Veliparib (ABT-888), a PARP inhibitor potentiates the cytotoxic activity of 5-fluorouracil by inhibiting MMR pathway through deregulation of MSH6 in colorectal cancer …

S Paul, S Chatterjee, S Sinha, SR Dash… - Expert Opinion on …, 2023 - Taylor & Francis
Objective Sensitization of mismatch repair (MMR)-deficient colorectal cancer (CRC) cells by
5-Fluorouracil (5-FU) is well-documented. But not much is known about the treatment of …

A mini review of novel topoisomerase II inhibitors as future anticancer agents

CO Okoro, TH Fatoki - International journal of molecular sciences, 2023 - mdpi.com
Several reviews of inhibitors of topoisomerase II have been published, covering research
before 2018. Therefore, this review is focused primarily on more recent publications with …

How to nurture natural products to create new therapeutics: Strategic innovations and molecule-to-medicinal insights into therapeutic advancements

A Acharya, M Nagpure, N Roy, V Gupta… - Drug Discovery …, 2024 - Elsevier
Highlights•Nurturing NPs to create new therapeutics has been discussed.•Various
innovative strategies important for successful discovery of drugs, clinical candidates, and …

Synthesis of amino juglone derivatives with adjuvant activity against clinical isolated methicillin-resistant staphylococcus aureus strains

C Majdi, M Seghir, Y Wegrich, D Behilil, D Bénimélis… - Bioorganic …, 2024 - Elsevier
naphthoquinones hydroxyderivatives belong to an important class of natural products and
have been known as a favored scaffold in medicinal chemistry due to their multiple …

Nitrogen‐containing heterocycles as topoisomerase II inhibitors for targeting cancer: Recent updates

C Sahu, A Chaurasiya… - Journal of Heterocyclic …, 2023 - Wiley Online Library
Cancer is a broad word for a set of diseases that can begin in virtually any organ or tissue of
the body and spread to other organs. In 2020, cancer was the largest cause of death …

Practical Access to Fused Carbazoles via Oxidative Benzannulation and their Photophysical Properties

S Rai, BE Patil, P Kumari, PS Mainkar… - The Journal of …, 2024 - ACS Publications
An aryne annulation strategy for the synthesis of fused carbazoles is developed using
indolyl β-ketonitrile in a cascade manner. The reaction sequence involves aryne-mediated …

Copper (I)-Mediated Divergent Synthesis of Pyrroquinone Derivatives and 2-Halo-3-amino-1, 4-quinones

B Wang, H Xu, FY Li, JY Wang - The Journal of Organic Chemistry, 2023 - ACS Publications
A divergent transformation of 2-amino-1, 4-quinones for the synthesis of pyrroquinone
derivatives and 2-halo-3-amino-1, 4-quinones was disclosed. The mechanistic study …

[HTML][HTML] Benzocarbazoledinones as SARS-CoV-2 Replication Inhibitors: Synthesis, Cell-Based Studies, Enzyme Inhibition, Molecular Modeling, and …

LG de Souza, EA Penna, AS Rosa, JC da Silva… - Viruses, 2024 - mdpi.com
Endemic and pandemic viruses represent significant public health challenges, leading to
substantial morbidity and mortality over time. The COVID-19 pandemic has underscored the …

Design, synthesis, and anticancer activity of some novel 1H-benzo [d] imidazole-5-carboxamide derivatives as fatty acid synthase inhibitors

S Singh, S Paul, NF Brás, CN Kundu, C Karthikeyan… - Bioorganic …, 2023 - Elsevier
Multiple malignancies exhibit aberrant FASN expression, associated with enhanced de novo
lipogenesis to meet the metabolic demands of rapidly proliferating tumour cells …

Molecular editing of NSC-666719 enabling discovery of benzodithiazinedioxide-guanidines as anticancer agents

VK Rao, S Paul, M Gulkis, Z Shen, H Nair… - RSC Medicinal …, 2024 - pubs.rsc.org
DNA polymerase β (Polβ) is crucial for the base excision repair (BER) pathway of DNA
damage repair and is an attractive target for suppressing tumorigenesis as well as …