Cimetidine Powder CAS 51481-61-9 Raw Material

CAS:51481-61-9

MF: C10H16N6S

MW:252.34

EINECS: 257-232-2

Specification​: 99% min Cimetidine 

Sample: Cimetidine Powder

Brand: Henrikang

Appearance: White Powder

Storage: Cool Dry Place

Shelf Life: 2 Years

Test Method: HPLC

Portal:https://henrikang.en.made-in-china.com/

Cimetidine Powder Usage and Synthesis.

Cimetidine Powder is an H2 receptor antagonist, which can significantly inhibit the secretion of gastric acid caused by food, histamine or pentagastrin stimulation and reduce its acidity.

Cimetidine CAS 51481-61-9 has a preventive and protective effect on corrosive gastritis caused by chemical stimulation, and also has significant Cimetidine CAS 581-61-9 has a preventive and protective effect on corrosive gastritis caused by chemical stimulation, and also has significant efficacy on stress gastric ulcer and upper gastrointestinal bleeding. 

Cimetidine Raw Material is mainly used for the treatment of peptic ulcer.

Cimetidine Raw Material has the effect of inhibiting the secretion of gastric acid and decreasing its acidity, which has a preventive and protective effect on corrosive gastritis. Cimetidine Raw Material has the effect of inhibiting the secretion of gastric acid and decreasing its acidity, which has a preventive and protective effect on corrosive gastritis caused by chemical irritation, and also has a significant effect on stress gastric ulcer and upper gastrointestinal It has a preventive and protective effect on corrosive gastritis caused by chemical irritation, and also has a significant effect on stress gastric ulcer and upper gastrointestinal bleeding.

Application/Function of Cimetidine Powder.

Cimetidine, marketed in 1975, is the first selective H2 receptor antagonist used in the treatment of peptic ulcer. It mainly has the effect of inhibiting the secretion of gastric acid and reducing its acidity, which has a preventive and protective effect on corrosive gastritis caused by chemical irritation, and also has a significant effect on stress gastric ulcer and upper gastrointestinal bleeding. Acid control and pain relief, stomach protection and muscle production, hemostasis. Histamine H2 receptor antagonist. It can inhibit gastric acid secretion induced by histamine stimulation, and also inhibit gastric acid secretion induced by food, pentagastrin, caffeine and insulin, etc. It can also inhibit basal gastric acid secretion. It is used for gastric and duodenal ulcer, peptic esophagitis, and Zhuo-Ai syndrome.

• 1. For stomach pain and acidity. This product is good at controlling acid and relieving pain, and also has the function of draining the liver and regulating qi and stomach, so it is a common medicine for liver and stomach disharmony, excessive acidity, stomach and epigastric pain, belching and swallowing acid.
• 2. For broken stomach muscle. It is used for stomach pain caused by broken stomach muscle, which can not only protect the stomach muscle but also harmonize the stomach to relieve pain.
• 3. Used for vomiting blood and blood in stool. This product has astringent and hemostatic effects, and is used for vomiting blood and blood in stool caused by injury to the stomach ligament.

Pharmacological Effects of Cimetidine Powder

This product is a histamine H2 receptor antagonist, which can reversibly inhibit the effect of histamine on H2 receptors. Therefore, it can inhibit the secretion of gastric acid caused by basic gastric acid and various stimuli, and prevent peptic ulcers. It can enhance cellular immune function, inhibit the activity of suppressive T cells, and have immunostimulatory effects on lymphocytes. It also has anti-androgenic effects, can block the binding of dihydrotestosterone to hair follicle receptors, and inhibit the secretion of skin glands.

It also has antiviral effect, local anesthetic and analgesic effect and antipruritic effect. It is rapidly absorbed after oral administration, with peak blood concentration in 60-90 minutes after administration and biological half-life of about 2 hours. The peak time is significantly delayed and the half-life is prolonged when the drug is taken during meals. When 0.4g is taken on an empty stomach, the effective blood concentration can be maintained for more than 4 hours, and the acid-suppressive effect lasts for 5-6 hours.

It can pass the blood-brain barrier, and the concentration in cerebrospinal fluid is about 1/4 of that in blood; it can also pass the placental barrier, and can be secreted into breast milk. 80% of the drug is excreted by kidney in its original form within 24 hours. In patients with renal insufficiency, excretion is reduced and the duration of drug action is prolonged.