About 6 results found for searched term "523-50-2" (0.119 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M4479 | Isopsoralen | Anti-infection |
| Angelicin | ||
| Isopsoralen (Angelicin) is a furocoumarin naturally occurring tricyclic aromatic compound which has anti-cancer, antiviral, anti-inflammatory activity. | ||
| M5345 | Ulixertinib (BVD-523) | ERK |
| VRT752271; BVD523, Ulixertinib | ||
| VRT752271 (BVD-523, Ulixertinib) is an orally available, highly selective, ATP-competitive, reversible ERK1/2 inhibitor with an IC50 of <0.3 nM for ERK2 inhibition. | ||
| M6152 | SF2523 | PI3K |
| SF2523 is a highly selective and potent inhibitor of PI3K with IC50 values of 34 nM, 158 nM, 9 nM, 241 nM and 280 nM for PI3Kα, PI3Kγ, DNA-PK, BRD4 and mTOR, respectively. | ||
| M14155 | Ulixertinib hydrochloride | ERK |
| BVD-523 hydrochloride; VRT752271 hydrochloride | ||
| Ulixertinib hydrochloride (BVD-523 hydrochloride) is a potent, orally active, highly selective, ATP-competitive and reversible covalent inhibitor of ERK1/2 kinases, with an IC50 of <0.3 nM against ERK2. | ||
| M30349 | L-873724 | Cathepsin |
| L-873724 is a potent, orally bioavailable, selective and reversible[2] non-basic cathepsin K inhibitor, with IC50s of 0.2, 178, 264, and 5239 nM for cathepsin K, cathepsin S, cathepsin L, cathepsin B, respectively. L-873724 also exhibits an IC50 of 0.5 nM for rabbit cathepsin K. L-873724 inhibits bone resorption. | ||
| M41263 | ZINC475239213 | Anti-infection |
| ZINC475239213 is an inhibitor of the SARS-CoV-2 Nsp14 N7-Methyltransferase (IC50: 20 μM). | ||
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