5241-58-7 | H-L-Phe-NH2

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$10.00	$7.00
10g	98%	in stock	$18.00	$13.00
25g	98%	in stock	$38.00	$27.00
100g	98%	in stock	$143.00	$101.00

Description

• Catalog Number: AB56070
• Chemical Name: H-L-Phe-NH2
• CAS Number: 5241-58-7
• Molecular Formula: C9H12N2O
• Molecular Weight: 164.2044
• MDL Number: MFCD00038146
• SMILES: N[C@H](C(=N)O)Cc1ccccc1

Computed Properties

• Complexity: 153
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: 0.1

Literature

• Antimicrobial chemical constituents from the endophytic fungus Phomopsis sp. from Notobasis syriaca.

  Natural product communications 20111201

• Biological properties of prolactin-releasing peptide analogs with a modified aromatic ring of a C-terminal phenylalanine amide.

  Peptides 20110901

• Discovery of dipeptides with high affinity to the specific binding site for substance P1-7.

  Journal of medicinal chemistry 20100325

• Biochemical properties and potential applications of a solvent-stable protease from the high-yield protease producer Pseudomonas aeruginosa PT121.

  Applied biochemistry and biotechnology 20100201

• Enhanced cell permeability of kojic acid-phenylalanine amide with metal complex.

  Bioorganic & medicinal chemistry letters 20100115

• Kojic acid-amino acid conjugates as tyrosinase inhibitors.

  Bioorganic & medicinal chemistry letters 20091001

• Enantioseparation of dansyl amino acids by ligand-exchange capillary electrophoresis with zinc(II)-L-phenylalaninamide complex.

  Journal of separation science 20090901

• Synthesis and assessment of molecular recognizability by RP-HPLC of an N-alkyl-beta-Ala-L: -Phe-derived organic phase with self-assembling ability.

  Analytical and bioanalytical chemistry 20081101

• A selective fluorescence reaction for peptides and chromatographic analysis.

  Peptides 20080301

• Structures of D-amino-acid amidase complexed with L-phenylalanine and with L-phenylalanine amide: insight into the D-stereospecificity of D-amino-acid amidase from Ochrobactrum anthropi SV3.

  Acta crystallographica. Section D, Biological crystallography 20080301

• Synthesis, self-assembling properties, and atom transfer radical polymerization of an alkylated L-phenylalanine-derived monomeric organogel from silica: a new approach to prepare packing materials for high-performance liquid chromatography.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20080101

• Comparative assessment of two indices of drug induced permeability changes in the perfused rat intestine.

  International journal of pharmaceutics 20060407

• L: -Stereoselective amino acid amidase with broad substrate specificity from Brevundimonas diminuta: characterization of a new member of the leucine aminopeptidase family.

  Applied microbiology and biotechnology 20060401

• Identification of specific calcitonin-like receptor residues important for calcitonin gene-related peptide high affinity binding.

  BMC pharmacology 20060101

• Application of Fourier transform infrared spectroscopy for monitoring hydrolysis and synthesis reactions catalyzed by a recombinant amidase.

  Analytical biochemistry 20051101

• Design of chiral monochloro-s-triazine reagents for the liquid chromatographic separation of amino acid enantiomers.

  Journal of chromatography. A 20030523

• Ni-to-Ni+ 3-ethylene-bridged partially modified retro-inverso tetrapeptide beta-turn mimetic: design, synthesis, and structural characterization.

  The Journal of organic chemistry 20020726

• Chemically modified chiral monolithic silica column prepared by a sol-gel process for enantiomeric separation by micro high-performance liquid chromatography.

  Journal of chromatography. A 20020104

• (R)-3-Amidinophenylalanine-derived inhibitors of factor Xa with a novel active-site binding mode.

  Biological chemistry 20020101

• In vitro selection of DNA aptamers that bind L-tyrosinamide.

  Bioorganic & medicinal chemistry 20011001

• Chemically L-phenylalaninamide-modified monolithic silica column prepared by a sol-gel process for enantioseparation of dansyl amino acids by ligand exchange-capillary electrochromatography.

  Analytical chemistry 20010715