| Weight | 179.219 g/mol |
|---|---|
| Formula | C10H13NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
4-Amino-3-phenylbutanoic acid (1078-21-3)
beta-(aminomethyl)hydrocinnamic acid · 4-amino-3-phenylbutyric acid hydrochloride · 4-amino-3-phenylbutyric acid, (DL)-(+-)-mixture
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- X-ray structure determination of (2S, 3R)-3-amino-2-hydroxy-4-phenylbutanoic acid, a new amino acid component of bestatin. (The Journal of Antibiotics, 1976)
- Analysis of amide bond formation with an alpha-hydroxy-beta-amino acid derivative, 3-amino-2-hydroxy-4-phenylbutanoic acid, as an acyl component: byproduction of homobislactone. (Journal of Organic Chemistry, 2001)
- Relationship between enhancement of morphine analgesia and inhibition of enkephalinase by 2S, 3R 3-amino-2-hydroxy-4-phenylbutanoic acid derivatives. (Life Sciences, 1982)
- 2S,3R 3-Amino-2-hydroxy-4-phenylbutanoic acid derivatives, enkephalinase inhibitors, augment Met5-enkephalin-induced antinociception (Japanese Journal of Pharmacology, 1988)
- A Convenient Preparation of (2SR,3S)-3-Amino-2-hydroxy-4-phenylbutanoic Acid; an Important Peptide Bond Isostere (Synthetic Communications, 1999)
- The synthesis and resolution of tritiated 4-amino-3-phenylbutanoic acid ([3H]R- and [3H]S--phenylgaba) (Journal of Labelled Compounds and Radiopharmaceuticals, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - beta-(aminomethyl)hydrocinnamic acid
- 4-amino-3-phenylbutyric acid hydrochloride
- 4-amino-3-phenylbutyric acid, (DL)-(+-)-mixture
- 4-amino-3-phenylbutyric acid, (L)-(-)-isomer
- beta-phenyl-gamma-aminobutyric acid
- 4-amino-3-phenylbutyric acid
- fenibut
- noophen
- fenibut citrate
- beta-(aminomethyl)benzenepropanoic acid
- phenybut
- citrocard
- phenibut
- phenyl-GABA
-
SMILESC1=CC=C(C=C1)C(CC(=O)O)CN
-
InChIKeyDAFOCGYVTAOKAJ-UHFFFAOYSA-N
- Pubchem - 4-Amino-3-phenylbutanoic acid
- Wikipedia - 4-amino-3-phenylbutyric acid
Phenibut, sold under the brand names Anvifen, Fenibut, and Noofen among others, is a central nervous system depressant with anxiolytic and sedative effects which is used in Russia, Ukraine, and Latvia for the treatment of anxiety, insomnia, and a variety of other indications. It is not approved for use in the United States or Europe, but it is sold over the Internet as a supplement and used as a recreational drug and purported nootropic. Phenibut is structurally related to the neurotransmitter -aminobutyric acid (GABA), and hence is a GABA analogue.
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Synthesis
benzene
+
Reactant
(Friedel-Crafts alkylation)
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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