Cetaben is a unique, PPAR??-independent peroxisome proliferator with hypolipidemic activity that inhibits cholesterol synthesis in the human hepatoma Hep-G2 cells resulting in reversible changes in Golgi morphology.
More Information Supplier PageINCB8761(PF-4136309) is a potent, selective, and orally bioavailable CCR2 antagonist.
More Information Supplier PageINCB8761(PF-4136309) is a potent, selective, and orally bioavailable CCR2 antagonist.
More Information Supplier PageINCB8761(PF-4136309) is a potent, selective, and orally bioavailable CCR2 antagonist.
More Information Supplier PageTOK-001 (Galeterone) is both an androgen receptor antagonist and CYP17A1 inhibitor.
More Information Supplier PageTOK-001 (Galeterone) is both an androgen receptor antagonist and CYP17A1 inhibitor.
More Information Supplier PageNPS-2143 is a selective Ca2+-sensing receptor antagonist, shown to block increases in cytoplasmic Ca2+ concentrations elicited by human Ca2+ receptors expressed in HEK293 cells with an IC50 of 43 nM.
More Information Supplier PageNPS-2143 is a selective Ca2+-sensing receptor antagonist, shown to block increases in cytoplasmic Ca2+ concentrations elicited by human Ca2+ receptors expressed in HEK293 cells with an IC50 of 43 nM.
More Information Supplier PageNPS-2143 is a selective Ca2+-sensing receptor antagonist, shown to block increases in cytoplasmic Ca2+ concentrations elicited by human Ca2+ receptors expressed in HEK293 cells with an IC50 of 43 nM.
More Information Supplier PageRetapamulin is an antibacterial agent, specifically a protein synthesis inhibitor
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