About 11 results found for searched term "HD5" (0.055 seconds)
Cat.No. | Name | Target |
---|---|---|
M7826 | 5-Hydroxydecanoic acid sodium salt | Potassium Channel |
5-HD; 5-hydroxydecanoate sodium salt | ||
5-hydroxydecanoate (5-HD) blocks post-ischemic actions of the K+ channel activator cromakalim. | ||
M8310 | CHD-5 | Others |
CHD-5 is a potent aryl hydrocarbon receptor antagonist. | ||
M28730 | CHDI-390576 | HDAC |
CHDI-390576, a potent, cell permeable and CNS penetrant class IIa histone deacetylase (HDAC) inhibitor with IC50s of 54 nM, 60 nM, 31 nM, 50 nM for class IIa HDAC4, HDAC5, HDAC7, HDAC9, respectively, shows >500-fold selectivity over class I HDACs (1, 2, 3) and ~150-fold selectivity over HDAC8 and the class IIb HDAC6 isoform. | ||
M41480 | HDAC-IN-56 | HDAC |
HDAC-IN-56 ((S)-17b) is an orally active class I histone deacetylase (HDAC) inhibitor. | ||
M41481 | HDAC-IN-57 | HDAC |
HDAC-IN-57 is an orally active inhibitor of histone deacetylases (HDAC), with IC50s of 2.07 nM, 4.71 nM, 2.4 nM and 107 nM for HDAC1, HDAC2, HDAC6, HDAC8, respectively. | ||
M41484 | HDAC-IN-53 | HDAC |
HDAC-IN-53 is an orally active, and selective HDAC1-3 inhibitor with IC50 values of 47 nM, 125 nM, and 450 nM, respectively. | ||
M41496 | HDAC-IN-59 | HDAC |
HDAC-IN-59 is a potent histone deacetylase (HDAC) inhibitor. | ||
M41506 | HDAC-IN-58 | HDAC |
HDAC-IN-58 is a HDAC inhibitor. | ||
M42906 | HDAC-IN-55 | Others |
HDAC-IN-55(8j) is a small molecular compound that can increase the expression of E-cadherin and inhibit the proliferation of cancer cells. | ||
M43355 | HD5 | Others |
HD5 is a biological active peptide. | ||
M54628 | hDHODH-IN-5 | DHODH |
hDHODH-IN-5 is a human dihydroorotic acid dehydrogenase (DHODH) inhibitor with an IC50 of 0.91 μM. hDHODH-IN-7 induces differentiation of acute myeloid leukemia cells. |
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