Pronunciation: [ʃˈɪkɪmˌɒlz] (IPA) 
The word "Shikimols" is spelled with the IPA phonetic transcription as /ʃɪkɪməʊlz/. The initial "sh" sound is followed by the "i" sound pronounced as "ih." The "k" is pronounced as "kuh," "i" as "ih," and "m" as "muh." The letter "o" is then pronounced as a long vowel sound "oh," followed by the letter "l" pronounced as "luh" with a soft "s" ending. Overall, the spelling of "Shikimols" closely matches its phonetic pronunciation.
Shikimols are a class of compounds that belong to the family of phenolic lignans. They are primarily found in a wide variety of plant species, including members of the Aristolochiaceae, Magnoliaceae, and Thymelaeaceae families. Shikimols are derived from the shikimic acid pathway, which is a metabolic pathway involved in the biosynthesis of aromatic compounds in plants.
Chemically, shikimols consist of a bicyclic structure, composed of three rings: a benzene ring and two oxygen-containing six-membered rings. The core structure of shikimols is known as tetrahydrofuran lignans, owing to the presence of a tetrahydrofuran ring fused to the benzene ring.
Shikimols possess significant biological activity, including antioxidant, anti-inflammatory, and anti-cancer properties. They have been studied for their potential therapeutic applications in various diseases, such as neurodegenerative disorders, cardiovascular diseases, and certain types of cancer. Shikimols are known to exhibit free radical scavenging activity, which helps in reducing oxidative stress and preventing cellular damage.
Due to their diverse pharmacological activities, shikimols have attracted attention from the scientific community as potential natural compounds for drug discovery and development. However, further research is required to fully understand the mechanisms of action and therapeutic potential of shikimols.
