A sensitive precolumn derivatization method has been developed to measure the 5-triphosphate of 2-fluoro-2,3-dideoxyadenosine (F-ddA, lodenosine), a new anti-HIV drug, in human lymphocytes by HPLC using fluorescence detection. Reaction of chloroacetaldehyde with F-ddA triphosphate in extracts from
Anti-human immunodeficiency virus activity of 3,4,5-tricaffeoylquinic acid in cultured cells of lettuce leaves
✍ Scribed by Hirotoshi Tamura; Takashi Akioka; Koichi Ueno; Takeshi Chujyo; Katsu-ichiro Okazaki; Peter J. King; W. Edward Robinson Jr.
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 581 KB
- Volume
- 50
- Category
- Article
- ISSN
- 1613-4125
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
3,4,5–Tricaffeoylquinic acid (TCQA) that is not found in intact plant of lettuce leaves was isolated from the cultured cells. The intact plant produced chicoric acid (dicaffeoyl tartaric acid: L‐CCA) as well as chlorogenic acid (3‐caffeoylquinic acid: 3‐CQA) as the major metabolites. After subculturing of the cells for 40 days, the amount of 3,4,5‐TCQA reached to 0.14 mg/g fresh weight. The inhibitory effect of 3,4,5‐TCQA for human immunodeficiency virus (HIV) Type 1 integrase was assayed. Anti‐HIV activity using HIV and MT‐2 cells was 1.15 μM and IC~50~ against HIV integrase was 0.063 μM whereas cell toxicity of this chemical was expressed as 5% death of all living cells to be 18.4 μM. The HIV inhibitory effect of 3,4,5‐TCQA was the highest in values among L‐CCA, and other dicaffeoylquinic acids. This data will provide a new possibility for creating a new drug design for HIV.
📜 SIMILAR VOLUMES