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Items: 6

1.

Axid

MedGen UID:
195694
Concept ID:
C0678129
Organic Chemical; Pharmacologic Substance
2.

LY-139037

MedGen UID:
163790
Concept ID:
C0877965
Organic Chemical; Pharmacologic Substance
3.

Nizatidine

A competitive and reversible histamine H2-receptor antagonist with antacid activity. Nizatidine inhibits the histamine H2-receptors located on the basolateral membrane of the gastric parietal cell, thereby reducing basal and nocturnal gastric acid secretion, resulting in a reduction in gastric volume, acidity, and amount of gastric acid released in response to stimuli. [from NCI]

MedGen UID:
43112
Concept ID:
C0085154
Organic Chemical; Pharmacologic Substance
4.

Subcutaneous heparin

MedGen UID:
579099
Concept ID:
C0353681
Organic Chemical; Pharmacologic Substance
5.

Ondansetron hydrochloride

The hydrochloride salt of the racemic form of ondansetron, a carbazole derivative and a selective, competitive serotonin 5-hydroxytryptamine type 3 (5-HT3) receptor antagonist with antiemetic activity. Although its mechanism of action has not been fully characterized, ondansetron appears to competitively block the action of serotonin at 5HT3 receptors peripherally in the gastrointestinal tract as well as centrally in the area postrema of the CNS, where the chemoreceptor trigger zone (CTZ) for vomiting is located, resulting in the suppression of chemotherapy- and radiotherapy-induced nausea and vomiting. [from NCI]

MedGen UID:
152157
Concept ID:
C0700478
Organic Chemical; Pharmacologic Substance
6.

Heparin sodium

The sodium salt form of heparin. As a glycosaminoglycan anticoagulant, heparin sodium binds to antithrombin III to form a heparin-antithrombin III complex. The complex binds to and irreversibly inactivates thrombin and other activated clotting factors IX, X, XI, and XII and prevents the transformation of fibrinogen to fibrin. (NCI) [from NCI]

MedGen UID:
11487
Concept ID:
C0037513
Organic Chemical; Pharmacologic Substance
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