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P3251

Sigma-Aldrich

Phe-Ala

≥98.0% (TLC)

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About This Item

Fórmula empírica (notación de Hill):
C12H16N2O3
Número de CAS:
3918-87-4
Peso molecular:
236.27
MDL number:
MFCD00037229
UNSPSC Code:
12352209
PubChem Substance ID:
24897876
NACRES:
NA.26

product name

Phe-Ala,

assay

≥98.0% (TLC)

form

powder

color

white

storage temp.

−20°C

SMILES string

C[C@H](NC(=O)[C@@H](N)Cc1ccccc1)C(O)=O

InChI

1S/C12H16N2O3/c1-8(12(16)17)14-11(15)10(13)7-9-5-3-2-4-6-9/h2-6,8,10H,7,13H2,1H3,(H,14,15)(H,16,17)/t8-,10-/m0/s1

InChI key

MIDZLCFIAINOQN-WPRPVWTQSA-N

Gene Information

human ... SLC15A1(6564)

Storage Class

11 - 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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F Döring et al.
Biochemical and biophysical research communications, 232(3), 656-662 (1997-03-27)
The methylotrophic yeast Pichia pastoris was used for heterologous expression of the rabbit intestinal peptide transporter PepT1 and its functional characterization. PepT1 mediates the electrogenic transmembrane transport of di- and tripeptides and peptido-mimetics such as beta-lactam antibiotics and ACE-inhibitors. Functional
Shu-Hui Chen et al.
Bioorganic & medicinal chemistry letters, 14(1), 245-250 (2003-12-20)
With the aim of reducing molecular weight and adjusting log D value of BACE inhibitors to more favorable range for BBB penetration and better bioavailability, we synthesized and evaluated several series of P3 cap modified BACE inhibitors obtained via replacement
C H Görbitz
Acta crystallographica. Section C, Crystal structure communications, 57(Pt 5), 575-576 (2001-05-16)
A new type of molecular arrangement for dipeptides is observed in the crystal structure of L-phenylalanyl-L-alanine dihydrate, C12H16N2O3-2H2O. Two L-Phe and two L-Ala side chains aggregate into large hydrophobic columns within a three-dimensional hydrogen-bond network.
I Knütter et al.
Biochemistry, 40(14), 4454-4458 (2001-04-04)
This study was initiated to develop inhibitors of the intestinal H(+)/peptide symporter. We provide evidence that the dipeptide derivative Lys[Z(NO(2))]-Pro is an effective competitive inhibitor of mammalian PEPT1 with an apparent binding affinity of 5-10 microM. Characterization of the interaction
Jaeseung Kim et al.
The Journal of organic chemistry, 70(15), 5781-5789 (2005-07-16)
Four stereoisomers of a Phe-Ala silanediol dipeptide mimic have been evaluated as inhibitors of angiotensin-converting enzyme (ACE) and compared to ketone-based inhibitors reported by Almquist et al. One stereogenic center of the isomers was derived from the individual enantiomers of
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