eponemycin: structure given in first source; isolated from Streptomyces hygroscpicus No. P247-71; active against B16 melanoma
ID Source | ID |
---|---|
PubMed CID | 10092280 |
SCHEMBL ID | 13523606 |
MeSH ID | M0174743 |
Synonym |
---|
eponemycin |
heptanamide, n-(1-(hydroxymethyl)-2-((1-((2-(hydroxymethyl)oxiranyl)carbonyl)-3-methyl-3-butenyl)amino)-2-oxoethyl)-6-methyl- |
antibiotic bu 3862t |
126509-46-4 |
1,2-epoxy-2-hydroxymethyl-4-(n-isooctanoylserylamino)-6-methylhept-6-ene-3-one |
SCHEMBL13523606 |
n-[(2s)-3-hydroxy-1-[[(2s)-1-[(2r)-2-(hydroxymethyl)oxiran-2-yl]-4-methyl-1-oxopent-4-en-2-yl]amino]-1-oxopropan-2-yl]-6-methylheptanamide |
Eponemycin is an α,β-epoxyketone natural product that inhibits the proteasome.
Excerpt | Reference | Relevance |
---|---|---|
"Eponemycin is an α,β-epoxyketone natural product that inhibits the proteasome " | ( Chemoenzymatic Synthesis of Novel Cytotoxic Epoxyketones Using the Eponemycin Biosynthetic Enzyme EpnF. Corless, BC; David, Y; Geißen, R; Prescott, NA; Scheinberg, DA; Tan, DS, 2023) | 2.59 |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 5 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (30.00) | 24.3611 |
2020's | 2 (20.00) | 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 moderate demand-to-supply ratio for research on this compound.
| This Compound (19.80) 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 | 10 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |