This product is a cholinesterase inhibitor, which has a selective inhibitory effect on true ChE and can easily pass through the blood-brain barrier. It has the effect of promoting memory reproduction and enhancing memory retention.

It has a layered structure and non-uniform charge distribution, and has a strong fixing and inhibitory effect on viruses, bacteria and the toxins and gases they produce in the digestive tract, making them lose their pathogenic effects; in addition, it has a strong covering and protective ability for the digestive tract mucosa, repairing and improving the defense function of the mucosal barrier against attacking factors, and has the effect of balancing normal flora and relieving local pain.

This product is graded based on natural montmorillonite, and has a layered structure and non-uniform charge distribution. It has a strong fixing and inhibitory effect on viruses, bacteria and the toxins and gases they produce in the digestive tract, making them lose their pathogenic effects. In addition, it has a strong covering and protective ability for the digestive tract mucosa, repairing and improving the defense function of the mucosal barrier against attacking factors, and has the effect of balancing normal flora and local analgesia.

This product is graded based on natural montmorillonite, and has a layered structure and non-uniform charge distribution. It has a strong fixing and inhibitory effect on viruses, bacteria and the toxins and gases they produce in the digestive tract, making them lose their pathogenic effects. In addition, it has a strong covering and protective ability for the digestive tract mucosa, repairing and improving the defense function of the mucosal barrier against attacking factors, and has the effect of balancing normal flora and local analgesia.

This product is graded based on natural montmorillonite, and has a layered structure and non-uniform charge distribution. It has a strong fixing and inhibitory effect on viruses, bacteria and the toxins and gases they produce in the digestive tract, making them lose their pathogenic effects. In addition, it has a strong covering and protective ability for the digestive tract mucosa, repairing and improving the defense function of the mucosal barrier against attacking factors, and has the effect of balancing normal flora and local analgesia.

Amoxicillin is a penicillin antibiotic that has good antibacterial activity against Streptococcus such as Streptococcus pneumoniae and hemolytic Streptococcus, aerobic Gram-positive cocci such as non-penicillinase-producing Staphylococci and Enterococcus faecalis, aerobic Gram-negative bacteria such as Escherichia coli, Proteus mirabilis, Salmonella, Haemophilus influenzae, Neisseria gonorrhoeae, and Helicobacter pylori. Amoxicillin exerts its bactericidal effect by inhibiting the synthesis of bacterial cell walls, which can quickly dissolve and rupture bacteria into spherical bodies.

A selective alpha 1 receptor antagonist that can inhibit the rise in blood pressure caused by alpha 1 receptors, has a hypotensive effect on a variety of hypertensive animal models, with a long duration of hypotensive effect, and does not cause reflex tachycardia during hypotensive treatment. No obvious first-dose effect or drug resistance was observed after multiple oral administrations. It can reduce the total peripheral resistance of anesthetized open-chest dogs, dilate peripheral blood vessels, and has no significant effect on cardiac output. It can also relieve the sympathetic tension of the prostate and urethra caused by the excitement of the receptor through the alpha 1 receptor blocking effect, reduce the intraurethral pressure, and improve symptoms such as urination disorders caused by benign prostatic hyperplasia.

This product is a prodrug, which is hydrolyzed into the active substance benazeprilat, which can inhibit angiotensin converting enzyme (ACE) and prevent angiotensin I from converting into angiotensin II. This can reduce a series of symptoms caused by angiotensin II, namely vasoconstriction and the production of aldosterone (the latter will lead to the reabsorption of sodium and water by the renal tubules and increase cardiac output). Lotensin reduces the reflex sympathetic excitatory heart rate increase caused by vasodilation. In addition, by inhibiting kininase and reducing the degradation of the vasodilator bradykinin, it helps to improve its antihypertensive effect. For patients with congestive heart failure, Lotensin can increase cardiac output and exercise tolerance, reduce pulmonary artery wedge pressure, systemic vascular resistance and blood pressure, slightly reduce heart rate, and improve NYHA class. In patients with progressive chronic renal insufficiency, Lotensin can significantly reduce proteinuria and delay the deterioration of renal function.