Multifunctional compounds: smart molecules for multifactorial diseases
- PMID: 24565571
- DOI: 10.1016/j.ejmech.2014.01.060
Multifunctional compounds: smart molecules for multifactorial diseases
Abstract
Multifunctional compounds (MFCs) are designed broadly as hybrid or conjugated drugs or as chimeric drugs from two or more pharmacophores/drugs having specific pharmacological activities. These are capable of eliciting multiple pharmacological actions and have emerged as magic bullets in treatment of multifactorial diseases. Many research articles disclosing the development of such compounds for treatment of multifactorial diseases are published during last 7 years. Some successful MFC candidates for multifactorial CNS disorders include ziprasidone, duloxetine, ladostigil and M-30 whereas sunitinib, lapatinib and synthetic oleandane triterpinoids are the successful MFC candidates for various cancers. Many more compounds derived from berberine, tacrine, artemisnin, quinine, NSAIDs, pralidoxine, donepezil, rivastigmine, curcumin and various antioxidants are under investigations for exploration of their multifunctional potential. In general, MFCs possess the advantages of reduced molecularity, no drug-drug interactions and improved pharmacokinetics and pharmacodynamics. A MFC derived from two or more different pharmacophores exerts its activities by interacting with respective receptors of its constituent pharmacophores. It may also exhibit additional binding interactions with the receptor sites that may be responsible for significantly improved or additional activities. The present review discusses various MFCs developed for specific class of disorders with an aim to provide an insight into the strategies in medicinal chemistry for development of such compounds.
Keywords: Chimeric; Hybrid; Multifactorial; Multifunctional; Multiple ligands; Multitarget.
Copyright © 2014. Published by Elsevier Masson SAS.
Similar articles
-
Hybrid compounds: from simple combinations to nanomachines.BioDrugs. 2012 Feb 1;26(1):21-31. doi: 10.2165/11597630-000000000-00000. BioDrugs. 2012. PMID: 22239618 Review.
-
Chimeric Structures in Mental Illnesses-"Magic" Molecules Specified for Complex Disorders.Int J Mol Sci. 2022 Mar 29;23(7):3739. doi: 10.3390/ijms23073739. Int J Mol Sci. 2022. PMID: 35409098 Free PMC article. Review.
-
Challenges in the design of multitarget drugs against multifactorial pathologies: a new life for medicinal chemistry?Future Med Chem. 2013 Jan;5(1):5-7. doi: 10.4155/fmc.12.193. Future Med Chem. 2013. PMID: 23256805 No abstract available.
-
Multicomponent phytotherapeutic approach gaining momentum: Is the "one drug to fit all" model breaking down?Phytomedicine. 2013 Dec 15;21(1):1-14. doi: 10.1016/j.phymed.2013.07.015. Epub 2013 Sep 12. Phytomedicine. 2013. PMID: 24035674 Review.
-
Molecular conceptor for training in medicinal chemistry, drug design, and cheminformatics.Chem Biol Drug Des. 2007 Jan;69(1):75-82. doi: 10.1111/j.1747-0285.2007.00465.x. Chem Biol Drug Des. 2007. PMID: 17313460
Cited by
-
Design, antiviral and cytostatic properties of isoxazolidine-containing amonafide analogues.Bioorg Med Chem. 2015 Jul 1;23(13):3135-46. doi: 10.1016/j.bmc.2015.04.079. Epub 2015 May 6. Bioorg Med Chem. 2015. PMID: 26001344 Free PMC article.
-
Synthesis and in-vitro anti-proliferative with antimicrobial activity of new coumarin containing heterocycles hybrids.Sci Rep. 2023 Dec 21;13(1):22791. doi: 10.1038/s41598-023-50170-9. Sci Rep. 2023. PMID: 38123695 Free PMC article.
-
Synthesis of novel perillyl-dihydropyrimidinone hybrids designed for antiproliferative activity.Medchemcomm. 2018 Jul 31;9(9):1553-1564. doi: 10.1039/c8md00270c. eCollection 2018 Sep 1. Medchemcomm. 2018. PMID: 30288229 Free PMC article.
-
Naphthoquinone-Quinolone Hybrids with Antitumor Effects on Breast Cancer Cell Lines-From the Synthesis to 3D-Cell Culture Effects.Int J Mol Sci. 2024 Jun 12;25(12):6490. doi: 10.3390/ijms25126490. Int J Mol Sci. 2024. PMID: 38928197 Free PMC article.
-
Advances in developing novel therapeutic strategies for Alzheimer's disease.Mol Neurodegener. 2018 Dec 12;13(1):64. doi: 10.1186/s13024-018-0299-8. Mol Neurodegener. 2018. PMID: 30541602 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources