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Das S, Borkotoky S, Rymbai M, Borah VV, Roy JD, Kaping S, Helissey P, Vishwakarma JN. Novel ferrocene-pyrazolo[1,5-a]pyrimidine hybrids: A facile environment-friendly regioselective synthesis, structure elucidation, and their antioxidant, antibacterial, and anti-biofilm activities. J Chem Sci 2022;134. [DOI: 10.1007/s12039-022-02064-y] [Reference Citation Analysis]
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Sharma A, Agrahari AK, Rajkhowa S, Tiwari VK. Emerging impact of triazoles as anti-tubercular agent. Eur J Med Chem 2022;238:114454. [PMID: 35597009 DOI: 10.1016/j.ejmech.2022.114454] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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Jayathuna MA, Ahmed S, Kim YG, Gajendiran M, Kim K, Rahiman AK. Ferrocenylimine-based homoleptic metal(II) complexes: Theoretical, biocompatibility, in vitro anti-proliferative, and in silico molecular docking and pharmacokinetics studies. Journal of Molecular Structure 2022;1250:131905. [DOI: 10.1016/j.molstruc.2021.131905] [Reference Citation Analysis]
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Pawlędzio S, Makal A, Plażuk D, Woźniak K. Experimental charge density of ferrocenyl derivative of β-lactam. Journal of Molecular Structure 2020;1217:128274. [DOI: 10.1016/j.molstruc.2020.128274] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
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Wang R, Chen H, Yan W, Zheng M, Zhang T, Zhang Y. Ferrocene-containing hybrids as potential anticancer agents: Current developments, mechanisms of action and structure-activity relationships. Eur J Med Chem 2020;190:112109. [PMID: 32032851 DOI: 10.1016/j.ejmech.2020.112109] [Cited by in Crossref: 71] [Cited by in F6Publishing: 77] [Article Influence: 23.7] [Reference Citation Analysis]
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Ludwig BS, Correia JD, Kühn FE. Ferrocene derivatives as anti-infective agents. Coordination Chemistry Reviews 2019;396:22-48. [DOI: 10.1016/j.ccr.2019.06.004] [Cited by in Crossref: 50] [Cited by in F6Publishing: 34] [Article Influence: 12.5] [Reference Citation Analysis]
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Mahapatra DK, Bharti SK, Asati V, Singh SK. Perspectives of medicinally privileged chalcone based metal coordination compounds for biomedical applications. European Journal of Medicinal Chemistry 2019;174:142-58. [DOI: 10.1016/j.ejmech.2019.04.032] [Cited by in Crossref: 53] [Cited by in F6Publishing: 55] [Article Influence: 13.3] [Reference Citation Analysis]
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Singh A, Lumb I, Mehra V, Kumar V. Ferrocene-appended pharmacophores: an exciting approach for modulating the biological potential of organic scaffolds. Dalton Trans 2019;48:2840-60. [DOI: 10.1039/c8dt03440k] [Cited by in Crossref: 76] [Cited by in F6Publishing: 78] [Article Influence: 19.0] [Reference Citation Analysis]
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Swetha Y, Reddy ER, Kumar JR, Trivedi R, Giribabu L, Sridhar B, Rathod B, Prakasham RS. Synthesis, characterization and antimicrobial evaluation of ferrocene–oxime ether benzyl 1 H -1,2,3-triazole hybrids. New J Chem 2019;43:8341-51. [DOI: 10.1039/c9nj00660e] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 4.8] [Reference Citation Analysis]
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Nalla V, Shaikh A, Bapat S, Vyas R, Karthikeyan M, Yogeeswari P, Sriram D, Muthukrishnan M. Identification of potent chromone embedded [1,2,3]-triazoles as novel anti-tubercular agents. R Soc Open Sci 2018;5:171750. [PMID: 29765644 DOI: 10.1098/rsos.171750] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 2.6] [Reference Citation Analysis]
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Singh A, Mehra V, Sadeghiani N, Mozaffari S, Parang K, Kumar V. Ferrocenylchalcone–uracil conjugates: synthesis and cytotoxic evaluation. Med Chem Res 2018;27:1260-8. [DOI: 10.1007/s00044-018-2145-5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
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| 12 |
Singh A, Saha ST, Perumal S, Kaur M, Kumar V. Azide-Alkyne Cycloaddition En Route to 1H-1,2,3-Triazole-Tethered Isatin-Ferrocene, Ferrocenylmethoxy-Isatin, and Isatin-Ferrocenylchalcone Conjugates: Synthesis and Antiproliferative Evaluation. ACS Omega 2018;3:1263-8. [PMID: 30023800 DOI: 10.1021/acsomega.7b01755] [Cited by in Crossref: 27] [Cited by in F6Publishing: 27] [Article Influence: 5.4] [Reference Citation Analysis]
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| 13 |
Singh A, Viljoen A, Kremer L, Kumar V. Azide-alkyne cycloaddition en route to 4-aminoquinoline-ferrocenylchalcone conjugates: synthesis and anti-TB evaluation. Future Med Chem 2017;9:1701-8. [PMID: 28869400 DOI: 10.4155/fmc-2017-0098] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
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Zhang S, Xu Z, Gao C, Ren QC, Chang L, Lv ZS, Feng LS. Triazole derivatives and their anti-tubercular activity. Eur J Med Chem 2017;138:501-13. [PMID: 28692915 DOI: 10.1016/j.ejmech.2017.06.051] [Cited by in Crossref: 274] [Cited by in F6Publishing: 284] [Article Influence: 45.7] [Reference Citation Analysis]
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Singh A, Gut J, Rosenthal PJ, Kumar V. 4-Aminoquinoline-ferrocenyl-chalcone conjugates: Synthesis and anti-plasmodial evaluation. European Journal of Medicinal Chemistry 2017;125:269-77. [DOI: 10.1016/j.ejmech.2016.09.044] [Cited by in Crossref: 47] [Cited by in F6Publishing: 51] [Article Influence: 7.8] [Reference Citation Analysis]
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Delpiccolo CM, Martinez-amezaga M, Mata EG. Recent Approaches Toward the Generation of Molecular Diversity Based on β-Lactam Structures. Beta-Lactams 2017. [DOI: 10.1007/978-3-319-55621-5_5] [Cited by in Crossref: 3] [Article Influence: 0.5] [Reference Citation Analysis]
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Bhalla A, Bari SS, Bhalla J. Synthesis of Diverse β-Lactams: Role of Appended Hetero Moiety on Its Activity. Beta-Lactams 2017. [DOI: 10.1007/978-3-319-55621-5_1] [Reference Citation Analysis]
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Bari SS, Bhalla A, Bhalla J. Role of Transition Metal Reagents in β-Lactam Synthesis: New Paradigms. Beta-Lactams 2017. [DOI: 10.1007/978-3-319-55621-5_2] [Reference Citation Analysis]
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Singh A, Biot C, Viljoen A, Dupont C, Kremer L, Kumar K, Kumar V. 1 H -1,2,3-triazole-tethered uracil-ferrocene and uracil-ferrocenylchalcone conjugates: Synthesis and antitubercular evaluation. Chem Biol Drug Des 2017;89:856-61. [DOI: 10.1111/cbdd.12908] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 3.4] [Reference Citation Analysis]
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Shaveta, Mishra S, Singh P. Hybrid molecules: The privileged scaffolds for various pharmaceuticals. Eur J Med Chem 2016;124:500-36. [PMID: 27598238 DOI: 10.1016/j.ejmech.2016.08.039] [Cited by in Crossref: 267] [Cited by in F6Publishing: 277] [Article Influence: 38.1] [Reference Citation Analysis]
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Błauż A, Rychlik B, Makal A, Szulc K, Strzelczyk P, Bujacz G, Zakrzewski J, Woźniak K, Plażuk D. Ferrocene-Biotin Conjugates: Synthesis, Structure, Cytotoxic Activity and Interaction with Avidin. ChemPlusChem 2016;81:1191-201. [DOI: 10.1002/cplu.201600320] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
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Liu C, Hou L, Meng A, Han G, Zhang W, Jiang S. Design, synthesis and bioactivity evaluation of Galf mimics as antitubercular agents. Carbohydr Res 2016;429:135-42. [PMID: 26706033 DOI: 10.1016/j.carres.2015.11.002] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
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Lozano-Cruz T, Ortega P, Batanero B, Copa-Patiño JL, Soliveri J, de la Mata FJ, Gómez R. Synthesis, characterization and antibacterial behavior of water-soluble carbosilane dendrons containing ferrocene at the focal point. Dalton Trans 2015;44:19294-304. [PMID: 26489707 DOI: 10.1039/c5dt02230d] [Cited by in Crossref: 21] [Cited by in F6Publishing: 20] [Article Influence: 2.6] [Reference Citation Analysis]
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Jarrahpour A, Shirvani P, Sinou V, Latour C, Brunel JM. Synthesis and biological evaluation of some new β-lactam-triazole hybrids. Med Chem Res 2016;25:149-62. [DOI: 10.1007/s00044-015-1474-x] [Cited by in Crossref: 26] [Cited by in F6Publishing: 18] [Article Influence: 3.3] [Reference Citation Analysis]
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Quintana C, Klahn AH, Artigas V, Fuentealba M, Biot C, Halloum I, Kremer L, Arancibia R. Cyrhetrenyl and ferrocenyl 1,3,4-thiadiazole derivatives: Synthesis, characterization, crystal structures and in vitro antitubercular activity. Inorganic Chemistry Communications 2015;55:48-50. [DOI: 10.1016/j.inoche.2015.03.008] [Cited by in Crossref: 18] [Cited by in F6Publishing: 15] [Article Influence: 2.3] [Reference Citation Analysis]
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Vandekerckhove S, D'hooghe M. Quinoline-based antimalarial hybrid compounds. Bioorg Med Chem 2015;23:5098-119. [PMID: 25593097 DOI: 10.1016/j.bmc.2014.12.018] [Cited by in Crossref: 138] [Cited by in F6Publishing: 122] [Article Influence: 15.3] [Reference Citation Analysis]
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Kamal A, Kumar K, Kumar V, Mahajan RK. Electrochemical and Chromogenic Sensors Based on Ferrocene Appended Chalcone for Selective Quantification of Copper (II). Electrochimica Acta 2014;145:307-13. [DOI: 10.1016/j.electacta.2014.08.068] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 2.4] [Reference Citation Analysis]
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Soldati R, Aliprandi A, Mauro M, De Cola L, Giacomini D. β-Lactam Bioconjugates Bearing Luminescent Platinum(II) Tags: Synthesis and Photophysical Characterization: β-Lactam Bioconjugates Bearing Luminescent Tags. Eur J Org Chem 2014;2014:7113-21. [DOI: 10.1002/ejoc.201402740] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.6] [Reference Citation Analysis]
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Li Y, de Kock C, Smith PJ, Chibale K, Smith GS. Synthesis and Evaluation of a Carbosilane Congener of Ferroquine and Its Corresponding Half-Sandwich Ruthenium and Rhodium Complexes for Antiplasmodial and β-Hematin Inhibition Activity. Organometallics 2014;33:4345-8. [DOI: 10.1021/om500622p] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 3.6] [Reference Citation Analysis]
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Kumar K, Schniper S, González-Sarrías A, Holder AA, Sanders N, Sullivan D, Jarrett WL, Davis K, Bai F, Seeram NP, Kumar V. Highly potent anti-proliferative effects of a gallium(III) complex with 7-chloroquinoline thiosemicarbazone as a ligand: synthesis, cytotoxic and antimalarial evaluation. Eur J Med Chem 2014;86:81-6. [PMID: 25147149 DOI: 10.1016/j.ejmech.2014.08.054] [Cited by in Crossref: 27] [Cited by in F6Publishing: 24] [Article Influence: 3.0] [Reference Citation Analysis]
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| 31 |
Raj R, Sharma V, Hopper MJ, Patel N, Hall D, Wrischnik LA, Land KM, Kumar V. Synthesis and preliminary in vitro activity of mono- and bis-1H-1,2,3-triazole-tethered β-lactam-isatin conjugates against the human protozoal pathogen Trichomonas vaginalis. Med Chem Res 2014;23:3671-80. [PMID: 32214766 DOI: 10.1007/s00044-014-0956-6] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 1.7] [Reference Citation Analysis]
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Muntaner JG, Casarrubios L, Sierra MA. Synthesis of new bioorganometallic Ir- and Rh-complexes having β-lactam containing ligands. Org Biomol Chem 2014;12:286-97. [DOI: 10.1039/c3ob41354c] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 0.9] [Reference Citation Analysis]
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de Carvalho da Silva F, Cardoso MFDC, Ferreira PG, Ferreira VF. Biological Properties of 1H-1,2,3- and 2H-1,2,3-Triazoles. Topics in Heterocyclic Chemistry 2014. [DOI: 10.1007/7081_2014_124] [Cited by in Crossref: 30] [Cited by in F6Publishing: 28] [Article Influence: 3.3] [Reference Citation Analysis]
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Liu Y, Zhang H, Yin D, Chen D. Synthesis, characterization, and antimicrobial activity of novel heterocyclic compounds containing a ferrocene unit via Michael addition reaction. Res Chem Intermed 2015;41:3793-801. [DOI: 10.1007/s11164-013-1489-1] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 0.5] [Reference Citation Analysis]
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Kumar K, Biot C, Carrère-kremer S, Kremer L, Guérardel Y, Roussel P, Kumar V. Base-Promoted Expedient Access to Spiroisatins: Synthesis and Antitubercular Evaluation of 1 H -1,2,3-Triazole-Tethered Spiroisatin–Ferrocene and Isatin–Ferrocene Conjugates. Organometallics 2013;32:7386-98. [DOI: 10.1021/om4009229] [Cited by in Crossref: 25] [Cited by in F6Publishing: 26] [Article Influence: 2.5] [Reference Citation Analysis]
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N’da DD, Smith PJ. Synthesis, in vitro antiplasmodial and antiproliferative activities of a series of quinoline–ferrocene hybrids. Med Chem Res 2014;23:1214-24. [DOI: 10.1007/s00044-013-0748-4] [Cited by in Crossref: 32] [Cited by in F6Publishing: 33] [Article Influence: 3.2] [Reference Citation Analysis]
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Baeza B, Casarrubios L, Sierra MA. Towards a General Synthesis of 3-Metal-Substituted β-Lactams. Chem Eur J 2013;19:11536-40. [DOI: 10.1002/chem.201301114] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 2.0] [Reference Citation Analysis]
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| 38 |
Raj R, Singh P, Singh P, Gut J, Rosenthal PJ, Kumar V. Azide-alkyne cycloaddition en route to 1 H -1,2,3-triazole-tethered 7-chloroquinoline-isatin chimeras: Synthesis and antimalarial evaluation. European Journal of Medicinal Chemistry 2013;62:590-6. [DOI: 10.1016/j.ejmech.2013.01.032] [Cited by in Crossref: 86] [Cited by in F6Publishing: 88] [Article Influence: 8.6] [Reference Citation Analysis]
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Kumar K, Carrère-kremer S, Kremer L, Guérardel Y, Biot C, Kumar V. 1 H -1,2,3-Triazole-Tethered Isatin–Ferrocene and Isatin–Ferrocenylchalcone Conjugates: Synthesis and in Vitro Antitubercular Evaluation. Organometallics 2013;32:5713-9. [DOI: 10.1021/om301157z] [Cited by in Crossref: 70] [Cited by in F6Publishing: 72] [Article Influence: 7.0] [Reference Citation Analysis]
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| 40 |
Raj R, Singh P, Haberkern NT, Faucher RM, Patel N, Land KM, Kumar V. Synthesis of 1H-1,2,3-triazole linked β-lactam-isatin bi-functional hybrids and preliminary analysis of in vitro activity against the protozoal parasite Trichomonas vaginalis. Eur J Med Chem 2013;63:897-906. [PMID: 23631874 DOI: 10.1016/j.ejmech.2013.03.019] [Cited by in Crossref: 34] [Cited by in F6Publishing: 34] [Article Influence: 3.4] [Reference Citation Analysis]
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| 41 |
Kumar K, Carrère-kremer S, Kremer L, Guérardel Y, Biot C, Kumar V. Azide–alkynecycloadditionen route towards 1H-1,2,3-triazole-tethered β-lactam–ferrocene and β-lactam–ferrocenylchalcone conjugates: synthesis and in vitro anti-tubercular evaluation. Dalton Trans 2013;42:1492-500. [DOI: 10.1039/c2dt32148c] [Cited by in Crossref: 44] [Cited by in F6Publishing: 45] [Article Influence: 4.4] [Reference Citation Analysis]
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| 42 |
Nisha, Mehra V, Hopper M, Patel N, Hall D, Wrischnik LA, Land KM, Kumar V. Design and synthesis of β-amino alcohol based β-lactam–isatin chimeras and preliminary analysis of in vitro activity against the protozoal pathogen Trichomonas vaginalis. Med Chem Commun 2013;4:1018. [DOI: 10.1039/c3md00057e] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 1.9] [Reference Citation Analysis]
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| 43 |
Li Y, de Kock C, Smith PJ, Guzgay H, Hendricks DT, Naran K, Mizrahi V, Warner DF, Chibale K, Smith GS. Synthesis, Characterization, and Pharmacological Evaluation of Silicon-Containing Aminoquinoline Organometallic Complexes As Antiplasmodial, Antitumor, and Antimycobacterial Agents. Organometallics 2013;32:141-50. [DOI: 10.1021/om300945c] [Cited by in Crossref: 43] [Cited by in F6Publishing: 43] [Article Influence: 3.9] [Reference Citation Analysis]
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| 44 |
Kumar K, Sagar S, Esau L, Kaur M, Kumar V. Synthesis of novel 1H-1,2,3-triazole tethered C-5 substituted uracil–isatin conjugates and their cytotoxic evaluation. European Journal of Medicinal Chemistry 2012;58:153-9. [DOI: 10.1016/j.ejmech.2012.10.008] [Cited by in Crossref: 45] [Cited by in F6Publishing: 45] [Article Influence: 4.1] [Reference Citation Analysis]
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| 45 |
Mehra V, Singh P, Kumar V. β-Lactam-synthon-interceded diastereoselective synthesis of functionally enriched thioxo-imidazolidines, imidazolidin-2-ones, piperazine-5,6-diones and 4,5-dihydroimidazoles. Tetrahedron 2012;68:8395-402. [DOI: 10.1016/j.tet.2012.08.005] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 1.8] [Reference Citation Analysis]
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| 46 |
Singh P, Sharma P, Anand A, Bedi PM, Kaur T, Saxena AK, Kumar V. Azide-alkyne cycloaddition en route to novel 1H-1,2,3-triazole tethered isatin conjugates with in vitro cytotoxic evaluation. Eur J Med Chem 2012;55:455-61. [PMID: 22818042 DOI: 10.1016/j.ejmech.2012.06.057] [Cited by in Crossref: 52] [Cited by in F6Publishing: 45] [Article Influence: 4.7] [Reference Citation Analysis]
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