About 7 results found for searched term "72-80-0" (0.13 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M2512 | Chlorquinaldol | Antibiotic |
| 5,7-Dichloro-8-hydroxy-2-methylquinoline | ||
| Chlorquinaldol is an antimicrobial agent used for local antisepsy. | ||
| M9964 | Panaxydol | Others |
| Panaxydol has significant anti-inflammatory, anti-platelet aggregation, inhibition of cell oxidase, inhibition of leukemia cell growth, and inhibition of thrombosis. | ||
| M50954 | Calpain substrate | Others |
| Calpain substrate is the membrane non-permeable fluorogenic calpain substrate and can be used in Calpain enzymatic activity assay. | ||
| M3783 | C7280948 | PRMTs |
| C7280948 is an inhibitor of histone arginine methyltransferase PRMT1 with IC50 values of 12.75 uM. | ||
| M10709 | TAS0728 | EGFR/HER2 |
| TAS0728 is an effective, selective, oral, irreversible, covalently bound HER2 inhibitor covalently bound to the C805 site of HER2, inhibiting its activity.IC50 The value is 13 nM. TAS0728 to BMX, HER4, BLK, EGFR, JAK3, SLK, LOK and HUMAN HER2 IC50 The values are 4.9, 8.5, 31, 65, 33, 25, 86, and 36 nM, respectively. TAS0728 simultaneously inhibits phosphorylation of HER2, HER3 and its downstream effector proteins. Has antitumor activity. | ||
| M30587 | Emprumapimod | p38 MAPK |
| PF-07265803 | ||
| Emprumapimod (PF-07265803) is a potent, orally active and selective inhibitor of p38α MAPK directly inhibits LPS-induced IL-6 production from RPMI-8226 cell (IC50=100 pM). Emprumapimod can be used for the research of dilated cardiomyopathy and acute inflammatory pain. | ||
| M42380 | PF-07238025 | Metabolite/Endogenous Metabolite |
| PF-07238025 is a BCKDC kinase (BDK) inhibitor (EC50=19 nM). | ||
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