About 11 results found for searched term "53-60-1" (0.055 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M4175 | 12-Acetyltrichilin-B | Others |
| 12-Acetyltrichilin-B | ||
| M5398 | Aliskiren Hemifumarate | Renin |
| CGP 60536; CGP60536B; SPP 100 | ||
| Aliskiren hemifumarate is a direct renin inhibitor with IC50 of 1.5 nM. | ||
| M5903 | Promazine HCl | Dopamine Receptor |
| Promazine (hydrochloride) is a D2 dopamine receptor antagonist, belongs to the phenothiazine class of antipsychotics, used to treat schizophrenia. | ||
| M7719 | CD437 | RAR/RXR |
| AHPN; Ro-472077 | ||
| CD437 is a retinoic acid receptor (RAR)γ-selective agonist, γ-selective retinoid; potent inducer of apoptosis. | ||
| M14530 | Aliskiren | Renin |
| CGP 60536; CGP60536B; SPP 100 | ||
| Aliskiren(CGP 60536) is a direct renin inhibitor with IC50 of 1.5 nM. | ||
| M16268 | Toddalosin ethyl ether | Coumarins |
| Toddalosin ethyl ether | ||
| M28935 | YM-53601 free base | Farnesyl Transferase |
| YM-53601 free base, a squalene synthase inhibitor, reduces plasma cholesterol and triglyceride levels in vivo. YM-53601 free base inhibits squalene synthase derived from human hepatoma cells with an IC50 of 79 nM. Lipid-lowering agent. YM-53601 free base is also an inhibitor of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) enzyme activity and abrogates HCV propagation. | ||
| M28936 | YM-53601 | Farnesyl Transferase |
| YM-53601, a squalene synthase inhibitor, reduces plasma cholesterol and triglyceride levels in vivo. YM-53601 inhibits squalene synthase derived from human hepatoma cells with an IC50 of 79 nM. Lipid-lowering agent. YM-53601 is also an inhibitor of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) enzyme activity and abrogates HCV propagation. | ||
| M39746 | 1-Hydroxyrutecarpine | Others |
| 1-Hydroxyrutaecarpine (compound 1a) is a hydroxy-derivative of rutaecarpine. 1-Hydroxyrutaecarpine shows cytotoxicities with ED50s of 3.72, 7.44 µg/mL for P-388 and HT-29 cells, respectively. 1-Hydroxyrutaecarpine shows antiplatelet activity. | ||
| M41022 | Cytochalasin H | Antibiotic |
| Cytochalasin H is a nature product that could be isolated from fungus Phomopsis sp. | ||
| M53095 | Ac-hMCH(6-16)-NH2 | GPR/FFAR |
| Ac-hMCH(6-16)-NH2 binds to and activates equally well both human MCH receptors present in the brain (non-selective agonist), with IC50 values of 0.16 nM and 2.7 nM for MCH-1R and MCH-2R. | ||
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