S44HP: structure in first source; an antifungal agent
ID Source | ID |
---|---|
PubMed CID | 86575038 |
MeSH ID | M0499464 |
Synonym |
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s44hp |
(1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,29r,32r,33r,35s,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-19,25,27,29,32,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaco |
16-decarboxy-16-methyl-28,29-didehydronystatin |
(7r,10r)-8,9-dideoxy-7,10-dihydroxyamphotericin b |
3D593A77J4 , |
823814-79-5 |
s-44hp |
amphotericin b, 8,9-dideoxy-7,10-dihydroxy-, (7r,10r)- |
unii-3d593a77j4 |
Excerpt | Reference | Relevance |
---|---|---|
" NYS exhibited the lowest acute toxicity in mice in these experiments, while both Amph-B and S44HP were shown to be 4 times more toxic as judged from the LD50 values." | ( [Comparative analysis of in vitro antifungal activity and in vivo acute toxicity of the nystatin analogue S44HP produced via genetic engineering]. Borgos, SE; Ellingsen, TE; Pereverzeva, EP; Sletta, H; Treshchalin, ID; Voeĭkova, TA; Zotchev, SB, 2005) | 0.76 |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 3 (50.00) | 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 (12.43) 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 | 6 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |