Name | OT-Key 21539 |
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Synonyms |
3-(3-Bromo-4-hydroxy-phenyl)-N-[2-(2-{3-(3-bromo-4-hydroxy-phenyl)-2-[(Z)-hydroxyimino]-propionylamino}-ethyldisulfanyl)-ethyl]-2-[(Z)-hydroxyimino]-propionamide
Li0061 bisprasin psammaplin A |
Description | Psammaplin A, a marine metabolite, is a potent inhibitor of HDAC and DNA methyltransferases. Psammaplin A ia a highly potent and selective DAC1 inhibitor with an IC50 of 0.9 nM. Psammaplin A possess the antimicrobial effect on the Gram-positive bacteria and inhibits DNA synthesis and DNA gyrase activity. Antitumor Activity[1][2]. |
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Related Catalog | |
Target |
IC50: 0.9 nM (DAC1)[1] |
References |
[2]. Psammaplin A, a Natural Bromotyrosine Derivative From a Sponge, Possesses the |
Molecular Formula | C22H24Br2N4O6S2 |
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Molecular Weight | 664.38700 |
Exact Mass | 661.95000 |
PSA | 214.44000 |
LogP | 4.46400 |
Hazard Codes | Xi |
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