Sedative and hypnotic, protect heart rhythm, prolong the sleep time of animals with sodium pentobarbital, tolerate hypoxia, promote the phagocytic function of mononuclear phagocytes, and protect against arrhythmias caused by aconitine

It has certain anti-inflammatory, liver cell membrane protection and liver function improvement effects. It can reduce the increase of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) caused by carbon tetrachloride, thioacetamide and D-aminogalactic acid, reduce the damage of D-aminogalactic acid to the liver and improve the chronic damage of immune factors to the liver.

This product is a potent, highly selective 5HT3 receptor antagonist with a strong antiemetic effect. It exerts an antiemetic effect by antagonizing the 5HT receptors of neurons located in the peripheral and central nervous systems, and is used to treat nausea and vomiting after chemotherapy, radiotherapy, and surgery. In addition, it can also inhibit nausea induced by opioids, but the specific mechanism is still unclear. Due to the high selectivity of this product, it does not have the side effects of other antiemetics, such as extrapyramidal reactions and excessive sedation.

It is an oxidized derivative of adrenaline and has no adrenaline-mimetic effect, so it does not affect blood pressure and heart rate, but it can enhance the resistance of capillaries to damage, stabilize the acidic mucopolysaccharides in blood vessels and surrounding tissues, reduce the permeability of capillaries, and enhance the retraction effect of damaged capillary ends, making it difficult for blood clots to fall off the tube wall, thereby shortening the hemostasis time, but it does not affect the coagulation process.