About 8 results found for searched term "50-41-9" (0.055 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M3564 | Clomifene citrate | Estrogen Receptor |
| Clomifene citrate is a selective estrogen receptor modulator. | ||
| M7223 | RS 45041-190 hydrochloride | Others |
| RS 45041-190 hydrochloride is a high affinity I 2 ligand. Highly selective. | ||
| M8619 | ASMI | Others |
| ASMI is a cell-permeable, non-toxic, biocompatible, photostable, positively charged, mitochondria targeting styryl-methylpyridinium based compound that acts as a rapid, cysteine selective, sensitive, and ratiometric (F 518 /F 452 nm) fluorescent turn-on probe (0. | ||
| M9214 | GC7 Sulfate | DNA/RNA Synthesis |
| GC7 Sulfate is a deoxyhypusine synthase (DHPS) inhibitor. | ||
| M13464 | Erianin | PD-1/PD-L1 |
| Erianin, a bibenzyl analog isolated from Dendrobium bulbosum, is also a PD-L1 inhibitor that exhibits potential antitumor activity in a variety of malignant tumors.Erianin regulates a variety of cancer-associated pathways in vitro and in vivo, including apoptosis, cell-cycle arrest, invasion, migration, and autophagy. In addition, Erianin inhibits indoleamine-2,3-dioxygenase (IDO)-induced tumor angiogenesis. | ||
| M18521 | 8-EPILOGANIC ACID | Others |
| 8-EPILOGANIC ACID | ||
| M29652 | DHODH-IN-21 | Dehydrogenase |
| DHODH-IN-21 (compound 19) is an orally active selective dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 value of 1.1 nM. DHODH-IN-21 has anticancer activity and can be used in studies of acute myeloid leukaemia (AML). | ||
| M49578 | JAK1-IN-9 | JAK |
| JAK1-IN-9 is a potent and selective JAK1 inhibitor with an IC50 of 72 nM. | ||
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