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      Synthesis biological evaluation and molecular docking of isatin hybrids as anti-cancer and anti-microbial agents

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          Abstract

          Isatin, known as 1 H-indole-2,3-dione, was originally recognised as a synthetic molecule until its discovery in the fruits of the cannonball tree, Couroupita guianensis. It is naturally occurring in plants of the genus Isatis and serves as a metabolic derivative of adrenaline in humans. Isatin possesses significant pharmacological importance, and its synthetic versatility has prompted extensive interest in its derivative compounds due to their diverse biological and pharmacological properties. These derivatives represent a valuable class of heterocyclic compounds with potential applications as precursors for synthesizing numerous valuable drugs. In the pursuit of advancing our research on isatin hybrids, we investigate the utilisation of readily available hydrazonoindolin-2-one and isatin as starting materials for the synthesis of a wide range of analogues. Characterisation of the synthesized compounds was carried out through various analytical techniques. Furthermore, the obtained compounds were subjected to extensive testing to evaluate their anticancer and antimicrobial activities. Specifically, their efficacy against key proteins, namely Staphylococcus aureus protein (PDB ID: 1JIJ), Escherichia coli protein (PDB ID: 1T9U), Pseudomonas aeruginosa protein (PDB ID: 2UV0), and Acinetobacter baumannii protein (PDB ID: 4HKG), was examined through molecular docking calculations. Several molecules, such as 3, 4, 6, 16, and 19, displayed remarkable activity against the renal cancer cell line UO-31. Additionally, the results of antimicrobial activity testing revealed that compound 16 exhibited significant cytotoxicity against Candida albicans and Cryptococcus neoformans. Subsequently, ADME/T calculations were performed to gain insights into the potential effects and reactions of these molecules within human metabolism. This comprehensive study provides valuable insights into the potential pharmacological applications of isatin derivatives and underscores their significance in drug development.

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          Most cited references43

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          Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings

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            Lead- and drug-like compounds: the rule-of-five revolution.

            Citations in CAS SciFinder to the rule-of-five (RO5) publication will exceed 1000 by year-end 2004. Trends in the RO5 literature explosion that can be discerned are the further definitions of drug-like. This topic is explored in terms of drug-like physicochemical features, drug-like structural features, a comparison of drug-like and non-drug-like in drug discovery and a discussion of how drug-like features relate to clinical success. Physicochemical features of CNS drugs and features related to CNS blood-brain transporter affinity are briefly reviewed. Recent literature on features of non-oral drugs is reviewed and how features of lead-like compounds differ from those of drug-like compounds is discussed. Most recently, partly driven by NIH roadmap initiatives, considerations have arisen as to what tool-like means in the search for chemical tools to probe biology space. All these topics frame the scope of this short review/perspective.: © 2004 Elsevier Ltd . All rights reserved.
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              Prediction of drug solubility from structure.

              The aqueous solubility of a drug is an important factor affecting its bioavailability. Numerous computational methods have been developed for the prediction of aqueous solubility from a compound's structure. A review is provided of the methodology and quality of results for the most useful procedures including the model implemented in the QikProp program. Viable methods now exist for predictions with less than 1 log unit uncertainty, which is adequate for prescreening synthetic candidates or design of combinatorial libraries. Further progress with predictive methods would require an experimental database of highly accurate solubilities for a large, diverse collection of drug-like molecules.
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                Author and article information

                Journal
                J Enzyme Inhib Med Chem
                J Enzyme Inhib Med Chem
                Journal of Enzyme Inhibition and Medicinal Chemistry
                Taylor & Francis
                1475-6366
                1475-6374
                11 December 2023
                2024
                11 December 2023
                : 39
                : 1
                : 2288548
                Affiliations
                [a ]Department of Pharmaceutics, College of Pharmacy, King Saud University , Riyadh, Saudi Arabia
                [b ]Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University , Riyadh, Saudi Arabia
                [c ]Plant and Animal Production Department, Technical Sciences Vocational School of Sivas, Sivas Cumhuriyet University , Sivas, Turkey
                [d ]College of Pharmacy, Central Laboratory, King Saud University , Riyadh, Saudi Arabia
                Author notes
                CONTACT Ahmed Bari abari@ 123456ksu.edu.sa Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University , P.O. Box 2457, Riyadh 11451, Saudi Arabia

                Supplemental data for this article is available online at https://doi.org/10.1080/14756366.2023.2288548

                Article
                2288548
                10.1080/14756366.2023.2288548
                11721758
                38073431
                86536555-cf1d-46de-bd85-b840206b1499
                © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.

                History
                Page count
                Figures: 7, Tables: 4, Pages: 14, Words: 8920
                Categories
                Research Article
                Research Article

                Pharmaceutical chemistry
                hydrazone–indolinone,antimicrobial,anticancer,oxindole,spiroxindole
                Pharmaceutical chemistry
                hydrazone–indolinone, antimicrobial, anticancer, oxindole, spiroxindole

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