L(-)-Glutathione(oxidised form) - high-purity , CAS No.27025-41-8

CAS: 27025-41-8 Cat. No.: L274260 Molecular Weight: 612.63 Beilstein Registry Number: 1718700 EC Number: 248-170-7
AVAILABLE TO ORDER
GRADE & PURITY High-purity ? High-purity grade with substantially reduced impurity levels. Use when trace contaminants would interfere with your measurement or process.
Synonyms
F20504 | OXIGLUTATIONE [ORANGE BOOK] | 4-{N-[(1R)-2-({(2R)-2-((4S)-4-Amino-4-carboxybutanoylamino)-2-[N-(carboxymethyl)carbamoyl]ethyl}disulfanyl)-1-[N-(carboxymethyl)carbamoyl]ethyl]carbamoyl}(2S)-2-aminobutanoic acid | Oxiglutationum [INN-Latin] | AS-14
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
L274260-1g
3
$99.90
5g
L274260-5g
3
$349.90
25g
L274260-25g
3
$1,199.90
100g
L274260-100g
2
$2,999.90
Enter a quantity for the sizes you want to add.
🧪

Why this grade

high-purity High-purity for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice 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 36 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
F20504 | OXIGLUTATIONE [ORANGE BOOK] | 4-{N-[(1R)-2-({(2R)-2-((4S)-4-Amino-4-carboxybutanoylamino)-2-[N-(carboxymethyl)carbamoyl]ethyl}disulfanyl)-1-[N-(carboxymethyl)carbamoyl]ethyl]carbamoyl}(2S)-2-aminobutanoic acid | Oxiglutationum [INN-Latin] | AS-14
Specifications & Purity
high-purity
Biochemical and Physiological Mechanisms
Oxidized L-glutathione is often measured as an oxidative stress indicator in the body. Oxidized L-glutathione can be converted into L-glutathione through various reduction systems.
Storage
Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
High-purity
Names and Identifiers
Pubchem Sid504753978
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504753978
Canonical SmilesN[C@@H](CCC(=O)N[C@@H](CSSC[C@H](NC(=O)CC[C@H](N)C(O)=O)C(=O)NCC(O)=O)C(=O)NCC(O)=O)C(O)=O
IUPAC Name(2S)-2-amino-5-[[(2R)-3-[[(2R)-2-[[(4S)-4-amino-4-carboxybutanoyl]amino]-3-(carboxymethylamino)-3-oxopropyl]disulfanyl]-1-(carboxymethylamino)-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
InChIKeyYPZRWBKMTBYPTK-BJDJZHNGSA-N
INCHI1S/C20H32N6O12S2/c21-9(19(35)36)1-3-13(27)25-11(17(33)23-5-15(29)30)7-39-40-8-12(18(34)24-6-16(31)32)26-14(28)4-2-10(22)20(37)38/h9-12H,1-8,21-22H2,(H,23,33)(H,24,34)(H,25,27)(H,26,28)(H,29,30)(H,31,32)(H,35,36)(H,37,38)/t9-,10-,11-,12-/m0/s1
Isomeric SMILES C(CC(=O)N[C@@H](CSSC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N)C(=O)NCC(=O)O)[C@@H](C(=O)O)N
WGK Germany 2
RTECS MC0556500
Molecular Weight 612.63
Beilstein 1718700
Reaxy-Rn 1718700
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1718700&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
SuperclassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Not available
Direct ParentPeptides
Alternative Parents Tetracarboxylic acids and derivatives  N-acyl-alpha amino acids  L-alpha-amino acids  Dialkyldisulfides  Amino acids  Sulfenyl compounds  Propargyl-type 1,3-dipolar organic compounds  Carboxylic acids  Carboximidic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents Alpha peptide - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Tetracarboxylic acid or derivatives - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Amino acid or derivatives - Amino acid - Dialkyldisulfide - Organic disulfide - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Amine - Hydrocarbon derivative - Organic oxide - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organopnictogen compound - Primary amine - Carbonyl group - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as peptides. These are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.
External Descriptors organic disulfide - glutathione derivative
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
INSR Tclin Insulin receptor (5558 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
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
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 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
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 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
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 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
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 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
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 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
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 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
CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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
Abcc1 Multidrug resistance-associated protein 1 (42 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
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Helicobacter pylori (3113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
fba Putative fructose-1,6-bisphosphate aldolase (15559 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ffp 4'-phosphopantetheinyl transferase ffp (24982 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 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
F2412061Certificate of AnalysisMar 17, 2026 L274260
G2201008Certificate of AnalysisJan 19, 2026 L274260
G2201009Certificate of AnalysisJan 19, 2026 L274260
G2201010Certificate of AnalysisJan 19, 2026 L274260
H2513585Certificate of AnalysisAug 04, 2025 L274260
H2513586Certificate of AnalysisAug 04, 2025 L274260
H2513782Certificate of AnalysisAug 04, 2025 L274260
B2505161Certificate of AnalysisJan 18, 2025 L274260
B2507044Certificate of AnalysisJan 18, 2025 L274260
B2507045Certificate of AnalysisJan 18, 2025 L274260
B2507046Certificate of AnalysisJan 18, 2025 L274260
G2201011Certificate of AnalysisApr 07, 2024 L274260
L2411171Certificate of AnalysisApr 07, 2024 L274260

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Chemical and Physical Properties
Specific Rotation[α]-105 ° (C=2, H2O)
Melt Point(°C)178°C
Molecular Weight612.600 g/mol
XLogP3-9.100
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count16
Rotatable Bond Count21
Exact Mass612.152 Da
Monoisotopic Mass612.152 Da
Topological Polar Surface Area368.000 Ų
Heavy Atom Count40
Formal Charge0
Complexity879.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Enzymes and dietary antioxidants
Biological enzyme catalysis technology and application
What is Glutathione?
High-Purity Reagents: Overview and Aladdin Product Selection Guide
Glutathione (GSH) Quantification: Method Systems, Experimental Workflows, and Key Quality-Control Considerations
Glutathione Reductase: A Flavin-Dependent Reductive System Maintaining GSH/GSSG Homeostasis, with Assays and Applications
Procyanidins: Structural Features and Key Points for Research and Application
Methionine: Biological Roles and Key Points for Research Application
Review of Glucose-6-phosphate Dehydrogenase (G6PD): Structural Features, Metabolic Functions, and Research Applications
Review of the Principles, Methods, and Application Considerations for Superoxide Dismutase Activity Determination
Cellular Electron Transfer Networks and Mechanisms of Metabolism-Signaling Coupling
Roles of One-Carbon Metabolism Enzymes in Oxidative Stress and Epigenetic Regulation in Cardiovascular Diseases
Antioxidant Enzyme Networks in Skin Cells and Their Applications in Skincare and Cosmetics
The Drug Target Potential of the GPX Family in Lipid Peroxidation Defense, Ferroptosis Regulation, and Organ Injury Protection
Progress in Research on the S-Adenosylmethionine Cycle and Regulatory Mechanisms of Methyltransfer Reactions
Progress in Research on Sugar-Nucleotide Metabolism Related to Ascorbate Biosynthesis in Plants
Galactose-Related Precursor Conversion and Redox Regulation in Plant Ascorbate Biosynthesis
Coupling Mechanisms Between Terminal Reducing-Power Allocation in Photosynthetic Electron Transport and Metabolic Demand
Thiol and Disulfide Status in Biological Samples: Detection Methods and Applications
Principles, Method Selection, and Result Interpretation for Malondialdehyde Content Detection
Citations of This Product
References
1. Jia Lin, Guoqing Yue, Kang Xiao, Deqing Yang, Xuxing Hao, Minlin Zheng, Pumo Cai, Qing'e Ji.  (2023)  Effects of low-concentration spinetoram wax-based bait stations on Bactrocera dorsalis (Diptera: Tephritidae).  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:38072558] [10.1016/j.pestbp.2023.105705]
2. Chen Na, Du Na, Shen Ruichen, He Tianpei, Xi Jing, Tan Jie, Bian Guangkai, Yang Yanbing, Liu Tiangang, Tan Weihong, Yu Lilei, Yuan Quan.  (2023)  Redox signaling-driven modulation of microbial biosynthesis and biocatalysis.  Nature Communications,  14  (1): (1-13).  [PMID:37884498] [10.1038/s41467-023-42561-3]
3. Xiaofang Wang, Huiming Wang, Meining Zhang.  (2023)  A multi-stimuli-responsive nanochannel inspired by biological disulfide bond.  TALANTA,      [PMID:37348351] [10.1016/j.talanta.2023.124785]
4. Luo Gu, Qiuyu Zhu, Xiaoyu Zou, Ru Song.  (2023)  Antibacterial Effect of Shrimp By-Products Hydrolysate on Specific Spoilage Organisms of Squid.  MOLECULES,  28  (10): (4105).  [PMID:37241846] [10.3390/molecules28104105]
5. Jia Kong, Jinyao Hu, Jia Li, Jiaxing Zhang, Yuhe Shen, Tianli Yue, Xihui Shen, Yuefei Wang, Zhonghong Li, Yinqiang Xia.  (2023)  Rethreading Design of Ratiometric roGFP2 Mimetic Peptide for Hydrogen Peroxide Sensing.  ANALYTICAL CHEMISTRY,      [PMID:37161261] [10.1021/acs.analchem.3c00486]
6. Yuwei Du, Lei Cao, Xinlu Li, Tongtong Zhu, Ruhong Yan, Wen-Fei Dong, Li Li.  (2023)  Preparation and application of high-brightness red carbon quantum dots for pH and oxidized L-glutathione dual response.  ANALYST,  148  (10): (2375-2386).  [PMID:37129055] [10.1039/D3AN00383C]
7. Mengfei Liu, Hong Mo, Qingyu Gao, Ling Yuan.  (2021)  The pH dependence of emulsifying properties for glutathione disulfide at oil-water interfaces.  BIOPHYSICAL CHEMISTRY,      [PMID:34959125] [10.1016/j.bpc.2021.106748]
8. Xiang-Rong Cheng, Piao-Han Tu, Wen-Le Dong, Bu-Tao Yu, Shu-Fang Xia, Mitchell N. Muskat, Bin Guan.  (2021)  Electrophilic thymol isobutyrate from Inula nervosa Wall. (Xiaoheiyao) ameliorates steatosis in HepG2 cells via Nrf2 activation.  Journal of Functional Foods,      [PMID:] [10.1016/j.jff.2021.104895]
9. Qianqian Zhang, Junhua Wang, Zhao Meng, Rui Ling, Hang Ren, Weidong Qin, Zhenglong Wu, Na Shao.  (2021)  Glutathione Disulfide as a Reducing, Capping, and Mass-Separating Agent for the Synthesis and Enrichment of Gold Nanoclusters.  Nanomaterials,  11  (9): (2258).  [PMID:34578574] [10.3390/nano11092258]
10. Yufen Lai, Mengyan Li, Xiaofei Liao, Li Zou.  (2021)  Smartphone-Assisted Colorimetric Detection of Glutathione and Glutathione Reductase Activity in Human Serum and Mouse Liver Using Hemin/G-Quadruplex DNAzyme.  MOLECULES,  26  (16): (5016).  [PMID:34443603] [10.3390/molecules26165016]
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12. Fengjiao Mao, Kai Yu, Jing He, Qi Zhou, Guangming Zhang, Wenxin Wang, Na Li, Hong Zhang, Jie Jiang.  (2019)  Real-time monitoring of electroreduction and labelling of disulfide-bonded peptides and proteins by mass spectrometry.  ANALYST,  144  (23): (6898-6904).  [PMID:31638109] [10.1039/C9AN01420A]
13. Wang Xiaoqing, Sun Qian, Zhao Liming, Gong Shuwen, Xu Li.  (2019)  Visualization of hydrogen polysulfides in living cells and in vivo via a near-infrared fluorescent probe.  JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY,  24  (7): (1077-1085).  [PMID:31515622] [10.1007/s00775-019-01718-6]
14. Jian-Yu Yang, Ting Yang, Xiao-Yan Wang, Yi-Ting Wang, Meng-Xian Liu, Ming-Li Chen, Yong-Liang Yu, Jian-Hua Wang.  (2019)  A Novel Three-Dimensional Nanosensing Array for the Discrimination of Sulfur-Containing Species and Sulfur Bacteria.  ANALYTICAL CHEMISTRY,      [PMID:30964645] [10.1021/acs.analchem.9b00476]
15. Chengfei Zhao, Xuewen Wang, Lina Wu, Wen Wu, Yanjie Zheng, Liqing Lin, Shaohuang Weng, Xinhua Lin.  (2019)  Nitrogen-doped carbon quantum dots as an antimicrobial agent against Staphylococcus for the treatment of infected wounds.  COLLOIDS AND SURFACES B-BIOINTERFACES,      [PMID:30928801] [10.1016/j.colsurfb.2019.03.042]
16. Xingqi Wang, Yong Zhang, Jie Huang, Mengqiu Xia, Liu Liu, Chunling Tian, Rongfeng Hu, Shuangying Gui, Xiaoqin Chu.  (2019)  Self-assembled hexagonal liquid crystalline gels as novel ocular formulation with enhanced topical delivery of pilocarpine nitrate.  INTERNATIONAL JOURNAL OF PHARMACEUTICS,      [PMID:30878587] [10.1016/j.ijpharm.2019.02.033]
17. Wang Xingqi, Zhang Yong, Huang Jie, Tian Chunling, Xia Mengqiu, Liu Liu, Li Zhengguang, Cao Jiaojiao, Gui Shuangying, Chu Xiaoqin.  (2019)  A Novel Phytantriol-Based Lyotropic Liquid Crystalline Gel for Efficient Ophthalmic Delivery of Pilocarpine Nitrate.  AAPS PHARMSCITECH,  20  (1): (1-14).  [PMID:30603986] [10.1208/s12249-018-1248-0]
18. Shanshan Wang, Xu Hun, Xiliang Luo.  (2018)  Photoelectrochemical endocrine-disrupting chemicals aptasenor based on resonance energy transfer between SnSe/GR and AuNPs along with GSSG for signal amplification.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2018.01.074]
19. Huili Ye, Hao Wang, Faqiong Zhao, Baizhao Zeng.  (2017)  A one-pot hydrothermal synthesis of graphene/CdS:Mn photocatalyst for photoelectrochemical sensing of glutathione.  RSC Advances,  (72): (45792-45798).  [PMID:] [10.1039/C7RA09075G]
20. Zihao Zhang, Yongjing Li, Jiaxun Wan, Peihua Long, Jia Guo, Guosong Chen, Changchun Wang.  (2017)  Preparation of Pt(IV)-crosslinked polymer nanoparticles with an anti-detoxifying effect for enhanced anticancer therapy.  Polymer Chemistry,  (15): (2410-2422).  [PMID:] [10.1039/C6PY02148D]
21. Lingzhi Zhao, Zhao Li, Liu Zhao, Chenxiao Zhang.  (2017)  In Vivo Determination of Reduced Thiols in Rat Cerebellum Paraflocculus Following Salicylate-Induced Tinnitus by Fluorescence.  ANALYTICAL LETTERS,      [PMID:] [10.1080/00032719.2016.1186170]
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