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MK-886 also decreases PPARα activation by fatty acids in the stable transfection system
when these are coexpressed with γ-2 in oocytes
acting as an antagonist of Smoothened
most likely through covalent interaction with Cys797 and Cys805 in the catalytic domains of EGFR and ErbB2
InChi: InChI=1S/C12H17NO4
PACAP (6-38), human, ovine, rat Size:Contact [email protected] for quotation MK-886 also decreases PPARα activationPACAP (6 38), human, ovine, rat is a potent PACAP receptor antagonist with IC50s of 30, 600, and 40 nM for PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2, respectively. Product information CAS Number: 143748 18 9 Molecular Weight: 4024. 74 Formula: C182H300N56O45S Chemical Name: (3S) 3 {[(1S) 1 {[(1S) 1 {[(1S) 1 {[(1S) 1 {[(1S) 1 {[(1S) 1 {[(1S) 5 amino 1 {[(1S) 1 {[(1S) 1 {[(1S) 1 {[(1S) 1 {[(1S) 5 amino 1 {[(1S)