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Tilianin: A Potential Natural Lead Molecule for New Drug Design and Development for the Treatment of Cardiovascular Disorders
Authors:Farrah Syazana Khattulanuar  Mahendran Sekar  Shivkanya Fuloria  Siew Hua Gan  Nur Najihah Izzati Mat Rani  Subban Ravi  Kumarappan Chidambaram  M Yasmin Begum  Abul Kalam Azad  Srikanth Jeyabalan  Arulmozhi Dhiravidamani  Lakshmi Thangavelu  Pei Teng Lum  Vetriselvan Subramaniyan  Yuan Seng Wu  Kathiresan V Sathasivam  Neeraj Kumar Fuloria
Abstract:Cardiovascular disorders (CVDs) are the leading risk factor for death worldwide, and research into the processes and treatment regimens has received a lot of attention. Tilianin is a flavonoid glycoside that can be found in a wide range of medicinal plants and is most commonly obtained from Dracocephalum moldavica. Due to its extensive range of biological actions, it has become a well-known molecule in recent years. In particular, numerous studies have shown that tilianin has cardioprotective properties against CVDs. Hence, this review summarises tilianin’s preclinical research in CVDs, as well as its mechanism of action and opportunities in future drug development. The physicochemical and drug-likeness properties, as well as the toxicity profile, were also highlighted. Tilianin can be a natural lead molecule in the therapy of CVDs such as coronary heart disease, angina pectoris, hypertension, and myocardial ischemia, according to scientific evidence. Free radical scavenging, inflammation control, mitochondrial function regulation, and related signalling pathways are all thought to play a role in tilianin’s cardioprotective actions. Finally, we discuss tilianin-derived compounds, as well as the limitations and opportunities of using tilianin as a lead molecule in drug development for CVDs. Overall, the scientific evidence presented in this review supports that tilianin and its derivatives could be used as a lead molecule in CVD drug development initiatives.
Keywords:tilianin  cardiovascular disorders  cardioprotection  molecular mechanism  drug-likeness  drug development
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