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For: Annunziata F, Pinna C, Dallavalle S, Tamborini L, Pinto A. An Overview of Coumarin as a Versatile and Readily Accessible Scaffold with Broad-Ranging Biological Activities. Int J Mol Sci 2020;21:E4618. [PMID: 32610556 DOI: 10.3390/ijms21134618] [Cited by in Crossref: 27] [Cited by in F6Publishing: 52] [Article Influence: 13.5] [Reference Citation Analysis]
Number Citing Articles
1 El-hussieny M, Elmansy MF, Ewies EF, El-rashedy AA, Ibrahim AY, El-sayed NF. Synthesis, biological evaluation, and molecular dynamics of novel coumarin based phosphorothioates as cholinesterase inhibitors. Journal of Molecular Structure 2023;1272:134214. [DOI: 10.1016/j.molstruc.2022.134214] [Reference Citation Analysis]
2 Halit S, Benazzouz-touami A, Makhloufi-chebli M, Bouaziz ST, Ighilahriz K, Robert A, Machado-rodrigues C. Design, Synthesis, Biological evaluation of Isonicotinoyl-pyrazolyl-coumarin derivatives and computational study. Journal of Molecular Structure 2022;1265:133487. [DOI: 10.1016/j.molstruc.2022.133487] [Reference Citation Analysis]
3 Mazur M, Masłowiec D. Antimicrobial Activity of Lactones. Antibiotics 2022;11:1327. [DOI: 10.3390/antibiotics11101327] [Reference Citation Analysis]
4 Thacker PS, Newaskar V, Angeli A, Sigalapalli DK, Goud NS, Chirra H, Shaik AB, Arifuddin M, Supuran CT. Synthesis and biological evaluation of coumarin-thiazole hybrids as selective carbonic anhydrase IX and XII inhibitors. Arch Pharm (Weinheim) 2022;:e2200232. [PMID: 36122182 DOI: 10.1002/ardp.202200232] [Reference Citation Analysis]
5 Topa-Skwarczyńska M, Świeży A, Krok D, Starzak K, Niezgoda P, Oksiuta B, Wałczyk W, Ortyl J. Novel Formulations Containing Fluorescent Sensors to Improve the Resolution of 3D Prints. Int J Mol Sci 2022;23:10470. [PMID: 36142382 DOI: 10.3390/ijms231810470] [Reference Citation Analysis]
6 Liu Y, Su S, Yu M, Zhai D, Hou Y, Zhao H, Ma X, Jia M, Xue X, Li M. Pyrancoumarin derivative LP4C targeting of pyrimidine de novo synthesis pathway inhibits MRSA biofilm and virulence. Front Pharmacol 2022;13:959736. [DOI: 10.3389/fphar.2022.959736] [Reference Citation Analysis]
7 Ji D, Li Q, Yang H, Fan Y, Wang T, Chen Y, Pacheco-fernández I. Determination of Five Coumarins in Angelicae Pubescentis Radix from Different Origins by HPTLC-Scanning. Journal of Analytical Methods in Chemistry 2022;2022:1-7. [DOI: 10.1155/2022/3415938] [Reference Citation Analysis]
8 Dai R, Sun Y, Su R, Gao H. Anti-Alzheimer's disease potential of traditional chinese medicinal herbs as inhibitors of BACE1 and AChE enzymes. Biomed Pharmacother 2022;154:113576. [PMID: 36007279 DOI: 10.1016/j.biopha.2022.113576] [Reference Citation Analysis]
9 Ruiz DM, Pasquale GA, Martínez JJ, Romanelli GP. Advances in novel activation methods to perform green organic synthesis using recyclable heteropolyacid catalysis. Green Processing and Synthesis 2022;11:766-809. [DOI: 10.1515/gps-2022-0068] [Reference Citation Analysis]
10 Patil SA, Kandathil V, Sobha A, Somappa SB, Feldman MR, Bugarin A, Patil SA. Comprehensive Review on Medicinal Applications of Coumarin-Derived Imine–Metal Complexes. Molecules 2022;27:5220. [DOI: 10.3390/molecules27165220] [Reference Citation Analysis]
11 He BT, Liu ZH, Li BZ, Yuan YJ. Advances in biosynthesis of scopoletin. Microb Cell Fact 2022;21:152. [PMID: 35918699 DOI: 10.1186/s12934-022-01865-7] [Reference Citation Analysis]
12 Assel A, Hajlaoui A, Lazrag H, Manachou M, Romdhane A, Kraiem J, Jannet HB. Synthesis of new sulfamate linked 4-hydroxycoumarine conjugates as potent anti-α-amylase agents: In vitro approach coupled with molecular docking, DFT calculation and chemoinformatics prediction. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.134020] [Reference Citation Analysis]
13 Bajalia EM, Azzouz FB, Chism DA, Giansiracusa DM, Wong CG, Plaskett KN, Bishayee A. Phytochemicals for the Prevention and Treatment of Renal Cell Carcinoma: Preclinical and Clinical Evidence and Molecular Mechanisms. Cancers 2022;14:3278. [DOI: 10.3390/cancers14133278] [Reference Citation Analysis]
14 Luo D, Zhang X, Li X, Zhen Y, Zeng X, Xiong Z, Zhang Y, Li H. Responsive Fluorescent Coumarin–Cinnamic Acid Conjugates for α-Glucosidase Detection. Front Chem 2022;10:927624. [DOI: 10.3389/fchem.2022.927624] [Reference Citation Analysis]
15 Kumar S, Saroha B, Kumar G, Lathwal E, Kumar S, Parshad B, Kumari M, Kumar N, Mphahlele-makgwane MM, Makgwane PR. Recent Developments in Nanocatalyzed Green Synthetic Protocols of Biologically Potent Diverse O-Heterocycles—A Review. Catalysts 2022;12:657. [DOI: 10.3390/catal12060657] [Reference Citation Analysis]
16 Natarajan P, Priya, Chuskit D. Persulfate-nitrogen doped graphene mixture as an oxidant for the synthesis of 3-nitro-4-aryl-2H-chromen-2-ones from aryl alkynoate esters and nitrite. Org Biomol Chem 2022;20:4616-24. [PMID: 35608321 DOI: 10.1039/d2ob00827k] [Reference Citation Analysis]
17 Abdou A, Mostafa HM, Abdel-mawgoud AM. Seven metal-based bi-dentate NO azocoumarine complexes: Synthesis, characterization, DFT calculations, Drug-Likeness, in vitro antimicrobial screening and molecular docking analysis. Inorganica Chimica Acta 2022. [DOI: 10.1016/j.ica.2022.121043] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
18 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]
19 Fu Z, Zhang L, Hang S, Wang S, Li N, Sun X, Wang Z, Sheng R, Wang F, Wu W, Guo R. Synthesis of Coumarin Derivatives: A New Class of Coumarin-Based G Protein-Coupled Receptor Activators and Inhibitors. Polymers 2022;14:2021. [DOI: 10.3390/polym14102021] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 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: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Ranđelović S, Bipat R. A Review of Coumarins and Coumarin-Related Compounds for Their Potential Antidiabetic Effect. Clin Med Insights Endocrinol Diabetes 2021;14:11795514211042023. [PMID: 35173509 DOI: 10.1177/11795514211042023] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
22 Qurat-Ul-Ain, Basu A, Choudhary MI, Scharffetter-Kochanek K. 3, 3'- (3, 5-DCPBC) Down-Regulates Multiple Phosphokinase Dependent Signal Transduction Pathways in Malignant Melanoma Cells through Specific Diminution of EGFRY1086 Phosphorylation. Molecules 2022;27:1172. [PMID: 35208960 DOI: 10.3390/molecules27041172] [Reference Citation Analysis]
23 Elleuch S, Ammar H, Abid Y. Spectroscopic and computational studies of the solid state photophysical properties of a biscoumarin dye. Spectrochim Acta A Mol Biomol Spectrosc 2022;266:120466. [PMID: 34637986 DOI: 10.1016/j.saa.2021.120466] [Reference Citation Analysis]
24 Heghes SC, Vostinaru O, Mogosan C, Miere D, Iuga CA, Filip L. Safety Profile of Nutraceuticals Rich in Coumarins: An Update. Front Pharmacol 2022;13:803338. [DOI: 10.3389/fphar.2022.803338] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
25 Kumar P, Tomar V, Kumar D, Joshi RK, Nemiwal M. Magnetically active iron oxide nanoparticles for catalysis of organic transformations: A review. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132641] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
26 Lee S, Kim H, Park E, Kim KJ, Bang M, Kim G, Jeon H, Lee C, Shin M, Kim D, Baek N. Antioxidant and anti-inflammatory effects in lipopolysaccharide-induced THP-1 cells of coumarins from the bark of Hesperethusa crenulata R. Appl Biol Chem 2021;64. [DOI: 10.1186/s13765-021-00665-8] [Reference Citation Analysis]
27 Sarmah M, Chutia K, Dutta D, Gogoi P. Overview of coumarin-fused-coumarins: synthesis, photophysical properties and their applications. Org Biomol Chem 2021;20:55-72. [PMID: 34854447 DOI: 10.1039/d1ob01876k] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
28 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 F6Publishing: 5] [Reference Citation Analysis]
29 Fuentes-Aguilar A, Merino-Montiel P, Montiel-Smith S, Meza-Reyes S, Vega-Báez JL, Puerta A, Fernandes MX, Padrón JM, Petreni A, Nocentini A, Supuran CT, López Ó, Fernández-Bolaños JG. 2-Aminobenzoxazole-appended coumarins as potent and selective inhibitors of tumour-associated carbonic anhydrases. J Enzyme Inhib Med Chem 2022;37:168-77. [PMID: 34894971 DOI: 10.1080/14756366.2021.1998026] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
30 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] [Reference Citation Analysis]
31 Borah B, Dhar Dwivedi K, Chowhan LR. 4‐Hydroxycoumarin: A Versatile Substrate for Transition‐metal‐free Multicomponent Synthesis of Bioactive Heterocycles. Asian J Org Chem 2021;10:3101-26. [DOI: 10.1002/ajoc.202100550] [Cited by in Crossref: 3] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
32 Fakri Mustafa Y, Riyadh Khalil R, Tareq Mohammed E, Bashir MK, Khudhayer Oglah M. Effects of Structural Manipulation on the Bioactivity of some Coumarin-Based Products. Arch Razi Inst 2021;76:1297-305. [PMID: 35355735 DOI: 10.22092/ari.2021.356100.1776] [Reference Citation Analysis]
33 Dorababu A. Pharmacological report of recently designed multifunctional coumarin and coumarin-heterocycle derivatives. Arch Pharm (Weinheim) 2021;:e2100345. [PMID: 34693550 DOI: 10.1002/ardp.202100345] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
34 Kozioł E, Jóźwiak K, Budzyńska B, de Witte PAM, Copmans D, Skalicka-Woźniak K. Comparative Antiseizure Analysis of Diverse Natural Coumarin Derivatives in Zebrafish. Int J Mol Sci 2021;22:11420. [PMID: 34768849 DOI: 10.3390/ijms222111420] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
35 Mohammad A, Mustafa HK. Unsymmetrical Coumarin based dimeric liquid crystals: Synthesis, Characterization, Mesomorphic investigation, Photoluminescence and Thermal conductivity. Liquid Crystals. [DOI: 10.1080/02678292.2021.1970835] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
36 Narayanan M, Krishnan L, Natarajan D, Kandasamy S, El Askary A, Elfasakhany A, Pugazhendhi A. Evaluation of antibacterial, antioxidant, and nephroprotective proficiency of methanol extract of Aerva lanata. Process Biochemistry 2021;109:98-103. [DOI: 10.1016/j.procbio.2021.07.004] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
37 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]
38 Kang JK, Chung YC, Hyun CG. Anti-Inflammatory Effects of 6-Methylcoumarin in LPS-Stimulated RAW 264.7 Macrophages via Regulation of MAPK and NF-κB Signaling Pathways. Molecules 2021;26:5351. [PMID: 34500784 DOI: 10.3390/molecules26175351] [Cited by in F6Publishing: 6] [Reference Citation Analysis]
39 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] [Reference Citation Analysis]
40 Toan VN, Thanh ND. Synthesis and antiproliferative activity of hybrid thiosemicarbazone derivatives bearing coumarin and d-galactose moieties with EGFR inhibitory activity and molecular docking study. Med Chem Res 2021;30:1868-85. [DOI: 10.1007/s00044-021-02773-y] [Reference Citation Analysis]
41 Sun M, Sun M, Zhang J. Osthole: an overview of its sources, biological activities, and modification development. Med Chem Res 2021;:1-28. [PMID: 34376964 DOI: 10.1007/s00044-021-02775-w] [Cited by in F6Publishing: 7] [Reference Citation Analysis]
42 Koyiparambath VP, Prayaga Rajappan K, Rangarajan TM, Al-Sehemi AG, Pannipara M, Bhaskar V, Nair AS, Sudevan ST, Kumar S, Mathew B. Deciphering the detailed structure-activity relationship of coumarins as Monoamine oxidase enzyme inhibitors-An updated review. Chem Biol Drug Des 2021. [PMID: 34233082 DOI: 10.1111/cbdd.13919] [Cited by in F6Publishing: 9] [Reference Citation Analysis]
43 Fiorito S, Epifano F, Marchetti L, Genovese S. Semisynthesis of Selenoauraptene. Molecules 2021;26:2798. [PMID: 34068532 DOI: 10.3390/molecules26092798] [Reference Citation Analysis]
44 Lai Y, Han T, Zhan S, Jiang Y, Liu X, Li G. Antiviral Activity of Isoimperatorin Against Influenza A Virus in vitro and its Inhibition of Neuraminidase. Front Pharmacol 2021;12:657826. [PMID: 33927632 DOI: 10.3389/fphar.2021.657826] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
45 Thacker PS, Tiwari PL, Angeli A, Srikanth D, Swain B, Arifuddin M, Supuran CT. Synthesis and Biological Evaluation of Coumarin-Linked 4-Anilinomethyl-1,2,3-Triazoles as Potent Inhibitors of Carbonic Anhydrases IX and XIII Involved in Tumorigenesis. Metabolites 2021;11:225. [PMID: 33917033 DOI: 10.3390/metabo11040225] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
46 Thacker PS, Srikanth D, Angeli A, Singh P, Chinchilli KK, Arifuddin M, Supuran CT. Coumarin-Thiourea Hybrids Show Potent Carbonic Anhydrase IX and XIII Inhibitory Action. ChemMedChem 2021;16:1252-6. [PMID: 33346945 DOI: 10.1002/cmdc.202000915] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
47 Wu T, Hu D, Wang Q. Noni fruit’s water spot appearance on the second day of harvest: a trade-off between resistance and energy. Chem Biol Technol Agric 2021;8. [DOI: 10.1186/s40538-020-00207-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
48 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: 4] [Cited by in F6Publishing: 29] [Article Influence: 4.0] [Reference Citation Analysis]
49 El-Sawy ER, Abdelwahab AB, Kirsch G. Synthetic Routes to Coumarin(Benzopyrone)-Fused Five-Membered Aromatic Heterocycles Built on the α-Pyrone Moiety. Part 1: Five-Membered Aromatic Rings with One Heteroatom. Molecules 2021;26:483. [PMID: 33477568 DOI: 10.3390/molecules26020483] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
50 Wróblewska-Łuczka P, Grabarska A, Florek-Łuszczki M, Plewa Z, Łuszczki JJ. Synergy, Additivity, and Antagonism between Cisplatin and Selected Coumarins in Human Melanoma Cells. Int J Mol Sci 2021;22:E537. [PMID: 33430369 DOI: 10.3390/ijms22020537] [Cited by in Crossref: 4] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
51 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: 1] [Article Influence: 4.0] [Reference Citation Analysis]
52 G Keller S, Kamiya M, Urano Y. Recent Progress in Small Spirocyclic, Xanthene-Based Fluorescent Probes. Molecules 2020;25:E5964. [PMID: 33339370 DOI: 10.3390/molecules25245964] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
53 Kaur G, Singh D, Singh A, Banerjee B. Camphor sulfonic acid catalyzed facile and general method for the synthesis of 3,3'-(arylmethylene) bis (4-hydroxy-2 H -chromen-2-ones), 3,3'-(arylmethylene) bis (2-hydroxynaphthalene-1,4-diones) and 3,3'-(2-oxoindoline-3,3-diyl) bis (2-hydroxynaphthalene-1,4-dione) derivatives at room temperature. Synthetic Communications 2021;51:1045-57. [DOI: 10.1080/00397911.2020.1856877] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 5.0] [Reference Citation Analysis]
54 Bakos É, Tusnády GE, Német O, Patik I, Magyar C, Németh K, Kele P, Özvegy-Laczka C. Synergistic transport of a fluorescent coumarin probe marks coumarins as pharmacological modulators of Organic anion-transporting polypeptide, OATP3A1. Biochem Pharmacol 2020;182:114250. [PMID: 32991865 DOI: 10.1016/j.bcp.2020.114250] [Cited by in Crossref: 2] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
55 Kang JK, Hyun CG. 4-Hydroxy-7-Methoxycoumarin Inhibits Inflammation in LPS-activated RAW264.7 Macrophages by Suppressing NF-κB and MAPK Activation. Molecules 2020;25:E4424. [PMID: 32993156 DOI: 10.3390/molecules25194424] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]