p-Aminophenylmercuric acetate 是一种有机汞基质金属蛋白酶 (MMP) 激活剂。p-Aminophenylmercuric acetate 通过攻击蛋白质巯基或诱导半胱氨酸转换反应，参与 MMP-8 的激活和抑制。p-Aminophenylmercuric acetate 促进了 β 纤维素素前体 (pro-BTC) 脱落。p-Aminophenylmercuric acetate 影响阿片类受体与其激动剂和拮抗剂的结合。 p-Aminophenylmercuric acetate is an organomercurial activator of matrix metalloproteinases (MMP). P-Aminophenylmercuric acetate participates in the activation and inhibition of MMP-8 by attacking protein sulfhydryl or inducing cysteine switching reaction. p-Aminophenylmercuric acetate promotes the shedding of betacellulin precursor (pro-BTC). p-Aminophenylmercuric acetate influences the binding of agonists and antagonists to the opiate receptor . In Vitro p-Aminophenylmercuric acetate (APMA) (0-30 µM; 20 min) decreases the apparent number of dihydromorphine binding sites and increases the sensitivity of agonist binding to the inhibitory effects of sodium in rat brain homogenate. p-Aminophenylmercuric acetate (0.5 mM; 30 min) activates the MMP-2 and MMP-9. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Form:Solid