Weight | 179.219 g/mol |
---|---|
Formula | C10H13NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 4 |
L-Homophenylalanine (943-73-7)
(S)-2-amino-4-phenylbutanoic acid · 2-amino-4-phenylbutanoic acid
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- Asymmetric synthesis of L-homophenylalanine by equilibrium-shift using recombinant aromatic L-amino acid transaminase (Biotechnology and Bioengineering, 2003)
- Simultaneous synthesis of 2phenylethanol and Lhomophenylalanine using aromatic transaminase with yeast Ehrlich pathway (Biotechnology and Bioengineering, 2009)
- 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)
- Enzyme-catalyzed asymmetric synthesis of (S)-2-amino-4-phenylbutanoic acid and (R)-2-hydroxy-4-phenylbutanoic acid (Bioorganic Chemistry, 1991)
- Asymmetrical synthesis of L-homophenylalanine using engineered Escherichia coli aspartate aminotransferase. (Biotechnology Progress, 2008)
- Novel Stereoselective Syntheses of the Fused Benzazepine Dopamine D1 Antagonist (6aS,13bR)-11-Chloro-6,6a,7,8,9,13b-hexahydro-7-methyl- 5H-benzo[d]naphth[2,1-b]azepin-12-ol (Sch 39166): 2. l-Homophenylalanine-Based Syntheses (Organic Process Research & Development, 1998)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - (S)-2-amino-4-phenylbutanoic acid
- 2-amino-4-phenylbutanoic acid
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SMILESC1=CC=C(C=C1)CCC(C(=O)O)N
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InChIKeyJTTHKOPSMAVJFE-UHFFFAOYSA-N
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