C5H4ClNO2

An inhibitor of dihydrodehydrogenase, one of the components of anticancer drug s-1 It can inhibit the toxic and side effects of tegafur

C8H14N3O6P

Antiviral drugs. Inhibit viral replication by selectively inhibiting the synthesis of viral DNA. Retinitis is used to treat AIDS.

C15H24N4O6S2.H2O

It is a new carbapenem antibiotic, which has a wide antibacterial spectrum and is resistant to most antibiotics β- Lactamases are stable, including penicillinase, cephalosporinase and extended spectrum β- Lactamases (ESBLs).

C11H14ClN

C20H34O5

Prostaglandin E1 is widely present in the body of biologically active substances, as one of the prostaglandin family, it is a recognized endogenous physiologically active substances. Prostaglandin E1 acts directly on vascular smooth muscle, dilates blood vessels, increases blood flow, improves microcirculation perfusion; and inhibits platelet aggregation and thromboxane A2 production, inhibits atherosclerosis, lipid plaque and immune complex formation

C22H32O4

A synthetic analogue of prostacyclin PGI2.

C25H34F2O5

A novel prostaglandin analogue, p-fluoroprostaglandin receptor PGF2 α It has high affinity. It is a selective FP receptor agonist for prostaglandins.

C24H29NaO5

It is the sodium salt form of anticoagulant beprost. This product can inhibit platelet aggregation, platelet adhesion and release reaction, expand arterioles and venules, especially pulmonary artery vascular bed, so as to reduce pulmonary artery pressure and pulmonary vascular resistance.

C23H38O5

Synthesis of derivatives of PGE1. It can strongly contract uterine smooth muscle, has little effect on gastrointestinal smooth muscle and blood pressure, and softens and dilates cervical canal.

C25H44O5

C22H36O5

A PGE1 analogue and an effective oral active vasodilator. It can increase blood flow and inhibit platelet aggregation. It can be used to relieve pain, has anti angina pectoris effect, and can be used to study ischemic symptoms.

C21H36O5.C4H11NO3

It's prostaglandin F2 α (prostaglandin F2 α) It can effectively promote the regular contraction of uterus and significantly reduce the amount of postpartum hemorrhage.

C22H28ClNaO6

A synthetic and effective prostaglandin analogue with luteal solubility, PGF2 α Receptor agonists.

C22H28ClNaO6

A highly active luteolytic prostaglandin analogue

C22H38O5

Chemically synthesized prostaglandin E1 anti ulcer drugs have strong effects on inhibiting gastric acid secretion and preventing ulcer formation