2922-40-9 | D,L-p-Nitrophenylalanine

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$12.00	$9.00
10g	97%	in stock	$22.00	$16.00
25g	97%	in stock	$45.00	$32.00
100g	97%	in stock	$151.00	$106.00
500g	97%	in stock	$493.00	$345.00

Description

• Catalog Number: AB36879
• Chemical Name: D,L-p-Nitrophenylalanine
• CAS Number: 2922-40-9
• Molecular Formula: C9H10N2O4
• Molecular Weight: 210.1867
• MDL Number: MFCD00007384
• SMILES: OC(=O)[C@H](Cc1ccc(cc1)[N+](=O)[O-])N

Computed Properties

• Complexity: 243
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: -1.2

Literature

• Comparison of fluorescence reagents for simultaneous determination of hydroxylated phenylalanine and nitrated tyrosine by high-performance liquid chromatography with fluorescence detection.

  Biomedical chromatography : BMC 20120101

• Nitro-phenylalanine: a novel sensor for heat transfer in peptides.

  The journal of physical chemistry. A 20110324

• Probing local environments with the infrared probe: L-4-nitrophenylalanine.

  The journal of physical chemistry. B 20110317

• Genetic incorporation of unnatural amino acids into proteins in Mycobacterium tuberculosis.

  PloS one 20100101

• 1H NMR determination of beta-N-methylamino-L-alanine (L-BMAA) in environmental and biological samples.

  Toxicon : official journal of the International Society on Toxinology 20090401

• 2-Ammonio-3-(4-nitro-phen-yl)propanoate monohydrate.

  Acta crystallographica. Section E, Structure reports online 20080801

• (S)-2-Ammonio-3-(4-nitro-phen-yl)propanoate monohydrate.

  Acta crystallographica. Section E, Structure reports online 20080601

• Profiling of proteolytic enzymes in the gut of the tick Ixodes ricinus reveals an evolutionarily conserved network of aspartic and cysteine peptidases.

  Parasites & vectors 20080101

• The genetic incorporation of a distance probe into proteins in Escherichia coli.

  Journal of the American Chemical Society 20060412

• Efficient incorporation of a nonnatural amino acid into a protein in an insect cell-free translation system.

  Nucleic acids symposium series (2004) 20060101

• Neighbouring group processes in the deamination of protonated phenylalanine derivatives.

  Organic & biomolecular chemistry 20051021

• Synthesis of new bivalent peptides for applications in the Affinity Enhancement System.

  Bioconjugate chemistry 20050101

• A novel competitive ELISA for both free and protein-bound nitrotyrosine.

  Hybridoma and hybridomics 20031201

• Position-specific incorporation of a fluorophore-quencher pair into a single streptavidin through orthogonal four-base codon/anticodon pairs.

  Journal of the American Chemical Society 20021211

• Influence of a ring substituent on the tendency to form H(2)O adducts to Ag(+) complexes with phenylalanine analogues in an ion trap mass spectrometer.

  Journal of mass spectrometry : JMS 20020401

• 6-hydroxydopamine increases the hydroxylation and nitration of phenylalanine in vivo: implication of peroxynitrite formation.

  Journal of neurochemistry 20010801

• Increase in fluorescence upon the hydrolysis of tyrosine peptides: application to proteinase assays.

  Analytical biochemistry 19950501

• Sensitive, soluble chromogenic substrates for HIV-1 proteinase.

  The Journal of biological chemistry 19900515

• Comparison of mu-, delta- and kappa-receptor binding sites through pharmacologic evaluation of p-nitrophenylalanine analogs of opioid peptides.

  Life sciences 19830101