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Cited by in F6Publishing
For: Wang X, Wei W, Wang P, Yi L, Shi W, Xie Y, Wu L, Tang N, Zhu L, Peng J, Liu C, Li X, Tang S, Xiao Z, Zhu H. Synthesis, molecular docking and biological evaluation of 3-arylfuran-2(5H)-ones as anti-gastric ulcer agent. Bioorganic & Medicinal Chemistry 2015;23:4860-5. [DOI: 10.1016/j.bmc.2015.05.026] [Cited by in Crossref: 18] [Cited by in F6Publishing: 15] [Article Influence: 2.6] [Reference Citation Analysis]
Number Citing Articles
1 Wusiman W, Zhang Z, Ding Q, Liu M. The pathophyiological role of aminoacyl-tRNA synthetases in digestive system diseases. Front Physiol 2022;13:935576. [DOI: 10.3389/fphys.2022.935576] [Reference Citation Analysis]
2 Liu ML, Li WY, Fang HL, Ye YX, Li SY, Song WQ, Xiao ZP, Ouyang H, Zhu HL. Synthesis and Biological Evaluation of Dithiobisacetamides as Novel Urease Inhibitors. ChemMedChem 2021. [PMID: 34687265 DOI: 10.1002/cmdc.202100618] [Reference Citation Analysis]
3 Ghobadi E, Ghanbarimasir Z, Emami S. A review on the structures and biological activities of anti-Helicobacter pylori agents. Eur J Med Chem 2021;223:113669. [PMID: 34218084 DOI: 10.1016/j.ejmech.2021.113669] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Choo JPS, Kammerer RA, Li X, Li Z. High‐Level Production of Phenylacetaldehyde using Fusion‐Tagged Styrene Oxide Isomerase. Adv Synth Catal 2021;363:1714-21. [DOI: 10.1002/adsc.202001500] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
5 Ni WW, Fang HL, Ye YX, Li WY, Yuan CP, Li DD, Mao SJ, Li SE, Zhu QH, Ouyang H, Xiao ZP, Zhu HL. N-monosubstituted thiosemicarbazide as novel Ure inhibitors: synthesis, biological evaluation and molecular docking. Future Med Chem 2020;12:1633-45. [PMID: 32892642 DOI: 10.4155/fmc-2020-0048] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Ferri M, Alunno M, Greco FA, Mammoli A, Saluti G, Carotti A, Sardella R, Macchiarulo A, Camaioni E, Liscio P. Fragment based drug design and diversity-oriented synthesis of carboxylic acid isosteres. Bioorg Med Chem 2020;28:115731. [PMID: 33007550 DOI: 10.1016/j.bmc.2020.115731] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Li WY, Ni WW, Ye YX, Fang HL, Pan XM, He JL, Zhou TL, Yi J, Liu SS, Zhou M, Xiao ZP, Zhu HL. N-monoarylacetothioureas as potent urease inhibitors: synthesis, SAR, and biological evaluation. J Enzyme Inhib Med Chem 2020;35:404-13. [PMID: 31880473 DOI: 10.1080/14756366.2019.1706503] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 3.5] [Reference Citation Analysis]
8 Shahbazi-alavi H, Khojasteh-khosro S, Safaei-ghomi J, Nazemzadeh SH. Sonosynthesis of furan-2(5H)-ones using nanosilica-tethered polyhedral oligomeric silsesquioxanes. J IRAN CHEM SOC 2019;16:2433-40. [DOI: 10.1007/s13738-019-01711-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
9 Husain A, Khan SA, Iram F, Iqbal MA, Asif M. Insights into the chemistry and therapeutic potential of furanones: A versatile pharmacophore. European Journal of Medicinal Chemistry 2019;171:66-92. [DOI: 10.1016/j.ejmech.2019.03.021] [Cited by in Crossref: 15] [Cited by in F6Publishing: 8] [Article Influence: 5.0] [Reference Citation Analysis]
10 Bao L, Wang S, Song D, Wang J, Cao X, Ke S. Synthesis and Bio-Evaluation of Natural Butenolides-Acrylate Conjugates. Molecules 2019;24:E1304. [PMID: 30987115 DOI: 10.3390/molecules24071304] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
11 Chu Y, Wang T, Ge X, Yang P, Li W, Zhao J, Zhu H. Synthesis, characterization and biological evaluation of naproxen Cu(II) complexes. Journal of Molecular Structure 2019;1178:564-9. [DOI: 10.1016/j.molstruc.2018.10.068] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
12 Liu Q, Ni W, Li Z, Bai C, Tan D, Pu C, Zhou D, Tian Q, Luo N, Tan K, Dai L, Yan Y, Pei Y, Li X, Xiao Z, Zhu H. Resolution and evaluation of 3-chlorophenyl-3-hydroxypropionylhydroxamic acid as antivirulence agent with excellent eradication efficacy in Helicobacter pylori infected mice. European Journal of Pharmaceutical Sciences 2018;121:293-300. [DOI: 10.1016/j.ejps.2018.05.029] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
13 Liu Q, Shi W, Ren S, Ni W, Li W, Chen H, Liu P, Yuan J, He X, Liu J, Cao P, Yang P, Xiao Z, Zhu H. Arylamino containing hydroxamic acids as potent urease inhibitors for the treatment of Helicobacter pylori infection. European Journal of Medicinal Chemistry 2018;156:126-36. [DOI: 10.1016/j.ejmech.2018.06.065] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 3.0] [Reference Citation Analysis]
14 Ni W, Liu Q, Ren S, Li W, Yi L, Jing H, Sheng L, Wan Q, Zhong P, Fang H, Ouyang H, Xiao Z, Zhu H. The synthesis and evaluation of phenoxyacylhydroxamic acids as potential agents for Helicobacter pylori infections. Bioorganic & Medicinal Chemistry 2018;26:4145-52. [DOI: 10.1016/j.bmc.2018.07.003] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
15 Wu S, Zhou Y, Seet D, Li Z. Regio- and Stereoselective Oxidation of Styrene Derivatives to Arylalkanoic Acids via One-Pot Cascade Biotransformations. Adv Synth Catal 2017;359:2132-41. [DOI: 10.1002/adsc.201700416] [Cited by in Crossref: 26] [Cited by in F6Publishing: 14] [Article Influence: 5.2] [Reference Citation Analysis]
16 Wei W, Liu Q, Li Z, Shi W, Fu X, Liu J, Zhu X, Wang X, Xu N, Li T, Jiang F, Xiao Z, Zhu H. Synthesis and evaluation of adenosine containing 3-arylfuran-2(5 H )-ones as tyrosyl-tRNA synthetase inhibitors. European Journal of Medicinal Chemistry 2017;133:62-8. [DOI: 10.1016/j.ejmech.2017.03.074] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
17 Safaei-ghomi J, Hatami A, Shahbazi-alavi H. A Highly Flexible Green Synthesis of 3,4,5-Substituted Furan-2(5 H )-ones Using Nano-CdZr 4 (PO 4 ) 6 as Catalyst under Microwave Irradiation. Polycyclic Aromatic Compounds 2017;37:407-14. [DOI: 10.1080/10406638.2015.1129975] [Cited by in Crossref: 3] [Article Influence: 0.5] [Reference Citation Analysis]
18 Manchoju A, Pansare SV. Catalytic Undirected Intermolecular C–H Functionalization of Arenes with 3-Diazofuran-2,4-dione: Synthesis of 3-Aryl Tetronic Acids, Vulpinic Acid, Pinastric Acid, and Methyl Isoxerocomate. Org Lett 2016;18:5952-5. [DOI: 10.1021/acs.orglett.6b03087] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 1.7] [Reference Citation Analysis]
19 Ali SM, Siddiqui R, Ong SK, Shah MR, Anwar A, Heard PJ, Khan NA. Identification and characterization of antibacterial compound(s) of cockroaches (Periplaneta americana). Appl Microbiol Biotechnol 2017;101:253-86. [PMID: 27743045 DOI: 10.1007/s00253-016-7872-2] [Cited by in Crossref: 33] [Cited by in F6Publishing: 33] [Article Influence: 5.5] [Reference Citation Analysis]
20 Shi W, Deng R, Wang P, Yue Q, Liu Q, Ding K, Yang M, Zhang H, Gong S, Deng M, Liu W, Feng Q, Xiao Z, Zhu H. 3-Arylpropionylhydroxamic acid derivatives as Helicobacter pylori urease inhibitors: Synthesis, molecular docking and biological evaluation. Bioorganic & Medicinal Chemistry 2016;24:4519-27. [DOI: 10.1016/j.bmc.2016.07.052] [Cited by in Crossref: 27] [Cited by in F6Publishing: 24] [Article Influence: 4.5] [Reference Citation Analysis]