An update on poly (ADP-ribose) polymerase-1 (PARP-1) inhibitors: opportunities and challenges in cancer therapy

YQ Wang, PY Wang, YT Wang, GF Yang… - Journal of medicinal …, 2016 - ACS Publications
Poly (ADP-ribose) polymerase-1 (PARP-1) is a critical DNA repair enzyme in the base
excision repair pathway. Inhibitors of this enzyme comprise a new type of anticancer drug …

G-quadruplexes in c-MYC promoter as targets for cancer therapy

B Bahls, IM Aljnadi, R Emídio, E Mendes, A Paulo - Biomedicines, 2023 - mdpi.com
Cancer is a societal burden demanding innovative approaches. A major problem with the
conventional chemotherapeutic agents is their strong toxicity and other side effects due to …

ABCB1 (MDR1) induction defines a common resistance mechanism in paclitaxel-and olaparib-resistant ovarian cancer cells

A Vaidyanathan, L Sawers, AL Gannon… - British journal of …, 2016 - nature.com
Background: Clinical response to chemotherapy for ovarian cancer is frequently
compromised by the development of drug-resistant disease. The underlying molecular …

Structural engineering in polymer semiconductors with aromatic N-heterocycles

J Huang, G Yu - Chemistry of Materials, 2021 - ACS Publications
The materials community has witnessed a complexity expansion in semiconducting
polymers by structural engineering. The most thriving area of polymeric semiconductors lies …

Diazaisoindigo-based polymers with high-performance charge-transport properties: from computational screening to experimental characterization

J Huang, Z Mao, Z Chen, D Gao, C Wei… - Chemistry of …, 2016 - ACS Publications
One of the major challenges confronting organic electronics is the development of high-
mobility semiconducting materials, especially n-channel and ambipolar semiconductors …

Discovery of novel bromophenol–thiosemicarbazone hybrids as potent selective inhibitors of poly (ADP-ribose) polymerase-1 (PARP-1) for use in cancer

C Guo, L Wang, X Li, S Wang, X Yu, K Xu… - Journal of Medicinal …, 2019 - ACS Publications
Poly (ADP-ribose) polymerase-1 (PARP-1) is a new potential target for anticancer drug
discovery. A series of bromophenol–thiosemicarbazone hybrids as PARP-1 inhibitors were …

Azaindole therapeutic agents

DR Motati, R Amaradhi, T Ganesh - Bioorganic & medicinal chemistry, 2020 - Elsevier
Azaindole structural framework is an integral part of several biologically active natural and
synthetic organic molecules; and several FDA approved drugs for various diseases. In the …

Olaparib hydroxamic acid derivatives as dual PARP and HDAC inhibitors for cancer therapy

Z Yuan, S Chen, Q Sun, N Wang, D Li, S Miao… - Bioorganic & medicinal …, 2017 - Elsevier
Olaparib was the first PARP inhibitor approved by the FDA for patients with BRCA-mutated
ovarian cancer. Recent studies have demonstrated enhanced anticancer effects of …

Recent developments in the synthesis of azaindoles from pyridine and pyrrole building blocks

DR Motati, R Amaradhi, T Ganesh - Organic Chemistry Frontiers, 2021 - pubs.rsc.org
The azaindole chemical scaffold is represented in many biologically active natural products
and synthetic derivatives. Recently, this chemical scaffold yielded several therapeutic agents …

Anticancer effects of new dibenzenesulfonamides by inducing apoptosis and autophagy pathways and their carbonic anhydrase inhibitory effects on hCA I, hCA II …

HI Gul, C Yamali, M Bulbuller, PB Kirmizibayrak… - Bioorganic …, 2018 - Elsevier
In this study, new dibenzensulfonamides, 7–9, having the chemical structure 4, 4′-(5′-
chloro-3′-methyl-5-aryl-3, 4-dihydro-1′ H, H-[3, 4′-bipyrazole]-1′, 2-diyl) …