About 9 results found for searched term "50-12-4" (0.052 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M1649 | Apixaban | Factor Xa |
| BMS-562247-01 | ||
| Apixaban is a highly selective, reversible and orally active direct factor Xa inhibitor with an IC50 of 0.22±0.02 µM. | ||
| M2320 | 17-AAG (Tanespimycin) | HSP |
| Tanespimycin; 17AAG; NSC 330507; CP 127374 | ||
| 17-AAG (Tanespimycin) is a potent HSP90 inhibitor with IC50of 5 nM. | ||
| M2550 | SB-505124 | TGF-β Receptor |
| Sb-505124 is a selective inhibitor of TGF-βI receptor (ALK4, ALK5, ALK7) with IC50 values of 129 nM and 47 nM for ALK4 and ALK5, respectively. Sb-505124 also inhibits ALK7, but not ALK1, 2, 3 and 6. | ||
| M10728 | Cyclo(RGDyK) trifluoroacetate | Integrin |
| Cyclo(RGDyK) trifluoroacetate is an effective selectivity αVβ3 integrin inhibitors,IC50 20 nM. | ||
| M10855 | Mephenytoin | Others |
| Mephenytoin is an anticonvulsant that is a substrate for CYP2C19 and CYP2B6. | ||
| M29975 | SB-505124 hydrochloride | TGF-β Receptor |
| SB-505124 hydrochloride is a selective inhibitor of TGF-β Receptor type I receptor (ALK4, ALK5, ALK7), with IC50s of 129 nM and 47 nM for ALK4, ALK5, respectively, but it does not inhibit ALK1, 2, 3, or 6. | ||
| M44030 | Octahydroisoindole | Others |
| Octahydroisoindole | ||
| M50721 | E(c(RGDfK))2 | Others |
| E(c(RGDfK)) is an αvβ3 integrin-specific binding moiety with tumor targeting properties. | ||
| M56606 | (3S,5S)-Atorvastatin | Cytochrome P450 (e.g. CYP17) |
| (3S,5S)-Atorvastatin is a inactive enantiomer of Atorvastatin. | ||
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