It binds to the 50S subunit of the ribosome of sensitive microorganisms, inhibits RNA-dependent protein synthesis and exerts an antibacterial effect

It binds to the 50S subunit of the ribosome of sensitive microorganisms, inhibits RNA-dependent protein synthesis and exerts an antibacterial effect

It binds to the 50S subunit of the ribosome of sensitive microorganisms, inhibits RNA-dependent protein synthesis and exerts an antibacterial effect

It binds to the 50S subunit of the ribosome of sensitive microorganisms, inhibits RNA-dependent protein synthesis and exerts an antibacterial effect

Omeprazole is a proton pump inhibitor that can irreversibly bind to the sulfhydryl group of the proton pump in the secretory membrane of gastric parietal cells, thereby inhibiting the activity of the enzyme and blocking the final step of gastric acid secretion. Therefore, this product has a strong and lasting inhibitory effect on gastric acid secretion caused by various reasons.

Its effect on intestinal smooth muscle is similar to that of opioids, which can inhibit the contraction of intestinal smooth muscle and reduce intestinal peristalsis; reduce the release of acetylcholine from intestinal wall nerve endings, and directly inhibit peristaltic reflexes through local interactions between cholinergic and non-cholinergic neurons; prolong the residence time of food in the small intestine, and promote the absorption of water, electrolytes and glucose; inhibit intestinal excessive secretion caused by prostaglandins, cholera toxin and other enterotoxins; increase the tension of the anal sphincter, and inhibit fecal incontinence or urgency.

This product is a broad-spectrum antibiotic, which has antibacterial activity against some Gram-positive and Gram-negative bacteria, especially against Streptococcus (except Enterococcus) and Pneumococcus among Gram-positive bacteria, and gonococci, Branhamella, Escherichia coli, Klebsiella, Serratia, Proteus, and influenza bacillus among Gram-negative bacteria. Its mechanism of action is to prevent the synthesis of bacterial cell walls, and it has a high affinity with 1 (la, lb, 1c) and 3 in penicillin-binding protein (PBP). It has extremely strong stability against β-lactamase produced by various bacteria, and shows excellent antibacterial power against bacteria producing β-lactamase.

Broad-spectrum semi-synthetic penicillin has antibacterial effects on hemolytic streptococci, viridans streptococci, pneumococci, penicillin G-sensitive Staphylococcus aureus, gonococci, Haemophilus influenzae, enterococci, Salmonella, Salmonella typhi and Proteus. It has no effect on Staphylococcus aureus that produces penicillinase. Bacteria have complete cross-resistance to this product and ampicillin.