Revealing quinquennial anticancer journey of morpholine: A SAR based review

F Arshad, MF Khan, W Akhtar, MM Alam… - European journal of …, 2019 - Elsevier
Morpholine, a six-membered heterocycle containing one nitrogen and one oxygen atom, is a
moiety of great significance. It forms an important intermediate in many industrial and …

High-efficiency transgene integration by homology-directed repair in human primary cells using DNA-PKcs inhibition

S Selvaraj, WN Feist, S Viel, S Vaidyanathan… - Nature …, 2024 - nature.com
Therapeutic applications of nuclease-based genome editing would benefit from improved
methods for transgene integration via homology-directed repair (HDR). To improve HDR …

Medicinal chemistry of oxazines as promising agents in drug discovery

DS Zinad, A Mahal, RK Mohapatra… - Chemical biology & …, 2020 - Wiley Online Library
Oxazines have brought much synthetic interest due to their extensive biological activities.
These are the important category of heterocycles, which may be formally derived from …

Development and evolution of DNA-dependent protein kinase inhibitors toward cancer therapy

Y Matsumoto - International Journal of Molecular Sciences, 2022 - mdpi.com
DNA double-strand break (DSB) is considered the most deleterious type of DNA damage,
which is generated by ionizing radiation (IR) and a subset of anticancer drugs. DNA …

Development and therapeutic potential of DNA-dependent protein kinase inhibitors

Z Hui, H Deng, X Zhang, C Garrido, F Lirussi, XY Ye… - Bioorganic …, 2024 - Elsevier
The deployment of DNA damage response (DDR) combats various forms of DNA damage,
ensuring genomic stability. Cancer cells' propensity for genomic instability offers therapeutic …

Design, synthesis, and biological evaluation of novel 3-substituted imidazo [1, 2-a] pyridine and quinazolin-4 (3H)-one derivatives as PI3Kα inhibitors

YH Fan, W Li, DD Liu, MX Bai, HR Song, YN Xu… - European Journal of …, 2017 - Elsevier
Abstract Phosphatidylinositol 3-kinase (PI3K) is a pivotal regulator of intracellular signaling
pathways and considered as a promising target in the development of a therapeutic …

An enolate ion as a synthon in biocatalytic synthesis of 3, 4-dihydro-2 (1 H)-quinoxalinones and 3, 4-dihydro-1, 4-benzoxazin-2-ones: lemon juice as an alternative to …

J Petronijević, Z Bugarčić, GA Bogdanović… - Green …, 2017 - pubs.rsc.org
Innovative, efficient, clean, experimentally simple and environmentally friendly one-pot
biocatalytic synthesis of two small libraries of 3, 4-dihydro-2 (1H)-quinoxalinones (4a–m) …

MK2 promotes Tfcp2l1 degradation via β-TrCP ubiquitin ligase to regulate mouse embryonic stem cell self-renewal

Y Zhang, H Ding, X Wang, X Wang, S Wan, A Xu… - Cell Reports, 2021 - cell.com
Tfcp2l1 can maintain mouse embryonic stem cell (mESC) self-renewal. However, it remains
unknown how Tfcp2l1 protein stability is regulated. Here, we demonstrate that β-transducin …

DNA‐PKc inhibition overcomes taxane resistance by promoting taxane‐induced DNA damage in prostate cancer cells

OS Chao, OB Goodman Jr - The Prostate, 2021 - Wiley Online Library
Background Overcoming taxane resistance remains a major clinical challenge in metastatic
castrate‐resistant prostate cancer (mCRPC). Loss of DNA repair proteins is associated with …

SCFβ-TrCP-mediated degradation of TOP2β promotes cancer cell survival in response to chemotherapeutic drugs targeting topoisomerase II

J Shu, D Cui, Y Ma, X Xiong, Y Sun, Y Zhao - Oncogenesis, 2020 - nature.com
Abstract Topoisomerase II (TOP2)-targeting anticancer chemotherapeutic drugs, termed
TOP2 poisons, are widely used and effective in the clinic by stabilizing TOP2-DNA covalent …