Literature DB >> 16114486

Synthesis and antifungal activity of naphthalene-1,4-diones modified at positions 2, 3, and 5.

Chung-Kyu Ryu1, Mi Jin Chae.   

Abstract

A series of 2-arylamino-5-hydroxy-naphthalene-1,4-diones, 3-arylamino-5-methoxy-naphthalene-1,4-diones, and 2-arylamino-3chloro-5-hydroxy-naphthalene-1,4-diones were synthesized and tested for in vitro antifungal activity against the species Candida and Aspergillus niger. Among those tested, 3-arylamino-5-methoxy-naphthalene-1,4-diones exhibited potent antifungal activity. In general, the 3-arylamino-5-methoxy-naphthalene-1,4-diones showed more potent antifungal activity than the 2-arylamino-5-hydroxy-naphthalene-1,4-diones and the 2-arylamino-3-chloro-5-hydroxy-naphthalene-1,4-diones.

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Year:  2005        PMID: 16114486     DOI: 10.1007/BF02977337

Source DB:  PubMed          Journal:  Arch Pharm Res        ISSN: 0253-6269            Impact factor:   4.946


  2 in total

1.  Chromatographic Characterization and GC-MS Evaluation of the Bioactive Constituents with Antimicrobial Potential from the Pigmented Ink of Loligo duvauceli.

Authors:  Smiline Girija; Veeramuthu Duraipandiyan; Pandi Suba Kuppusamy; Hariprasad Gajendran; Raghuraman Rajagopal
Journal:  Int Sch Res Notices       Date:  2014-11-10

2.  2-Methoxy-7-Acetonyljuglone Isolated from Reynoutria japonica Increases the Activity of Nuclear Factor Erythroid 2-Related Factor-2 through Inhibition of Ubiquitin Degradation in HeLa Cells.

Authors:  Jung-Hwan Kim; Atif Ali Khan Khalil; Hye-Jin Kim; Sung-Eun Kim; Mi-Jeong Ahn
Journal:  Antioxidants (Basel)       Date:  2019-09-14
  2 in total

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