Weight | 128.087 g/mol |
---|---|
Formula | C4H4N2O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
BARBITURIC ACID (67-52-7, 4390-16-3)
barbiturate · sodium barbiturate · barbituric acid, monosodium salt
Score:
#797 in Neuroscience
,
#3494 in Biology
,
#4371 in Chemistry
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- Steroid hormone metabolites are barbiturate-like modulators of the GABA receptor (Science, 1986)
- GABA-Benzodiazepine-Barbiturate Receptor Interactions (Journal of Neurochemistry, 1981)
- High-dose barbiturate control of elevated intracranial pressure in patients with severe head injury (Journal of Neurosurgery, 1988)
- A 24-HOUR PERIODICITY IN THE LH-RELEASE APPARATUS OF FEMALE RATS, DISCLOSED BY BARBITURATE SEDATION1 (Endocrinology, 1950)
- Neuropsychiatric complications after cardiopulmonary bypass: cerebral protection by a barbiturate. (Anesthesiology, 1985)
- Barbiturate Protection in Acute Focal Cerebral Ischemia (Stroke, 1974)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - barbiturate
- sodium barbiturate
- barbituric acid, monosodium salt
-
SMILESC1C(=O)NC(=O)NC1=O
-
InChIKeyHNYOPLTXPVRDBG-UHFFFAOYSA-N
- Pubchem - BARBITURIC ACID
- Wikipedia - barbituric acid
Barbituric acid or malonylurea or 6-hydroxyuracil is an organic compound based on a pyrimidine heterocyclic skeleton. It is an odorless powder soluble in water. Barbituric acid is the parent compound of barbiturate drugs, although barbituric acid itself is not pharmacologically active.
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pyrrolidine-1-carboxamide
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1-(4-methylphenyl)pyrimidine-2,4,6(1H,3H,5H)-trione
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3-(4,4-dimethyl-2,5-dioxoimidazolidin-1-yl)propanoic acid
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