Dihydropyrimidinones as potent anticancer agents : medicinal chemistry perspective / edited by Mashooq Ahmad Bhat, Muneeb U. Rehman, Amita Verma.

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Bibliographic Details
Online Access: Full Text (via ScienceDirect)
Other Authors: Bhat, Mashooq Ahmad (Editor), Rehman. Muneeb U. (Editor), Verma, Amita (Editor)
Format: Electronic eBook
Language:English
Published: Amsterdam, Netherlands ; Cambridge, MA : Elsevier, [2023]
Subjects:

MARC

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245 0 0 |a Dihydropyrimidinones as potent anticancer agents :  |b medicinal chemistry perspective /  |c edited by Mashooq Ahmad Bhat, Muneeb U. Rehman, Amita Verma. 
264 1 |a Amsterdam, Netherlands ;  |a Cambridge, MA :  |b Elsevier,  |c [2023] 
300 |a 1 online resource (xiii, 279 pages) 
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504 |a Includes bibliographical references and index. 
505 0 |a Front Cover -- Dihydropyrimidinones as Potent Anticancer Agents -- Copyright Page -- Contents -- List of contributors -- 1 Introduction of dihydropyrimidinones: a medicinal chemistry perspective -- 1.1 Introduction -- 1.2 History -- 1.3 Separation of isomers -- 1.4 Synthesis -- 1.4.1 Chemistry and biological activities -- 1.4.2 New derivative: biphenyl dihydropyrimidinone -- 1.5 Future perspective -- 1.6 Conclusion -- References -- 2 Synthetic strategies of dihydropyrimidinones -- 2.1 Introduction -- 2.2 Synthetic strategies for dihydropyrimidinones 
505 8 |a 2.2.1 Classical methods to synthesize dihydropyrimidinones -- 2.2.2 Nonclassical methods to synthesize dihydropyrimidinones -- 2.2.2.1 Microwave-assisted synthesis -- 2.2.2.2 Ultrasonication-assisted synthesis -- 2.2.2.3 Synthesis using ionic liquids as catalysts -- 2.2.2.4 Synthesis using nanomaterial-assisted catalysts -- 2.2.2.5 Synthesis under green conditions and chiral catalysts -- 2.2.2.6 Synthesis using miscellaneous strategies -- 2.3 Conclusion -- References -- 3 Biological activities of dihydropyrimidinones -- 3.1 Introduction -- 3.1.1 Antiinflammatory activity 
505 8 |a 4.2 Synthetic strategies -- 4.3 Pharmacological potential of dihydropyrimidinones -- 4.3.1 Antifilarial activity -- 4.3.2 Antitubercular activity -- 4.3.3 Antihypertensive activity -- 4.3.4 Antibacterial activity -- 4.3.5 Anticancer activity -- 4.3.6 Antiinflammatory activity -- 4.3.7 Anti-HIV -- 4.3.8 Analgesic activity -- 4.3.9 Antifungal activity -- 4.3.10 Antihyperglycemic activity -- 4.3.11 Antisevere acute respiratory syndrome activity -- 4.3.12 Antioxidant activity -- 4.3.13 Anticonvulsant activity -- 4.3.14 Anti-Alzheimer's activity -- 4.3.15 Antihepatitis activity -- 4.4 Conclusion 
505 8 |a Acknowledgment -- Conflict of interest -- Funding -- References -- 5 Dihydropyrimidinones scaffold and potential anticancer targets -- 5.1 Introduction -- 5.2 Biological activities -- 5.2.1 Anticancer properties -- 5.2.2 Dihydropyrimidin-2(1H)-one (or thione) scaffolds potent against different cancers -- 5.2.2.1 Diarylpyrazole-ligated dihydropyrimidinones are potent scaffolds against breast cancer -- 5.2.2.1.1 Dihydropyrimidinone-based scaffolds are effective against breast cancer -- 5.2.2.1.2 DHPM-based scaffolds block kinesin Eg5 
588 |a Description based on online resource; title from digital title page (viewed on September 21, 2023). 
650 0 |a Antineoplastic agents  |x Therapeutic use. 
650 0 |a Dihydropyridine  |x Therapeutic use. 
700 1 |a Bhat, Mashooq Ahmad,  |e editor. 
700 1 |a Rehman. Muneeb U.,  |e editor. 
700 1 |a Verma, Amita,  |e editor. 
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776 0 8 |i Print version:  |z 0443190941  |z 9780443190940  |w (OCoLC)1360286365 
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