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For: Fan YL, Jin XH, Huang ZP, Yu HF, Zeng ZG, Gao T, Feng LS. Recent advances of imidazole-containing derivatives as anti-tubercular agents. Eur J Med Chem 2018;150:347-65. [PMID: 29544148 DOI: 10.1016/j.ejmech.2018.03.016] [Cited by in Crossref: 71] [Cited by in F6Publishing: 49] [Article Influence: 17.8] [Reference Citation Analysis]
Number Citing Articles
1 Yao L, Zhang G, Yu L, Liu S, Wang X, Fan T, Kang H, Feng W. Development of 1,3,4-Oxadiazole Derived Antifungal Agents and Their Application in Maize Diseases Control. Front Plant Sci 2022;13:912091. [PMID: 35599869 DOI: 10.3389/fpls.2022.912091] [Reference Citation Analysis]
2 Katariya KD, Reddy DV. Oxazolyl-Pyrimidines As Antibacterial And Antitubercular Agents: Synthesis, Biological Evaluation, in-silico ADMET And Molecular Docking Study. Journal of Molecular Structure 2022;1253:132240. [DOI: 10.1016/j.molstruc.2021.132240] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Yan M, Xu L, Wang Y, Wan J, Liu T, Liu W, Wan Y, Zhang B, Wang R, Li Q. Opportunities and challenges of using five-membered ring compounds as promising antitubercular agents. Drug Dev Res 2020;81:402-18. [PMID: 31904877 DOI: 10.1002/ddr.21638] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
4 Ren Z, Cai S, Liu Y, Xie Y, Yuan D, Lei M, He P, Wang L. C(sp 2 )–H Functionalization of Imidazole at the C2- and C4-Position via Palladium-Catalyzed Isocyanide Insertion Leading to Indeno[1,2- d ]imidazole and Imidazo[1,2- a ]indole Derivatives. J Org Chem 2020;85:11014-24. [DOI: 10.1021/acs.joc.0c01454] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
5 Satyam K, Murugesh V, Suresh S. The base-free van Leusen reaction of cyclic imines on water: synthesis of N-fused imidazo 6,11-dihydro β-carboline derivatives. Org Biomol Chem 2019;17:5234-8. [PMID: 31074750 DOI: 10.1039/c9ob00660e] [Cited by in Crossref: 8] [Cited by in F6Publishing: 1] [Article Influence: 2.7] [Reference Citation Analysis]
6 Sharma P, LaRosa C, Antwi J, Govindarajan R, Werbovetz KA. Imidazoles as Potential Anticancer Agents: An Update on Recent Studies. Molecules 2021;26:4213. [PMID: 34299488 DOI: 10.3390/molecules26144213] [Reference Citation Analysis]
7 Gao F, Ye L, Kong F, Huang G, Xiao J. Design, synthesis and antibacterial activity evaluation of moxifloxacin-amide-1,2,3-triazole-isatin hybrids. Bioorg Chem 2019;91:103162. [PMID: 31382058 DOI: 10.1016/j.bioorg.2019.103162] [Cited by in Crossref: 16] [Cited by in F6Publishing: 10] [Article Influence: 5.3] [Reference Citation Analysis]
8 Xu Z, Zhao S, Deng J, Wang Q, Lv Z, Fan Y. Design, Synthesis, and Evaluation of Tetraethylene Glycol Tethered Isatin-Coumarin Hybrids as Novel Anticancer Agents: Design, Synthesis, and Evaluation of Tetraethylene Glycol Tethered Isatin-Coumarin Hybrids as Novel Anticancer Agents. J Heterocyclic Chem 2019;56:400-5. [DOI: 10.1002/jhet.3411] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.8] [Reference Citation Analysis]
9 Kerru N, Gummidi L, Maddila S, Jonnalagadda SB. A Review of Recent Advances in the Green Synthesis of Azole- and Pyran-based Fused Heterocycles Using MCRs and Sustainable Catalysts. COC 2021;25:4-39. [DOI: 10.2174/1385272824999201020204620] [Cited by in Crossref: 8] [Article Influence: 8.0] [Reference Citation Analysis]
10 Wei L, Li Q, Chen Y, Zhang J, Mi Y, Dong F, Lei C, Guo Z. Enhanced antioxidant and antifungal activity of chitosan derivatives bearing 6-O-imidazole-based quaternary ammonium salts. Carbohydr Polym 2019;206:493-503. [PMID: 30553350 DOI: 10.1016/j.carbpol.2018.11.022] [Cited by in Crossref: 31] [Cited by in F6Publishing: 23] [Article Influence: 7.8] [Reference Citation Analysis]
11 Maddili SK, Li Z, Kannekanti VK, Bheemanaboina RRY, Tuniki B, Tangadanchu VKR, Zhou C. Azoalkyl ether imidazo[2,1- b ]benzothiazoles as potentially antimicrobial agents with novel structural skeleton. Bioorganic & Medicinal Chemistry Letters 2018;28:2426-31. [DOI: 10.1016/j.bmcl.2018.06.016] [Cited by in Crossref: 27] [Cited by in F6Publishing: 23] [Article Influence: 6.8] [Reference Citation Analysis]
12 Hou Y, Shang C, Wang H, Yun J. Isatin-azole hybrids and their anticancer activities. Arch Pharm (Weinheim) 2020;353:e1900272. [PMID: 31691360 DOI: 10.1002/ardp.201900272] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 5.7] [Reference Citation Analysis]
13 Nayak S, Gaonkar SL, Musad EA, Dawsar AMA. 1,3,4-Oxadiazole-containing hybrids as potential anticancer agents: Recent developments, mechanism of action and structure-activity relationships. Journal of Saudi Chemical Society 2021;25:101284. [DOI: 10.1016/j.jscs.2021.101284] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
14 Zinad DS, Mahal A, Shareef OA. Antifungal activity and theoretical study of synthesized pyrazole-imidazole hybrids. IOP Conf Ser : Mater Sci Eng 2020;770:012053. [DOI: 10.1088/1757-899x/770/1/012053] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
15 Gao C, Fan YL, Zhao F, Ren QC, Wu X, Chang L, Gao F. Quinolone derivatives and their activities against methicillin-resistant Staphylococcus aureus (MRSA). Eur J Med Chem 2018;157:1081-95. [PMID: 30179746 DOI: 10.1016/j.ejmech.2018.08.061] [Cited by in Crossref: 49] [Cited by in F6Publishing: 37] [Article Influence: 12.3] [Reference Citation Analysis]
16 Dong H, Wu J, Huo G. Design, synthesis and biological studies of some new imidazole-1,2,3-triazole hybrid derivatives. Journal of Molecular Structure 2022;1256:132516. [DOI: 10.1016/j.molstruc.2022.132516] [Reference Citation Analysis]
17 Gao C, Chang L, Xu Z, Yan XF, Ding C, Zhao F, Wu X, Feng LS. Recent advances of tetrazole derivatives as potential anti-tubercular and anti-malarial agents. Eur J Med Chem 2019;163:404-12. [PMID: 30530192 DOI: 10.1016/j.ejmech.2018.12.001] [Cited by in Crossref: 49] [Cited by in F6Publishing: 36] [Article Influence: 12.3] [Reference Citation Analysis]
18 Guo H. Isatin derivatives and their anti-bacterial activities. European Journal of Medicinal Chemistry 2019;164:678-88. [DOI: 10.1016/j.ejmech.2018.12.017] [Cited by in Crossref: 55] [Cited by in F6Publishing: 32] [Article Influence: 18.3] [Reference Citation Analysis]
19 Elsaman T, Mohamed MS, Mohamed MA. Current development of 5-nitrofuran-2-yl derivatives as antitubercular agents. Bioorg Chem 2019;88:102969. [PMID: 31077910 DOI: 10.1016/j.bioorg.2019.102969] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
20 Bhati S, Kumar V, Singh S, Singh J. Synthesis, biological activities and docking studies of piperazine incorporated 1, 3, 4-oxadiazole derivatives. Journal of Molecular Structure 2019;1191:197-205. [DOI: 10.1016/j.molstruc.2019.04.106] [Cited by in Crossref: 20] [Cited by in F6Publishing: 5] [Article Influence: 6.7] [Reference Citation Analysis]
21 Romo PE, Insuasty B, Abonia R, Crespo MDP, Quiroga J. Synthesis of New Oxindoles and Determination of Their Antibacterial Properties. Heteroatom Chemistry 2020;2020:1-9. [DOI: 10.1155/2020/8021920] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Zhang L, Xu Z. Coumarin-containing hybrids and their anticancer activities. Eur J Med Chem 2019;181:111587. [PMID: 31404864 DOI: 10.1016/j.ejmech.2019.111587] [Cited by in Crossref: 50] [Cited by in F6Publishing: 32] [Article Influence: 16.7] [Reference Citation Analysis]
23 Dhameliya TM, Bhakhar KA, Gajjar ND, Patel KA, Devani AA, Hirani RV. Recent advancements and developments in search of anti-tuberculosis agents: A quinquennial update and future directions. Journal of Molecular Structure 2022;1248:131473. [DOI: 10.1016/j.molstruc.2021.131473] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 8.0] [Reference Citation Analysis]
24 Lamberth C. Imidazole Chemistry in Crop Protection. HETEROCYCLES 2021;102:1449. [DOI: 10.3987/rev-20-948] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Xu Z, Zhao S, Lv Z, Feng L, Wang Y, Zhang F, Bai L, Deng J. Benzofuran derivatives and their anti-tubercular, anti-bacterial activities. Eur J Med Chem 2019;162:266-76. [PMID: 30448416 DOI: 10.1016/j.ejmech.2018.11.025] [Cited by in Crossref: 45] [Cited by in F6Publishing: 26] [Article Influence: 11.3] [Reference Citation Analysis]
26 Akinpelu OI, Lawal MM, Kumalo HM, Mhlongo NN. Drug repurposing: Fusidic acid as a potential inhibitor of M. tuberculosis FtsZ polymerization – Insight from DFT calculations, molecular docking and molecular dynamics simulations. Tuberculosis 2020;121:101920. [DOI: 10.1016/j.tube.2020.101920] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
27 Chen R, Zhang H, Ma T, Xue H, Miao Z, Chen L, Shi X. Ciprofloxacin-1,2,3-triazole-isatin hybrids tethered via amide: Design, synthesis, and in vitro anti-mycobacterial activity evaluation. Bioorganic & Medicinal Chemistry Letters 2019;29:2635-7. [DOI: 10.1016/j.bmcl.2019.07.041] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 2.7] [Reference Citation Analysis]
28 Soni J, Sethiya A, Sahiba N, Agarwal DK, Agarwal S. Contemporary Progress in the Synthetic Strategies of Imidazole and its Biological Activities. Curr Org Synth 2019;16:1078-104. [PMID: 31984918 DOI: 10.2174/1570179416666191007092548] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
29 Wang H, Wei C, Zou H, Linghu C, Wang Z, Wang J, Chen Y, Zhang L. Transition-metal-free, direct C-H radical trifluoromethylation of nitroimidazoles with Togni’s reagent. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.153659] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Bai MJ, Liu NZ, Zhou YL, Liu J, Zou J, Tan WJ, Huang XT, Mei WJ. Synthesis of Fluorinated Imidazole[4,5f][1,10]phenanthroline Derivatives as Potential Inhibitors of Liver Cancer Cell Proliferation by Inducing Apoptosis via DNA Damage. ChemMedChem 2021. [PMID: 34713586 DOI: 10.1002/cmdc.202100537] [Reference Citation Analysis]
31 Zhang J, Ba Y, Wang S, Yang H, Hou X, Xu Z. Nitroimidazole-containing compounds and their antibacterial and antitubercular activities. Eur J Med Chem 2019;179:376-88. [PMID: 31260891 DOI: 10.1016/j.ejmech.2019.06.068] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
32 Chu XM, Wang C, Wang WL, Liang LL, Liu W, Gong KK, Sun KL. Triazole derivatives and their antiplasmodial and antimalarial activities. Eur J Med Chem 2019;166:206-23. [PMID: 30711831 DOI: 10.1016/j.ejmech.2019.01.047] [Cited by in Crossref: 67] [Cited by in F6Publishing: 39] [Article Influence: 22.3] [Reference Citation Analysis]
33 Antoci V, Cucu D, Zbancioc G, Moldoveanu C, Mangalagiu V, Amariucai-Mantu D, Aricu A, Mangalagiu II. Bis-(imidazole/benzimidazole)-pyridine derivatives: synthesis, structure and antimycobacterial activity. Future Med Chem 2020;12:207-22. [PMID: 31916456 DOI: 10.4155/fmc-2019-0063] [Cited by in Crossref: 13] [Cited by in F6Publishing: 5] [Article Influence: 6.5] [Reference Citation Analysis]
34 Gapanenok D, Makhmet A, Peshkov AA, Smirnova D, Amire N, Peshkov VA, Spiridonova D, Dar'in D, Balalaie S, Krasavin M. Multicomponent Assembly of Trisubstituted Imidazoles and Their Photochemical Cyclization into Fused Polyheterocyclic Scaffolds. J Org Chem 2022;87:7838-51. [PMID: 35675099 DOI: 10.1021/acs.joc.2c00475] [Reference Citation Analysis]
35 Ghoneim AA, Ali Hassan AG. An Efficient Procedure of Synthesis Acyclic C -Glycosides of Thiazolo [4, 5- b ]Pyrazine and Imidazo[4,5-d]Thiazole with Expected Anti-Cancer Activities. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2020.1866035] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
36 Xu Z, Zhao SJ, Liu Y. 1,2,3-Triazole-containing hybrids as potential anticancer agents: Current developments, action mechanisms and structure-activity relationships. Eur J Med Chem 2019;183:111700. [PMID: 31546197 DOI: 10.1016/j.ejmech.2019.111700] [Cited by in Crossref: 105] [Cited by in F6Publishing: 70] [Article Influence: 35.0] [Reference Citation Analysis]
37 Gao T, Hu W, Zeng Z, Sun S, Wang R. Design, Synthesis, and Evaluation of Tetraethylene Glycol Tethered Ciprofloxacin–Isatin Hybrids as Novel Antitubercular Agents. J Heterocyclic Chem 2019;56:306-11. [DOI: 10.1002/jhet.3338] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
38 Xu Z, Zhao SJ, Lv ZS, Gao F, Wang Y, Zhang F, Bai L, Deng JL. Fluoroquinolone-isatin hybrids and their biological activities. Eur J Med Chem 2019;162:396-406. [PMID: 30453247 DOI: 10.1016/j.ejmech.2018.11.032] [Cited by in Crossref: 61] [Cited by in F6Publishing: 39] [Article Influence: 15.3] [Reference Citation Analysis]
39 Krasavin M, Lukin A, Vedekhina T, Manicheva O, Dogonadze M, Vinogradova T, Zabolotnykh N, Rogacheva E, Kraeva L, Yablonsky P. Conjugation of a 5-nitrofuran-2-oyl moiety to aminoalkylimidazoles produces non-toxic nitrofurans that are efficacious in vitro and in vivo against multidrug-resistant Mycobacterium tuberculosis. European Journal of Medicinal Chemistry 2018;157:1115-26. [DOI: 10.1016/j.ejmech.2018.08.068] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
40 Xu W, Yao H, Zhang X, Peng C, Li L, Zhang Y, Qian S, Yang L, Wang Z. K2CO3 Promoted Cascade Reaction for the Preparation of 1H-Imidazol-4- yl-1-amine Derivatives. LOC 2020;17:127-32. [DOI: 10.2174/1570178616666190226144620] [Reference Citation Analysis]
41 Adeniji AA, Knoll KE, Loots DT. Potential anti-TB investigational compounds and drugs with repurposing potential in TB therapy: a conspectus. Appl Microbiol Biotechnol 2020;104:5633-62. [PMID: 32372202 DOI: 10.1007/s00253-020-10606-y] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
42 Gao F, Zhang X, Wang T, Xiao J. Quinolone hybrids and their anti-cancer activities: An overview. European Journal of Medicinal Chemistry 2019;165:59-79. [DOI: 10.1016/j.ejmech.2019.01.017] [Cited by in Crossref: 71] [Cited by in F6Publishing: 52] [Article Influence: 23.7] [Reference Citation Analysis]
43 Zhao S, Lv Z, Deng J, Gao F, Zhang G, Xu Z. Design, Synthesis, and In Vitro Anti‐mycobacterial Activities of 1,2,3‐Triazole‐tetraethylene Glycol Tethered Isatin Dimers. J Heterocyclic Chem 2018;55:3006-10. [DOI: 10.1002/jhet.3349] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
44 Lal K, Poonia N, Rani P, Kumar A, Kumar A. Design, synthesis, antimicrobial evaluation and docking studies of urea-triazole-amide hybrids. Journal of Molecular Structure 2020;1215:128234. [DOI: 10.1016/j.molstruc.2020.128234] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 3.5] [Reference Citation Analysis]
45 Dubovtsev AY, Dar'in DV, Krasavin M, Kukushkin VY. Gold-Catalyzed Oxidation of Internal Alkynes into Benzils and its Application for One-Pot Synthesis of Five-, Six-, and Seven-Membered Azaheterocycles: Gold-Catalyzed Oxidation of Internal Alkynes into Benzils and its Application for One-Pot Synthesis of Five-, Six-, and Seven-Membered Azaheterocycles. Eur J Org Chem 2019;2019:1856-64. [DOI: 10.1002/ejoc.201900108] [Cited by in Crossref: 25] [Cited by in F6Publishing: 11] [Article Influence: 8.3] [Reference Citation Analysis]
46 Głuszyńska A, Juskowiak B, Rubiś B. Binding Study of the Fluorescent Carbazole Derivative with Human Telomeric G-Quadruplexes. Molecules 2018;23:E3154. [PMID: 30513661 DOI: 10.3390/molecules23123154] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.5] [Reference Citation Analysis]
47 Toosi MR, Pordel M, Bozorgmehr MR. Synthesis of Heterocyclic Systems 3H-furo[2,3-b]imidazo[4,5-f]quinolines and 3H-furo[2,3-b]pyrazolo[4,3-f]quinolines as New Antibacterial Agents. Pharm Chem J. [DOI: 10.1007/s11094-022-02622-1] [Reference Citation Analysis]
48 Lin Y, Li E, Wu X, Wang L, Wang H, Li X, Kang H, Zhou L, Shen G, Lv X. One-pot synthesis of 2-azolylimidazole derivatives through a domino addition/A3 coupling/cyclization process under copper catalysis. Org Biomol Chem 2020;18:1476-86. [PMID: 32026913 DOI: 10.1039/c9ob02532d] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
49 Guo H. Design, Synthesis, and In Vitro Anti‐mycobacterial Activities of Propylene Tethered Benzofuran–Isatin Hybrids. J Heterocyclic Chem 2019;56:338-42. [DOI: 10.1002/jhet.3387] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
50 Amosova SV, Filippov AS, Potapov VA, Makhaeva NA, Albanov AI. Unexpected Regioselective Reactions of 2-(Bromomethyl)-1,3-thiaselenole with 1-Methyl-1H-imidazol-2-thiol, Accompanied by Rearrangements. Russ J Org Chem 2018;54:1697-701. [DOI: 10.1134/s107042801811012x] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
51 Yang X, Sun H, Maddili SK, Li S, Yang R, Zhou C. Dihydropyrimidinone imidazoles as unique structural antibacterial agents for drug-resistant gram-negative pathogens. European Journal of Medicinal Chemistry 2022;232:114188. [DOI: 10.1016/j.ejmech.2022.114188] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
52 Nandikolla A, Srinivasarao S, Khetmalis YM, Kumar BK, Murugesan S, Shetye G, Ma R, Franzblau SG, Sekhar KVGC. Design, synthesis and biological evaluation of novel 1,2,3-triazole analogues of Imidazo-[1,2-a]-pyridine-3-carboxamide against Mycobacterium tuberculosis. Toxicol In Vitro 2021;74:105137. [PMID: 33684466 DOI: 10.1016/j.tiv.2021.105137] [Reference Citation Analysis]
53 Pattanayak P, Kaliyaperumal S. Design, Synthesis, Characterization and IN VITRO Antimicrobial and Anthelmintic Evaluation of Metronidazole Derivatives Modified at Position 1. Pharm Chem J. [DOI: 10.1007/s11094-022-02620-3] [Reference Citation Analysis]
54 Punia S, Verma V, Kumar D, Kumar A, Deswal L. Facile synthesis, antimicrobial evaluation and molecular docking studies of pyrazole-imidazole-triazole hybrids. Journal of Molecular Structure 2021;1223:129216. [DOI: 10.1016/j.molstruc.2020.129216] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 7.0] [Reference Citation Analysis]
55 Tao X, Gao C, Huang ZG, Luo W, Liu KL, Peng CT, Ding CZ, Li J, Chen SH, Yu LT. Discovery and evaluation of novel nitrodihydroimidazooxazoles as promising anti-tuberculosis agents. Bioorg Med Chem Lett 2019;29:2511-5. [PMID: 31353295 DOI: 10.1016/j.bmcl.2019.06.055] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
56 Xu Z, Zhao S, Lv Z, Gao F, Wang Y, Zhang F, Bai L, Deng J, Wang Q, Fan Y. Design, Synthesis, and Evaluation of Tetraethylene Glycol‐Tethered Isatin–1,2,3‐Triazole–Coumarin Hybrids as Novel Anticancer Agents. J Heterocyclic Chem 2019;56:1127-32. [DOI: 10.1002/jhet.3475] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
57 Fan YL, Wu JB, Ke X, Huang ZP. Design, synthesis and evaluation of oxime-functionalized nitrofuranylamides as novel antitubercular agents. Bioorg Med Chem Lett 2018;28:3064-6. [PMID: 30119957 DOI: 10.1016/j.bmcl.2018.07.046] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
58 Gao F, Xiao J, Huang G. Current scenario of tetrazole hybrids for antibacterial activity. European Journal of Medicinal Chemistry 2019;184:111744. [DOI: 10.1016/j.ejmech.2019.111744] [Cited by in Crossref: 17] [Cited by in F6Publishing: 10] [Article Influence: 5.7] [Reference Citation Analysis]
59 Agrwal A, Juneja S, Dwivedi S, Kasana V. Molecular docking and antimicrobial analyses of synthesized imidazole derivatives in solvent less condition, adjacent to human pathogenic bacterial strains. Materials Today: Proceedings 2022;57:2250-4. [DOI: 10.1016/j.matpr.2021.12.452] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
60 Zhao S, Lv Z, Deng J, Zhang G, Xu Z. Pyrrolidine‐containing or Piperazine‐containing Nitrofuranylamides: Design, Synthesis, and In Vitro Anti‐mycobacterial Activities. J Heterocyclic Chem 2018;55:2996-3000. [DOI: 10.1002/jhet.3340] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
61 Zheng X, Ma Z, Zhang D. Synthesis of Imidazole-Based Medicinal Molecules Utilizing the van Leusen Imidazole Synthesis. Pharmaceuticals (Basel) 2020;13:E37. [PMID: 32138202 DOI: 10.3390/ph13030037] [Cited by in Crossref: 20] [Cited by in F6Publishing: 8] [Article Influence: 10.0] [Reference Citation Analysis]
62 Gupta PK, Azzam MA, Saquib M, Hussain MK. A Highly Efficient and Eco-Friendly Synthesis of Disubstituted Imidazoles in Ionic Liquid from Gem -Dibromo Vinylarenes and Amidines. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2022.2061532] [Reference Citation Analysis]
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64 Gao F, Ye L, Wang Y, Kong F, Zhao S, Xiao J, Huang G. Benzofuran-isatin hybrids and their in vitro anti-mycobacterial activities against multi-drug resistant Mycobacterium tuberculosis. Eur J Med Chem 2019;183:111678. [PMID: 31525660 DOI: 10.1016/j.ejmech.2019.111678] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 2.3] [Reference Citation Analysis]
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