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author:

Wang, R. (Wang, R..) [1] | Xu, K. (Xu, K..) [2] | Shi, W. (Shi, W..) [3]

Indexed by:

Scopus

Abstract:

Acquired immune deficiency syndrome (AIDS)/human immunodeficiency virus (HIV) is one of the largest and most devastating public health pandemics throughout the world. The global pandemic of drug-sensitive HIV and the increasing threat from drug-resistant HIV result in an urgent need to develop more effective anti-HIV candidates. Quinolone represents a significant class of privileged heterocycles, and its derivatives possess promising in vitro and in vivo anti-HIV properties. The 4-quinolone elvitegravir has already been approved for the treatment of HIV; thus, quinolone derivatives might be promising candidates with anti-HIV activity. This review emphasizes quinolone derivatives with potential anti-HIV activity, covering articles published between 1992 and 2019. The structure-activity relationship is also discussed to provide insights for further development of more active quinolone derivatives. © 2019 Deutsche Pharmazeutische Gesellschaft

Keyword:

AIDS; HIV; hybrid compounds; quinolone; structure-activity relationship

Community:

  • [ 1 ] [Wang, R.]College of Chemistry, Fuzhou University, Fuzhou, Fujian, China
  • [ 2 ] [Xu, K.]College of Chemistry, Fuzhou University, Fuzhou, Fujian, China
  • [ 3 ] [Shi, W.]College of Chemistry, Fuzhou University, Fuzhou, Fujian, China

Reprint 's Address:

  • [Wang, R.]College of Chemistry, Fuzhou UniversityChina

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Source :

Archiv der Pharmazie

ISSN: 0365-6233

Year: 2019

Issue: 9

Volume: 352

2 . 5 9

JCR@2019

4 . 3 0 0

JCR@2023

ESI HC Threshold:136

JCR Journal Grade:2

CAS Journal Grade:4

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 3

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