Pyrimidine: a review on anticancer activity with key emphasis on SAR

A Mahapatra, T Prasad, T Sharma - Future journal of pharmaceutical …, 2021 - Springer
Background Cancer is a global health challenge, it impacts the quality of life and its
treatment is associated with several side effects. Resistance of the cancer cells to the …

Thiophene-based derivatives as anticancer agents: An overview on decade's work

S Pathania, PA Chawla - Bioorganic Chemistry, 2020 - Elsevier
Heterocyclic compounds hold a pivotal place in medicinal chemistry due to their wide range
of biological activities and thus, are exhaustively explored in the field of drug design and …

Expedition of sulfur‐containing heterocyclic derivatives as cytotoxic agents in medicinal chemistry: A decade update

K Laxmikeshav, P Kumari… - Medicinal Research …, 2022 - Wiley Online Library
This review article proposes a comprehensive report of the design strategies engaged in the
development of various sulfur‐bearing cytotoxic agents. The outcomes of various studies …

Thieno [2, 3-d] pyrimidine as a promising scaffold in medicinal chemistry: Recent advances

EMH Ali, MS Abdel-Maksoud, CH Oh - Bioorganic & medicinal chemistry, 2019 - Elsevier
Thienopyrimidine scaffold is a fused heterocyclic ring system that structurally can be
considered as adenine, the purine base that is found in both DNA and RNA-bioisosteres …

Design, synthesis, anticancer and antioxidant activities of amide linked 1, 4-disubstituted 1, 2, 3-triazoles

CP Kaushik, J Sangwan, R Luxmi, D Kumar… - Journal of Molecular …, 2021 - Elsevier
To explore anticancer and antioxidant agents with improved potency, we synthesized a
series of amide linked 1, 4-disubstituted 1, 2, 3-triazoles through click chemistry approach …

Design, synthesis and biological evaluation of novel uracil derivatives bearing 1, 2, 3-triazole moiety as thymidylate synthase (TS) inhibitors and as potential antitumor …

G Lu, X Li, D Wang, F Meng - European journal of medicinal chemistry, 2019 - Elsevier
Research on thymidylate synthase inhibitors has been a hot spot for anticancer drug
development. Here, based on the structures and pharmacological properties of two types of …

Synthesis and evaluation of novel α-substituted chalcones with potent anti-cancer activities and ability to overcome multidrug resistance

S Riaz, M Iqbal, R Ullah, R Zahra, GA Chotana… - Bioorganic …, 2019 - Elsevier
A series of forty α-substituted chalcones were synthesized and screened for their
antiproliferative activities against HCT116 (colorectal) and HCC1954 (breast) cancer cell …

Oxovanadium (IV) complexes with tetradentate thiosemicarbazones. Synthesis, characterization, anticancer enzyme inhibition and in vitro cytotoxicity on breast cancer …

O Ertik, FD Kalındemirtaş, B Kaya, R Yanardag… - Polyhedron, 2021 - Elsevier
Five oxovanadium (IV) complexes were synthesized using acetyl-and benzoylacetone-S-
alkyl-thiosemicarbazones (alkyl= methyl, ethyl, propyl or butyl) and salicylaldehyde …

Recent development in the synthesis of heterocycles by 2-naphthol-based multicomponent reactions

A Chaudhary - Molecular Diversity, 2021 - Springer
Naphthol or β-naphthol is an important starting material that has drawn great attention in
various organic transformations because of its attributes, such as low cost, easy to handle …

Diverse thiophenes as scaffolds in anti-cancer drug development: A concise review

NV Bhilare, PB Auti, VS Marulkar… - Mini Reviews in …, 2021 - ingentaconnect.com
Thiophenes are one of the abundantly found heterocyclic ring systems in many biologically
active compounds. Moreover, various substituted thiophenes exert numerous …