Marine Diterpenes: Molecular Modeling of Thrombin Inhibitors with Potential Biotechnological Application as an Antithrombotic

• Published in: Marine drugs 2017-03, Vol.15 (3), p.79
• Main Authors: Pereira, Rebeca Cristina Costa, Lourenço, André Luiz, Terra, Luciana, Abreu, Paula Alvarez, Laneuville Teixeira, Valéria, Castro, Helena Carla
• Format: Article
• Language: English
• Subjects: Algae; anticoagulant; Anticoagulants - chemistry; Anticoagulants - pharmacology; antithrombotic; Aquatic Organisms - chemistry; Binding; Biotechnology; Blood Coagulation - drug effects; Brazil; Catalysis; Catalytic activity; Coagulation; Complementarity; Dictyota menstrualis; Dipole moments; Diterpenes; Diterpenes - chemistry; Diterpenes - pharmacology; Drugs; Enzymes; Fibrinolytic Agents - chemistry; Fibrinolytic Agents - pharmacology; Hemorrhage; marine products; Metabolites; Modelling; Models, Molecular; Molecular docking; Molecular Docking Simulation - methods; Molecular modelling; Molecular structure; Phaeophyceae - chemistry; Plant culture; Side effects; Structure-Activity Relationship; Thrombin; Thrombin - antagonists & inhibitors; Thromboembolism; Thrombosis; Thrombosis - drug therapy
• ISSN: 1660-3397; 1660-3397
• DOI: 10.3390/md15030079

Thrombosis related diseases are among the main causes of death and incapacity in the world. Despite the existence of antithrombotic agents available for therapy, they still present adverse effects like hemorrhagic risks which justify the search for new options. Recently, pachydictyol A, isopachydictyol A, and dichotomanol, three diterpenes isolated from Brazilian marine brown alga were identified as potent antithrombotic molecules through inhibition of thrombin, a key enzyme of coagulation cascade and a platelet agonist. Due to the biotechnological potential of these marine metabolites, in this work we evaluated their binding mode to thrombin in silico and identified structural features related to the activity in order to characterize their molecular mechanism. According to our theoretical studies including structure-activity relationship and molecular docking analysis, the highest dipole moment, polar surface area, and lowest electronic density of dichotomanol are probably involved in its higher inhibition percentage towards thrombin catalytic activity compared to pachydictyol A and isopachydictyol A. Interestingly, the molecular docking studies also revealed a good shape complementarity of pachydictyol A and isopachydictyol A and interactions with important residues and regions (e.g., H57, S195, W215, G216, and loop-60), which probably justify their thrombin inhibitor effects demonstrated in vitro. Finally, this study explored the structural features and binding mode of these three diterpenes in thrombin which reinforced their potential to be further explored and may help in the design of new antithrombotic agents.