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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2008-2-18
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pubmed:abstractText |
The alkenyldiarylmethanes (ADAMs) are currently being investigated as non-nucleoside HIV-1 reverse transcriptase inhibitors (NNRTIs) of potential value in the treatment of HIV infection and AIDS. During the course of these studies, a number of ADAM analogues have been identified that protect HIV-infected cells from the cytopathic effects of the virus by an unknown, HIV-1 RT-independent mechanism. Since the phosphodiesterase 4 family is required for HIV infection, the effect of various ADAMs on the activity of PDE4B2 was investigated in an effort to determine if the ADAMs could possibly be targeting phosphodiesterases. Six compounds representative of the ADAM class were tested for inhibition of cAMP hydrolysis by PDE4B2 enzymatic activity. Four ADAMs were found to be weak inhibitors of PDE4B2 and two of them were inactive. The experimental results are consistent with an antiviral mechanism that does not include inhibition of PDE4 isoforms.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-10579849,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-10712916,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-10925252,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-11096104,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-11306681,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-11708913,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-1281479,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-15163195,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-15738310,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-15887951,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-16162014,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-16321539,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-16389458,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-16424030,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-16913721,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-1701568,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-1712395,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-17191775,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-2184033,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-2460479,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-8519449,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-8759644,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-8940140,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-9369477,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-9371714,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-9622549,
http://linkedlifedata.com/resource/pubmed/commentcorrection/18222088-9677330
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Alkenes,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic Nucleotide...,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Reverse Transcriptase,
http://linkedlifedata.com/resource/pubmed/chemical/Methane,
http://linkedlifedata.com/resource/pubmed/chemical/Oxazoles,
http://linkedlifedata.com/resource/pubmed/chemical/PDE4B protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphodiesterase 4 Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphodiesterase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Reverse Transcriptase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/reverse transcriptase, Human...
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1464-3405
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1530-3
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:18222088-Alkenes,
pubmed-meshheading:18222088-Cell Line, Tumor,
pubmed-meshheading:18222088-Cyclic Nucleotide Phosphodiesterases, Type 4,
pubmed-meshheading:18222088-HIV Reverse Transcriptase,
pubmed-meshheading:18222088-Humans,
pubmed-meshheading:18222088-Inhibitory Concentration 50,
pubmed-meshheading:18222088-Methane,
pubmed-meshheading:18222088-Oxazoles,
pubmed-meshheading:18222088-Phosphodiesterase 4 Inhibitors,
pubmed-meshheading:18222088-Phosphodiesterase Inhibitors,
pubmed-meshheading:18222088-Reverse Transcriptase Inhibitors,
pubmed-meshheading:18222088-Structure-Activity Relationship
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pubmed:year |
2008
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pubmed:articleTitle |
Investigation of the alkenyldiarylmethane non-nucleoside reverse transcriptase inhibitors as potential cAMP phosphodiesterase-4B2 inhibitors.
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pubmed:affiliation |
Department of Medicinal Chemistry and Molecular Pharmacology, School of Pharmacy and Pharmaceutical Sciences, and the Purdue Cancer Center, Purdue University, West Lafayette, IN 47907, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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