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Cited by in F6Publishing
For: Peng Y, Zhao S, Wu Y, Cao H, Xu Y, Liu X, Shui W, Cheng J, Zhao S, Shen L, Ma J, Quinn RJ, Stevens RC, Zhong G, Liu ZJ. Identification of natural products as novel ligands for the human 5-HT2C receptor. Biophys Rep 2018;4:50-61. [PMID: 29577069 DOI: 10.1007/s41048-018-0047-1] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Mao Q, Zhang B, Tian S, Qin W, Chen J, Huang X, Xin Y, Yang H, Zhen X, Shui W, Ye N. Structural optimizations and bioevaluation of N-H aporphine analogues as Gq-biased and selective serotonin 5-HT2C receptor agonists. Bioorganic Chemistry 2022. [DOI: 10.1016/j.bioorg.2022.105795] [Reference Citation Analysis]
2 Yuen H, Hung A, Yang AWH, Lenon GB. Mechanisms of Action of Cassiae Semen for Weight Management: A Computational Molecular Docking Study of Serotonin Receptor 5-HT2C. Int J Mol Sci 2020;21:E1326. [PMID: 32079105 DOI: 10.3390/ijms21041326] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
3 Lu Y, Liu H, Yang D, Zhong L, Xin Y, Zhao S, Wang MW, Zhou Q, Shui W. Affinity Mass Spectrometry-Based Fragment Screening Identified a New Negative Allosteric Modulator of the Adenosine A2A Receptor Targeting the Sodium Ion Pocket. ACS Chem Biol 2021;16:991-1002. [PMID: 34048655 DOI: 10.1021/acschembio.0c00899] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
4 Chung JY, Jeong JH, Song J. Resveratrol Modulates the Gut-Brain Axis: Focus on Glucagon-Like Peptide-1, 5-HT, and Gut Microbiota. Front Aging Neurosci 2020;12:588044. [PMID: 33328965 DOI: 10.3389/fnagi.2020.588044] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
5 Bruder M, Polo G, Trivella DBB. Natural allosteric modulators and their biological targets: molecular signatures and mechanisms. Nat Prod Rep 2020;37:488-514. [PMID: 32048675 DOI: 10.1039/c9np00064j] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
6 Xia L, Ma Z, Tong J, Tang Y, Li S, Qin S, Lou R, Zhao S, Lei X, Shui W. Evaluation of chemical cross-linkers for in-depth structural analysis of G protein-coupled receptors through cross-linking mass spectrometry. Analytica Chimica Acta 2020;1102:53-62. [DOI: 10.1016/j.aca.2019.12.036] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Hothersall JD, Jones AY, Dafforn TR, Perrior T, Chapman KL. Releasing the technical 'shackles' on GPCR drug discovery: opportunities enabled by detergent-free polymer lipid particle (PoLiPa) purification. Drug Discov Today 2020:S1359-6446(20)30337-8. [PMID: 32835806 DOI: 10.1016/j.drudis.2020.08.006] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
8 Kirchweger B, Rollinger JM. A Strength-Weaknesses-Opportunities-Threats (SWOT) Analysis of Cheminformatics in Natural Product Research. Prog Chem Org Nat Prod 2019;110:239-71. [PMID: 31621015 DOI: 10.1007/978-3-030-14632-0_7] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Veeramachaneni GK, Thunuguntla VBSC, Bhaswant M, Mathai ML, Bondili JS. Pharmacophore Directed Screening of Agonistic Natural Molecules Showing Affinity to 5HT2C Receptor. Biomolecules 2019;9:E556. [PMID: 31581577 DOI: 10.3390/biom9100556] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
10 Motevalli SM, Eltahan AS, Liu L, Magrini A, Rosato N, Guo W, Bottini M, Liang X. Co-encapsulation of curcumin and doxorubicin in albumin nanoparticles blocks the adaptive treatment tolerance of cancer cells. Biophys Rep 2019;5:19-30. [DOI: 10.1007/s41048-018-0079-6] [Cited by in Crossref: 24] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
11 Mao Q, Zhang B, Li W, Tian S, Shui W, Ye N. Identification of Novel 1-O-Substituted Aporphine Analogues as Potent 5-HT2C Receptor Agonists. ACS Chem Neurosci 2020;11:549-59. [PMID: 31968160 DOI: 10.1021/acschemneuro.9b00563] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
12 Zhang B, Zhao S, Yang D, Wu Y, Xin Y, Cao H, Huang X, Cai X, Sun W, Ye N, Xu Y, Peng Y, Zhao S, Liu Z, Zhong G, Wang M, Shui W. A Novel G Protein-Biased and Subtype-Selective Agonist for a G Protein-Coupled Receptor Discovered from Screening Herbal Extracts. ACS Cent Sci 2020;6:213-25. [DOI: 10.1021/acscentsci.9b01125] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
13 Garcia CS, Besckow EM, da Silva Espíndola CN, D'Avila Nunes G, Zuge NP, de Azeredo MP, Rocha MJD, Carraro Junior LR, Penteado F, Gomes CS, Lenardão EJ, Bortolatto CF, Brüning CA. Antidepressant-Like Effect of a Selenoindolizine in Mice: In Vivo and In Silico Evidence for the Involvement of the Serotonergic 5-HT2A/C Receptors. ACS Chem Neurosci 2022. [PMID: 35605134 DOI: 10.1021/acschemneuro.2c00129] [Reference Citation Analysis]
14 Xu Y, Sromek AW, Neumeyer JL. Identification of fluorinated (R)-(−)-aporphine derivatives as potent and selective ligands at serotonin 5-HT2C receptor. Bioorganic & Medicinal Chemistry Letters 2019;29:230-3. [DOI: 10.1016/j.bmcl.2018.11.050] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Pawłowicz K, Sip S, Plech T, Kaproń B, Kobus-cisowska J, Cielecka-piontek J. Aloe arborescens: In Vitro Screening of Genotoxicity, Effective Inhibition of Enzyme Characteristics for Disease Etiology, and Microbiological Activity. Molecules 2022;27:2323. [DOI: 10.3390/molecules27072323] [Reference Citation Analysis]