| Weight | 111.148 g/mol |
|---|---|
| Formula | C5H9N3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
BETAZOLE (105-20-4)
Histalog · Ametazole · 105-20-4
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- BASAL AND HISTALOG-STIMULATED GASTRIC SECRETION IN CONTROL SUBJECTS AND IN PATIENTS WITH PEPTIC ULCER OR GASTRIC CANCER. (Gastroenterology, 1963)
- Maximal histalog test in control subjects and patients with peptic ulcer. (Gut, 1965)
- Comparison of Histalog and Histamine as Stimulants for Maximal Gastric Secretion in Human Subjects and in Dogs (Gastroenterology, 1963)
- A comparative study of the effects of gastrin, histamine, histalog, and mechothane on the secretory capacity of the human stomach in two normal subjects over 20 months. (Gut, 1965)
- The gastric secretory response to histalog: one-hour basal and histalog secretion in normal persons and in patients with duodenal ulcer and gastric ulcer. (Journal of Laboratory and Clinical Medicine, 1955)
- Inhibition of Basal and Betazole- and Sham-Feeding-Induced Acid Secretion by Omeprazole in Man (Scandinavian Journal of Gastroenterology, 1986)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Histalog
- Ametazole
- 105-20-4
- 2-(1H-pyrazol-5-yl)ethanamine
- Lilly 96791
- Betazole Monohydrochloride
- Betazole Dihydrochloride
-
SMILESC1=C(NN=C1)CCN
-
InChIKeyJXDFEQONERDKSS-UHFFFAOYSA-N
- Pubchem - BETAZOLE
- Wikipedia - betazole
Betazole (also known as ametazole) is a histamine H2 receptor agonist. Betazole hydrochloride is known as gastramine and histalog. It has been used as a gastric stimulant to test for maximal production of gastric secretion activity.
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Alternate Names
Estimated Properties
| Boiling Point | 253.59 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 263.5 C | EPI Suite |
| Density | 1.15 g/cm3 | EPA T.E.S.T. |
| Flash Point | 132.07 C | EPA T.E.S.T. |
| Melting Point | 62.36 C | EPI Suite |
| Water Solubility | 16690.5 mg/L | EPA T.E.S.T. |
| Water Solubility | 1e+06 mg/L | EPI Suite |
External Links
Synthesis
Similar Compounds
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4-Bromo-3-ethyl-5-methyl-1H-pyrazole
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4-BROMO-3-ISOPROPYL-1H-PYRAZOLE
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3-Amino-5-tert-butylpyrazole
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4,5,6,7-Tetrahydro-1H-pyrazolo[4,3-c]pyridine Dihydrochloride
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4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
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5-ISOBUTYL-1H-PYRAZOLE-3-CARBALDEHYDE
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3-tert-butyl-1H-pyrazole-5-carbaldehyde
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[(3-tert-butyl-1H-pyrazol-5-yl)methyl]methylamine hydrochloride
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4-Bromo-5-cyclopropyl-1H-pyrazole
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3-Amino-5-methylpyrazole
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1-(5-CYCLOPROPYL-1H-PYRAZOL-3-YL)-N-METHYLMETHANAMINE
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4-fluoro-3,5-dimethyl-1H-pyrazole
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4-chloro-3,5-dimethyl-1H-pyrazole
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3-Isopropyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine dihydrochloride
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MolPort-029-906-622
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2-(3,5-dimethyl-1H-pyrazol-4-yl)ethanamine
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3-acetyl-1H-pyrazole-5-carboxylic acid
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5-cyclopropyl-3-(trifluoromethyl)-1H-pyrazole
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4-Ethyl-3,5-dimethyl-1H-pyrazole
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3,5-bis(difluoromethyl)-1H-pyrazole
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3,5-dimethyl-1H-pyrazol-4-ol
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1-(1-Methyl-1H-pyrazol-5-yl)propan-1-amine
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5-(chloromethyl)-1-methyl-1H-pyrazole
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5-(chloromethyl)-1-methyl-1H-pyrazole hydrochloride
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4-(2-chloroethyl)-3,5-dimethyl-1H-pyrazole
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2-(2-Aminoethyl)pyridine
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3-cyclopropyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine dihydrochloride
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3-Cyclopropyl-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine
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4,5,6,7-tetrahydro-1H-indazol-5-amine dihydrochloride
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2-methoxy-1-(1-methyl-1H-pyrazol-5-yl)ethanamine
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3,5-dimethyl-4-propyl-1H-pyrazole
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3,5-Bis(trifluoromethyl)-1H-pyrazole
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3-(3,5-dimethyl-1H-pyrazol-4-yl)propan-1-amine
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5-Amino-1,3-dimethylpyrazole
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1-(2-chloroethyl)-3-methyl-1H-pyrazole
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5-bromo-3-cyclopropyl-1-methyl-1H-pyrazole
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1-(4-chloro-1-methyl-1H-pyrazol-3-yl)ethanone
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2,3-Dimethyl-3-pyrazolin-5-one
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BETAZOLE
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