| Weight | 115.132 g/mol |
|---|---|
| Formula | C5H9NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
2-aminopent-4-enoic acid (7685-44-1)
Allylglycine · 2-Amino-4-Pentenoic Acid
Score:
#1157 in Neuroscience
,
#2591 in Biochemistry
,
#5004 in Biology
,
#6444 in Chemistry
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- Intracellular calcium accumulation in rat hippocampus during seizures induced by bicuculline orl-allylglycine (Neuroscience, 1983)
- Seizures induced by allylglycine, 3-mercaptopropionic acid and 4-deoxypyridoxine in mice and photosensitive baboons, and different modes of inhibition of cerebral glutamic acid decarboxylase (British Journal of Pharmacology, 1973)
- Epileptic Brain Damage in Adolescent Baboons Following Seizures Induced by Allylglycine (Brain, 1974)
- Glutamic acid decarboxylase inhibition and ultrastructural changes by the convulsant drug allylglycine (Biochemical Pharmacology, 1969)
- D AND LSTEREOISOMERS OF ALLYLGLYCINE: CONVULSIVE ACTION AND INHIBITION OF BRAIN LGLUTAMATE DECARBOXYLASE (Journal of Neurochemistry, 1977)
- Zn-catalyzed asymmetric allylation for the synthesis of optically active allylglycine derivatives. Regio- and stereoselective formal alpha-addition of allylboronates to hydrazono esters. (Journal of the American Chemical Society, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Allylglycine
- 2-Amino-4-Pentenoic Acid
-
SMILESC=CCC(C(=O)O)N
-
InChIKeyWNNNWFKQCKFSDK-UHFFFAOYSA-N
- Pubchem - 2-aminopent-4-enoic acid
- Wikipedia - Allylglycine
Allylglycine is a glycine derivative. It is an inhibitor of glutamate decarboxylase. Inhibition of glutamate decarboxylase blocks GABA biosynthesis, leading to lower levels of the neurotransmitter.
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