943-73-7 | L-Homophenylalanine

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$8.00	$5.00
10g	98%	in stock	$9.00	$6.00
25g	98%	in stock	$10.00	$7.00
100g	98%	in stock	$35.00	$24.00

Description

• Catalog Number: AB42967
• Chemical Name: L-Homophenylalanine
• CAS Number: 943-73-7
• Molecular Formula: C10H13NO2
• Molecular Weight: 179.2157
• MDL Number: MFCD00002619
• SMILES: N[C@H](C(=O)O)CCc1ccccc1

Computed Properties

• Complexity: 164
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4
• XLogP3: -1.2

Literature

• Simultaneous synthesis of 2-phenylethanol and L-homophenylalanine using aromatic transaminase with yeast Ehrlich pathway.

  Biotechnology and bioengineering 20090401

• Sustainable biocatalytic synthesis of L-homophenylalanine as pharmaceutical drug precursor.

  Biotechnology advances 20090101

• Asymmetrically simultaneous synthesis of L-homophenylalanine and N6-protected-2-oxo-6-amino-hexanoic acid by engineered Escherichia coli aspartate aminotransferase.

  Biotechnology progress 20090101

• A novel hydantoinase process using recombinant Escherichia coli cells with dihydropyrimidinase and L-N-carbamoylase activities as biocatalyst for the production of L-homophenylalanine.

  Journal of biotechnology 20080430

• mGluR7 undergoes rapid internalization in response to activation by the allosteric agonist AMN082.

  Neuropharmacology 20070101

• 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.

  Biotechnology progress 20060101

• Asymmetrical synthesis of L-homophenylalanine using engineered Escherichia coli aspartate aminotransferase.

  Biotechnology progress 20050101

• Enantioselective synthesis of (S)-2-amino-4-phenylbutanoic acid by the hydantoinase method.

  Chirality 20031001

• Asymmetric synthesis of L-homophenylalanine by equilibrium-shift using recombinant aromatic L-amino acid transaminase.

  Biotechnology and bioengineering 20030720

• Concise synthesis and enzymatic resolution of L-(+)-homophenylalanine hydrochloride.

  Enantiomer 20020101