Recent advances in the discovery of small molecule c-Met Kinase inhibitors

PK Parikh, MD Ghate - European journal of medicinal chemistry, 2018 - Elsevier
Abstract c-Met is a prototype member of a subfamily of heterodimeric receptor tyrosine
kinases (RTKs) and is the receptor for hepatocyte growth factor (HGF). Binding of HGF to its …

Oleocanthal, an antioxidant phenolic compound in extra virgin olive oil (EVOO): a comprehensive systematic review of its potential in inflammation and Cancer

M González-Rodríguez, D Ait Edjoudi… - Antioxidants, 2023 - mdpi.com
Background: The Mediterranean diet is linked to various health benefits, especially the
consumption of olive oil as a key component. Multiple studies highlight its advantages …

The biological activities of oleocanthal from a molecular perspective

KL Pang, KY Chin - Nutrients, 2018 - mdpi.com
Oleocanthal is a minor constituent of olive oil with strong anti-inflammatory activities. Since
the pathogenesis of many chronic diseases involves inflammatory and oxidative …

[HTML][HTML] Phytochemicals, withaferin A and carnosol, overcome pancreatic cancer stem cells as c-Met inhibitors

S Aliebrahimi, SM Kouhsari, SS Arab… - Biomedicine & …, 2018 - Elsevier
Receptor tyrosine kinases (RTKs) are pharmaceutically attractive targets due to their
fundamental role in tumor formation. The hallmark of pancreatic cancer is its high mortality …

The olive oil phenolic (-)-oleocanthal modulates estrogen receptor expression in luminal breast cancer in vitro and in vivo and synergizes with tamoxifen treatment

NM Ayoub, AB Siddique, HY Ebrahim… - European journal of …, 2017 - Elsevier
Luminal breast cancer represents a therapeutic challenge in terms of aggressive disease
and emerging resistance to targeted therapy.(-)-Oleocanthal has demonstrated anticancer …

Comprehensive study of Anthriscus sylvestris lignans

D Orčić, S Berežni, D Škorić, N Mimica-Dukić - Phytochemistry, 2021 - Elsevier
Wild chervil (Anthriscus sylvestris) is a widespread, wild-growing herbaceous plant from
Apiaceae family, known for high content of lignans related to podophyllotoxin, and thus …

Recent advances of RAF (rapidly accelerated fibrosarcoma) inhibitors as anti-cancer agents

UM Ammar, MS Abdel-Maksoud, CH Oh - European Journal of Medicinal …, 2018 - Elsevier
Frequent oncogenic mutations have been identified in MAPK (mitogen-activated protein
kinase) signaling pathway components. As a result, MAPK pathway is associated with …

Synthesis of amide and ester derivatives of cinnamic acid and its analogs: evaluation of their free radical scavenging and monoamine oxidase and cholinesterase …

K Takao, K Toda, T Saito, Y Sugita - Chemical and Pharmaceutical …, 2017 - jstage.jst.go.jp
A series of cinnamic acid derivatives, amides (1–12) and esters (13–22), were synthesized,
and structure–activity relationships for antioxidant activity, and monoamine oxidases (MAO) …

Identification of phytochemicals targeting c-Met kinase domain using consensus docking and molecular dynamics simulation studies

S Aliebrahimi, S Montasser Kouhsari, SN Ostad… - Cell biochemistry and …, 2018 - Springer
Abstract c-Met receptor tyrosine kinase is a proto-oncogene whose aberrant activation is
attributed to a lower rate of survival in most cancers. Natural product-derived inhibitors …

Synthesis and biological evaluation of new MET inhibitors with 1, 6-naphthyridinone scaffold

MS Wang, LS Zhuo, FP Yang, WJ Wang… - European journal of …, 2020 - Elsevier
A potent and novel MET inhibitor, 5-((4-((2-amino-3-chloropyridin-4-yl) oxy)-3-fluorophenyl)
amino)-3-(4-fluorophenyl)-1, 6-naphthyridin-4 (1H)-ones (8), was designed and synthesized …