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For: Hao M, Li Y, Liu L, Yuan X, Gao Y, Guan Z, Li W. The design and synthesis of a novel compound of berberine and baicalein that inhibits the efficacy of lipid accumulation in 3T3-L1 adipocytes. Bioorganic & Medicinal Chemistry 2017;25:5506-12. [DOI: 10.1016/j.bmc.2017.08.013] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Tian J, Jin Y, Yu E, Sun J, Xia Y, Zhang K, Li Z, Gong W, Wang G, Xie J. Intestinal farnesoid X receptor mediates the effect of dietary berberine on lipid accumulation in grass carp (Ctenopharyngodon idella). Aquaculture 2022;553:738055. [DOI: 10.1016/j.aquaculture.2022.738055] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
2 Meenu MT, Cherian AR, Sherin DR, Nair AR, Manojkumar TK, Radhakrishnan KV, Varghese A. A protoberberine alkaloid based ratiometric pH-responsive probe for the detection of diabetic ketoacidosis. Dyes and Pigments 2021;194:109636. [DOI: 10.1016/j.dyepig.2021.109636] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
3 Xu Y, Yu T, Ma G, Zheng L, Jiang X, Yang F, Wang Z, Li N, He Z, Song X, Wen D, Kong J, Yu Y, Cao L. Berberine modulates deacetylation of PPARγ to promote adipose tissue remodeling and thermogenesis via AMPK/SIRT1 pathway. Int J Biol Sci 2021;17:3173-87. [PMID: 34421358 DOI: 10.7150/ijbs.62556] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
4 Li DD, Yu P, Xiao W, Wang ZZ, Zhao LG. Berberine: A Promising Natural Isoquinoline Alkaloid for the Development of Hypolipidemic Drugs. Curr Top Med Chem 2020;20:2634-47. [PMID: 32901585 DOI: 10.2174/1568026620666200908165913] [Cited by in Crossref: 6] [Cited by in F6Publishing: 9] [Article Influence: 6.0] [Reference Citation Analysis]
5 Gaba S, Saini A, Singh G, Monga V. An insight into the medicinal attributes of berberine derivatives: A review. Bioorg Med Chem 2021;38:116143. [PMID: 33848698 DOI: 10.1016/j.bmc.2021.116143] [Cited by in Crossref: 6] [Cited by in F6Publishing: 25] [Article Influence: 6.0] [Reference Citation Analysis]
6 Baradaran Rahimi V, Askari VR, Hosseinzadeh H. Promising influences of Scutellaria baicalensis and its two active constituents, baicalin, and baicalein, against metabolic syndrome: A review. Phytother Res 2021;35:3558-74. [PMID: 33590943 DOI: 10.1002/ptr.7046] [Cited by in Crossref: 2] [Cited by in F6Publishing: 11] [Article Influence: 2.0] [Reference Citation Analysis]
7 Li DD, Yu P, Wang ZZ, Xiao W, Zhou XH, Zhao LG. Discovery of 7,9-Disulfatetrahydroberberine as Novel Lipid-Lowering Agents. ACS Omega 2020;5:30836-48. [PMID: 33324793 DOI: 10.1021/acsomega.0c03253] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
8 Li G, Wang T, Zhang X, Zhao S, Wang Y, Wu J, Peng S, Zhao M. Development of 13-Cys-BBR as an Agent Having Dual Action of Anti-Thrombosis and Anti-Inflammation. Drug Des Devel Ther 2020;14:2187-97. [PMID: 32581515 DOI: 10.2147/DDDT.S249228] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Asbaghi O, Ghanbari N, Shekari M, Reiner Ž, Amirani E, Hallajzadeh J, Mirsafaei L, Asemi Z. The effect of berberine supplementation on obesity parameters, inflammation and liver function enzymes: A systematic review and meta-analysis of randomized controlled trials. Clin Nutr ESPEN 2020;38:43-9. [PMID: 32690176 DOI: 10.1016/j.clnesp.2020.04.010] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
10 Habtemariam S. The Quest to Enhance the Efficacy of Berberine for Type-2 Diabetes and Associated Diseases: Physicochemical Modification Approaches. Biomedicines 2020;8:E90. [PMID: 32325761 DOI: 10.3390/biomedicines8040090] [Cited by in Crossref: 4] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
11 Fang P, Yu M, Shi M, Bo P, Gu X, Zhang Z. Baicalin and its aglycone: a novel approach for treatment of metabolic disorders. Pharmacol Rep 2020;72:13-23. [PMID: 32016847 DOI: 10.1007/s43440-019-00024-x] [Cited by in Crossref: 19] [Cited by in F6Publishing: 28] [Article Influence: 9.5] [Reference Citation Analysis]
12 Li G, Ren Y, Zhang X, Zhao S, Wang Y, Wu J, Peng S, Zhao M. 13-[CH2CO-Cys-(Bzl)-OBzl]-Berberine: Exploring The Correlation Of Anti-Tumor Efficacy With ROS And Apoptosis Protein. Onco Targets Ther 2019;12:10651-62. [PMID: 31824172 DOI: 10.2147/OTT.S231035] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
13 Payab M, Hasani-Ranjbar S, Baeeri M, Rahimifard M, Arjmand B, Haghi-Aminjan H, Abdollahi M, Larijani B. Development of a Novel Anti-Obesity Compound with Inhibiting Properties on the Lipid Accumulation in 3T3-L1 Adipocytes. Iran Biomed J 2020;24:155-63. [PMID: 31952433 [PMID: 31952433 DOI: 10.29252/ibj.24.3.155] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
14 Yuan F, Wang D, Ma L, Qin X, Gong J, Hu M, Su H, Dong H, Lu F. Effects of Huanglian-Renshen-Decoction, a Fixed Mixture of Traditional Chinese Medicine, on the Improvement of Glucose Metabolism by Maintenance of Pancreatic β Cell Identity in db/db Mice. Evid Based Complement Alternat Med 2019;2019:1232913. [PMID: 31015847 DOI: 10.1155/2019/1232913] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
15 Qiu R, Luo G, Cai X, Liu L, Chen M, Chen D, You Q, Xiang H. Structure-guided design and synthesis of isoflavone analogs of GW4064 with potent lipid accumulation inhibitory activities. Bioorganic & Medicinal Chemistry Letters 2018;28:3726-30. [DOI: 10.1016/j.bmcl.2018.10.021] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
16 Luo G, Qian Z, Qiu R, You Q, Xiang H. Lipid reducing activity of novel cholic acid (CA) analogs: Design, synthesis and preliminary mechanism study. Bioorg Chem 2018;80:396-407. [PMID: 29986186 DOI: 10.1016/j.bioorg.2018.07.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
17 Gu Z, Wu L, Duan Y, Wang J, Zhou S, Li J, Chen K, Li J, Liu H. Design, synthesis, and structure-activity relationships of novel 4,7,12,12a-tetrahydro-5H-thieno[3′,2′:3,4]pyrido[1,2-b]isoquinoline and 5,8,12,12a-tetrahydro-6H-thieno[2′,3′:4,5]pyrido[2,1-a]isoquinoline derivatives as cellular activators of adenosine 5′-monophosphate-activated protein kinase (AMPK). Bioorganic & Medicinal Chemistry 2018;26:2017-27. [DOI: 10.1016/j.bmc.2018.02.052] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
18 Tsai FJ, Li TM, Cheng CF, Wu YC, Lai CH, Ho TJ, Liu X, Tsang H, Lin TH, Liao CC, Huang SM, Li JP, Lin JC, Lin CC, Liang WM, Lin YJ. Effects of Chinese herbal medicine on hyperlipidemia and the risk of cardiovascular disease in HIV-infected patients in Taiwan. J Ethnopharmacol 2018;219:71-80. [PMID: 29530610 DOI: 10.1016/j.jep.2018.03.006] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]