Aspergillomarasmine A

From WikiMD's Food, Medicine & Wellness Encyclopedia

Aspergillomarasmine_A.svg

Aspergillomarasmine A is a naturally occurring compound produced by certain species of the Aspergillus genus of fungi. It is classified as a type of marasmine, which are secondary metabolites known for their diverse biological activities.

Structure and Properties[edit | edit source]

Aspergillomarasmine A is a complex molecule characterized by its unique chemical structure. It contains multiple functional groups, including carboxyl and hydroxyl groups, which contribute to its biological activity. The exact molecular formula and structural details are crucial for understanding its interactions and mechanisms of action.

Biological Activity[edit | edit source]

Aspergillomarasmine A has garnered significant interest due to its potential antibiotic properties. It has been shown to inhibit the activity of certain beta-lactamase enzymes, which are responsible for antibiotic resistance in various bacteria. This inhibition can restore the efficacy of beta-lactam antibiotics against resistant bacterial strains.

Mechanism of Action[edit | edit source]

The primary mechanism by which Aspergillomarasmine A exerts its effects is through the chelation of zinc ions. Beta-lactamase enzymes require zinc as a cofactor for their activity. By binding to zinc, Aspergillomarasmine A effectively inactivates these enzymes, thereby preventing the degradation of beta-lactam antibiotics.

Applications in Medicine[edit | edit source]

The potential use of Aspergillomarasmine A in clinical settings is being explored, particularly as an adjuvant therapy to combat antibiotic-resistant infections. Its ability to inhibit beta-lactamase enzymes makes it a promising candidate for combination therapies with existing antibiotics.

Research and Development[edit | edit source]

Ongoing research is focused on optimizing the production and purification of Aspergillomarasmine A, as well as understanding its pharmacokinetics and pharmacodynamics. Studies are also investigating its efficacy in vivo and its potential side effects.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


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Contributors: Prab R. Tumpati, MD