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For: De Almeida Barros TA, De Freitas LAR, Filho JMB, Nunes XP, Giulietti AM, De Souza GE, Dos Santos RR, Soares MBP, Villarreal CF. Antinociceptive and anti-inflammatory properties of 7-hydroxycoumarin in experimental animal models: potential therapeutic for the control of inflammatory chronic pain. Journal of Pharmacy and Pharmacology 2010;62:205-13. [DOI: 10.1211/jpp.62.02.0008] [Cited by in Crossref: 43] [Cited by in F6Publishing: 42] [Article Influence: 3.6] [Reference Citation Analysis]
Number Citing Articles
1 Zagaja M, Zagaja A, Szala-Rycaj J, Szewczyk A, Lemieszek MK, Raszewski G, Andres-Mach M. Influence of Umbelliferone on the Anticonvulsant and Neuroprotective Activity of Selected Antiepileptic Drugs: An In Vivo and In Vitro Study. Int J Mol Sci 2022;23:3492. [PMID: 35408852 DOI: 10.3390/ijms23073492] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Channabasappa V, Kumara K, Kariyappa AK. Design, synthesis of coumarin tethered 1,2,3-triazoles analogues, evaluation of their antimicrobial and α-amylase inhibition activities. J Chem Sci 2021;133. [DOI: 10.1007/s12039-021-01997-0] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
3 Cai L, Zong P, Zhou MY, Liu FY, Meng B, Liu MM, Li Z, Li R. 7-Hydroxycoumarin mitigates the severity of collagen-induced arthritis in rats by inhibiting proliferation and inducing apoptosis of fibroblast-like synoviocytes via suppression of Wnt/β-catenin signaling pathway. Phytomedicine 2021;94:153841. [PMID: 34752968 DOI: 10.1016/j.phymed.2021.153841] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
4 Kaur T, Singh D, Pathak D, Singh AP, Singh B. Umbelliferone attenuates glycerol-induced myoglobinuric acute kidney injury through peroxisome proliferator-activated receptor-γ agonism in rats. J Biochem Mol Toxicol 2021;35:e22892. [PMID: 34409680 DOI: 10.1002/jbt.22892] [Reference Citation Analysis]
5 Sharma P, Singh M, Mathew B. An Update of Synthetic Approaches and Structure‐Activity Relationships of Various Classes of Human MAO‐B Inhibitors. ChemistrySelect 2021;6:1404-29. [DOI: 10.1002/slct.202004188] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Chandrakar K, Patel JL, Mahapatra SP, Penta S. Recent Advances in On-Water Multicomponent Synthesis of Coumarin Derivatives. COC 2020;24:2601-11. [DOI: 10.2174/1385272824999201013164825] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
7 Zhang H, Li Q, Yin Y, Kim JK, Huang M, Li Y, Wu Y. The light “on-off” stepwise one-pot method for 3,4-diaryl coumarins with potential AIE properties. Tetrahedron 2020;76:131677. [DOI: 10.1016/j.tet.2020.131677] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
8 Zhang S, Tan X, Liang C, Zhang W. Design, synthesis, and antifungal evaluation of novel coumarin‐pyrrole hybrids. J Heterocyclic Chem 2021;58:450-8. [DOI: 10.1002/jhet.4180] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
9 Darweesh AF, Salama SK, Abdelhamid IA, Elwahy AHM. Bis(aldehydes): Versatile precursors for novel bis ( 14 H ‐dibenzo[ a , j ]xanthenes), bis (pyrano[3,2‐ c :5,6‐ c ']dichromenedione), and bis (dihydrobenzo[ a ]xanthenones) via multicomponent reactions. J Heterocyclic Chem 2021;58:315-28. [DOI: 10.1002/jhet.4170] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
10 Shahraki J, Rezaee R, Mohammadzehi Kenar S, Setoodeh Nezhad S, Bagheri G, Jahantigh H, Tsarouhas K, Hashemzaei M. Umbelliprenin relieves paclitaxel-induced neuropathy. J Pharm Pharmacol 2020;72:1822-9. [PMID: 32930406 DOI: 10.1111/jphp.13365] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
11 Alves QL, Moraes RDA, Froes TQ, Castilho MS, Aquino de Araújo RS, Barbosa-Filho JM, Meira CS, Pereira Soares MB, Silva DF. Inhibition of intracellular Ca2+ mobilization and potassium channels activation are involved in the vasorelaxation induced by 7-hydroxycoumarin. Eur J Pharmacol 2020;887:173525. [PMID: 32889064 DOI: 10.1016/j.ejphar.2020.173525] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Santos DS, Lauria PSS, Evangelista AF, Azeredo FJ, Costa JAV, Soares MBP, Druzian JI, Villarreal CF. Beyond inflammation: Centrally mediated antinociceptive properties of Spirulina platensis LEB-18 biomass via the opioid system. Journal of Functional Foods 2020;72:104083. [DOI: 10.1016/j.jff.2020.104083] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
13 Pires CT, Scodro RB, Cortez DA, Brenzan MA, Siqueira VL, Caleffi-Ferracioli KR, Vieira LC, Monteiro JL, Corrêa AG, Cardoso RF. Structure-activity relationship of natural and synthetic coumarin derivatives against Mycobacterium tuberculosis. Future Med Chem 2020;12:1533-46. [PMID: 32820960 DOI: 10.4155/fmc-2018-0281] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
14 Shaikh S, Pavale G, Ramana MMV. Synthesis and biological evaluation of novel N-substituted (3-(1-aminoethylidene)-2-oxochroman-4-yl)phosphonic acid diethyl ester derivatives as anti-Alzheimer agent. Chem Pap 2020;74:2555-71. [DOI: 10.1007/s11696-020-01099-0] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Regal MKA, Shaban SS, El-metwally SA. Synthesis and Antimicrobial Activity of Some New Coumarin and Dicoumarol Derivatives. Russ J Bioorg Chem 2020;46:438-47. [DOI: 10.1134/s1068162020030176] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
16 Pasricha S, Gahlot P. Synthetic Strategies and Biological Potential of Coumarin-Chalcone Hybrids: A New Dimension to Drug Design. COC 2020;24:402-38. [DOI: 10.2174/1385272824666200219091830] [Reference Citation Analysis]
17 Regal MK, Shaban SS, El‐metwally SA. Synthesis and antimicrobial activity of some new coumarin and dicoumarol derivatives. J Heterocyclic Chem 2020;57:1368-78. [DOI: 10.1002/jhet.3873] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Lee B, Yeom M, Shim I, Lee H, Hahm D. Umbelliferone modulates depression-like symptoms by altering monoamines in a rat post-traumatic stress disorder model. J Nat Med 2020;74:377-86. [DOI: 10.1007/s11418-019-01373-w] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
19 Abreu LS, Alves IM, Espírito Santo RFD, Nascimento YMD, Dantas CAG, Dos Santos GGL, Le Hyaric M, Guedes MLS, da Silva MS, Villarreal CF, Velozo EDS, Tavares JF. Antinociceptive compounds and LC-DAD-ESIMSn profile from Dictyoloma vandellianum leaves. PLoS One 2019;14:e0224575. [PMID: 31661523 DOI: 10.1371/journal.pone.0224575] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.7] [Reference Citation Analysis]
20 Kwak SC, Baek JM, Lee CH, Yoon KH, Lee MS, Kim JY. Umbelliferone Prevents Lipopolysaccharide-Induced Bone Loss and Suppresses RANKL-Induced Osteoclastogenesis by Attenuating Akt-c-Fos-NFATc1 Signaling. Int J Biol Sci 2019;15:2427-37. [PMID: 31595160 DOI: 10.7150/ijbs.28609] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
21 Perumal R, Bathrinarayanan B, Ghashang M, Mansoor SS. An Efficient One‐Pot Synthesis of 7,7‐Dimethyl‐2‐(2‐oxo‐2 H ‐chromen‐3‐yl)‐4‐aryl‐7,8‐dihydroquinolin‐5(6 H )‐one Derivatives Using Chitosan–SO 3 H as Biodegradable Organocatalyst. J Heterocyclic Chem 2019;56:947-55. [DOI: 10.1002/jhet.3473] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 1.3] [Reference Citation Analysis]
22 Yusufzai SK, Khan MS, Sulaiman O, Osman H, Lamjin DN. Molecular docking studies of coumarin hybrids as potential acetylcholinesterase, butyrylcholinesterase, monoamine oxidase A/B and β-amyloid inhibitors for Alzheimer's disease. Chem Cent J 2018;12:128. [PMID: 30515636 DOI: 10.1186/s13065-018-0497-z] [Cited by in Crossref: 18] [Cited by in F6Publishing: 24] [Article Influence: 4.5] [Reference Citation Analysis]
23 Rahimi S, Khoee S, Ghandi M. Development of photo and pH dual crosslinked coumarin-containing chitosan nanoparticles for controlled drug release. Carbohydrate Polymers 2018;201:236-45. [DOI: 10.1016/j.carbpol.2018.08.074] [Cited by in Crossref: 19] [Cited by in F6Publishing: 24] [Article Influence: 4.8] [Reference Citation Analysis]
24 Taha M, Adnan Ali Shah S, Afifi M, Imran S, Sultan S, Rahim F, Hadiani Ismail N, Mohammed Khan K. Synthesis, molecular docking study and thymidine phosphorylase inhibitory activity of 3-formylcoumarin derivatives. Bioorganic Chemistry 2018;78:17-23. [DOI: 10.1016/j.bioorg.2018.02.028] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
25 Ashok D, Gundu S, Aamate VK, Devulapally MG, Bathini R, Manga V. Dimers of coumarin-1,2,3-triazole hybrids bearing alkyl spacer: Design, microwave-assisted synthesis, molecular docking and evaluation as antimycobacterial and antimicrobial agents. Journal of Molecular Structure 2018;1157:312-21. [DOI: 10.1016/j.molstruc.2017.12.080] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 6.0] [Reference Citation Analysis]
26 Sasaki T, Moriyama K, Togo H. One-pot preparation of 4-aryl-3-bromocoumarins from 4-aryl-2-propynoic acids with diaryliodonium salts, TBAB, and Na2S2O8. Beilstein J Org Chem 2018;14:345-53. [PMID: 29507639 DOI: 10.3762/bjoc.14.22] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
27 Sharma A, Gudala S, Ambati SR, Penta S, Bomma Y, Janapala VR, Jha A, Kumar A. Synthesis, Anticancer Evaluation, and Molecular Docking Studies of Novel (4-Hydroxy-2-Thioxo-3,4-Dihydro-2 H -[1,3]Thiazin-6-Yl)-Chromen-2-Ones via a Multicomponent Approach. Journal of the Chinese Chemical Society 2018;65:810-21. [DOI: 10.1002/jccs.201700340] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 3.5] [Reference Citation Analysis]
28 Liao M, Diao X, Cheng X, Sun Y, Zhang L. Nontargeted SWATH acquisition mode for metabolites identification of osthole in rats using ultra-high-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry. RSC Adv 2018;8:14925-35. [DOI: 10.1039/c8ra01221k] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
29 Subramaniam SR, Ellis EM. Umbelliferone and esculetin protect against N-nitrosodiethylamine-induced hepatotoxicity in rats: Umbelliferone and esculetin protect against liver toxicity. Cell Biol Int 2016;40:761-9. [DOI: 10.1002/cbin.10611] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 2.7] [Reference Citation Analysis]
30 Medina FG, Marrero JG, Macías-Alonso M, González MC, Córdova-Guerrero I, Teissier García AG, Osegueda-Robles S. Coumarin heterocyclic derivatives: chemical synthesis and biological activity. Nat Prod Rep 2015;32:1472-507. [PMID: 26151411 DOI: 10.1039/c4np00162a] [Cited by in Crossref: 252] [Cited by in F6Publishing: 253] [Article Influence: 36.0] [Reference Citation Analysis]
31 Yin D, Liu Y, Wang T, Hu Z, Qu W, Chen J, Cheng N, Huang Z. Paeoniflorin exerts analgesic and hypnotic effects via adenosine A1 receptors in a mouse neuropathic pain model. Psychopharmacology 2016;233:281-93. [DOI: 10.1007/s00213-015-4108-6] [Cited by in Crossref: 24] [Cited by in F6Publishing: 28] [Article Influence: 3.4] [Reference Citation Analysis]
32 Roussaki M, Zelianaios K, Kavetsou E, Hamilakis S, Hadjipavlou-Litina D, Kontogiorgis C, Liargkova T, Detsi A. Structural modifications of coumarin derivatives: Determination of antioxidant and lipoxygenase (LOX) inhibitory activity. Bioorg Med Chem 2014;22:6586-94. [PMID: 25456384 DOI: 10.1016/j.bmc.2014.10.008] [Cited by in Crossref: 40] [Cited by in F6Publishing: 43] [Article Influence: 5.7] [Reference Citation Analysis]
33 Emami S, Dadashpour S. Current developments of coumarin-based anti-cancer agents in medicinal chemistry. European Journal of Medicinal Chemistry 2015;102:611-30. [DOI: 10.1016/j.ejmech.2015.08.033] [Cited by in Crossref: 252] [Cited by in F6Publishing: 255] [Article Influence: 36.0] [Reference Citation Analysis]
34 Keri RS, Sasidhar BS, Nagaraja BM, Santos MA. Recent progress in the drug development of coumarin derivatives as potent antituberculosis agents. Eur J Med Chem 2015;100:257-69. [PMID: 26112067 DOI: 10.1016/j.ejmech.2015.06.017] [Cited by in Crossref: 123] [Cited by in F6Publishing: 115] [Article Influence: 17.6] [Reference Citation Analysis]
35 Liu YY, Yin D, Chen L, Qu WM, Chen CR, Laudon M, Cheng NN, Urade Y, Huang ZL. Piromelatine exerts antinociceptive effect via melatonin, opioid, and 5HT1A receptors and hypnotic effect via melatonin receptors in a mouse model of neuropathic pain. Psychopharmacology (Berl) 2014;231:3973-85. [PMID: 24700387 DOI: 10.1007/s00213-014-3530-5] [Cited by in Crossref: 24] [Cited by in F6Publishing: 27] [Article Influence: 3.0] [Reference Citation Analysis]
36 Sarithakumari C, Kurup GM. Alginic acid isolated from Sargassum wightii exhibits anti-inflammatory potential on type II collagen induced arthritis in experimental animals. International Immunopharmacology 2013;17:1108-15. [DOI: 10.1016/j.intimp.2013.09.012] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
37 Patil PO, Bari SB, Firke SD, Deshmukh PK, Donda ST, Patil DA. A comprehensive review on synthesis and designing aspects of coumarin derivatives as monoamine oxidase inhibitors for depression and Alzheimer’s disease. Bioorganic & Medicinal Chemistry 2013;21:2434-50. [DOI: 10.1016/j.bmc.2013.02.017] [Cited by in Crossref: 132] [Cited by in F6Publishing: 133] [Article Influence: 14.7] [Reference Citation Analysis]
38 Cavalcante-Silva LH, da Matta CB, de Araújo MV, Barbosa-Filho JM, de Lira DP, de Oliveira Santos BV, de Miranda GE, Alexandre-Moreira MS. Antinociceptive and anti-inflammatory activities of crude methanolic extract of red alga Bryothamnion triquetrum. Mar Drugs 2012;10:1977-92. [PMID: 23118715 DOI: 10.3390/md10091977] [Cited by in Crossref: 16] [Cited by in F6Publishing: 10] [Article Influence: 1.6] [Reference Citation Analysis]
39 Anand P, Singh B, Singh N. A review on coumarins as acetylcholinesterase inhibitors for Alzheimer's disease. Bioorg Med Chem 2012;20:1175-80. [PMID: 22257528 DOI: 10.1016/j.bmc.2011.12.042] [Cited by in Crossref: 305] [Cited by in F6Publishing: 309] [Article Influence: 27.7] [Reference Citation Analysis]
40 Qin P, Ma T, Wu L, Shan F, Ren G. Identification of tartary buckwheat tea aroma compounds with gas chromatography-mass spectrometry. J Food Sci 2011;76:S401-7. [PMID: 22417522 DOI: 10.1111/j.1750-3841.2011.02223.x] [Cited by in Crossref: 37] [Cited by in F6Publishing: 37] [Article Influence: 3.4] [Reference Citation Analysis]
41 de Lima FO, Nonato FR, Couto RD, Barbosa Filho JM, Nunes XP, Ribeiro dos Santos R, Soares MBP, Villarreal CF. Mechanisms Involved in the Antinociceptive Effects of 7-Hydroxycoumarin. J Nat Prod 2011;74:596-602. [DOI: 10.1021/np100621c] [Cited by in Crossref: 30] [Cited by in F6Publishing: 30] [Article Influence: 2.7] [Reference Citation Analysis]
42 Corsi L, Zavatti M, Geminiani E, Zanoli P, Baraldi M. Anti-inflammatory activity of the non-peptidyl low molecular weight radical scavenger IAC in carrageenan-induced oedema in rats. J Pharm Pharmacol. 2011;63:417-422. [PMID: 21749390 DOI: 10.1111/j.2042-7158.2010.01233.x] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 0.9] [Reference Citation Analysis]