | Phlo
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
Potent, competitive SGLT inhibitor (IC 50 values are 400 and 65 nM for SGLT1 and SLGT2 respectively). Induces renal glycosuria and blocks intestinal glucose absorption in vivo. Orally active.
Storage
Room temperature
Shipped In
Normal
Grade
Moligand™
Action Type
INHIBITOR
Mechanism of action
Inhibitor of major facilitator superfamily domain containing 4B;Inhibitor of SGLT6;Inhibitor of SMIT
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%
Names and Identifiers
Canonical SmilesC1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O
IUPAC Name1-[2,4-dihydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-(4-hydroxyphenyl)propan-1-one
InChIKeyIOUVKUPGCMBWBT-QNDFHXLGSA-N
INCHI1S/C21H24O10/c22-9-16-18(27)19(28)20(29)21(31-16)30-15-8-12(24)7-14(26)17(15)13(25)6-3-10-1-4-11(23)5-2-10/h1-2,4-5,7-8,16,18-24,26-29H,3,6,9H2/t16-,18-,19+,20-,21-/m1/s1
Isomeric SMILES C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O)O)O
WGK Germany 3
PubChem CID 6072
Molecular Weight 436.45
Beilstein 66621

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
ClassFlavonoids
SubclassFlavonoid glycosides
Intermediate Tree Nodes Not available
Direct ParentFlavonoid O-glycosides
Alternative Parents 2'-Hydroxy-dihydrochalcones  Cinnamylphenols  Phenolic glycosides  Alkyl-phenylketones  Hexoses  Butyrophenones  O-glycosyl compounds  Phenol ethers  Resorcinols  Benzoyl derivatives  Aryl alkyl ketones  Phenoxy compounds  1-hydroxy-4-unsubstituted benzenoids  1-hydroxy-2-unsubstituted benzenoids  Oxanes  Vinylogous acids  Secondary alcohols  Oxacyclic compounds  Acetals  Polyols  Organic oxides  Hydrocarbon derivatives  Primary alcohols  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Flavonoid o-glycoside - 2'-hydroxy-dihydrochalcone - Linear 1,3-diarylpropanoid - Cinnamylphenol - Phenolic glycoside - Alkyl-phenylketone - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Butyrophenone - Phenylketone - Aryl alkyl ketone - Aryl ketone - Benzoyl - Resorcinol - Phenoxy compound - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Benzenoid - Monocyclic benzene moiety - Monosaccharide - Oxane - Vinylogous acid - Secondary alcohol - Ketone - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Primary alcohol - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as flavonoid o-glycosides. These are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
External Descriptors dihydrochalcones - Chalcones and dihydrochalcones
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
SLC5A4 Tchem Solute carrier family 5 member 4 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLC5A11 Tchem Sodium/myo-inositol cotransporter 2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLC5A2 Tclin Sodium/glucose cotransporter 2 (21 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLC5A3 Tbio Sodium/myo-inositol cotransporter (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
SLC5A1 Tclin Sodium/glucose cotransporter 1 (18 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MFSD4B Tdark Sodium-dependent glucose transporter 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EPHX2 Tchem Epoxide hydratase (3844 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEK293 (82097 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC28A1 Tbio Sodium/nucleoside cotransporter 1 (13 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC28A2 Tchem Sodium/nucleoside cotransporter 2 (91 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC28A3 Tchem Solute carrier family 28 member 3 (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AKR1B10 Tchem Aldo-keto reductase family 1 member B10 (300 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC5A4 Tchem Low affinity sodium-glucose cotransporter (30 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc5a1 Sodium/glucose cotransporter 1 (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Slc5a2 Sodium/glucose cotransporter 2 (17 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
3T3-L1 (3664 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Intestine (514 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PNLIP Pancreatic triacylglycerol lipase (476 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

13 results found

Lot NumberCertificate TypeDateItem
C2412392Certificate of AnalysisDec 10, 2025 P139206
C2412396Certificate of AnalysisDec 10, 2025 P139206
G2518484Certificate of AnalysisJul 09, 2025 P139206
G2518485Certificate of AnalysisJul 09, 2025 P139206
G2518486Certificate of AnalysisJul 09, 2025 P139206
A2517420Certificate of AnalysisJan 09, 2025 P139206
A2517423Certificate of AnalysisJan 09, 2025 P139206
A2517437Certificate of AnalysisJan 09, 2025 P139206
A2517438Certificate of AnalysisJan 09, 2025 P139206
C2412397Certificate of AnalysisMar 06, 2024 P139206
J2209518Certificate of AnalysisSep 22, 2022 P139206
J2209519Certificate of AnalysisSep 22, 2022 P139206
J2209520Certificate of AnalysisSep 22, 2022 P139206

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Chemical and Physical Properties
SolubilitySoluble in DMSO (100 mM), methanol, acetone, ethanol (100 mM), and water (partly).
Refractive Index1.69
Melt Point(°C)113-114°C
Molecular Weight436.400 g/mol
XLogP31.200
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count10
Rotatable Bond Count7
Exact Mass436.137 Da
Monoisotopic Mass436.137 Da
Topological Polar Surface Area177.000 Ų
Heavy Atom Count31
Formal Charge0
Complexity581.000
Isotope Atom Count0
Defined Atom Stereocenter Count5
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Chengyun He, Lu Bai, Daqun Liu, Benguo Liu.  (2023)  Interaction mechanism of okra (Abelmoschus esculentus L.) seed protein and flavonoids: Fluorescent and 3D-QSAR studies.  Food Chemistry-X,      [PMID:38144792] [10.1016/j.fochx.2023.101023]
2. Jing Zhang, Yali Song, Xia Hu, Zhen Zeng, Jie Hu, Tingting Zeng, Fang Geng, Di Wu.  (2023)  Nanoparticles loaded with phlorizin fabricate a fortified yogurt with antioxidant potential.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2023.102849]
3. Yang Liu, Jiali Lin, Tiantian Cheng, Yangjie Liu, Fuliang Han.  (2022)  Methylation, Hydroxylation, Glycosylation and Acylation Affect the Transport of Wine Anthocyanins in Caco-2 Cells.  Foods,  11  (23): (3793).  [PMID:36496602] [10.3390/foods11233793]
4. Zhang Hongzhen, Zhang Chenghua, Xiang Xiaolong, Zhang Qilun, Zhao Wei, Wei Guoyu, Hu Anlong.  (2022)  Uptake and transport of antibiotic kasugamycin in castor bean (Ricinus communis L.) seedlings.  Frontiers in Microbiology,      [PMID:36033898] [10.3389/fmicb.2022.948171]
5. Haoyu Zhou, Changzhong Liu, Sheng Geng.  (2021)  Laccase Catalyzed Oxidative Polymerization of Phloridzin: Polymer Characterization, Antioxidant Capacity and α-Glucosidase Inhibitory Activity.  Natural Product Communications,      [PMID:] [10.1177/1934578X211052373]
6. Lijuan Wang, Liji Huang, Nan Li, Junjun Miao, Wei Liu, Jiangyi Yu.  (2019)  Ameliorative effect of polydatin on hyperglycemia and renal injury in streptozotocin-induced diabetic rats.  CELLULAR AND MOLECULAR BIOLOGY,  65  (7):   [PMID:] [10.14715/cmb/2019.65.7.10]
7. Yufeng Chen, Fan Xue, Guobin Xia, Zhenlei Zhao, Chun Chen, Yunhong Li, Ying Zhang.  (2019)  Transepithelial transport mechanisms of 7,8-dihydroxyflavone, a small molecular TrkB receptor agonist, in human intestinal Caco-2 cells.  Food & Function,  10  (8): (5215-5227).  [PMID:31384856] [10.1039/C9FO01007F]
8. Yurong Ma, Qingfeng Ban, Jingying Shi, Tiantian Dong, Cai-Zhong Jiang, Qingguo Wang.  (2018)  1-Methylcyclopropene (1-MCP), storage time, and shelf life and temperature affect phenolic compounds and antioxidant activity of ‘Jonagold’ apple.  POSTHARVEST BIOLOGY AND TECHNOLOGY,      [PMID:] [10.1016/j.postharvbio.2018.12.015]
9. Yongsheng Chen, Jiangwei Liu, Sheng Geng, Yonglan Liu, Hanjun Ma, Jie Zheng, Benguo Liu, Guizhao Liang.  (2018)  Lipase-catalyzed synthesis mechanism of tri-acetylated phloridzin and its antiproliferative activity against HepG2 cancer cells.  FOOD CHEMISTRY,      [PMID:30502134] [10.1016/j.foodchem.2018.10.111]
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11. Wang Qian-Wen, Liu Jia-Jia, Liu Xiong, Zha Hong-Wei, Ren Na.  (2014)  Purification of phloridzin from Lithocarpus polystachyus Rehd leaves using polymeric adsorbents functionalized with glucosamine and β-cyclodextrin.  CHEMICAL PAPERS,  68  (11): (1521-1531).  [PMID:] [10.2478/s11696-014-0615-x]
12. Jie Wang, Zhiwei Lei, Yingjie Wen, Genlin Mao, Hanxiang Wu, Hanhong Xu.  (2014)  A Novel Fluorescent Conjugate Applicable To Visualize the Translocation of Glucose–Fipronil.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:25134020] [10.1021/jf502838m]
13. Muhammad Abid, Saqib Jabbar, Tao Wu, Malik Muhammad Hashim, Bing Hu, Shicheng Lei, Xiaoxiong Zeng.  (2013)  Sonication enhances polyphenolic compounds, sugars, carotenoids and mineral elements of apple juice.  ULTRASONICS SONOCHEMISTRY,      [PMID:23835397] [10.1016/j.ultsonch.2013.06.002]
14. Xiaomeng Zhang, Xinquan Tian, Junyu Luo, Xiaoyang Wang, Shoupu He, Gaofei Sun, Ruidan Dong, Panhong Dai, Xiao Wang, Zhaoe Pan, Baojun Chen, Daowu Hu, Liru Wang, Baoyin Pang, Aishuang Xing, Guoyong Fu, Baoquan Wang, Jinjie Cui, Lei Ma, Xiongming Du.  (2025)  Identification of UDP-glucosyltransferase involved in the biosynthesis of phloridzin in Gossypium hirsutum.  PLANT JOURNAL,  121  (3): (e17248).  [PMID:39935137] [10.1111/tpj.17248]
15. Zhengming Qian, Qinggui Lei, Dan Tang, Guoying Tan, Qi Huang, Fucai Zhou, Wenhao Wang.  (2024)  Rapid and green quantification of phloridzin and trilobatin in Lithocarpus litseifolius (Hance) Chun (sweet tea) using an online pressurized liquid extraction high-performance liquid chromatography at equal absorption wavelength method.  Analytical Methods,  16  (16): (2513-2521).  [PMID:38587209] [10.1039/D4AY00170B]
16. Zhixiao Liu, Yuhang Zhao, Mingli Yi, Lintao Liao, Yangyang Huang, Guangqiu Lei, Gao Hu, Mayu Lan, Huiping Li, Zhiming Mi.  (2025)  Preparation of high-permeance polyester nanofiltration membranes utilizing biobased phloretin derivatives for antibiotic separation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2025.124458]
17. Chen-Xin Guo, Jiyan Li, Yu Wang, Tang Li, Heng Yin.  (2025)  Functional characterization of a Stevia rebaudiana flavonoid glycosyltransferase.  ENZYME AND MICROBIAL TECHNOLOGY,      [PMID:40639146] [10.1016/j.enzmictec.2025.110708]
18. Mengyu Yang, Pengyuan Liu, Pei Cheng, Chenghao Li, Jingmei Liu, Haifeng Sun, Fangxia Guan, Minghao Yao.  (2025)  Naturally derived hydrogel with antioxidant, angiogenesis and photothermal effect to accelerate infected diabetic wound healing and reduce scar formation.  Theranostics,  15  (18): (9838).  [PMID:41041060] [10.7150/thno.117179]
19. Xiaochun Wu, Yan Xu, Dandan Zhu, Weiye Zhang, Yanjun Yang, Liang Feng, Bing Yang, Xiaobin Jia.  (2025)  Oral absorption mechanisms of Astragalus polysaccharides and potential as an excipient to increase the absorption of flavonoids.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41033508] [10.1016/j.ijbiomac.2025.147977]
20. Zepeng Yang, Huangling Wang, Chen Huang, Cui Wang, Zimeng Geng, Fei Lyu.  (2025)  Size-structured flavonoid distribution in Salix babylonica branches modulates Anoplophora glabripennis feeding behavior: A novel mechanistic target for eco-friendly antifeedant development.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:41461405] [10.1016/j.pestbp.2025.106711]
21. Shuwen Li, Zhiguo Wang, Siyi Chen, Jialin Gu, Yanping Ma, Jiangang Jiang, Rui Zhang, Dan Zhang, Yiping Wang, He Wang.  (2022)  Ratiometric fluorescence sensing based on rare-earth upconversion nanoparticles for the rapid identification of antioxidant capacity.  NEW JOURNAL OF CHEMISTRY,  47  (4): (2079-2085).  [PMID:] [10.1039/D2NJ05429A]
22. Zhang Guorong, Wang Qin, Tao Wanyin, Jiang Wei, Elinav Eran, Wang Yucai, Zhu Shu.  (2022)  Glucosylated nanoparticles for the oral delivery of antibiotics to the proximal small intestine protect mice from gut dysbiosis.  Nature Biomedical Engineering,  (7): (867-881).  [PMID:35798834] [10.1038/s41551-022-00903-4]
23. Fang Li, Yachao Xi, Jianming Jiang, Hao Peng, Bing Li, Jianbo He, Jiangnan Shu, Hua Cui.  (2022)  O-Fluorobenzoic Acid-Mediated Construction of Porous Graphitic Carbon Nitride with Nitrogen Defects for Multicolor Electrochemiluminescence Imaging Sensing.  ANALYTICAL CHEMISTRY,      [PMID:35738019] [10.1021/acs.analchem.2c00702]
24. Zhang Haipin, Song Huijia, Tian Xuemeng, Wang Yue, Hao Yi, Wang Wenting, Gao Ruixia, Yang Wan, Ke YuShen, Tang Yuhai.  (2021)  Magnetic imprinted nanoparticles with synergistic tailoring of covalent and non-covalent interactions for purification and detection of procyanidin B2.  MICROCHIMICA ACTA,  188  (1): (1-12).  [PMID:33403455] [10.1007/s00604-020-04693-x]
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27. Yue Yuan, Rong Zhou, Dongliang Li, Cheng Luo, Guoyou Li.  (2017)  Simultaneous quantitative assessment of nine glycosides in tobacco by liquid chromatography–tandem mass spectrometry.  JOURNAL OF SEPARATION SCIENCE,  41  (5): (1009-1016).  [PMID:29178289] [10.1002/jssc.201700880]
28. Tong Wang, Hai-Long Wu, Li-Xia Xie, Li Zhu, Zhi Liu, Xiao-Dong Sun, Rong Xiao, Ru-Qin Yu.  (2017)  Fast and simultaneous determination of 12 polyphenols in apple peel and pulp by using chemometrics-assisted high-performance liquid chromatography with diode array detection.  JOURNAL OF SEPARATION SCIENCE,  40  (8): (1651-1659).  [PMID:28217915] [10.1002/jssc.201601293]
29. Mengru Bai, Qian Shen, Yong Wu, Zhiyuan Ma, Yuqing Wang, Mingyang Chen, Dan Liu, Lin Zhou.  (2024)  Evaluation of transport mechanisms of methotrexate in human choriocarcinoma cell lines by LC-MS/MS.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:38823222] [10.1016/j.jpba.2024.116268]
30. Zhengming Xu, Kseniya Hileuskaya, Aliaksandr Kraskouski, Yujiao Yang, Zhe Huang, Zhengang Zhao.  (2024)  Inhibition of α-glucosidase activity and intestinal glucose transport to assess in vivo anti-hyperglycemia potential of dodecyl-acylated phlorizin and polydatin derivatives.  Food & Function,      [PMID:38511466] [10.1039/D3FO05233H]
31. Xia Yang, Yun Wang, Yan Sun, Jiali Guo, Zhaojun Geng, Bingyao Wei, Peiqin Li, Guanghui Tang.  (2025)  Integrated transcriptomics and metabolomics revealed the role of the flavonoid pathway in the resistance of Zanthoxylum bungeanum against leaf rust.  SCIENTIA HORTICULTURAE,      [PMID:] [10.1016/j.scienta.2025.113990]
32. Yushi Wei, Jianmei Wu, Xi Peng, Xing Hu, Deming Gong, Guowen Zhang.  (2024)  Protein glycosylation inhibitory effects and mechanisms of phloretin and phlorizin.  Food Bioscience,      [PMID:] [10.1016/j.fbio.2024.104971]
33. Huayang Xu, Hongzhen Zhang, Guoyu Wei, Yuling Jiang, Meto Yao Charles, Anlong Hu.  (2024)  Uptake and transport of antibiotic kasugamycin from leaves to roots in rice (Oryza sativa L.) seedlings.  ANNALS OF APPLIED BIOLOGY,  185  (3): (360-370).  [PMID:] [10.1111/aab.12928]
34. Xiaolun Peng, Ruijie Xu, Liang Zhang, Xingyao Li, Junhui Xu, Dongyun Huang, Yazhen Wang.  (2026)  Construction of multi-component CuO/ZIF-8@CNTs modified electrode for sensitive electrochemical detection of neohesperidin dihydrochalcone in liquor samples.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2026.108987]
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