What is caffeic acid phenethyl ester used for?
Caffeic acid phenethyl ester (CAPE) has been reported to possess a variety of biological and pharmacological activities such as anti-inflammatory, antiproliferative, antioxidant, antiviral, antibacterial, and antifungal properties.
Where is caffeic acid phenethyl ester found?
Caffeic acid phenethyl ester (CAPE) is a natural bioactive compound. It occurs in many plants [1]. It is acquired from propolis obtained through extraction from honeybee hives [2].
What is Cape synthesis?
In addition to traditional one-step organic synthesis laboratories, a multistep natural product synthesis is an interesting experiment to challenge students. The proposed three-step synthesis describes the total synthesis of the caffeic acid phenethyl ester (CAPE), a potent 5-lipoxygenase inhibitor from honeybee hives.
What is the molecular formula for caffeine acid phenethyl ester?
Caffeic acid phenethyl ester. PubChem CID. 5281787. Structure. Find Similar Structures. Chemical Safety. Laboratory Chemical Safety Summary (LCSS) Datasheet. Molecular Formula. C17H16O4.
What is the formula for caffeine in LCSs?
Laboratory Chemical Safety Summary (LCSS) Datasheet. Molecular Formula. C17H16O4. Synonyms. Caffeic acid phenethyl ester. Phenethyl caffeate. 104594-70-9. CAPE.
What is the HPLC for caffeine acid?
U2S3A33KVM Caffeic acid, purum, >=95.0% (HPLC) Caffeic acid, matrix substance for MALDI-MS, >=99.0% (HPLC), powder, light beige 3,4-dihydroxycinnamic acid appears as yellow prisms or plates (from chloroform or ligroin) or pale yellow granules. Alkaline solutions turn from yellow to orange.
What is the structure of caffeine acid?
Caffeic acid is a hydroxycinnamic acid that is cinnamic acid in which the phenyl ring is substituted by hydroxy groups at positions 3 and 4. It exists in cis and trans forms; the latter is the more common.