## Abstract Starting from 5‐nitro‐2‐furoyl azide **(1)**, some new 5‐nitro‐2‐furamides **2a–d**, __O__‐alkyl __N__‐(5‐nitro‐2‐furyl)carbamates **3a,b** and 5‐nitro‐2‐ureidofurans **4a,b** were synthesized and tested for in vitro antimicrobial activity. Compounds **2c** and **2d** exhibited apprecia
Cytotoxicity and Antimicrobial Activity of Some Naphthol Derivatives
✍ Scribed by Ai Yu Shen; Mei Han Hwang; Steve Roffler; Chia Fu Chen
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 448 KB
- Volume
- 328
- Category
- Article
- ISSN
- 0365-6233
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✦ Synopsis
Abstract
2‐Hydroxymethyl‐1‐naphthol diacetate (TAC) and sixteen Mannich base derivatives of naphthol were prepared and examined for cytotoxicity and antimicrobial activity. Cytotoxicity was examined against four human carcinoma cell lines. Several derivatives were effective at concentrations < 4 μg/ml. TAC showed the highest cytotoxicity. Inhibition of DNA‐, RNA‐, and protein synthesis by TAC was also studied and discussed. TAC also exhibits potent antimicrobial activity against Enterobacter clocae 23355, Klebsiella pneumonia 13883, Proteus vulgaris 13315, Pseudomonas aeruginosa 27853, Candida parapsilosis, Candida tropicalis, Trichosposon beigelli, and Rhodotorul spp. with minimum inhibitory concentrations of 0.1 ∼ 0.4 μM. These results indicate that esterification by Bruson reaction of 1‐naphthol Mannich base to TAC enhances the cytotoxicity and antimicrobial activity.
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