About 8 results found for searched term "Qc1" (0.121 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M8361 | Qc1 | Others |
| Qc1 is a reversible inhibitor of threonine dehydroxygenase (TDH). | ||
| M57168 | QC-01–175 | PROTAC |
| QC-01-175 is a heterobifunctional molecule, which degrades aberrant tau. | ||
| M8368 | BQCA | Others |
| BQCA is a potent muscarinic M1 receptor positive allosteric modulator with selectivity for M1 over M2-M5. | ||
| M10877 | QCA570 | Others |
| QCA570 is made up of Cereblon ligands and BET ligands connected to PROTAC, which is paired with the BRD4 BD1 protein IC50 The value is 10 nM. | ||
| M20810 | PBD-150 | Amyloid |
| PBD-150 is a potent human glutaminyl cyclase (hQC) Y115E-Y117E variant inhibitor with Ki of 60 nM. | ||
| M27841 | PQCA | AChR/AChE |
| PQCA is a highly selective and potent muscarinic M1 receptor positive allosteric modulator. PQCA has an EC50 value of 49 nM and 135 nM on rhesus and human M1 receptor, respectively. PQCA is inactive for other muscarinic receptors. PQCA has potential to reduce the cognitive deficits associated with Alzheimer's disease. | ||
| M56052 | Zavondemstat | Histone demethylase |
| Zavondemstat (QC8222; TACH 101) is an inhibitor of histone lysine demethylase 4D (KDM4D) with antineoplastic activity. | ||
| M56051 | Zavondemstat L-lysine | Histone demethylase |
| Zavondemstat (QC8222; TACH 101) (L-lysine) is an inhibitor of histone lysine demethylase 4D (KDM4D) with antineoplastic activity. | ||
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