| Literature DB >> 10482451 |
P Barraja1, P Diana, A Lauria, A Passannanti, A M Almerico, C Minnei, S Longu, D Congiu, C Musiu, P La Colla.
Abstract
A series of indolo[3,2-c]cinnoline derivatives was prepared and tested to evaluate their biological activity. Most of them inhibited the proliferation of leukemia, lymphoma and solid tumor-derived cell lines at micromolar concentrations, whereas none of the compounds were active against HIV-1. With the exception of 7g, all title compounds showed antibacterial activity against gram-positive bacteria, being up to 200 times more potent than the reference drug streptomycin. Some of the indolo[3,2-c]cinnolines were also endowed with good antifungal activity, particularly against Criptococcus neoformans.Entities:
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Year: 1999 PMID: 10482451 DOI: 10.1016/s0968-0896(99)00096-6
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641