SB-705498 10mM * 1mL in DMSO 10mM * 1mL in DMSO | Purity Not Available
Adooq Bioscience
SB-705498 is a potent, selective and orally bioavailable TRPV1 antagonist.
More Information Supplier PageSB-705498 is a potent, selective and orally bioavailable TRPV1 antagonist.
More Information Supplier PageSB-705498 is a potent, selective and orally bioavailable TRPV1 antagonist.
More Information Supplier PageSB-705498 is a potent, selective and orally bioavailable TRPV1 antagonist.
More Information Supplier PagePF 431396 is a dual focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (PYK2) inhibitor (IC50 values are 2 and 11 nM respectively).
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 PageCetaben 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 PageCetaben 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 PageCetaben 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 PageCetaben 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 Page