The First Affiliated Hospital of Jinan University

China

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A61P 31/10 - Antimycotics 2
C07D 295/194 - Radicals derived from thio- or thiono carboxylic acids 2
A61K 31/496 - Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin 1
A61K 9/00 - Medicinal preparations characterised by special physical form 1
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Found results for  patents

1.

APPLICATION OF POLYCYCLIC AROMATIC COMPOUND IN THE PREPARATION OF ANTIFUNGAL DRUGS

      
Document Number 03224558
Status Pending
Filing Date 2022-05-24
Open to Public Date 2023-01-19
Owner THE FIRST AFFILIATED HOSPITAL OF JINAN UNIVERSITY (China)
Inventor
  • Zhang, Hong
  • Ye, Wencai
  • Zhang, Yishan
  • Hu, Lijun
  • Li, Shuixiu
  • Zhao, Yajing
  • Tang, Chuanyan
  • Weng, Luobang

Abstract

The present invention provides a polycyclic aryl compound S1 for preparing a drug for antifungal infection. The structural formula of the polycyclic compound is S1. The polycyclic aryl compound having the shell-core structure and represented by S1 in the present invention is suitable for preparing drugs for anti-Candida, Aspergillus, Mucor and other pathogenic fungal infections, and has the following beneficial effects: the compound S1 of the present application has a broad-spectrum antifungal effect on pathogenic fungi including, but not limited to, Candida, Aspergillus, Mucor, etc., is effective against azole resistant Candida, is low in toxicity to mammals, and can treat systemic fungal infection by oral administration, and can also be used locally to treat mucosal Candida infection.

IPC Classes  ?

2.

APPLICATION OF POLYCYCLIC ARYL COMPOUND IN PREPARATION OF ANTIFUNGAL DRUG

      
Application Number CN2022094745
Publication Number 2023/284420
Status In Force
Filing Date 2022-05-24
Publication Date 2023-01-19
Owner THE FIRST AFFILIATED HOSPITAL OF JINAN UNIVERSITY (China)
Inventor
  • Zhang, Hong
  • Ye, Wencai
  • Zhang, Yishan
  • Hu, Lijun
  • Li, Shuixiu
  • Zhao, Yajing
  • Tang, Chuanyan
  • Weng, Luobang

Abstract

The present invention provides a polycyclic aryl compound S1 for preparing a drug for antifungal infection. The structural formula of the polycyclic compound is S1. The polycyclic aryl compound having the shell-core structure and represented by S1 in the present invention is suitable for preparing drugs for anti-Candida, Aspergillus, Mucor and other pathogenic fungal infections, and has the following beneficial effects: the compound S1 of the present application has a broad-spectrum antifungal effect on pathogenic fungi including, but not limited to, Candida, Aspergillus, Mucor, etc., is effective against azole resistant Candida, is low in toxicity to mammals, and can treat systemic fungal infection by oral administration, and can also be used locally to treat mucosal Candida infection.

IPC Classes  ?

  • C07D 295/194 - Radicals derived from thio- or thiono carboxylic acids
  • A61K 31/496 - Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
  • A61K 9/00 - Medicinal preparations characterised by special physical form
  • A61P 31/10 - Antimycotics