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For: 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]
Number Citing Articles
1 Ali G, Cuny GD. An efficient synthesis of an 8-phenoxy aporphine derivative utilizing mono-ligated palladium ortho-phenol arylation. Tetrahedron 2019;75:4318-24. [DOI: 10.1016/j.tet.2019.04.011] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 2.7] [Reference Citation Analysis]
2 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]
3 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]
4 Karki A, Juarez R, Namballa HK, Alberts I, Harding WW. Identification of C10 nitrogen-containing aporphines with dopamine D1 versus D5 receptor selectivity. Bioorg Med Chem Lett 2020;30:127053. [PMID: 32107165 DOI: 10.1016/j.bmcl.2020.127053] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
5 Lv J, Li ZH, Deng AJ, Qin HL. A unified total synthesis of benzo[d][1,3]dioxole-type benzylisoquinoline alkaloids of aporphines, coptisines, and dibenzopyrrocolines. Org Biomol Chem 2021. [PMID: 34951439 DOI: 10.1039/d1ob02258j] [Reference Citation Analysis]