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For: Qin H, Zhang Z, Ravindar L, Rakesh K. Antibacterial activities with the structure-activity relationship of coumarin derivatives. European Journal of Medicinal Chemistry 2020;207:112832. [DOI: 10.1016/j.ejmech.2020.112832] [Cited by in Crossref: 24] [Cited by in F6Publishing: 43] [Article Influence: 12.0] [Reference Citation Analysis]
Number Citing Articles
1 Liu H, Chen Y, Cui F, Liao Y, Wang X. Synthesis, docking studies, biological activity of carbon monoxide release molecules based on coumarin derivatives. Front Chem 2022;10:996079. [DOI: 10.3389/fchem.2022.996079] [Reference Citation Analysis]
2 Mali G, Maji S, Chavan KA, Shukla M, Kumar M, Bhattacharyya S, Erande RD. Effective Synthesis and Biological Evaluation of Functionalized 2,3-Dihydrofuro[3,2- c ]coumarins via an Imidazole-Catalyzed Green Multicomponent Approach. ACS Omega. [DOI: 10.1021/acsomega.2c05361] [Reference Citation Analysis]
3 Shang H, Hu Y, Li J, Li L, Tian Y, Li X, Wu Q, Zou Z. The Synthesis and Biological Evaluation of Aloe-Emodin-Coumarin Hybrids as Potential Antitumor Agents. Molecules 2022;27:6153. [DOI: 10.3390/molecules27196153] [Reference Citation Analysis]
4 Pérez-anzúrez G, Olmedo-juárez A, von-Son de Fernex E, Alonso-díaz MÁ, Delgado-núñez EJ, López-arellano ME, González-cortázar M, Zamilpa A, Ocampo-gutierrez AY, Paz-silva A, Mendoza-de Gives P. Arthrobotrys musiformis (Orbiliales) Kills Haemonchus contortus Infective Larvae (Trichostronylidae) through Its Predatory Activity and Its Fungal Culture Filtrates. Pathogens 2022;11:1068. [DOI: 10.3390/pathogens11101068] [Reference Citation Analysis]
5 Fetzer DE, Kanda LRS, Xavier LA, da Cruz PN, Errico M, Corazza ML. Lipids and coumarin extraction from cumaru seeds (Dipteryx odorata) using sequential supercritical CO2+solvent and pressurized ethanol. The Journal of Supercritical Fluids 2022;188:105688. [DOI: 10.1016/j.supflu.2022.105688] [Reference Citation Analysis]
6 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]
7 Zhang Y, Tian X, Teng A, Li Y, Jiao Y, Zhao K, Wang Y, Li R, Yang N, Wang W. Polyphenols and polyphenols-based biopolymer materials: Regulating iron absorption and availability from spontaneous to controllable. Critical Reviews in Food Science and Nutrition. [DOI: 10.1080/10408398.2022.2101092] [Reference Citation Analysis]
8 Houshmand A, Heroux D, Liu DY, Zhou W, Linington RG, Bally M, Warren JJ, Walsby CJ. Ferrocene-appended anthraquinone and coumarin as redox-active cytotoxins. Dalton Trans 2022. [PMID: 35822497 DOI: 10.1039/d2dt01251k] [Reference Citation Analysis]
9 Yang X, Hu C, Zhang P, Li S, Hu C, Geng R, Zhou C. Coumarin thiazoles as unique structural skeleton of potential antimicrobial agents. Bioorganic Chemistry 2022;124:105855. [DOI: 10.1016/j.bioorg.2022.105855] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 7.0] [Reference Citation Analysis]
10 Hosseini Nasab N, Azimian F, Kruger HG, Kim SJ. 3‐Bromoacetylcoumarin, a Crucial Key for Facial Synthesis of Biological Active Compounds. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201734] [Reference Citation Analysis]
11 Ragab A, Abusaif MS, Aboul-Magd DS, Wassel MMS, Elhagali GAM, Ammar YA. A new exploration toward adamantane derivatives as potential anti-MDR agents: Design, synthesis, antimicrobial, and radiosterilization activity as potential topoisomerase IV and DNA gyrase inhibitors. Drug Dev Res 2022. [PMID: 35716118 DOI: 10.1002/ddr.21960] [Reference Citation Analysis]
12 Fan X, Song H, Xu X, Lu X, Wang Y, Duan X. Subchronic Oral Toxicity of Sodium p-Hydroxybenzoate in Sprague-Dawley Rats. Front Pharmacol 2022;13:843368. [PMID: 35355716 DOI: 10.3389/fphar.2022.843368] [Reference Citation Analysis]
13 Keri RS, Budagumpi S, Balappa Somappa S. Synthetic and natural coumarins as potent anticonvulsant agents: A review with structure-activity relationship. J Clin Pharm Ther 2022. [PMID: 35288962 DOI: 10.1111/jcpt.13644] [Reference Citation Analysis]
14 Yang X, Zhang P, Kumar KV, Li S, Geng R, Zhou C. Discovery of unique thiazolidinone-conjugated coumarins as novel broad spectrum antibacterial agents. European Journal of Medicinal Chemistry 2022;232:114192. [DOI: 10.1016/j.ejmech.2022.114192] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 10.0] [Reference Citation Analysis]
15 Hamzehniya M, Mobinikhaledi A, Ahadi N, Sameri F. Zn complexed on CaO coated with walnut husk extract as an efficient and reusable catalyst for the green synthesis of benzylpyrazolyl coumarin derivatives. Reac Kinet Mech Cat 2022;135:897-914. [DOI: 10.1007/s11144-022-02186-x] [Reference Citation Analysis]
16 Xiang YZ, Wu G, Yang LY, Yang XJ, Zhang YM, Lin LB, Deng XY, Zhang QL. Antibacterial effect of bacteriocin XJS01 and its application as antibiofilm agents to treat multidrug-resistant Staphylococcus aureus infection. Int J Biol Macromol 2022;196:13-22. [PMID: 34838856 DOI: 10.1016/j.ijbiomac.2021.11.136] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 Pan Y, Liu T, Wang X, Sun J. Research progress of coumarins and their derivatives in the treatment of diabetes. Journal of Enzyme Inhibition and Medicinal Chemistry 2022;37:616-28. [DOI: 10.1080/14756366.2021.2024526] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
18 Horchani M, Edziri H, Harrath AH, Jannet HB, Romdhane A. Access to new Schiff bases tethered with pyrazolopyrimidinone as antibacterial agents: Design and synthesis, molecular docking and DFT analysis. Journal of Molecular Structure 2022;1248:131523. [DOI: 10.1016/j.molstruc.2021.131523] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Behboodyzad F, Mohseniabbasabadi T, Ghanemnia N, Balali E. Structural analysis of dexrazoxane: Exploring tautomeric conformations. MGC 2021. [DOI: 10.3233/mgc-210158] [Reference Citation Analysis]
20 Harismah K, Da’i M, Azimzadeh-sadeghi S, Poursafa P, Mirzaei M, Salarrezaei E. Interactions of coumarin derivatives with monoamine oxidase biomarkers: In silico approach. MGC 2021. [DOI: 10.3233/mgc-210162] [Reference Citation Analysis]
21 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: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
22 Othman IM, Mahross MH, Gad-elkareem MA, Rudrapal M, Gogoi N, Chetia D, Aouadi K, Snoussi M, Kadri A. Toward a treatment of antibacterial and antifungal infections: Design, synthesis and in vitro activity of novel arylhydrazothiazolylsulfonamides analogues and their insight of DFT, docking and molecular dynamic simulations. Journal of Molecular Structure 2021;1243:130862. [DOI: 10.1016/j.molstruc.2021.130862] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 7.0] [Reference Citation Analysis]
23 Sarkar M, Nath A, Kumer A, Mallik C, Akter F, Moniruzzaman M, Ali M. Synthesis, molecular docking screening, ADMET and dynamics studies of synthesized 4-(4-methoxyphenyl)-8-methyl-3,4,5,6,7,8-hexahydroquinazolin-2(1H)-one and quinazolinone derivatives. Journal of Molecular Structure 2021;1244:130953. [DOI: 10.1016/j.molstruc.2021.130953] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
24 Carmel Yesudass S, Ranjan P, Suresh HP. Synthesis, antimicrobial/radical scavenging, and in‐silico investigations of a novel class of 4‐[(4 ‐hydroxymethylphenyl)‐ 1 H ‐1 ,2 ,3 ‐triazol‐1‐yl‐methyl]‐ 2 H ‐chromen‐2‐ones. J Heterocyclic Chem. [DOI: 10.1002/jhet.4385] [Reference Citation Analysis]
25 Ma Y, Yao A, Chen X, Wang L, Ma C, Xi X, Chen T, Shaw C, Zhou M. Generation of truncated derivatives through in silico enzymatic digest of peptide GV30 target MRSA both in vitro and in vivo. Comput Struct Biotechnol J 2021;19:4984-96. [PMID: 34584638 DOI: 10.1016/j.csbj.2021.08.039] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
26 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]
27 Chen K, Wu W, Hou X, Yang Q, Li Z. A review: antimicrobial properties of several medicinal plants widely used in Traditional Chinese Medicine. Food Quality and Safety 2021;5:fyab020. [DOI: 10.1093/fqsafe/fyab020] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
28 Akpunar C, Özdemir N, Karataş MO, Alıcı B, Özdemir İ. Synthesis, crystal structures and catalytic activities of palladium complexes with coumarin-functionalised N-heterocyclic carbene ligands. Inorganic Chemistry Communications 2021;131:108755. [DOI: 10.1016/j.inoche.2021.108755] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
29 Simic M, Petkovic M, Jovanovic P, Jovanovic M, Tasic G, Besu I, Zizak Z, Aleksic I, Nikodinovic-Runic J, Savic V. Fragment-type 4-azolylcoumarin derivatives with anticancer properties. Arch Pharm (Weinheim) 2021;:e2100238. [PMID: 34374111 DOI: 10.1002/ardp.202100238] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
30 Chen YS, Zheng Y, Chen ZJ, Xie ZZ, He XC, Xiao JA, Chen K, Xiang HY, Yang H. A phosphine-catalysed one-pot domino sequence to access cyclopentene-fused coumarins. Org Biomol Chem 2021;19:7074-80. [PMID: 34342319 DOI: 10.1039/d1ob01143j] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
31 Moreira NM, Martelli LSR, Corrêa AG. Asymmetric organocatalyzed synthesis of coumarin derivatives. Beilstein J Org Chem 2021;17:1952-80. [PMID: 34386105 DOI: 10.3762/bjoc.17.128] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
32 Gao L, Wang F, Chen Y, Li F, Han B, Liu D. The antithrombotic activity of natural and synthetic coumarins. Fitoterapia 2021;154:104947. [PMID: 34352355 DOI: 10.1016/j.fitote.2021.104947] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
33 Salem MA, Abbas SY, Helal MH, Alzahrani AY. Synthesis and antimicrobial evaluation of new 2‐pyridinone and 2‐iminochromene derivatives containing morpholine moiety. J Heterocyclic Chem 2021;58:2117-23. [DOI: 10.1002/jhet.4335] [Reference Citation Analysis]
34 Targhi AA, Moammeri A, Jamshidifar E, Abbaspour K, Sadeghi S, Lamakani L, Akbarzadeh I. Synergistic effect of curcumin-Cu and curcumin-Ag nanoparticle loaded niosome: Enhanced antibacterial and anti-biofilm activities. Bioorg Chem 2021;115:105116. [PMID: 34333420 DOI: 10.1016/j.bioorg.2021.105116] [Cited by in F6Publishing: 20] [Reference Citation Analysis]
35 Konidala SK, Kotra V, Danduga RCSR, Kola PK, Bhandare RR, Shaik AB. Design, multistep synthesis and in-vitro antimicrobial and antioxidant screening of coumarin clubbed chalcone hybrids through molecular hybridization approach. Arabian Journal of Chemistry 2021;14:103154. [DOI: 10.1016/j.arabjc.2021.103154] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
36 Verma SK, Verma R, Kumar KSS, Banjare L, Shaik AB, Bhandare RR, Rakesh KP, Rangappa KS. A key review on oxadiazole analogs as potential methicillin-resistant Staphylococcus aureus (MRSA) activity: Structure-activity relationship studies. Eur J Med Chem 2021;219:113442. [PMID: 33878562 DOI: 10.1016/j.ejmech.2021.113442] [Cited by in Crossref: 3] [Cited by in F6Publishing: 17] [Article Influence: 3.0] [Reference Citation Analysis]
37 Badran A, Ibrahim MA, Ahmed A. Nucleophilic reactions with the novel condensation product derived from 3-formylchromone and 4-hydroxycoumarin. Synthetic Communications 2021;51:1868-81. [DOI: 10.1080/00397911.2021.1910961] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
38 Wang H, Zuo J, Zha L, Jiang X, Wu C, Yang YA, Tang W, Shi T. Design and synthesis of novel glycyrrhetin ureas as anti-inflammatory agents for the treatment of acute kidney injury. Bioorg Chem 2021;110:104755. [PMID: 33652342 DOI: 10.1016/j.bioorg.2021.104755] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
39 Al-Khattaf FS, Mani A, Atef Hatamleh A, Akbar I. Antimicrobial and cytotoxic activities of isoniazid connected menthone derivatives and their investigation of clinical pathogens causing infectious disease. J Infect Public Health 2021;14:533-42. [PMID: 33744741 DOI: 10.1016/j.jiph.2020.12.033] [Reference Citation Analysis]
40 Liu J, Wang T, Huang B, Zhuang Y, Hu Y, Fei P. Pectin modified with phenolic acids: Evaluation of their emulsification properties, antioxidation activities, and antibacterial activities. Int J Biol Macromol 2021;174:485-93. [PMID: 33548307 DOI: 10.1016/j.ijbiomac.2021.01.190] [Cited by in F6Publishing: 6] [Reference Citation Analysis]
41 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]
42 Emam SH, Sonousi A, Osman EO, Hwang D, Kim GD, Hassan RA. Design and synthesis of methoxyphenyl- and coumarin-based chalcone derivatives as anti-inflammatory agents by inhibition of NO production and down-regulation of NF-κB in LPS-induced RAW264.7 macrophage cells. Bioorg Chem 2021;107:104630. [PMID: 33476864 DOI: 10.1016/j.bioorg.2021.104630] [Cited by in Crossref: 3] [Cited by in F6Publishing: 18] [Article Influence: 3.0] [Reference Citation Analysis]
43 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]
44 Verma R, Verma SK, Rakesh KP, Girish YR, Ashrafizadeh M, Sharath Kumar KS, Rangappa KS. Pyrazole-based analogs as potential antibacterial agents against methicillin-resistance staphylococcus aureus (MRSA) and its SAR elucidation. Eur J Med Chem 2021;212:113134. [PMID: 33395624 DOI: 10.1016/j.ejmech.2020.113134] [Cited by in Crossref: 9] [Cited by in F6Publishing: 36] [Article Influence: 4.5] [Reference Citation Analysis]
45 Kumar Verma S, Verma R, Xue F, Kumar Thakur P, Girish Y, Rakesh K. Antibacterial activities of sulfonyl or sulfonamide containing heterocyclic derivatives and its structure-activity relationships (SAR) studies: A critical review. Bioorganic Chemistry 2020;105:104400. [DOI: 10.1016/j.bioorg.2020.104400] [Cited by in Crossref: 6] [Cited by in F6Publishing: 21] [Article Influence: 3.0] [Reference Citation Analysis]