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For: Leino TO, Turku A, Yli-kauhaluoma J, Kukkonen JP, Xhaard H, Wallén EA. Azulene-based compounds for targeting orexin receptors. European Journal of Medicinal Chemistry 2018;157:88-100. [DOI: 10.1016/j.ejmech.2018.07.040] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Bakun P, Czarczynska-Goslinska B, Goslinski T, Lijewski S. In vitro and in vivo biological activities of azulene derivatives with potential applications in medicine. Med Chem Res 2021;:1-13. [PMID: 33551629 DOI: 10.1007/s00044-021-02701-0] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
2 Turku A, Leino TO, Karhu L, Yli-Kauhaluoma J, Kukkonen JP, Wallén EAA, Xhaard H. Structure-Activity Relationships of 1-Benzoylazulenes at the OX1 and OX2 Orexin Receptors. ChemMedChem 2019;14:965-81. [PMID: 30892823 DOI: 10.1002/cmdc.201900074] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Williams GE, Kociok-Köhn G, James TD, Lewis SE. C4-aldehyde of guaiazulene: synthesis and derivatisation. Org Biomol Chem 2021;19:2502-11. [PMID: 33661271 DOI: 10.1039/d0ob02567d] [Reference Citation Analysis]
4 Rinne M, Tanoli ZU, Khan A, Xhaard H. Cartography of rhodopsin-like G protein-coupled receptors across vertebrate genomes. Sci Rep 2019;9:7058. [PMID: 31064998 DOI: 10.1038/s41598-018-33120-8] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
5 Leino TO, Sieger P, Yli-kauhaluoma J, Wallén EA, Kley JT. The azulene scaffold from a medicinal chemist's perspective: Physicochemical and in vitro parameters relevant for drug discovery. European Journal of Medicinal Chemistry 2022;237:114374. [DOI: 10.1016/j.ejmech.2022.114374] [Reference Citation Analysis]
6 Carvalho MSS, Andrade-vieira LF, Santos FED, Correa FF, das Graças Cardoso M, Vilela LR. Allelopathic potential and phytochemical screening of ethanolic extracts from five species of Amaranthus spp. in the plant model Lactuca sativa. Scientia Horticulturae 2019;245:90-8. [DOI: 10.1016/j.scienta.2018.10.001] [Cited by in Crossref: 17] [Cited by in F6Publishing: 6] [Article Influence: 5.7] [Reference Citation Analysis]
7 Shoji T, Sugiyama S, Kobayashi Y, Yamazaki A, Ariga Y, Katoh R, Wakui H, Yasunami M, Ito S. Direct synthesis of 2-arylazulenes by [8+2] cycloaddition of 2H-cyclohepta[b]furan-2-ones with silyl enol ethers. Chem Commun (Camb) 2020;56:1485-8. [PMID: 31912824 DOI: 10.1039/c9cc09376a] [Cited by in Crossref: 13] [Cited by in F6Publishing: 4] [Article Influence: 6.5] [Reference Citation Analysis]
8 Dale NC, Hoyer D, Jacobson LH, Pfleger KDG, Johnstone EKM. Orexin Signaling: A Complex, Multifaceted Process. Front Cell Neurosci 2022;16:812359. [DOI: 10.3389/fncel.2022.812359] [Reference Citation Analysis]
9 Kukkonen JP. Allosteric interactions via the orthosteric ligand binding sites in a constitutive G-protein-coupled receptor homodimer. Pharmacol Res 2021;166:105116. [PMID: 32783977 DOI: 10.1016/j.phrs.2020.105116] [Reference Citation Analysis]
10 Fried R, Oprea I, Fleck K, Rudroff F. Biogenic colourants in the textile industry – a promising and sustainable alternative to synthetic dyes. Green Chem 2022;24:13-35. [DOI: 10.1039/d1gc02968a] [Reference Citation Analysis]
11 Giardinetti M, Jessen NI, Christensen ML, Jørgensen KA. Organocatalytic [10+4] cycloadditions for the synthesis of functionalised benzo[ a ]azulenes. Chem Commun 2019;55:202-5. [DOI: 10.1039/c8cc08551j] [Cited by in Crossref: 13] [Cited by in F6Publishing: 3] [Article Influence: 4.3] [Reference Citation Analysis]