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For: Nath R, Pathania S, Grover G, Akhtar MJ. Isatin containing heterocycles for different biological activities: Analysis of structure activity relationship. Journal of Molecular Structure 2020;1222:128900. [DOI: 10.1016/j.molstruc.2020.128900] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Asiri M, Abdulsalam AG, Kahtan M, Alsaikhan F, Farhan I, Mutlak DA, Hadrawi SK, Suliman M, Di Lorenzo R, Laneri S. Synthesis of New Zirconium Magnetic Nanocomposite as a Bioactive Agent and Green Catalyst in the Four-Component Synthesis of a Novel Multi-Ring Compound Containing Pyrazole Derivatives. Nanomaterials (Basel) 2022;12. [PMID: 36558322 DOI: 10.3390/nano12244468] [Reference Citation Analysis]
2 Reiland KM, Eckroat TJ. Selective butyrylcholinesterase inhibition by isatin dimers and 3-indolyl-3-hydroxy-2-oxindole dimers. Bioorganic & Medicinal Chemistry Letters 2022;77:129037. [DOI: 10.1016/j.bmcl.2022.129037] [Reference Citation Analysis]
3 Len’shina NA, Arsenyev MV, Fagin AA, Bogdanov AV, Chesnokov SA. Photoreduction and Photoinitiating Ability of 1-Hexadecyl Isatin Derivatives Containing Chemically Different Substituents in the 5-Position. High Energy Chem 2022;56:315-9. [DOI: 10.1134/s0018143922050095] [Reference Citation Analysis]
4 Nchioua I, Alsubari A, Mague JT, Ramli Y. Crystal structure and Hirshfeld surface analysis of N-(2,6-dimethylphenyl)-2-[3-hydroxy-2-oxo-3-(2-oxopropyl)indolin-1-yl]acetamide. Acta Cryst E 2022;78:922-925. [DOI: 10.1107/s2056989022007848] [Reference Citation Analysis]
5 Parakkal SC, Datta R, Muthu S, Irfan A, Jeelani A. Computational investigation into structural, topological, electronic properties, and biological evaluation of spiro[1H-indole-3,2′-3H-1,3-benzothiazole]-2-one. Journal of Molecular Liquids 2022;359:119234. [DOI: 10.1016/j.molliq.2022.119234] [Reference Citation Analysis]
6 Kariuki BM, Abdel-wahab BF, Farahat AA, El-hiti GA. Synthesis and Structure Determination of 1-(4-Methoxyphenyl)-5-methyl-N’-(2-oxoindolin-3-ylidene)-1H-1,2,3-triazole-4-carbohydrazide. Molbank 2022;2022:M1374. [DOI: 10.3390/m1374] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 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]
8 Eldeeb M, Sanad EF, Ragab A, Ammar YA, Mahmoud K, Ali MM, Hamdy NM. Anticancer Effects with Molecular Docking Confirmation of Newly Synthesized Isatin Sulfonamide Molecular Hybrid Derivatives against Hepatic Cancer Cell Lines. Biomedicines 2022;10:722. [DOI: 10.3390/biomedicines10030722] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 6.0] [Reference Citation Analysis]
9 Malah TE, Farag H, Hemdan BA, Abdel Mageid RE, Abdelrahman MT, El-manawaty MA, Nour HF. Synthesis, in vitro antimicrobial evaluation, and molecular docking studies of new isatin-1,2,3-triazole hybrids. Journal of Molecular Structure 2022;1250:131855. [DOI: 10.1016/j.molstruc.2021.131855] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
10 Kancharla SK, Birudaraju S, Pal A, Krishnakanth Reddy L, Reddy ER, Vagolu SK, Sriram D, Bonige KB, Korupolu RB. Synthesis and biological evaluation of isatin oxime ether-tethered aryl 1 H -1,2,3-triazoles as inhibitors of Mycobacterium tuberculosis. New J Chem 2022;46:2863-74. [DOI: 10.1039/d1nj05171g] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Manchala L, Reddy Tatipelly M, Andole S, Manda S, Prasad Devarakonda K, Arukula R, Gangarapu K. Synthesis and biological evaluation of new bis isatin derivatives for CNS activity. Materials Today: Proceedings 2022;64:903-908. [DOI: 10.1016/j.matpr.2022.06.052] [Reference Citation Analysis]
12 Ismail R, Yunarti RT, Cahyana AH. Synthesis Schiff base of isatin derivatives catalyzed by iron (III) trifluoromethanesulfonate. THE 9TH INTERNATIONAL CONFERENCE OF THE INDONESIAN CHEMICAL SOCIETY ICICS 2021: Toward a Meaningful Society 2022. [DOI: 10.1063/5.0104134] [Reference Citation Analysis]
13 Mehreen S, Zia M, Khan A, Hussain J, Ullah S, Anwar MU, Al-harrasi A, Naseer MM. Phenoxy pendant isatins as potent α-glucosidase inhibitors: reciprocal carbonyl⋯carbonyl interactions, antiparallel π⋯π stacking driven solid state self-assembly and biological evaluation. RSC Adv 2022;12:20919-28. [DOI: 10.1039/d2ra03307k] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
14 Gideon DA, Annadurai P, Nirusimhan V, Parashar A, James J, Dhayabaran VV. Evaluation of the Anticancer Activities of Isatin-Based Derivatives. Handbook of Oxidative Stress in Cancer: Therapeutic Aspects 2022. [DOI: 10.1007/978-981-16-1247-3_51-1] [Reference Citation Analysis]
15 Gideon DA, Annadurai P, Nirusimhan V, Parashar A, James J, Dhayabaran VV. Evaluation of the Anticancer Activities of Isatin-Based Derivatives. Handbook of Oxidative Stress in Cancer: Therapeutic Aspects 2022. [DOI: 10.1007/978-981-16-5422-0_51] [Reference Citation Analysis]
16 Muthumanickam S, Thennila M, Yuvaraj P, Lingam KAP, Selvakumar K. An Efficient Synthesis of Heterogeneous and Hard Bound Ti IV ‐MCM‐41 Catalyzed Mannich Bases and π‐Conjugated Imines. ChemistrySelect 2021;6:14071-6. [DOI: 10.1002/slct.202103547] [Reference Citation Analysis]
17 Ali A, Ali A, Tahir A, Bakht MA, Ahsan MJ. Ultrasound promoted green synthesis, anticancer evaluation, and molecular docking studies of hydrazines: a pilot trial. J Enzyme Inhib Med Chem 2022;37:135-44. [PMID: 34894970 DOI: 10.1080/14756366.2021.1995727] [Reference Citation Analysis]
18 Quadri TW, Olasunkanmi LO, Akpan ED, Ebenso EE. Indole and Its Derivatives as Corrosion Inhibitors. Organic Corrosion Inhibitors 2021. [DOI: 10.1002/9781119794516.ch9] [Reference Citation Analysis]
19 Kumar G, Singh NP, Kumar K. Recent Advancement of Synthesis of Isatins as a Versatile Pharmacophore: A review. Drug Res (Stuttg) 2021;71:115-21. [PMID: 33296925 DOI: 10.1055/a-1238-2639] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]