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Antifungal Agents01:15

Antifungal Agents

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Amphotericin B is a broad-spectrum antifungal agent that exploits structural differences between fungal and mammalian cell membranes. Its amphipathic structure—featuring a hydrophobic polyene-lactone ring and a hydrophilic region containing mycosamine and carboxylic acid groups—enables selective binding to ergosterol, a sterol predominantly found in fungal plasma membranes. This selective interaction underlies the drug’s antifungal activity, although weak binding to...
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Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
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Theophylline, a member of the methylxanthine class of bronchodilators, has long been used in asthma management. While its exact mechanism of action is not fully understood, it is believed to have multiple effects on various cellular processes.
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The group Stramenopiles include some phototrophic microorganisms. Members of this group possess flagella covered in numerous short, hairlike extensions, a feature that inspired the group's name, derived from the Latin words for "straw" and "hair." Some of the main categories of Stramenopiles include diatoms, golden algae, and brown algae.Diatoms are unicellular, photosynthetic eukaryotes, with over 200 known genera. They play a key role in the planktonic communities of both marine and...
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Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
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Histochemical Staining of Arabidopsis thaliana Secondary Cell Wall Elements
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Two new compounds from Xanthium strumarium.

Rong-Hua Yin1,2, Xue Bai1, Tao Feng3

  • 1a State Key Laboratory of Phytochemistry and Plant Resources in West China , Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201 , China.

Journal of Asian Natural Products Research
|December 3, 2015
PubMed
Summary

Researchers isolated new compounds from Xanthium strumarium seeds. These compounds, including fructusol A and 2-hydroxy-xanthiazone, showed no significant antifungal activity against Candida albicans in vitro.

Keywords:
2-hydroxy-xanthiazoneXanthium strumariumantifungal activitiesfructusol A

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Area of Science:

  • Natural Product Chemistry
  • Pharmacognosy
  • Mycology

Background:

  • Xanthium strumarium seeds are a source of bioactive natural products.
  • Lignans and thiazine derivatives are classes of compounds with diverse biological activities.
  • Investigating novel compounds for potential therapeutic applications is ongoing.

Purpose of the Study:

  • To isolate and characterize new chemical constituents from Xanthium strumarium seeds.
  • To evaluate the in vitro antifungal activity of isolated compounds against Candida albicans.

Main Methods:

  • Isolation of compounds using chromatographic techniques.
  • Structure elucidation of new compounds via extensive spectroscopic analysis (NMR, MS).
  • Antifungal activity testing using broth microdilution method.

Main Results:

  • One new lignan, fructusol A (1), and one new thiazine derivative, 2-hydroxy-xanthiazone (2), were identified.
  • Eight known compounds were also isolated from the plant extract.
  • Compounds 1-3 exhibited no significant antifungal activity against Candida albicans, with minimum inhibitory concentrations (MIC90) greater than 128 μg/ml.

Conclusions:

  • The new compounds fructusol A and 2-hydroxy-xanthiazone were structurally characterized.
  • The tested compounds from Xanthium strumarium seeds do not possess potent in vitro antifungal activity against Candida albicans.