L-Buthionine-sulfoximine(L-BSO) - ≥95% , CAS No.83730-53-4

CAS: 83730-53-4 Cat. No.: B305771 Molecular Weight: 222.31 Beilstein Registry Number: 2367136 EC Number: 690-151-4
AVAILABLE TO ORDER
GRADE & PURITY ≥95%
Synonyms
CHEBI:94288 | A864195 | Butanoic acid, 2-amino-4-((R)-S-butylsulfonimidoyl)-, (2S)-rel- | L-Buthionine-sulfoximine | s9728 | 2-amino-4-(S-butylsulfonimidoyl)butanoate | Butanoic acid, 2-amino-4-(S-butylsulfonimidoyl)-, (R*,S*)-(+-)- | Buthionine-S,R-sulfo
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
250mg
B305771-250mg
3
$169.90
500mg
B305771-500mg
4
$279.90
1g
B305771-1g
3
$449.90
5g
B305771-5g
2
$1,699.90
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 21 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

A glutathione-synthesis inhibitor that activates oxidative stress. 

Used to induce experimental glutathione deficiency, to investigate roles of glutathione in cellular processes.


Application:

L-Buthionine-sulfoximine has been used:

as a selective activator for the induction of ferroptosis in rat apoptotic cells

as an inhibitor of γ-glutamylcysteine synthetase to study its effects on the viability and effectiveness of microspore embryogenesis (ME) induction in triticale and barley

as a glutathione synthesis blocker to study its effects on auranofin (AFN)-mediated interleukin-1β expression in murine alveolar macrophages


Specifications

Synonyms
CHEBI:94288 | A864195 | Butanoic acid, 2-amino-4-((R)-S-butylsulfonimidoyl)-, (2S)-rel- | L-Buthionine-sulfoximine | s9728 | 2-amino-4-(S-butylsulfonimidoyl)butanoate | Butanoic acid, 2-amino-4-(S-butylsulfonimidoyl)-, (R*, S*)-(+-)- | Buthionine-S, R-sulfo
Specifications & Purity
≥95%
Biochemical and Physiological Mechanisms
Buthionine-sulfoximine (BSO) is a glutathione-synthesis inhibitor that activates oxidative stress through irreversibly inhibiting γ-GCSc (γ-glutamylcysteine synthetase). Studies show methylglyoxal (MG) activated caspase-3 is enhanced in the presence of BS
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
ACTIVATOR
Purity
≥95%
Names and Identifiers
Pubchem Sid488187607
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488187607
Canonical SmilesCCCCS(=N)(=O)CCC(C(=O)O)N
IUPAC Name(2S)-2-amino-4-(butylsulfonimidoyl)butanoic acid
InChIKeyKJQFBVYMGADDTQ-CVSPRKDYSA-N
INCHI1S/C8H18N2O3S/c1-2-3-5-14(10,13)6-4-7(9)8(11)12/h7,10H,2-6,9H2,1H3,(H,11,12)/t7-,14?/m0/s1
Isomeric SMILES CCCCS(=N)(=O)CC[C@@H](C(=O)O)N
WGK Germany 3
RTECS EK7713440
Molecular Weight 222.31
Beilstein 2367136
Reaxy-Rn 2367136
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2367136&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 Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids
Direct ParentL-alpha-amino acids
Alternative Parents Thia fatty acids  Carbo-azosulfones  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAliphatic acyclic compounds
Substituents L-alpha-amino acid - Thia fatty acid - Fatty acid - Fatty acyl - Carbo-azosulfone - Amino acid - Carboxylic acid - Monocarboxylic acid or derivatives - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Primary amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Carbonyl group - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
A498 (42825 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHN (49357 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAKI-1 (44928 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCRF-CEM (65223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
COLO 205 (50209 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DLD-1 (17511 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DMS-273 (14108 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DU-145 (51482 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HT-29 (80576 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KM12 (47707 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
M14 (47487 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MOLT-4 (49676 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-3 (48710 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-4 (44535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-5 (45555 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OVCAR-8 (47708 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-3 (62116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RPMI-8226 (44974 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXF 393 (41971 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-295 (48000 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-2 (46422 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-28 (48833 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-MEL-5 (47095 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-OV-3 (52876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SN12C (47755 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNB-19 (46794 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNB-78 (14240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TK-10 (45540 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-251 (51189 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-257 (46019 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UACC-62 (47335 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
UO-31 (46270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
XF498 (12972 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
786-0 (47912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI/ADR-RES (33767 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
T47D (39041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EKVX (44102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H322M (45589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCC 2998 (41480 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HCT-116 (91556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HOP-18 (11577 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HOP-92 (41141 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hs-578T (29457 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H460 (60772 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SF-268 (49410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
IGROV-1 (47897 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
P388 (20296 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
P388/ADR (1216 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Txnrd1 Thioredoxin reductase 1, cytoplasmic (45279 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Gclc Glutamate--cysteine ligase catalytic subunit (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
gcs-1 Glutamate--cysteine ligase (130 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.

16 results found

Lot NumberCertificate TypeDateItem
E2608257Certificate of AnalysisApr 09, 2026 B305771
E2608258Certificate of AnalysisApr 09, 2026 B305771
E2608259Certificate of AnalysisApr 09, 2026 B305771
E2407076Certificate of AnalysisJun 06, 2023 B305771
F2403373Certificate of AnalysisJun 06, 2023 B305771
F2518153Certificate of AnalysisJun 06, 2023 B305771
G2310014Certificate of AnalysisJun 06, 2023 B305771
G2310015Certificate of AnalysisJun 06, 2023 B305771
G2310016Certificate of AnalysisJun 06, 2023 B305771
G2310019Certificate of AnalysisJun 06, 2023 B305771
G2310020Certificate of AnalysisJun 06, 2023 B305771
G2310021Certificate of AnalysisJun 06, 2023 B305771
G2310023Certificate of AnalysisJun 06, 2023 B305771
G2310027Certificate of AnalysisJun 06, 2023 B305771
H2508084Certificate of AnalysisJun 06, 2023 B305771
G2208126Certificate of AnalysisJul 12, 2022 B305771

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Chemical and Physical Properties
SolubilitySoluble in water (>25 mg/mL), aqueous acid, and 1N HCl.
Melt Point(°C)234-235°C
Molecular Weight222.310 g/mol
XLogP3-0.600
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count5
Rotatable Bond Count7
Exact Mass222.104 Da
Monoisotopic Mass222.104 Da
Topological Polar Surface Area113.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity284.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Yufen Liao, Xin Wang, Guangyun Ran, Shiyu Zhang, Chutian Wu, Rong Tan, Ying Liu, Yan He, Ting Liu, Zhongxiu Wu, Ying Peng, Weiwei Li, Jiang Zheng.  (2023)  DNA damage and up-regulation of PARP-1 induced by columbin in vitro and in vivo.  TOXICOLOGY LETTERS,      [PMID:36905973] [10.1016/j.toxlet.2023.03.003]
2. Liu Wang, Kang Wang, Xiaohui Wang, Ruyan Niu, Xiaohui Chen, Ying Zhu, Zixin Sun, Jichun Yang, Guoxiang Liu, Yang Luo.  (2023)  Intelligent Dual-Lock Deoxyribonucleic Acid Automatons Boosting Precise Tumor Imaging.  ACS Applied Materials & Interfaces,      [PMID:36625537] [10.1021/acsami.2c20024]
3. Chengcheng Wang, Jiao Wang, Xue Pan, Shuang Yu, Meiqi Chen, Yan Gao, Zilin Song, Haiyang Hu, Xiuli Zhao, Dawei Chen, Fei Han, Mingxi Qiao.  (2022)  Reversing ferroptosis resistance by MOFs through regulation intracellular redox homeostasis.  Asian Journal of Pharmaceutical Sciences,      [PMID:36660553] [10.1016/j.ajps.2022.11.004]
4. Tao Liu, Cheng-Feng Xiong, Lin-Jun Zhang, Guan-Hua Jiao, Hui Shi, Jun Feng, Xian-Zheng Zhang.  (2022)  Boosting Doxorubicin-Induced Mitochondria Apoptosis for the Monodrug-Mediated Combination of Chemotherapy and Chemodynamic Therapy.  Advanced Healthcare Materials,  12  (3): (2202045).  [PMID:36239177] [10.1002/adhm.202202045]
5. Mingyu Zhang, Yaodong Hu, Wei Li, Chen Sun, Chunjing Guan, Ying Peng, Jiang Zheng.  (2022)  In Vitro and In Vivo Metabolic Activation and Hepatotoxicity of Environmental Pollutant 2,6-Dimethylphenol.  CHEMICAL RESEARCH IN TOXICOLOGY,      [PMID:35583464] [10.1021/acs.chemrestox.2c00048]
6. Shiyu Zhang, Ying Liu, Ting Liu, Jie Pan, Rong Tan, Zixia Hu, Bowen Gong, Yufen Liao, Peng Luo, Qibing Zeng, Weiwei Li, Jiang Zheng.  (2022)  DNA damage by reactive oxygen species resulting from metabolic activation of 8-epidiosbulbin E acetate in vitro and in vivo.  TOXICOLOGY AND APPLIED PHARMACOLOGY,      [PMID:35367474] [10.1016/j.taap.2022.116007]
7. Yue Zhang, Shibo Sun, Weiping Xu, Rui Yang, Yijia Yang, Jianli Guo, Kun Ma, Jianqiang Xu.  (2021)  Thioredoxin reductase 1 inhibitor shikonin promotes cell necroptosis via SecTRAPs generation and oxygen-coupled redox cycling.  FREE RADICAL BIOLOGY AND MEDICINE,      [PMID:34973363] [10.1016/j.freeradbiomed.2021.12.314]
8. Qiang Chu, Shuang Zhang, Xin Yu, Yaxuan Wang, Mingkui Zhang, Xiaodong Zheng.  (2021)  Fecal microbiota transplantation attenuates nano-plastics induced toxicity in Caenorhabditis elegans.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:33744565] [10.1016/j.scitotenv.2021.146454]
9. Hong Lin, Chen Jundixia, Wu Fang, Wu Fengjiao, Shen Xin, Zheng Peisen, Shao Rongrong, Lu Kongqin, Liu Zhiguo, Chen Daoxing, Liang Guang, Cai Yuepiao, Zou Peng, Xia Yiqun.  (2020)  Isodeoxyelephantopin Inactivates Thioredoxin Reductase 1 and Activates ROS-Mediated JNK Signaling Pathway to Exacerbate Cisplatin Effectiveness in Human Colon Cancer Cells.  Frontiers in Cell and Developmental Biology,      [PMID:33072762] [10.3389/fcell.2020.580517]
10. Shuting Xiao, Yao Lu, Miao Feng, Ming Dong, Zhong Cao, Xiaoge Zhang, You Chen, Jie Liu.  (2020)  Multifunctional FeS2 theranostic nanoparticles for photothermal-enhanced chemodynamic/photodynamic cancer therapy and photoacoustic imaging.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2020.125294]
11. Zhongyin Chen, Lihui Wan, Ye Yuan, Ying Kuang, Xiangyu Xu, Tao Liao, Jia Liu, Zi-Qiang Xu, Bingbing Jiang, Cao Li.  (2020)  pH/GSH-Dual-Sensitive Hollow Mesoporous Silica Nanoparticle-Based Drug Delivery System for Targeted Cancer Therapy.  ACS Biomaterials Science & Engineering,      [PMID:33463161] [10.1021/acsbiomaterials.0c00073]
12. Jinbo Lu, Bichu Luo, Zhongyin Chen, Ye Yuan, Ying Kuang, Lihui Wan, Li Yao, Xueqin Chen, Bingbing Jiang, Jia Liu, Cao Li.  (2020)  Host-guest fabrication of dual-responsive hyaluronic acid/mesoporous silica nanoparticle based drug delivery system for targeted cancer therapy.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:31911174] [10.1016/j.ijbiomac.2019.12.265]
13. Cheng Li, Lindan Sun, Hanzuo Lin, Zhendong Qin, Jiagang Tu, Jun Li, Keping Chen, Sarath Babu V, Li Lin.  (2018)  Glutamine starvation inhibits snakehead vesiculovirus replication via inducing autophagy associated with the disturbance of endogenous glutathione pool.  FISH & SHELLFISH IMMUNOLOGY,      [PMID:30590160] [10.1016/j.fsi.2018.12.041]
14. Min Zhang, Jia Liu, Ying Kuang, Qilin Li, Hongyu Chen, Haifeng Ye, Li Guo, Yanglin Xu, Xueqin Chen, Cao Li, Bingbing Jiang.  (2016)  “Stealthy” chitosan/mesoporous silica nanoparticle based complex system for tumor-triggered intracellular drug release.  Journal of Materials Chemistry B,  (19): (3387-3397).  [PMID:32263274] [10.1039/C5TB02548F]
15. Qi Shen, Minjuan Zuo, Li Ma, Ye Tian, Lu Wang, Huidi Jiang, Quan Zhou, Hui Zhou, Lushan Yu, Su Zeng.  (2014)  Demethylation of neferine in human liver microsomes and formation of quinone methide metabolites mediated by CYP3A4 accentuates its cytotoxicity.  CHEMICO-BIOLOGICAL INTERACTIONS,      [PMID:25451576] [10.1016/j.cbi.2014.10.014]
16. Yong Li, Jing Wang, Tao Zhu, Ying Zhan, Xiaoli Tang, Jianying Xi, Xiaohui Zhu, Yong Zhang, Jinliang Liu.  (2024)  A ROS storm generating nanocomposite for enhanced chemodynamic therapy through H2O2 self-supply, GSH depletion and calcium overload.  Nanoscale,      [PMID:38590261] [10.1039/D3NR06422K]
17. Xueqi Hu, Dongdong Zhang, Linjie Huang, Zheng Zeng, Yina Su, Shanshan Chen, Xiahui Lin, Shanni Hong.  (2024)  Construction of a Functional Nucleic Acid-Based Artificial Vesicle-Encapsulated Composite Nanoparticle and Its Application in Retinoblastoma-Targeted Theranostics.  ACS Biomaterials Science & Engineering,      [PMID:38408449] [10.1021/acsbiomaterials.3c01972]
18. Yang Chen, Wenzhe Xu, Hao Jin, Mengsi Zhang, Shuwei Liu, Yi Liu, Hao Zhang.  (2024)  Nutritional Glutamine-Modified Iron-Delivery System with Enhanced Endocytosis for Ferroptosis Therapy of Pancreatic Tumors.  ACS Nano,      [PMID:39512234] [10.1021/acsnano.4c08083]
19. Huimei Zhao, Haiyan Zhang, Jianyu Shi, Yanru Liu, Jingao Yu, Yuangui Yang, Jingyu Weng, Zhongxing Song, Rui Zhou, Hong Min, Jian Yao, Mei Wang, Zhen Zhang.  (2025)  Wuwei Shaji powder alleviates OVA-induced allergic asthma by protecting bronchial epithelial cells from ferroptosis via the S-sulfhydration of Keap1.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:40222689] [10.1016/j.jep.2025.119649]
20. Jiajian Wang, Lanqing Zhang, Runfang Li, Rui Yang, Fan Yang, Fei Yu, Jihong Zhang.  (2025)  Gambogic acid restores wild-type-like p53 functions to induce ferroptosis in mutant p53 cancer cells.  BIOCHEMICAL PHARMACOLOGY,      [PMID:41213406] [10.1016/j.bcp.2025.117533]
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