About 6 results found for searched term "51-03-6" (0.054 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M8577 | BAY-678 | Others |
| BAY-678 is an orally available, highly potent and selective inhibitor of human neutrophil elastase (HNE). | ||
| M8650 | ML264 | KLF |
| CID-51003603 | ||
| ML264 is a potent and selective inhibitor of Kruppel-like factor 5 (KLF5) expression. | ||
| M17059 | 3,8-Di-O-methylellagic acid 2-O-glucoside | Phenols |
| 3,8-Di-O-methylellagic acid 2-O-glucoside | ||
| M20901 | Piperonyl butoxide | Others |
| Butacide, Ethanol butoxide, Pyrenone 606 | ||
| Piperonyl butoxide (PBO) is a man-made pesticide synergist, working with insect killers to increase their effectiveness. | ||
| M24956 | Cendakimab | IL Receptor/Related |
| RPC 4046; ABT 308; CC-93538 | ||
| Cendakimab (RPC4046; ABT 308; CC-93538) is a selective, humanized, recombinant monoclonal antibody against the IL-13 molecule. Cendakimab has a high affinity and potency for both human wild-type and variant IL-13 and blocks binding of IL-13 to both IL-13Rα1 and IL-13Rα2 with IC50s of 352 pM and 631 pM by ELISA, respectively. | ||
| M28553 | MC-DOXHZN | Topoisomerase |
| (E/Z)-Aldoxorubicin; Doxorubicin(6-maleimidocaproyl)hydrazone | ||
| MC-DOXHZN ((E/Z)-Aldoxorubicin) is an albumin-binding proagent of Doxorubicin (DNA topoisomerase II inhibitor), with acid-sensitive properties. | ||
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