About 11 results found for searched term "92-62-6" (0.054 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M4392 | Scutellarin-methylester | Others |
| Scutellarin Methyl ester is a component of breviscapine, a crude extract of several flavonoids in breviscapine. | ||
| M6782 | H2L5186303 | LPL Receptor |
| H2L5186303 is a potent and selective LPA2 receptor antagonist with an IC50 of 9 nM. | ||
| M9480 | BG45 | HDAC |
| BG45 is a potent and selective HDAC3 inhibitor with selectivity for HDAC3 (IC50 = 289 nM) over HDAC1, 2, 6. | ||
| M10181 | STK321130 | FLT3 |
| FLT3-IN-2 | ||
| STK321130, also known as FLT3-IN-2, is potent FLT3 inhibitor with IC50 of <1 μM. | ||
| M13732 | SAR407899 hydrochloride | ROCK |
| SAR407899 hydrochloride is a selective, potent and ATP-competitive ROCK inhibitor, with an IC50 of 135 nM for ROCK-2, and Kis of 36 nM and 41 nM for human and rat ROCK-2, respectively. | ||
| M14305 | Cysteine Protease inhibitor | Cathepsin |
| Cysteine Protease inhibitor is an inhibitor of cysteine protease. IC50 & Target: Cysteine Protease | ||
| M20940 | Proflavine | Anti-infection |
| 3,6-Diaminoacridine | ||
| Proflavine is a disinfectant bacteriostatic against many gram-positive bacteria. It is a topical antiseptic used mainly in wound dressings. | ||
| M29025 | G-9791 | PAK |
| G-9791, a poyridone side chain analogue, is a potent PAK inhibitor with Ki values of 0.95 nM and 2.0 nM for PAK1 and PAK2, respectively. | ||
| M39105 | alpha-D-glucose | Metabolite/Endogenous Metabolite |
| alpha-D-glucose is an endogenous metabolite. | ||
| M40548 | Troriluzole Hydrochloride | EAAT |
| BHV-4157 hydrochloride; Trigriluzole hydrochloride | ||
| Troriluzole Hydrochloride is the hydrochloride form of Troriluzole, and is also an excitatory amino acid transporter protein 2 (EAAT2) modulator, which increases glutamate uptake at neuronal synapses by increasing the expression of EAAT in neuroglia and enhancing its function, thereby decreasing glutamate levels in neuronal synapses. It can be used in studies related to spinocerebellar ataxia (SCA) and anxiety disorders. | ||
| M41408 | ATR-IN-23 | ATM/ATR |
| ATR-IN-23 is a potent and selective ATR inhibitor with an IC50 of 1.5 nM. | ||
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