| Weight | 126.115 g/mol |
|---|---|
| Formula | C5H6N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Imidazole-4-acetic acid (645-65-8)
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- Nonpeptide angiotensin II receptor antagonists. I. Pharmacological characterization of 2-n-butyl-4-chloro-1-(2-chlorobenzyl)imidazole-5-acetic acid, sodium salt (S-8307). (Journal of Pharmacology and Experimental Therapeutics, 1988)
- SCAVENGING OF SINGLET MOLECULAR OXYGEN BY IMIDAZOLE COMPOUNDS: HIGH and SUSTAINED ACTIVITIES OF CARBOXY TERMINAL HISTIDINE DIPEPTIDES and EXCEPTIONAL ACTIVITY OF IMIDAZOLE4ACETIC ACID (Photochemistry and Photobiology, 1990)
- Neuropharmacological studies of imidazole-4-acetic acid actions in the mouse and rat (Neuropharmacology, 1971)
- Urinary Excretion of a Metabolite of Histamine (1,4methylimidazoleaceticacid) in Painful Bladder Disease (BJUI, 1987)
- Some properties of cyclic 3, 5-nucleotide phosphodiesterase of mouse brain: effects of imidazole-4-acetic acid, chlorpromazine, cyclic 3,5-GMP, and other substances (Brain Research, 1970)
- A comparison of gamma-aminobutyric acid and the semi-rigid analogues 4-aminotetrolic acid, 4-aminocrotonic acid and imidazole-4-acetic acid on the isolated superior cervical ganglion of the rat. (British Journal of Pharmacology, 1976)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=C(NC=N1)CC(=O)O
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InChIKeyPRJKNHOMHKJCEJ-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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