Abstract |
A series of 2-(2-aminothiazol-4-yl) benzo[b]furan and 3-(2-aminothiazol-4-yl) benzo[b]furan derivatives were prepared, and their leukotriene B(4) inhibitory activity and growth inhibitory activity in cancer cell lines were evaluated. Several compounds showed strong inhibition of calcium mobilization in CHO cells overexpressing human BLT(1) and BLT(2) receptors and growth inhibition to human pancreatic cancer cells MIA PaCa-2. 3-(4-Chlorophenyl)-2-[5-formyl-2-[(dimethylamino)methyleneamino]thiazol-4-yl]-5-methoxybenzo[b] furan 8b showed the most potent and selective inhibition for the human BLT(2) receptor, and its IC(50) value was smaller than that of the selected positive control compound, ZK-158252. 3-(4-Chlorophenyl)-2-[2-[(dimethylamino)methyleneamino]-5-(2-hydroxyethyliminomethyl)thiazol-4-yl]-5-methoxybenzo[b] furan 9a displayed growth inhibitory activity towards MIA PaCa-2.
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Authors | Mari Kuramoto, Yoko Sakata, Kumi Terai, Ikuo Kawasaki, Jun-Ichi Kunitomo, Takahiro Ohishi, Takehiko Yokomizo, Seiichi Takeda, Shuichi Tanaka, Yoshitaka Ohishi |
Journal | Organic & biomolecular chemistry
(Org Biomol Chem)
Vol. 6
Issue 15
Pg. 2772-81
(Aug 07 2008)
ISSN: 1477-0520 [Print] England |
PMID | 18633535
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Benzofurans
- Receptors, Leukotriene B4
- Thiazoles
- 2-aminothiazole
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Topics |
- Animals
- Antineoplastic Agents
(chemistry, therapeutic use)
- Benzofurans
(chemistry, therapeutic use)
- CHO Cells
- Cell Line, Tumor
- Cricetinae
- Cricetulus
- Drug Screening Assays, Antitumor
- Humans
- Inhibitory Concentration 50
- Molecular Structure
- Pancreatic Neoplasms
(drug therapy)
- Receptors, Leukotriene B4
(antagonists & inhibitors, drug effects)
- Thiazoles
(chemistry)
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