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Therapeutic potential of boswellic acids: an update patent review (2016–2023)

Hidayat HussainDepartment of Bioorganic Chemistry, Leibniz Institute of Plant Biochemistry, Halle (Saale), GermanyDaijie WangInternational Joint Laboratory of Medicinal Food Development and Health Products Creation, Biological Engineering Technology Innovation Center of Shandong Province, Heze Branch of Qilu University of Technology (Shandong Academy of Sciences), Heze, ChinaHesham R. El‐SeediChemistry Department, Faculty of Science, Islamic University of Madinah, Madinah, Saudi ArabiaLuay RashanDhofar University Research Center, Salalah, OmanIshtiaq AhmedDepartment of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge, UKMuzaffar AbbasFaculty of Pharmacy, Capital University of Science & Technology, Islamabad, PakistanNilufar Z. MamadalievaInstitute of the Chemistry of Plant Substances of the Academy Sciences of Uzbekistan, Tashkent, UzbekistanHaider N. SultaniDepartment of Bioorganic Chemistry, Leibniz Institute of Plant Biochemistry, Halle (Saale), GermanyMuhammad Iftikhar HussainDepartment of Plant Biology & Soil Science, Universidad de Vigo, Vigo, SpainSyed Tasadaque Ali ShahDepartment of Education, Sukkur IBA University, Sukkur, Pakistan
ABI

Аннотация

INTRODUCTION: Boswellic acids (BAs) are a group of pentacyclic triterpenoids of the ursane and oleanane type. They have shown very interesting biological properties that have led to the development of a number of synthesis protocols. Both natural BAs and their synthetic derivatives may be useful in the treatment of a variety of cancers, viral infections and inflammatory diseases. AREAS COVERED: This review covers patents relating to the therapeutic activities of natural BAs and their synthetic derivatives. The latest patented studies of boswellic acids (are summarized by using the keywords 'boswellic acid,' in SciFinder, PubMed, and Google Patents and databases in the year from 2016 to 2023. EXPERT OPINION: H functional groups. In particular, the C-24 amide and amino analogues have shown enhanced anticancer effects compared to the parent AKBA. In addition, BAs have the ability to form conjugates with other antiviral, anti-inflammatory and anticancer drugs that synergistically enhance their biological efficacy. In addition, this conjugation strategy will increase the solubility and bioavailability of BAs, which is one of the most important issues in the development of BAs.

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