Anticancer peptide: Physicochemical property, functional aspect and trend in clinical application
W Chiangjong… - … journal of oncology, 2020 - spandidos-publications.com
Cancer is currently ineffectively treated using therapeutic drugs, and is also able to resist
drug action, resulting in increased side effects following drug treatment. A novel therapeutic …
drug action, resulting in increased side effects following drug treatment. A novel therapeutic …
Covalent inhibitors design and discovery
S De Cesco, J Kurian, C Dufresne… - European Journal of …, 2017 - Elsevier
In the history of therapeutics, covalent drugs occupy a very distinct category. While
representing a significant fraction of the drugs on the market, very few have been …
representing a significant fraction of the drugs on the market, very few have been …
Anticancer peptides mechanisms, simple and complex
P Norouzi, M Mirmohammadi, MHH Tehrani - Chemico-Biological …, 2022 - Elsevier
Peptide therapy has started since 1920s with the advent of insulin application, and now it
has emerged as a new approach in treatment of diseases including cancer. Using anti …
has emerged as a new approach in treatment of diseases including cancer. Using anti …
Next-generation proteasome inhibitors for cancer therapy
Over 2 decades ago, the proteasome was considered a risky or even untenable therapeutic
target. Today, proteasome inhibitors are a mainstay in the treatment of multiple myeloma …
target. Today, proteasome inhibitors are a mainstay in the treatment of multiple myeloma …
Proteasome activation as a new therapeutic approach to target proteotoxic disorders
Proteasomes are multienzyme complexes that maintain protein homeostasis (proteostasis)
and important cellular functions through the degradation of misfolded, redundant, and …
and important cellular functions through the degradation of misfolded, redundant, and …
Silver complexes as anticancer agents: A perspective review
SK Raju, A Karunakaran, S Kumar, P Sekar… - German Journal of …, 2022 - gjpb.de
Metal complexes gained more attention in the medical field, particularly cancer treatment,
due to their enhanced potential and redox ability. These complexes exhibited more …
due to their enhanced potential and redox ability. These complexes exhibited more …
Immunoproteasome-selective and non-selective inhibitors: A promising approach for the treatment of multiple myeloma
R Ettari, M Zappalà, S Grasso, C Musolino… - Pharmacology & …, 2018 - Elsevier
The ubiquitin-proteasome system (UPS) is the major non-lysosomal proteolytic system for
the degradation of abnormal or damaged proteins no longer required. The proteasome is …
the degradation of abnormal or damaged proteins no longer required. The proteasome is …
Antimicrobial/anticancer peptides: Bioactive molecules and therapeutic agents
K Kardani, A Bolhassani - Immunotherapy, 2021 - Taylor & Francis
Antimicrobial peptides (AMPs) have been known as host-defense peptides. These cationic
and amphipathic peptides are relatively short (∼ 5–50 L-amino acids) with molecular weight …
and amphipathic peptides are relatively short (∼ 5–50 L-amino acids) with molecular weight …
Structure-based optimization and discovery of M3258, a specific inhibitor of the immunoproteasome subunit LMP7 (β5i)
M Klein, M Busch, M Friese-Hamim… - Journal of medicinal …, 2021 - ACS Publications
Proteasomes are broadly expressed key components of the ubiquitin-dependent protein
degradation pathway containing catalytically active subunits (β1, β2, and β5). LMP7 (β5i) is …
degradation pathway containing catalytically active subunits (β1, β2, and β5). LMP7 (β5i) is …
Develo** natural product drugs: Supply problems and how they have been overcome
DJ Newman - Pharmacology & therapeutics, 2016 - Elsevier
The development of natural product-derived drugs has some unique problems associated
with the process, which can be best described as the “problem of supply”. In this short …
with the process, which can be best described as the “problem of supply”. In this short …