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Journal ArticleDOI

Synthesis of Halogen Derivatives of Benzo[h]chromene and Benzo[a]anthracene with Promising Antimicrobial Activities.

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TLDR
In this paper, the synthesis of novel 7-(4-halophenyl)-8,9-dihydro-7H-12-oxa-9,11-diaza-benzo[a]anthracene derivatives has been reported.
Abstract
The synthesis of novel 7-(4-halophenyl)-8,9-dihydro-7H-12-oxa-9,11-diaza-benzo[a]anthracene derivatives has been reported. The key intermediate 3-amino-9-chloro-1-(4-halophenyl)-1H-benzo[h]chromene-2-carbonitrile (3) was obtained by treating 4-halobenzylidenmalononitriles (1a-c) and ethyl 4-halobenzylidenmalonates (1d-f) with 4-chloro-1-naphthol (2) in ethanolic piperidine solution. Antimicrobial activity was shown for most of the synthesized compounds.

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Identification and characterization of antibacterial compound(s) of cockroaches (Periplaneta americana)

TL;DR: In this paper, the authors characterized antibacterial properties in extracts of various body organs of cockroaches (Periplaneta americana) and showed potent antibacterial activity in crude brain extract against methicillin-resistant Staphylococcus aureus and neuropathogenic Escherichia coli K1.
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Studies on the synthesis, in vitro antitumor activity of 4H-benzo[h]chromene, 7H-benzo[h]chromene[2,3-d]pyrimidine derivatives and structure–activity relationships of the 2-,3- and 2,3-positions

TL;DR: The structure–activity relationship (SAR) study revealed that the antitumor activity on 4H-benzo[h]chromenes with modification at the 2-,3- and 2,3-positions were significantly affected by the lipophilicity (hydrophobic or hydrophilic).
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Synthesis, antitumor activity, and structure–activity relationship of some 4H-pyrano[3,2-h]quinoline and 7H-pyrimido[4′,5′:6,5]pyrano[3,2-h]quinoline derivatives

TL;DR: In this paper, several 4H-pyrano[3,2-h]quinoline derivatives were obtained by treatment of 8-hydroxyquinoline with α-cyano-p-chloro/bromocinnamonitrile.
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Design of New Benzo[h]chromene Derivatives: Antitumor Activities and Structure-Activity Relationships of the 2,3-Positions and Fused Rings at the 2,3-Positions.

TL;DR: The structure–activity relationships (SAR) study highlights that the antitumor activity of the target compounds was significantly affected by the lipophilicity of the substituent at 2- or 3- and fused rings at the 2,3-positions.
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Cytotoxic and apoptotic effects of synthetic benzochromene derivatives on human cancer cell lines.

TL;DR: The results of apoptosis evaluation suggested that the cytotoxic activity of these compounds in breast cancer cells occurs via apoptosis, and Cytotoxic and apoptotic effects of these drugs indicated that they can be a good candidate for further pharmacological studies to discover effective anticancer agents.
References
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Journal ArticleDOI

Synthesis of halogen derivatives of benzo[h]chromene and benzo[a]anthracene with promising antimicrobial activities.

TL;DR: The synthesis of novel 7-(4-halophenyl)-8,9-dihydro-7H-12-oxa-9,11-diaza-benzo[a]anthracene derivatives has been reported and antimicrobial activity was shown for most of the synthesized compounds.