期刊
BIOORGANIC & MEDICINAL CHEMISTRY
卷 28, 期 7, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2020.115398
关键词
Antifungal agents; Antifungal targets; Minimum Inhibitory Concentration (MIC); Structure activity relationships (SARs); Zone of inhibition (Z.I)
资金
- Sri Sathya Sai Institute of Higher Learning, Andhra Pradesh, India
In the recent past, prevalence of life threatening fungal diseases have increased rapidly in immune-compromised cases such as acquired immunodeficiency syndrome (AIDS), cancer, organ transplant etc. Side by side, the appearance of drug resistance to the presently available antifungal therapeutics is on a rapid rise. It has become a top priority for the academia and pharmaceutical industries to develop new antifungal agents able to combat this resistance, and at the same time, possess potential broad spectrum of activity and minimum toxicity. An understanding of the pharmacological interactions between antifungal agents and their targets offers opportunities for design of new therapeutics. This review discusses the various methodology of drug design, structure activity relationships (SARs), and mode of action of variety of new antifungal agents.
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