Factor XIa inhibitors in anticoagulation therapy: recent advances and perspectives

Z Xie, Z Meng, X Yang, Y Duan, Q Wang… - Journal of medicinal …, 2023 - ACS Publications
Factor XIa (FXIa) in the intrinsic pathway of the coagulation process has been proven to be
an effective and safe target for anticoagulant discovery with limited or no bleeding …

Structural studies of plasmin inhibition

G Wu, AJ Quek, TT Caradoc-Davies… - Biochemical Society …, 2019 - portlandpress.com
Plasminogen (Plg) is the zymogen form of the serine protease plasmin (Plm), and it plays a
crucial role in fibrinolysis as well as wound healing, immunity, tissue remodeling and …

Fibrinolysis inhibitors: Potential drugs for the treatment and prevention of bleeding

T Steinmetzer, O Pilgram, BM Wenzel… - Journal of Medicinal …, 2019 - ACS Publications
Hyperfibrinolytic situations can lead to life-threatening bleeding, especially during cardiac
surgery. The approved antifibrinolytic agents such as tranexamic acid, ε-aminocaproic acid …

[HTML][HTML] Design and Synthesis of Small Molecule Probes of MDA-9/Syntenin

NV Sankaranarayanan, BK Villuri, B Nagarajan… - Biomolecules, 2024 - mdpi.com
MDA-9/Syntenin, a key scaffolding protein and a molecular hub involved in a diverse range
of cell signaling responses, has proved to be a challenging target for the design and …

A unique nonsaccharide mimetic of heparin hexasaccharide inhibits colon cancer stem cells via p38 MAP kinase activation

RS Boothello, NJ Patel, C Sharon, EI Abdelfadiel… - Molecular cancer …, 2019 - AACR
Targeting of cancer stem cells (CSC) is expected to be a paradigm-shifting approach for the
treatment of cancers. Cell surface proteoglycans bearing sulfated glycosaminoglycan (GAG) …

Highly potent and selective plasmin inhibitors based on the sunflower trypsin inhibitor-1 scaffold attenuate fibrinolysis in plasma

JE Swedberg, G Wu, T Mahatmanto… - Journal of medicinal …, 2018 - ACS Publications
Antifibrinolytic drugs provide important pharmacological interventions to reduce morbidity
and mortality from excessive bleeding during surgery and after trauma. Current drugs used …

Design of small-molecule active-site inhibitors of the S1A family proteases as procoagulant and anticoagulant drugs

PM Fischer - Journal of Medicinal Chemistry, 2017 - ACS Publications
Vitamin K antagonists (VKA) have long been the default drugs for anticoagulant
management in venous thrombosis. While efficacious, they are difficult to use due to …

Thermodynamics, kinetics and mechanisms of noncompetitive allosteric inhibition of chymotrypsin by dihydrolipoic acid-coated gold nanoclusters

WQ Chen, MM Yin, PJ Song, XH He, Y Liu, FL Jiang - Langmuir, 2020 - ACS Publications
Enzymes are an important class of biomacromolecules which catalyze many metabolic
processes in living systems. Nanomaterials can be synthesized with tailored sizes as well as …

Inhibition of herpes simplex virus-1 entry into human cells by nonsaccharide glycosaminoglycan mimetics

RN Gangji, NV Sankaranarayanan, J Elste… - ACS Medicinal …, 2018 - ACS Publications
Although heparan sulfate (HS) has been implicated in facilitating entry of enveloped viruses
including herpes simplex virus (HSV), small molecules that effectively compete with this …

Designing Smaller, Synthetic, Functional Mimetics of Sulfated Glycosaminoglycans as Allosteric Modulators of Coagulation Factors

EI Abdelfadiel, R Gunta, BK Villuri… - Journal of Medicinal …, 2023 - ACS Publications
Natural glycosaminoglycans (GAGs) are arguably the most diverse collection of natural
products. Unfortunately, this bounty of structures remains untapped. Decades of research …