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H-L-Phe-NH2

CAS No.:
5241-58-7
Catalog Number:
AG003CKU
Molecular Formula:
C9H12N2O
Molecular Weight:
164.2044
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$13
- +
5g
97%
In Stock USA
United States
$17
- +
25g
97%
In Stock USA
United States
$61
- +
100g
97%
In Stock USA
United States
$181
- +
500g
97%
In Stock USA
United States
$725
- +
Product Description
Catalog Number:
AG003CKU
Chemical Name:
H-L-Phe-NH2
CAS Number:
5241-58-7
Molecular Formula:
C9H12N2O
Molecular Weight:
164.2044
MDL Number:
MFCD00038146
IUPAC Name:
(2S)-2-amino-3-phenylpropanamide
InChI:
InChI=1S/C9H12N2O/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5,8H,6,10H2,(H2,11,12)/t8-/m0/s1
InChI Key:
OBSIQMZKFXFYLV-QMMMGPOBSA-N
SMILES:
N[C@H](C(=N)O)Cc1ccccc1
UNII:
PV9T9B2S11
Properties
Complexity:
153  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
164.095g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
164.208g/mol
Monoisotopic Mass:
164.095g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
69.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.1  
Literature
Title Journal
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
Properties