MGCD0103 10mg 10mg | Purity Not Available
Adooq Bioscience
MGCD0103 (Mocetinostat) is a benzamide histone deacetylase inhibitor by inhibiting mainly histone deacetylase 1 (HDAC1), but also HDAC2, HDAC3, and HDAC11.
More Information Supplier PageMGCD0103 (Mocetinostat) is a benzamide histone deacetylase inhibitor by inhibiting mainly histone deacetylase 1 (HDAC1), but also HDAC2, HDAC3, and HDAC11.
More Information Supplier PageMetolazone and the other thiazide diuretics inhibit the function of the sodium-chloride symporter and prevent sodium and chloride, water as well, from leaving the lumen to enter the tubule cell.
More Information Supplier PageMGCD265 is a multitargeted tyrosine kinase inhibitor that binds to and inhibits the phosphorylation of several RTKs, including the c-Met receptor (HGFR); the Tek/Tie-2 receptor; VEGFR types 1, 2, and 3; and MST1R.
More Information Supplier PageMGCD265 is a multitargeted tyrosine kinase inhibitor that binds to and inhibits the phosphorylation of several RTKs, including the c-Met receptor (HGFR); the Tek/Tie-2 receptor; VEGFR types 1, 2, and 3; and MST1R.
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMifepristone, an antioxidant and glucocorticoid receptor antagonist, demonstrates the ability to suppress activation of NF??B, a nuclear transcription factor that affects the expression of various adhesion molecules and several inflammatory genes.
More Information Supplier PageMianserin hydrochloride is a 5-HT2/5-HT1 antagonist. Has moderate affinity for 5-ht6 Non-selective 5-HT2 receptor antagonist. Has moderate affinity for 5-HT6. Antidepressant.
More Information Supplier PageMianserin hydrochloride is a 5-HT2/5-HT1 antagonist. Has moderate affinity for 5-ht6 Non-selective 5-HT2 receptor antagonist. Has moderate affinity for 5-HT6. Antidepressant.
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