About 9 results found for searched term "59-32-5" (0.099 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M8649 | GSK591 | PRMTs |
| GSK-591; GSK3203591; EPZ015866 | ||
| GSK591 (EPZ015866) is a potent and selective inhibitor of protein methyltransferase 5 (PRMT5) with an IC50 of 4 nM. | ||
| M9420 | GSK3326595 | PRMTs |
| EPZ015938; GSK-3326595 | ||
| GSK3326595 is a potent, reversible and selective protein arginine methyltransferase 5 (PRMT5) inhibitor with broad antiproliferative activity for studies related to lymphoma and leukemia. | ||
| M20469 | Nicardipine | Others |
| YC-93 | ||
| Nicardipine(YC-93) is a calcium channel blocker that has been widely used to control blood pressure in severe hypertension following events such as ischemic stroke, traumatic brain injury, and intracerebral hemorrhage. | ||
| M28639 | Bizine | Histone demethylase |
| Bizine, a Phenelzine analogue, is a potent and selective LSD1 inhibitor, with a b>Ki of 59 nM. Bizine can modulate bulk histone methylation in cancer cells. Bizine shows neuroprotective effects. | ||
| M30334 | Chloropyramine | Apoptosis |
| Chloropyramine is competitive reversible H1 receptor antagonist. Chloropyramine also has anti-tumour activity in breast cancer. Chloropyramine can be used for the research of allergic conditions, such as conjunctivitis and bronchial asthma. | ||
| M30335 | DCH36_06 | Histone Acetyltransferase |
| DCH36_06 is a potent and selective p300/CBP inhibitor with IC50s of 0.6 μM and 3.2 μM for p300 and CBP, respectively. DCH36_06 mediated p300/CBP inhibition leading to hypoacetylation on H3K18 in leukemic cells. Anti-tumor activity. | ||
| M44298 | 6-Hydroxytropinone | Others |
| 6-Hydroxytropinone | ||
| M56492 | MPDC | GlyT |
| MPDC is a potent and competitive inhibitor of the Na+-dependent high-affinity glutamate transporter in forebrain synaptosomes. | ||
| M56388 | NSC622608 | PD-1/PD-L1 |
| NSC622608 is a V-domain Ig suppressor of T-cell activation (VISTA) ligand with an IC50 value of 4.8 μM. | ||
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