Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H13NO2 |
| Molecular Weight | 179.2157 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@@H](CCC1=CC=CC=C1)C(O)=O
InChI
InChIKey=JTTHKOPSMAVJFE-VIFPVBQESA-N
InChI=1S/C10H13NO2/c11-9(10(12)13)7-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)/t9-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Asymmetrically simultaneous synthesis of L-homophenylalanine and N6-protected-2-oxo-6-amino-hexanoic acid by engineered Escherichia coli aspartate aminotransferase. | 2009-09-22 |
|
| Simultaneous synthesis of 2-phenylethanol and L-homophenylalanine using aromatic transaminase with yeast Ehrlich pathway. | 2009-04-01 |
|
| Sustainable biocatalytic synthesis of L-homophenylalanine as pharmaceutical drug precursor. | 2008-09-19 |
|
| A novel hydantoinase process using recombinant Escherichia coli cells with dihydropyrimidinase and L-N-carbamoylase activities as biocatalyst for the production of L-homophenylalanine. | 2008-04-30 |
|
| Enantioselective synthesis of L-homophenylalanine by whole cells of recombinant Escherichia coli expressing L-aminoacylase and N-acylamino acid racemase genes from Deinococcus radiodurans BCRC12827. | 2006-12-02 |
|
| Asymmetrical synthesis of L-homophenylalanine using engineered Escherichia coli aspartate aminotransferase. | 2005-04-02 |
|
| Asymmetric synthesis of L-homophenylalanine by equilibrium-shift using recombinant aromatic L-amino acid transaminase. | 2003-07-20 |
|
| Concise synthesis and enzymatic resolution of L-(+)-homophenylalanine hydrochloride. | 2002-06-05 |
Patents
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| Code System | Code | Type | Description | ||
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943-73-7
Created by
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213-403-3
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DTXSID001315729
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2724505
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43103
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8JYL44CC06
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admin on Mon Mar 31 22:15:22 GMT 2025 , Edited by admin on Mon Mar 31 22:15:22 GMT 2025
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SUBSTANCE RECORD
