Adenine - Moligand™, ≥99.5%(HPLC) , CAS No.73-24-5

CAS: 73-24-5 Cat. No.: A108805 Peso molecular: 135.13 Beilstein Registry Number: 5777 Número EC: 200-796-1
Disponible para pedir
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. ≥99.5%(HPLC)
Synonyms
bmse000861 | Adenine, United States Pharmacopeia (USP) Reference Standard | Spectrum_001106 | Vitamin B 4 | 9H-Purin-6-amine | 3H-Purin-6(7H)-imine | Adenine, 1 | MFCD00041790 | SCHEMBL8110 | 1wei | 3,6-Dihydro-6-iminopurine | 6-Amino-1H-purine | ADENINE
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
A108805-5g
2
15,90US$
25g
A108805-25g
3
49,90US$
100g
A108805-100g
1
148,90US$
250g
A108805-250g
2
339,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Moligand™, ≥99.5%(HPLC) 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 269 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
bmse000861 | Adenine, United States Pharmacopeia (USP) Reference Standard | Spectrum_001106 | Vitamin B 4 | 9H-Purin-6-amine | 3H-Purin-6(7H)-imine | Adenine, 1 | MFCD00041790 | SCHEMBL8110 | 1wei | 3, 6-Dihydro-6-iminopurine | 6-Amino-1H-purine | ADENINE
Especificaciones y pureza
Moligand™, ≥99.5%(HPLC)
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Grado
Moligand™
Pureza
≥99.5%(HPLC)
Nombres e identificadores
Pubchem Sid504750360
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504750360
Sonrisas canónicasNc1ncnc2[nH]cnc12
IUPAC Name7H-purin-6-amine
InChIKeyGFFGJBXGBJISGV-UHFFFAOYSA-N
INCHI1S/C5H5N5/c6-4-3-5(9-1-7-3)10-2-8-4/h1-2H,(H3,6,7,8,9,10)
Isómeros SMILES C1=NC2=NC=NC(=C2N1)N
WGK Alemania 3
RTECS AU6125000
Número ONU 2811
Grupo de embalaje III
Peso molecular 135.13
Beilstein 5777
Reaxy-Rn 608603

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
SuperclassOrganoheterocyclic compounds
ClaseImidazopyrimidines
SubclassPurines and purine derivatives
Intermediate Tree Nodes Not available
Direct Parent6-aminopurines
Alternative Parents Aminopyrimidines and derivatives  Imidolactams  Imidazoles  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 6-aminopurine - Aminopyrimidine - Imidolactam - Pyrimidine - Heteroaromatic compound - Imidazole - Azole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors a ring
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
XDH Tclin Xanthine dehydrogenase (1038 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2B Tclin Serotonin 2b (5-HT2b) receptor (10323 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IGF1R Tclin Insulin-like growth factor I receptor (8605 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EDNRA Tclin Endothelin receptor ET-A (5008 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA2A Tclin Adenosine A2a receptor (16305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA3 Tchem Adenosine A3 receptor (15931 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIK3CA PI3-kinase p110-alpha subunit (51 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pde4d Phosphodiesterase 4D (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp2 Matrix metalloproteinase-2 (12 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
P388 (20296 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
P388/ADR (1216 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Streptavidin (24 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Camk2a Ca2+/calmodulin-dependent protein kinase II (CaM kinase II) (58 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 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.

39 results found

Lot NumberCertificate TypeFechaArticulo
D2608183Certificate of AnalysisMar 27, 2026 A108805
D2608182Certificate of AnalysisMar 27, 2026 A108805
D2608179Certificate of AnalysisMar 27, 2026 A108805
D2608178Certificate of AnalysisMar 27, 2026 A108805
C2609400Certificate of AnalysisMar 03, 2026 A108805
C2609423Certificate of AnalysisMar 03, 2026 A108805
C2609424Certificate of AnalysisMar 03, 2026 A108805
L2512190Certificate of AnalysisDec 04, 2025 A108805
L2512133Certificate of AnalysisDec 04, 2025 A108805
L2512132Certificate of AnalysisDec 04, 2025 A108805
L2512131Certificate of AnalysisDec 04, 2025 A108805
A2521059Certificate of AnalysisJan 07, 2025 A108805
J2513013Certificate of AnalysisJan 07, 2025 A108805
A2521058Certificate of AnalysisJan 07, 2025 A108805
A2521063Certificate of AnalysisJan 07, 2025 A108805
A2521070Certificate of AnalysisJan 07, 2025 A108805
F2415308Certificate of AnalysisJun 12, 2024 A108805
F2415314Certificate of AnalysisJun 12, 2024 A108805
F2415352Certificate of AnalysisJun 12, 2024 A108805
L2312224Certificate of AnalysisNov 23, 2023 A108805
L2312223Certificate of AnalysisNov 23, 2023 A108805
L2312222Certificate of AnalysisNov 23, 2023 A108805
L2312221Certificate of AnalysisNov 23, 2023 A108805
L2312220Certificate of AnalysisNov 23, 2023 A108805
L2312219Certificate of AnalysisNov 23, 2023 A108805
D2328079Certificate of AnalysisMay 06, 2023 A108805
K2315039Certificate of AnalysisMay 06, 2023 A108805
D2328068Certificate of AnalysisMay 06, 2023 A108805
D2328073Certificate of AnalysisMay 06, 2023 A108805
D2328077Certificate of AnalysisMay 06, 2023 A108805
C2329631Certificate of AnalysisMar 13, 2023 A108805
C2329632Certificate of AnalysisMar 13, 2023 A108805
C2329634Certificate of AnalysisMar 13, 2023 A108805
J2228205Certificate of AnalysisOct 20, 2022 A108805
J2228202Certificate of AnalysisOct 20, 2022 A108805
J2228201Certificate of AnalysisOct 20, 2022 A108805
J2228200Certificate of AnalysisOct 20, 2022 A108805
C2310603Certificate of AnalysisOct 20, 2022 A108805
J2220028Certificate of AnalysisNov 04, 2021 A108805

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Propiedades químicas y físicas
Punto de fusión (°C)360 °C
Peso molecular135.130 g/mol
XLogP3-0.100
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count0
Exact Mass135.054 Da
Monoisotopic Mass135.054 Da
Topological Polar Surface Area80.500 Ų
Heavy Atom Count10
Formal Charge0
Complexity127.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Han Lu, Dan Wang, Guangfei Huang, Qilin Ma, Yuan Zhang, Mingliang Jin, Lingling Shui.  (2023)  Label-free identification of DNA single-base mutation for clinical diagnostics based on plasmonic SiNW@AgNP arrays.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2023.135005]
2. Mukaram Amatjan, Na Li, Pengke He, Boheng Zhang, Xianyan Mai, Qianle Jiang, Haochen Xie, Xiaoni Shao.  (2023)  A Novel Approach Based on Gut Microbiota Analysis and Network Pharmacology to Explain the Mechanisms of Action of Cichorium intybus L. Formula in the Improvement of Hyperuricemic Nephropathy in Rats.  Drug Design Development and Therapy,      [PMID:36712944] [10.2147/DDDT.S389811]
3. Shuanghui Lu, Xiu Chen, Yujia Chen, Yingqiong Zhang, Jun Luo, Huidi Jiang, Luo Fang, Hui Zhou.  (2023)  Downregulation of PDZK1 by TGF-β1 promotes renal fibrosis via inducing epithelial-mesenchymal transition of renal tubular cells.  BIOCHEMICAL PHARMACOLOGY,      [PMID:38158021] [10.1016/j.bcp.2023.116015]
4. Liu Jie, Lin Chenshi, Wu Man, Wang Yingjie, Chen Shenyu, Yang Taiwang, Xie Chenlu, Kong Yue, Wu Wenliang, Wang Jiaping, Ma Xiaonan, Teng Chao.  (2023)  Co-delivery of indomethacin and uricase as a new strategy for inflammatory diseases associated with high uric acid.  Drug Delivery and Translational Research,      [PMID:38127247] [10.1007/s13346-023-01487-5]
5. Xiaofei Zhou, Bowei Zhang, Xiuli Zhao, Pixian Zhang, Jingting Guo, Yuan Zhuang, Shuo Wang.  (2023)  Coffee Leaf Tea Extracts Improve Hyperuricemia Nephropathy and Its Associated Negative Effect in Gut Microbiota and Amino Acid Metabolism in Rats.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:37936369] [10.1021/acs.jafc.3c02797]
6. Yali Yang, Yan Li, Zelong Long, Lingling Han, Kaijun Quan, Jia Chen, Xiuhui Liu, Hongdeng Qiu.  (2023)  A C4-modified bipyridinium multi-mode stationary phase for reversed phase, hydrophilic interaction and ion exchange chromatography.  Analytical Methods,  15  (45): (6286-6293).  [PMID:37965679] [10.1039/D3AY01796F]
7. Pu Li, Chen Luo, Xiaoxiao Chen, Chaobiao Huang.  (2023)  A novel “off-on” ratiometric fluorescent aptasensor for adenosine detection based on FRET between quantum dots and graphene oxide.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:37866265] [10.1016/j.saa.2023.123557]
8. Dai Di Chen, Qingxin Li, Jin Chuan Wu.  (2023)  Efficient removal of purine compounds from solutions via biomass carbons derived from pomelo peel.  JOURNAL OF BIOSCIENCE AND BIOENGINEERING,      [PMID:37775439] [10.1016/j.jbiosc.2023.09.002]
9. Dai Shuyu, Guo Yun, Mao Hongyan, Wei Xiaohui, Zhang Wenfen, Chen Xin, Zhao Wuduo, Zhang Shusheng.  (2023)  Sulfonic acid functionalized monolithic column for high selectivity capillary electrochromatography separation.  MICROCHIMICA ACTA,  190  (10): (1-10).  [PMID:37726434] [10.1007/s00604-023-05994-7]
10. Qiangqiang Jia, Zufan Yang, Qian Wang, Haishan Yang, Xiaofeng Tang, Hongyang Zhang, Lingling Cao, Gong Zhang.  (2023)  A liquid chromatography-tandem mass spectrometry method for comprehensive determination of metabolites in the purine pathway of rat plasma and its application in anti-gout effects of Lycium ruthenicum Murr..  JOURNAL OF SEPARATION SCIENCE,  46  (21): (2300090).  [PMID:37688342] [10.1002/jssc.202300090]
11. Meng Dong, Feng Liang, Shuang Cui, Bing-Bing Mao, Xu-Hui Huang, Lei Qin.  (2023)  Insights into the effects of steaming on organoleptic quality of salmon (Salmo salar) integrating multi-omics analysis and electronic sensory system.  FOOD CHEMISTRY,      [PMID:37741235] [10.1016/j.foodchem.2023.137372]
12. Yangcenzi Xie, Mingyang Chen, Xinyu Liu, Xiaoming Su, Ming Li.  (2023)  Artificial Intelligence-Assisted Label-Free Spectroscopic Quantification of Global DNA Cytosine Methylation in a Miniature Plasmonic Pickering Emulsion.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202307091]
13. Xing Chenyu, Chen Gaoyu, Zhu Xia, An Jiakun, Bao Jianchun, Wang Xuan, Zhou Xiuqing, Du Xiuli, Xu Xiangxing.  (2023)  Synthesis of carbon dots with predictable photoluminescence by the aid of machine learning.  Nano Research,      [PMID:] [10.1007/s12274-023-5893-6]
14. Chi Zhang, Man Fang, Yuanbo Gao, Yunchao Li, Louzhen Fan, Xiaohong Li.  (2023)  Valence-Engineered Oxidase-Mimicking Nanozyme with Specificity for Aromatic Amine Oxidation and Identification.  ANALYTICAL CHEMISTRY,      [PMID:37402320] [10.1021/acs.analchem.3c01488]
15. Handan Lei, Nan Yao, Saisai Wang, Xinzi Fang, Jiang Wu, Guang Yang, Zan Hua.  (2023)  Plant oil-based branched polymer coatings enhanced with nucleobases for achieving strong adhesion and outstanding environmental tolerance.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.144602]
16. Ziqiang Li, Shuang Liang, Li Zhou, Fengjian Luo, Zhengyun Lou, Zongmao Chen, Xinzhong Zhang, Mei Yang.  (2023)  A Turn-On Fluorescence Sensor Based on Nitrogen-Doped Carbon Dots and Cu2+ for Sensitively and Selectively Sensing Glyphosate.  Foods,  12  (13): (2487).  [PMID:37444225] [10.3390/foods12132487]
17. Lihui Feng, Xiaofei Zhang, Zhekuang Jin, Jiashang Chen, Xing Duan, Shiyu Ma, Tifeng Xia.  (2023)  An Anionic Porous Indium-Organic Framework with Nitrogen-Rich Linker for Efficient and Selective Removal of Trace Cationic Dyes.  MOLECULES,  28  (13): (4980).  [PMID:37446641] [10.3390/molecules28134980]
18. Fei Wang, Fan Yang, Jiawei Liu, Quan Bai.  (2023)  Studies on the retention mechanism of solutes in hydrophilic interaction chromatography using stoichiometric displacement theory II. HILIC/RPLC dual-retention mechanism of solutes in hydrophilic interaction chromatography over the entire range of water concentration in mobile phase.  TALANTA,      [PMID:37385194] [10.1016/j.talanta.2023.124858]
19. Yudan Mei, Xiaoyu Tong, Yumei Hu, Wenjun Liu, Jiajia Wang, Kaihong Lv, Xu Li, Liang Cao, Zhenzhong Wang, Wei Xiao, Xia Gao.  (2023)  Comparative pharmacokinetics of six bioactive components of Shen-Wu-Yi-Shen tablets in normal and chronic renal failure rats based on UPLC-TSQ-MS/MS.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:37348793] [10.1016/j.jep.2023.116818]
20. Xiao-Dong Cheng, Zheng Zhang, Yun-Ping Li.  (2023)  A facile approach to undecylenic acid-functionalized stationary phases for per aqueous liquid chromatography.  ANALYTICA CHIMICA ACTA,      [PMID:37230580] [10.1016/j.aca.2023.341337]
21. Zhengqi Zha, Xiaoning Wang, Guoqing Wang, Hongping Yin, Hang Wang.  (2023)  Synthesis and structural characterization of xylan acetate ester and its antinephritic effects in rats with experimental chronic kidney disease.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:37059278] [10.1016/j.ijbiomac.2023.124413]
22. Sun Hao-Fei, Cui Yuan-Yuan, Li Hong-Liang, Yang Cheng-Xiong.  (2023)  Click postsynthesis of microporous organic network@silica composites for reversed-phase/hydrophilic interaction mixed-mode chromatography.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  415  (18): (4533-4543).  [PMID:37017725] [10.1007/s00216-023-04680-0]
23. Jun Ma, Jiahe Zhang, Ye Yuan, Yunqi Zhou, Shenzhen Cong, Guangyu Xing, Jixiao Wang, Zhi Wang.  (2023)  HOF-21 nanofillers incorporated mixed matrix membranes for high-performance N2/CH4 separation.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2023.121626]
24. Na Li, Gengsheng Xu, Manqing Yan, Bensong Chen, Yupeng Yuan, Chuhong Zhu.  (2023)  Fabrication of Vertically Aligned ZnO Nanorods Modified with Dense Silver Nanoparticles as Effective SERS Substrates.  Chemosensors,  11  (4): (210).  [PMID:] [10.3390/chemosensors11040210]
25. Ran Xin, Meng Dong, Yu-Ying Zhang, Xu-Hui Huang, Xiu-Ping Dong, Lei Qin.  (2023)  Development and validation of a HILIC-MS/MS method for simultaneous quantitative of taste-active compounds in foods.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2023.105302]
26. Xiaojuan Xie, Jing Jiang, Jiali Ma, Chenjie Gu, Tao Jiang, Jinjie Zhang.  (2023)  Quantitative detection of purine from food products with different water activities using needle-based surface-enhanced Raman scattering sensors.  FOOD CHEMISTRY,      [PMID:37001358] [10.1016/j.foodchem.2023.136011]
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