Source:http://linkedlifedata.com/resource/pubmed/id/12098751
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2002-7-5
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pubmed:abstractText |
A convenient synthesis of the new enamine derivatives 2-(4-morpholinyl)-3-(3-methyl-2-butenyl)-1,4-naphthalenedione, 2-(1-piperidinyl)-3-(3-methyl-2-butenyl)-1,4-naphtalenedione and 2-(1-pyrrolidinyl)-3-(3-methyl-2-butenyl)-1,4-naphthalenedione was carried out from natural 2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthalenedione (lapachol) and morpholine, piperidine and pyrrolidine. The structures of the products were established mainly by NMR analysis, including 2D experiments. Biological activities of these products were evaluated against Artemia salina, Aedes aegypti and cytotoxicity using A549 human breast cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0001-3765
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
74
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
211-21
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12098751-Aedes,
pubmed-meshheading:12098751-Amines,
pubmed-meshheading:12098751-Animals,
pubmed-meshheading:12098751-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:12098751-Artemia,
pubmed-meshheading:12098751-Breast Neoplasms,
pubmed-meshheading:12098751-Drug Evaluation, Preclinical,
pubmed-meshheading:12098751-Female,
pubmed-meshheading:12098751-Humans,
pubmed-meshheading:12098751-Magnetic Resonance Spectroscopy,
pubmed-meshheading:12098751-Naphthoquinones,
pubmed-meshheading:12098751-Tumor Cells, Cultured
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pubmed:year |
2002
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pubmed:articleTitle |
New enamine derivatives of lapachol and biological activity.
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pubmed:affiliation |
Departamento de Química Orgânica e Inorgânica, Universidade Federal do Ceará, Fortaleza, Ceará, Brazil.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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