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For: Wang D, Gao F. Quinazoline derivatives: synthesis and bioactivities. Chem Cent J 2013;7:95. [PMID: 23731671 DOI: 10.1186/1752-153X-7-95] [Cited by in Crossref: 92] [Cited by in F6Publishing: 93] [Article Influence: 10.2] [Reference Citation Analysis]
Number Citing Articles
1 Alharthi AA, Alotaibi M, Shalwi MN, Qahtan TF, Ali I, Alshehri F, Afroz Bakht M. Photocatalytic-driven three-component synthesis of 1,2,3,4-tetrahydropyrimidine-5-carbonitrile derivatives: A comparative study of organocatalysts and photocatalysts. Journal of Photochemistry and Photobiology A: Chemistry 2023;436:114358. [DOI: 10.1016/j.jphotochem.2022.114358] [Reference Citation Analysis]
2 Zayed MF. Medicinal Chemistry of Quinazolines as Analgesic and Anti-Inflammatory Agents. ChemEngineering 2022;6:94. [DOI: 10.3390/chemengineering6060094] [Reference Citation Analysis]
3 De S, Aamna B, Sahu R, Parida S, Behera SK, Dan AK. Seeking heterocyclic scaffolds as antivirals against dengue virus. European Journal of Medicinal Chemistry 2022. [DOI: 10.1016/j.ejmech.2022.114576] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
4 Taayoshi F, Iraji A, Moazzam A, Soleimani M, Asadi M, Pedrood K, Akbari M, Salehabadi H, Larijani B, Adibpour N, Mahdavi M. Synthesis, molecular docking, and cytotoxicity of quinazolinone and dihydroquinazolinone derivatives as cytotoxic agents. BMC Chem 2022;16:35. [PMID: 35585608 DOI: 10.1186/s13065-022-00825-x] [Reference Citation Analysis]
5 Kommula D, Chintakunta PK, Garikapati K, Murty MSR. Nano-CuFe2O3-catalyzed green synthesis of novel quinazolinone-tetrazole hybrids as anti-cancer agents. Mol Divers 2022. [PMID: 35503155 DOI: 10.1007/s11030-022-10432-6] [Reference Citation Analysis]
6 Yamamoto Y, Yamakawa C, Nishimura R, Dong C, Kodama S, Nomoto A, Ueshima M, Ogawa A. Metal-Free Synthesis of 2-Substituted Quinazolines via Green Oxidation of o-Aminobenzylamines: Practical Construction of N-Containing Heterocycles Based on a Salicylic Acid-Catalyzed Oxidation System. Front Chem 2022;9:822841. [DOI: 10.3389/fchem.2021.822841] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
7 Sohrabi M, Nazari Montazer M, Farid SM, Tanideh N, Dianatpour M, Moazzam A, Zomorodian K, Yazdanpanah S, Asadi M, Hosseini S, Biglar M, Larijani B, Amanlou M, Barazandeh Tehrani M, Iraji A, Mahdavi M. Design and synthesis of novel nitrothiazolacetamide conjugated to different thioquinazolinone derivatives as anti-urease agents. Sci Rep 2022;12:2003. [PMID: 35132095 DOI: 10.1038/s41598-022-05736-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
8 Carreira MA, Oliveira MC, Fernandes AC. One-pot sustainable synthesis of valuable nitrogen compounds from biomass resources. Molecular Catalysis 2022;518:112094. [DOI: 10.1016/j.mcat.2021.112094] [Reference Citation Analysis]
9 Truong CC, Mishra DK. Organic base-mediated fixation of CO2 into value-added chemicals. Carbon Dioxide Capture and Conversion 2022. [DOI: 10.1016/b978-0-323-85585-3.00010-9] [Reference Citation Analysis]
10 Cao T, Martini ML, Park K, Kaniskan HÜ, Jin J. Pyrimidines and Their Benzo Derivatives. Comprehensive Heterocyclic Chemistry IV 2022. [DOI: 10.1016/b978-0-12-818655-8.00041-x] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Das Adhikary N, Mandal S, Jana A, Pramanik A. Diaryliodonium salt as oxidant in sp3 C-H activation and synthesis of quinazolin-4(3H)-ones. Results in Chemistry 2022;4:100270. [DOI: 10.1016/j.rechem.2021.100270] [Reference Citation Analysis]
12 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: 6] [Cited by in F6Publishing: 4] [Article Influence: 6.0] [Reference Citation Analysis]
13 Karan R, Agarwal P, Sinha M, Mahato N. Recent Advances on Quinazoline Derivatives: A Potential Bioactive Scaffold in Medicinal Chemistry. ChemEngineering 2021;5:73. [DOI: 10.3390/chemengineering5040073] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
14 Mirgany TO, Abdalla AN, Arifuzzaman M, Motiur Rahman AFM, Al-Salem HS. Quinazolin-4(3H)-one based potential multiple tyrosine kinase inhibitors with excellent cytotoxicity. J Enzyme Inhib Med Chem 2021;36:2055-67. [PMID: 34551654 DOI: 10.1080/14756366.2021.1972992] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
15 Komkov AV, Kozlov MA, Linitskii YA, Vasil’ev LS, Dmitrenok AS, Zavarzin IV. Synthesis of new 5-hydroxyquinazoline derivatives from functionalized 5-acetyl-6-methylpyrimidines. Chem Heterocycl Comp 2021;57:772-86. [DOI: 10.1007/s10593-021-02981-9] [Reference Citation Analysis]
16 Ahmed U, Anwar A, Ong SK, Anwar A, Khan NA. Applications of medicinal chemistry for drug discovery against Acanthamoeba infections. Med Res Rev 2022;42:462-512. [PMID: 34472107 DOI: 10.1002/med.21851] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Rehuman NA, Al‐sehemi AG, Parambi DGT, Rangarajan TM, Nicolotti O, Kim H, Mathew B. Current Progress in Quinazoline Derivatives as Acetylcholinesterase and Monoamine Oxidase Inhibitors. ChemistrySelect 2021;6:7162-82. [DOI: 10.1002/slct.202101077] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
18 De La Cruz JA, Ganesh T, Diebold BA, Cao W, Hofstetter A, Singh N, Kumar A, McCoy J, Ranjan P, Smith SME, Sambhara S, Lambeth JD, Gangappa S. Quinazolin-derived myeloperoxidase inhibitor suppresses influenza A virus-induced reactive oxygen species, pro-inflammatory mediators and improves cell survival. PLoS One 2021;16:e0254632. [PMID: 34280220 DOI: 10.1371/journal.pone.0254632] [Reference Citation Analysis]
19 Hasan HA, Salman A, Emilia A. Anticancer Activity and High Content Screening of New 6-Substituted-5,6-dihydrobenzo[4,5]imidazo[1,2-c]quinazoline Derivatives. RJPT 2021. [DOI: 10.52711/0974-360x.2021.00423] [Reference Citation Analysis]
20 Banerjee M, Panjikar PC, Bhutia ZT, Bhosle AA, Chatterjee A. Micellar nanoreactors for organic transformations with a focus on “dehydration” reactions in water: A decade update. Tetrahedron 2021;88:132142. [DOI: 10.1016/j.tet.2021.132142] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
21 Faisal M, Saeed A. Chemical Insights Into the Synthetic Chemistry of Quinazolines: Recent Advances. Front Chem 2020;8:594717. [PMID: 33585397 DOI: 10.3389/fchem.2020.594717] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 18.0] [Reference Citation Analysis]
22 Yamamoto Y. Copper-mediated synthesis of quinazolines and related benzodiazines. Copper in N-Heterocyclic Chemistry 2021. [DOI: 10.1016/b978-0-12-821263-9.00008-4] [Reference Citation Analysis]
23 Deharkar P, Satpute S, Panhekar D. Review on Synthesis Route of Quinazoline Based Hybrid Derivatives. Asian J Chem 2021;33:2525-2547. [DOI: 10.14233/ajchem.2021.23373] [Reference Citation Analysis]
24 Moussa A, Rahmati A. Synthesis and characterization of silica‐coated Fe 3 O 4 nanoparticle@silylpropyl triethylammonium polyoxometalate as an organic–inorganic hybrid heterogeneous catalyst for the one‐pot synthesis of tetrahydrobenzimidazo[2,1‐ b ]quinazolin‐1(2 H )‐ones. Appl Organomet Chem 2020;34. [DOI: 10.1002/aoc.5894] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
25 Sheng ZZ, Huang MM, Xue T, Xia F, Wu HH. Alcohol amine-catalyzed CO2 conversion for the synthesis of quinazoline-2,4-(1H,3H)-dione in water. RSC Adv 2020;10:34910-5. [PMID: 35514399 DOI: 10.1039/d0ra06439d] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
26 Geesi MH, Riadi Y, Kaiba A, Anouar EH, Ouerghi O, Ibnouf EO, Guionneau P. Synthesis, antibacterial evaluation, Raman, Crystal Structure and Hirshfeld Surface analysis of a new 3-(4-fluorophenyl)-6-methyl-2-(propylthio)quinazolin-4(3H)-one. Journal of Molecular Structure 2020;1215:128265. [DOI: 10.1016/j.molstruc.2020.128265] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
27 Perupogu N, Krishna CM, Ramachandran D. Design, synthesis and anticancer evaluation of 1,2,4-thiadiazole linked benzoxazole-quinazoline derivatives. Chemical Data Collections 2020;28:100482. [DOI: 10.1016/j.cdc.2020.100482] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
28 Geesi MH. Synthesis, antibacterial evaluation, Crystal Structure and Hirshfeld surface analysis of a new 2-Benzylsulfanyl-3-(4-fluoro-phenyl)-6-methyl-3H-quinazolin-4-one. Journal of Molecular Structure 2020;1208:127894. [DOI: 10.1016/j.molstruc.2020.127894] [Cited by in Crossref: 8] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
29 Rahmannejadi N, Yavari I, Khabnadideh S. Synthesis and antitumor activities of novel bis‐quinazolin‐4(3 H )‐ones. J Heterocyclic Chem 2020;57:978-82. [DOI: 10.1002/jhet.3749] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
30 Masri A, Anwar A, Khan NA, Shahbaz MS, Khan KM, Shahabuddin S, Siddiqui R. Antibacterial Effects of Quinazolin-4(3H)-One Functionalized-Conjugated Silver Nanoparticles. Antibiotics (Basel) 2019;8:E179. [PMID: 31600971 DOI: 10.3390/antibiotics8040179] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
31 Rothan HA, Faraj FL, Teoh TC, Yusof R. Novel Quinazoline derivatives inhibited HCV Serine protease and viral replication in Huh-7 cells.. [DOI: 10.1101/671313] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
32 Chen C, Zhu G, Xie T, Jiang P, Wang J, Jiang Z. A phenanthroindolizidine glycoside with HIF-1 inhibitory activity from Tylophora atrofolliculata. Phytochemistry Letters 2019;31:39-42. [DOI: 10.1016/j.phytol.2019.03.003] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
33 Chernyshov VV, Yarovaya OI, Fadeev DS, Gatilov YV, Esaulkova YL, Muryleva AS, Sinegubova KO, Zarubaev VV, Salakhutdinov NF. Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity. Mol Divers 2020;24:61-7. [PMID: 30820742 DOI: 10.1007/s11030-019-09932-9] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 4.7] [Reference Citation Analysis]
34 Herrera-vázquez FS, Hernández-luis F, Medina Franco JL. Quinazolines as inhibitors of chromatin-associated proteins in histones. Med Chem Res 2019;28:395-416. [DOI: 10.1007/s00044-019-02300-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
35 Paracha TU, Pobsuk N, Salaloy N, Suphakun P, Pekthong D, Hannongbua S, Choowongkomon K, Khorana N, Temkitthawon P, Ingkaninan K, Gleeson MP, Chootip K. Elucidation of Vasodilation Response and Structure Activity Relationships of N²,N-Disubstituted Quinazoline 2,4-Diamines in a Rat Pulmonary Artery Model. Molecules 2019;24:E281. [PMID: 30646523 DOI: 10.3390/molecules24020281] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
36 Kitanosono T, Cho SM, Kobayashi S. A convenient and mild cyclocondensation using water-soluble aldehydes in water. Tetrahedron 2018;74:7237-41. [DOI: 10.1016/j.tet.2018.10.023] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
37 Osarumwense PO. Analgesic activity of newly synthesized 7-chloro–2–methyl-4H–benzo[d] [1,3]–oxazin–4–one and 3–amino-7-chloro-2–methyl-quinazolin-4(3H)–one. Ovidius University Annals of Chemistry 2018;29:25-28. [DOI: 10.2478/auoc-2018-0003] [Reference Citation Analysis]
38 Barakat A, Al-Majid AM, Al-Qahtany BM, Ali M, Teleb M, Al-Agamy MH, Naz S, Ul-Haq Z. Synthesis, antimicrobial activity, pharmacophore modeling and molecular docking studies of new pyrazole-dimedone hybrid architectures. Chem Cent J 2018;12:29. [PMID: 29541952 DOI: 10.1186/s13065-018-0399-0] [Cited by in Crossref: 18] [Cited by in F6Publishing: 19] [Article Influence: 4.5] [Reference Citation Analysis]
39 Saikia UP, Borah G, Pahari P. Lewis-Acid-Catalysed Activation of Nitriles: A Microwave-Assisted Solvent-Free Synthesis of 2,4-Disubstituted Quinazolines and 1,3-Diazaspiro[5.5]undec-1-enes: Lewis-Acid-Catalysed Activation of Nitriles: A Microwave-Assisted Solvent-Free Synthesis of 2,4-Disubstituted Quinazolines and 1,3-Diazaspiro[5.5]unde. Eur J Org Chem 2018;2018:1211-7. [DOI: 10.1002/ejoc.201701585] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 3.3] [Reference Citation Analysis]
40 Toze FAA, Zaytsev VP, Chervyakova LV, Kvyatkovskaya EA, Dorovatovskii PV, Khrustalev VN. Crystal structure of 3-benzyl-2-[(E)-2-(furan-2-yl)ethen-yl]-2,3-di-hydro-quinazolin-4(1H)-one and 3-benzyl-2-[(E)-2-(thio-phen-2-yl)ethen-yl]-2,3-di-hydro-quinazolin-4(1H)-one from synchrotron X-ray diffraction. Acta Crystallogr E Crystallogr Commun 2018;74:10-4. [PMID: 29416882 DOI: 10.1107/S2056989017017479] [Reference Citation Analysis]
41 Solomos MA, Bertke JA, Swift JA. One step synthesis of a fused four-ring heterocycle. New J Chem 2018;42:7125-7129. [DOI: 10.1039/c8nj00629f] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
42 Kant S, Asthana S, Missiakas D, Pancholi V. A novel STK1-targeted small-molecule as an "antibiotic resistance breaker" against multidrug-resistant Staphylococcus aureus. Sci Rep 2017;7:5067. [PMID: 28698584 DOI: 10.1038/s41598-017-05314-z] [Cited by in Crossref: 29] [Cited by in F6Publishing: 30] [Article Influence: 5.8] [Reference Citation Analysis]
43 Fröhlich T, Reiter C, Ibrahim MM, Beutel J, Hutterer C, Zeitträger I, Bahsi H, Leidenberger M, Friedrich O, Kappes B, Efferth T, Marschall M, Tsogoeva SB. Synthesis of Novel Hybrids of Quinazoline and Artemisinin with High Activities against Plasmodium falciparum, Human Cytomegalovirus, and Leukemia Cells. ACS Omega 2017;2:2422-31. [PMID: 30023664 DOI: 10.1021/acsomega.7b00310] [Cited by in Crossref: 53] [Cited by in F6Publishing: 54] [Article Influence: 10.6] [Reference Citation Analysis]
44 Fleeman R, Van Horn KS, Barber MM, Burda WN, Flanigan DL, Manetsch R, Shaw LN. Characterizing the Antimicrobial Activity of N2,N4-Disubstituted Quinazoline-2,4-Diamines toward Multidrug-Resistant Acinetobacter baumannii. Antimicrob Agents Chemother 2017;61:e00059-17. [PMID: 28289036 DOI: 10.1128/AAC.00059-17] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 3.4] [Reference Citation Analysis]
45 Kumar P, Matta A, Singh S, Van der Eycken J, Len C, Parmar VS, Van der Eycken EV, Singh BK. Facile, catalyst-free, microwave-assisted access toward the synthesis of 2-aryl/alkyl-3-(1 H -benzo[ d ]imidazol-2-yl)-2, 3-dihydroquinazolin-4(1 H )-ones. Synthetic Communications 2017;47:756-63. [DOI: 10.1080/00397911.2016.1277761] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.2] [Reference Citation Analysis]
46 Asadi P, Khodarahmi G, Farrokhpour H, Hassanzadeh F, Saghaei L. Quantum mechanical/molecular mechanical and docking study of the novel analogues based on hybridization of common pharmacophores as potential anti-breast cancer agents. Res Pharm Sci 2017;12:233-40. [PMID: 28626481 DOI: 10.4103/1735-5362.207204] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 1.6] [Reference Citation Analysis]
47 Marinho E, Proença MF. Reactivity and regioselectivity in the acylation of 2,4-diaminoquinazolines. Tetrahedron 2016;72:4383-4389. [DOI: 10.1016/j.tet.2016.06.003] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
48 Vlachou I, Kourtidou E, Papasotiriou I. 9-(4-Methoxyquinazolin-2-yl)-9H-purin-6-amine. Molbank 2016;2016:M885. [DOI: 10.3390/m885] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
49 Šačkus A, Kriščiūnienė V, Matulevičiūtė G, Paliulis O. Conversion of 2-Thioxo-2,3-dihydroquinazolin-4(1H)-ones to N(3)-Unsubstituted 2-(Het)Arylquinazolin-4(3H)-ones by Copper-Mediated Pd-Catalysed Cross-Coupling Reactions. HETEROCYCLES 2016;93:150. [DOI: 10.3987/com-15-s(t)12] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
50 Cundell D, Piechoski M. Antiprotozoal agents derived from natural soil and aquatic actinobacteria: Fighting one microbe with another. Antimicrobials 2015. [DOI: 10.1201/b19224-29] [Reference Citation Analysis]
51 Feng J, Wu X. Oxidative Synthesis of Quinazolinones under Metal-free Conditions: Oxidative Synthesis of Quinazolinones under Metal-free Conditions. J Heterocyclic Chem 2017;54:794-8. [DOI: 10.1002/jhet.2562] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
52 Mphahlele MJ, Maluleka MM. Advances in metal-catalyzed cross-coupling reactions of halogenated quinazolinones and their quinazoline derivatives. Molecules 2014;19:17435-63. [PMID: 25356566 DOI: 10.3390/molecules191117435] [Cited by in Crossref: 22] [Cited by in F6Publishing: 23] [Article Influence: 2.8] [Reference Citation Analysis]
53 Wang D, Gao F. ChemInform Abstract: Quinazoline Derivatives. Synthesis and Bioactivities. ChemInform 2014;45:no-no. [DOI: 10.1002/chin.201429286] [Reference Citation Analysis]