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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
Source :
Molecules, Vol 27, Iss 3, p 673 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

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.

Details

Language :
English
ISSN :
14203049
Volume :
27
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Molecules
Publication Type :
Academic Journal
Accession number :
edsdoj.700aead579847079737847f40497371
Document Type :
article
Full Text :
https://doi.org/10.3390/molecules27030673