2922-41-0 | P-Amino-DL-phenylalanine

Packsize	Purity	Availability	Price	Discounted Price
1g	99%	in stock	$36.00	$25.00
5g	99%	in stock	$143.00	$100.00
25g	95%	in stock	$573.00	$402.00

Description

• Catalog Number: AB36878
• Chemical Name: P-Amino-DL-phenylalanine
• CAS Number: 2922-41-0
• Molecular Formula: C9H12N2O2
• Molecular Weight: 180.2038
• MDL Number: MFCD00007917
• SMILES: N[C@H](C(=O)O)Cc1ccc(cc1)N

Computed Properties

• Complexity: 177
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: -2.2

Literature

• Model-driven engineering of RNA devices to quantitatively program gene expression.

  Science (New York, N.Y.) 20111223

• 4-aminophenylalanine as a biocompatible nucleophilic catalyst for hydrazone ligations at low temperature and neutral pH.

  Bioconjugate chemistry 20111019

• catena-Poly[[aqua-bis-(N-benzyl-adenine-κN)copper(II)]-μ-benzene-1,4-dicarboxyl-ato-κO:O].

  Acta crystallographica. Section E, Structure reports online 20110901

• Position-specific incorporation of biotinylated non-natural amino acids into a protein in a cell-free translation system.

  Biochemical and biophysical research communications 20070928

• 4-aminophenylalanine and 4-aminocyclohexylalanine derivatives as potent, selective, and orally bioavailable inhibitors of dipeptidyl peptidase IV.

  Bioorganic & medicinal chemistry letters 20070515

• Further studies of tyrosine surrogates in opioid receptor peptide ligands.

  Bioorganic & medicinal chemistry letters 20070501

• Rational design of MOFs constructed from modified aromatic amino acids.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

• FRET analysis of protein conformational change through position-specific incorporation of fluorescent amino acids.

  Nature methods 20061101

• Development of a highly enantioselective capacitive immunosensor for the detection of alpha-amino acids.

  Analytical chemistry 20061101

• Synthesis and sequence optimization of GFP mutants containing aromatic non-natural amino acids at the Tyr66 position.

  Protein engineering, design & selection : PEDS 20050601

• Site-specific replacement of a conserved tyrosine in ribonucleotide reductase with an aniline amino acid: a mechanistic probe for a redox-active tyrosine.

  Journal of the American Chemical Society 20041229

• An expanding genetic code.

  Trends in genetics : TIG 20041201

• Effect of 3-5 monocyclizations of angiotensin II and 4-aminoPhe6-Ang II on AT2 receptor affinity.

  Bioorganic & medicinal chemistry 20030703

• Evolution of protein amino acids.

  Science (New York, N.Y.) 20030530

• Scientists expand the genetic code.

  Drug discovery today 20030315

• Metabolic engineering. Researchers create first autonomous synthetic life form.

  Science (New York, N.Y.) 20030131

• Generation of a bacterium with a 21 amino acid genetic code.

  Journal of the American Chemical Society 20030129

• Metabolites of a blocked chloramphenicol producer.

  Journal of natural products 20030101