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author:

Wang, Ruo (Wang, Ruo.) [1] | Xu, Kai (Xu, Kai.) [2] | Shi, Weixiong (Shi, Weixiong.) [3]

Indexed by:

Scopus SCIE

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.

Keyword:

AIDS HIV hybrid compounds quinolone structure-activity relationship

Community:

  • [ 1 ] [Wang, Ruo]Fuzhou Univ, Coll Chem, Fuzhou 350116, Fujian, Peoples R China
  • [ 2 ] [Xu, Kai]Fuzhou Univ, Coll Chem, Fuzhou 350116, Fujian, Peoples R China
  • [ 3 ] [Shi, Weixiong]Fuzhou Univ, Coll Chem, Fuzhou 350116, Fujian, Peoples R China

Reprint 's Address:

  • 王若

    [Wang, Ruo]Fuzhou Univ, Coll Chem, Fuzhou 350116, Fujian, Peoples R China

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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 Discipline: PHARMACOLOGY & TOXICOLOGY;

ESI HC Threshold:136

JCR Journal Grade:2

CAS Journal Grade:4

Cited Count:

WoS CC Cited Count: 36

SCOPUS Cited Count: 38

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 4

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