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Coenzyme Q10 - 98%, high purity , CAS No.303-98-0

25 Citations COA COA
    Grade & Purity:
  • ≥98%
In stock
Item Number
C111044
Grouped product items
SKU Size
Availability
 Price Qty
C111044-250mg
250mg
3
$48.90
C111044-1g
1g
2
$162.90
C111044-5g
5g
2
$238.90
C111044-25g
25g
1
$1,075.90
C111044-100g
100g
2
$3,871.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet

Antioxidant

View related series
Apoptosis (4276) Chemical preventive agent (37) Endogenous Metabolite (959) Ferroptosis (356) Glucose Metabolism (1943) Immunology/Inflammation (1929) Metabolic Enzyme/Protease (4860) Metabolite (5307) NF-κB (747) Reactive Oxygen Species (309) terpenes (123)

Basic Description

Synonyms all-trans-ubiquinone | EJ27X76M46 | NCGC00159429-02 | Aqua Q10 | Luvacor | NSC 140865 | Ubiquinone 50 | Q-Gel 100 | Ubidecarenone [INN:BAN:JAN:NF] | UBIDECARENONE [MART.] | Ubidecarenonum [Latin] | 2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Component of the mitochondrial transporter chain that behaves as a powerful antioxidant. Displays neuroprotective activity. Ferroptosis inhibitor.
Storage Temp Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Application

It is used as a component of electron transport chain and in aerobic cellular respiration, Coenzyme Q10 can protect human endothelial cells from oxidative damage by modulating the nitric oxide pathway. In addition, Coenzyme Q10 inhibits LDL oxidation, a major process in the development of atherosclerosis. Coenzyme Q10 is known to suppress the down regulation of NOS and up-regulation of NOS2. As a result of its ability to bind Ca2+, Coenzyme Q10 can transport this cation across artificial biomimetic membranes.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Lipids and lipid-like molecules
Class Prenol lipids
Subclass Quinone and hydroquinone lipids
Intermediate Tree Nodes Prenylquinones
Direct Parent Ubiquinones
Alternative Parents Polyterpenoids  Polyprenylbenzoquinones  P-benzoquinones  Vinylogous esters  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aliphatic homomonocyclic compounds
Substituents Polyterpenoid - Polyprenylbenzoquinone - Ubiquinone skeleton - Quinone - P-benzoquinone - Vinylogous ester - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as ubiquinones. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methyl(1,4-benzoquinone) moiety to which an isoprenyl group is attached at ring position 2(or 6).
External Descriptors Ubiquinones

Product Properties

ALogP 19.4

Associated Targets(Human)

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
ADRB2 Tclin Beta-2 adrenergic receptor (11824 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
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
CNR1 Tclin Cannabinoid CB1 receptor (20913 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
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
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 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
HRH1 Tclin Histamine H1 receptor (7573 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
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 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
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 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
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CHRM3 Tclin Muscarinic acetylcholine receptor M3 (7750 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
HRH3 Tclin Histamine H3 receptor (10389 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
LMNA Tbio Prelamin-A/C (36751 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PMP22 Tbio Peripheral myelin protein 22 (699 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PSAP Tbio Prosaposin (12 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Pde4d Phosphodiesterase 4D (4 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Micrococcus luteus (7463 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Proteus mirabilis (3894 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Serratia marcescens (3237 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PC-12 (7051 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HT-22 (3261 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
Coptotermes formosanus (677 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SARS-CoV-2 (38078 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

IUPAC Name 2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
INCHI InChI=1S/C59H90O4/c1-44(2)24-15-25-45(3)26-16-27-46(4)28-17-29-47(5)30-18-31-48(6)32-19-33-49(7)34-20-35-50(8)36-21-37-51(9)38-22-39-52(10)40-23-41-53(11)42-43-55-54(12)56(60)58(62-13)59(63-14)57(55)61/h24,26,28,30,32,34,36,38,40,42H,15-23,25,27,29,31,33,35,37,39,41,43H2,1-14H3/b45-26+,46-28+,47-30+,48-32+,49-34+,50-36+,51-38+,52-40+,53-42+
InChIKey ACTIUHUUMQJHFO-UPTCCGCDSA-N
Smiles CC1=C(C(=O)C(=C(C1=O)OC)OC)CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C
Isomeric SMILES CC1=C(C(=O)C(=C(C1=O)OC)OC)C/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CC/C=C(\C)/CCC=C(C)C
WGK Germany 3
RTECS DK3900000
Molecular Weight 863.34
Beilstein 1900141
Reaxy-Rn 1900140
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1900140&ln=

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.

21 results found

Lot Number Certificate Type Date Item
G2503041 Certificate of Analysis Jul 05, 2025 C111044
E2521033 Certificate of Analysis May 27, 2025 C111044
E2507027 Certificate of Analysis May 15, 2025 C111044
L2402046 Certificate of Analysis Dec 09, 2024 C111044
H2415055 Certificate of Analysis Aug 29, 2024 C111044
K2211217 Certificate of Analysis Aug 22, 2024 C111044
K2211222 Certificate of Analysis Aug 22, 2024 C111044
K2211225 Certificate of Analysis Aug 22, 2024 C111044
K2211223 Certificate of Analysis Aug 22, 2024 C111044
H2415017 Certificate of Analysis Aug 20, 2024 C111044
L2402135 Certificate of Analysis Mar 30, 2024 C111044
K2125827 Certificate of Analysis Aug 21, 2023 C111044
K2125895 Certificate of Analysis Aug 21, 2023 C111044
K21251086 Certificate of Analysis Aug 21, 2023 C111044
K2125953 Certificate of Analysis Aug 21, 2023 C111044
K2427160 Certificate of Analysis Aug 21, 2023 C111044
K2125869 Certificate of Analysis Aug 21, 2023 C111044
L2022079 Certificate of Analysis Sep 21, 2022 C111044
L2022078 Certificate of Analysis Sep 21, 2022 C111044
L2022077 Certificate of Analysis Sep 21, 2022 C111044
K2330176 Certificate of Analysis Aug 03, 2022 C111044

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Chemical and Physical Properties

Solubility Solvent:ethanol, Max Conc. mg/mL: 4.32, Max Conc. mM: 5 with gentle warming; Solvent:chloroform, Max Conc. mg/mL: 43.17, Max Conc. mM: 50
Sensitivity Light Sensitive,Air Sensitive,Heat Sensitive
Melt Point(°C) 49°C
Molecular Weight 863.300 g/mol
XLogP3 19.400
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 31
Exact Mass 862.684 Da
Monoisotopic Mass 862.684 Da
Topological Polar Surface Area 52.600 Ų
Heavy Atom Count 63
Formal Charge 0
Complexity 1840.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 9
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 9
Covalently-Bonded Unit Count 1

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Yuan Shun, Che Yanjia, Wang Zhiwei, Xing Kai, Xie Xiaoping, Chen Yuanyang.  (2023)  Mitochondrion-targeted carboxymethyl chitosan hybrid nanoparticles loaded with Coenzyme Q10 protect cardiac grafts against cold ischaemia‒reperfusion injury in heart transplantation.  Journal of Translational Medicine,  21  (1): (1-23). 
2. Xiang Luo, Sha Ao, Hongze Wu, David Julian McClements, Likun Fang, Mengyu Huang, Yanyan Zhou, Xuguang Yin, Meiyang Xi, Tao Cai, Kewu Zhu.  (2023)  Hyaluronic Acid Poly(glyceryl)10-Stearate Derivatives: Novel Emulsifiers for Improving the Gastrointestinal Stability and Bioaccessibility of Coenzyme Q10 Nanoemulsions.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  71  (29): (11180–11194). 
3. Tiantian Chen, Yan Qin, Yao Li, Yaru Li, Jiajia Luo, Lanlan Fan, Meiyu Feng, Zheng Wang, Yanjun Zhao.  (2023)  Chiral Polymer Micelles Alleviate Adriamycin Cardiotoxicity via Iron Chelation and Ferroptosis Inhibition.  ADVANCED FUNCTIONAL MATERIALS,    (2300689). 
4. Shuoye Yang, Yakun Niu, Siqi Li, Mingzhen Lv, Jiaxin Liu, Lu Zhang, Lan Cui, Lingbo Qu.  (2023)  TPGS and Doca dual-modified mesoporous silica nanoparticle-supported lipid bilayers enhance the efficient delivery and in vivo absorption of Coenzyme Q10.  JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY,  81  (104243). 
5. Xuan Ma, Hui Chen, Lixing Cao, Shuang Zhao, Chong Zhao, Shutao Yin, Lihong Fan, Hongbo Hu.  (2022)  18β-glycyrrhetinic acid protects neuronal cells from ferroptosis through inhibiting labile iron accumulation and preventing coenzyme Q10 reduction.  BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,  635  (57). 
6. Yaqin Wang, Lingjia Fan, Jintao Huang, Jingjing Liang, Xingnan Wang, Yichen Ren, Hongcai Li, Tianli Yue, Zhenpeng Gao.  (2023)  Evaluation of chemical composition, antioxidant activity, and gut microbiota associated with pumpkin juice fermented by Rhodobacter sphaeroides.  FOOD CHEMISTRY,  401  (134122). 
7. Mohsen Sheykhhasan, Razieh Amini, Sara Soleimani Asl, Massoud Saidijam, Seyed Mahmoud Hashemi, Rezvan Najafi.  (2022)  Neuroprotective effects of coenzyme Q10-loaded exosomes obtained from adipose-derived stem cells in a rat model of Alzheimer's disease.  BIOMEDICINE & PHARMACOTHERAPY,  152  (113224). 
8. Yuan Liu, Yaxin Yao, Wenjing Tao, Feng Liu, Songbai Yang, Ayong Zhao, Dan Song, Xiangchen Li.  (2021)  Coenzyme Q10 ameliorates BPA-induced apoptosis by regulating autophagy-related lysosomal pathways.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,  221  (112450). 
9. Yang Shuoye, Niu Yakun, Li Luheng, Liu Jiaxin, Ma Mengjin, Duan Xiaoyu, Zhang Lu, Wang Le, Qu Lingbo.  (2021)  PEG-conjugated single-walled carbon nanotubes enhance the cellular uptake of Coenzyme Q10: in vitro evaluation and mechanism study.  JOURNAL OF NANOPARTICLE RESEARCH,  23  (5): (1-14). 
10. Peiwen Zhang, Shen Chen, Huanwen Tang, Wanjun Fang, Ke Chen, Xu Chen.  (2021)  CoQ10 protects against acetaminophen-induced liver injury by enhancing mitophagy.  TOXICOLOGY AND APPLIED PHARMACOLOGY,  410  (115355). 
11. Wenqi Cao, Linfan Shi, Gengxin Hao, Jun Chen, Wuyin Weng.  (2021)  Effect of molecular weight on the emulsion properties of microfluidized gelatin hydrolysates.  FOOD HYDROCOLLOIDS,  111  (106267). 
12. Meng Jiang, Xiong Zheng, Yinguang Chen.  (2020)  Enhancement of denitrification performance with reduction of nitrite accumulation and N2O emission by Shewanella oneidensis MR-1 in microbial denitrifying process.  WATER RESEARCH,  169  (115242). 
13. Liu Ze, Li Zonglin, Wu Ya’Nan, Song Shaohui, Yang Huijuan, Cai Wei, Weidong Li, Guoyang Liao.  (2019)  Application of a novel nanoemulsion adjuvant for rabies vaccine which stabilizes a Krebs cycle intermediate (SDH) in an animal model.  Human Vaccines & Immunotherapeutics,  15  (2): (388-396). 
14. Shuoye Yang.  (2017)  Preparation, in vitro Characterization and Pharmacokinetic Study of Coenzyme Q10 Long-Circulating Liposomes.  Drug Research,  68  (5): (270-279). 
15. Ting Yue, He-Lin Xu, Pian-Pian Chen, Lei Zheng, Qun Huang, Wen-Shuang Sheng, Yuan-Di Zhuang, Li-Zhuo Jiao, Ting-Ting Chi, De-Li ZhuGe, Jin-Jin Liu, Ying-Zheng Zhao, Li Lan.  (2017)  Combination of coenzyme Q10-loaded liposomes with ultrasound targeted microbubbles destruction (UTMD) for early theranostics of diabetic nephropathy.  INTERNATIONAL JOURNAL OF PHARMACEUTICS,  528  (664). 
16. Huibin Li, Fang Chen.  (2017)  Preparation and quality evaluation of coenzyme Q10 long-circulating liposomes.  SAUDI JOURNAL OF BIOLOGICAL SCIENCES,  24  (797). 
17. Peng Xin, Sun Yinhe, Qi Wei, Su Rongxin, He Zhimin.  (2014)  Study of the Interaction Between Coenzyme Q10 and Human Serum Albumin: Spectroscopic Approach.  JOURNAL OF SOLUTION CHEMISTRY,  43  (3): (585-607). 
18. Xiaoling Lin, Meier Chen, Pedro Rodriguez Gonzalez, Dganit Danino, Harold Corke.  (2024)  Advancing coenzyme Q10 delivery with plant protein-based nanoparticle-mediated nanosuspensions.  FOOD RESEARCH INTERNATIONAL,    (115120). 
19. Zheng Delu, Cui Chenli, Ye Chengsong, Shao Chen, Zha Xiujing, Xu Ying, Liu Xu, Wang Can.  (2024)  Coenzyme Q10 prevents RANKL-induced osteoclastogenesis by promoting autophagy via inactivation of the PI3K/AKT/mTOR and MAPK pathways.  BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH,  57  (e13474). 
20. Bo Yang, Xu Zhang, Liguo Zhang, Jinjin Wu, Wei Wang, Qiaomei Huang, Zhenyuan Wang, Jichuan Zhang, Tongjie Xu, Chengyu Wu, Jiaheng Zhang.  (2024)  Ionic Liquid-Based Grapeseed Oil Emulsion for Enhanced Anti-Wrinkle Treatment.  Pharmaceuticals,  17  (10): (1273). 
21. Haiyan Zhu, Yijing Yang, Yenan Duan, Xin Zheng, Zixiong Lin, Jie Zhou.  (2024)  Nrf2/FSP1/CoQ10 axis-mediated ferroptosis is involved in sodium aescinate-induced nephrotoxicity.  ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS,  759  (110100). 
22. Zhou Qu, Yanni Liu, Haoran Wang, Qianxi Yang, Hongwei Fan, Hong Meng.  (2025)  One-dimensional confinement-induced MOF-in-COF layer on polymeric substrate for helium separation.  SEPARATION AND PURIFICATION TECHNOLOGY,  366  (132782). 
23. Zhili Xu, Fan Zhang, Dewei Cheng, Qianyun Ma, Wenxiu Wang, Jie Wang, Jianfeng Sun.  (2025)  Physical stability of oil-in-water multi-layered coenzyme Q10 nano-emulsions.  FOOD CHEMISTRY,  464  (141860). 
24. Ning Xia, Fengli Gao, Gang Liu, Yong Chang, Lin Liu.  (2025)  Pyrroloquinoline quinone exhibiting peroxidase-mimicking property for colorimetric assays.  ANALYTICA CHIMICA ACTA,  1335  (343468). 
25. Mengcheng Jin, Tangbin Zou, Hairong Huang, Ming Chen, Haoqi Zou, Baoyan Chen, Chengze Lai, Huawen Li, Peiwen Zhang.  (2024)  The Effect of Coenzyme Q10 Supplementation on Bile Acid Metabolism: Insights from Network Pharmacology, Molecular Docking, and Experimental Validation.  MOLECULAR NUTRITION & FOOD RESEARCH,    (2400147). 

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