Therapeutic journery of nitrogen mustard as alkylating anticancer agents: Historic to future perspectives
Cancer is considered as one of the most serious health problems today. The discovery of
nitrogen mustard as an alkylating agent in 1942, opened a new era in the cancer …
nitrogen mustard as an alkylating agent in 1942, opened a new era in the cancer …
Exploiting tumour hypoxia in cancer treatment
Solid tumours contain regions at very low oxygen concentrations (hypoxia), often
surrounding areas of necrosis. The cells in these hypoxic regions are resistant to both …
surrounding areas of necrosis. The cells in these hypoxic regions are resistant to both …
Selected organophosphorus compounds with biological activity. Applications in medicine
S Demkowicz, J Rachon, M Daśko, W Kozak - RSC advances, 2016 - pubs.rsc.org
The purpose of this article is to provide an overview of the latest applications of
organophosphorus compounds (OPs) that exhibit biological activity. A large family of OPs …
organophosphorus compounds (OPs) that exhibit biological activity. A large family of OPs …
Prodrugs of phosphates and phosphonates
SJ Hecker, MD Erion - Journal of medicinal chemistry, 2008 - ACS Publications
Phosphonic acids are rarely found in drug candidate molecules, despite the potential of this
functional group to provide unique binding interactions with a target enzyme or receptor …
functional group to provide unique binding interactions with a target enzyme or receptor …
Prodrugs of biologically active phosphate esters
C Schultz - Bioorganic & medicinal chemistry, 2003 - Elsevier
Bioactivatable protecting groups represent an enormously powerful tool to increase
bioavailability or to generally help deliver drugs to cells. This approach is particularly …
bioavailability or to generally help deliver drugs to cells. This approach is particularly …
Potent and highly selective hypoxia-activated achiral phosphoramidate mustards as anticancer drugs
JX Duan, H Jiao, J Kaizerman, T Stanton… - Journal of medicinal …, 2008 - ACS Publications
A series of achiral hypoxia-activated prodrugs were synthesized on the basis of the DNA
cross-linking toxin of the prodrug, ifosfamide. The hypoxia-selective cytotoxicity of several of …
cross-linking toxin of the prodrug, ifosfamide. The hypoxia-selective cytotoxicity of several of …
Design of anticancer prodrugs for reductive activation
Y Chen, L Hu - Medicinal research reviews, 2009 - Wiley Online Library
Anticancer prodrugs designed to target specifically tumor cells should increase therapeutic
effectiveness and decrease systemic side effects in the treatment of cancer. Over the last 20 …
effectiveness and decrease systemic side effects in the treatment of cancer. Over the last 20 …
An enolase inhibitor for the targeted treatment of ENO1-deleted cancers
Inhibiting glycolysis remains an aspirational approach for the treatment of cancer. We have
previously identified a subset of cancers harbouring homozygous deletion of the glycolytic …
previously identified a subset of cancers harbouring homozygous deletion of the glycolytic …
Why great mitotic inhibitors make poor cancer drugs
VC Yan, HE Butterfield, AH Poral, MJ Yan, KL Yang… - Trends in cancer, 2020 - cell.com
Chemotherapy is central to oncology, perceived to operate only on prolific cancerous tissue.
Yet, many non-neoplastic tissues are more prolific compared with typical tumors …
Yet, many non-neoplastic tissues are more prolific compared with typical tumors …
Single-and two-electron reduction of nitroaromatic compounds by flavoenzymes: Mechanisms and implications for cytotoxicity
N Čėnas, A Nemeikaitė-Čėnienė… - International journal of …, 2021 - mdpi.com
Nitroaromatic compounds (ArNO2) maintain their importance in relation to industrial
processes, environmental pollution, and pharmaceutical application. The manifestation of …
processes, environmental pollution, and pharmaceutical application. The manifestation of …