76963-41-2
76963-41-2
Chemical Structure
Nizatidine
- CAS No.: 76963-41-2
- Formula:C12H21N5O2S2
- Molecular Weight:331.46
IUPAC Name: (E)-N-(2-(((2-((dimethylamino)methyl)thiazol-4-yl)methyl)thio)ethyl)-N'-methyl-2-nitroethene-1,1-diamine
InChIKey: SGXXNSQHWDMGGP-IZZDOVSWSA-N
SMILES: CN/C(NCCSCC1=CSC(CN(C)C)=N1)=C\[N+]([O-])=O
Biological Activity: Nizatidine is a potent and orally active histamine H2 receptor antagonist, can be used for the research of stomach and intestines ulcers. Nizatidine works by decreasing the secretion of gastric acid the stomach makes and prevent ulcers from coming back after they have healed in animal models[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Nizatidine | 98.94% | Nizatidine is a potent and orally active histamine H2 receptor antagonist, can be used for the research of stomach and intestines ulcers. Nizatidine works by decreasing the secretion of gastric acid the stomach makes and prevent ulcers from coming back after they have healed in animal models. | ||||||||||||||||||||
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Nizatidine (Standard) | ≥98% | Nizatidine (Standard) is the analytical standard of Nizatidine. This product is intended for research and analytical applications. Nizatidine is a potent and orally active histamine H2 receptor antagonist, can be used for the research of stomach and intestines ulcers. Nizatidine works by decreasing the secretion of gastric acid the stomach makes and prevent ulcers from coming back after they have healed in animal models. | ||||||||||||||||||||
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Nizatidine-d3 | 98.80% | Nizatidine-d3 is the deuterium labeled Nizatidine. Nizatidine is a potent and orally active histamine H2 receptor antagonist, can be used for the research of stomach?and?intestines ulcers. Nizatidine works by decreasing the secretion of gastric?acid the stomach makes and prevent ulcers from coming back after they have healed in animal models. | ||||||||||||||||||||
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Tiotidine (Standard) | ≥98% | Tiotidine (Standard) is the analytical standard of Tiotidine. This product is intended for research and analytical applications. Tiotidine (ICI 125211) is a potent and selective antagonist of histamine H2-receptor (pA2=7.3-7.8 for guinea-pig right atrium). Tiotidine has low affinity for both the H1 and the H3 receptors. | ||||||||||||||||||||
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Ranitidine impurity 12 | Ranitidine impurity 12 is an impurity of Ranitidine. | |||||||||||||||||||||
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Ranitidine hydrochloride | 99.86% | Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine hydrochloride antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA2 values of 7.2 and 6.95, respectively. Ranitidine hydrochloride inhibits breast tumor development and spread in mice. | ||||||||||||||||||||
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Ranitidine-d6 hydrochloride | 97.00% | Ranitidine-d6 hydrochloride is the deuterium labeled Ranitidine hydrochloride (HY-B0281A). Ranitidine hydrochloride is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine hydrochloride antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA2 values of 7.2 and 6.95, respectively. Ranitidine hydrochloride inhibits breast tumor development and spread in mice. | ||||||||||||||||||||
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Ranitidine | 99.9% | Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA2 values of 7.2 and 6.95, respectively. Ranitidine inhibits breast tumor development and spread in mice. | ||||||||||||||||||||
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Ranitidine-d6 | Ranitidine-d6 is the deuterium labeled Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist that inhibits gastric secretion. Ranitidine antagonizes Histamine (HY-B1204)-induced increases of the guinea-pig isolated rat atrium and Histamine-induced relaxations of the rat isolated uterine horn, with pA2 values of 7.2 and 6.95, respectively. Ranitidine inhibits breast tumor development and spread in mice. | |||||||||||||||||||||
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Ranitidine S-oxide (Standard) | ≥98% | Ranitidine S-oxide (Standard) is the analytical standard of Ranitidine S-oxide. This product is intended for research and analytical applications. Ranitidine S-oxide is the metabolite of Ranitidine (HY-B0693). Ranitidine is a potent, selective and orally active histamine H2-receptor antagonist with an IC50 of 3.3 μM that inhibits gastric secretion. | ||||||||||||||||||||
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Famotidine impurity 8 | Famotidine impurity 8 (Famotidine propionic acid) is an impurity of Famotidine. | |||||||||||||||||||||
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Famotidine impurity 10 | Famotidine impurity 10 is an impurity of Famotidine. | |||||||||||||||||||||
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