Abstract |
To search for possible antitumor promoters, we carried out a primary screening of fifty-one quinones ( anthraquinones, naphthoquinones, azaanthraquinones, and azafluorenones) and related compounds, using their possible inhibitory effects on Epstein-Barr virus early antigen ( EBV-EA) activation induced by 12-O-tetradecanoylphorbol-13-acetate (TPA) in Raji cells. Some of these quinones, notably 5-hydroxy-1,2-methylenedioxy-anthraquinone [9], shikonin [29], 2-acetylfuranonaphthoquinone [32], 5,8-dihydroxycleistopholine [37], and 5,8-dihydroxy-2-methyl-1-azaanthraquinone [45], were observed to significantly inhibit the EBV-EA activation at low doses. The position and number of hydroxyl groups on phenyl rings of these quinones affected the inhibitory activity on EBV-EA activation. The investigation indicates that 9, 29, 32, 37, and 45 might be valuable anti- tumor promoters.
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Authors | T Konoshima, M Kozuka, J Koyama, T Okatani, K Tagahara, H Tokuda |
Journal | Journal of natural products
(J Nat Prod)
1989 Sep-Oct
Vol. 52
Issue 5
Pg. 987-95
ISSN: 0163-3864 [Print] United States |
PMID | 2558164
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents, Phytogenic
- Quinones
- Tetradecanoylphorbol Acetate
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Topics |
- Animals
- Antineoplastic Agents, Phytogenic
(metabolism, pharmacology)
- Drug Screening Assays, Antitumor
- Female
- Herpesvirus 4, Human
(drug effects, physiology)
- Magnetic Resonance Spectroscopy
- Mice
- Mice, Inbred ICR
- Quinones
(pharmacology)
- Structure-Activity Relationship
- Tetradecanoylphorbol Acetate
(metabolism)
- Tumor Cells, Cultured
- Virus Activation
(drug effects)
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