jesterone: structure in first source
ID Source | ID |
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PubMed CID | 10515747 |
MeSH ID | M0393746 |
Synonym |
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jesterone |
(1r,5s,6r)-5-hydroxy-4-(hydroxymethyl)-1-(3-methylbut-2-enyl)-3-[(e)-prop-1-enyl]-7-oxabicyclo[4.1.0]hept-3-en-2-one |
Jesterone dimer (JD) is a synthetic derivative of the natural fungal metabolite jesterone. JD has previously been shown to be cytotoxic in select tumor cell lines.
Excerpt | Reference | Relevance |
---|---|---|
"Jesterone dimer (JD) is a synthetic derivative of the natural fungal metabolite jesterone, and JD has previously been shown to be cytotoxic in select tumor cell lines." | ( Jesterone dimer, a synthetic derivative of the fungal metabolite jesterone, blocks activation of transcription factor nuclear factor kappaB by inhibiting the inhibitor of kappaB kinase. Bardhan, S; Gilmore, TD; Li, C; Liang, MC; Pace, EA; Porco, JA, 2003) | 2.48 |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 5 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.56) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 5 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |