Icariin - ≥96% , CAS No.489-32-7

CAS: 489-32-7 Cat. No.: I141014 Peso molecular: 676.66 Número EC: 610-440-0 PubChem CID: 5318997
Disponible para pedir
GRADE & PURITY ≥96%
Synonyms
3-((6-Deoxymannopyranosyl)oxy)-7-(glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one | 5-HYDROXY-2-(4-METHOXYPHENYL)-8-(3-METHYLBUT-2-EN-1-YL)-7-{[3,4,5-TRIHYDROXY-6-(HYDROXYMETHYL)OXAN-2-YL]OXY}-3-[(3,4,5-TRIHYD
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
250mg
I141014-250mg
7
10,90US$
1g
I141014-1g
10
26,90US$
5g
I141014-5g
2
120,90US$
25g
I141014-25g
1
479,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥96% 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 38 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
3-((6-Deoxymannopyranosyl)oxy)-7-(glucopyranosyloxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one | 5-HYDROXY-2-(4-METHOXYPHENYL)-8-(3-METHYLBUT-2-EN-1-YL)-7-{[3, 4, 5-TRIHYDROXY-6-(HYDROXYMETHYL)OXAN-2-YL]OXY}-3-[(3, 4, 5-TRIHYD
Especificaciones y pureza
≥96%
Mecanismos bioquímicos y fisiológicos
Selective cGMP specific PDE5 inhibitor (IC 50 = 0.4 and 74 μM for PDE5 and PDE4 respectively). Shows anti-inflammatory and antitumor effects in vivo . Orally active.
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Nota
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.
Pureza
≥96%
Nombres e identificadores
Pubchem Sid488195337
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488195337
Sonrisas canónicasCOc1ccc(cc1)C2=C(O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)C(=O)c4c(O)cc(O[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)c(C\C=C(\C)C)c4O2
IUPAC Name5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
InChIKeyTZJALUIVHRYQQB-XLRXWWTNSA-N
INCHI1S/C33H40O15/c1-13(2)5-10-17-19(45-33-28(42)26(40)23(37)20(12-34)46-33)11-18(35)21-24(38)31(48-32-27(41)25(39)22(36)14(3)44-32)29(47-30(17)21)15-6-8-16(43-4)9-7-15/h5-9,11,14,20,22-23,25-28,32-37,39-42H,10,12H2,1-4H3/t14-,20+,22-,23+,25+,26-,27+,28+,32-,33+/m0/s1
Isómeros SMILES C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O
WGK Alemania 3
PubChem CID 5318997
Peso molecular 676.66

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
ClaseFlavonoids
SubclassFlavonoid glycosides
Intermediate Tree Nodes Flavonoid O-glycosides
Direct ParentFlavonoid-7-O-glycosides
Alternative Parents 8-prenylated flavones  Flavonoid-3-O-glycosides  4'-O-methylated flavonoids  5-hydroxyflavonoids  Phenolic glycosides  Chromones  O-glycosyl compounds  Anisoles  Methoxybenzenes  Phenoxy compounds  1-hydroxy-2-unsubstituted benzenoids  Alkyl aryl ethers  Pyranones and derivatives  Monosaccharides  Oxanes  Vinylogous acids  Heteroaromatic compounds  Secondary alcohols  Polyols  Acetals  Oxacyclic compounds  Hydrocarbon derivatives  Primary alcohols  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents 8-prenylated flavone - Flavonoid-3-o-glycoside - Flavonoid-7-o-glycoside - 4p-methoxyflavonoid-skeleton - Hydroxyflavonoid - Flavone - 5-hydroxyflavonoid - Phenolic glycoside - Glycosyl compound - O-glycosyl compound - Chromone - Benzopyran - 1-benzopyran - Methoxybenzene - Phenol ether - Phenoxy compound - Anisole - Alkyl aryl ether - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Pyran - Monosaccharide - Oxane - Benzenoid - Heteroaromatic compound - Vinylogous acid - Secondary alcohol - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Ether - Organic oxide - Organic oxygen compound - Primary alcohol - Alcohol - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.
External Descriptors Flavones and Flavonols
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLB Tchem DNA polymerase beta (23632 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM1A Tchem Lysine-specific histone demethylase 1 (3916 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
IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic (40980 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
PDE6C Phosphodiesterase 6C (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 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.

28 results found

Lot NumberCertificate TypeFechaArticulo
D2607408Certificate of AnalysisJun 09, 2026 I141014
D2607407Certificate of AnalysisJun 09, 2026 I141014
D2607406Certificate of AnalysisJun 09, 2026 I141014
D2607405Certificate of AnalysisJun 09, 2026 I141014
L2509104Certificate of AnalysisAug 18, 2025 I141014
H2511399Certificate of AnalysisAug 18, 2025 I141014
H2511398Certificate of AnalysisAug 18, 2025 I141014
H2511397Certificate of AnalysisAug 18, 2025 I141014
H2511396Certificate of AnalysisAug 18, 2025 I141014
L2420771Certificate of AnalysisJan 04, 2025 I141014
L2420770Certificate of AnalysisJan 04, 2025 I141014
E2409238Certificate of AnalysisOct 25, 2024 I141014
E2409237Certificate of AnalysisOct 25, 2024 I141014
E2409236Certificate of AnalysisOct 25, 2024 I141014
A2403397Certificate of AnalysisJan 10, 2024 I141014
D2429035Certificate of AnalysisJan 09, 2024 I141014
A2403401Certificate of AnalysisJan 09, 2024 I141014
A2403402Certificate of AnalysisJan 09, 2024 I141014
D2328291Certificate of AnalysisAug 14, 2023 I141014
D2328286Certificate of AnalysisAug 14, 2023 I141014
D2328287Certificate of AnalysisAug 14, 2023 I141014
D2328288Certificate of AnalysisAug 14, 2023 I141014
D2328290Certificate of AnalysisAug 14, 2023 I141014
E2304051Certificate of AnalysisMay 10, 2023 I141014
E2304011Certificate of AnalysisMay 10, 2023 I141014
A2306218Certificate of AnalysisJan 11, 2023 I141014
C2204417Certificate of AnalysisMar 10, 2022 I141014
C2204421Certificate of AnalysisMar 10, 2022 I141014

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Propiedades químicas y físicas
SensibilidadHeat Sensitive
Rotación específica [α]-84° (C=1,Pyridine)
Punto de fusión (°C)235 - 239°C
Peso molecular676.700 g/mol
XLogP31.700
Hydrogen Bond Donor Count8
Hydrogen Bond Acceptor Count15
Rotatable Bond Count9
Exact Mass676.237 Da
Monoisotopic Mass676.237 Da
Topological Polar Surface Area234.000 Ų
Heavy Atom Count48
Formal Charge0
Complexity1170.000
Isotope Atom Count0
Defined Atom Stereocenter Count10
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
Referencias
1. Bin Wang, Yanbin Zhao, Yangyang Li, Chengliang Tang, Peng He, Xiaowei Liu, Junyan Yao, Chenglin Chu, Bin Xu.  (2023)  NIR-responsive injectable magnesium phosphate bone cement loaded with icariin promotes osteogenesis.  Journal of the Mechanical Behavior of Biomedical Materials,      [PMID:38048713] [10.1016/j.jmbbm.2023.106256]
2. Jia Ji, Zhao Xing-an, Tao Si-ming, Wang Jun-wen, Zhang Rong-liang, Dai Hua-lei, Zhang Xin-jin, Han Ming-hua, Yang Bei, Li Yu, Li Jin-tao.  (2023)  Icariin improves cardiac function and remodeling via the TGF-β1/Smad signaling pathway in rats following myocardial infarction.  EUROPEAN JOURNAL OF MEDICAL RESEARCH,  28  (1): (1-12).  [PMID:38115154] [10.1186/s40001-023-01588-4]
3. Jinping Wang, Lingrong Wen, Yueming Jiang, Hong Zhu, Weizheng Sun, Guangyi Dai, Bao Yang.  (2023)  Structure, bioavailability and physicochemical properties of icariin-soymilk nanoparticle.  Food Science and Human Wellness,      [PMID:] [10.26599/FSHW.2022.9250083]
4. Wanwu Dai, Pan Jin, Xingyan Li, Jinmin Zhao, Ying Lan, Hongmian Li, Li Zheng.  (2023)  A carrier-free nano-drug assembled via π–π stacking interaction for the treatment of osteoarthritis.  BIOMEDICINE & PHARMACOTHERAPY,      [PMID:37210895] [10.1016/j.biopha.2023.114881]
5. Lin Yu, Chen Wen-wen, Ding Bo, Guo Man, Liang Meng, Pang Hao, Wei Yu-tuo, Huang Ri-bo, Du Li-qin.  (2023)  Highly efficient bioconversion of icariin to icaritin by whole-cell catalysis.  Microbial Cell Factories,  22  (1): (1-11).  [PMID:37016390] [10.1186/s12934-023-02068-4]
6. Simin Deng, Yuan Xu, Binbin Gao, Tingting Yu, Lun Kuang, Bo’ang Han, Shaolun Feng, Haodong Chi, Qing Cao, Shen Yue, Chen Liu.  (2023)  Anemarrhenasaponin I suppresses ovarian cancer progression via inhibition of SHH signaling pathway.  Oncologie,  25  (3): (233-243).  [PMID:] [10.1515/oncologie-2022-1001]
7. Yang Du, Fengjiao Zhao, Junpeng Xing, Zhiqiang Liu, Meng Cui.  (2023)  Stabilization of Labile Lysozyme–Ligand Interactions in Native Electrospray Ionization Mass Spectrometry.  JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY,      [PMID:36735536] [10.1021/jasms.2c00238]
8. Ruiyi Fan, Congyi Zhu, Diyang Qiu, Genlin Mao, Bernd Mueller-Roeber, Jiwu Zeng.  (2023)  Integrated transcriptomic and metabolomic analyses reveal key genes controlling flavonoid biosynthesis in Citrus grandis ‘Tomentosa’ fruits.  PLANT PHYSIOLOGY AND BIOCHEMISTRY,      [PMID:36724705] [10.1016/j.plaphy.2023.01.050]
9. Yu Li-Ming, Dong Xue, Huang Tao, Zhao Ji-Kai, Zhou Zi-Jun, Huang Yu-Ting, Xu Yin-Li, Zhao Qiu-Sheng, Wang Zhi-Shang, Jiang Hui, Yin Zong-Tao, Wang Hui-Shan.  (2023)  Inhibition of ferroptosis by icariin treatment attenuates excessive ethanol consumption-induced atrial remodeling and susceptibility to atrial fibrillation, role of SIRT1.  APOPTOSIS,  28  (3): (607-626).  [PMID:36708428] [10.1007/s10495-023-01814-8]
10. LI Gang, GE Xiaohong.  (2023)  Interaction mechanism of icariin and whey protein based on spectrofluorimetry and molecular docking.  Food Science and Technology,      [PMID:] [10.1590/fst.102822]
11. Jinping Wang, Hong Zhu, Yueming Jiang, Jianbo Xiao, Bao Yang, Lingrong Wen.  (2022)  Fabrication of icariin-soymilk nanoparticles with ultrasound-assisted treatment.  ULTRASONICS SONOCHEMISTRY,      [PMID:36436486] [10.1016/j.ultsonch.2022.106230]
12. Li-Ming Yu, Xue Dong, Yin-Li Xu, Zi-Jun Zhou, Yu-Ting Huang, Ji-Kai Zhao, Deng-Yue Xu, Xiao-Dong Xue, Qiu-Sheng Zhao, Tao Liu, Zong-Tao Yin, Hui Jiang, Hui-Shan Wang.  (2022)  Icariin attenuates excessive alcohol consumption-induced susceptibility to atrial fibrillation through SIRT3 signaling.  BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE,      [PMID:35798229] [10.1016/j.bbadis.2022.166483]
13. Cui Zhanding, Wang Qian, Li Dengliang, Zhao Shihui, Zhang Qian, Tan Yuxin, Gong Qianwen, Liu Ting, Shao Jiang, Zhang Shuang, Huang Hailong, Wang Junzheng, Pei Zhihua, Dong Hao, Wang Kai, Hu Guixue, Li Zhiyong.  (2021)  Icariin, Formononetin and Caffeic Acid Phenethyl Ester Inhibit Feline Calicivirus Replication In Vitro.  ARCHIVES OF VIROLOGY,  166  (9): (2443-2450).  [PMID:34173062] [10.1007/s00705-021-05107-w]
14. Li Chunyang, Yang Shuangqing, Ma Huaqing, Ruan Mengjia, Fang Luyan, Cheng Jing.  (2021)  Influence of icariin on inflammation, apoptosis, invasion, and tumor immunity in cervical cancer by reducing the TLR4/MyD88/NF-κB and Wnt/β-catenin pathways.  Cancer Cell International,  21  (1): (1-14).  [PMID:33849528] [10.1186/s12935-021-01910-2]
15. Xiaoang Li, Imran Khan, Wenrui Xia, Guoxin Huang, Liang Liu, Betty Yuen Kwan Law, Lin Yin, Weilin Liao, Waikit Leong, Ruixuan Han, Vincent Kam Wai Wong, Chenglai Xia, Xiaoling Guo, W.L. Wendy Hsiao.  (2021)  Icariin enhances youth-like features by attenuating the declined gut microbiota in the aged mice.  PHARMACOLOGICAL RESEARCH,      [PMID:33798737] [10.1016/j.phrs.2021.105587]
16. Yanzheng Xie, Lei Xie, Ailan Chen, Shengnan Wu, Yuxiao Mo, Xiaoqiang Guo, Changchun Zeng, Xinan Huang, Jinyang He.  (2020)  Anti-HIV/SIV activity of icariin and its metabolite anhydroicaritin mainly involve reverse transcriptase.  EUROPEAN JOURNAL OF PHARMACOLOGY,      [PMID:32726656] [10.1016/j.ejphar.2020.173327]
17. Wenbin Hua, Shuai Li, Rongjin Luo, Xinghuo Wu, Yukun Zhang, Zhiwei Liao, Yu Song, Kun Wang, Kangcheng Zhao, Shuhua Yang, Cao Yang.  (2019)  Icariin protects human nucleus pulposus cells from hydrogen peroxide-induced mitochondria-mediated apoptosis by activating nuclear factor erythroid 2-related factor 2.  BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE,      [PMID:31666206] [10.1016/j.bbadis.2019.165575]
18. Yuanlong Xie, Wenchao Sun, Feifei Yan, Huowen Liu, Zhouming Deng, Lin Cai.  (2019)  Icariin-loaded porous scaffolds for bone regeneration through the regulation of the coupling process of osteogenesis and osteoclastic activity.  International Journal of Nanomedicine,      [PMID:31534334] [10.2147/IJN.S203859]
19. Zhou Mengmeng, Jiang Zehua, Zhang Maosen, Feng Sa, Ma Boyuan, Kan Shunli, Fu Xuanhao, Zhu Rusen.  (2025)  Exploring the molecular mechanism of icariin improving spinal cord injury through network pharmacology combined with experimental verification.  NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY,      [PMID:40014127] [10.1007/s00210-025-03904-7]
20. Nannan Ding, Shanyue Sun, Shuting Zhou, Zhimei Lv, Rong Wang.  (2024)  Icariin alleviates renal inflammation and tubulointerstitial fibrosis via Nrf2-mediated attenuation of mitochondrial damage.  CELL BIOCHEMISTRY AND FUNCTION,  42  (3): (e4005).  [PMID:38583082] [10.1002/cbf.4005]
21. Huizhen Tian, Qigang Pan, Jianfeng Wu, Juanjuan Liao, Yuwei Wan, Ke Pei, Qiong Liu, Lingbing Zeng, Yanli Cao, Qiaofa shi, Nanzhen Kuang, LiJuan Sun, Xiaomin Yu, Xiaotian Huang.  (2024)  Icariin ameliorates Coxsackievirus B3-induced viral myocarditis by modulating the S100 calcium binding protein A6/β-catenin/c-Myc signaling pathway.  PHYTOMEDICINE,      [PMID:39522251] [10.1016/j.phymed.2024.156214]
22. Wang Haoyue, Sun Kexiang, Tan Wei Shan, Gao Jiamin, Yuan Luyun, Wen Junkai, Deng Wanli.  (2024)  Icariin promoted ferroptosis by activating mitochondrial dysfunction to inhibit colorectal cancer and synergistically enhanced the efficacy of PD-1 inhibitors.  PHYTOMEDICINE,      [PMID:39642461] [10.1016/j.phymed.2024.156224]
23. Feng Sa, Liu Linyan, Cheng Yuelin, Zhou Mengmeng, Zhu Haoqiang, Zhao Xinyan, Chen Ziyu, Kan Shunli, Fu Xuanhao, Hu Wei, Zhu Rusen.  (2024)  Icariin promotes functional recovery in rats after spinal cord injury by inhibiting YAP and regulating PPM1B ubiquitination to inhibiting the activation of reactive astrocytes.  Frontiers in Pharmacology,      [PMID:39439899] [10.3389/fphar.2024.1434652]
24. Song Wang, Xinnan Chang, Jing Li, Zuoqiao Shi, Guowen Li.  (2025)  Identification of chemical components and metabolites in rats after oral administration of Epimedium-Astragalus granule pair by liquid chromatography-high resolution mass spectrometry combined with diagnostic fragment ions and mass defect filtering.  JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS,      [PMID:40014893] [10.1016/j.jpba.2025.116768]
25. Jiaojiao Ding, Tiexiang Gao, Songlin Liu, Zhezhe Li, Baifei Hu, Junping Zhen, Xiaowei Yao, Hongtao Liu, Haiming Hu.  (2025)  Rhamnosidase from Parabacteroides distasonis exhibit the catabolism of epimedin C in the human gut microbiota.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40157660] [10.1016/j.ijbiomac.2025.142481]
26. Jiayi Zhang, Jingzhi Wang, Junfeng Wang, Weifeng Ni, Shichao Liu, Daqing Zhao, Zhengqi Dong, Shiting Yu, Siming Wang, Weinan Wang, Meichen Liu.  (2025)  Integrated multi-omics and machine learning reveal the intrinsic relationship between color and flavor variations in processed ginseng products through major pigment dynamics and non-enzymatic pathways.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2025.118161]
27. Yimin Sun, Xuetao Yang, Yin Liu, Chenxi Zhang, Huiyu Feng, Dongdong Wu, Ling Ye, Fanyuan Yu, Feifei Li.  (2025)  Adaptive Cationic Peptide Bundles Hydrogel for the Repair of Infected Mandibular Defects.  BIOMATERIALS,      [PMID:40818323] [10.1016/j.biomaterials.2025.123613]
28. Qingdi Qu, Qian Zhang, Mengyuan Wang, Shuang Zhao, Ping Li, Chenxi Shang, Yumei Niu, Shuang Zhang, Shuang Pan.  (2025)  Study on the effect of sustained -release icariin-loaded Graphene oxide-hydrogel composite scaffold on bone defect repair.  Biomedical Physics & Engineering Express,  11  (5): (055018).  [PMID:40774284] [10.1088/2057-1976/adf8ee]
29. Hongxia Fan, Jiansong Zhao, Zhencheng Gao, Yinling Mu, Xiaoman Zhang, Wanbing Pan, Sishu Li, Haibing He, Jingxin Gou, Xing Tang, Tian Yin, Yu Zhang.  (2025)  Injectable self-healing hydrogel loaded PLGA nanoparticles for long-term osteoarthritis therapy.  Biomaterials Advances,      [PMID:41005083] [10.1016/j.bioadv.2025.214506]
30. Han Yan, Yuhao Liao, Weixiong Chen, Junnan Luo, Dongdong Li, Jilong Wang, Faxin Liu.  (2025)  Bone-targeted nanomedicine based on red blood cell membrane-coated polymeric carriers for effective osteoporosis reversal.  JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.jddst.2025.107063]
31. Wei Hu, Chen Li, Chenguang Wang, Wei Liu, Chuntong Li, Lihua Mu, Kun Wang, Mengli Chen.  (2025)  Exploring the therapeutic mechanism of Miao nationality medicine Qijiao Shengbai capsule on leukopenia based on multi-omics, network pharmacology and experimental verification.  PHYTOMEDICINE,      [PMID:40513324] [10.1016/j.phymed.2025.156935]
32. Wei Yusen, Mao Jiangdi, Tang Wenjie, Ma Yanfei, Li Jiachen, Su Songtao, Ni Zhixiang, Wu Jinhong, Liu Daren, Wang Haifeng.  (2025)  Targeting Catenibacterium mitsuokai with icariin modulates gut microbiota and improves hepatic lipid metabolism in intrauterine growth restriction.  ISME Journal,      [PMID:40607758] [10.1093/ismejo/wraf141]
33. Yongbin Wang, Han Zhang, Zhili Xu, Weihang Zhu, Sheng Chang, Jiahao Wei, Shuqing Chen, Yong Liu, Weiqing Kong, Jianwei Guo.  (2025)  Icariin-loaded GelMa Hydrogel Encapsulated Potassium Sodium Niobate Biomimetic Piezoelectric Scaffold Regulates Macrophage Polarization to Accelerate Bone Defect Repair.  Materials Today Bio,      [PMID:41281663] [10.1016/j.mtbio.2025.102476]
34. Yongmei Chen, Qingwen Wei, Jing Wang, Chuanyao Huang, Zhenghao Wang, Yuchun Liu.  (2025)  Studies on the Flavonoid Composition of Pleioblastus amarus Leaves and Shoots Based on Targeted Metabolomics.  Metabolites,  15  (11): (709).  [PMID:41295295] [10.3390/metabo15110709]
35. Jingfeng Sun, Jinying Li, Peining She, Yang Xiao, Tao Zhang, Guorui Li, Jiaming Ye, Zhanlun Ou, Jianghao Bi, Shaochuan Li.  (2025)  Polydopamine coating for anchoring icariin-regulated CF/PEEK with enhanced cytocompatibility and osteogenic activity.  Journal of Materials Chemistry B,      [PMID:41246930] [10.1039/D5TB02014J]
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