| Literature DB >> 26521858 |
Nobuko Mibu1, Kazumi Yokomizo, Hatsumi Aki, Norimasa Ota, Hiroyuki Fujii, Ai Yuzuriha, Shiori Saneyoshi, Aoi Tanaka, Airi Koga, Jianrong Zhou, Takeshi Miyata, Kunihiro Sumoto.
Abstract
As one of our projects, we here report some new molecular modifications of 2,4,6-trichloro-1,3,5-triazine (TCTAZ: 1) to symmetrical 2,4,6-trialkoxy- or 2,4,6-triaryloxy-substituted 1,3,5-triazine (TAZ) molecules, as well as the results of anti-herpes simplex virus type 1 (anti-HSV-1) activity evaluation of synthesized 2,4,6-trisubstituted TAZ derivatives. Among the tested 2,4,6-trisubstituted TAZ derivatives, we reconfirmed that a C3-symmetrical TAZ derivative, 4e, shows the highest level of anti-HSV-1 activity with a good selectivity index. In this paper, we also report the results of the preparation of newly targeted TAZ derivatives and the structure-activity relationships (SARs) of these trialkoxy-substituted TAZ derivatives and related compounds. The sugar recognition properties of C3-symmetrical TAZ derivative 4e are also described.Entities:
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Year: 2015 PMID: 26521858 DOI: 10.1248/cpb.c15-00309
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645