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For: Feng LS, Xu Z, Chang L, Li C, Yan XF, Gao C, Ding C, Zhao F, Shi F, Wu X. Hybrid molecules with potential in vitro antiplasmodial and in vivo antimalarial activity against drug-resistant Plasmodium falciparum. Med Res Rev 2020;40:931-71. [PMID: 31692025 DOI: 10.1002/med.21643] [Cited by in Crossref: 33] [Cited by in F6Publishing: 34] [Article Influence: 11.0] [Reference Citation Analysis]
Number Citing Articles
1 Khwaza V, Buyana B, Nqoro X, Peter S, Mbese Z, Feketshane Z, Alven S, Aderibigbe BA. Strategies for delivery of antiviral agents. Viral Infections and Antiviral Therapies 2023. [DOI: 10.1016/b978-0-323-91814-5.00018-0] [Reference Citation Analysis]
2 Seghetti F, Belluti F, Rampa A, Gobbi S, Legac J, Parapini S, Basilico N, Bisi A. Hitting drug-resistant malaria infection with triazole-linked flavonoid–chloroquine hybrid compounds. Future Medicinal Chemistry 2022. [DOI: 10.4155/fmc-2022-0173] [Reference Citation Analysis]
3 Chopin N, Bosson J, Iikawa S, Picot S, Bienvenu AL, Lavoignat A, Bonnot G, Riou M, Beaugé C, Guillory V, Biot C, Pilet G, Chessé M, Davioud-Charvet E, Elhabiri M, Bouillon JP, Médebielle M. Evaluation of ferrocenyl-containing γ-hydroxy-γ-lactam-derived tetramates as potential antiplasmodials. Eur J Med Chem 2022;243:114735. [PMID: 36122550 DOI: 10.1016/j.ejmech.2022.114735] [Reference Citation Analysis]
4 Reddivari CKR, Devineni SR, Nemallapudi BR, Sravya G, Avula B, Shaik N, Badavath VN, Zyryanov GV, Yellalavenkata RR, Chamarthi NR. Design, Synthesis, Biological Evaluation and Molecular Docking Studies of 1,4-Disubstituted 1,2,3-Triazoles: PEG-400:H2O Mediated Click Reaction of Fluorescent Organic Probes under Ultrasonic Irradiation. Polycyclic Aromatic Compounds 2022;42:3953-3974. [DOI: 10.1080/10406638.2021.1878246] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Feng LS, Cheng JB, Su WQ, Li HZ, Xiao T, Chen DA, Zhang ZL. Cinnamic acid hybrids as anticancer agents: A mini-review. Arch Pharm (Weinheim) 2022;:e2200052. [PMID: 35419808 DOI: 10.1002/ardp.202200052] [Reference Citation Analysis]
6 Fang J, Song F, Wang F. The antimalarial activity of 1,2,4-trioxolane/trioxane hybrids and dimers: A review. Arch Pharm (Weinheim) 2022;:e2200077. [PMID: 35388499 DOI: 10.1002/ardp.202200077] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Roy D, Anas M, Manhas A, Saha S, Kumar N, Panda G. Synthesis, biological evaluation, Structure − Activity relationship studies of quinoline-imidazole derivatives as potent antimalarial agents. Bioorganic Chemistry 2022;121:105671. [DOI: 10.1016/j.bioorg.2022.105671] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Li Y, Cardoso-silva J, Papageorgiou LG, Tsoka S. Optimisation-based modelling for drug discovery in malaria.. [DOI: 10.1101/2022.02.12.479469] [Reference Citation Analysis]
9 Alekseyev RS, Aliyev FN, Terenin VI. Methods for the synthesis of 3H-pyrrolo[2,3-c]quinolines. Chem Heterocycl Comp. [DOI: 10.1007/s10593-021-03036-9] [Reference Citation Analysis]
10 Hou H, Qu B, Su C, Hou G, Gao F. Design, Synthesis and Anti-Lung Cancer Evaluation of 1, 2, 3-Triazole Tethered Dihydroartemisinin-Isatin Hybrids. Front Pharmacol 2021;12:801580. [PMID: 34975498 DOI: 10.3389/fphar.2021.801580] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
11 Gehrmann R, Hertlein T, Hopke E, Ohlsen K, Lalk M, Hilgeroth A. Novel Small-Molecule Hybrid-Antibacterial Agents against S. aureus and MRSA Strains. Molecules 2021;27:61. [PMID: 35011293 DOI: 10.3390/molecules27010061] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Jaiswal MK, Singh S, Singh RP. Enantioselective vinylogous aldol reaction of acylphosphonates with 3-alkylidene oxindoles. Org Biomol Chem 2021;19:7861-6. [PMID: 34476434 DOI: 10.1039/d1ob00140j] [Reference Citation Analysis]
13 Ouyang Y, Li J, Chen X, Fu X, Sun S, Wu Q. Chalcone Derivatives: Role in Anticancer Therapy. Biomolecules 2021;11:894. [PMID: 34208562 DOI: 10.3390/biom11060894] [Cited by in Crossref: 27] [Cited by in F6Publishing: 33] [Article Influence: 27.0] [Reference Citation Analysis]
14 Liang T, Sun X, Li W, Hou G, Gao F. 1,2,3-Triazole-Containing Compounds as Anti-Lung Cancer Agents: Current Developments, Mechanisms of Action, and Structure-Activity Relationship. Front Pharmacol 2021;12:661173. [PMID: 34177578 DOI: 10.3389/fphar.2021.661173] [Cited by in Crossref: 15] [Cited by in F6Publishing: 17] [Article Influence: 15.0] [Reference Citation Analysis]
15 Prinčič GG, Lozinšek M, Iskra J. Expanding the boron peroxide chemistry on BODIPY scaffold. Dyes and Pigments 2021;190:109290. [DOI: 10.1016/j.dyepig.2021.109290] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Ouji M, Nguyen M, Mustière R, Jimenez T, Augereau JM, Benoit-Vical F, Deraeve C. Novel molecule combinations and corresponding hybrids targeting artemisinin-resistant Plasmodium falciparum parasites. Bioorg Med Chem Lett 2021;39:127884. [PMID: 33636304 DOI: 10.1016/j.bmcl.2021.127884] [Cited by in Crossref: 2] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
17 Bhanot A, Sundriyal S. Physicochemical Profiling and Comparison of Research Antiplasmodials and Advanced Stage Antimalarials with Oral Drugs. ACS Omega 2021;6:6424-37. [PMID: 33718733 DOI: 10.1021/acsomega.1c00104] [Reference Citation Analysis]
18 Tan Z, Deng J, Ye Q, Zhang Z. Triazole-containing hybrids with anti-Mycobacterium tuberculosis potential - Part I: 1,2,3-Triazole. Future Med Chem 2021;13:643-62. [PMID: 33619989 DOI: 10.4155/fmc-2020-0301] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
19 Xu Z, Chen Q, Zhang Y, Liang C. Coumarin-based derivatives with potential anti-HIV activity. Fitoterapia 2021;150:104863. [PMID: 33582266 DOI: 10.1016/j.fitote.2021.104863] [Cited by in Crossref: 21] [Cited by in F6Publishing: 11] [Article Influence: 21.0] [Reference Citation Analysis]
20 Shalini, Kumar S, Gendrot M, Fonta I, Mosnier J, Cele N, Awolade P, Singh P, Pradines B, Kumar V. Amide Tethered 4-Aminoquinoline-naphthalimide Hybrids: A New Class of Possible Dual Function Antiplasmodials. ACS Med Chem Lett 2020;11:2544-52. [PMID: 33335678 DOI: 10.1021/acsmedchemlett.0c00536] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
21 Fonte M, Tassi N, Fontinha D, Bouzón-Arnáiz I, Ferraz R, Araújo MJ, Fernàndez-Busquets X, Prudêncio M, Gomes P, Teixeira C. 4,9-Diaminoacridines and 4-Aminoacridines as Dual-Stage Antiplasmodial Hits. ChemMedChem 2021;16:788-92. [PMID: 33217195 DOI: 10.1002/cmdc.202000740] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
22 Uddin A, Chawla M, Irfan I, Mahajan S, Singh S, Abid M. Medicinal chemistry updates on quinoline- and endoperoxide-based hybrids with potent antimalarial activity. RSC Med Chem 2021;12:24-42. [PMID: 34046596 DOI: 10.1039/d0md00244e] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
23 Liu W, Liang Y, Si X. Hydroxamic acid hybrids as the potential anticancer agents: An Overview. European Journal of Medicinal Chemistry 2020;205:112679. [DOI: 10.1016/j.ejmech.2020.112679] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
24 Meng T, Hou Y, Shang C, Zhang J, Zhang B. Recent advances in indole dimers and hybrids with antibacterial activity against methicillin-resistant Staphylococcus aureus. Arch Pharm (Weinheim) 2021;354:e2000266. [PMID: 32986279 DOI: 10.1002/ardp.202000266] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
25 Feng LS, Zheng MJ, Zhao F, Liu D. 1,2,3-Triazole hybrids with anti-HIV-1 activity. Arch Pharm (Weinheim) 2021;354:e2000163. [PMID: 32960467 DOI: 10.1002/ardp.202000163] [Cited by in Crossref: 30] [Cited by in F6Publishing: 33] [Article Influence: 15.0] [Reference Citation Analysis]
26 Li J, Sun X, Li J, Yu F, Zhang Y, Huang X, Jiang F. The antimalarial activity of indole alkaloids and hybrids. Arch Pharm 2020;353:2000131. [DOI: 10.1002/ardp.202000131] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
27 Xu Z. 1,2,3-Triazole-containing hybrids with potential antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA). Eur J Med Chem 2020;206:112686. [PMID: 32795773 DOI: 10.1016/j.ejmech.2020.112686] [Cited by in Crossref: 37] [Cited by in F6Publishing: 39] [Article Influence: 18.5] [Reference Citation Analysis]
28 Wen X, Zhou Y, Zeng J, Liu X. Recent Development of 1,2,4-triazole-containing Compounds as Anticancer Agents. CTMC 2020;20:1441-60. [DOI: 10.2174/1568026620666200128143230] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 9.0] [Reference Citation Analysis]
29 Song F, Li Z, Bian Y, Huo X, Fang J, Shao L, Zhou M. Indole/isatin-containing hybrids as potential antibacterial agents. Arch Pharm (Weinheim) 2020;353:e2000143. [PMID: 32667714 DOI: 10.1002/ardp.202000143] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
30 Gao F, Huang G, Xiao J. Chalcone hybrids as potential anticancer agents: Current development, mechanism of action, and structure-activity relationship. Med Res Rev 2020;40:2049-84. [PMID: 32525247 DOI: 10.1002/med.21698] [Cited by in Crossref: 31] [Cited by in F6Publishing: 34] [Article Influence: 15.5] [Reference Citation Analysis]
31 Xiao J, Sun Z, Kong F, Gao F. Current scenario of ferrocene-containing hybrids for antimalarial activity. Eur J Med Chem 2020;185:111791. [PMID: 31669852 DOI: 10.1016/j.ejmech.2019.111791] [Cited by in Crossref: 41] [Cited by in F6Publishing: 31] [Article Influence: 13.7] [Reference Citation Analysis]