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For: Carneiro A, Matos MJ, Uriarte E, Santana L. Trending Topics on Coumarin and Its Derivatives in 2020. Molecules 2021;26:501. [PMID: 33477785 DOI: 10.3390/molecules26020501] [Cited by in Crossref: 38] [Cited by in F6Publishing: 40] [Article Influence: 38.0] [Reference Citation Analysis]
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1 Shakiba S, Shariati S, Wu H, Astete CE, Cueto R, Fini EH, Rodrigues DF, Sabliov CM, Louie SM. Distinguishing nanoparticle drug release mechanisms by asymmetric flow field–flow fractionation. Journal of Controlled Release 2022;352:485-496. [DOI: 10.1016/j.jconrel.2022.10.034] [Reference Citation Analysis]
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12 Korkmaz A. Synthesis, Characterization, ADMET prediction, and Molecular Docking Studies of Novel Coumarin Sulfonate Derivatives. Journal of the Institute of Science and Technology. [DOI: 10.21597/jist.1089701] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
13 Johan AN, Li Y. Development of Photoremovable Linkers as a Novel Strategy to Improve the Pharmacokinetics of Drug Conjugates and Their Potential Application in Antibody–Drug Conjugates for Cancer Therapy. Pharmaceuticals 2022;15:655. [DOI: 10.3390/ph15060655] [Reference Citation Analysis]
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15 Mlakić M, Faraho I, Odak I, Talić S, Vukovinski A, Raspudić A, Bosnar M, Zadravec R, Ratković A, Lasić K, Marinić Ž, Barić D, Škorić I. Synthesis, photochemistry and computational study of novel 1,2,3-triazole heterostilbenes: Expressed biological activity of their electrocyclization photoproducts. Bioorganic Chemistry 2022;121:105701. [DOI: 10.1016/j.bioorg.2022.105701] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
16 Rather IA, Ali R. An Efficient and Versatile Deep Eutectic Solvent-Mediated Green Method for the Synthesis of Functionalized Coumarins. ACS Omega 2022;7:10649-59. [PMID: 35382332 DOI: 10.1021/acsomega.2c00293] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
17 Rashid P, Sanjayan GJ. A multi-purpose synthetic α-amino acid featuring coumarin and ureidopyrimidinone motifs on its backbone: Synthesis and peptide formation. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.153695] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Patil SB. Medicinal significance of novel coumarin analogs: Recent Studies. Results in Chemistry 2022. [DOI: 10.1016/j.rechem.2022.100313] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Mellado M, González C, Mella J, Aguilar LF, Celik I, Borges F, Uriarte E, Delogu G, Viña D, Matos MJ. Coumarin-Resveratrol-Inspired Hybrids as Monoamine Oxidase B Inhibitors: 3-Phenylcoumarin versus trans-6-Styrylcoumarin. Molecules 2022;27:928. [DOI: 10.3390/molecules27030928] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
20 El-mahalawy AM, Abdou MM, Wassel AR. Physical and optoelectronic characteristics of novel low-cost synthesized coumarin dye-based metal-free thin films for light sensing applications. Materials Science in Semiconductor Processing 2022;137:106225. [DOI: 10.1016/j.mssp.2021.106225] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 10.0] [Reference Citation Analysis]
21 Balewski Ł, Szulta S, Jalińska A, Kornicka A. A Mini-Review: Recent Advances in Coumarin-Metal Complexes With Biological Properties. Front Chem 2021;9:781779. [PMID: 34926402 DOI: 10.3389/fchem.2021.781779] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 8.0] [Reference Citation Analysis]
22 Kashirin AO, Krylova IB, Selina EN, Polukeev VA, Zarubina IV, Bychkov ER, Shabanov PD. Antihypoxic effect of new synthetic derivatives of 7-alkoxycoumarin and 4-aminocoumarin in acute hypobaric hypoxia in rats. Rev Clin Pharm Drug Ther 2021;19:413-420. [DOI: 10.17816/rcf194413-420] [Reference Citation Analysis]
23 Khomenko TM, Shtro AA, Galochkina AV, Nikolaeva YV, Petukhova GD, Borisevich SS, Korchagina DV, Volcho KP, Salakhutdinov NF. Monoterpene-Containing Substituted Coumarins as Inhibitors of Respiratory Syncytial Virus (RSV) Replication. Molecules 2021;26:7493. [PMID: 34946573 DOI: 10.3390/molecules26247493] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
24 Skarga VV, Negrebetsky VV, Baukov YI, Malakhov MV. Twice as Nice: The Duff Formylation of Umbelliferone Revised. Molecules 2021;26:7482. [PMID: 34946562 DOI: 10.3390/molecules26247482] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Ortega-Forte E, Rovira A, Gandioso A, Bonelli J, Bosch M, Ruiz J, Marchán V. COUPY Coumarins as Novel Mitochondria-Targeted Photodynamic Therapy Anticancer Agents. J Med Chem 2021;64:17209-20. [PMID: 34797672 DOI: 10.1021/acs.jmedchem.1c01254] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
26 Abdou MM, Abu-Rayyan A, Bedir AG, Abdel-Fattah S, Omar AMA, Ahmed AA, El-Desoky EI, Ghaith EA. 3-(Bromoacetyl)coumarins: unraveling their synthesis, chemistry, and applications. RSC Adv 2021;11:38391-433. [PMID: 35493203 DOI: 10.1039/d1ra05574g] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
27 Maračić S, Grbčić P, Shammugam S, Radić Stojković M, Pavelić K, Sedić M, Kraljević Pavelić S, Raić-Malić S. Amidine- and Amidoxime-Substituted Heterocycles: Synthesis, Antiproliferative Evaluations and DNA Binding. Molecules 2021;26:7060. [PMID: 34834151 DOI: 10.3390/molecules26227060] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Dalpozzo R, Mancuso R. Copper-Catalyzed Synthesis of Coumarins. A Mini-Review. Catalysts 2021;11:1382. [DOI: 10.3390/catal11111382] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Matos MJ. Coumarin and Its Derivatives-Editorial. Molecules 2021;26:6320. [PMID: 34684900 DOI: 10.3390/molecules26206320] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
30 Katopodi A, Tsotsou E, Iliou T, Deligiannidou GE, Pontiki E, Kontogiorgis C, Tsopelas F, Detsi A. Synthesis, Bioactivity, Pharmacokinetic and Biomimetic Properties of Multi-Substituted Coumarin Derivatives. Molecules 2021;26:5999. [PMID: 34641543 DOI: 10.3390/molecules26195999] [Reference Citation Analysis]
31 Sierra EJT, Cordeiro CF, de Figueiredo Diniz L, Caldas IS, Hawkes JA, Carvalho DT. Coumarins as Potential Antiprotozoal Agents: Biological Activities and Mechanism of Action. Rev Bras Farmacogn 2021;31:592-611. [DOI: 10.1007/s43450-021-00169-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
32 Goswami M, Dutta A, Paul P, Nongkhlaw R. Recent Developments on Catalyst‐Free, Visible‐Light‐Triggered Synthesis of Heterocyclic Scaffolds and Their Mechanistic Study. ChemistrySelect 2021;6:9684-700. [DOI: 10.1002/slct.202102696] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
33 Sokol I, Toma M, Krnić M, Macan AM, Drenjančević D, Liekens S, Raić-Malić S, Gazivoda Kraljević T. Transition metal-catalyzed synthesis of new 3-substituted coumarin derivatives as antibacterial and cytostatic agents. Future Med Chem 2021;13:1865-84. [PMID: 34533068 DOI: 10.4155/fmc-2021-0161] [Reference Citation Analysis]
34 Karcz D, Starzak K, Ciszkowicz E, Lecka-Szlachta K, Kamiński D, Creaven B, Jenkins H, Radomski P, Miłoś A, Ślusarczyk L, Matwijczuk A. Novel Coumarin-Thiadiazole Hybrids and Their Cu(II) and Zn(II) Complexes as Potential Antimicrobial Agents and Acetylcholinesterase Inhibitors. Int J Mol Sci 2021;22:9709. [PMID: 34575894 DOI: 10.3390/ijms22189709] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
35 Niinivehmas S, Pentikäinen OT. Coumarins as Tool Compounds to Aid the Discovery of Selective Function Modulators of Steroid Hormone Binding Proteins. Molecules 2021;26:5142. [PMID: 34500576 DOI: 10.3390/molecules26175142] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
36 Serdyukov A, Kosenko I, Druzina A, Grin M, Mironov AF, Bregadze VI, Laskova J. Anionic polyhedral boron clusters conjugates with 7-diethylamino-4-hydroxycoumarin. Synthesis and lipophilicity determination. Journal of Organometallic Chemistry 2021;946-947:121905. [DOI: 10.1016/j.jorganchem.2021.121905] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
37 Konkoľová E, Hudáčová M, Hamuľaková S, Jendželovský R, Vargová J, Ševc J, Fedoročko P, Kožurková M. Tacrine-Coumarin Derivatives as Topoisomerase Inhibitors with Antitumor Effects on A549 Human Lung Carcinoma Cancer Cell Lines. Molecules 2021;26:1133. [PMID: 33672694 DOI: 10.3390/molecules26041133] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
38 Mathivanan M, Tharmalingam B, Anitha O, Lin C, Thiagarajan V, Murugesapandian B. All-in-one type ESIPT-active multi-stimuli responsive 7-diethylamino-4-hydroxycoumarin-rhodamine B hydrazone as molecular switches and the reversible photochromic features of its zinc ensemble. Mater Chem Front 2021;5:8183-96. [DOI: 10.1039/d1qm00782c] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
39 Tan L, Liang D, Cheng Y, Xiao W, Chen J. Visible-light-induced tandem radical addition/cyclization of 2-alkenylphenols and CBr 4 for the synthesis of 4-arylcoumarins. Org Chem Front 2021;8:5052-7. [DOI: 10.1039/d1qo00831e] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]