Source:http://linkedlifedata.com/resource/pubmed/id/14575937
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2003-10-24
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pubmed:abstractText |
Several podophyllotoxin derivatives modified in the E-ring were prepared and evaluated for their cytotoxicity on four neoplastic cell lines (P-388, A-549, HT-29 and MEL-28) and for their antiherpetic activity against Herpes simplex virus type II. The trimethoxyphenyl moiety was oxidized to ortho-quinone and further condensed with diamines and enamines to form different heterocycles. Most of the compounds maintained their cytotoxicity at the muM level and some of them showed antiherpetic activity.
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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 |
Oct
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pubmed:issn |
0223-5234
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
38
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
899-911
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14575937-Animals,
pubmed-meshheading:14575937-Antiviral Agents,
pubmed-meshheading:14575937-Cell Line, Tumor,
pubmed-meshheading:14575937-Cell Survival,
pubmed-meshheading:14575937-Cercopithecus aethiops,
pubmed-meshheading:14575937-Herpesvirus 2, Human,
pubmed-meshheading:14575937-Humans,
pubmed-meshheading:14575937-Magnetic Resonance Spectroscopy,
pubmed-meshheading:14575937-Molecular Structure,
pubmed-meshheading:14575937-Podophyllotoxin,
pubmed-meshheading:14575937-Structure-Activity Relationship,
pubmed-meshheading:14575937-Vero Cells
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pubmed:year |
2003
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pubmed:articleTitle |
Synthesis, cytotoxicity and antiviral activity of podophyllotoxin analogues modified in the E-ring.
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pubmed:affiliation |
Departamento de Química Farmacéutica, Facultad de Farmacia, Universidad de Salamanca, 37007 Salamanca, Spain. macg@usal.es
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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