| pubmed-article:14742233 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:14742233 | lifeskim:mentions | umls-concept:C0682458 | lld:lifeskim |
| pubmed-article:14742233 | lifeskim:mentions | umls-concept:C0332307 | lld:lifeskim |
| pubmed-article:14742233 | lifeskim:mentions | umls-concept:C1524059 | lld:lifeskim |
| pubmed-article:14742233 | lifeskim:mentions | umls-concept:C0031327 | lld:lifeskim |
| pubmed-article:14742233 | lifeskim:mentions | umls-concept:C1328819 | lld:lifeskim |
| pubmed-article:14742233 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:14742233 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:14742233 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:14742233 | pubmed:dateCreated | 2004-1-26 | lld:pubmed |
| pubmed-article:14742233 | pubmed:abstractText | A class of betulinic acid derivatives was synthesized to target two critical steps in the human immunodeficiency virus type 1 (HIV-1) replication cycle, entry and maturation. Each mechanism of HIV-1 inhibition is distinct from clinically available anti-HIV therapeutics. The viral determinants of the antientry and antimaturation activities are the bridging sheet of HIV-1 gp120 and the P24/p2 cleavage site, respectively. | lld:pubmed |
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| pubmed-article:14742233 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:14742233 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:14742233 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:14742233 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:14742233 | pubmed:issn | 0066-4804 | lld:pubmed |
| pubmed-article:14742233 | pubmed:author | pubmed-author:AikenChristop... | lld:pubmed |
| pubmed-article:14742233 | pubmed:author | pubmed-author:HuangLiL | lld:pubmed |
| pubmed-article:14742233 | pubmed:author | pubmed-author:ChenChin HoCH | lld:pubmed |
| pubmed-article:14742233 | pubmed:author | pubmed-author:XiongYuanY | lld:pubmed |
| pubmed-article:14742233 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:14742233 | pubmed:volume | 48 | lld:pubmed |
| pubmed-article:14742233 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:14742233 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:14742233 | pubmed:pagination | 663-5 | lld:pubmed |
| pubmed-article:14742233 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
| pubmed-article:14742233 | pubmed:meshHeading | pubmed-meshheading:14742233... | lld:pubmed |
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| pubmed-article:14742233 | pubmed:meshHeading | pubmed-meshheading:14742233... | lld:pubmed |
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| pubmed-article:14742233 | pubmed:meshHeading | pubmed-meshheading:14742233... | lld:pubmed |
| pubmed-article:14742233 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:14742233 | pubmed:articleTitle | Bifunctional anti-human immunodeficiency virus type 1 small molecules with two novel mechanisms of action. | lld:pubmed |
| pubmed-article:14742233 | pubmed:affiliation | Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA. | lld:pubmed |
| pubmed-article:14742233 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:14742233 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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