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About This Item
Empirical Formula (Hill Notation):
C9H12N2O
CAS Number:
Molecular Weight:
164.20
Beilstein/REAXYS Number:
6270941
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.26
Recommended Products
assay
≥98%
form
powder
color
white to off-white
mp
92.8 °C
application(s)
detection
SMILES string
N[C@@H](Cc1ccccc1)C(N)=O
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
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Biochem/physiol Actions
L-Phenylalaninamide is a chiral selector.
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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M Mizanur Rahman et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(4), 1312-1321 (2007-11-23)
The monomer N'-octadecyl-N(alpha)-(4-vinyl)-benzoyl-L-phenylalanineamide (4) based on L-phenylalanine has been simply but effectively synthesized, and its self-assembling properties have been investigated. FTIR and a variable-temperature (1)H NMR spectroscopic investigation demonstrated that the aggregation of compound 4 in various organic solvents is
J F Rehfeld
Clinical chemistry, 44(5), 991-1001 (1998-05-20)
Shortage of reliable plasma assays has hampered studies of cholecystokinin (CCK). The assay problems are low plasma concentrations, extensive molecular heterogeneity, and close homology of CCK to gastrin, which circulates in higher concentrations. To develop an accurate CCK RIA, antibodies
K Morihara
Biomedica biochimica acta, 50(10-11), S15-S18 (1991-01-01)
The semisynthesis of C-terminal peptides of gastrin, calcitonin gene-related peptides (rat and human), and cholecystokinin, or of human neuropeptide Y was achieved by introduction of Phe-NH2 or Tyr-NH2 at their carboxyl termini, respectively. Thermolysin or the related enzyme was used
Seon-Yeong Kwak et al.
Bioorganic & medicinal chemistry letters, 20(2), 738-741 (2009-12-08)
Kojic acid-phenylalanine amide (KA-F-NH(2)), which showed an excellent tyrosinase inhibitory activity, did not inhibit melanogenesis in melanocyte due to its low cell permeability. To enhance its cell permeability by increasing lipophilicity, we prepared metal coordination compounds of KA-F-NH(2) and characterized
Lenka Maletínská et al.
Peptides, 32(9), 1887-1892 (2011-08-30)
Prolactin-releasing peptide (PrRP)-induced secretion of prolactin is not currently considered a primary function of PrRP, but the development of late-onset obesity in both PrRP and PrRP receptor knock-out mice indicates the unique anorexigenic properties of PrRP. In our recent study
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